Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: BMPR1B ENSSSCG00000029621

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Description

bone morphogenetic protein receptor type 1B [Source:NCBI gene (formerly Entrezgene);Acc:396691]

Gene Synonyms

BMPR-IB

Location

Primary_assembly 8: 124,536,653-124,759,406 reverse strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 2 transcripts (splice variants), 285 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000028459.4	BMPR1B-201	5552	532aa	ENSSSCP00000023827.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UG71 A0A5K1UKI8	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSSSCT00000034827.4	BMPR1B-202	5476	502aa	ENSSSCP00000030296.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UG64 Q95L23	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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Summary

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