Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: GRWD1 ENSPTRG00000011236

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Description

glutamate rich WD repeat containing 1 [Source:VGNC Symbol;Acc:VGNC:11124]

Location

Chromosome 19: 50,613,708-50,622,567 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 1 transcript (splice variant), 179 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000020881.4	GRWD1-201	3210	446aa	ENSPTRP00000019277.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XDU2 K7CMK2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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