Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Phenotypes
Genetic Variation
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Gene: C19h1orf131 ENSRNOG00000019169

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Description

similar to human chromosome 1 open reading frame 131 [Source:RGD Symbol;Acc:1562218]

Gene Synonyms

MGC124748, RGD1562218

Location

Primary_assembly 19: 69,705,321-69,720,093 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 1 transcript (splice variant) and 190 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025948.7	C19h1orf131-201	4469	370aa	ENSRNOP00000025948.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3KRF3	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data