ZMP
PHKA2
Ensembl ID:
Description:
phosphorylase kinase, alpha 2 (liver) [Source:HGNC Symbol;Acc:8926]
Human Orthologue:
PHKA2
Human Description:
phosphorylase kinase, alpha 2 (liver) [Source:HGNC Symbol;Acc:8926]
Mouse Orthologue:
Phka2
Mouse Description:
phosphorylase kinase alpha 2 Gene [Source:MGI Symbol;Acc:MGI:97577]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14109 | Nonsense | Available for shipment | Available now |
sa21943 | Essential Splice Site | Available for shipment | Available now |
sa10546 | Nonsense | Available for shipment | Available now |
sa16397 | Essential Splice Site | Available for shipment | Available now |
sa11966 | Essential Splice Site | Available for shipment | Available now |
sa45433 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14109
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078202 | Nonsense | 240 | 1161 | 9 | 32 |
Genomic Location (Zv9):
Chromosome 11 (position 34739205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33640142 |
GRCz11 | 11 | 33902944 |
KASP Assay ID:
2260-4502.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTGCTTTTTCATTTCATGKTTAKAACAGGACCCYACTYGAYTTCACTA[T/G]GACCCTGCCGAGCTGAAGCTCTTTGARAACATTGAATGTGAATGGCCAGT
Long Flanking Sequence:
TGCAAAACACTGTACCTCCTGGGATGTATTTTGCCATCACCAAAAATGTATATAGGGCTACGTTTTCAGAATGAGCCTGTGTTGCATATTTCAATGTTTATTTTTTTTTTTTAAAGTAAAAACACTTTTATGAGGGAACAAAAAAAATTGCCGGAATACATGAGGTTTTTTAAATAAACACAATTATTTTGTGAGGAAGCATTAAAATATAAATTTCCCATCTCATGTCCTCTTAGCATCTCTGCAGTTCCCTTCTGTGGTTGCTAGTTTTATTGCAAGTTTAATCATCGATTTCAATTATTTTAGGGACGTTATGGCTGTTGTCGATTTATCCGAGATGGATACAGGACTCCAAAAGAGGTAACCAGATATAACTTGAATTTACACACACACACAAAGTAATAATAAATTGGCAATAATAAGTAATAATTATTTTGTGACCAGTTCTCTGTCTGCTTTTTCATTTCATGTTTATAACAGGACCCTACTCGACTTCACTA[T/G]GACCCTGCCGAGCTGAAGCTCTTTGAGAACATTGAATGTGAATGGCCAGTGTTTTGGACTTATCTAATACTCGATGGCATCTTCAATGCAGATCATGAACAGGTATGAAAATAATCATCTGTATACTCTGAAAGCATCTGCAGTACATCTGAGGGGAAAAATTATGGGATATTTCCCCCCAAAAATGAAAATTTGAGTATATTAGTAAATTTTTGGGTGAACTATCTTTTATCTCCAGATGGAGGCAGTGTAGCAATGATTGATGGCTGTGCTGTTCCTCATAGGTGGAGGAATACAGAGAGGCTCTGGATGGGGTTTTGATCAGGGGCAAACATGGTATCCGTCTGGTGCCTGAACTCTACGCTGTACCTGCTGACAAAGTGAGTTTAACTTTTTAAACTAGCACAGGAACTCCTTTTATATTTAATTACATGCAATGGTATTGTAATAGGTTCACAATAAAGTGAGCGAGATTGAATTAAAGTGCTGATTTGAGGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21943
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078202 | Essential Splice Site | 413 | 1161 | 13 | 32 |
Genomic Location (Zv9):
Chromosome 11 (position 34736585)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33637522 |
GRCz11 | 11 | 33900324 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCCGGGTTATGCCAGCTCGCATCCTGAGCCACATTTATGTGAAACTGG[G/A]TGAGTGTTCAGATCCAGATGGCGTAAATGAGGATATCTGTGAAATTTAGA
Long Flanking Sequence:
TATTTTTTATTTGTTTGTAAAGCCCTCATACTGTACAGACACATGGCTTTTTGTAAAATATTTAAAACTATTTCATTATTTCATTTAATGTTTAATTTACAGCAGTTTTTGTTAGAGTTTTTACTCTGAAAATACTAGTAAATGTCTATTTAAATTTAATTATAAAAAAAATACTTGGAGGGGAAACAATATTGCAAATGTATGCAAATCTATCACAATGTAGAAACGACCCAGCTGGTTGCTTTGCTCTGAAGTCCATTTAAGGTTCATTACTTGAAACTCAATTTTGAATTGAATCTTGCCACTATAATTTGCTGCACAGAGAAAGCTGATCTTTTGCCAGCGGCTGTATTTGTTCTGTTTAGTGAGTGTAGTGGCTGAGTCAGTGCAGATCCAGCAGCTGCTGAGGGATCATGGGATTGAGGTTCAGACCGTCTCTGATGTATCGCCCATCCGGGTTATGCCAGCTCGCATCCTGAGCCACATTTATGTGAAACTGG[G/A]TGAGTGTTCAGATCCAGATGGCGTAAATGAGGATATCTGTGAAATTTAGACTCAATTTCCTTTTTGCTTTTCACAGGAAACTGTAAAAAACTCAACTTGAGTGGACGACCGTACAGGCACATTGGCGTTCTGGGAACTTCAAAGTTTTATGAGATCAGAAATGGCACTTACACTTTTACTCCACAGGTAAGTGAAATTTCTGCCTTGAAACTCTTTAGAAAGAAAATATTATCTACATGGCACAGGAGATTGGTTGCTGTCTCCTCGGCAGCCAATGAGCTTGAACTTCATGGGTGCATGCTCCACGTCATTTTAAGCTGTCAAGCTACAGCGCGTTTTTGAAGACCCTCCTCCACCCCAGCTCCACCTGTGTTTAGATACTGCTTACATGTATACTATGTTTGCAGCAGGAGCGTGTTATATTTTTTAGACGGCATGTCTGTGTGTATACTGGCAGTAGCAGGTCTCAGTACTTCCTCTGCCATAATTATCAAAGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10546
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 |
---|---|---|---|---|---|
ENSDART00000078202 | Nonsense | 424 | 1161 | 14 | 32 |
Genomic Location (Zv9):
Chromosome 11 (position 34736479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33637416 |
GRCz11 | 11 | 33900218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCCTTTTTBNCTTTYCACAGGAAACTGTAAAAAACTSAACTTGAGTGGA[C/T]GACCGTACAGGCACATTGGCGTTCTGGGAACTTCAAAGTTTTATGAGATC
Long Flanking Sequence:
TTTTGTTAGAGTTTTTACTCTGAAAATACTAGTAAATGTCTATTTAAATTTAATTATAAAAAAAATACTTGGAGGGGAAACAATATTGCAAATGTATGCAAATCTATCACAATGTAGAAACGACCCAGCTGGTTGCTTTGCTCTGAAGTCCATTTAAGGTTCATTACTTGAAACTCAATTTTGAATTGAATCTTGCCACTATAATTTGCTGCACAGAGAAAGCTGATCTTTTGCCAGCGGCTGTATTTGTTCTGTTTAGTGAGTGTAGTGGCTGAGTCAGTGCAGATCCAGCAGCTGCTGAGGGATCATGGGATTGAGGTTCAGACCGTCTCTGATGTATCGCCCATCCGGGTTATGCCAGCTCGCATCCTGAGCCACATTTATGTGAAACTGGGTGAGTGTTCAGATCCAGATGGCGTAAATGAGGATATCTGTGAAATTTAGACTCAATTTCCTTTTTGCTTTTCACAGGAAACTGTAAAAAACTCAACTTGAGTGGA[C/T]GACCGTACAGGCACATTGGCGTTCTGGGAACTTCAAAGTTTTATGAGATCAGAAATGGCACTTACACTTTTACTCCACAGGTAAGTGAAATTTCTGCCTTGAAACTCTTTAGAAAGAAAATATTATCTACATGGCACAGGAGATTGGTTGCTGTCTCCTCGGCAGCCAATGAGCTTGAACTTCATGGGTGCATGCTCCACGTCATTTTAAGCTGTCAAGCTACAGCGCGTTTTTGAAGACCCTCCTCCACCCCAGCTCCACCTGTGTTTAGATACTGCTTACATGTATACTATGTTTGCAGCAGGAGCGTGTTATATTTTTTAGACGGCATGTCTGTGTGTATACTGGCAGTAGCAGGTCTCAGTACTTCCTCTGCCATAATTATCAAAGCAGCAGCAGTGTAGCAGGTCTATACCGCTAAGACAAAATACATCAACACTGCCATATACATAATAATTATACTAAATCCTGGGATCCTGGGACACTAATCCTATTAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16397
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078202 | Essential Splice Site | 450 | 1161 | 14 | 32 |
Genomic Location (Zv9):
Chromosome 11 (position 34736398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33637335 |
GRCz11 | 11 | 33900137 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCAGAAATGGCACTTACACTTTTACTCCACAG[G/T]TAAGWGAAATTTCTGCCTTGAAAYTCTTTAGAAAGAAAAKATTAWCTACA
Long Flanking Sequence:
AATATTGCAAATGTATGCAAATCTATCACAATGTAGAAACGACCCAGCTGGTTGCTTTGCTCTGAAGTCCATTTAAGGTTCATTACTTGAAACTCAATTTTGAATTGAATCTTGCCACTATAATTTGCTGCACAGAGAAAGCTGATCTTTTGCCAGCGGCTGTATTTGTTCTGTTTAGTGAGTGTAGTGGCTGAGTCAGTGCAGATCCAGCAGCTGCTGAGGGATCATGGGATTGAGGTTCAGACCGTCTCTGATGTATCGCCCATCCGGGTTATGCCAGCTCGCATCCTGAGCCACATTTATGTGAAACTGGGTGAGTGTTCAGATCCAGATGGCGTAAATGAGGATATCTGTGAAATTTAGACTCAATTTCCTTTTTGCTTTTCACAGGAAACTGTAAAAAACTCAACTTGAGTGGACGACCGTACAGGCACATTGGCGTTCTGGGAACTTCAAAGTTTTATGAGATCAGAAATGGCACTTACACTTTTACTCCACAG[G/T]TAAGTGAAATTTCTGCCTTGAAACTCTTTAGAAAGAAAATATTATCTACATGGCACAGGAGATTGGTTGCTGTCTCCTCGGCAGCCAATGAGCTTGAACTTCATGGGTGCATGCTCCACGTCATTTTAAGCTGTCAAGCTACAGCGCGTTTTTGAAGACCCTCCTCCACCCCAGCTCCACCTGTGTTTAGATACTGCTTACATGTATACTATGTTTGCAGCAGGAGCGTGTTATATTTTTTAGACGGCATGTCTGTGTGTATACTGGCAGTAGCAGGTCTCAGTACTTCCTCTGCCATAATTATCAAAGCAGCAGCAGTGTAGCAGGTCTATACCGCTAAGACAAAATACATCAACACTGCCATATACATAATAATTATACTAAATCCTGGGATCCTGGGACACTAATCCTATTAGTGTTCATGAAAATTACATCAAATGACAGGAAGTTCATTACAGAGTTAAAACTAATTTACTAACCGTCTGATCATCTAAAGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11966
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078202 | Essential Splice Site | 713 | 1161 | 21 | 32 |
Genomic Location (Zv9):
Chromosome 11 (position 34723442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33624379 |
GRCz11 | 11 | 33887181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAACCCTGCAGGAYCAGGCCGATAWCCTCTATGTCCTCTATGCTATGAA[G/A]TGAGAGACTATTGTGCATATCTATTTTGATWTCTGCTTCATCCAATAGTY
Long Flanking Sequence:
AGTTTATTAATTCTTAAATGCGAGGCTGACAGAAATGAAAATGGCTGAACGGAGCATACACTAATCCTATTATTCATTTTATTCAATATTATTTAATCACAAGATGGCGCCACACAGTCAAAAGCATCAGCCAAACAGAATCTTAAACATATGAATGTGGATGTATGTATATGATGTGAACGTATTCATTTAGAGTCAAGGTGATTCAAAGTATCTAGACGAGCATGTTTTATTAGCTTTAGTGGTTGTTATCTGGAAATAACTGATTGACCAATCAGAATCAAGTATTCCAGAGAGCCGTGCAATTAAAAAAGCGCAAAGAAGAATCAAAATAAACAGCTGTAGTTTGTGGTTTTGTCTCTTTAGGCTGATAACGTTGACCTGCATTTACCACGCGATTCTCATGGAAACACAGACTTTGTTCATCTGGTGGATCAGCTTAAGCACTGTCCAACCCTGCAGGACCAGGCCGATATCCTCTATGTCCTCTATGCTATGAA[G/A]TGAGAGACTATTGTGCATATCTATTTTGATTTCTGCTTCATCCAATAGTTTAATAATCGTTCTCTTCCTGATGTGTATGTGTATATAGAGGCCCGAACTGGGTGGTGAGTTTGTCAGGACAGGGTGAGGCGACAGTTCGCTCTCTGCTGGAGGAGCTGTACGTTCGGGCAGGAGCGTGTAAGGAATGGGGCCTCATCCGCTACATCTCCGGCATCCTGAAGAAGAGGGTGGAAGTCCTTGCTGAAGTGAGACTCTTGTTAATCTATGCATTTATTGTCAACTTGACAATATTAATTATTGTTGTTTGATTAATTCATATATAATACAGTATGTGAATCTAGACCAGGGGTGTAAAAACTCGGTCCTGGGGGGCCGGTGTCCCTCACAGTTTAGCTCCAACTTGCTTCTACACACCTACCAGAAAGTTGCTAGTATATCTAGTAAGAGCTTGATTAGCTGGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAACTTTCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45433
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078202 | Essential Splice Site | 792 | 1161 | 23 | 32 |
Genomic Location (Zv9):
Chromosome 11 (position 34721264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33622201 |
GRCz11 | 11 | 33885003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGACAGTGGGTCTTCCTCCTGAACCCAGAGAGAAAGTCATCACGGTG[T/C]GAGTGTCTTTTCACATGTTCCTTTTAAAATAATTTTAATATTCCTCCAAT
Long Flanking Sequence:
TTTTTGGTCAAAGTAATTGAATTGCTAATATGATGTGCTGATTTGCTCCTTAAGAAACATTGCTAACAACCAGAGACATTTTTTCAAAATCCTTTGTAAGATTATAAATGTCCGCATCACTTTTGATCGTTTTGAACGTTTCATGTTTTTGTTTCTCATCAAGTTAACAAATTATTTATTTTTACTCCTTATCCAGACCCAAACATCTGTTCATATCTATGAAAATCCATCATAAAATGTAAATTATTATATTGATGAAACTATGATAAGCTAAACAGAGTACAAATCGGTGATGTCATGCCAAGTCACATTTATAGTAATTAGATGGTTTCTTTTGGACTAATATCTTGAACTTACATACCTGTGAGTTGTCCAACATTTGCATTAATATGCTTTTTGTTGGCATCTTATGCAATTAGGCCTGCACAGATCTGATCTCTCATCATAAACAGCTGACAGTGGGTCTTCCTCCTGAACCCAGAGAGAAAGTCATCACGGTG[T/C]GAGTGTCTTTTCACATGTTCCTTTTAAAATAATTTTAATATTCCTCCAATACCTAACCAGGTTCTTATTTTTAGTCCTCTTCCTCCTGAAGAATTGATCAGCTTGATCTACGAGGCCAGCGGACAAGACATCAGCATTGCAGTCCTCACACAGGTACTGTTGATTTGTAAGCCTTAGGGCCCTATCATAAACCTGGCTCAGTGTTTTTCTCCGGTTTCAAATTGGTGCAGGTATAATTTTCATGTCCTGTGCCACTTTGTTTAAATTTGTGCACCCATGAGTGTGCTGGTCTGAAAAGCAGGTCTGTTGGTAAAGCATTTCTATTGTGACGCAACTGAAAAAGACCACACCATTGACCAACTAAAAGTCAATAGGGCATTTCTTTTTGTTGTTCTTGTTATTTAAACAATGTGTTGACAAACAGTGCCTATGTGCAGGTCCATGTGTGTACTTGTTGCTTATTACACACGCAGGGATGCACAGCAGCACACAAACATCTT
Associated Phenotype:
Not determined