ZMP

prkcq

Ensembl ID:

ENSDARG00000034173

ZFIN ID:

ZDB-GENE-041210-195

Description:

protein kinase C, theta [Source:RefSeq peptide;Acc:NP_001082839]

Human Orthologue:

PRKCQ

Human Description:

protein kinase C, theta [Source:HGNC Symbol;Acc:9410]

Mouse Orthologue:

Prkcq

Mouse Description:

protein kinase C, theta Gene [Source:MGI Symbol;Acc:MGI:97601]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa7269	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa20289	Nonsense	Available for shipment	Available now
sa2170	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa7269

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
ENSDART00000046253	Essential Splice Site	39	721	2	17
ENSDART00000123680	None	None	709	None	17

Genomic Location (Zv9):

Chromosome 4 (position 24502308)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	25425977
GRCz11	4	25415175

KASP Assay ID:

554-5178.1 (used for ordering genotyping assays)

KASP Sequence:

ATAGTGTTTTTCTGTTCAGCCAGTRAAACTTACTGCAGAATTTATCTTAT[A/T]TATTTGTGTGCATCTCTAGAAAAGGGTCAAGTGTACAAACAGAAGCGGCC

Long Flanking Sequence:

TAAACACAAAATAAGTAATTTTTTTTTAAAGATGTTGGAAACAATTAACTATTAACTTCCATAATAATTTGTTTTACTATTATGAATGCCAATGGTCTCCAGTTTTCAACATTTTTGAAATATTGTCTTTTGTGTTTAACAGAATTAAAAGAAACTCATTAGGATTTAGAAACACTTGAGGGGGAAAGTAATTTGTGAATACATTTTTATTTTGGGCGAACTATTCTTTTAAGAAAATAAAACAGGGCAGTCAAAGTCCCTTTGACTTTAACTAAGGGAAAATGTTGACATTCTACCCAAATTGCATGATTTCTTTTGCACAGGACTGTATTTGTTTCAATGCACAGCTGTCAGATTACAATCAAACAATTAGATCTTTGTGTCATTTAAGTAGTATCAGTTTCAGATCCGGTAAATCCACAGTTGGAGTGATGTAAAACACACCGCAGCATAGTGTTTTTCTGTTCAGCCAGTGAAACTTACTGCAGAATTTATCTTAT[A/T]TATTTGTGTGCATCTCTAGAAAAGGGTCAAGTGTACAAACAGAAGCGGCCCACCATGTATCCCCCGTGGAGCAGCACTTTTGACGCTCACGTCCACAAAGGACGAGTGATGCATGTGGTGGTCAAGGACAAAACAGCTGAGCTAAAGACGGAGGCTACAGTCCAGCTCGACACCCTCGCTTCACGTTGCAAGAAAGAGAACGGCAAACTGGAGATATGGGTGAGTGATATCTACTGTATATCAAAAATAAATGTGCAGAGATTAAACGCACAAAGGCCTGGCTCCACGGGGGTTGGGCCTGACCCACCCCATCAGGAGCCTGGCCTACTTTGGCCCCATATGAGATAACAAAAAAAATGCGATAAATGTGACATAAAATGTGACAGTGATCTTTTAAAAACATGTTTTAAGCAGCCAGGCTCATTTACAACCAGTGTTGTGGGTAACACATTACAAGTAGCACGAGTTACACAATAATAATATTTTTTAAGTAACGAGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20289

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000046253	Nonsense	494	721	12	17
ENSDART00000123680	Nonsense	482	709	12	17

Genomic Location (Zv9):

Chromosome 4 (position 24521126)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	25444795
GRCz11	4	25433993

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGGCGACTTAATGTTCCACATCCAGACCTGTCACAGATTTGACCTCCCA[C/T]GATCCACGTGAGCTACATACAGCCCCCACACACAGATTTTTAAAGGCCTA

Long Flanking Sequence:

TATTGCAATATTGTGCAGCCTGACTTCACTTAAACAAGTGAGTAAACCTGTTGTTTTTAAAGTAATTATTTGACAAAGTGAGTAAATCGGTTGTCTTATAAATTACTAAGAATGAACAGTGCATAACTATGTAAATTAAATTAAACCAACTTCCAAGTTCCAACAGGTTTAGTCACTTTTTATATGTAAAACCACATGATGACTTTAAAGCAGCAGGTTTATTCACTTTAAGTAAGGTAACTAATTGTTTTTTTGTTTTTTTTACAGTGAGTGATAGCCATAAAATTCTATGAGATACTATGCTTTTTGACATTCTGCCAAACCCCCATGACACACATTGAGTCACTCTTGTTATTAAAGTACTGTGCTTTTGTTTGACCAGCCTGAACTGCTCTGCTTCTGTATCTTTTCTAAAGGAAAATCTTTTCTTTGTGATGGAGTACTTAAACGGAGGCGACTTAATGTTCCACATCCAGACCTGTCACAGATTTGACCTCCCA[C/T]GATCCACGTGAGCTACATACAGCCCCCACACACAGATTTTTAAAGGCCTAGTCTGCCTACTCTGTTTTTCACTCTCACATCTCCTCTTCTCTGTGTCAATAGGTTCTATGCAGCAGAGATCATCTGTGGACTGCAGTTTCTACACTCTAAAGGCATTGTGTACAGGTATGCGCTACTGTAAAAACTATATCAATCAAAGTATAGTGAGGTTATCTGGCTAGAAACTGACTTCGAATGTGCAACCATTTTTTTTATCATCTATCATCTTTTTTCATCTATTTTATCTATTTACATTTTTGGGGTTGATCTTGGTCCTGGTGCACAAACTGCAATGCATTCATTTTCCAAAACGGTATTTGTGTGGATATATTCCATAAAAAAGGATAAAAACAAGTCAAAACAGAGTCGCACCTACATACAAAATCGTCACCTTAGAATTATAAGGTTCTATCTGACATTTTCGTCAAATATGAGTTATTGACATATTCTTATTAAATGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa2170

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000046253	Essential Splice Site	626	721	15	17
ENSDART00000123680	Essential Splice Site	614	709	15	17

Genomic Location (Zv9):

Chromosome 4 (position 24525508)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	25449177
GRCz11	4	25438375

KASP Assay ID:

554-3308.1 (used for ordering genotyping assays)

KASP Sequence:

TTGTTACCCACGCTGGTTAACTAGAGATGCACGAGACATTCTTGTGAAGG[T/A]ATATCTGAACTAGAGATCAATATAAGACTTGYGATTCTGTTATGAACTAT

Long Flanking Sequence:

TATTTTGTGGTCCGTTTGTTAAATTTAAATTACATTGCATCTACATGCCAACTAATTCTCATAAGGTTACAAGTAGTAGACATGTACATGCAAAGTTCCTTATAGTCAGTTAAATGTGTTGAAGAAGCAGTATCAATAGATATAAAGCAGACAGTCTACTAAAACTCAAATGGAACATCAAAATAAAGTGTTACCAAATTACACACCCCTAAAACTCCATTCACAATAGTTTTAAGTTAGATACCTAAACCATGCAAATAAGTGAATAAAAGTTATTTGTAATACATAATGTGCACTTTATACCTCACAGATACTGCTTGGTCAGAAATATGGGACATCTGTAGACTGGTGGTCATTTGGCGTCCTACTTTACGAGATGCTGATTGGCCAGTCTCCATTTCATGGGCACGATGAAGAAGAGCTGTTTCAGTCAATTCGCACAGATGACCCTTGTTACCCACGCTGGTTAACTAGAGATGCACGAGACATTCTTGTGAAGG[T/A]ATATCTGAACTAGAGATCAATATAAGACTTGTGATTCTGTTATGAACTATAACAGTGTTTGTATATAAAATAACACAGTAAAACACTGATTGGTTTTAGCTGTTTGTCCGGGAGCCAGAGCGAAGGCTGGGCGTGAAAGGGAATATACGGCAACATCCCTTCTTTAGAGAAACAGACTGGAGCGCGCTGGAGGAACGACAGGTGGAGCCACCCTTCAAGCCCACTGTGGTAAGTTCATTACAGACCACAACGATTGTCATTTCTGCTCTAAAACCTGATGGGCTGTTGATATGGATAACATTTAAATGCTAATTAACAGCGCACAAACGCCAATAAACAATTTGTCGGATCAGTCGGCATCTGTTGCCATTGATCGGAGTTTTGTTTTCACCCAAATTAACATGTTTAATCTGCGTTTGTTAAATTGTGGATCACTGATTTTACAGTACAACTAAATACAATAGTTAATTTGCTTGTTGCCATTTGTCTGTGAAGTGTGA

Associated Phenotype:

Not determined