Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: C15h14orf119 ENSRNOG00000029146

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Description

similar to human chromosome 14 open reading frame 119 [Source:RGD Symbol;Acc:1308430]

Gene Synonyms

LOC361038, RGD1308430

Location

Primary_assembly 15: 32,116,021-32,122,416 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 3 transcripts (splice variants), 180 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000095147.2	C15h14orf119-202	2025	274aa	ENSRNOP00000080052.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0BN25	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,
ENSRNOT00000104680.2	C15h14orf119-203	2305	142aa	ENSRNOP00000080456.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZNS3 B0BN25	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,
ENSRNOT00000049927.5	C15h14orf119-201	1074	142aa	ENSRNOP00000045776.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZNS3 B0BN25	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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