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

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Gene: RHBG ENSBTAG00000012234

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Description

Rh family B glycoprotein [Source:VGNC Symbol;Acc:VGNC:55671]

Location

Primary_assembly 3: 14,441,110-14,453,808 reverse strand.

ARS-UCD1.3:CM008170.2

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000050191.5	RHBG-201	1733	455aa	ENSBTAP00000046932.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q95M77	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,
ENSBTAT00000016227.6	RHBG-202	1637	423aa	ENSBTAP00000016227.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BGB6	-

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Summary

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