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: Rnaseh2b ENSRNOG00000009192

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Description

ribonuclease H2, subunit B [Source:RGD Symbol;Acc:1359710]

Gene Synonyms

MGC94780

Location

Primary_assembly 15: 40,717,232-40,770,825 forward strand.

GRCr8:CM070405.1

About this gene

This gene has 7 transcripts (splice variants), 222 orthologues and is associated with 8 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000012231.6	Rnaseh2b-201	1509	334aa	ENSRNOP00000012231.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q5D7	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000122637.1	Rnaseh2b-202	1881	280aa	ENSRNOP00000110574.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000131730.1	Rnaseh2b-203	1577	298aa	ENSRNOP00000111961.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000168846.1	Rnaseh2b-207	1497	302aa	ENSRNOP00000107248.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000164657.1	Rnaseh2b-206	1478	327aa	ENSRNOP00000099248.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000148528.1	Rnaseh2b-205	1350	280aa	ENSRNOP00000104857.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000145208.1	Rnaseh2b-204	1304	283aa	ENSRNOP00000103384.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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