ZMP

LOC556339

Ensembl ID:

ENSDARG00000062839

Human Orthologue:

PRKG2

Human Description:

protein kinase, cGMP-dependent, type II [Source:HGNC Symbol;Acc:9416]

Mouse Orthologue:

Prkg2

Mouse Description:

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
sa31905	Essential Splice Site	Available for shipment	Available now
sa22218	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa31905

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

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091271	Essential Splice Site	593	763	13	18

Genomic Location (Zv9):

Chromosome 13 (position 7501987)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	7806597
GRCz11	13	8138799

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTGAAGCCAGAGAATCTTCTTCTGGATGCCGAAGGCTATGTCAAAATGG[T/C]TATTTCACTTGAACTACTAAAAGCTTAAGTGCATAAGTAAATATTGAGGT

Long Flanking Sequence:

CACATGTGAGCCACAGACCCATATTACCCTTAAATGACTATGCCACATTTTTGCCAACTGTGGCCTACATTTGTCCTCCATCATTTGGGCTAAATTGATCATTTTCCACATGGGCCCCATTAGACCCACATTCAGATTACATTTTGCCATAAGTGCCAAATCTTTGCCTTAAATTGCCCATATATGAATTTAACTCTTTGGCCCCCCTCTGCCATTGTACAGGTGGGCCACTTTAGGGTCACATTAATTTTGTCTGGGCTAAAGGAATACCACAATTGCCTAAAGTGGCCAACATTTGAATGCTATCTGGGATATGTTTGCTAAATTAGGATGCCATGATGTTTTGATTTTATTTAGGAGTTGCTTTGATGAGCCCACGGCCCGCTTCTGCACTGGATGTGTGCTGGAGGCTTTTGATTATCTTCATGGCAAAGGCATCGTCTACCGAGACCTGAAGCCAGAGAATCTTCTTCTGGATGCCGAAGGCTATGTCAAAATGG[T/C]TATTTCACTTGAACTACTAAAAGCTTAAGTGCATAAGTAAATATTGAGGTTCTAATAGACAATTCTAAATTTATATTCCAATTTTTGTCAACCTTTTGAATACTTTGTCCAAGTGAGTCTTCAAAGGACTTTCATTTCTAAGCTGATATTGCACAGACTAATAGCAGGCTTAAGTTTAGAAATGGGATAGTATTAAGAGATGTCAGTTTTTGCCATTTAGAATAAGACATTAAAGGGTTAGTTACCCCAAAAGCAAAAATTCTTGTATTAAATGCCATCATGTCTGTCAGTCCCCTGAGACCTTTCATTTTGCGAACACAAATTACAATATTTAAGTACAAACCTAAGAGTTCTCTGATGCTCCATAGACCAGTGGTTTCCATAGTGGAGGTCACAGGACAATGCGGGAGGCTTGCTTGGCAATCTCCAAAAATCAAATAAATTTTCTTAAACTATTAGAATGACCATTACCACATTGACTTTATGGTAAGGTCATACTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22218

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
Order Allele From EZRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000091271	Nonsense	713	763	17	18

Genomic Location (Zv9):

Chromosome 13 (position 7515770)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	7820380
GRCz11	13	8152582

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCCGAATTATTGAGGCTTAGTTTGTTCTGTTATTTTCCCACAGATGGTTT[C/T]AAGGTTTCAACTGGGAAGGATTGAGACGCCGGAAGCTGATGTCTCCTCTA

Long Flanking Sequence:

CTGGTTTGAGCCTTGGCTTGGTCAGTTCGCATTTCTATGTGGAGTTTGCATGTTCTCCCCGTGTTCATGTGGGTTTTCTCTGGGGGCTCCGGTTTCCCCCACAGTCCAAAGACATACGGTACAGGTGAATTGGGTAAGCTAAATTGACCATAGTGTATGTGTGTGCATGTCAGTTTGTATGGGTGTTTCTCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCCTAAAACTGGATAAGTTGGTGGTTCATTCTGCAGACCTCTGATTAATAAAAGGGACTAATCTGAAAATAAAATGAATGAATTATAAAACTTTCTAGCTGGTTTTATTATTGAATGCATGATCATTCCTGTAAAGCTGCATGCTTTTACACAATTTGCATTGTATAAAGCACCACTGAAATAAGTGACTTGATTTAACTTGGCATGTGTCGAAGATTTAGCCAGATCCCGAATTATTGAGGCTTAGTTTGTTCTGTTATTTTCCCACAGATGGTTT[C/T]AAGGTTTCAACTGGGAAGGATTGAGACGCCGGAAGCTGATGTCTCCTCTAAGGAGAGAGGTGAAGAATGGATTAAACATAGTTTTTACAGTATTTTCACATGAAAGCCTGATCTCTTACACTTGTATATTTTCTTCTGTTCCAACATTGGTTTTCCCAGCTCAAGGGACCTCTGGATCACAGCTATTTTGACATGTTTCCCCCTGAGCTCGAAGAGCCTCCAGATGAATTCTCTGGCTGGGATAAAGACTTCTGAAAAACAAGCTGTTTTCATAGCTTTGCTCAACTTACTTTTTTCATACACGATTGATTTTGTAAGTGCTCAGAAGCTCAAAGGAGTTCTCATCTAAAGTGATGGTGGACTTTGTCTGTGCTGGACAACCAAATGACTTGTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGAATTC

Associated Phenotype:

Not determined