Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: C1h9orf85 ENSRNOG00000027161

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Description

similar to human chromosome 9 open reading frame 85 [Source:RGD Symbol;Acc:1359158]

Gene Synonyms

MGC94797, RGD1359158

Location

Primary_assembly 1: 228,564,731-228,624,278 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 212 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000112470.2	C1h9orf85-201	1348	155aa	ENSRNOP00000094802.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I0M5 Q68FU5	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,
ENSRNOT00000132807.1	C1h9orf85-202	415	35aa	ENSRNOP00000112039.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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