ZMP

ppp6c

Ensembl ID:

ENSDARG00000002949

ZFIN ID:

ZDB-GENE-040426-949

Description:

serine/threonine-protein phosphatase 6 catalytic subunit [Source:RefSeq peptide;Acc:NP_957299]

Human Orthologue:

PPP6C

Human Description:

protein phosphatase 6, catalytic subunit [Source:HGNC Symbol;Acc:9323]

Mouse Orthologue:

Ppp6c

Mouse Description:

protein phosphatase 6, catalytic subunit Gene [Source:MGI Symbol;Acc:MGI:1915107]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11395	Essential Splice Site	Available for shipment	Available now
sa7567	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11395

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
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Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007458	Essential Splice Site	127	305	None	7

The following transcripts of ENSDARG00000002949 do not overlap with this mutation:

ENSDART00000136124

Genomic Location (Zv9):

Chromosome 5 (position 33622118)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31384350
GRCz11	5	31984503

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGTGGCAATCACGAGAGTAGGCAGATTACACAGGTYTATGGCTTTTATGG[T/C]AAGGCTGCAGAAATCAGAGATNNNTTTGAAATATTTTGTTTTKAATTTACTTG

Long Flanking Sequence:

CTGCTTGAGGAATCAAATGTACAGCCAGTATCCACTCCAGTCACTGTATGCGGGGACATTCATGGACAGGTGTGTGTGCAGGCTCCATTAATGCATCCCTGGTATTGATGTTGAGCTGATGTCGTGTTTTTGTAAAAACATGCATACTGACTAAGCTTTTTTTTTTCTTTTATAAATAGTTTTATGACCTATGTGAACTCTTTAGAACTGGGGGCCAAGTACCAGATACAAACTACATTTTCATGGTGAAGTATATTACAACAATAATTTTAATTGATGATTTGTGATTAGTACTGCGTTGGAAATTGTTCCACCATCATCTATTGAGGAGACATTGGTATGTTTTCTTTCATCCAGGGTGACTTTGTTGACCGAGGATATTACAGCTTAGAAACATTCACATATTTGCTAGCACTTAAAGCAAAGTGGCCTGACCGCATCACACTGTTGCGTGGCAATCACGAGAGTAGGCAGATTACACAGGTCTATGGCTTTTATGG[T/C]AAGGCTGCAGAAATCAGAGATTTTGAAATATTTTGTTTTGAATTTACTTGGGATTTTAATTGTTTTGGCTTTCTGTCTACAGATGAGTGCCAAACTAAATATGGAAATGCTAATGCCTGGCGATACTGCACTAAAGTATTCGACATGCTCACTGTTGCTGCCGTAAGTGTTGATTTTGGAATACCTATCTGTCTGTCTATCTGTCTGTCTGTCTATCTATCAATCACACATCTCAACATTATCAATATTTGTTTTGGTCTTCTTACTAATGGGCCTCACTCAGGAAACACATGTTTTTGTTTAAATCAAATAATTTTAGGATGTTTTTGTTTAAATCAAATAATTTTTGGATTAATGAAACTGTTTATATTTCTAAGTATGAATTGGTATAAAAGAAATGTAGGAAACTATACATCCAGTTATTGTCTTGCGCTTATCCGGAGCTAGGTCATTGGGGCAGCAGTCTCAGGAGAGAACCTCATACTTCCCTCTCTCTGGGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7567

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007458	Missense	220	305	6	7

The following transcripts of ENSDARG00000002949 do not overlap with this mutation:

ENSDART00000136124

Genomic Location (Zv9):

Chromosome 5 (position 33631409)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	31393641
GRCz11	5	31993794

KASP Assay ID:

554-4015.1 (used for ordering genotyping assays)

KASP Sequence:

CACCTGGGCTATCAGTCCAAGAGGAGCTGGCTGGCTGTTTGGTGCTAAGG[T/G]CACTAATGAGGTAAAAATCGCTCTCAAARTGCACAGTCTGCNTTTGTTTTT

Long Flanking Sequence:

ATTTATTGATTATGAATGTTATTTCAAATGGCTTTTGATACTATGAATCTGAATATTTTTTTATTTTTAAATGGAAAGAACTGTCATTAGTAGTTTATAGAATTAAAAACAAATCAATTGATCTTTTTCAATTGTGTACATAAATTACACAGATTCGGGATATTATTTATTGTTGCAATACATCATTGCAGAACTAGCATAAAATGGTTGCAATATATTCAGTGCTTCAAACTAAAAATCATATCGATTGGCTAGTTTAACTTGTCAATTATCTAATAATTGTTGTTTGTTTCTCCCACAGTTGATAGATGAGCAGATCCTTTGTGTACATGGTGGCCTTTCACCTGACATCAAAACTCTGGACCAGATACGCACCATTGAACGCAATCAGGAGATCCCTCACAAGGGAGCATTTTGTGACCTTGTTTGGTCCGACCCAGAGGACGTGGACACCTGGGCTATCAGTCCAAGAGGAGCTGGCTGGCTGTTTGGTGCTAAGG[T/G]CACTAATGAGGTAAAAATCGCTCTCAAAGTGCACAGTCTGCTTTGTTTTTGGCTTTTATAACACTTCCCTATGGAAGATACTATTGCTCTGTAATTACAGATTGAGGTCTGCTAATTATTTGTTGATTCTAGGCATGGGCCTGTATAAGTTTTGCACGGTACGATAAACTTGGATAAAAATACCACTGTTTCACGTTGTTGCGATTACTGCTTTAAAATAAGTTAACTTTAATTTTTTTTTTGCCGTATTAAACACAAAATATTTAATTTTAGTAGACATTTATAATATTTTGGAACACTAAACATGTCAGGCTAAATAATTAAAATGCACCATTGACCTCTGCACTCTTCATATGTTTCAAAAACACAGATTAATTTACAAAACACAAAAAAAAAAACATTTAAAAAAAGCTTGCATATACCTTAGAAATGGTACGACAGTAAATATTAGCGGTTTTAAAATCAAACCATGGTAAACCCTGAAACTGCTTATCATCCCA

Associated Phenotype:

Not determined