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:0001744 | Splenomegaly |
HP:0001892 | Abnormal bleeding |
HP:0001928 | Abnormality of coagulation |
HP:0002014 | Diarrhea |
HP:0002024 | Malabsorption |
HP:0002239 | Gastrointestinal hemorrhage |
HP:0002240 | Hepatomegaly |
HP:0002570 | Steatorrhea |
HP:0002630 | Fat malabsorption |
HP:0002748 | Rickets |
Disease ID | Disease Name |
---|---|
OMIM:607765 |
|
ORPHA:79301 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
113883941 | BOBOX17903 | ||
105871052 | MICMU10257 | ||
100946229 | OTOGA07029 | ||
102025133 | CHILA19772 | ||
105729290 | AOTNA37739 | ||
110223144 | PHACI08615 | ||
101043229 | SAIBB16850 | ||
101960771 | ICTTR12784 | ||
101611951 | JACJA23137 | ||
102442201 | MYOLU14936 |
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Last updated: August 19, 2024