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: Molecular function
- GO: Cellular component
- GO: Biological process
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: C19h16orf86 ENSRNOG00000017867

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Description

similar to human chromosome 16 open reading frame 86 [Source:RGD Symbol;Acc:1561415]

Gene Synonyms

LOC498943

Location

Primary_assembly 19: 50,505,546-50,508,414 forward strand.

GRCr8:CM070409.1

About this gene

This gene has 2 transcripts (splice variants) and 89 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000099052.2	C19h16orf86-202	1362	343aa	ENSRNOP00000076658.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5YBT7	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,
ENSRNOT00000024125.6	C19h16orf86-201	1411	318aa	ENSRNOP00000024125.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHP2	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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