Busch Lab

ZMP

LOC562087

Ensembl ID:
ENSDARG00000076011
Human Orthologue:
PPM1K
Human Description:
protein phosphatase, Mg2+/Mn2+ dependent, 1K [Source:HGNC Symbol;Acc:25415]
Mouse Orthologue:
Ppm1k
Mouse Description:
protein phosphatase 1K (PP2C domain containing) Gene [Source:MGI Symbol;Acc:MGI:2442111]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa24411 Essential Splice Site Available for shipment Available now
sa18150 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24411
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113757 Essential Splice Site 222 358 3 6
Genomic Location (Zv9):
Chromosome 23 (position 43984816)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 44014983
GRCz11 23 43816501
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAACTCACAGACGATCACACTCCGGAGAGAAAAGACGAGAAACACAGG[T/C]ACACACACACTTACACATACACAGATACTTGCATAGTTGTACTGACACTA
Long Flanking Sequence:
TGTGTGTTTTATTCGACTGCACAGAGCAGCATTATAACGGAAACCTAAAATGTATTTAGTGTGATAAAACAGTGCTGTACTGTGGTATAATAAAAGCTCCTCTACTTTCGTATTTTGTATACAATTTTCTTAGCCACGCCACTCTTACCATTACTTTGCTATGAGGGAATGATGCAGAAAATAAAGCCCCGCCCCCTACTCAATATTCAGCTTTCATTGGAAGAACATCGACATAGTGAAATATAAGTCTCAGCAATTTCCACATAACACAGACTTTATTTAAAGTAAACAACATAATGAAATGACTTTAAATTATGCGTGTTTGCTGTTCAGCCTCCCTCATGATGGTGGGCACGACGGCGACAGTGGCTCTGCTTCGGGACGGCATTGAGCTGGTGGTCGGCAGCGTTGGAGACAGTCGAGCTCTGCTGTGTAGGAAAGGAAAATCACGCAAACTCACAGACGATCACACTCCGGAGAGAAAAGACGAGAAACACAGG[T/C]ACACACACACTTACACATACACAGATACTTGCATAGTTGTACTGACACTACACGACCTGACAAGCAGCAAAGTTGCTTCTAGTTGATGTGTAAAAGTGTCAGAAGGTGGATTTTTCTGTTGTATCATCTGTTCTGCATCCCGATCATTACCAATACTGCAGAAGACCTACTGGAACCCACATGGAGCCAAGATCCTCACAGAAATCAGTCAAGTTTGGTGAAGGAAAAATCATGGTTTGGGATTACATTCAGTATGGGGGTGTGCGAGAGATCTGCAACATTAACAGCCTGAGGTATCAAGACATCTGTGCTGCCCATTACATTACAAACCACAGGAGAGGGACAATTCTCCAGCAGGATAGCGCTCCTTCTCATACTTCAGCCTCCACATCAAAGCTCCTGAAAGCAAAGAAGGTGAAGCTGCTCTAGGATTGGCCAGCCCAGTCACCAGATACGAACATTATTGAGCATGTCTGGGGTAAGATGAAGGAGGAGGCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18150
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113757 Nonsense 256 358 4 6
Genomic Location (Zv9):
Chromosome 23 (position 43991655)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 44021822
GRCz11 23 43823340
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGTTAACGGCCGCTTGGCAATGACCCGCAGCATCGGAGACTTTGACTTG[A/T]AAAAAAGTGGCGTGATCGCTGAACCAGAGATCACACRGACTCTAGTATGT
Long Flanking Sequence:
CTTTGGCTCTGGATGGCCACAGTCCTCCACTGTACCTTGGTCCCGCATTTATTTCAAAGGAGCGCTACCCTGTAGCAAGATGGAGGCGCTATTGACGCATTCCGTCCAATAGACTAAAATAGGCCAGGCGACATCTAATGTATATATCTATGACTGAATACTAGTATCCTGAAGAATATCTAATCAAATATTATGTGCTGTCATGATGGCAAATATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGGAAAAAAATCTGCTCTCTGTTAAACAGAAATTGGGGAAAAATATACAGGGGGGGGCTAATAATTCTGACCTCAATGGTATATATAACTATTATTATTAAATAATTTAACTAATATGTCTTTTGTAGGATCCGTCAGAGTGGTGGGTTCGTGACCTGGAACAGCGTCGGCCAGGCTAACGTTAACGGCCGCTTGGCAATGACCCGCAGCATCGGAGACTTTGACTTG[A/T]AAAAAAGTGGCGTGATCGCTGAACCAGAGATCACACGGACTCTAGTATGTGCTTTTCACATTATTTCATCCCTATGACTTTTAAAATGTATTCCCTCATTGTTTGACATGAAACCAGGGTGTGGATTACTGGGTGTATGGGTATTTAAGTCCTTTAAAATTGAGAAATAGCTTGCTGTTATTCATTCATTTTCCTTCAGGTTAGTCCCTTTATTCACAGCGGAATGACTCACTAATTTATCCAGCACATGTTTTACACAGCGGATGCTCTTCCAGCTGCAACCCAGTACAGGGAAACACCCATACACACTCATTCACACACATACACTACAGCCAATTAAGTTTATTCAATTCACCTATAGCGCATGTGTTTGGACTGTGGGGGACCCAGCCAGGGCTCAAACCAGTGACCTTCTTGCTGTGAGGCCACAGTGCTAACCACTGAGCCACTGTGTTCTCCCAGTTTGCTGTTAACTTTGTCTTAAATAATAATTTAATAGT
Associated Phenotype:
Not determined