Gene: Bmpr1a ENSMUSG00000021796

Description

bone morphogenetic protein receptor, type 1A [Source:MGI Symbol;Acc:MGI:1338938]

Gene Synonyms

1110037I22Rik, ALK3, BMPR-IA, Bmpr

Location

Chromosome 14: 34,132,691-34,225,298 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 4 transcripts (splice variants), 221 orthologues, 11 paralogues and is associated with 13 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000049005.15	Bmpr1a-201	5956	532aa	ENSMUSP00000035900.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26938	P36895 Q53Z43	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, 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, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000165280.8	Bmpr1a-202	1945	500aa	ENSMUSP00000131984.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q60607	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:1,
ENSMUST00000171343.9	Bmpr1a-203	748	108aa	ENSMUSP00000126852.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PW65	TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000171551.2	Bmpr1a-204	641	38aa	ENSMUSP00000129927.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9Q2G5	TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

Gene: Bmpr1a ENSMUSG00000021796

Summary

About Us

Get help

Our sister sites

Follow us

Favourite species

All species

Recent locations

Gene: Bmpr1a ENSMUSG00000021796

Summary

About Us

Get help

Our sister sites

Follow us