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

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Gene: CCDC167 ENSPTRG00000018123

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Description

coiled-coil domain containing 167 [Source:VGNC Symbol;Acc:VGNC:52004]

Location

Chromosome 6: 37,887,602-37,904,678 reverse strand.

Pan_tro_3.0:CM000320.3

About this gene

This gene has 2 transcripts (splice variants) and 168 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000057323.3	CCDC167-201	612	97aa	ENSPTRP00000050190.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2YA01 K7C7M4	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,
ENSPTRT00000088840.1	CCDC167-202	285	94aa	ENSPTRP00000087644.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TEF7	-

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Summary

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