abnormality of the gallbladder Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the gallbladder. (Human Phenotype Ontology, HP_0005264)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005264
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Genes

36 genes associated with the abnormality of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
AIRE autoimmune regulator
ALAS2 5'-aminolevulinate synthase 2
ALDOA aldolase A, fructose-bisphosphate
AMACR alpha-methylacyl-CoA racemase
ANK1 ankyrin 1, erythrocytic
ARSA arylsulfatase A
B3GALTL beta 1,3-galactosyltransferase-like
BLVRA biliverdin reductase A
BPGM 2,3-bisphosphoglycerate mutase
BRAF B-Raf proto-oncogene, serine/threonine kinase
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
DHCR7 7-dehydrocholesterol reductase
DMPK dystrophia myotonica-protein kinase
FECH ferrochelatase
FOXF1 forkhead box F1
FUCA1 fucosidase, alpha-L- 1, tissue
GPI glucose-6-phosphate isomerase
HBB hemoglobin, beta
HK1 hexokinase 1
HOXD13 homeobox D13
LETM1 leucine zipper-EF-hand containing transmembrane protein 1
NELFA negative elongation factor complex member A
PEX19 peroxisomal biogenesis factor 19
PFKM phosphofructokinase, muscle
PIEZO1 piezo-type mechanosensitive ion channel component 1
PKLR pyruvate kinase, liver and RBC
RFX6 regulatory factor X, 6
SC5D sterol-C5-desaturase
SEC23B Sec23 homolog B (S. cerevisiae)
TBX1 T-box 1
TPI1 triosephosphate isomerase 1
UROS uroporphyrinogen III synthase
WHSC1 Wolf-Hirschhorn syndrome candidate 1