ZMP
bmp7b
Ensembl ID:
ZFIN ID:
Description:
bone morphogenetic protein 7 [Source:RefSeq peptide;Acc:NP_001070614]
Human Orthologue:
BMP7
Human Description:
bone morphogenetic protein 7 [Source:HGNC Symbol;Acc:1074]
Mouse Orthologue:
Bmp7
Mouse Description:
bone morphogenetic protein 7 Gene [Source:MGI Symbol;Acc:MGI:103302]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37612 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17005 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37612
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092214 | Essential Splice Site | 248 | 427 | 3 | 8 |
ENSDART00000138020 | Essential Splice Site | 248 | 427 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 6494190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 6509405 |
GRCz11 | 23 | 6443377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCGGGCCGTAACCTGGGCCTGCAGCTGGCTCTGGACAGTCTGGACGG[T/A]GAGCAAAATGAGCAATGCATTCACAAATCTGCCATTCAGAGAGCACGCAG
Long Flanking Sequence:
TGCGCTGTTTCATTTGCACACATACATAAGTGCTCGCTCGCTCGGGAGTAGGGAGCAATATTGCTAGAATATTCGCAGGTCGCAGAAATCTGGTCGGGTCCCGTGGAAGACCTCTACTAAGGGGTAGAATTGGGATTGGGCCTAAATAGTGAGTAAATTTTCATTTTTGGGTGAACTATCTCTTTATTTTTCATATAAAATATCATAGAATGTAAAATATGCACAAAAAGTCATTTGACAGGTTATCTCTATCTTTCCTTCATGCTGTAATGACTTGATTTGTGTGATATGTTTGATGTGTTACGCTGGTCTTTTCTTCATCATCATCTCGCTCTCTGTCTGTCGATCAGGGATTCAGATTTGTTCCTGCTGGACTCGCGGGTGATCTGGGCAGCAGAAGAGGGCTGGCTGGTTTTTGACATCACAGTCACCAGTAACCACTGGGTGCTGAACCCGGGCCGTAACCTGGGCCTGCAGCTGGCTCTGGACAGTCTGGACGG[T/A]GAGCAAAATGAGCAATGCATTCACAAATCTGCCATTCAGAGAGCACGCAGAGAGCACGCTATGCTTCCACACACATATTTTTATGCACATTTTGGAATATTGCATAAAAATGCTGACCGGGAATGCCAGGATGTGTGTAAATTTAGAAAAAAATTACAATGAAAACACATTTACTGCAAAAAAGTGTATAGATTCCAGCAGGTGCATCAAAAATGTCATGTGATTTGTAAATGTAGCTTTGGTCATTTTAAAGTGCCTTAGCTGAAGTCCGTCATCAAAGTGGTTCAGTGCACTTTAGTGGGCTTTTGTACTTTCATAATGTGCTTTTCAGTTTAATGTTAAGCATTTACGTTTTTAGATATAACCTTTAAGTGCTTCATAACCTTTGTTTTGTGTCGATTAAAACTGCAATACATATTTTTTAAAGGTGGTTTTCTCAAAATTAGTTATTCCCCATACATCCACATCAAAATCAGAATCAGTTTTATTGCCAAGTGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17005
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092214 | Nonsense | 267 | 427 | 4 | 8 |
ENSDART00000138020 | Nonsense | 267 | 427 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 23 (position 6488739)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 6503954 |
GRCz11 | 23 | 6437926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGAACCCCTGGGTGGCGGGACTGGTGGGGCGCAGTGGCCCTCAGAGC[A/T]AACAGCCCTTCATGGTGGCCTTCTTCAAAGCCACGGAGGTCCACATCCGC
Long Flanking Sequence:
AAAAAAAAGGCACATATGGTATGAAAAAGAGTTATAAAACATTAGTTGCGGGATGTTTCGAGCTAAAATTTCACATACGCACTCTAGGGACATCAGAGATTTACGATCTTGTAAAAAGAAGTATAATAGTTCCCCTTTAACAAAAATGATTTGATGTAAAGTTGCAATTACAAATTCATGATAGAAGTCAATATATTCTGCTGCAGAAATTGCTCACCCACAGTAATATCCGATTCAAACTCACACTAAAAATGTTTGTCACCCATTATCCAGATGAAAAAGATCTTGTATAACTTTACAGTACTGCTTTCCCTCATGGATTTGTACCTGTCAACATTTCCACTAACAATCTCAAGATGTATTTCTCTCCTCTATTATCTCAGCATCATAAATGATTGTTGTGAAATGATGAACTGTGAAATCTCTCTCTGTCTCCCCCTGCAGGTCAGAGTGTGAACCCCTGGGTGGCGGGACTGGTGGGGCGCAGTGGCCCTCAGAGC[A/T]AACAGCCCTTCATGGTGGCCTTCTTCAAAGCCACGGAGGTCCACATCCGCAGCATCCGCTCCGCTCAGGGCGGAAACAAGCAGCGCAATCCCAACCGCTCCAAAACCGCCAAGGGCCAGGAGGCGCTGCGTGTAGCCAATATTGCAGGTGTGTGTGGCTGACGTGTATTGAAGGAGGCAGGTGAAGAAAGACATATAGTAAGACCAAACTGAGAGAAAGGCACTTAGTATAGTTCTGTGCCACCCTGAAAATAAAAAAAAATATATATGGAAAAACCATTATTTATAATATATGCTAAAGGAATTAGGAATATTCACGTGGAAAAGAAGTGTACTGAAGTGTGACACTATTTATTATGCAAACTTGTAGTGTACTGCAAATTCACAATATATTTTTATACACACTGTATACTATTTTTAATGCTCTTAATTAAAAAAAAATACTGTTTCAAAACAAGTATATACACTGTACAAATAATCCGTAATTTTACATTTGTAATG
Associated Phenotype:
Not determined