ZMP

ppp2r5c

Ensembl ID:

ENSDARG00000031200

ZFIN ID:

ZDB-GENE-041014-4

Description:

serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform [Source:RefSeq pept

Human Orthologue:

PPP2R5C

Human Description:

protein phosphatase 2, regulatory subunit B', gamma [Source:HGNC Symbol;Acc:9311]

Mouse Orthologue:

Ppp2r5c

Mouse Description:

protein phosphatase 2, regulatory subunit B (B56), gamma isoform Gene [Source:MGI Symbol;Acc:MGI:134

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa3085	Essential Splice Site	F2 line generated	Not yet available
sa17560	Essential Splice Site, Missense	Available for shipment	Available now
sa29479	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa3085

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000020266	None	30	578	3	19
ENSDART00000052781	None	None	420	None	12
ENSDART00000109320	None	30	578	3	18
ENSDART00000110252	Essential Splice Site	30	577	3	17

Genomic Location (Zv9):

Chromosome 20 (position 54313398)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	54168801
GRCz11	20	53958247

KASP Assay ID:

554-3272.1 (used for ordering genotyping assays)

KASP Sequence:

TTTAGAGAGGTGATGTTAAAGTRTGAARTGTCCTTTGTTTTTCGTCAGCA[G/A]GCTTCGAATAAGAAGGGTGGGAACAGCGTCCCGCCGGCCACACAGCTGCT

Long Flanking Sequence:

AACCTAAGGATGTTCCATATTGAATCTAGTTTCGTTATGTAACTATTTATAGTATAGTAAATATTTATATCTATTTTTTACTGAGGATTTGCACCATGTTTATTTGGACTTTGACACATTATTTATTATTTTCCTATTTTTTTATTTGTTCATTGTAAGTGGTGTTGTTCATAGCAACTGAAAATATATTATTTGGAAAAAGTCAAATTTGCTTCACTGTTCTATTATTTTGTAACATTTGTAACATACCGTATACCGCGAAACCGTCAAACCGTGGTATTGTTTTAGACGATTATCATACCGTAAAAAATTCATACCGTTACAACCCTACTTCAGCTTCACACAAATGTAAGCAGTCAAATGTAAAAAAATAAATAAATAAAAAAATCAAAAAAAATTTTAAATGCATGAAATGTTTTTGCATTTCTCTGATGTTTTCTGCGCTCTTTCTTTAGAGAGGTGATGTTAAAGTATGAAATGTCCTTTGTTTTTCGTCAGCA[G/A]GCTTCGAATAAGAAGGGTGGGAACAGCGTCCCGCCGGCCACACAGCTGCTGAAGGGTAAGCAGTCTGGATCTCAGACTCCAGTCAAGAAAGAAAAGCGTCCGAACTCCTCCAGATTCAGCCTCAGCAACAACCGAGAGCTTCAGAAGCTGCCCGTTTTCACAGGTGAGACGCCGAACATGATTTATGCTGAGTTTCCATATGAAGATGCTGGAATATTGCATTAAACATTTGCAAATAAAGCAGCGTTTCCAGTCAGTGATGAACAGAAGAGAACAAAACCAGCACGTCCTGATCTGTTGAAGAGCTTCTATTCTGTCCCTTTAAAATGCATCGCTGCTGTCTCTTGAGTGTGTAGTTTAGTGAAGTTTGACATAATGCTCTCTAAGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTCCGAAACAGAGATTACAAATGTTACATTGTTGCTCTTTGCTCTTGGAGCGGTTCGCTTTCACACGGCAAAGTTTCTAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17560

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:

T > C

Consequence:

Essential Splice Site, Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000020266	Essential Splice Site	471	578	None	19
ENSDART00000052781	Missense	419	420	11	12
ENSDART00000109320	Essential Splice Site	471	578	None	18
ENSDART00000110252	Essential Splice Site	470	577	None	17

Genomic Location (Zv9):

Chromosome 20 (position 54261525)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	54116928
GRCz11	20	53906374

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGAAGCTGTTTGAKGACTGCACACAGCAGTTCAGAGCCGAGAAAAACAAG[T/C]AGGAAGAGCTTTCAGTAACTCTCACACACTGTCACGAGCTCWCTTCACTC

Long Flanking Sequence:

TTGCACAATAATAAAGAACTGTCGGTCAGTAATGTCTATCCAAAATCCTCAGATATAAAAACTAGACATTTTAAGCTTTCAGTTGATATATAGTTGGTCATGATTGCTTTATGGGTAGATTTTATAATATTATGGTTTAAAAATATATTCATAAATGCTCCCACAGGTTGTTGGCTGACAGTAAATGTGCTTTAATCTGTTGCTCTTCCTATGTAACTAAAAACTGAGGTGAAAGATGTATTCAGAAGTCCTGGACCTTTCCGCTGATATATAGTGTGTCGTGATTGGATTAGGGTTTAGTTGTAAAAATGTGATGTAAGTTAAAGTGATGTTTAATGGGTTAAAACACAACAAAACAAGCACAGAACTAAAGACGGTTTCCTCTTCCTGTTTTGAGGACGATTCACGGGCTGATCTACAACGCTCTGAAGCTGTTTATGGAGATGAACCAGAAGCTGTTTGATGACTGCACACAGCAGTTCAGAGCCGAGAAAAACAAG[T/C]AGGAAGAGCTTTCAGTAACTCTCACACACTGTCACGAGCTCTCTTCACTCAGTTTTTACTCTTCTCTGTGTGTGAAACTAGAGAGAAAGCCAAGTGGAAAGAGCGCGAGGAGGCCTGGATCAAGATCGAGAATCTCGCCAAATCAAACCCACAGGTGAGCGCATCTCATTACCAGTGCATGAATATTCATAACACTTCTTGTGATCTTCTCATCAATTAAAATTTTCTGCATTTAATTTAATTTTAATTTAATTAATTACTTTATTGATTTTTTTTTGTTTTCTGTCTGTATGGCTGGCTATATCTAACTTTTTTATTCTATTTTTATATTCATTTCATTTATATTTTTTTAGATGATTATTTAAATTTATTTTTTATATTATTATTATTTTATATTTTTTTTCTTATTTTTTATTTAATTTTTATTAATTTTAATTTATTAAATCTATCTATCCATCAATCCACCCATCCATCAATCCACCCATCCATCCGTCCATCCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29479

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000020266	None	None	578	16	19
ENSDART00000052781	None	None	420	None	12
ENSDART00000109320	None	None	578	16	18
ENSDART00000110252	Essential Splice Site	None	577	16	17

Genomic Location (Zv9):

Chromosome 20 (position 54259036)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	54114439
GRCz11	20	53903885

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAGAGGACACAAGCACATGCACACACAAATACACACACACACACACACA[T/A]CTCAAACCAAACCCGGTGTTCTGACGATATGTGCTAAACCCTCAGAGTGT

Long Flanking Sequence:

GGACATGGAGACTGATGGGCCGATGCTTGAAGACGTCCTGATGCTGAAGAAAACTGTAGAAGAAGAAGCCACTCCAGTAAGAAACAAGCCTCTTGCTCAACAAAGCTGCATTTATTCAATTTAAAATCATGAAAATATTATTGAAAATTTAAAAATGTGAATATCTAGTAAGATGTAAATCATAGTTTGTTGATACACAAGCATCACTTGATCTTTCCGAAATCACAGTATGCAGTTGAGGGCAAGAGTAATTTTTCATTATGCTTAAACTGTGTGTTTATATAGACGTAATCTTGTGTGTGTTGTTGTGTGTGTTCAGTTGCACAGAGAGCAGCGTAAGGAGCGTCCGCTGATGCGGCGTAAGTCTGAGCTTCCTCAGGACACGAGCACCGTGAAGGCGCTGGAAACACACCGGCGTGCAGAGGACATGATCGGCACTCAGGATGGCCACTAGAGGACACAAGCACATGCACACACAAATACACACACACACACACACA[T/A]CTCAAACCAAACCCGGTGTTCTGACGATATGTGCTAAACCCTCAGAGTGTATCTAAATCTGTCATGTTTCATCTAAAAACACAGGGGCTCTATCACAACTTCTCTGCTTCAAATGTGTTAGAGTTAACTTCCACCTTAAATTAGAACTTCCACTTTGAATTAGGACTTCCACCTTAAATTAGAACTTCCACTTTGAATTAGGACTTCCACCTTAAATTAGGACTTCCACTTTAAAATTGGACTTCCACCTTAAATTAGGACTTCCACCTTAAATTTGGACTTTTACCTTAAATTAGGACTTCCACCTTAAATTAGGACTTCCACTTTAAATTTGGACTTCCACCTTAAATTTGGACTTCCACCTTAAATTAGGACTTCCACTTTAAATTTGGACTTCCACCTTAAATTAGGACTTCCACTTTAAAATTGGACTTCCACCTTAAATTAGGACTTCCACCTTAAATTAGGACTTCCACCTTAAATTTGGACTTCCACCTTAA

Associated Phenotype:

Not determined