Name

BMIQ6 Gene

body mass index QTL 6

BMIQ5 Gene

body mass index QTL 5

BMIQ2 Gene

body mass index QTL 2

BMIQ3 Gene

body mass index QTL 3

BMIQ1 Gene

body mass index QTL 1

BMIQ15 Gene

Body mass index QTL 15

BMIQ8 Gene

body mass index quantitative trait locus 8

BMIQ14 Gene

Body mass index QTL14

BMIQ13 Gene

Body mass index QTL13

LBMQTL1 Gene

Lean body mass QTL 1

BDLN1 Gene

body length, human homolog of mouse body length 1

FTO Gene

fat mass and obesity associated

This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011]

FTOP1 Gene

fat mass and obesity associated pseudogene 1

BW1 Gene

Body weight QTL 1

BW2 Gene

Body weight QTL 2

BW3 Gene

Body weight QTL 3

BW4 Gene

Body weight QTL 4

BW6 Gene

Body weight QTL 6

BW7 Gene

Body weight QTL 7

BW8 Gene

Body weight QTL 8

BW9 Gene

Body weight QTL 9

BW27 Gene

Body weight QTL 27

BW26 Gene

Body weight QTL 26

BW24 Gene

Body weight QTL 24

BW23 Gene

Body weight QTL 23

BW22 Gene

Body weight QTL 22

BW20 Gene

Body weight QTL 20

BW29 Gene

Body weight QTL 29

BW28 Gene

Body weight QTL 28

BFD1 Gene

Body fluid distribution QTL 1

BFD3 Gene

Body fluid distribution QTL 3

BFD4 Gene

Body fluid distribution QTL 4

BFD5 Gene

Body fluid distribution QTL 5

BW56 Gene

Body weight QTL 56

BW57 Gene

Body weight QTL 57

BW54 Gene

Body weight QTL 54

BW55 Gene

Body weight QTL 55

BW52 Gene

Body weight QTL 52

BW53 Gene

Body weight QTL 53

BW58 Gene

Body weight QTL 58

BW59 Gene

Body weight QTL 59

BW15 Gene

Body weight QTL 15

BW36 Gene

Body weight QTL 36

BW37 Gene

Body weight QTL 37

BW88 Gene

Body weight QTL 88

BW35 Gene

Body weight QTL 35

BW30 Gene

Body weight QTL 30

BW33 Gene

Body weight QTL 33

BW5 Gene

Body weight QTL 5

BW25 Gene

Body weight QTL 25

BW69 Gene

Body weight QTL 69

BW68 Gene

Body weight QTL 68

BW63 Gene

Body weight QTL 63

BW62 Gene

Body weight QTL 62

BW61 Gene

Body weight QTL 61

BW60 Gene

Body weight QTL 60

BW67 Gene

Body weight QTL 67

BW66 Gene

Body weight QTL 66

BW65 Gene

Body weight QTL 65

BW64 Gene

Body weight QTL 64

BW11 Gene

Body weight QTL 11

BFD2 Gene

Body fluid distribution QTL 2

BW12 Gene

Body weight QTL 12

BW13 Gene

Body weight QTL 13

BW10 Gene

Body weight QTL 10

BW16 Gene

Body weight QTL 16

BW17 Gene

Body weight QTL 17

BW14 Gene

Body weight QTL 14

BW18 Gene

Body weight QTL 18

BW19 Gene

Body weight QTL 19

BW34 Gene

Body weight QTL 34

BW31 Gene

Body weight QTL 31

BW32 Gene

Body weight QTL 32

BW70 Gene

Body weight QTL 70

BW71 Gene

Body weight QTL 71

BW72 Gene

Body weight QTL 72

CHMP1B Gene

charged multivesicular body protein 1B

CHMP1B belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]

CHMP3 Gene

charged multivesicular body protein 3

This gene encodes a protein that sorts transmembrane proteins into lysosomes/vacuoles via the multivesicular body (MVB) pathway. This protein, along with other soluble coiled-coil containing proteins, forms part of the ESCRT-III protein complex that binds to the endosomal membrane and recruits additional cofactors for protein sorting into the MVB. This protein may also co-immunoprecipitate with a member of the IFG-binding protein superfamily. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ring finger protein 103 (RNF103) gene. [provided by RefSeq, Nov 2010]

CHMP7 Gene

charged multivesicular body protein 7

Involved in several processes, including midbody abscission; mitotic nuclear division; and vacuolar transport. Located in chromatin; cytosol; and nucleus. Part of several cellular components, including bounding membrane of organelle; kinetochore microtubule; and midbody. [provided by Alliance of Genome Resources, Mar 2025]

CHMP5 Gene

charged multivesicular body protein 5

CHMP5 belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]

CHMP4A Gene

charged multivesicular body protein 4A

CHMP4A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]

CHMP4B Gene

charged multivesicular body protein 4B

This gene encodes a member of the chromatin-modifying protein/charged multivesicular body protein (CHMP) protein family. The protein is part of the endosomal sorting complex required for transport (ESCRT) complex III (ESCRT-III), which functions in the sorting of endocytosed cell-surface receptors into multivesicular endosomes. The ESCRT machinery also functions in the final abscisson stage of cytokinesis and in the budding of enveloped viruses such as HIV-1. The three proteins of the CHMP4 subfamily interact with programmed cell death 6 interacting protein (PDCD6IP, also known as ALIX), which also functions in the ESCRT pathway. The CHMP4 proteins assemble into membrane-attached 5-nm filaments that form circular scaffolds and promote or stabilize outward budding. These polymers are proposed to help generate the luminal vesicles of multivesicular bodies. Mutations in this gene result in autosomal dominant posterior polar cataracts.[provided by RefSeq, Oct 2009]

CHMP4C Gene

charged multivesicular body protein 4C

CHMP4C belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]

LOC100130209 Gene

charged multivesicular body protein 4A pseudogene

SP140L Gene

SP140 nuclear body protein-like

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

CHMP6 Gene

charged multivesicular body protein 6

This gene encodes a member of the chromatin-modifying protein/charged multivesicular body protein family. Proteins in this family are part of the ESCRT-III (endosomal sorting complex required for transport III) which degrades surface receptors, and in biosynthesis of endosomes. [provided by RefSeq, Mar 2012]

CHMP1A Gene

charged multivesicular body protein 1A

This gene encodes a member of the CHMP/Chmp family of proteins which are involved in multivesicular body sorting of proteins to the interiors of lysosomes. The initial prediction of the protein sequence encoded by this gene suggested that the encoded protein was a metallopeptidase. The nomenclature has been updated recently to reflect the correct biological function of this encoded protein. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

CHMP2B Gene

charged multivesicular body protein 2B

This gene encodes a component of the heteromeric ESCRT-III complex (Endosomal Sorting Complex Required for Transport III) that functions in the recycling or degradation of cell surface receptors. ESCRT-III functions in the concentration and invagination of ubiquitinated endosomal cargos into intralumenal vesicles. The protein encoded by this gene is found as a monomer in the cytosol or as an oligomer in ESCRT-III complexes on endosomal membranes. It is expressed in neurons of all major regions of the brain. Mutations in this gene result in one form of familial frontotemporal lobar degeneration. [provided by RefSeq, Jul 2008]

CHMP2A Gene

charged multivesicular body protein 2A

CHMP2A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008]

LOC100420338 Gene

charged multivesicular body protein 5 pseudogene

SCARNA27 Gene

small Cajal body-specific RNA 27

SCARNA22 Gene

small Cajal body-specific RNA 22

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA23 Gene

small Cajal body-specific RNA 23

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA20 Gene

small Cajal body-specific RNA 20

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA21 Gene

small Cajal body-specific RNA 21

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

CHMP4BP1 Gene

charged multivesicular body protein 4B pseudogene 1

Predicted to be involved in late endosome to vacuole transport via multivesicular body sorting pathway and vesicle budding from membrane. Predicted to be located in several cellular components, including bounding membrane of organelle; kinetochore microtubule; and midbody. Predicted to be part of ESCRT III complex. Predicted to be active in cytoplasmic side of plasma membrane and multivesicular body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA5 Gene

small Cajal body-specific RNA 5

Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA4 Gene

small Cajal body-specific RNA 4

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA2 Gene

small Cajal body-specific RNA 2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

VTA1P2 Gene

vesicle (multivesicular body) trafficking 1 pseudogene 2

NOLC1 Gene

nucleolar and coiled-body phosphoprotein 1

Enables molecular function inhibitor activity; protein heterodimerization activity; and protein-macromolecule adaptor activity. Involved in neural crest cell development; neural crest formation; and regulation of translation. Acts upstream of or within axonogenesis and regulation of synaptic plasticity. Located in fibrillar center. [provided by Alliance of Genome Resources, Mar 2025]

MHB Gene

myopathy, hyaline body, autosomal recessive

LOC100420317 Gene

charged multivesicular body protein 5 pseudogene

LOC392426 Gene

nucleolar and coiled-body phosphoprotein 1 pseudogene

SCARNA9L Gene

small Cajal body-specific RNA 9-like

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA13 Gene

small Cajal body-specific RNA 13

Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA12 Gene

small Cajal body-specific RNA 12

This gene produces a small nuclear RNA that localizes specifically to Cajal bodies, which are conserved subnuclear organelles that are present in the nucleoplasm. This RNA is processed from an intron of the prohibitin 2 host gene. It includes both an H/ACA box and a C/D box, and is thought to guide the pseudouridylation of residue U46 in the U5 small nuclear RNA. [provided by RefSeq, Jun 2010]

SCARNA11 Gene

small Cajal body-specific RNA 11

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA10 Gene

small Cajal body-specific RNA 10

Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA17 Gene

small Cajal body-specific RNA 17

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA16 Gene

small Cajal body-specific RNA 16

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA15 Gene

small Cajal body-specific RNA 15

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA14 Gene

small Cajal body-specific RNA 14

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA18 Gene

small Cajal body-specific RNA 18

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

VTA1 Gene

vesicle (multivesicular body) trafficking 1

C6ORF55 encodes a protein involved in trafficking of the multivesicular body, an endosomal compartment involved in sorting membrane proteins for degradation in lysosomes (Ward et al., 2005 [PubMed 15644320]).[supplied by OMIM, Mar 2008]

SCARNA9 Gene

small Cajal body-specific RNA 9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA8 Gene

small Cajal body-specific RNA 8

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA7 Gene

small Cajal body-specific RNA 7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA3 Gene

small Cajal body-specific RNA 3

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA1 Gene

small Cajal body-specific RNA 1

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

CHMP1AP1 Gene

charged multivesicular body protein 1A pseudogene 1

LOC100129367 Gene

nucleolar and coiled-body phosphoprotein 1 pseudogene

CHMP1B2P Gene

charged multivesicular body protein 1B2, pseudogene

PARK3 Gene

Parkinson disease 3 (autosomal dominant, Lewy body)

SP140 Gene

SP140 nuclear body protein

This gene encodes a member of the SP100 family of proteins, which are share common domains including an N-terminal homogeneously staining region domain followed by a SP100/autoimmune regulator/NucP41/P75/deformed epidermal autoregulatory factor domain, a plant homeobox zinc finger, and a bromodomain. The encoded protein is interferon-inducible and is expressed at high levels in the nuclei of leukocytes. Variants of this gene have been associated with multiple sclerosis, Crohn's disease, and chronic lymphocytic leukemia. Alternative splicing results in multiple variants. [provided by RefSeq, Aug 2016]

SCARNA6 Gene

small Cajal body-specific RNA 6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

MVB12B Gene

multivesicular body subunit 12B

The protein encoded by this gene is a component of the ESCRT-I complex, a heterotetramer, which mediates the sorting of ubiquitinated cargo protein from the plasma membrane to the endosomal vesicle. ESCRT-I complex plays an essential role in HIV budding and endosomal protein sorting. Depletion and overexpression of this and related protein (MVB12A) inhibit HIV-1 infectivity and induce unusual viral assembly defects, indicating a role for MVB12 subunits in regulating ESCRT-mediated virus budding. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]

MVB12A Gene

multivesicular body subunit 12A

Enables lipid binding activity and ubiquitin binding activity. Involved in regulation of epidermal growth factor receptor signaling pathway. Located in several cellular components, including centrosome; cytosol; and vesicle. Part of ESCRT I complex. [provided by Alliance of Genome Resources, Mar 2025]

SP110 Gene

SP110 nuclear body protein

The nuclear body is a multiprotein complex that may have a role in the regulation of gene transcription. This gene is a member of the SP100/SP140 family of nuclear body proteins and encodes a leukocyte-specific nuclear body component. The protein can function as an activator of gene transcription and may serve as a nuclear hormone receptor coactivator. In addition, it has been suggested that the protein may play a role in ribosome biogenesis and in the induction of myeloid cell differentiation. Alternative splicing has been observed for this gene and three transcript variants, encoding distinct isoforms, have been identified. [provided by RefSeq, Jul 2008]

NBDY Gene

negative regulator of P-body association

Involved in negative regulation of cytoplasmic mRNA processing body assembly and nuclear-transcribed mRNA catabolic process. Located in P-body. [provided by Alliance of Genome Resources, Mar 2025]

BBOF1 Gene

basal body orientation factor 1

Predicted to be involved in sperm axoneme assembly. Predicted to act upstream of or within several processes, including cilium movement involved in cell motility; negative regulation of microtubule depolymerization; and protein stabilization. Predicted to be located in axoneme; ciliary basal body; and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025]

AASTH40 Gene

Allergic/atopic asthma related QTL 40

AASTH45 Gene

Allergic/atopic asthma related QTL 45

BP49 Gene

Blood pressure QTL 49

HRTRT1 Gene

Heart rate QTL 1

CRCL Gene

Creatinine clearance QTL

BP24 Gene

Blood pressure QTL 24

BP25 Gene

Blood pressure QTL 25

BP26 Gene

Blood pressure QTL 26

BP27 Gene

Blood pressure QTL 27

BP20 Gene

Blood pressure QTL 20

BP21 Gene

Blood pressure QTL 21

BP22 Gene

Blood pressure QTL 22

BP23 Gene

Blood pressure QTL 23

BP28 Gene

Blood pressure QTL 28

BP29 Gene

Blood pressure QTL 29

COHEN1 Gene

Cohen syndrome QTL 1

FGQTL4 Gene

Fasting plasma glucose level QTL 4

FGQTL6 Gene

Fasting plasma glucose level QTL 6

FGQTL1 Gene

Fasting plasma glucose level QTL 1

RA26 Gene

Rheumatoid arthritis QTL 26

COPD14 Gene

Chronic obstructive pulmonary disease QTL 14

ADIPQTL2 Gene

Circulating adiponectin QTL on chromosome 5

BMND9 Gene

Bone mineral density QTL 9

BMND6 Gene

Bone mineral density QTL 6

BMND5 Gene

Bone mineral density variation QTL 5

RA6 Gene

Rheumatoid arthritis QTL 06

RA7 Gene

Rheumatoid arthritis QTL 07

RA4 Gene

Rheumatoid arthritis QTL 04

RA5 Gene

Rheumatoid arthritis QTL 01

RA2 Gene

Rheumatoid arthritis QTL 01

RA3 Gene

Rheumatoid arthritis QTL 02

RA1 Gene

Rheumatoid arthritis QTL 01

RA8 Gene

Rheumatoid arthritis QTL 08

AASTH18 Gene

Allergic/atopic asthma related QTL 18

AASTH13 Gene

Allergic/atopic asthma related QTL 13

AASTH15 Gene

Allergic/atopic asthma related QTL 15

AASTH14 Gene

Allergic/atopic asthma related QTL 14

AASTH16 Gene

Allergic/atopic asthma related QTL 16

SLEP3 Gene

Serum leptin concentration QTL 3

SLEP2 Gene

Serum leptin concentration QTL 2

SLEP1 Gene

Serum leptin concentration QTL 1

HDLCQ6 Gene

High density lipoprotein cholesterol level QTL 6

HDLCQ1 Gene

high density lipoprotein cholesterol level QTL 1

AASTH38 Gene

Allergic/atopic asthma related QTL 38

AASTH37 Gene

Allergic/atopic asthma related QTL 37

COPD3 Gene

Chronic obstructive pulmonary disease QTL 3

COPD2 Gene

Chronic obstructive pulmonary disease QTL 2

COPD1 Gene

Chronic obstructive pulmonary disease QTL 1

COPD6 Gene

Chronic obstructive pulmonary disease QTL 6

COPD5 Gene

Chronic obstructive pulmonary disease QTL 5

COPD4 Gene

Chronic obstructive pulmonary disease QTL 4

COPD8 Gene

Chronic obstructive pulmonary disease QTL 8

OA10 Gene

Osteoarthritis QTL 10

BSZQTL Gene

Bone size QTL

CPROTQ Gene

C-reactive protein QTL

BP1 Gene

Blood pressure QTL 1

BP3 Gene

Blood pressure QTL 3

BP2 Gene

Blood pressure QTL 2

BP5 Gene

Blood pressure QTL 5

BP4 Gene

Blood pressure QTL 4

BP7 Gene

Blood pressure QTL 7

BP6 Gene

Blood pressure QTL 6

BP9 Gene

Blood pressure QTL 9

BP8 Gene

Blood pressure QTL 8

OA30 Gene

Osteoarthritis QTL 29

SLI2 Gene

Specific language impairment QTL, 2

SLI3 Gene

Specific language impairment QTL, 3

SLI1 Gene

Specific language impairment QTL, 1

ALPQTL2 Gene

Alkaline phosphatase, plasma level of, QTL 2

AASTH48 Gene

Allergic/atopic asthma related QTL 48

AASTH49 Gene

Allergic/atopic asthma related QTL 49

RA24 Gene

Rheumatoid arthritis QTL 24

MENOQ1 Gene

menopause, natural, age at, QTL

CLQTL2 Gene

Cholesterol level QTL 2

TST2 Gene

Tuberculin skin test reactivity QTL

RA21 Gene

Rheumatoid arthritis QTL 21

RA20 Gene

Rheumatoid arthritis QTL 20

RA23 Gene

Rheumatoid arthritis QTL 23

RA22 Gene

Rheumatoid arthritis QTL 22

RA25 Gene

Rheumatoid arthritis QTL 25

RA27 Gene

Rheumatoid arthritis QTL 27

RA29 Gene

Rheumatoid arthritis QTL 29

RA28 Gene

Rheumatoid arthritis QTL 28

AASTH42 Gene

Allergic/atopic asthma related QTL 42

AASTH43 Gene

Allergic/atopic asthma related QTL 43

AASTH47 Gene

Allergic/atopic asthma related QTL 47

AASTH44 Gene

Allergic/atopic asthma related QTL 44

TSHQTL1 Gene

Thyroid-stimulating hormone level QTL 1

COHEN2 Gene

Cohen syndrome QTL 2

OSTEAR3_H Gene

Osteoarthritis QTL 3

COPD17 Gene

Chronic obstructive pulmonary disease QTL 17

AASTH9 Gene

Allergic/atopic asthma related QTL 9

AASTH8 Gene

Allergic/atopic asthma related QTL 8

AASTH7 Gene

Allergic/atopic asthma related QTL 7

AASTH6 Gene

Allergic/atopic asthma related QTL 6

AASTH1 Gene

Allergic/atopic asthma related QTL 1

AASTH3 Gene

Allergic/atopic asthma related QTL 3

AASTH2 Gene

Allergic/atopic asthma related QTL 2

RA18 Gene

Rheumatoid arthritis QTL 18

RA19 Gene

Rheumatoid arthritis QTL 19

RA10 Gene

Rheumatoid arthritis QTL 10

RA11 Gene

Rheumatoid arthritis QTL 11

RA12 Gene

Rheumatoid arthritis QTL 12

RA13 Gene

Rheumatoid arthritis QTL 13

RA14 Gene

Rheumatoid arthritis QTL 14

RA15 Gene

Rheumatoid arthritis QTL 15

RA16 Gene

Rheumatoid arthritis QTL 16

RA17 Gene

Rheumatoid arthritis QTL 17

BP51 Gene

Blood pressure QTL 51

BP50 Gene

Blood pressure QTL 50

BP53 Gene

Blood pressure QTL 53

BP52 Gene

Blood pressure QTL 52

BP55 Gene

Blood pressure QTL 55

BP54 Gene

Blood pressure QTL 54

STQTL23 Gene

Stature QTL 23

STQTL20 Gene

Stature QTL 20

COPD7 Gene

Chronic obstructive pulmonary disease QTL 7

COPD9 Gene

Chronic obstructive pulmonary disease QTL 9

AASTH29 Gene

Allergic/Atopic asthma related QTL 29

AASTH24 Gene

Allergic/atopic asthma related QTL 24

AASTH26 Gene

Allergic/atopic asthma related QTL 25

AASTH27 Gene

Allergic/atopic asthma related QTL 27

AASTH20 Gene

Allergic/atopic asthma related QTL 20

AASTH21 Gene

Allergic/atopic asthma related QTL 21

AASTH22 Gene

Allergic/atopic asthma related QTL 22

OA26 Gene

Osteoarthritis QTL 26

OA25 Gene

Osteoarthritis QTL 25

OA27 Gene

Osteoarthritis QTL 27

OA24 Gene

Osteoarthritis QTL 24

OA22 Gene

Osteoarthritis QTL 22

OA23 Gene

Osteoarthritis QTL 23

OA20 Gene

Osteoarthritis QTL 20

OA21 Gene

Osteoarthritis QTL 21

OA28 Gene

Osteoarthritis QTL 28

OA29 Gene

Osteoarthritis QTL 29

AASTH41 Gene

Allergic/Atopic asthma related QTL 41

AASTH46 Gene

Allergic/atopic asthma related QTL 46

STQTL17 Gene

Stature QTL 17

UAE1 Gene

Urinary albumin excretion QTL 1

UAE2 Gene

Urinary albumin excretion QTL 2

STQTL15 Gene

Stature QTL 15

STQTL13 Gene

Stature QTL 13

BMND10 Gene

Bone mineral density QTL 10

BMND11 Gene

Bone mineral density QTL 11

BMND13 Gene

Bone mineral density QTL 13

BMND14 Gene

Bone mineral density QTL 14

AASTH25 Gene

Allergic/atopic asthma related QTL 25

BSZQTL2 Gene

Bone size QTL

ADIPQTL3 Gene

Circulating adiponectin QTL on chromosome 14

AASTH55 Gene

Allergic/atopic asthma related QTL 5

AASTH54 Gene

Allergic/atopic asthma related QTL 54

AASTH56 Gene

Allergic/Atopic asthma related QTL 56

AASTH51 Gene

Allergic/atopic asthma related QTL 51

AASTH53 Gene

Allergic/atopic asthma related QTL 53

AASTH52 Gene

Allergic/atopic asthma related QTL 52

BMND4 Gene

Bone mineral density variation QTL 4

AASTH4 Gene

Allergic/atopic asthma related QTL 4

RA9 Gene

Rheumatoid arthritis QTL 09

BP37 Gene

Blood pressure QTL 37

BP36 Gene

Blood pressure QTL 36

BP35 Gene

Blood pressure QTL 35

BP34 Gene

Blood pressure QTL 34

BP33 Gene

Blood pressure QTL 33

BP32 Gene

Blood pressure QTL 32

BP31 Gene

Blood pressure QTL 31

BP30 Gene

Blood pressure QTL 30

BP39 Gene

Blood pressure QTL 39

BP38 Gene

Blood pressure QTL 38

BP18 Gene

Blood pressure QTL 18

BP14 Gene

Blood pressure QTL 14

AASTH11 Gene

Allergic/atopic asthma related QTL 11

AASTH12 Gene

Allergic/atopic asthma related QTL 12

AASTH17 Gene

Allergic/atopic asthma related QTL 17

RA30 Gene

Rheumatoid arthritis QTL 30

RA31 Gene

Rheumatoid arthritis QTL 31

HBFQTL4 Gene

Fetal hemoglobin QTL on chromosome 8

AASTH19 Gene

Allergic/atopic asthma related QTL 19

AASTH10 Gene

Allergic/atopic asthma related QTL 10

STQTL16 Gene

Stature QTL 16

STQTL14 Gene

Stature QTL 14

STQTL12 Gene

Stature QTL 12

STQTL10 Gene

Stature QTL 10

MUSQTL1 Gene

Musical aptitude QTL 1

STQTL11 Gene

Stature QTL 11

STQTL18 Gene

Stature QTL 18

STQTL19 Gene

Stature QTL 19

AASTH50 Gene

Allergic/atopic asthma related QTL 50

BP46 Gene

Blood pressure QTL 46

BP47 Gene

Blood pressure QTL 47

BP45 Gene

Blood pressure QTL 45

BP48 Gene

Blood pressure QTL 48

BWQTL2 Gene

Birth weight QTL 2

COPD13 Gene

Chronic obstructive pulmonary disease QTL 13

COPD12 Gene

Chronic obstructive pulmonary disease QTL 12

COPD11 Gene

Chronic obstructive pulmonary disease QTL 11

COPD10 Gene

Chronic obstructive pulmonary disease QTL 10

COPD16 Gene

Chronic obstructive pulmonary disease QTL 16

COPD15 Gene

Chronic obstructive pulmonary disease QTL 15

COPD19 Gene

Chronic obstructive pulmonary disease QTL 19

COPD18 Gene

Chronic obstructive pulmonary disease QTL 18

OA7 Gene

Osteoarthritis QTL 7

OA6 Gene

Osteoarthritis QTL 6

OA5 Gene

Osteoarthritis QTL 5

OA4 Gene

Osteoarthritis QTL 4

OA2 Gene

Osteoarthritis QTL 2

OA1 Gene

Osteoarthritis QTL 1

OA9 Gene

Osteoarthritis QTL 9

OA8 Gene

Osteoarthritis QTL 8

AASTH39 Gene

Allergic/atopic asthma related QTL 39

AASTH36 Gene

Allergic/atopic asthma related QTL 36

AASTH35 Gene

Allergic/atopic asthma related QTL 35

AASTH34 Gene

Allergic/atopic asthma related QTL 34

AASTH33 Gene

Allergic/atopic asthma related QTL 33

AASTH32 Gene

Allergic/Atopic asthma related QTL 32

AASTH31 Gene

Allergic/atopic asthma related QTL 31

AASTH30 Gene

Allergic/atopic asthma related QTL 30

AASTH5 Gene

Allergic/atopic asthma related QTL 5

B6QTL1 Gene

Vitamin B6 plasma level QTL 1

STQTL24 Gene

Stature QTL 24

STQTL21 Gene

Stature QTL 21

MENAQ1 Gene

Menarche, age at, QTL

HDLCQ4 Gene

High density lipoprotein cholesterol level QTL 4

HDLCQ5 Gene

High density lipoprotein cholesterol level QTL 5

HDLCQ2 Gene

High density lipoprotein cholesterol level QTL on chromosome 8

AASTH28 Gene

Allergic/Atopic asthma related QTL 28

AASTH23 Gene

Allergic/atopic asthma related QTL 23

STQTL22 Gene

Stature QTL 22

BP19 Gene

Blood pressure QTL 19

BP15 Gene

Blood pressure QTL 15

BP17 Gene

Blood pressure QTL 17

BP16 Gene

Blood pressure QTL 16

BP11 Gene

Blood pressure QTL 11

BP10 Gene

Blood pressure QTL 10

BP13 Gene

Blood pressure QTL 13

BP12 Gene

Blood pressure QTL 12

OA19 Gene

Osteoarthritis QTL 19

OA18 Gene

Osteoarthritis QTL 18

OA13 Gene

Osteoarthritis QTL 13

OA12 Gene

Osteoarthritis QTL 12

OA11 Gene

Osteoarthritis QTL 11

OA17 Gene

Osteoarthritis QTL 17

OA16 Gene

Osteoarthritis QTL 16

OA15 Gene

Osteoarthritis QTL 15

OA14 Gene

Osteoarthritis QTL 14

COPD28 Gene

Chronic obstructive pulmonary disease QTL 28

COPD29 Gene

Chronic obstructive pulmonary disease QTL 29

COPD22 Gene

Chronic obstructive pulmonary disease QTL 22

COPD23 Gene

Chronic obstructive pulmonary disease QTL 23

COPD20 Gene

Chronic obstructive pulmonary disease QTL 20

COPD21 Gene

Chronic obstructive pulmonary disease QTL 21

COPD26 Gene

Chronic obstructive pulmonary disease QTL 26

COPD27 Gene

Chronic obstructive pulmonary disease QTL 27

COPD24 Gene

Chronic obstructive pulmonary disease QTL 24

COPD25 Gene

Chronic obstructive pulmonary disease QTL 25

SXGQTL1 Gene

Sex hormone-binding blobulin circulating level QTL 1