ZMP
prkci
Ensembl ID:
ZFIN ID:
Description:
Protein kinase C iota type [Source:UniProtKB/Swiss-Prot;Acc:Q90XF2]
Human Orthologue:
PRKCI
Human Description:
protein kinase C, iota [Source:HGNC Symbol;Acc:9404]
Mouse Orthologue:
Prkci
Mouse Description:
protein kinase C, iota Gene [Source:MGI Symbol;Acc:MGI:99260]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14108 | Nonsense | Available for shipment | Available now |
sa17535 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14108
Status:
Available for shipment
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:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015723 | Nonsense | 37 | 588 | 2 | 18 |
The following transcripts of ENSDARG00000021225 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37114342)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37411052 |
GRCz11 | 2 | 37393509 |
KASP Assay ID:
2259-2347.1 (used for ordering genotyping assays)
KASP Sequence:
CACTTTTTTTNNNTGTTTTAGGGACATCATGATCACACATTTTGAGCCTT[C/A]GATCTCCTATGAGGGACTCTGCAATGAGGTGCGKGATATGTGCTCCATGG
Long Flanking Sequence:
AGTAGGGCTGCACAATATATTGTTTTAACATTGATATTGAAATATGTGCATCTGTAGTAGTCAGATTGCAGGATCTGCAATGTTGAATTTGTGAATATAGTTTACCATGAGCCACAGTTATTGAAGATTTATTCCATAATAAAGCAAAAGTTTTTTATTTGCATGTGTTTTTCAGGCCTGTGATTAAAGCATATACAAGAGAGTTTAAAGCATTCAGGCATGAAAATTGTACCAGTCTTTAATAAAAAATATTCAATTGATTTATTTATGCAATAAAATCTAAGCACTGCTATTTTACATTTGATTAAATTCTGTATATGCTTTCATACCAAATCGAGGTATTTAAAGTCATCTGGGGAAATTATATACACATCACAGAAAAACAAAACATTGCATTGTCAGATTTTTCTAATATCGTGCAGCCCTAAAATGTAGGATTTTAATGAATGTCACTTTTTTTTCCTGTTTTAGGGACATCATGATCACACATTTTGAGCCTT[C/A]GATCTCCTATGAGGGACTCTGCAATGAGGTGCGGGATATGTGCTCCATGGACAATGACCAGCTCTTCACCATGAAATGGATTGATGAGGAAGGTTTGTTGTTTCATTTTTGTGTCTCTTTGCTCTATTCACAGTAGGTGTTGGCATCTGTCTCAGGTGATCTGATCTCAGTCAGTCGAGACAGATTGACATTTACTCCTGGTTAACACAAATCTCCAGTGACTTCTTTAGATCAGGTTTCACTAAAGAGAACCTCTCACTCGTTTCATGATTACACACAGCGTGTTAAACCAAAGAGAGCTTTTACTTGTTAAAACTGAATTTTGGCTATTACAGTTAATTGACCCATTTTTCTAAATGAGCTGTTTTATAGGCTATCGTCTTAGTTGCTTGAGAATAAGGGTCACTTCATGAATAGTTTAATGTTTATTTTACTGTTTAACAATAAAATGCACTTTTCGATGTTATACTAATGCTGAACGGCCATATTAGTGCCAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17535
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015723 | Nonsense | 167 | 588 | 6 | 18 |
The following transcripts of ENSDARG00000021225 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37108338)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37405048 |
GRCz11 | 2 | 37387505 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGATCGTATCTGGGGTCTGGGCAGGCAGGGATACAAGTGTATCAACTG[T/A]AAGCTTCTGGTGCATAAGAAATGCCATAAGCTGGTCACAGTAGAATGTGG
Long Flanking Sequence:
CCGCTGTCAGACGAGGAGAGGTCACAGAGGGGTCATGCAGGAGCTGTTTTTTCACAATCTCTCTCTCTCTCCAGTGTTTCCTTGTGTCCCTGAAAAACCTGGCATGCCCTGTCCTGGAGAAGACAGTATGTGTGTTTTCTGATATTTATATCATATTTAAAAAAAAAATACATTTTGTGGCTGCATTGATTCTGTGTAAGTGGTGCATAGATTTTATTGACTTGTTGTACTCAGAGTCTATATACCGGCGGGGAGCTCGACGTTGGAGGAAACTCTACTATGCCACTGGACATGCGTTTCAGGCCAAACGCTTTAACAGGGTATATGCTCTTATTATATATATATATATATATATATATATATATATTCTTAATTTCTCTGTAGTATGTTGTGTTTGCTTTAATTTGCCTGTCACTTTGTTTTGTACAGCGTGCTCATTGTGCCATCTGCACAGATCGTATCTGGGGTCTGGGCAGGCAGGGATACAAGTGTATCAACTG[T/A]AAGCTTCTGGTGCATAAGAAATGCCATAAGCTGGTCACAGTAGAATGTGGTAGACAGGTAATACAGGTGAGGCATTCGCATGGTCAGAAGTTTGCTTTTCTAATAGTTTGCACCATTTGCCTTCTCTGTTGATTTCCATTGAGCTTTTATTATCATGATCTTATCAATTGTGTCAAATCCTTCAATTAATTAACCCTTTATAGGCCACTCATTGTAATGCTCATTGAAAAAATGAGTGGAATATTACTAGGGTAACTTTTAAGGCTTAAAATAAAAATAATAATGTAATTAGTATCAATGAAGTTACAATTTAAGGTTTCTATGGTTAAAACTATTAGCAATTAAAAATGAACAATAAAAAGTGATTAACAAACTGTTTTAAACAGTGGTAGGGAACCTATGGCTCGCTAGCCACATATGGCTATTTGACCAAAAATATGTGGCTCTCCAGGTGTCTAGCTTCAATTATATTTTGCAGTTTAAAAAATAATAACCATCAC
Associated Phenotype:
Not determined