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:0008065 | Aplasia/Hypoplasia of the skin |
HP:0008070 | Sparse hair |
HP:0009773 | Symphalangism affecting the phalanges of the hand |
HP:0009843 | Aplasia/Hypoplasia of the middle phalanges of the hand |
HP:0010554 | Cutaneous finger syndactyly |
HP:0010627 | Anterior pituitary hypoplasia |
HP:0010628 | Facial palsy |
HP:0011001 | Increased bone mineral density |
HP:0011002 | Osteopetrosis |
HP:0011220 | Prominent forehead |
Disease ID | Disease Name |
---|---|
ORPHA:2658 |
|
OMIM:151050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
176776 | WB:WBGene00012095 | ||
181211 | WB:WBGene00013920 | ||
40281 | FB:FBgn0287585 | ||
100179127 | CIOIN15552 | ||
103175125 | CALMI06976 | ||
102367168 | LATCH05569 | ||
559442 | ZFIN:ZDB-GENE-081031-18 | DANRE15421 | |
393931 | ZFIN:ZDB-GENE-040426-837 | ||
108257397 | ICTPU18873 | ||
113586998 | ELEEL38562 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024