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Standards Ontologies Notations
Guidelines
MIRAGE
GREB1 like retinoic acid receptor coactivator

Summary
Gene Symbol
  • GREB1L
Organism
Homo sapiens (human)
NCBI Gene
80000
PubChem
80000
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Developmental protein
  • Disease variant
  • Non-syndromic deafness
  • Proteomics identification
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
Q9C091
  • Growth regulation by estrogen in breast cancer 1-like protein
J3QQW0
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 11 in total
GO Term Evidence Code PMID
metanephros development
branching involved in ureteric bud morphogenesis
kidney development
kidney development
kidney development
GO Hierarchy
Displaying 1 entry
GO Term Evidence Code PMID
membrane
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
GREB1
Functional Category
  • I: Lipid transport and metabolism
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Displaying all 6 entries
InterPro
GREB1, N-terminal domain
GREB1-like, C-terminal domain
GREB1-like, circularly permuted SF2 helicase domain
GREB1-like, second domain
GREB1
TET-Associated Glycosyltransferase
Disease
Disease Ontology
Displaying all 2 entries
DO ID Disease Name Source
DOID:0070602 autosomal dominant nonsyndromic deafness 80
DOID:14766 renal agenesis
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025