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: 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: C19h16orf95 ENSRNOG00000050028

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Description

similar to human chromosome 16 open reading frame 95 [Source:RGD Symbol;Acc:1584205]

Gene Synonyms

LOC687560

Location

Primary_assembly 19: 66,514,447-66,527,014 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 2 transcripts (splice variants) and 56 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000102294.2	C19h16orf95-202	1078	233aa	ENSRNOP00000095688.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLR4	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,
ENSRNOT00000071344.3	C19h16orf95-201	1092	214aa	ENSRNOP00000067089.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IZP1 M0RBY7	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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