ZMP
phkg1b
Ensembl ID:
ZFIN ID:
Description:
Zgc:110610 protein [Source:UniProtKB/TrEMBL;Acc:Q503G9]
Human Orthologue:
PHKG1
Human Description:
phosphorylase kinase, gamma 1 (muscle) [Source:HGNC Symbol;Acc:8930]
Mouse Orthologue:
Phkg1
Mouse Description:
phosphorylase kinase gamma 1 Gene [Source:MGI Symbol;Acc:MGI:97579]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43652 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43651 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43652
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101205 | Essential Splice Site | 28 | 394 | 2 | 10 |
| ENSDART00000129619 | Essential Splice Site | 28 | 44 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 25065386)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 25648723 |
| GRCz11 | 21 | 25685328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGACAAGAATTTTATGACAAATATGATCCAAAGGAGATCTTGGGAAG[G/T]TTAGTGTCACCCTGATGAATTTGTGTCTGCAATCTATGACAAAATTAATA
Long Flanking Sequence:
GTTCGACCGAAACAATTCGACTGATTCACTAAAATGATCCGACTCGTAAGAACGATTCGCGACACTGACATCGCTGTTTTACAGCCAAAGTCAAGTCTTCTGGGCAGAGAACTGGAGCACAATTAAAGGCTGTATAAAGAAACGACAAAAATAATCAACTTCTGAAGCGGTTTGTTCTTGGAGGTGTTGTTTATGAGCGTCGTCTGTTGTTATGAGCTACAACTGAGGCATAAAAAGGTTACTGAAGGACGAACGGCTAGGTGAGTGAATTCAGTTCGACTCAATTACATTTTGCAGGAAAACAATCATTAAAATCATTATTATTTATTAGTATTCAATGAAATACTGGTATGCACATGTCTGTGTCTGTGTGTTAAACTTTAAGGCATTATTTTGAAGCACGTCCAATTCATCAGAATGACAAAAGAAGAGGAAAACCCTGACTGGGTTGGTGGACAAGAATTTTATGACAAATATGATCCAAAGGAGATCTTGGGAAG[G/T]TTAGTGTCACCCTGATGAATTTGTGTCTGCAATCTATGACAAAATTAATAGCATAAATGCAAGTCTTACATCAAAAAATAGGCTATTTTAAATATGGGATTTGAAGTCTTGGGTTTGTTTTGAATTTTTCTCCCAGGGGTGTGAGCAGTGTAGTTCGCAGATGTGTGGATAAACGGACTGGTCAGGAATATGCAGTAAAGATCATAGACATCACACCATCAGACAAAATGACACCCCAAGAGATACAAGAAATCCAGCAGGCCACTGTGAAAGAGATCGACATTCTTCGAAAAGTGTCTGGACAAAAGAACATAAGTATGACTATCTACTGCCCCTCAAAGACTTTCACATCACATTCAACAAAATCGAAGGTTATGGCTCTATAATATAAAAAAATCTATTTCATTACAAAAGTAAAAACTGCAATTGTTTTTTTTGTAACAACATACAAATGTAGGTTTTGTTTGTCCCTGGTAGTTCAACTCAAGGATTGCTTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43651
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101205 | Essential Splice Site | 88 | 394 | 4 | 10 |
| ENSDART00000129619 | None | None | 44 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 25064909)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 25648246 |
| GRCz11 | 21 | 25684851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTTTTTTTGTAACAACATACAAATGTAGGTTTTGTTTGTCCCTGGTA[G/T]TTCAACTCAAGGATTGCTTTGAATCAAAGGCCTTCTTCTTTTTGGTATTT
Long Flanking Sequence:
GATCCAAAGGAGATCTTGGGAAGGTTAGTGTCACCCTGATGAATTTGTGTCTGCAATCTATGACAAAATTAATAGCATAAATGCAAGTCTTACATCAAAAAATAGGCTATTTTAAATATGGGATTTGAAGTCTTGGGTTTGTTTTGAATTTTTCTCCCAGGGGTGTGAGCAGTGTAGTTCGCAGATGTGTGGATAAACGGACTGGTCAGGAATATGCAGTAAAGATCATAGACATCACACCATCAGACAAAATGACACCCCAAGAGATACAAGAAATCCAGCAGGCCACTGTGAAAGAGATCGACATTCTTCGAAAAGTGTCTGGACAAAAGAACATAAGTATGACTATCTACTGCCCCTCAAAGACTTTCACATCACATTCAACAAAATCGAAGGTTATGGCTCTATAATATAAAAAAATCTATTTCATTACAAAAGTAAAAACTGCAATTGTTTTTTTTGTAACAACATACAAATGTAGGTTTTGTTTGTCCCTGGTA[G/T]TTCAACTCAAGGATTGCTTTGAATCAAAGGCCTTCTTCTTTTTGGTATTTGATCTGTAAGTAAACCTTTTTTTCTTTCATTGCATGCAACTTTCATGTCTGTGCCTCATTATTTTTATTGACAAAACACATCAAGGACTTGAGTTAAAAAAAAAGTCTAAGTAAAAAAGTGCTTTTAGTATAAAGTATTAAGATTATATAAAAAAACATTAAAAACAAATCTTAAAATTAACGGAAATAAAACAGCAGCTGTGATTTTACGGTAAATAACCAGAGCTTTTTTTATACCAAAGTTTTGAAGAACAAACATCTGCACAACTTAACATTGGTTCATAGATAATACACAACCATAAGCAGGTTTGGATGAGAAAGTCATATGGTGACCCAATGCCCATCACAACTTTTCCTACAAGCAAAGAAATATACTAATTAGGGCTGGGCGATTAATCGAAAAGTCATCGAAATTGACATTCATAATCTAAAATCGATCAAATTTTTATA
Associated Phenotype:
Not determined