Failure To Thrive In Infant Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3887638
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Genes

77 genes associated with the disease Failure To Thrive In Infant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACAD8 acyl-CoA dehydrogenase family, member 8
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain
ALDOB aldolase B, fructose-bisphosphate
APOB apolipoprotein B
ASXL1 additional sex combs like transcriptional regulator 1
ASXL3 additional sex combs like transcriptional regulator 3
C5 complement component 5
CD19 CD19 molecule
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CIT citron rho-interacting serine/threonine kinase
CSF2 colony stimulating factor 2 (granulocyte-macrophage)
CSF3 colony stimulating factor 3 (granulocyte)
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DGAT1 diacylglycerol O-acyltransferase 1
DGUOK deoxyguanosine kinase
EEF1A2 eukaryotic translation elongation factor 1 alpha 2
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
FBXL4 F-box and leucine-rich repeat protein 4
FCGR2B Fc fragment of IgG, low affinity IIb, receptor (CD32)
FH fumarate hydratase
FOXP3 forkhead box P3
G6PC glucose-6-phosphatase, catalytic subunit
G6PC3 glucose 6 phosphatase, catalytic, 3
GDF15 growth differentiation factor 15
GH1 growth hormone 1
GLI1 GLI family zinc finger 1
HIP1 huntingtin interacting protein 1
HRAS Harvey rat sarcoma viral oncogene homolog
HSD17B8 hydroxysteroid (17-beta) dehydrogenase 8
IGF1 insulin-like growth factor 1 (somatomedin C)
IGFALS insulin-like growth factor binding protein, acid labile subunit
IL7 interleukin 7
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KRT6A keratin 6A, type II
LAMA2 laminin, alpha 2
LAMC2 laminin, gamma 2
LEMD3 LEM domain containing 3
MBTPS2 membrane-bound transcription factor peptidase, site 2
MC3R melanocortin 3 receptor
MC4R melanocortin 4 receptor
MKRN3 makorin ring finger protein 3
MPV17 MpV17 mitochondrial inner membrane protein
MRC1 mannose receptor, C type 1
MRGPRF MAS-related GPR, member F
MTO1 mitochondrial tRNA translation optimization 1
NLRP12 NLR family, pyrin domain containing 12
NR3C2 nuclear receptor subfamily 3, group C, member 2
NR4A1 nuclear receptor subfamily 4, group A, member 1
NSD2 nuclear receptor binding SET domain protein 2
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PAX7 paired box 7
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
POFUT1 protein O-fucosyltransferase 1
PYCR2 pyrroline-5-carboxylate reductase family, member 2
PYY peptide YY
RAG1 recombination activating gene 1
RAG2 recombination activating gene 2
RBFOX2 RNA binding protein, fox-1 homolog (C. elegans) 2
RNF2 ring finger protein 2
SAR1B secretion associated, Ras related GTPase 1B
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC5A1 solute carrier family 5 (sodium/glucose cotransporter), member 1
SPINK5 serine peptidase inhibitor, Kazal type 5
SPINT2 serine peptidase inhibitor, Kunitz type, 2
STXBP2 syntaxin binding protein 2
SURF1 surfeit 1
TRMT10A tRNA methyltransferase 10 homolog A (S. cerevisiae)
TSHR thyroid stimulating hormone receptor
TTC19 tetratricopeptide repeat domain 19
UBA5 ubiquitin-like modifier activating enzyme 5
VARS2 valyl-tRNA synthetase 2, mitochondrial
WAS Wiskott-Aldrich syndrome