abnormal gallbladder morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A structural anomaly of the gallbladder. (Human Phenotype Ontology, HP_0012437)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012437
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Genes

26 genes associated with the abnormal gallbladder morphology 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
ANK1 ankyrin 1, erythrocytic
B3GALTL beta 1,3-galactosyltransferase-like
BLVRA biliverdin reductase A
BPGM 2,3-bisphosphoglycerate mutase
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
DMPK dystrophia myotonica-protein kinase
FECH ferrochelatase
GPI glucose-6-phosphate isomerase
HBB hemoglobin, beta
HK1 hexokinase 1
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