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: c1qtnf6b ENSDARG00000006544

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Description

C1q and TNF related 6b [Source:ZFIN;Acc:ZDB-GENE-080411-1]

Gene Synonyms

c1qntf1, c1qntf6b, c1qtnf1l

Location

Chromosome 6: 214,269-218,882 reverse strand.

GRCz11:CM002890.2

About this gene

This gene has 1 transcript (splice variant), 79 orthologues and 32 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000008398.7	c1qtnf6b-201	2173	244aa	ENSDARP00000013553.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1R342	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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