ZMP

bmpr1ba

Ensembl ID:

ENSDARG00000005600

ZFIN ID:

ZDB-GENE-991208-8

Description:

bone morphogenetic protein receptor type-1B [Source:RefSeq peptide;Acc:NP_571532]

Human Orthologue:

BMPR1B

Human Description:

bone morphogenetic protein receptor, type IB [Source:HGNC Symbol;Acc:1077]

Mouse Orthologue:

Bmpr1b

Mouse Description:

bone morphogenetic protein receptor, type 1B Gene [Source:MGI Symbol;Acc:MGI:107191]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13912	Nonsense	Available for shipment	Available now
sa20343	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa13912

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027129	Nonsense	120	504	4	10

Genomic Location (Zv9):

Chromosome 5 (position 8836830)

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTGTGTGTGTGTGTGYGTGCGTGCGNNNNNNNNCGNNTGCGTGCAGGTTA[T/A]GTGGTTGGAGACATTCATCATATCGCTCTGCTCATCTCWGTGAGCGTCTG

Long Flanking Sequence:

ATTGTTATTATTATTATTATTTTATTTTTATATAGATCCTTTTTTAATTTAACTTTAAAATTAAGTTAGACTAAATTCTACAATTAACAATTGTCTTCCCTTGATACAGTGTATATTTTATTTTATGAGGCAGCCCAAAACACCCCAAACACACTAAACACACTCACACAAAGTCACACCTCTGCTTAAAAGCAAGAGATGGCATCACACACACACGCACGCACGCACACAAACACACGCGCACACACACTAACACTAACATATCCACACACACACACACACACACACACATACATACATACATATACATACACACACAAACACACACACACACACACACAAATCAGTGTTATGGTGCAGAGTTTATGTTTGACATGCAATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGTGCGTGCGTGCGTGCAGGTTA[T/A]GTGGTTGGAGACATTCATCATATCGCTCTGCTCATCTCAGTGAGCGTCTGTAGCTTCATCCTCACCTTCATCATCATCTTCTGTTACTTCAGGTGTGTAAGTTACAGCAGAAACACAAACACACTGCCTTTACCCATAGAAATGATTATCAGTAAAGCCTCTGTCGTTTTGTACCCACAAAGTACAACCTATCACTTAGATTGTGTTGCGTTTTCAACTCATTTGTATAAATATTAATAACTTGGATGCCATTGAAATGTTACCAGAGAATTGTTACTATATAAATGTTCCTATAGGCAGATTTTGATGTAAACTCTAAAACTCTTCAAACTGACCCTGACTGCAAACTTTGAATCCACTACATTAGTTTATTTTAATATAATTTGTCTCTCAGTGATCACCATGTACACATCAGTATTATATAGTTTTGGAGTTTTAGTGTAGATTCTGTCTCATGTTTTCTGTGCCGTGTGTGTGTGTGTACATTTCAGATATAAGCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20343

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000027129	Nonsense	425	504	9	10

Genomic Location (Zv9):

Chromosome 5 (position 8824634)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	7003718
GRCz11	5	7494873

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTGAAGTGAGATGTTGTGTGTTGTTTGTGCAGGTATAGTAGAGGAGTA[T/A]CAGCTGCCGTATCATGATCATGTTCCCAATGACCCGTCATATGAAGACAT

Long Flanking Sequence:

AATGTGTTTGGTCATTATCAATGTACTGTCACTTTAAATGAGCGTGTGCAGCGCGTCAAAAATAGACCCGGCGCCGAAACTATCGCTGCACTGCTGCTTTGCTGACGCTCACGCCTCGCTCTGAAGCGCTGCTGCTGCGTGCTGTATGAAAGCTCTAATCTGTTAACATGGACGCCGAAAACACACGCGCCGCTGATGCTTGCGGTGTGAAACAGGCGTAAGAGCAATTTTAAATGTGGTTTTAGGATGCCAAAAACACCAAAAAACACAATTAGGATCAAAACCTAAAGGAGTCAGTTTCAAAGAGTTATAAAACATTATCAGTGTGGTATTTTGAACTGAATCTTTACATACACACTCTAAGATTATCAGAAACTGATTTTACATCTTGTAAAAAGCAGCATAATAGGTCCCCTTAAGTTTTACATAATTTGACATGTAGGAGAATTTGTCTGAAGTGAGATGTTGTGTGTTGTTTGTGCAGGTATAGTAGAGGAGTA[T/A]CAGCTGCCGTATCATGATCATGTTCCCAATGACCCGTCATATGAAGACATGAGAGAGGTGGTCTGCATCAAGAGGATACGACCCTCCTTCCCCAACCGCTGGAGCAGTGATGAGGTACGTTTTAGCTAACTACAAAAAAAATAATTATATCTATATACAGTTAGAATTATCAGCCCCCCTGTTTATTTTTTCCCCAATTTCTGTTTAACGGAGAGAAGATTTTCTAAACACATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGGTTTATTTTATTTTTGCCGTGATGACAGTAAATAATATTTTACTAGATATTTTCCAAGACACTGCTATACAGCTTAAAGGGTCACGAAACACCAAAACACATTTTTTGAGCTGTTGACAGTCGTATATGTGTCCCACACTGCTAAAAACACTATTAGGACACCTATATTTCACTAAAAAGTGTAAATTGGTTGTTTTTGCGTTATTTCAAGCAAATTTGTACTTCC

Associated Phenotype:

Not determined