| Name |
|---|
BMIQ6 Genebody mass index QTL 6 |
BMIQ5 Genebody mass index QTL 5 |
BMIQ2 Genebody mass index QTL 2 |
BMIQ3 Genebody mass index QTL 3 |
BMIQ1 Genebody mass index QTL 1 |
BMIQ15 GeneBody mass index QTL 15 |
BMIQ8 Genebody mass index quantitative trait locus 8 |
BMIQ14 GeneBody mass index QTL14 |
BMIQ13 GeneBody mass index QTL13 |
LBMQTL1 GeneLean body mass QTL 1 |
BDLN1 Genebody length, human homolog of mouse body length 1 |
FTO Genefat 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 Genefat mass and obesity associated pseudogene 1 |
BW1 GeneBody weight QTL 1 |
BW2 GeneBody weight QTL 2 |
BW3 GeneBody weight QTL 3 |
BW4 GeneBody weight QTL 4 |
BW6 GeneBody weight QTL 6 |
BW7 GeneBody weight QTL 7 |
BW8 GeneBody weight QTL 8 |
BW9 GeneBody weight QTL 9 |
BW27 GeneBody weight QTL 27 |
BW26 GeneBody weight QTL 26 |
BW24 GeneBody weight QTL 24 |
BW23 GeneBody weight QTL 23 |
BW22 GeneBody weight QTL 22 |
BW20 GeneBody weight QTL 20 |
BW29 GeneBody weight QTL 29 |
BW28 GeneBody weight QTL 28 |
BFD1 GeneBody fluid distribution QTL 1 |
BFD3 GeneBody fluid distribution QTL 3 |
BFD4 GeneBody fluid distribution QTL 4 |
BFD5 GeneBody fluid distribution QTL 5 |
BW56 GeneBody weight QTL 56 |
BW57 GeneBody weight QTL 57 |
BW54 GeneBody weight QTL 54 |
BW55 GeneBody weight QTL 55 |
BW52 GeneBody weight QTL 52 |
BW53 GeneBody weight QTL 53 |
BW58 GeneBody weight QTL 58 |
BW59 GeneBody weight QTL 59 |
BW15 GeneBody weight QTL 15 |
BW36 GeneBody weight QTL 36 |
BW37 GeneBody weight QTL 37 |
BW88 GeneBody weight QTL 88 |
BW35 GeneBody weight QTL 35 |
BW30 GeneBody weight QTL 30 |
BW33 GeneBody weight QTL 33 |
BW5 GeneBody weight QTL 5 |
BW25 GeneBody weight QTL 25 |
BW69 GeneBody weight QTL 69 |
BW68 GeneBody weight QTL 68 |
BW63 GeneBody weight QTL 63 |
BW62 GeneBody weight QTL 62 |
BW61 GeneBody weight QTL 61 |
BW60 GeneBody weight QTL 60 |
BW67 GeneBody weight QTL 67 |
BW66 GeneBody weight QTL 66 |
BW65 GeneBody weight QTL 65 |
BW64 GeneBody weight QTL 64 |
BW11 GeneBody weight QTL 11 |
BFD2 GeneBody fluid distribution QTL 2 |
BW12 GeneBody weight QTL 12 |
BW13 GeneBody weight QTL 13 |
BW10 GeneBody weight QTL 10 |
BW16 GeneBody weight QTL 16 |
BW17 GeneBody weight QTL 17 |
BW14 GeneBody weight QTL 14 |
BW18 GeneBody weight QTL 18 |
BW19 GeneBody weight QTL 19 |
BW34 GeneBody weight QTL 34 |
BW31 GeneBody weight QTL 31 |
BW32 GeneBody weight QTL 32 |
BW70 GeneBody weight QTL 70 |
BW71 GeneBody weight QTL 71 |
BW72 GeneBody weight QTL 72 |
CHMP1B Genecharged 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 Genecharged 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 Genecharged 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 Genecharged 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 Genecharged 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 Genecharged 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 Genecharged 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 Genecharged multivesicular body protein 4A pseudogene |
SP140L GeneSP140 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 Genecharged 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 Genecharged 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 Genecharged 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 Genecharged 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 Genecharged multivesicular body protein 5 pseudogene |
SCARNA27 Genesmall Cajal body-specific RNA 27 |
SCARNA22 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genecharged 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 Genesmall 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 Genesmall 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 Genesmall 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 Genevesicle (multivesicular body) trafficking 1 pseudogene 2 |
NOLC1 Genenucleolar 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 Genemyopathy, hyaline body, autosomal recessive |
LOC100420317 Genecharged multivesicular body protein 5 pseudogene |
LOC392426 Genenucleolar and coiled-body phosphoprotein 1 pseudogene |
SCARNA9L Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genevesicle (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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genecharged multivesicular body protein 1A pseudogene 1 |
LOC100129367 Genenucleolar and coiled-body phosphoprotein 1 pseudogene |
CHMP1B2P Genecharged multivesicular body protein 1B2, pseudogene |
PARK3 GeneParkinson disease 3 (autosomal dominant, Lewy body) |
SP140 GeneSP140 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 Genesmall 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 Genemultivesicular 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 Genemultivesicular 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 GeneSP110 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 Genenegative 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 Genebasal 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 GeneAllergic/atopic asthma related QTL 40 |
AASTH45 GeneAllergic/atopic asthma related QTL 45 |
BP49 GeneBlood pressure QTL 49 |
HRTRT1 GeneHeart rate QTL 1 |
CRCL GeneCreatinine clearance QTL |
BP24 GeneBlood pressure QTL 24 |
BP25 GeneBlood pressure QTL 25 |
BP26 GeneBlood pressure QTL 26 |
BP27 GeneBlood pressure QTL 27 |
BP20 GeneBlood pressure QTL 20 |
BP21 GeneBlood pressure QTL 21 |
BP22 GeneBlood pressure QTL 22 |
BP23 GeneBlood pressure QTL 23 |
BP28 GeneBlood pressure QTL 28 |
BP29 GeneBlood pressure QTL 29 |
COHEN1 GeneCohen syndrome QTL 1 |
FGQTL4 GeneFasting plasma glucose level QTL 4 |
FGQTL6 GeneFasting plasma glucose level QTL 6 |
FGQTL1 GeneFasting plasma glucose level QTL 1 |
RA26 GeneRheumatoid arthritis QTL 26 |
COPD14 GeneChronic obstructive pulmonary disease QTL 14 |
ADIPQTL2 GeneCirculating adiponectin QTL on chromosome 5 |
BMND9 GeneBone mineral density QTL 9 |
BMND6 GeneBone mineral density QTL 6 |
BMND5 GeneBone mineral density variation QTL 5 |
RA6 GeneRheumatoid arthritis QTL 06 |
RA7 GeneRheumatoid arthritis QTL 07 |
RA4 GeneRheumatoid arthritis QTL 04 |
RA5 GeneRheumatoid arthritis QTL 01 |
RA2 GeneRheumatoid arthritis QTL 01 |
RA3 GeneRheumatoid arthritis QTL 02 |
RA1 GeneRheumatoid arthritis QTL 01 |
RA8 GeneRheumatoid arthritis QTL 08 |
AASTH18 GeneAllergic/atopic asthma related QTL 18 |
AASTH13 GeneAllergic/atopic asthma related QTL 13 |
AASTH15 GeneAllergic/atopic asthma related QTL 15 |
AASTH14 GeneAllergic/atopic asthma related QTL 14 |
AASTH16 GeneAllergic/atopic asthma related QTL 16 |
SLEP3 GeneSerum leptin concentration QTL 3 |
SLEP2 GeneSerum leptin concentration QTL 2 |
SLEP1 GeneSerum leptin concentration QTL 1 |
HDLCQ6 GeneHigh density lipoprotein cholesterol level QTL 6 |
HDLCQ1 Genehigh density lipoprotein cholesterol level QTL 1 |
AASTH38 GeneAllergic/atopic asthma related QTL 38 |
AASTH37 GeneAllergic/atopic asthma related QTL 37 |
COPD3 GeneChronic obstructive pulmonary disease QTL 3 |
COPD2 GeneChronic obstructive pulmonary disease QTL 2 |
COPD1 GeneChronic obstructive pulmonary disease QTL 1 |
COPD6 GeneChronic obstructive pulmonary disease QTL 6 |
COPD5 GeneChronic obstructive pulmonary disease QTL 5 |
COPD4 GeneChronic obstructive pulmonary disease QTL 4 |
COPD8 GeneChronic obstructive pulmonary disease QTL 8 |
OA10 GeneOsteoarthritis QTL 10 |
BSZQTL GeneBone size QTL |
CPROTQ GeneC-reactive protein QTL |
BP1 GeneBlood pressure QTL 1 |
BP3 GeneBlood pressure QTL 3 |
BP2 GeneBlood pressure QTL 2 |
BP5 GeneBlood pressure QTL 5 |
BP4 GeneBlood pressure QTL 4 |
BP7 GeneBlood pressure QTL 7 |
BP6 GeneBlood pressure QTL 6 |
BP9 GeneBlood pressure QTL 9 |
BP8 GeneBlood pressure QTL 8 |
OA30 GeneOsteoarthritis QTL 29 |
SLI2 GeneSpecific language impairment QTL, 2 |
SLI3 GeneSpecific language impairment QTL, 3 |
SLI1 GeneSpecific language impairment QTL, 1 |
ALPQTL2 GeneAlkaline phosphatase, plasma level of, QTL 2 |
AASTH48 GeneAllergic/atopic asthma related QTL 48 |
AASTH49 GeneAllergic/atopic asthma related QTL 49 |
RA24 GeneRheumatoid arthritis QTL 24 |
MENOQ1 Genemenopause, natural, age at, QTL |
CLQTL2 GeneCholesterol level QTL 2 |
TST2 GeneTuberculin skin test reactivity QTL |
RA21 GeneRheumatoid arthritis QTL 21 |
RA20 GeneRheumatoid arthritis QTL 20 |
RA23 GeneRheumatoid arthritis QTL 23 |
RA22 GeneRheumatoid arthritis QTL 22 |
RA25 GeneRheumatoid arthritis QTL 25 |
RA27 GeneRheumatoid arthritis QTL 27 |
RA29 GeneRheumatoid arthritis QTL 29 |
RA28 GeneRheumatoid arthritis QTL 28 |
AASTH42 GeneAllergic/atopic asthma related QTL 42 |
AASTH43 GeneAllergic/atopic asthma related QTL 43 |
AASTH47 GeneAllergic/atopic asthma related QTL 47 |
AASTH44 GeneAllergic/atopic asthma related QTL 44 |
TSHQTL1 GeneThyroid-stimulating hormone level QTL 1 |
COHEN2 GeneCohen syndrome QTL 2 |
OSTEAR3_H GeneOsteoarthritis QTL 3 |
COPD17 GeneChronic obstructive pulmonary disease QTL 17 |
AASTH9 GeneAllergic/atopic asthma related QTL 9 |
AASTH8 GeneAllergic/atopic asthma related QTL 8 |
AASTH7 GeneAllergic/atopic asthma related QTL 7 |
AASTH6 GeneAllergic/atopic asthma related QTL 6 |
AASTH1 GeneAllergic/atopic asthma related QTL 1 |
AASTH3 GeneAllergic/atopic asthma related QTL 3 |
AASTH2 GeneAllergic/atopic asthma related QTL 2 |
RA18 GeneRheumatoid arthritis QTL 18 |
RA19 GeneRheumatoid arthritis QTL 19 |
RA10 GeneRheumatoid arthritis QTL 10 |
RA11 GeneRheumatoid arthritis QTL 11 |
RA12 GeneRheumatoid arthritis QTL 12 |
RA13 GeneRheumatoid arthritis QTL 13 |
RA14 GeneRheumatoid arthritis QTL 14 |
RA15 GeneRheumatoid arthritis QTL 15 |
RA16 GeneRheumatoid arthritis QTL 16 |
RA17 GeneRheumatoid arthritis QTL 17 |
BP51 GeneBlood pressure QTL 51 |
BP50 GeneBlood pressure QTL 50 |
BP53 GeneBlood pressure QTL 53 |
BP52 GeneBlood pressure QTL 52 |
BP55 GeneBlood pressure QTL 55 |
BP54 GeneBlood pressure QTL 54 |
STQTL23 GeneStature QTL 23 |
STQTL20 GeneStature QTL 20 |
COPD7 GeneChronic obstructive pulmonary disease QTL 7 |
COPD9 GeneChronic obstructive pulmonary disease QTL 9 |
AASTH29 GeneAllergic/Atopic asthma related QTL 29 |
AASTH24 GeneAllergic/atopic asthma related QTL 24 |
AASTH26 GeneAllergic/atopic asthma related QTL 25 |
AASTH27 GeneAllergic/atopic asthma related QTL 27 |
AASTH20 GeneAllergic/atopic asthma related QTL 20 |
AASTH21 GeneAllergic/atopic asthma related QTL 21 |
AASTH22 GeneAllergic/atopic asthma related QTL 22 |
OA26 GeneOsteoarthritis QTL 26 |
OA25 GeneOsteoarthritis QTL 25 |
OA27 GeneOsteoarthritis QTL 27 |
OA24 GeneOsteoarthritis QTL 24 |
OA22 GeneOsteoarthritis QTL 22 |
OA23 GeneOsteoarthritis QTL 23 |
OA20 GeneOsteoarthritis QTL 20 |
OA21 GeneOsteoarthritis QTL 21 |
OA28 GeneOsteoarthritis QTL 28 |
OA29 GeneOsteoarthritis QTL 29 |
AASTH41 GeneAllergic/Atopic asthma related QTL 41 |
AASTH46 GeneAllergic/atopic asthma related QTL 46 |
STQTL17 GeneStature QTL 17 |
UAE1 GeneUrinary albumin excretion QTL 1 |
UAE2 GeneUrinary albumin excretion QTL 2 |
STQTL15 GeneStature QTL 15 |
STQTL13 GeneStature QTL 13 |
BMND10 GeneBone mineral density QTL 10 |
BMND11 GeneBone mineral density QTL 11 |
BMND13 GeneBone mineral density QTL 13 |
BMND14 GeneBone mineral density QTL 14 |
AASTH25 GeneAllergic/atopic asthma related QTL 25 |
BSZQTL2 GeneBone size QTL |
ADIPQTL3 GeneCirculating adiponectin QTL on chromosome 14 |
AASTH55 GeneAllergic/atopic asthma related QTL 5 |
AASTH54 GeneAllergic/atopic asthma related QTL 54 |
AASTH56 GeneAllergic/Atopic asthma related QTL 56 |
AASTH51 GeneAllergic/atopic asthma related QTL 51 |
AASTH53 GeneAllergic/atopic asthma related QTL 53 |
AASTH52 GeneAllergic/atopic asthma related QTL 52 |
BMND4 GeneBone mineral density variation QTL 4 |
AASTH4 GeneAllergic/atopic asthma related QTL 4 |
RA9 GeneRheumatoid arthritis QTL 09 |
BP37 GeneBlood pressure QTL 37 |
BP36 GeneBlood pressure QTL 36 |
BP35 GeneBlood pressure QTL 35 |
BP34 GeneBlood pressure QTL 34 |
BP33 GeneBlood pressure QTL 33 |
BP32 GeneBlood pressure QTL 32 |
BP31 GeneBlood pressure QTL 31 |
BP30 GeneBlood pressure QTL 30 |
BP39 GeneBlood pressure QTL 39 |
BP38 GeneBlood pressure QTL 38 |
BP18 GeneBlood pressure QTL 18 |
BP14 GeneBlood pressure QTL 14 |
AASTH11 GeneAllergic/atopic asthma related QTL 11 |
AASTH12 GeneAllergic/atopic asthma related QTL 12 |
AASTH17 GeneAllergic/atopic asthma related QTL 17 |
RA30 GeneRheumatoid arthritis QTL 30 |
RA31 GeneRheumatoid arthritis QTL 31 |
HBFQTL4 GeneFetal hemoglobin QTL on chromosome 8 |
AASTH19 GeneAllergic/atopic asthma related QTL 19 |
AASTH10 GeneAllergic/atopic asthma related QTL 10 |
STQTL16 GeneStature QTL 16 |
STQTL14 GeneStature QTL 14 |
STQTL12 GeneStature QTL 12 |
STQTL10 GeneStature QTL 10 |
MUSQTL1 GeneMusical aptitude QTL 1 |
STQTL11 GeneStature QTL 11 |
STQTL18 GeneStature QTL 18 |
STQTL19 GeneStature QTL 19 |
AASTH50 GeneAllergic/atopic asthma related QTL 50 |
BP46 GeneBlood pressure QTL 46 |
BP47 GeneBlood pressure QTL 47 |
BP45 GeneBlood pressure QTL 45 |
BP48 GeneBlood pressure QTL 48 |
BWQTL2 GeneBirth weight QTL 2 |
COPD13 GeneChronic obstructive pulmonary disease QTL 13 |
COPD12 GeneChronic obstructive pulmonary disease QTL 12 |
COPD11 GeneChronic obstructive pulmonary disease QTL 11 |
COPD10 GeneChronic obstructive pulmonary disease QTL 10 |
COPD16 GeneChronic obstructive pulmonary disease QTL 16 |
COPD15 GeneChronic obstructive pulmonary disease QTL 15 |
COPD19 GeneChronic obstructive pulmonary disease QTL 19 |
COPD18 GeneChronic obstructive pulmonary disease QTL 18 |
OA7 GeneOsteoarthritis QTL 7 |
OA6 GeneOsteoarthritis QTL 6 |
OA5 GeneOsteoarthritis QTL 5 |
OA4 GeneOsteoarthritis QTL 4 |
OA2 GeneOsteoarthritis QTL 2 |
OA1 GeneOsteoarthritis QTL 1 |
OA9 GeneOsteoarthritis QTL 9 |
OA8 GeneOsteoarthritis QTL 8 |
AASTH39 GeneAllergic/atopic asthma related QTL 39 |
AASTH36 GeneAllergic/atopic asthma related QTL 36 |
AASTH35 GeneAllergic/atopic asthma related QTL 35 |
AASTH34 GeneAllergic/atopic asthma related QTL 34 |
AASTH33 GeneAllergic/atopic asthma related QTL 33 |
AASTH32 GeneAllergic/Atopic asthma related QTL 32 |
AASTH31 GeneAllergic/atopic asthma related QTL 31 |
AASTH30 GeneAllergic/atopic asthma related QTL 30 |
AASTH5 GeneAllergic/atopic asthma related QTL 5 |
B6QTL1 GeneVitamin B6 plasma level QTL 1 |
STQTL24 GeneStature QTL 24 |
STQTL21 GeneStature QTL 21 |
MENAQ1 GeneMenarche, age at, QTL |
HDLCQ4 GeneHigh density lipoprotein cholesterol level QTL 4 |
HDLCQ5 GeneHigh density lipoprotein cholesterol level QTL 5 |
HDLCQ2 GeneHigh density lipoprotein cholesterol level QTL on chromosome 8 |
AASTH28 GeneAllergic/Atopic asthma related QTL 28 |
AASTH23 GeneAllergic/atopic asthma related QTL 23 |
STQTL22 GeneStature QTL 22 |
BP19 GeneBlood pressure QTL 19 |
BP15 GeneBlood pressure QTL 15 |
BP17 GeneBlood pressure QTL 17 |
BP16 GeneBlood pressure QTL 16 |
BP11 GeneBlood pressure QTL 11 |
BP10 GeneBlood pressure QTL 10 |
BP13 GeneBlood pressure QTL 13 |
BP12 GeneBlood pressure QTL 12 |
OA19 GeneOsteoarthritis QTL 19 |
OA18 GeneOsteoarthritis QTL 18 |
OA13 GeneOsteoarthritis QTL 13 |
OA12 GeneOsteoarthritis QTL 12 |
OA11 GeneOsteoarthritis QTL 11 |
OA17 GeneOsteoarthritis QTL 17 |
OA16 GeneOsteoarthritis QTL 16 |
OA15 GeneOsteoarthritis QTL 15 |
OA14 GeneOsteoarthritis QTL 14 |
COPD28 GeneChronic obstructive pulmonary disease QTL 28 |
COPD29 GeneChronic obstructive pulmonary disease QTL 29 |
COPD22 GeneChronic obstructive pulmonary disease QTL 22 |
COPD23 GeneChronic obstructive pulmonary disease QTL 23 |
COPD20 GeneChronic obstructive pulmonary disease QTL 20 |
COPD21 GeneChronic obstructive pulmonary disease QTL 21 |
COPD26 GeneChronic obstructive pulmonary disease QTL 26 |
COPD27 GeneChronic obstructive pulmonary disease QTL 27 |
COPD24 GeneChronic obstructive pulmonary disease QTL 24 |
COPD25 GeneChronic obstructive pulmonary disease QTL 25 |
SXGQTL1 GeneSex hormone-binding blobulin circulating level QTL 1 |