UniProt | Protein Name |
---|---|
P48651 |
|
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylserine biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
L-serine-phosphatidylethanolamine phosphatidyltransferase activity | ||
transferase activity |
|
|
L-serine-phosphatidylcholine phosphatidyltransferase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0070133 | autosomal recessive cutis laxa type IB | |
DOID:0070134 | autosomal recessive cutis laxa type IIA | |
DOID:0070135 | autosomal recessive cutis laxa type IA | |
DOID:0070136 | autosomal dominant cutis laxa 2 | |
DOID:0070137 | autosomal recessive cutis laxa type IIB | |
DOID:0070138 | autosomal recessive cutis laxa type IIIB | |
DOID:0070140 | autosomal recessive cutis laxa type IIC | |
DOID:0070141 | autosomal recessive cutis laxa type II classic type | |
DOID:0070142 | autosomal dominant cutis laxa | |
DOID:0080334 | aortic valve disease 2 |
HPO ID | HPO Term |
---|---|
HP:0000316 | Hypertelorism |
HP:0000337 | Broad forehead |
HP:0000347 | Micrognathia |
HP:0000400 | Macrotia |
HP:0000407 | Sensorineural hearing impairment |
HP:0000452 | Choanal stenosis |
HP:0000453 | Choanal atresia |
HP:0000614 | Abnormal nasolacrimal system morphology |
HP:0000682 | Abnormal dental enamel morphology |
HP:0000885 | Broad ribs |
Disease ID | Disease Name |
---|---|
ORPHA:2658 |
|
OMIM:151050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
112931317 | VULVU02806 | ||
123797862 | URSAM04144 | ||
100468000 | AILME11006 | ||
101679721 | MUSPF06489 | ||
101091087 | FELCA37821 | ||
122210485 | PANLE18534 | ||
118883673 | BALMU01449 | ||
100670511 | LOXAF16431 | ||
100059691 | HORSE42402 | ||
100156809 | PIGXX23115 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024