UniProt | Protein Name |
---|---|
Q9P2K1 |
|
GO Term | Evidence Code | PMID |
---|---|---|
smoothened signaling pathway | ||
protein localization to ciliary transition zone | ||
heart development | ||
cilium assembly | ||
camera-type eye development |
GO Term | Evidence Code | PMID |
---|---|---|
MKS complex | ||
ciliary transition zone | ||
cytoskeleton | ||
cytosol |
Gene Ontology |
---|
protein localization to ciliary transition zone |
InterPro |
---|
C2 domain superfamily |
CC2D2A, N-terminal, C2 domain |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050545 | visceral heterotaxy | |
DOID:0050777 | Joubert syndrome | |
DOID:0050778 | Meckel syndrome | |
DOID:0060340 | ciliopathy | |
DOID:0070120 | Meckel syndrome 6 | |
DOID:0111004 | Joubert syndrome 9 | |
DOID:10584 | retinitis pigmentosa | |
DOID:1059 | intellectual disability |
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
101142483 | 9595_0:0016ee | GORGO31463 | ||
101160942 | ORYLA07852 | |||
101571912 | OCTDE01571 | |||
101594467 | JACJA07437 | |||
101682465 | MUSPF04429 | |||
101814023 | FICAL02064 | |||
101933977 | CHRPI22565 | |||
102017335 | CHILA18107 | |||
102120746 | MACFA33468 | |||
102171228 | CAPHI26766 |
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GlyCosmos Portal v4.1.0
Last updated: December 9, 2024