UniProt | Protein Name |
---|---|
Q75T13 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of ER to Golgi vesicle-mediated transport | ||
embryonic pattern specification | ||
sensory perception of sound | ||
GPI anchor metabolic process | ||
anterior/posterior axis specification |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol deacylase activity | ||
hydrolase activity, acting on ester bonds |
|
DO ID | Disease Name | Source |
---|---|---|
DOID:0060284 | paroxysmal nocturnal hemoglobinuria | |
DOID:0060308 | autosomal recessive intellectual developmental disorder | |
DOID:0060810 | syndromic X-linked intellectual disability type 10 | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0110881 | holoprosencephaly 1 | |
DOID:1059 | intellectual disability | |
DOID:10907 | microcephaly | |
DOID:11832 | visual epilepsy | |
DOID:12139 | dysthymic disorder | |
DOID:12859 | choreatic disease |
HPO ID | HPO Term |
---|---|
HP:0001257 | Spasticity |
HP:0001263 | Global developmental delay |
HP:0001270 | Motor delay |
HP:0001274 | Agenesis of corpus callosum |
HP:0001276 | Hypertonia |
HP:0001319 | Neonatal hypotonia |
HP:0001320 | Cerebellar vermis hypoplasia |
HP:0001344 | Absent speech |
HP:0001347 | Hyperreflexia |
HP:0001508 | Failure to thrive |
Disease ID | Disease Name |
---|---|
OMIM:615802 |
|
ORPHA:401820 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101331305 | TURTR16061 | ||
118898419 | BALMU00550 | ||
100666144 | LOXAF18837 | ||
100070459 | HORSE13538 | ||
100620753 | PIGXX09715 | ||
504677 | BOVIN24493 | ||
102170473 | CAPHI20586 | ||
101120808 | SHEEP09616 | ||
100348476 | RABIT11878 | ||
105995540 | DIPOR00392 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024