Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
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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

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Gene: C19h19orf67 ENSRNOG00000005533

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Description

similar to human chromosome 19 open reading frame 67 [Source:RGD Symbol;Acc:1586683]

Gene Synonyms

LOC686013

Location

Primary_assembly 19: 41,051,577-41,054,955 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 1 transcript (splice variant) and 170 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000007407.6	C19h19orf67-201	1413	355aa	ENSRNOP00000007407.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A283	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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