UniProt | Protein Name |
---|---|
Q9UJA2 |
|
GO Term | Evidence Code | PMID |
---|---|---|
response to phosphatidylethanolamine | ||
cardiolipin biosynthetic process | ||
phosphatidylglycerol acyl-chain remodeling |
|
|
response to thyroxine |
GO Term | Evidence Code | PMID |
---|---|---|
mitochondrial inner membrane | ||
mitochondrion |
GO Term | Evidence Code | PMID |
---|---|---|
cardiolipin synthase (CMP-forming) | ||
1-acylglycerol-3-phosphate O-acyltransferase activity |
|
|
2-acylglycerol-3-phosphate O-acyltransferase activity |
|
DO ID | Disease Name | Source |
---|---|---|
DOID:0060180 | colitis | |
DOID:0060189 | ileitis | |
DOID:0060190 | ileocolitis | |
DOID:0060284 | paroxysmal nocturnal hemoglobinuria | |
DOID:0070430 | combined oxidative phosphorylation deficiency 57 | |
DOID:10354 | breast fibrocystic disease | |
DOID:10690 | mastitis | |
DOID:12139 | dysthymic disorder | |
DOID:1324 | lung cancer | |
DOID:1325 | bronchus cancer |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000407 | Sensorineural hearing impairment |
HP:0000639 | Nystagmus |
HP:0000710 | Hyperorality |
HP:0000863 | Central diabetes insipidus |
HP:0000873 | Diabetes insipidus |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001332 | Dystonia |
Disease ID | Disease Name |
---|---|
OMIM:620167 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
184910 | WB:WBGene00017763 | ||
43104 | FB:FBgn0039360 | ||
405867 | ZFIN:ZDB-GENE-040426-2519 | ||
779375 | Xenbase:XB-GENE-6252450 | ||
780303 | Xenbase:XB-GENE-979013 | ||
109319037 | CROPO06896 | ||
100543402 | MELGA05568 | ||
100083897 | ORNAN26906 | ||
100406450 | CALJA32699 | ||
105582101 | CERAT03133 |
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Last updated: August 19, 2024