UniProt | Protein Name |
---|---|
Q9H2F3 |
|
GO Term | Evidence Code | PMID |
---|---|---|
bile acid biosynthetic process |
|
|
B cell chemotaxis |
GO Term | Evidence Code | PMID |
---|---|---|
lipid droplet | ||
endoplasmic reticulum membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
cholest-5-ene-3-beta,7-alpha-diol 3-beta-dehydrogenase activity | ||
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | ||
3-beta-hydroxy-delta5-steroid dehydrogenase activity | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050534 | congenital stationary night blindness | |
DOID:0050674 | congenital bile acid synthesis defect | |
DOID:0060262 | gallbladder disease | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0070221 | progressive familial intrahepatic cholestasis | |
DOID:0070224 | progressive familial intrahepatic cholestasis 4 | |
DOID:0070226 | progressive familial intrahepatic cholestasis 1 | |
DOID:0110870 | congenital stationary night blindness 1A |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000662 | Nyctalopia |
HP:0000939 | Osteoporosis |
HP:0000952 | Jaundice |
HP:0000989 | Pruritus |
HP:0001080 | Biliary tract abnormality |
HP:0001394 | Cirrhosis |
HP:0001399 | Hepatic failure |
HP:0001406 | Intrahepatic cholestasis |
HP:0001508 | Failure to thrive |
Disease ID | Disease Name |
---|---|
OMIM:607765 |
|
ORPHA:79301 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100385140 | CALJA05973 | ||
105599353 | CERAT36624 | ||
714136 | MACMU27041 | ||
105482944 | MACNE37162 | ||
101021257 | PAPAN16636 | ||
105541459 | MANLE13918 | ||
101148659 | GORGO10808 | ||
100986476 | PANPA15041 | ||
454059 | PANTR12198 | ||
100460204 | PONAB10691 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024