Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: zgc:100846 ENSDARG00000011837

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Description

zgc:100846 [Source:ZFIN;Acc:ZDB-GENE-040801-47]

Gene Synonyms

C9orf72, c13h9orf72

Location

Chromosome 13: 12,761,707-12,778,947 forward strand.

GRCz11:CM002897.2

About this gene

This gene has 1 transcript (splice variant), 205 orthologues and is associated with 14 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000015127.7	zgc:100846-201	2427	462aa	ENSDARP00000005597.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6TLH8	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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