UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
amino acid metabolic process |
|
|
protein transport | ||
monoatomic ion transport |
|
|
long-term memory | ||
positive regulation of thyroid hormone generation |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
melanosome | ||
plasma membrane | ||
lysosomal membrane | ||
early endosome |
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050336 | hypophosphatemia | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080001 | bone disease | |
DOID:0080348 | Alzheimer's disease 1 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 |
HPO ID | HPO Term |
---|---|
HP:0000821 | Hypothyroidism |
HP:0000823 | Delayed puberty |
HP:0000832 | Primary hypothyroidism |
HP:0000897 | Rachitic rosary |
HP:0000966 | Hypohidrosis |
HP:0001010 | Hypopigmentation of the skin |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001263 | Global developmental delay |
HP:0001507 | Growth abnormality |
Disease ID | Disease Name |
---|---|
OMIM:219800 |
|
ORPHA:411629 |
|
OMIM:219900 |
|
ORPHA:411641 |
|
ORPHA:411634 |
|
OMIM:219750 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100669881 | LOXAF07846 | ||
100060554 | HORSE03110 | ||
100515235 | PIGXX03131 | ||
613527 | BOVIN12569 | ||
102187709 | CAPHI10245 | ||
101122533 | SHEEP02647 | ||
105983465 | DIPOR08657 | ||
83429 | MGI:1932872 | MOUSE07194 | |
287478 | RGD:1308466 | RATNO00724 | |
101721174 | HETGA14366 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024