UniProt | Protein Name |
---|---|
P21964 |
|
A0A140VJG8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
renin secretion into blood stream | ||
response to inorganic substance | ||
artery development | ||
prostaglandin metabolic process | ||
multicellular organism growth |
GO Term | Evidence Code | PMID |
---|---|---|
magnesium ion binding | ||
L-dopa O-methyltransferase activity |
|
|
orcinol O-methyltransferase activity |
|
|
protein binding | ||
catechol O-methyltransferase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060256 | Dowling-Degos disease | |
DOID:0060258 | reticulate acropigmentation of Kitamura | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis | |
DOID:0060262 | gallbladder disease | |
DOID:0060306 | Meier-Gorlin syndrome | |
DOID:0060320 | inguinal hernia | |
DOID:0060321 | umbilical hernia | |
DOID:0060326 | myelomeningocele | |
DOID:0060327 | omphalocele |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000023 | Inguinal hernia |
HP:0000028 | Cryptorchidism |
HP:0000047 | Hypospadias |
HP:0000076 | Vesicoureteral reflux |
HP:0000089 | Renal hypoplasia |
HP:0000113 | Polycystic kidney dysplasia |
HP:0000130 | Abnormality of the uterus |
HP:0000160 | Narrow mouth |
HP:0000164 | Abnormality of the dentition |
Disease ID | Disease Name |
---|---|
OMIM:181500 |
|
ORPHA:567 |
|
OMIM:167870 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
104681986 | RHIRO39893 | ||
114586245 | PODMU27645 | ||
107553993 | SINGR08682 | ||
107584930 | SINGR34375 | ||
107601759 | SINGR65043 | ||
116819462 | CHEAB13616 | ||
115043895 | ECHNA05008 | ||
115388414 | SALFA35247 | ||
113485994 | ATHCN16216 | ||
109098298 | CYPCA119631 |
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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