Busch Lab

ZMP

si:dkey-109i21.1

Ensembl ID:
ENSDARG00000043806
ZFIN ID:
ZDB-GENE-091113-23
Human Orthologue:
POSTN
Human Description:
periostin, osteoblast specific factor [Source:HGNC Symbol;Acc:16953]
Mouse Orthologue:
Postn
Mouse Description:
periostin, osteoblast specific factor Gene [Source:MGI Symbol;Acc:MGI:1926321]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa34911 Nonsense Mutation detected in F1 DNA Not yet available
sa34910 Nonsense Mutation detected in F1 DNA Not yet available
sa34909 Nonsense Mutation detected in F1 DNA Not yet available
sa41666 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34911
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017240 Nonsense 116 1016 4 26
ENSDART00000134176 None None 153 None 7
ENSDART00000147677 Nonsense 116 695 6 20
Genomic Location (Zv9):
Chromosome 10 (position 26430120)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 25833977
GRCz11 10 25795690
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGTTTATGGCACCTTGGATCTGGTAAAAGCCAAAACCACTCAGCAATA[T/G]GCGGATCAATCCAAACTGAGGGAAGAAATTGCGGGAGAAGGATCTTATAC
Long Flanking Sequence:
TAGATTGTAATATTTTGCTTGGCTTATCATCCACTGCTCAATAACTGCATATCATGAGGTGTCTGTTGTACAAATACTTTAAAATTCAATGCTGAATGTTAATATATATGGTTATTTATATTGGTATATGCCAACAATTACTGCACATTCGACTTCATTTTAAGGTCATGCTTGGATTAAATGTCAGGTTATTCATTGACTTGGAGTTCAGCAGAGGAGAACCTTAGATTTTGTTCTATAAACAAGACCTGAATCCAGCTGGCTGTATAGTTAAACATGAGGTTAATGTGCCACAGCTAGTCTTGAAGGTTCACATCTTCTGAATGGAGCCTGACTTTGGATTATGTGTTGTATTGTTACTCTGTCTATTTGCTGGAAACCTACATGAGAGTCTTTGTGCTAATGTGAACTCTGTAAACTTTGCTCTTTCACCCAGTGGCCCCCATTGACAGCGTTTATGGCACCTTGGATCTGGTAAAAGCCAAAACCACTCAGCAATA[T/G]GCGGATCAATCCAAACTGAGGGAAGAAATTGCGGGAGAAGGATCTTATACAATATTTGCGCCCAGTGACGATGCCTGGGAAGAGTTAGATCCTGTGAGTCACTTCTTTCAAGCCGCAGTATTTGCATGCTGTTTAAATCGCTGATCCAATGTGTGTGTTACTAATAAGCATGTTAGAGCTCTCAGTGGAACTTATTCAAAAGAAATAAATTCAGGAACATGTAGTCATGCTTTTCAGATTTTTTCCCAGTGCAAAGCTCTCACGATTGATCAATGTCTTTATATTTGCAGGCATCGAAGGCTGCTGTGATCAGCCTTGGAAACACTGAGCTTTACAATGCACTTCACTATCACATGGTCAGCAAACGGTTTCTCACCAAGGACTTGAAGAATGATATGACCCTGGAGTCCATGTTTAACAAACAAGGCCTCCATATCAATCACTACTCCAATGGAGTATGTTTCTCTTTCCTTCTGATTCACTGTGTGTGAATGAAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34910
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017240 Nonsense 162 1016 5 26
ENSDART00000134176 None None 153 None 7
ENSDART00000147677 Nonsense 162 695 7 20
Genomic Location (Zv9):
Chromosome 10 (position 26429785)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 25833642
GRCz11 10 25795355
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCAGGCATCGAAGGCTGCTGTGATCAGCCTTGGAAACACTGAGCTTTA[C/A]AATGCACTTCACTATCACATGGTCAGCAAACGGTTTCTCACCAAGGACTT
Long Flanking Sequence:
TTTGGATTATGTGTTGTATTGTTACTCTGTCTATTTGCTGGAAACCTACATGAGAGTCTTTGTGCTAATGTGAACTCTGTAAACTTTGCTCTTTCACCCAGTGGCCCCCATTGACAGCGTTTATGGCACCTTGGATCTGGTAAAAGCCAAAACCACTCAGCAATATGCGGATCAATCCAAACTGAGGGAAGAAATTGCGGGAGAAGGATCTTATACAATATTTGCGCCCAGTGACGATGCCTGGGAAGAGTTAGATCCTGTGAGTCACTTCTTTCAAGCCGCAGTATTTGCATGCTGTTTAAATCGCTGATCCAATGTGTGTGTTACTAATAAGCATGTTAGAGCTCTCAGTGGAACTTATTCAAAAGAAATAAATTCAGGAACATGTAGTCATGCTTTTCAGATTTTTTCCCAGTGCAAAGCTCTCACGATTGATCAATGTCTTTATATTTGCAGGCATCGAAGGCTGCTGTGATCAGCCTTGGAAACACTGAGCTTTA[C/A]AATGCACTTCACTATCACATGGTCAGCAAACGGTTTCTCACCAAGGACTTGAAGAATGATATGACCCTGGAGTCCATGTTTAACAAACAAGGCCTCCATATCAATCACTACTCCAATGGAGTATGTTTCTCTTTCCTTCTGATTCACTGTGTGTGAATGAAATCATGCCATTGTATTGCAGTTATTTATGTCATATTTATAAATATTTTGAATATATTCATTTTTAGATTTTCAATTTTCCCTTTATTTAGGTTTCGGTTTTAGAAATGATATTTTATCTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTCAGCTTTTCTTTTTTTATGAATGTAATCTAATTTTAGTGATTTTTATCAGTTTAACTTAATTTGACTTTAACTTTTTAGTCTAAATGCATTATTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34909
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017240 Nonsense 586 1016 13 26
ENSDART00000134176 None None 153 None 7
ENSDART00000147677 Nonsense 586 695 15 20
Genomic Location (Zv9):
Chromosome 10 (position 26415801)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 25819658
GRCz11 10 25781371
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGCATCTTTATTAACGGAGGTCTGGAGGGTGGAGTGACTAACCTCCTC[A/T]AGACCATACAGGGAAACAACCTTCAAGTGCTGTCTGTAAGTAGACAGTTA
Long Flanking Sequence:
TGATTATTGTTTATACACAAACATAATATTGTATAGTATCCTATAGAAAATGTAATAAATGAAAAGAGAGATCTGAGGGGTGTACTAATTTAAGCTGGACACTAATTATAGTATTGTATTTAAACATTGAAATAAAAAAATTATAATCCACCAACTGTCTGAATCTTTCCAGAATCTTCCTATCTCTGATGGAGAGTGCTGGACTGACAGATCTTCTCAAGCAGGATGGATCCTACACACTCTTTGCTCCTATAGATGCTGCCTTTGGCTCTCTGACAAAGGACGACCTTGCTCTTTTAAAAAGTAAATCTTTTTAATCGTTATTATTTTCAACATTATTTCTGTGACTAGATCAACTTTTGCTTAGTCTATTGTCCATTCACACTGTGGCTGTTTGTTATCCAGGTGACATCAATGTTCTCAGAACAATCCTGCTGTATCACTTCAGCAACGGCATCTTTATTAACGGAGGTCTGGAGGGTGGAGTGACTAACCTCCTC[A/T]AGACCATACAGGGAAACAACCTTCAAGTGCTGTCTGTAAGTAGACAGTTATTCGTTCATTAATTTTCTGCATGCCCTTCTAGCTGCAACCCTTCACAGGGAAACACCCATACACTCTCATTCACACTCATACACTACGGACAATTTACAGTAGCTTACCCAATTCATCTACAGCGCATGAAACCCACGTGAACACGGAAAGAACATGCAAACTTCACACAGAAATGCTAACTGATCCAGCCAAGGCTCAAAACAGTGATCTTCTTTCTGTGAGGCGACATCGCTACCCACTGCGCCACCACGTTGCCCTGTGCACAGTTATATTTAGATAAAATTTGTACCAGCTGAGGTTTTAAGGGCCTTATCCAATACCACAATTAGCAAAAAATGTAGCCGTTTCCTCAAATATCAGCCTTTTTCCTAAAAGCGATTGTTAAAAGTGACTAATAATGAGCTTTTCCAGTCACATGATTAATGTTTTCACACTCCCCAACAAAACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41666
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017240 Nonsense 662 1016 16 26
ENSDART00000134176 None None 153 None 7
ENSDART00000147677 Nonsense 662 695 18 20
Genomic Location (Zv9):
Chromosome 10 (position 26409417)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 25813274
GRCz11 10 25774987
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTTTGTATGTGTGTGTGTGTAGTTTGTATCTGGATACACCTAT[C/T]GAGACATTCCACTTACATTTATCAGTAAGTTTAGTTTTATTCTTCTTTCA
Long Flanking Sequence:
TAAATTCAGTGGATGTTCCAGATTTTGATCTTATGGCATCCAATGGAGTAGTCCATGTTGTGAAAACCTTATTATATCCTCAAGGTAAAGTTATGCAAGGAATTTGTGTTTAGATGCACATACATATATAAATATATATTTAGATGCACAAAGTCAAAATCAGTTGCGTAGATCAAGTTTATCGTAGTAATACCTGGATTTTCCACAGTTATATAACCATACAATTCCTGAGACATAAGACACAGTCCCTTGAGCTTAATAGAAAATTTTACTGCATTTCACAGATCTGCCAGTTGGCCGTGAAGACATATTGATTCTGCTGAAGAGACTCATCAAATACATGCAGCTGAAGGTACAGCAGAACACACATCATATCTGAACACTGACTCACATTATATAACAGATCCATCATGGTCACCAAACAAACACATAGCATTTTATCTTTTTTTGTGTGTGTGTTTGTATGTGTGTGTGTGTAGTTTGTATCTGGATACACCTAT[C/T]GAGACATTCCACTTACATTTATCAGTAAGTTTAGTTTTATTCTTCTTTCATTTTTGTCTTTAAGTTACACTTAACCTAACATCATCAGCAACAGCATCTGGAATTAATTTGATATGCTTTATTTATTTATTCATTTATTCATTTATTCATTTATTTATTTATTTATTTATTTATTTGTTTATTTATTTATTTATTTATTTATTTATTTATTTGTTTATTTTTTATTTATTTTTTATTTATTTATTTATTTTTTATAATAACTGTTGTTTTCTTGTCTTGCAGAGAGGACTATAACTACTCATGTCATTGAGAGAGGTAATACATTATTATATTAATGTATTTTTTTATTATTATTATTTTTAGTCACCTTTGAAAAAACACTTTTTAATTTAATTTAATTTAATTTTACCTCCGTATAACCACTGTATACTTTATTTTCATTTTCTTTTCGGCTGAGTCCTTTTATTAATCTGGGGTTGCCACAGCTGAATGAATCGCCA
Associated Phenotype:
Not determined