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

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Gene: crlf1b ENSDARG00000006368

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Description

cytokine receptor-like factor 1b [Source:ZFIN;Acc:ZDB-GENE-080108-1]

Gene Synonyms

clf-1b, zgc:172222

Location

Chromosome 22: 21,152,847-21,165,192 forward strand.

GRCz11:CM002906.2

About this gene

This gene has 2 transcripts (splice variants), 70 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000007321.10	crlf1b-201	1584	416aa	ENSDARP00000011541.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8JL58	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSDART00000166342.2	crlf1b-202	1377	431aa	ENSDARP00000134377.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4IHT8	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,

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Summary

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