UniProt | Protein Name |
---|---|
O75787 |
|
GO Term | Evidence Code | PMID |
---|---|---|
Golgi lumen acidification |
|
|
synaptic vesicle lumen acidification | ||
central nervous system maturation | ||
head morphogenesis | ||
angiotensin maturation |
GO Term | Evidence Code | PMID |
---|---|---|
autophagosome membrane | ||
clathrin-coated vesicle membrane | ||
vacuolar proton-transporting V-type ATPase, V0 domain | ||
external side of plasma membrane | ||
axon |
GO Term | Evidence Code | PMID |
---|---|---|
signaling receptor activity | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050571 | congenital disorder of glycosylation type II | |
DOID:0050678 | Blau syndrome | |
DOID:0050848 | obstructive sleep apnea | |
DOID:0060135 | apraxia | |
DOID:0060224 | atrial fibrillation | |
DOID:0060249 | scoliosis | |
DOID:0060262 | gallbladder disease | |
DOID:0060309 | syndromic X-linked intellectual disability | |
DOID:0060318 | acute promyelocytic leukemia |
HPO ID | HPO Term |
---|---|
HP:0000047 | Hypospadias |
HP:0000298 | Mask-like facies |
HP:0000338 | Hypomimic face |
HP:0000341 | Narrow forehead |
HP:0000347 | Micrognathia |
HP:0000369 | Low-set ears |
HP:0000750 | Delayed speech and language development |
HP:0000952 | Jaundice |
HP:0000973 | Cutis laxa |
HP:0001249 | Intellectual disability |
Disease ID | Disease Name |
---|---|
ORPHA:363654 |
|
OMIM:300911 |
|
OMIM:301045 |
|
OMIM:300423 |
|
ORPHA:93952 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
174109 | WB:WBGene00020500 | ||
181526 | WB:WBGene00010993 | ||
41104 | FB:FBgn0037671 | ||
103183828 | CALMI03163 | ||
102360219 | LATCH14143 | ||
406296 | ZFIN:ZDB-GENE-040426-1960 | DANRE22794 | |
103046401 | ASTMX10533 | ||
108259516 | ICTPU22329 | ||
100195062 | SALSA77940 | ||
115156323 | SALTR09087 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024