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: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: C14h5orf52 ENSRNOG00000004112

.

Description

similar to human chromosome 5 open reading frame 52 [Source:RGD Symbol;Acc:1308775]

Gene Synonyms

LOC305476, RGD1308775

Location

Primary_assembly 14: 83,004,906-83,013,549 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 1 transcript (splice variant) and 76 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000005514.6	C14h5orf52-201	2518	167aa	ENSRNOP00000005514.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IKD0 D3ZFB8	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,

.

Summary

.

.