Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
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Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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Pathway
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Gene: Chchd4-ps1 ENSRNOG00000022466

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Description

coiled-coil-helix-coiled-coil-helix domain containing 4, pseudogene 1 [Source:RGD Symbol;Acc:2319280]

Gene Synonyms

LOC100361898, LOC312559, MGC109542

Location

Primary_assembly 4: 123,968,265-123,977,414 reverse strand.

mRatBN7.2:CM026977.1

About this gene

This gene has 2 transcripts (splice variants), 301 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000116715.1	Chchd4-ps1-202	1171	140aa	ENSRNOP00000098005.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AU06	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,
ENSRNOT00000038096.5	Chchd4-ps1-201	1354	139aa	ENSRNOP00000038359.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5BJN5	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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