ZMP
si:ch73-9j13.1
Ensembl ID:
ZFIN ID:
Description:
LOC563577 protein [Source:UniProtKB/TrEMBL;Acc:Q5D017]
Human Orthologue:
PPP1R13B
Human Description:
protein phosphatase 1, regulatory (inhibitor) subunit 13B [Source:HGNC Symbol;Acc:14950]
Mouse Orthologue:
Ppp1r13b
Mouse Description:
protein phosphatase 1, regulatory (inhibitor) subunit 13B Gene [Source:MGI Symbol;Acc:MGI:1336199]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18096 | Nonsense | Available for shipment | Available now |
sa23020 | Nonsense | Available for shipment | Available now |
sa15553 | Nonsense | Available for shipment | Available now |
sa17119 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18096
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037371 | Nonsense | 63 | 1110 | 2 | 18 |
The following transcripts of ENSDARG00000004377 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 14505639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14656467 |
GRCz11 | 17 | 14664400 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATAATCAACAGTTGCTGACCGAGGTGCCCATTACYCCAGAGACGCTCTG[T/A]AARGATGTGGTGGARTTCTGTAAGGAGGCCGGAGAGAGCGGCTGCCACCT
Long Flanking Sequence:
GTTTAAGCCTCTTTAATAAAAACCCTGCTGGATGATCCTTAAAGTATCATCTAATGCCAGGATTAAATAACTCTTACATTGTCGTCTGGGTATGACACAAAATAGGTTGTCCTTTCCAAAGTTTTGACATTTTCCATTTTGTGTGCTTAAAGTCTTCTCGCCAATATGCTTGGTTTTGGTATGTAGGAGATAATAGCTCAGAAATAATGATTACTTATTCTTGAATAAACATGCAATTCCCTTGATTTCAACTCAACTTGTGAATGTCCTTTAATTGGCCTTCGTCTGCCTTTGCAACTCATTTGACCACTGGAATAATGAATGTAAACAGTTTGAGAATTATAAGGCTAAGATGAAGCCCACACAGTCAAAAATGAGAGGCTGTAAGTTGACTCAGATAACCTCAATATTCTTTCCTCTTTGCAGACGATTCTGACCGTATTCCTGAGTGATAATCAACAGTTGCTGACCGAGGTGCCCATTACTCCAGAGACGCTCTG[T/A]AAGGATGTGGTGGAGTTCTGTAAGGAGGCCGGAGAGAGCGGCTGCCACCTCGCTGAAGTCTGGAAAGGAAAAGGTACCCATCTACCACCCTACAGTGCCTATAGAAAGTAATATTTGAAATAAGTACCTCCGTGAAGTTGGCACCCCATAAAAACAAATAATCCCCAAAACTATGCCATTCGTTTGTGCAACGTTTGTGTTGATTTGTGCCGCAAAAACGAACGTTTGAGCTGGTTTGGGGTCTGAGATATTAAGCATTATTTTTTTTGACCGTGTGACGTCACTCTCCACCCCTTGTTGTGCAAATGACTTCAAAACAGCACAGGTCGTTTGTGCTCGGTTTGTGCTGGTTTGTGTCGTTAAAACGAACACGGTATCCGTTTTCCTCCTTTCGATATAAGCAAAATATTTCGGGAGCCGTGACGTCACTCTCCACCCCATTTCCTCTAAATCACACAAAACTGGTCTCATTCGTTAGTGCTGGATTTGTGCTGGTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23020
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 |
---|---|---|---|---|---|
ENSDART00000037371 | Nonsense | 187 | 1110 | 6 | 18 |
The following transcripts of ENSDARG00000004377 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 14468676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14619504 |
GRCz11 | 17 | 14627437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCCTCTCCTGTCCTCTCCTCCCATTTCCGCTCCGTCTTTTAGGAGCAA[C/T]GATTGCGGTATCTCAAGCAGCAGGACCCATGTCAGGGCCAGTCTGCGTCT
Long Flanking Sequence:
ATTTGCTCATTCTTAAGCAGACCTGAAAGTGCTAGTCAGCATGACCGCCTATGCTTCCCTCTGCTTTCTATTTTAGTCCCATTCATCATGCATTCACTTTTTGGTTGTGTAATGTTGTAATATCTCAAATATCTGAATCTTTCATACTGTTTGGGTAATTAGTGTTTGATTTTTCTCCCTTTTTTGTTGTAAGATGCATCTTTCATCGTCTCTGCTGACGTTAAATCTTAGTATTCATATTCTGTGAGGCCACTGGAATTAAATATATGTTCTTTTTTATTTCCTCTCTCTATTTTACCCACTCCTTCCTTATTGGCTTCATCCCATTCTTGTGAAGCTCTCCATTGTGCGTAGTGAGGTGTGTGTGAAAGGGCTTTTGTTGATCGGTTGCAAGATTGTTTTGATGATCAGTCAGTGCAGCATGTTCCTTCCCATTCCGTAATTGACCGTCACCCTCTCCTGTCCTCTCCTCCCATTTCCGCTCCGTCTTTTAGGAGCAA[C/T]GATTGCGGTATCTCAAGCAGCAGGACCCATGTCAGGGCCAGTCTGCGTCTGAGAGTGACAAGCTCCAGAGGTTGAGGGAAAGAGTGGAGAATCAAGAAGCCAAACTCAAAAAGGTCCGTGCCATGAGGGGTCAAGTGGACTACAGCAAACTCATCAATGGCAACCTGTGTACGTACAACCATGTAAATTTCAAATGTTTTAAAGTTCCAATTCACATTTGTAGACTGTATAAACAGATGCTATTATTTGTCAAAGGATGTCCAGGCTGTGTTTTTAAGGTGGTGGGGTATTGCAGATAAATAGGTCGTTGAATGCCAAAAATGCCAATTTACTCACCATTTACCACCCTTATCCTAATCCTGCATGAGTTTGTTTCTTCTGCTGAAGATATTCTTTAAAATGTTGATAACCCAAAAGTTGACAGCTGCTGACGCTAGTAGCCTTGTGGTTAGTGTGCCAACCTATAGCACTAAGGGCGTACTCACACTAGGTACAGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15553
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 |
---|---|---|---|---|---|
ENSDART00000037371 | Nonsense | 638 | 1110 | 13 | 18 |
The following transcripts of ENSDARG00000004377 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 14459973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14610801 |
GRCz11 | 17 | 14618734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTCCTYATTTTAAACTTTATTTATTTTAATTTTCTTACAGTATATGGA[A/T]AACCAGTCCTACCAGGCTCCACCTCTCCRTCTCCAGTTCCACTCTACCAG
Long Flanking Sequence:
CAGTAACAGCATTGTCTAAGCAGCCTCCACCCATCTATGGAACCTATCCCAGTGCAGGCCATCACTCCACAGTCTGTGCTACCAGCTCTTTGCCCCGCTCTGCTCCTGGCACCCTAGGTTGGCAGAGAGCACCCCCCACCTCTGGTTCCACTTCACAACAAATCCAACAGCGGATTACTGTGCCTCCCAGTCCTACGCCTGGGTCAGCTCTTTTTCCTCACGGTGAGAGAACAGAACCTCCTCTTGCTGTTGCGGTGCGTCCCTTTATTCCAGACAGAGGTTCCAGGCCCCAATCTCCAAGGAAGGGCCCTGCCACGATGAACTCCAGCTCAATCTACAATATGTACCTGCAGCAGCCTACAGCCAAAAACTACTCCGGTAGCAGCAGAACTGCTGTTAAAGCAGGTAAGATGCAGTTGCAGCTAAGCAGGAAATTAGCTTAGACTACACGTTTCCTTATTTTAAACTTTATTTATTTTAATTTTCTTACAGTATATGGA[A/T]AACCAGTCCTACCAGGCTCCACCTCTCCGTCTCCAGTTCCACTCTACCAGCAGTCATCCACAGATGAGACAGACAGAGAGGCAGCCCAAGAGAACCATCCCTTACCTCCTTCTAGTGTGGAAAACATCCCTCGCCCTCTCAGCCCTACCAAGCTGACCCCTGTTGCCCACTCCCCTCTCCGTTACCAAAGTGACATTGATTTGGAGGTGCTAAGAAGGAAGTTATCCAATGCTCCCCGACCACTGAAGAAGAGAAGCTCCATCACAGAACCAGAAGGCCCCAGTGGGCCTAACATCCAGAAGCTCCTGTACCAACGATTCAACACCCTTGCAGGGGGTATTGAGAGTGGAGTAGGTGGTACACCCTTCTACCAGCCTGACAGTCCTCTGAACTACATGGCCACTGCTTTGGGCAATGTAGACACAGCTAATGGGAACCTGATGGAGTCAAGCATGTTAGTTGAGCCTTCAGCAGAGCTGGTAATGGTTCCTCCTCCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17119
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 |
---|---|---|---|---|---|
ENSDART00000037371 | Nonsense | 743 | 1110 | 13 | 18 |
The following transcripts of ENSDARG00000004377 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 14459658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 14610486 |
GRCz11 | 17 | 14618419 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAACCAGAAGGCCCCAGTGGGCCTAACATCCAGAAGCTCCTGTACCAA[C/T]GATTCAACACCCTTGCAGGGGGTATTGAGAGTGGAGTRGGTGGTACACCC
Long Flanking Sequence:
CGATGAACTCCAGCTCAATCTACAATATGTACCTGCAGCAGCCTACAGCCAAAAACTACTCCGGTAGCAGCAGAACTGCTGTTAAAGCAGGTAAGATGCAGTTGCAGCTAAGCAGGAAATTAGCTTAGACTACACGTTTCCTTATTTTAAACTTTATTTATTTTAATTTTCTTACAGTATATGGAAAACCAGTCCTACCAGGCTCCACCTCTCCGTCTCCAGTTCCACTCTACCAGCAGTCATCCACAGATGAGACAGACAGAGAGGCAGCCCAAGAGAACCATCCCTTACCTCCTTCTAGTGTGGAAAACATCCCTCGCCCTCTCAGCCCTACCAAGCTGACCCCTGTTGCCCACTCCCCTCTCCGTTACCAAAGTGACATTGATTTGGAGGTGCTAAGAAGGAAGTTATCCAATGCTCCCCGACCACTGAAGAAGAGAAGCTCCATCACAGAACCAGAAGGCCCCAGTGGGCCTAACATCCAGAAGCTCCTGTACCAA[C/T]GATTCAACACCCTTGCAGGGGGTATTGAGAGTGGAGTAGGTGGTACACCCTTCTACCAGCCTGACAGTCCTCTGAACTACATGGCCACTGCTTTGGGCAATGTAGACACAGCTAATGGGAACCTGATGGAGTCAAGCATGTTAGTTGAGCCTTCAGCAGAGCTGGTAATGGTTCCTCCTCCCACCGCTTCTGTGTCTCCTACAGCTGATGACAATGAGAACAAGTTGACACATCTTTCTAGTGACTCAGGGGGTGCCCAGTCTGCTGATGCCTTAGAACATTCTCTTAAAGACACCCATGAGGACAATCATAACAACAACCACACAAATGTCACGGACACACAACCTAGTTCAGTACCAGAACCCCACTCCCCTGCAGAGGAAGACATCACAGCACAGTCGGGAATGTCTCCTGGTTTATCTACCGTGAGTTTGCGATAGCATGTTGTCTAGATGTAGATGTACCCTCTTTATCTAATATAACACTTATTCATTGTATTC
Associated Phenotype:
Not determined