ZMP
bmpr1ab
Ensembl ID:
ZFIN ID:
Description:
bone morphogenetic protein receptor, type 1ab [Source:RefSeq peptide;Acc:NP_001004585]
Human Orthologue:
BMPR1A
Human Description:
bone morphogenetic protein receptor, type IA [Source:HGNC Symbol;Acc:1076]
Mouse Orthologue:
Bmpr1a
Mouse Description:
bone morphogenetic protein receptor, type 1A Gene [Source:MGI Symbol;Acc:MGI:1338938]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16062 | Essential Splice Site | Available for shipment | Available now |
sa22103 | Nonsense | Available for shipment | Available now |
sa28 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16062
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105621 | Essential Splice Site | 24 | 534 | 3 | 13 |
ENSDART00000125839 | Essential Splice Site | 25 | 535 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 27555350)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25891258 |
GRCz11 | 12 | 25982618 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTCWTTGGCGTTTTAGTAGCTGCTGTCCTCCTCTCACCAYTGGCCGAGG[G/A]TAAGTCCAATTCATTACTATAAAGTGCCTACATTTGCCCATTGCKTTATT
Long Flanking Sequence:
GTCCTAATTAAATAATTAAAAATCAAGGCATGATCATATTTTATTTTGTTAAAATAAGTGTAACCTAGAGGCCTTTGCCTTTCATATTAGGCACTTTTGATACCGAATGATCAACTAGAAGTCAAGTTATTATTTGTTGTTCCTAAAACTTATATAGAGGACAATAATTTTGTCAGGTAGTGTCGTCTTTAAATGTCAATATTGCATATGTCTTTTGTACATCATGATTGTTCAGAAATTAATAAGTGTCTCTCTCTTTATTACAGGGTTTTCCACAAGAGGAGACTGTAAAGAGGCCTTAGAGAAGTCTTCATACTCTTACCGTGTCCATTCATCTTCACAACTGATTGGATACTTCAGTAATTCAAAAGTGGTGCAGTACATCACAACCAAAACAGCCATACAGTTCCACAACTCGACCTTCATGATGAAAAGCACCTTCACGATCATCGTCATTGGCGTTTTAGTAGCTGCTGTCCTCCTCTCACCATTGGCCGAGG[G/A]TAAGTCCAATTCATTACTATAAAGTGCCTACATTTGCCCATTGCGTTATTCCCAGTGGATACAGATGCTTGTCAGTAACCTCAGTGTGTGTCTTTTGGATCGTAAACAAAAATGTGTTTTTTGTTTGGCCTTGATTTGAGTGAAGGAAGAAGGCGAAAACTGATAGGGTCATCTGTTTTGTTTCATCTGGATGCTTAATAGAAATCCAACAGCAATTTATAATACAAAGCAGACTGAGACAGCAGGAGAATTGATTTCGCCGTGTTTGGATGATACCCAGTGTTAGCAGAAGCCTGTTTTAATGGATGGTGGCCTTTAAAAACATGGCGTGGTAATGGCCTCGCTTTTTATTCTCATCAGGCCCCGAATGCTCTGGATCCGTCTCCTCACATTTGCGATGCATTAGCAAACAAACACTATCTGCCAGGATATTCATCTGAATTACATTATTTAATTTTATTGATTTGATGCCCTTGTGATCTTCTCTCAGATGGGTCGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22103
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105621 | Nonsense | 27 | 534 | 4 | 13 |
ENSDART00000125839 | Nonsense | 28 | 535 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 27532586)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGGATATCTAAAAAAAATCTGATTTCCTCTATTTTAACCTTAGGTGGA[C/T]AAAACCCAGACTACATGCTTCATGGCACTGGAGTCAAGCCTGGATCAGAT
Long Flanking Sequence:
AGTACGGCGCTTGCAGGCAAACTGTCATATTTACAGTTTGTTTTGCTGAACAAAGTTTTTTTGACGCTTTGTAAGATTACAGTTGAAACACTGAAGTTACATAGAATGTTTTGACAATGTTTTTGGTTCTTTGTCTGAGCTTTAAATATCTCAGGGCCGTATGGAGGATGAGAGAGATCTCTGATTTCATCTAAAATATTGTAATTTGTCTCAGGGGTTTGGAATGACATGGGGTTGAGTAAATAACAGAACTTTCATTTTTGGATGAACGAAACCTTTAACTTTATGATATCAAGATCACTGAGTGAAATGAACAGCAATACTAATCGTACATTTTGGTTTTATTGGTTTGAAATGCTTTGACACAATGATTTCTCTAGCAAGATTTGATTCATCACGATTGCATAAATATAGACGAGTAATGATGAAAATACTATGGACAGTCACATTCTGGGATATCTAAAAAAAATCTGATTTCCTCTATTTTAACCTTAGGTGGA[C/T]AAAACCCAGACTACATGCTTCATGGCACTGGAGTCAAGCCTGGATCAGATCCAAGGCGAGCTCAGGCAGGAGACGGGTCCACCGTGGCCCCAGAGGATGCTGCCCGCTTCCTTAGCTGCTACTGTTCAGGCCACTGCCCAGAAGATGCCACAAACAACACCTGCGAGTGAGTACACTATCCTCATCTCACTTCTTCTCAATTAAATGTGAACAATCTGAATTAAACTACCTTTGTGTGTTTGCCCAGGACAAACGGCCATTGTTTTGCTATCATAGAGGAGGATGAGCACGGCGAGGCGATGCTGACCTCAGGCTGCATGAAGTACGAGGGATCCCACTTCCAGTGCAAGGTAATTCATGAACGAGACAGTGAGGAATAGATGTTAAGTGCTAAGGCATTAAGATTGACTGAATGTGGTTATTGTCGTCTAGGACTCTCCTAATGCTCAGACCAGACGGACCATTGAGTGCTGCTCCACAGATTTCTGTAATAGAGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105621 | Nonsense | 108 | 534 | 5 | 13 |
ENSDART00000125839 | Nonsense | 109 | 535 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 27532260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 25867278 |
GRCz11 | 12 | 25958638 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGGATGAGCACGGCGAGGCGATGCTGACCTCAGGCTGCATGAAGTA[C/A]GAGGGATCCCACTTCCAGTGCAAGGTAATTCATGAACGAGACAGTGAGGA
Long Flanking Sequence:
TCGTACATTTTGGTTTTATTGGTTTGAAATGCTTTGACACAATGATTTCTCTAGCAAGATTTGATTCATCACGATTGCATAAATATAGACGAGTAATGATGAAAATACTATGGACAGTCACATTCTGGGATATCTAAAAAAAATCTGATTTCCTCTATTTTAACCTTAGGTGGACAAAACCCAGACTACATGCTTCATGGCACTGGAGTCAAGCCTGGATCAGATCCAAGGCGAGCTCAGGCAGGAGACGGGTCCACCGTGGCCCCAGAGGATGCTGCCCGCTTCCTTAGCTGCTACTGTTCAGGCCACTGCCCAGAAGATGCCACAAACAACACCTGCGAGTGAGTACACTATCCTCATCTCACTTCTTCTCAATTAAATGTGAACAATCTGAATTAAACTACCTTTGTGTGTTTGCCCAGGACAAACGGCCATTGTTTTGCTATCATAGAGGAGGATGAGCACGGCGAGGCGATGCTGACCTCAGGCTGCATGAAGTA[C/A]GAGGGATCCCACTTCCAGTGCAAGGTAATTCATGAACGAGACAGTGAGGAATAGATGTTAAGTGCTAAGGCATTAAGATTGACTGAATGTGGTTATTGTCGTCTAGGACTCTCCTAATGCTCAGACCAGACGGACCATTGAGTGCTGCTCCACAGATTTCTGTAATAGAGACCTACAGCCCACACTTCCACCTCCTATTCCAGGAAGTAAGTGTAACGCTGCTCGAGAACCTTAATATAATAAATATATGAAAACGTCACTCTACAGTGTGGAAATTACTCGGTGTGACCATGAAAAACTATTACCAAATTATAGCACATTAACCATTATATAAATATAATTGGATTAAAACATCTACATTGTAGGCCTGTCACAATAATCAATATACCTACTTATCGCACAATACATGGACATGACCTCAGTCATTTTTGGTGATGCAATATACTGTATATCACCCATACATAAAACCAAATCTAGCAACATTTTAGCTAATTGCACCA
Associated Phenotype:
Not determined