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
- 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: CCDC141 ENSPTRG00000012693

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Description

coiled-coil domain containing 141 [Source:VGNC Symbol;Acc:VGNC:10631]

Location

Chromosome 2B: 69,163,849-69,357,338 reverse strand.

Pan_tro_3.0:CM000316.3

About this gene

This gene has 1 transcript (splice variant), 180 orthologues and 9 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000023534.6	CCDC141-201	3073	955aa	ENSPTRP00000021704.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WNT3 H2QJ25	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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