Busch Lab

ZMP

prkchb

Ensembl ID:
ENSDARG00000043243
ZFIN ID:
ZDB-GENE-041001-104
Description:
protein kinase C, eta, b [Source:RefSeq peptide;Acc:NP_001038271]
Human Orthologue:
PRKCH
Human Description:
protein kinase C, eta [Source:HGNC Symbol;Acc:9403]
Mouse Orthologue:
Prkch
Mouse Description:
protein kinase C, eta Gene [Source:MGI Symbol;Acc:MGI:97600]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa29336 Nonsense Mutation detected in F1 DNA Not yet available
sa43415 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43414 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa29336
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063483 Nonsense 97 676 1 14
Genomic Location (Zv9):
Chromosome 20 (position 20481901)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 20510068
GRCz11 20 20409741
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACAGCACTCGTTTAGGATACGACACGTTTGTGGCTAATTGCAGAATC[C/T]AGCTTAAGGAAATCACAACGACACCAGGCACAAAGCCAAAATTTGAAGGA
Long Flanking Sequence:
AGAAAGAGAGAGAGAGAATTTTTTACAGACGATTTCCTGCATAAGACGAGAGTTCAGCTCTTTTTATATTACGTAAATACTTAATTTGTGTTTAATACGTTCCTTAAACGTTAATTTTGACTTAGTGCCAATTACGTTAAACGTTTTTGTTTTAAACTAATGCATATTTAGTGTAGTAAACCTAAAATTAGCTTAATACTGAAGCTTCGACTATGAAATTCAACGGATATTTGAGACTGCATATTCGCGAGGCGGTGGATTTAAAACCGACGAGGTTTTCAACTCGACACACATTTAATAGGAAAATCCAGTTGGATCCTTACATCGTTGTTAAAGTCGACAATGTAAAACATGCGAAGACCGCCACAAAACCGAAGACCAACAAACCGACTTTCAATGAGGAGTTCTGCCCGTACATCTCCAACGGTGTGGAGCTGGAGCTGGCTGTTTTCCACAGCACTCGTTTAGGATACGACACGTTTGTGGCTAATTGCAGAATC[C/T]AGCTTAAGGAAATCACAACGACACCAGGCACAAAGCCAAAATTTGAAGGATGGGTGAGTTATAATAAAGTTACAGCAAGTACATCTAGAATTAGATAAAATATAAAGCAAATGATGCATTCATAAAATCAATGACAAAATGGAAGGAGAAAAAAGTAAACCTTTTTAAAAATTTATGTATATTGTGAATTAATGGTGTAATTGATGTAGTTAATGGAAAAGTAATAGCAAACACTACAGAAATATCAAGATATTTGGCAGAATTCTACACTGAGAAAAATTATTTAAAGATGTTGGGTTTATTCAATTTATTTAAGTTAAATGGTTGTAAACAATTTATTTGGACTGAATTTAAACAAACAAATTAAGTTGTACATTGCTAAATTTAATTTGTTTAAATTCAACACATTGTTTGCAGAAATTTATATTTTTTCAGTGAATGAAAATCTATATTGGGATAACTACAAATGATGTAATACTCAGAATATATTAACGAGGACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43415
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
ENSDART00000063483 Essential Splice Site 268 676 7 14
Genomic Location (Zv9):
Chromosome 20 (position 20463220)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 20491387
GRCz11 20 20391060
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGTACATGAAAACACATGGACAAATCTGTTTTGTGTGTAATTATGCA[G/T]TTTGTAAGATGAACATCCACAAACGCTGTGAACAAAATGTCGCACCTAAT
Long Flanking Sequence:
GTGTATATTATACAATGTATTAGGCAAATATAAACTGAAAATGCAATGGAAGGTTGAACAAAATCTTGTTATTGTAGTTAATCAAGAAACAATAATGGAATCCCTTTCTTATAAAAAAAGAAAAATTTTTTATTATTTTTCCTATTCAGGCATAAACACTTAATGTGTAAGCAAACTGCCAATAGACATTAAAAGGTTTTGCATTGTTAGTTGAAAATGTTGTTGTGTATATAGACCCATAAAACATTTGTGATTGAATGCTTTGAGATCAGCCTTCTGCTTAATCCAGTTATCCAATCTCACGATCTGTTGAGAAAAGTCACATGAGATTTTTGTTGTGAAATATGGAATTTATTTGATAATTGTGTTTCCAATGCAAATTGCATATCTTTCCATCTTCTAAAAATATACCACAATTGAGTTTATTCAGCATTTTTATATGTTAATCCAGAATGTACATGAAAACACATGGACAAATCTGTTTTGTGTGTAATTATGCA[G/T]TTTGTAAGATGAACATCCACAAACGCTGTGAACAAAATGTCGCACCTAATTGTGGAGTGGACAATGCTGAGCTGGCCAGCAAACTGTCAGAGATTGGACTGCTCAACACAATCTCCAAACGAAAGTCTCAGGTAGTGTCACCATCTTAAAAATCTTATTAGAAAACACTTGGTTTTTTTACATTTACATTTATTTTCTGTTAAAGACAGTATCAGATTTGCATTTGAGTGCATTTCTTTGTGTTTTTAACAGGGTTCGCTGCACATGTCAAGTGTAAGGAGTCAGAGCTCCACTACTAGCATAGAGACAACTGAGGAGGAGTCAGATGAGGAGGCTGTAAAAGTTTGCCTGGAAGATTTCAGTTTCTTGCAGGTGCTGGGGAAAGGAAGCTTTGGCAAGGTGAGACAGATTGGTATTGGTAGATTATTGGCAAGTCTCACTCTTAAAGAGATAGTTCACCCAAAATGAAAGATTGTTGTTAATTTACTGTTGTTGTTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43414
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063483 Nonsense 277 676 7 14
Genomic Location (Zv9):
Chromosome 20 (position 20463191)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 20491358
GRCz11 20 20391031
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGTGTGTAATTATGCAGTTTGTAAGATGAACATCCACAAACGCTG[T/A]GAACAAAATGTCGCACCTAATTGTGGAGTGGACAATGCTGAGCTGGCCAG
Long Flanking Sequence:
ATAAACTGAAAATGCAATGGAAGGTTGAACAAAATCTTGTTATTGTAGTTAATCAAGAAACAATAATGGAATCCCTTTCTTATAAAAAAAGAAAAATTTTTTATTATTTTTCCTATTCAGGCATAAACACTTAATGTGTAAGCAAACTGCCAATAGACATTAAAAGGTTTTGCATTGTTAGTTGAAAATGTTGTTGTGTATATAGACCCATAAAACATTTGTGATTGAATGCTTTGAGATCAGCCTTCTGCTTAATCCAGTTATCCAATCTCACGATCTGTTGAGAAAAGTCACATGAGATTTTTGTTGTGAAATATGGAATTTATTTGATAATTGTGTTTCCAATGCAAATTGCATATCTTTCCATCTTCTAAAAATATACCACAATTGAGTTTATTCAGCATTTTTATATGTTAATCCAGAATGTACATGAAAACACATGGACAAATCTGTTTTGTGTGTAATTATGCAGTTTGTAAGATGAACATCCACAAACGCTG[T/A]GAACAAAATGTCGCACCTAATTGTGGAGTGGACAATGCTGAGCTGGCCAGCAAACTGTCAGAGATTGGACTGCTCAACACAATCTCCAAACGAAAGTCTCAGGTAGTGTCACCATCTTAAAAATCTTATTAGAAAACACTTGGTTTTTTTACATTTACATTTATTTTCTGTTAAAGACAGTATCAGATTTGCATTTGAGTGCATTTCTTTGTGTTTTTAACAGGGTTCGCTGCACATGTCAAGTGTAAGGAGTCAGAGCTCCACTACTAGCATAGAGACAACTGAGGAGGAGTCAGATGAGGAGGCTGTAAAAGTTTGCCTGGAAGATTTCAGTTTCTTGCAGGTGCTGGGGAAAGGAAGCTTTGGCAAGGTGAGACAGATTGGTATTGGTAGATTATTGGCAAGTCTCACTCTTAAAGAGATAGTTCACCCAAAATGAAAGATTGTTGTTAATTTACTGTTGTTGTTTGACAATCCATAGAACAGCAGCAAATTAATTT
Associated Phenotype:
Not determined