ZMP
pnck
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate pregnancy upregulated non-ubiquitously expressed CaM kinase (PNC
Human Orthologue:
PNCK
Human Description:
pregnancy up-regulated non-ubiquitously expressed CaM kinase [Source:HGNC Symbol;Acc:13415]
Mouse Orthologue:
Pnck
Mouse Description:
pregnancy upregulated non-ubiquitously expressed CaM kinase Gene [Source:MGI Symbol;Acc:MGI:1347357]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45311 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38671 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45311
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000064090 | Essential Splice Site | 69 | 316 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 9697532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9114114 |
GRCz11 | 8 | 9152699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAAGGGAAAAGAATCCATGCTGGAGAATGAGGTTGCGGTATTACGCAG[G/A]TCAGTTATTTGGCAAACAGCGTTCTTGACTGATTGGTTAAATTTCTTGAC
Long Flanking Sequence:
GAATGAATGAATGTCACATCCATAACGCTGGAATTGCTCATCTGCAGATTTTATGGTGCACAGATTCAATGTTTTCCTACCAATGATATATATAGCAGGAAAAGCAAATACTATGGAAGTCAATGGTTACAGGATTCCAACAATTTTCAAAATGTCTTCTTTTGTGTTTAACATAAGGGACTCCATCAAATGTGAAACAAATAAAGGGTGAGTAAATGAGTTCATTTTTGGGCGAACTGTCCCTTTAAGAAGGCTCTGGAGACTCCTATTTTTCACAGTGCGCCCACAGCACTTGTCATTAAGGATTAATTGTGAACGAAACTCATTAGGGGCTGAATTATAAATAATATAAAGGTGTAACGTCTCAGGGGCTCGTTCTCTGAGGTTCGAGTGGCTCAGCACAGATGCACCCAGAAGCTGGTGGCTGTCAAGTGCATCCGGAAGAGAGCGCTAAAGGGAAAAGAATCCATGCTGGAGAATGAGGTTGCGGTATTACGCAG[G/A]TCAGTTATTTGGCAAACAGCGTTCTTGACTGATTGGTTAAATTTCTTGACTTTACAAAGCGCTTTTGTGTGCATTTTCTAGGTTGTTATTAGCGTAGAGCTGCATTTTACATACATTTTTTTGATTTGATGGTACGAAGGGAATGATTTTTTTATATGTGTCCCCTGTGATTTCTTCACAGAATAAATCACGAAAATATTGTGTCCCTGGAGGAAACCTTTGAGACTCCTACTAAACTGTATTTGGTAATGACACTGTGAGTGGAGCAGAGTGTGGAAATGAATATAGTGCAGTTCAAAATCCATAATGCTATAAATAGTTGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATATAGATGACACTGACAGAATCAAAATACACTGACAGATAGATACAGAAGACACTGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38671
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000064090 | Essential Splice Site | 140 | 316 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 8 (position 9699574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9116156 |
GRCz11 | 8 | 9154741 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCGTGAAGTATCTGCATCAGCTGGGCGTCGTGCATCGCGATCTAAAG[G/A]TAGCCGAGAACAAAACATAACACTTCCGTCTCGAGATTTTTAGTTTCAGA
Long Flanking Sequence:
GACACTGACAGACAGACAGAAGACACTGACAGACAGACAGAAGACACTGACAGACAGACAGAAGACACTGACAGACAGACAGACAGACAGACAGACAGACAGACGGACAGACAGACAGAAGACACTGACAGACAGACAGACAGACAGACAGACGGACAGACAGACAGACAGACAGGTAGATAGAAAAACAGACAGACATACAGACAGAAGATACTGACAGACAAACTGAAGACAGACAGACAGACAGATAGAGGACACTGACGGACAGACAGATGACACTGACAAATAGACAGAGAGATGACACAGAATAACAGACGACACTGACAGACAGACAGACAGCTGATTTGAGTTTATTGCGCAGGCTGACAGGAGGTGAGCTGCTGAACAGGATTCTGGAGAGAGGCAGTTACACAGAGAAAGATGCCAGTCGGGTCATTTACCAGGTGCTGCAAGCCGTGAAGTATCTGCATCAGCTGGGCGTCGTGCATCGCGATCTAAAG[G/A]TAGCCGAGAACAAAACATAACACTTCCGTCTCGAGATTTTTAGTTTCAGAGCAACACTCATGCTGAGCATCTCTCCATTAGCCTGAGAATTTAATATTTGAGACTCCATTAGAAGACTCCAAAATTGTCATCAGTGACTTTGGCCTGTCTAAAATGGAAGAGCAGGGGGCTCTGTCCACCGCATGTGGGACTCCAGCATATGTCGGTAAGAGAAACCGTTTATGATCATGTTTATAAACAAATATTTTGCACAGTTACATACAGAATCAAGATTATTTAGTTCAACACAAAATAAACTCTAATGCTTAAAAAAACAAACAAAATGCACAGATCTGAAGCTGGTATAATGTGACAAGCATATCTGTTTAATCTTCTATGGGTTAATACCATATATAACAATTAAAGGTTAAGATCAAACAAAAATATACATTTGCTGTTCATTTTTTTACCCTCAGGCCATCAAGGCCATAATTTTTTTTTCTCTTCAGTAGATTTTTTTT
Associated Phenotype:
Not determined