ZMP

ppm1g

Ensembl ID:

ENSDARG00000075559

ZFIN ID:

ZDB-GENE-030425-4

Description:

protein phosphatase 1G (formerly 2C), magnesium-dependent, gamma isoform [Source:RefSeq peptide;Acc

Human Orthologue:

PPM1G

Human Description:

protein phosphatase, Mg2+/Mn2+ dependent, 1G [Source:HGNC Symbol;Acc:9278]

Mouse Orthologue:

Ppm1g

Mouse Description:

protein phosphatase 1G (formerly 2C), magnesium-dependent, gamma isoform Gene [Source:MGI Symbol;Acc

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35411	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35412	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35411

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109665	Essential Splice Site	400	495	9	12

Genomic Location (Zv9):

Chromosome 13 (position 5877044)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	6071069
GRCz11	13	6199529

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTAATTGAATGCATTTTCATTATTGCATGACTAATGGCTGGGTTTCATGT[A/T]GGCGATCACTTTTACAAAAGAAACAAAGCTCTTCCCGCTGAGGAACAGAT

Long Flanking Sequence:

TGTGTGAACCGAACCGTGACCACTGAATTTAGTTGTTTTGATGAACAGATTATTAATCACAGTTGCCGTGTACATTGGAATATAGTGCACAAGGAGCAGAACACACAAACTTATGATACATACTGGTGCGGAGTCATTTTTGCTGACCATTTTTCATCTCCGTTATCCAGCCAGGTTCAGACAGTGGCACTACAGCTGTAGTTGCTCTTATTCGTGGGAAGCAGCTGATCGTGGCCAACGCTGGAGACTCCAGATGTGTGGTGTCTGAAAAGGGAAAAGCGTTAGACATGTCCTACGACCACAAGCCGGAGGATGAGCTCGAGCTGGCCAGAATAAAGAATGCTGGTGGAAAGGTGACCATGGACGGTCGTGTCAATGGAGGACTGAACCTCTCCAGAGCTATCGGTAATGTGGAATACTCTGATTTTTTTATTTATTTATTTTAAATCATTAATTGAATGCATTTTCATTATTGCATGACTAATGGCTGGGTTTCATGT[A/T]GGCGATCACTTTTACAAAAGAAACAAAGCTCTTCCCGCTGAGGAACAGATGATCTCCGCTCTCCCTGATGTCAAAGTGCTGACTCTCAACGATGATCATGAGTTCATGGTTATTGCATGTGATGGCATTTGGTAAGACTTTTTTTTTTTTATTGATCCAAAGTATGTTAGTAGTTTCATCATTCATATTAAGCCCCAAATGGAAGTCATGCACTTCAGTGGCTGTAAAAAAACAATAATGCTTTGTTTCTCTTTGGAGATTCAAGAGATTATTTCAGATTTTTCTAAAAAAATAATTTTGGCTCAACCTCTGTCCTTCCTCTGAAATTAACGTGTACTTTAACATATAAAATTCCTACAATGACAACAGTATCAGTTGTAAGTCATTTGAAGTTAAATGTTTCTTACCACTTTTGTTTTTTTTTTTCGAGAGTAGACATGACCATAATGTTTACTTAAGATTCTGATTTGGTTAATATTGGCAGCTTGAGAGAGCCAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35412

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109665	Essential Splice Site	400	495	9	12

Genomic Location (Zv9):

Chromosome 13 (position 5877045)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	6071070
GRCz11	13	6199530

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAATTGAATGCATTTTCATTATTGCATGACTAATGGCTGGGTTTCATGTA[G/T]GCGATCACTTTTACAAAAGAAACAAAGCTCTTCCCGCTGAGGAACAGATG

Long Flanking Sequence:

GTGTGAACCGAACCGTGACCACTGAATTTAGTTGTTTTGATGAACAGATTATTAATCACAGTTGCCGTGTACATTGGAATATAGTGCACAAGGAGCAGAACACACAAACTTATGATACATACTGGTGCGGAGTCATTTTTGCTGACCATTTTTCATCTCCGTTATCCAGCCAGGTTCAGACAGTGGCACTACAGCTGTAGTTGCTCTTATTCGTGGGAAGCAGCTGATCGTGGCCAACGCTGGAGACTCCAGATGTGTGGTGTCTGAAAAGGGAAAAGCGTTAGACATGTCCTACGACCACAAGCCGGAGGATGAGCTCGAGCTGGCCAGAATAAAGAATGCTGGTGGAAAGGTGACCATGGACGGTCGTGTCAATGGAGGACTGAACCTCTCCAGAGCTATCGGTAATGTGGAATACTCTGATTTTTTTATTTATTTATTTTAAATCATTAATTGAATGCATTTTCATTATTGCATGACTAATGGCTGGGTTTCATGTA[G/T]GCGATCACTTTTACAAAAGAAACAAAGCTCTTCCCGCTGAGGAACAGATGATCTCCGCTCTCCCTGATGTCAAAGTGCTGACTCTCAACGATGATCATGAGTTCATGGTTATTGCATGTGATGGCATTTGGTAAGACTTTTTTTTTTTTATTGATCCAAAGTATGTTAGTAGTTTCATCATTCATATTAAGCCCCAAATGGAAGTCATGCACTTCAGTGGCTGTAAAAAAACAATAATGCTTTGTTTCTCTTTGGAGATTCAAGAGATTATTTCAGATTTTTCTAAAAAAATAATTTTGGCTCAACCTCTGTCCTTCCTCTGAAATTAACGTGTACTTTAACATATAAAATTCCTACAATGACAACAGTATCAGTTGTAAGTCATTTGAAGTTAAATGTTTCTTACCACTTTTGTTTTTTTTTTTCGAGAGTAGACATGACCATAATGTTTACTTAAGATTCTGATTTGGTTAATATTGGCAGCTTGAGAGAGCCAACAT

Associated Phenotype:

Not determined