ZMP
gkap1
Ensembl ID:
ZFIN ID:
Description:
G kinase-anchoring protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q6NWC9]
Human Orthologue:
GKAP1
Human Description:
G kinase anchoring protein 1 [Source:HGNC Symbol;Acc:17496]
Mouse Orthologue:
Gkap1
Mouse Description:
G kinase anchoring protein 1 Gene [Source:MGI Symbol;Acc:MGI:1891694]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34498 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa7621 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa34497 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34498
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028009 | Essential Splice Site | None | 377 | 1 | 13 |
| ENSDART00000098319 | Essential Splice Site | None | 368 | 1 | 12 |
| ENSDART00000135675 | None | None | 168 | None | 4 |
| ENSDART00000135714 | None | None | 207 | None | 6 |
| ENSDART00000138810 | Essential Splice Site | None | 28 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 51989497)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49739884 |
| GRCz11 | 8 | 49728653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCAGTTTCCACTTGCACGAAGCCGAAGGTACCGACAAGTCCTAACCAG[G/A]TGAAAGTTTGCTTAGTAAATTATAACACCGCCGTTATTATAATCCCTACA
Long Flanking Sequence:
ACGCTGGATAAGTTGGCGGTTCATTCCACTGTGGCGACCTATGATAAATAAAGGGACTAAGCCGAAGGAAAATGAATGAATAATACTAATTGTTTACTGGAAAAACAGTGGACAATGCGTCTCAGGATTCTTAACGTCACGTGGTATGTGTTACATTTCTCATCTTTAATTATGATCGCAGTCGTGATTACTGAATAAACATTTGTTTAATTTTCGTAACATGATATATTTTACCAGAGGTGACAACACCATGTATGTCAGGTATTCACAGAATTAATTAATATATTTTAAGGAAACATTCAACGACAAACAAATAGTTCTCATCTGTTATTCTGAGCCATAGAGCGCCACCTAAAGGGAGCACGTATTGGCAGTTACTGACAACATTTCCACTCAATAATAACCACTGAAGCTTTTATGTCCGTTCAGGCCGCCATACTCACGTCTGTGTAGCAGTTTCCACTTGCACGAAGCCGAAGGTACCGACAAGTCCTAACCAG[G/A]TGAAAGTTTGCTTAGTAAATTATAACACCGCCGTTATTATAATCCCTACACGTTTGCAGAATACGTGTGTTAAAGGTAGAAACGCGCTGAGGGAATATTACTGTAAACAGGGCGCCTTTGTTACTTGTTTTCAACACCAGCGAGCTAAAAAAAGTCAATGCTAGCGACATTTTAGGTAGCGAATTGTATAATGACTAAAAACTACATTATATCAGGGTGTAATTATTATTTAAACGTATATTACATAACGACGAGTAACGTTACATCTGAAGCGGTTGTTCAGCGAGCACTACAAGCTCCACTCGATTATATACTACATCTTCTAATTGTCAAGTGCTTTGTGTTTATTCAGTGAACAATGCTTATTAAACCTGTTTTTATTTGTTTATTTAAGTCTAGCATGCTAACACATTCAAACGTTATCCGCAAAGTTGTTATGGTAGATGTACGTTAGCACTGATTTTTCAATGCTATAATTTGCTAGTCCCAGAGACGCCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7621
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:
C > T
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028009 | Missense | 14 | 377 | 2 | 13 |
| ENSDART00000098319 | Missense | 14 | 368 | 2 | 12 |
| ENSDART00000135675 | Missense | 14 | 168 | 1 | 4 |
| ENSDART00000135714 | Missense | 14 | 207 | 2 | 6 |
| ENSDART00000138810 | Missense | 14 | 28 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 51985985)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49736372 |
| GRCz11 | 8 | 49725141 |
KASP Assay ID:
554-4022.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGGTCTAGGATGGCATCAGCAGTGATCTCCGTGCCCACCACCGCCTCA[C/T]GCTTCGCCCTGCTGCAGGTCGACTCTGATTCGGACTCAGATTCAGATGTA
Long Flanking Sequence:
GCGCAACATTTTCACGCTAGAAAACGTTTTATGCAGGAATGTAACTGATAATGCTGCTCCTTTAAATATGAGATCAATGTTGCGAGTTTTGACGCTCTCGCCGCAGGAGCTGAAGGCAGAGAGTGTTGTCGCCAGGGCGGCCAGAGCGACCTTGGACGCTCTCGCCGCTTTCGGTGTGAACGTACGGTAAGAATGCATTTAGGTGCCACTGCAACTTTTTCCATCATCATTATATTTACAGGGAAGCCAAAATGCTTTCATACATGTGATTTTAAATGATGCGGGAGGTGATCTCTTTGCGACTGTATAGTTCAAAAAAAGTTCTTAATCAACACGTTACTTGCGTTCCAAACCGTGGGTTCCTAGTTAATAATGAAACCGGTTAATCGTTGCATCCCTACTTTATTTTTCGTCAAGTAAATGTTGCACTGACTGGTGTTGGTGTGATTGGCAGGTCTAGGATGGCATCAGCAGTGATCTCCGTGCCCACCACCGCCTCA[C/T]GCTTCGCCCTGCTGCAGGTCGACTCTGATTCGGACTCAGATTCAGATGTAGGAAAGCCGAAGGCGGCGGGTCGAGGAGCAGGGAAGCCCCGGTCGGGGAAATCGCCTAGCGGGAAGAACAGCCAAAATAACGAGAAAAAGAAGGAAAAGAGGAGACGGAAGAAGGAACAGCAGCAGAGTGAAGCTAATGAGGTGACAGAAAACAAATATGTATATGTTTGTCTGTCTGTCAGTCTGTCTACTTATAAACCTTTTTCTTGGAACGCAAAATTACCCATTATGCTTTGCGTGTATGCGCAAGGCGAATGCAAAGAACTTCCGGTCGGCAGCTGATGCGTGTAAACAGTTACATTTGGACAGCTTTGAAACGATAGTTTTAATCTGTTTTACCAGCTTTTATCCTCTTTGAACTAATACTGTTGTCCATCAGCAGCATCTCCTGGACTGATCATTTAAAGAAATGCAATCTAATAGGATGGAAAACAGCTGCTGTGAGGCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34497
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028009 | Nonsense | 282 | 377 | 8 | 13 |
| ENSDART00000098319 | Nonsense | 282 | 368 | 8 | 12 |
| ENSDART00000135675 | None | None | 168 | None | 4 |
| ENSDART00000135714 | None | None | 207 | None | 6 |
| ENSDART00000138810 | None | None | 28 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 51974405)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 49724792 |
| GRCz11 | 8 | 49713561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGGAGAAGAAAGACCAGGAAATCGCAAAGTTGAAAAAGACAATTTCA[C/T]AATGGGAGGTAAGATGAAATGAGAAATGCTGCAGCAGCAGTAGTGAAGAC
Long Flanking Sequence:
GAATTTTAGCTCATAACTACTGATTATCTGCTAATTAATAGCTTGAAAAGGTGGCAGTTGGATTAGGGACACTTAAGATCATAGTTTAATAAGTGCTGATAAAGAGTTAAGATCCTAACAATAGGCAGGTAATAAGCTAGTTGTTAATGGTATGAATTGTTACTAAAGTGTTACCCTGTTGTTTTCCATAGCCTGTAAATCCAGCGCTCCGCGATGACAAGTTCTTTAACAAGCTAGAGGATGACGTGAGTAAAATCGTCCAGCGCGACAAACGCAGAGAGCAGTACAGCAACAGCGCCGGGCAGGAGGTCAACACGTCCTCAGAGCACGAGCAGGTCCGGCTTTCTCACTGCACATCATAATGTGATCTCAAAGTGGAGAATGCAGCTAAATATAACACCAAAACTGTTTTCAACTTCCAGGATGTGAGAACTGAGCAGCTGAAATACGAACTGGAGAAGAAAGACCAGGAAATCGCAAAGTTGAAAAAGACAATTTCA[C/T]AATGGGAGGTAAGATGAAATGAGAAATGCTGCAGCAGCAGTAGTGAAGACGGTAATAATACTAGATAATAGAATAATGCATATCAGCTACTGTACAATGGGTACAAAGGAAAGCATTTTTATTGATCTGTACTTGTGTGGAAACAACAAGCAGTGTTTTAAACAGGGGCCTGTTTTAGTAAGGTTTAACCGACTGAGTTTAAACTTGAACTTTGAGTTGATTTACAGAGAATAAAAACTCAGAGTTTTCGGTTTCAGAACAGCTCATCTGAGTTGGGTCAATCAACTTTGAGTCGGCCAACTCAGAGTTAAGCGCGCACACTGTGACTATAAAAAGGCATTATTAATGGAGCGCAGATATTATGAGTGGCCATGGCAACCTCTGAAAAAAGAGATCAGCATTTCTTTCTCCAGCTGAACTTGGTGTGCTCATGCAAAGTTAGAGCAAATATGAGCGTATATATTTAAAAAAGCAACACCACTGCATCAGTGAACAACAGA
Associated Phenotype:
Not determined