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

Gene: C7h22orf23 ENSRNOG00000011170

Description

similar to human chromosome 22 open reading frame 23 [Source:RGD Symbol;Acc:1359634]

Gene Synonyms

MGC93972, RGD1359634

Location

GRCr8:CM070397.1

About this gene

This gene has 3 transcripts (splice variants) and 184 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014878.7	C7h22orf23-201	1933	220aa	ENSRNOP00000014878.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HSP8 F7FLU1	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,
ENSRNOT00000104629.2	C7h22orf23-202	1668	155aa	ENSRNOP00000082303.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZXN7 A6HSP9	-
ENSRNOT00000105348.2	C7h22orf23-203	1589	195aa	ENSRNOP00000088958.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AAJ3	-

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