ZMP
si:dkey-121j17.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate protein kinase, cGMP-dependent, type I (PRKG1) [Source:UniProtKB
Human Orthologues:
PRKG1, PRKG2
Human Descriptions:
protein kinase, cGMP-dependent, type I [Source:HGNC Symbol;Acc:9414]
protein kinase, cGMP-dependent, type II [Source:HGNC Symbol;Acc:9416]
protein kinase, cGMP-dependent, type II [Source:HGNC Symbol;Acc:9416]
Mouse Orthologues:
Prkg1, Prkg2
Mouse Descriptions:
protein kinase, cGMP-dependent, type I Gene [Source:MGI Symbol;Acc:MGI:108174]
protein kinase, cGMP-dependent, type II Gene [Source:MGI Symbol;Acc:MGI:108173]
protein kinase, cGMP-dependent, type II Gene [Source:MGI Symbol;Acc:MGI:108173]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10460 | Nonsense | Available for shipment | Available now |
sa16085 | Nonsense | Available for shipment | Available now |
sa16040 | Nonsense | Available for shipment | Available now |
sa13353 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10460
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 |
---|---|---|---|---|---|
ENSDART00000017857 | Nonsense | 72 | 571 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 656109)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 649384 |
GRCz11 | 20 | 639231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTAGCGGGRGAGCTGAAGGTTACTCAGGCTGGWCGTGATTTGCGTATTT[T/A]GAGCCYTGGAGATATGTTCGGGGAACTGGCCATTCTATACAACTGCAAAC
Long Flanking Sequence:
TGTGGGTTTCCTTCAGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTATGAGTTTTTGAGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATGTGCTGCGAAAAAATGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGACGATCCCAGATTAATAAAGGGACTAAGCCGACAAGAGAATGAATGAATGACTATATGGTTGGGGTTAGAATGTGGGGTAGGTTTAGGGGTAGCTACATGTAAGTATGCATAATTCATCATAATTACAGTAAGTGCATGGCACATGTGCAACTACGTCACCTTAAATCAAAGTGTTACAACAACCCAAACCTCTTTCATATGTGAATAAAAGACAGTGTATAAGTTTGTAAGGATAAACTTTTGAGTTTTTTAATTCTAGCGGGGGAGCTGAAGGTTACTCAGGCTGGACGTGATTTGCGTATTT[T/A]GAGCCCTGGAGATATGTTCGGGGAACTGGCCATTCTATACAACTGCAAACGAACAGCATCAGTCAAAGGTCAGTTGCCATCGTGGAGGGATGAAAGGCCATGAGTTATTTGAGTCGCCCTCTGCTGGTGGGATCAATGGTTAACTGTTTTCCCCACAGCCATCTCTGCGGTAAAGTTATGGTGTATCGAGAGACAAACGTATCGGAGCATCATGACCAACAAATCCAAGATGAAACGAGAGCAGCTGATGGGCTTCCTGAAAACGTACGACATTCTGGTGACACTTCAAGTCAGACGCTTACTCACTGTGGATTATGCTTAAGTGAGTTTTACTGTTGTTTTCATCAGGGCGCGCACTTTGAAGGCTCTGAATGATGTGCAGTTGTCAAAAATCATCGACTCCATGGAAGAAGTAGGTGTGATTTTTTAAAATAATAATATAATAAATACCAGTTGCTTTCTAAATCTTTTAGTTTCATGATTACGTGTGTGATTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16085
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017857 | Nonsense | 106 | 571 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 655918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 649193 |
GRCz11 | 20 | 639040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACTGTTTTCCCCMCAGCCATYTCTGCGGTAAAGTTATGGYGTATYGWG[A/T]GACAAACGTAWCGGAGCATCATGACCAACWAATCCAAGWTGAAACGAGAG
Long Flanking Sequence:
TGTGACGATCCCAGATTAATAAAGGGACTAAGCCGACAAGAGAATGAATGAATGACTATATGGTTGGGGTTAGAATGTGGGGTAGGTTTAGGGGTAGCTACATGTAAGTATGCATAATTCATCATAATTACAGTAAGTGCATGGCACATGTGCAACTACGTCACCTTAAATCAAAGTGTTACAACAACCCAAACCTCTTTCATATGTGAATAAAAGACAGTGTATAAGTTTGTAAGGATAAACTTTTGAGTTTTTTAATTCTAGCGGGGGAGCTGAAGGTTACTCAGGCTGGACGTGATTTGCGTATTTTGAGCCCTGGAGATATGTTCGGGGAACTGGCCATTCTATACAACTGCAAACGAACAGCATCAGTCAAAGGTCAGTTGCCATCGTGGAGGGATGAAAGGCCATGAGTTATTTGAGTCGCCCTCTGCTGGTGGGATCAATGGTTAACTGTTTTCCCCACAGCCATCTCTGCGGTAAAGTTATGGTGTATCGAG[A/T]GACAAACGTATCGGAGCATCATGACCAACAAATCCAAGATGAAACGAGAGCAGCTGATGGGCTTCCTGAAAACGTACGACATTCTGGTGACACTTCAAGTCAGACGCTTACTCACTGTGGATTATGCTTAAGTGAGTTTTACTGTTGTTTTCATCAGGGCGCGCACTTTGAAGGCTCTGAATGATGTGCAGTTGTCAAAAATCATCGACTCCATGGAAGAAGTAGGTGTGATTTTTTAAAATAATAATATAATAAATACCAGTTGCTTTCTAAATCTTTTAGTTTCATGATTACGTGTGTGATTTGTGTTAAAGAAATGCAATCTGGTAAATAAAGGACAGACAGAAAGAGGTGACATAAGGGGAAAACTTGTACATATAAACAAACTGTAACTTAAAAATGTAAGTTTATATCAATTAGATTTATAATAGCCCTTAGTGTCTTTACCCCAAAGGGCCCTTTCAGCTGAAATAGTAGCGTATGGGTCTTTCTGAAAGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16040
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017857 | Nonsense | 116 | 571 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 655888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 649163 |
GRCz11 | 20 | 639010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNGATGGYGTATYGWGWGACAAACGTAWCGGAGCATCATGACCAAC[A/T]AATCCAAGWTGAAACGAGAGCAGCTGATGGGCTTCCTGAAAACGTACGAC
Long Flanking Sequence:
AGCCGACAAGAGAATGAATGAATGACTATATGGTTGGGGTTAGAATGTGGGGTAGGTTTAGGGGTAGCTACATGTAAGTATGCATAATTCATCATAATTACAGTAAGTGCATGGCACATGTGCAACTACGTCACCTTAAATCAAAGTGTTACAACAACCCAAACCTCTTTCATATGTGAATAAAAGACAGTGTATAAGTTTGTAAGGATAAACTTTTGAGTTTTTTAATTCTAGCGGGGGAGCTGAAGGTTACTCAGGCTGGACGTGATTTGCGTATTTTGAGCCCTGGAGATATGTTCGGGGAACTGGCCATTCTATACAACTGCAAACGAACAGCATCAGTCAAAGGTCAGTTGCCATCGTGGAGGGATGAAAGGCCATGAGTTATTTGAGTCGCCCTCTGCTGGTGGGATCAATGGTTAACTGTTTTCCCCACAGCCATCTCTGCGGTAAAGTTATGGTGTATCGAGAGACAAACGTATCGGAGCATCATGACCAAC[A/T]AATCCAAGATGAAACGAGAGCAGCTGATGGGCTTCCTGAAAACGTACGACATTCTGGTGACACTTCAAGTCAGACGCTTACTCACTGTGGATTATGCTTAAGTGAGTTTTACTGTTGTTTTCATCAGGGCGCGCACTTTGAAGGCTCTGAATGATGTGCAGTTGTCAAAAATCATCGACTCCATGGAAGAAGTAGGTGTGATTTTTTAAAATAATAATATAATAAATACCAGTTGCTTTCTAAATCTTTTAGTTTCATGATTACGTGTGTGATTTGTGTTAAAGAAATGCAATCTGGTAAATAAAGGACAGACAGAAAGAGGTGACATAAGGGGAAAACTTGTACATATAAACAAACTGTAACTTAAAAATGTAAGTTTATATCAATTAGATTTATAATAGCCCTTAGTGTCTTTACCCCAAAGGGCCCTTTCAGCTGAAATAGTAGCGTATGGGTCTTTCTGAAAGACCATTATAAATTATCAAAACATGAATGAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13353
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017857 | Nonsense | 555 | 571 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 20 (position 633682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 626957 |
GRCz11 | 20 | 616804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTTCGGTTTTCAGGGTCCTTGCTATWTMAACTTCGACCGYTTTCCTTA[T/G]GACAAGACCCAGGCGGAGGAGGAATTCTCAGGCTGGGATTGTGACTTCTG
Long Flanking Sequence:
ACCAAACTCAACTAGATTAGCCACTCAACTGACAAACCGTAAAATACTTACATTTCCTCGTGAGAACATTCTGGTTTTTCTGTTGTTTTAGGAGAGGGTTGGGCTTAGCCTTGAAAGTTCAACACTAAAGTCTCCTATTTATATGTTTTTAATAATACTATTTATTTTGGATAACAAGAAGCTCTTCGGTTCTGTAGCTGAGTGTGACAAAACACGTCTGCCTGTTCAAAAGTACAGACAGAAGCAAGCACTGGGGATTTGTTATTAATCCTGAGGTAATAAACTCTTATCGAACTGTGACCGAGGAACGTACCGAAACGTGACTTCTGTGTACTGTTACACCCCTGATATCCATCTTTTACAACATCTGATCTCAAATTTTCTTCTGTGATAACGTTCAGAAATGTAAATTATATCTTAAGGTTTTTTTCATTAATTATGGCTTTGCGTGCTTTCGGTTTTCAGGGTCCTTGCTATATAAACTTCGACCGCTTTCCTTA[T/G]GACAAGACCCAGGCGGAGGAGGAATTCTCAGGCTGGGATTGTGACTTCTGAACAACTGCCAAGTAGTCTTAAGATCTCCAACATATCTCAAACTCTCAGGTTATCTCATGTTTAACACCCATAGCATATCTTAGTGGAAGATCAGTACTTTCTGACGATTGGTATATGACCGAACTTTAGTATCTTTCCACAAAGAGAAAGTAAAAGAGTTCTTTGCAGGACTTGTGCTAGTGAGGTGTCAAATGCCCATTTCAAATGCATTGTTTTTATTCTGAAGTGATTTCAGACACTGTGATTCATAGGAGCTAGAGAAAACTGGAGCCAACTTTGCACTAGAAACAGTGAAAATTATTATTATTTTTCAATGTAATGTAAAAATAGACATTGGGATTTGTCTCCATTGTCGTACACGATACCTTATGTACATGCACTTGTCAGACTATTCATGTTTAGGCGAATCAGTCAGATTATAATGTACATTCTTTATTTACTTGTTTAAT
Associated Phenotype:
Not determined