ZMP
LOC556339
Ensembl ID:
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 |
---|---|---|---|
sa35418 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45481 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31905 | Essential Splice Site | Available for shipment | Available now |
sa35419 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22218 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35418
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091271 | Nonsense | 239 | 763 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 7480330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7784940 |
GRCz11 | 13 | 8117142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAGGTCAGATGCGTCCTGGAACAGCCTTCGGAGAGCTGGCCATTCTCTA[T/A]AACTGTAAAAGAACTGCTACGGTCAAAGGTAGATTTTATTATGCTTGAGT
Long Flanking Sequence:
TTCATAATAAAATTATAAAATTTGAATCTCCACTGGATATAACAACACATAAAAAAAAAAACACCAAGCGTCACTTAAATTTTAATTCTTTCTTTTCCTTCGTCTTATAGCACTAAGAAACTGATAAATGAAGCCCTCATGAAGAATGACTTCCTGAAGAAGCTGGAACCTCAGCACACTAGAGAGATGGTGGACTGTATGTATGAGAAAATCTATGGGGCTGAGCAGCTGGTTATCCAGGAGGGAGAGCCGGGGAACTTTCTCTATGTGCTTGCTGGTATGGTACAGGCACTTTATTCTTTCATATGTTCATATCAACATATTTTAATAAGAATAGTCAGATAATATCCTGCACTCCACTTTTATGTGTTGTTTAAATTTAATTTTGCCCATTTCTGTAATTTTATTTGGTCAGAGGGCTTATTAGAGGTCATTCAAAATGGAAAGTTCCTAGGTCAGATGCGTCCTGGAACAGCCTTCGGAGAGCTGGCCATTCTCTA[T/A]AACTGTAAAAGAACTGCTACGGTCAAAGGTAGATTTTATTATGCTTGAGTATTTTTGTGTTTAACCAAAATGTTTAAAGGGATGGTTTACCCAAAATTGTAATTCTGCCATTATTCACTGATCCTTCATTTTTAAAAACAAAGTTTTGTTTTTCTGTTGAACTCAAAACAAGTCATTTTTTAAAAATGCAGGTTGTTGGCACTCATTGGCTGTTTCTCAATTCCAAGAACACAGAGAACGGACTTGCGTTCTTGTGGAGACCAGTCTTGCCAGGTGTCCTCGGAAGAACGAACTCAGGAGACCATGAGGGCAGAGAATGCATCCTTTGAAAACTGAGATGCTGCGTTCTTCCTGATGGTCACATGACCTTCACGCATTTTAAATAGTAAATTATTTAAACATTACAGCATTCATAGAACGATTTATTGTTTTTCCCTTTTTCAAAATATATACTTTGCATAAAAACATTATAACTATACACTGCACAATTTAAATAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45481
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091271 | Essential Splice Site | 546 | 763 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 7501842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7806452 |
GRCz11 | 13 | 8138654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGGATATGTTTGCTAAATTAGGATGCCATGATGTTTTGATTTTATTT[A/C]GGAGTTGCTTTGATGAGCCCACGGCCCGCTTCTGCACTGGATGTGTGCTG
Long Flanking Sequence:
GTTTTAAAATAACTGGGCCATATTTTCCAGATTTTCTCTGGGCCACATTAGGCTCACAGCCACAATAGCCAGAGCTTACTTTGCCAAATATTTGCCAAAAGTGGCCCACATATGTCTTAAGATAACTGGGCCACATTTGCCCTTACACATGTGAGCCACAGACCCATATTACCCTTAAATGACTATGCCACATTTTTGCCAACTGTGGCCTACATTTGTCCTCCATCATTTGGGCTAAATTGATCATTTTCCACATGGGCCCCATTAGACCCACATTCAGATTACATTTTGCCATAAGTGCCAAATCTTTGCCTTAAATTGCCCATATATGAATTTAACTCTTTGGCCCCCCTCTGCCATTGTACAGGTGGGCCACTTTAGGGTCACATTAATTTTGTCTGGGCTAAAGGAATACCACAATTGCCTAAAGTGGCCAACATTTGAATGCTATCTGGGATATGTTTGCTAAATTAGGATGCCATGATGTTTTGATTTTATTT[A/C]GGAGTTGCTTTGATGAGCCCACGGCCCGCTTCTGCACTGGATGTGTGCTGGAGGCTTTTGATTATCTTCATGGCAAAGGCATCGTCTACCGAGACCTGAAGCCAGAGAATCTTCTTCTGGATGCCGAAGGCTATGTCAAAATGGTTATTTCACTTGAACTACTAAAAGCTTAAGTGCATAAGTAAATATTGAGGTTCTAATAGACAATTCTAAATTTATATTCCAATTTTTGTCAACCTTTTGAATACTTTGTCCAAGTGAGTCTTCAAAGGACTTTCATTTCTAAGCTGATATTGCACAGACTAATAGCAGGCTTAAGTTTAGAAATGGGATAGTATTAAGAGATGTCAGTTTTTGCCATTTAGAATAAGACATTAAAGGGTTAGTTACCCCAAAAGCAAAAATTCTTGTATTAAATGCCATCATGTCTGTCAGTCCCCTGAGACCTTTCATTTTGCGAACACAAATTACAATATTTAAGTACAAACCTAAGAGTTCTC
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa35419
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091271 | Essential Splice Site | 689 | 763 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 7508121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7812731 |
GRCz11 | 13 | 8144933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCTAAATGAGAACAGTCAGAAACTCTTTTGTCTCATTTATTCTCTCC[A/G]GACTCAATCCAGCAGAACGGCTTGGGAATAAAAAGAATGGCATCATAGAT
Long Flanking Sequence:
TCATCTTTGCTCCTATGGTACAAGACCTATTTTAGATGCTGCTTTTGTACCAAACCATAATTACAATCACCTGTTGACATCACCTGTTTCAAATAACATCATTATTTAACCAATTTACCTGACTACTAGCCCTAATTTGCTCCGGTCCCAACTTTCTTTGGAATAAGTTGCAGCTCTGAATGACAGGGAAAGATGGATATTTGAAAATAAAATCAAGTTGACCAGACAAACTATTTAATATCTTGCGTTCAAATTGTCTGCAATGAAATACAAATCAAAGTAAATTTGGAAATAACTACTTTCTTTTTTATTTGTGTTTTCCATACTGTCCCAGAGATGTTCTTTACATCTGACTGTTCTCATTAAATGCTGTTTGATGTTTCCTGCACATGTCAGTGTACATGTGTACCTGTCAGTGTATGTTTATTGTTGTAGCCTTTTTCTATTGTTCCACCTAAATGAGAACAGTCAGAAACTCTTTTGTCTCATTTATTCTCTCC[A/G]GACTCAATCCAGCAGAACGGCTTGGGAATAAAAAGAATGGCATCATAGATATAAAGAAACACAAGTAAGCCATTTCTTTCTTTCATCCTGGTGAGCACATTGAGACAAAACAATGGCACTAAAGTGTTCAAATGTATAGCCTTATATTCCAAGGGTATACATCACAGTGGAGTGCTCATAAATGTCACTGTCACTGAGTAGAAGAAAATGCTGAATGTAGTTGTTATTTTTGTTTTATGTGCACACAAAAGTATTACCGTAGCTTGAGAATATTTCAATTTAATCACTGAAAGGTTTAAGTCTAGCCTGTAAAACCAGGGGTATATGTTACAGATTAAACATTTACATTTAACATTTAGGGCTCTATTTTGATTGTCCATGCGCAAAGTGCAGAGCGCAAACCAAGGGTGTAGAATTGGCATGGGCGGAGGGGTTGTGTCCCCACCAATATCCATCAATTACTAAAATGTCCCTACTAATAATTTAATCGACTTTAAAAT
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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