Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RNASEH2C ENSECAG00000017289

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Description

ribonuclease H2 subunit C [Source:VGNC Symbol;Acc:VGNC:69332]

Location

Primary_assembly 12: 29,538,061-29,578,856 reverse strand.

EquCab3.0:CM009159.1

About this gene

This gene has 2 transcripts (splice variants) and 87 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSECAT00000083143.1	RNASEH2C-202	1596	176aa	ENSECAP00000074041.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSECAT00000018200.4	RNASEH2C-201	8303	166aa	ENSECAP00000014836.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6WNX0	-

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Summary

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