Busch Lab

ZMP

si:ch1073-219n12.1

Ensembl ID:
ENSDARG00000063580
ZFIN ID:
ZDB-GENE-091204-412
Human Orthologues:
PPP1R9A, SAMD14
Human Descriptions:
protein phosphatase 1, regulatory (inhibitor) subunit 9A [Source:HGNC Symbol;Acc:14946]
sterile alpha motif domain containing 14 [Source:HGNC Symbol;Acc:27312]
Mouse Orthologues:
Ppp1r9a, Ppp1r9b, Samd14
Mouse Descriptions:
protein phosphatase 1, regulatory (inhibitor) subunit 9A Gene [Source:MGI Symbol;Acc:MGI:2442401]
protein phosphatase 1, regulatory subunit 9B Gene [Source:MGI Symbol;Acc:MGI:2387581]
sterile alpha motif domain containing 14 Gene [Source:MGI Symbol;Acc:MGI:2384945]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa733 Nonsense Available for shipment Available now
sa38721 Nonsense Mutation detected in F1 DNA Not yet available
sa34545 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa733
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000093021 Nonsense 252 1317 1 18
ENSDART00000139476 None None 145 None 3
ENSDART00000146148 None None 308 None 7
Genomic Location (Zv9):
Chromosome 9 (position 3054949)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3050421
GRCz11 9 3056441
KASP Assay ID:
554-0640.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGTGGTGATGATAAAGAGTCAACRCAAGTAATCCCTGAGAAATCGAGC[A/T]GACCTATACAGGYAAGTTTCCAAAAAACAAGCTCACCTGCAACTGATTCA
Long Flanking Sequence:
ATGCTTCTCCGGTATCCCCAGTATCTCCAGTGTCCAAGTTTGCAGTTAACACCAACAAACCAAATAGTGCCAACAGCCAAGAACCGCAGAACACTGACAGAAAAGCAGAGGAAGTGGAGATCGATAAAGTCGCCCTGGCGGAGAAATTCTCAGTGACCAGAAAGCTCTTCGAGAGAGGCATTAAGGATCAGCCTGCTACAGAAAGGCCGATCCCTGGAAGAACATCAACCCGACTGTCCCACGGGAAAGTTCCCGATGATGCAGTCCGTGGGTCCAGGAGATCCTTTGGATCTTCAGAAAGCATGAACACCAATAGTGCCATTAAAACCCCTCCAATATCACCTGTAAGGAGCGTCTCAGATGAAAAGGGCATTGATGAGTCCAAACAGGTCAACCGATTATCACTAAACGCCGGACCCATTTCCAGACGACTGGAGAACTTCATTGTGGATGGTGGTGATGATAAAGAGTCAACACAAGTAATCCCTGAGAAATCGAGC[A/T]GACCTATACAGGCAAGTTTCCAAAAAACAAGCTCACCTGCAACTGATTCAACACAGAAACCCCTGAACGCTGACTCTTCACACGAACTATCCTCGCCTAAATCCGACCCAATATCCAACATCAGCCCAATTTCAATCAAGCTATCCTCCTCGTCCAGCACTGGTGAGCTTAATTCGCCGTCCACCAATCACATCCCGTTTAAACGTTCATCGTCATCATCCGGGAGTGATTTGGTCAAACCATCCGCCACAAACGAATCCACAAAAGATCCCAAATCACCTAGTAGTCCCTGTAACTCGTCCCAGAGTCCGGAGGAACCCAAAAGTGATAACCACATCATTGGCAGTTCCTCTCGTGAGCAGTGTTTGGACCCCGCTGGGGCAGGAATGGTACGGGCTGAGCTGGTGGTGGTCCAGAATGAATCCTCAGAGAGTGATGATGATGAGGATGAGGATTTATTGGAGGATGTTATGACTGAGGTGAAGCTTCAAAGGGAACTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38721
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000093021 Nonsense 784 1317 7 18
ENSDART00000139476 None None 145 None 3
ENSDART00000146148 Nonsense 231 308 6 7
Genomic Location (Zv9):
Chromosome 9 (position 3098732)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3094204
GRCz11 9 3100224
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCCAGATAAAGCACACCATCGCAGAAGCTGAAGTGGATGAGCTGAAA[G/T]AGAGAGTATGAACCTGTAAACCATTTACATTTGAAATCAGAATCATTAGC
Long Flanking Sequence:
AAATAAAGCTCAGATTTGATAGACGAGACCAGCAGAAGCATCAAGAGTTTGACACTCTGTTGGAGTCTGTGTACAACTCACACCTGAGCAATGCATGTGACTTCATTCCCCATATGAGAGGCGTCTTTAAGCTGCAGCACCAAAAAAAGCCTCTTATATAAAGTATTAAACACATTTCAGTAGTTCAGGACTTTCTCCTTGTGTCATTCCACTGTTATCACACACAACCTTTTTTTCCGTTTTGTTTTTGTTTTTTGTATGTGTGTATATTTACAATAAAATATGGTCTATATTGTGCTTTAATTTCAGCTACTTTGTACTTAATTTAAACATATTTCCATATATTTTTGTAATTCTGTGCATATTGTGCTTTAATTTTAGCTACATTTCACTGTCTGTTAACATATTTCTATTAGTTTTGTAACTCTGTCTATATTGTGCTTTAATTTCAGCTCCAGATAAAGCACACCATCGCAGAAGCTGAAGTGGATGAGCTGAAA[G/T]AGAGAGTATGAACCTGTAAACCATTTACATTTGAAATCAGAATCATTAGCCCTCCTGAATTTGAAGGACCCTATATTTCCCCTAATTTCTGTTTAACAGAAAGAAGATTTTTTACCACATTTCTAATCATAATAGTTTTAAAAATTCCTTTCTAATAACTGATTTATTTTATCCTTGCCATGATGACAGCAAATAATATTTTACTAGATATTTCAAGACACTTCTATACAGATTAAAGTGACATTTAAAGGCTTAACTAGGTTAAATTAGGTTAAAGTTAAATATTGTCTTGTAGATCTTAAATAATTTTAAATGCCTCTTAATTTTTCCTTTGTTTATGTAAAGCTTCCCAATCGATCCAACACACATCCAATCACCAATACATTTCGCTAAAACTTTTAGAAAAACTTCATATATAACTAATGTTTGAACATATCTGTTGTGTTTTTAAAGTTATGTTGAAAATATAGTATGTATAAAACTAGGGTCTGCTTATTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34545
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
ENSDART00000093021 Nonsense 893 1317 9 18
ENSDART00000139476 None None 145 None 3
ENSDART00000146148 None None 308 None 7
Genomic Location (Zv9):
Chromosome 9 (position 3104539)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 3100011
GRCz11 9 3106031
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGGATGAAAGAGAGAGCGCATATAAGAGTCAGATCGAGGATCTGCAG[C/T]GAAGGGTGAGAACTCACATCATACAGACAAAATCACTCGCACATAAAGCA
Long Flanking Sequence:
ATGGGGTCTTTTTGCGTATGATCACCCTTATGTATCCCTTTTAAATGTAAGAGTGTTGCATAAAATAATAAAGTAGTTTTAATTTATAGTGACATTCTTTGCTGCCTCACACTTATACACTACGGACAATTTAGCCTACCCAATTCACCTGTACTGCATGTCTTTGGACTGTGGGGAAAACGGGAGCATCCGGAGGAAACCCACGCGAACGCAGGTAGAACATGCAAACTCCACATAGAAATGCCAACTGATCCAGCTGAGGCTCAAACCAGCGACCTTCTTGCTGTGAGGCGAGAGCACTACCTACTGCGCCGCCGCATCACCTGTACATAGTATTTTAGCTTGTAATTTATAAATGTAATGATTAGTACAACTTTTCTGATTGGCTGGACGTGTTTGTGTCCTGTAGAGAGGCGGAGTTTGAGCAGAGGGAGGAGGAGTTAAAGAGGTCTCTGGATGAAAGAGAGAGCGCATATAAGAGTCAGATCGAGGATCTGCAG[C/T]GAAGGGTGAGAACTCACATCATACAGACAAAATCACTCGCACATAAAGCATCCATGTTTTCTGATACCCGTCTCTCCATTTCTCTGAATAGCTGGCGAAACTCGAATCTGGCCGTGGTCATAATGAGTCTTCATTGTCGGGCAGCAAGTCTGCAGATTCACTTCTGCTGGGTGAGTTACTGTAAAGCTGATTTTTAATGCCTTTTTAATTAATTTTGGCAATGTAAATGTGTATTATGTCATTTTAATTAGTTTTTATTTAAATGACTATACAATTTAAATTTATTTTTAATTGAGCTTTAGTTTTAGTTTGTTACATATTATATTTATATAGTACTTTTCCATTATTGTTATATTGTTAGTTTACTATAATAATCCTACAGACAAGATACAAAGCACATGATTATTTGTATAGGATTTTTTGGCTGTTCATAAAAAATTCACCATCACAGCAAAGTTTGTCACTATTTGCACCTCCCCCAATTTTTTCATCTGTGCCAA
Associated Phenotype:
Not determined