ZMP

D1LXJ4_DANRE

Ensembl ID:

ENSDARG00000031702

Description:

cGMP dependent protein kinase I [Source:UniProtKB/TrEMBL;Acc:D1LXJ4]

Human Orthologue:

PRKG1

Human Description:

protein kinase, cGMP-dependent, type I [Source:HGNC Symbol;Acc:9414]

Mouse Orthologue:

Prkg1

Mouse Description:

protein kinase, cGMP-dependent, type I Gene [Source:MGI Symbol;Acc:MGI:108174]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa16398	Nonsense	Available for shipment	Available now
sa41962	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa16398

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
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Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043236	Nonsense	21	684	1	18

Genomic Location (Zv9):

Chromosome 12 (position 6897597)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	6180517
GRCz11	12	6214101

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TACGCGATCTCCAGTACGCGTTACAGGAGAAGATTGAAGAATTGAGACAG[A/T]GAGACGCGCTTATCGACGAGCTGGAGTTGGAGCTCGACCARAAAGACGAA

Long Flanking Sequence:

AAAACGGAGCATTTGTTGAGGTAAAAGTGTGGCTGTGTGCTCGTGTATACGGGAGCGCACATGAAAGCTCTCCGCGGCCGCTACAGGTGCGCGCTCGCGTCTTCCCTCATTGGCTCATCGGGGACTCGCGTTCACTGCGCGCTCATGGCGTTACACTCGCGCTCGACGCGCACCACAGCTGCGACTGACGTATTTGGACAAGAAATTAATGCCCTGTGAAACTTCGGCTCCCGAATGTGATGTTTGCAGACGCCGTGGGTGTTTCCCCGCTCATTCCTCCGCTTTAACTAGCCCGAAAGCACGCCGGTGGATCTACACGGCGAAATCTGAAGGACGTTCTCGGAAAAAAACACGAACTAAAGCGGTTTTCTTGTCTGAGAGCGTGGATTTACCGTTATCCAAGTTGGTAACGGCTGCAGGAGCACTGACTGTGGGGAGAAATGGGCACTTTACGCGATCTCCAGTACGCGTTACAGGAGAAGATTGAAGAATTGAGACAG[A/T]GAGACGCGCTTATCGACGAGCTGGAGTTGGAGCTCGACCAGAAAGACGAACTCATACAGAAGCTACAGAATGAGTTAGACAAGTACCGATCCGTGATAAGACCCGCAACTCAACAAGTCCACAAGCAGAGTGCCCTTCAGGAGCACCAGAGGACCAAGAGACAGGCGATCTCAGCCGAACCCACAGCCTTTGATATCCAAGACCTCAGTCACGTCACTCTGCCTTTCTACCCAAAGAGTCCACAGTAGGTGCCGCTTAAACAGATTTTACTATGATGGTTTCCATCAAACGGTGCTGATGATTTGCATTACTGATGCTATTATGTCAGTGCAGTCTTGTTATGACACGTGAATCACTTTCTGTTGCGCTGTTCTCATTTTAAGCGAGAAATCTTGGTCAGTAGGACACCTTGAGTTGTGTGTGGTGTGGGTAATAATCATAAGCATCCATCAAACCTGTCTCCGCATCTATGCCTTCATTACTTTGCTAATGTGATGCAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41962

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000043236	Essential Splice Site	231	684	4	18

Genomic Location (Zv9):

Chromosome 12 (position 7042329)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	6325249
GRCz11	12	6358752

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAGGACAGGACTCATCAAACATGCAGAGTACATGGAGTTCCTGAAGAG[G/A]TGAGCCCTCACTGCTTTCATTTCTATTCATTCATCTCCAACCCCTGATGC

Long Flanking Sequence:

ATTGGATGTTCTATTCGTGTTGTCGTGGGTTTTCTCCAGGTGCTCTGGTTTCCCTCAGAGTCCAAAGACATGCGCTATGGATGAACTAATTAAACTAAATTGGCCGCAGTGTATGGGTGTGTGTTTGTGAATGAATACTGAATGTTTCTCAGTACTGGGCTGCGGCTGGAAGGACACCTGCTGTGTAAAGCATATGCCAGAATAGTTGGTGGTTCATTCTGCTGTGGTGACCCCTGATAAACAAGAGACCAAACCGAAGGAAAATGAACGAATAAATAATTTTAAGTGACAATGACTGCACAGCTAATGTATATGACTGATAAAAAGAAGCACTTGCTTGTGTGTTTTGCGTGGGCATTATTTACTTACTTCTTTTCAAATTTTTATTCCTCAGCCCTCACAAATGTGAAGTTATGGGCCATTGACCGGCAGTGTTTCCAGACCATCATGATGAGGACAGGACTCATCAAACATGCAGAGTACATGGAGTTCCTGAAGAG[G/A]TGAGCCCTCACTGCTTTCATTTCTATTCATTCATCTCCAACCCCTGATGCAAGAGGTCTGTCCCTCACCAGTATGCAATAAAAAGAAATTGATTTTCATCATGAATGGATAACACAGGAGTCAGCGCTTACACAATCGCAGACTTTACACTCGCTGTCCTTTGCAATGTGTGCGCCGTTAATTTCCCGGGTGATGGGTTTTGATTCGAACAGTTAGAAAGGTGAAACGTCATATTGCTCTCGAATGTTTCTAATCAACTGTTGTTATATTTCGTCAGGTTTTTCTTGAGGAAAGCGAAAGGTATTGGTTAGAGAGCAGGTAATGATTAGAGTGCTGCTGCTTTCTGCTTGTTTGAGTCTAATTCATCTCCTTCCACACACTTATAGTGGCGAGATATTGATTTTTAAGCCATGAGCTGTTTGTGAATAGCTTTGCTCAGATAGAACGTACTTAGTTTTATTATTTGATATCGATTAGTCTACTTTCTGTCAGTAATGTTG

Associated Phenotype:

Not determined