Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: agfg1a ENSDARG00000030020

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Description

ArfGAP with FG repeats 1a [Source:ZFIN;Acc:ZDB-GENE-030131-5808]

Gene Synonyms

agfg1, hrb, wu:fb14f05, wu:fi19d11

Location

Chromosome 15: 35,156,414-35,212,462 reverse strand.

GRCz11:CM002899.2

About this gene

This gene has 2 transcripts (splice variants), 210 orthologues and 34 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000043960.8	agfg1a-201	2581	556aa	ENSDARP00000043959.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R9R7	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,
ENSDART00000144944.2	agfg1a-202	785	225aa	ENSDARP00000117201.1	Nonsense mediated decay	F1QPM2	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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