UniProt | Protein Name |
---|---|
P07602 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of beta-galactosidase activity | ||
epithelial cell differentiation involved in prostate gland development | ||
sphingolipid metabolic process | ||
prostate gland growth | ||
regulation of autophagy |
|
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
azurophil granule membrane |
|
|
extracellular region | ||
plasma membrane |
|
|
collagen-containing extracellular matrix |
GO Term | Evidence Code | PMID |
---|---|---|
ganglioside GM1 binding | ||
ganglioside GM3 binding | ||
protein homodimerization activity | ||
ganglioside GT1b binding | ||
scaffold protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110512 | autosomal recessive nonsyndromic deafness 6 | |
DOID:0110513 | autosomal recessive nonsyndromic deafness 61 | |
DOID:0110514 | autosomal recessive nonsyndromic deafness 62 | |
DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | |
DOID:0110516 | autosomal recessive nonsyndromic deafness 65 | |
DOID:0110517 | autosomal recessive nonsyndromic deafness 66 | |
DOID:0110518 | autosomal recessive nonsyndromic deafness 67 | |
DOID:0110519 | autosomal recessive nonsyndromic deafness 68 | |
DOID:0110520 | autosomal recessive nonsyndromic deafness 7 | |
DOID:0110521 | autosomal recessive nonsyndromic deafness 70 |
HPO ID | HPO Term |
---|---|
HP:0004302 | Functional motor deficit |
HP:0004326 | Cachexia |
HP:0004343 | Abnormal glycosphingolipid metabolism |
HP:0004466 | Delayed brainstem auditory evoked response conduction time |
HP:0004926 | Orthostatic hypotension due to autonomic dysfunction |
HP:0004975 | Erlenmeyer flask deformity of the femurs |
HP:0005968 | Temperature instability |
HP:0006897 | Abducens palsy |
HP:0007103 | Hypointensity of cerebral white matter on MRI |
HP:0007133 | Progressive peripheral neuropathy |
Disease ID | Disease Name |
---|---|
OMIM:611721 |
|
ORPHA:139406 |
|
ORPHA:309271 |
|
OMIM:611722 |
|
ORPHA:206436 |
|
ORPHA:309263 |
|
OMIM:610539 |
|
ORPHA:309256 |
|
OMIM:619491 |
|
OMIM:249900 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115055704 | ECHNA10443 | ||
115399205 | SALFA53463 | ||
113481820 | ATHCN18638 | ||
105825471 | PROCO08336 | ||
109062214 | CYPCA63937 | ||
109062217 | CYPCA78568 | ||
103736967 | NANGA13901 | ||
116447216 | CORMO25684 | ||
103257021 | CARSF10010 | ||
115608990 | STRHB03871 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024