ZMP
PYGL
Ensembl ID:
Description:
phosphorylase, glycogen, liver [Source:HGNC Symbol;Acc:9725]
Human Orthologue:
PYGL
Human Description:
phosphorylase, glycogen, liver [Source:HGNC Symbol;Acc:9725]
Mouse Orthologue:
Pygl
Mouse Description:
liver glycogen phosphorylase Gene [Source:MGI Symbol;Acc:MGI:97829]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16886 | Nonsense | Available for shipment | Available now |
sa6325 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12138 | Nonsense | Available for shipment | Available now |
sa38964 | Missense | Mutation detected in F1 DNA | Not yet available |
sa38963 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16886
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 |
---|---|---|---|---|---|
ENSDART00000023449 | Nonsense | 161 | 965 | 4 | 31 |
Genomic Location (Zv9):
Chromosome 13 (position 37263010)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36735312 |
GRCz11 | 13 | 36861144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTAGACTCAATGGCRACTCTGGGTCTGGCAGCCTATGGATATGGGATA[C/T]GATATGAATATGGAATATTCAACCAGAAGATTAAAGATGGCWGGCAGGTG
Long Flanking Sequence:
TTAAACTAAATGTAGACAATCTACTATGCAAAATCCTGGAAATCTCCATTTCTCACTAGAAAGTTGTTTTTCCCTCTGTGTGCTTCAGCGTGTTTATTACCTCTCACTGGAGTTCTACATGGGTCGCACGCTCCAGAACACCATGATCAATCTGGGTCTGCAGAACGCCTGTGATGAGGCCATCTATCAGGTCAGGGAACACAAAAACACTCATTTGTCTGTGCGTCTGTTTGCCTATCAGTCTGTAATCCTCTTGTTCTCCTTCCAGCTGGGCTTGGACATGGAGGATCTGGAGGAGATGGAAGAAGATGCTGGATTAGGCAATGGAGGCCTGGGCAGATTAGCAGGTCTCACTTTCTCTCTCTCTGAAATACACTGAACAAATAATATCATGATACAAGTTATATTGAAATTTATTTATGTGTGTGTGTGTGTGATTCACAGCATGTTTTCTAGACTCAATGGCGACTCTGGGTCTGGCAGCCTATGGATATGGGATA[C/T]GATATGAATATGGAATATTCAACCAGAAGATTAAAGATGGCTGGCAGGTGAATAAGATGGCTGACCGAATTAGCCAAATTTCCTGAATATTTGTAAACGTTGGTGACCTGATACTGATATTTAGAGTAATTCTGACCTATATTCCACAAATATTTATTTAAGAATACACAAAAAAAGAGATGAAATATATTTAAATACTTTGTTACATAAAATTTTATATTAATTATAATTATCAGAATTAATCTCCTATTATATATTATATTATATTATTATATATTATATTATATATTATAATTATAATTAAAGCATATCCCATAATGCAACAAATTGCTTAAATTTATTGATAATAGAGATTTTAAAATATATTAGCACAAATACAGTTGAATTATTAGCTCCCCTATATATTTATTATTATTATATGTTATTATAAATTTTTGAGTTACTTGAGTTTTACGTGATTCATATTGCATTTACATATATGTGACCTAGTTTGCAGTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6325
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023449 | Nonsense | 264 | 965 | 7 | 31 |
Genomic Location (Zv9):
Chromosome 13 (position 37259199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36731501 |
GRCz11 | 13 | 36857333 |
KASP Assay ID:
554-5215.1 (used for ordering genotyping assays)
KASP Sequence:
TTAWAAATTCTTTATAAACTSTATTTATTTACAGTTAAYGTGGGTGATTA[C/A]ATTCAGGCAGTTTTGGACCGTAACTTAGCAGAAAACATTTCSCGTGTGCT
Long Flanking Sequence:
TATTTTTAAATATAGTGATAGATGATATGAATTTCATATGAAGTATATCTTGAAGCGCATTCAATACATGTGGAGCATATTTAGAGAATGCAGATCGACCTTTAATTCTATCATTTTTATTTGTTAGTTTTAATATTTTTATTTAAAATTAAATGAATAAAATATTATTTAATATAATACAAAACTACAATTATAAATATTAGTTAGCATTATTTCATTATTGTTTTATTTACAGTAACAACAATATTTTAATTAGGATTTAATAAGTATTCATCAAGATAATAACATAAAATAGTATATAAAATAAGAATTAAATAAAAAGGGTTTGAGCTGCGTGCATAAATAAAATCAAGCCTTTATGTATTTATTTATTTTCTGATTTTAGTTATTCCAGAAAAATTAGTTGTTGCTACTGTTATTTATACTAAATTATATATTTTTTAAATGTATTTATAAATTCTTTATAAACTCTATTTATTTACAGTTAACGTGGGTGATTA[C/A]ATTCAGGCAGTTTTGGACCGTAACTTAGCAGAAAACATTTCCCGTGTGCTTTATCCAAATGACAATGTAAGTTCCTTTTTTTATGTCTTGCCTTTGAGGTTTAAATGCCTTTTATGTAATTAAACTGCATAAATGTCTATTAGTTATTGTGTGCTTGAAGATTTTAATAATCCAGTAGACTTTAACCTTGAACATACTCTATGGCATTCATTTGTAGTTTTTTTGCATCCATTTGTAGTTTTTTACATCCATTTGTAGTTTTTTGACTCTACACCTTCTGTGATTTGTAGTTTTTTGAGGGAAAGGAGCTGCGTTTAAAGCAGGAATATTTTGTGGTGGCAGCAACTTTACAAGATGTGATTCGACGCTTTAAGACCTCGAAGAGAAACACTTCTGGACCGTTGTCATTCGACAGCTTCCCTGATAAGGTCTGACTTTGATGCAAATTCTCTAGACTCAATGCAACCATTTGACACTTCAGAGCATATATTTAATTCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12138
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023449 | Nonsense | 387 | 965 | 10 | 31 |
Genomic Location (Zv9):
Chromosome 13 (position 37256148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36728450 |
GRCz11 | 13 | 36854282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACRTTTGCYTACACAAACCACACGGTTCTGCCAGAGGCTCTGGAACGCTG[G/A]CCAGTTGATCTGATGGAGAAACTCTTACCGCGACACCTGCAGATCATATA
Long Flanking Sequence:
GAATCGAATATTAAAATTAATGTAGAATAGGACATAACTCAGCAGCCCCTCAGCATAAGTCAAATTGAAATATTTTGGTTGTAAAAACACACTTTCGGTTACCAAAACTTGCAAATTGGTCAAGCAACGAGTAACCATAATAACAAACAAACATCCAAGGAAACATAGGAAATGCACAAAACAAATTACTGACAAAGTCTGCAAAGCAAAACTGAAACCAAACTGGCTCACTGTAAAAAGCAGTAGCCTCTTTTTTTAAATTTATTTATTATTTATTTTTAATAAAGTTATTTAAGCTTAAAATGAGTACTGTATGGGTATAAATGAAATCTATTTAGTTTAATTGAATGATGCAGATTTTTAACAGTATGTTAGCTTTGTGAAGGCGACATGATTCCTGAAAATAAGTTGCTCTGTGTGAGTGTCTAGGCCTGGGATATCACCAAGCGAACGTTTGCTTACACAAACCACACGGTTCTGCCAGAGGCTCTGGAACGCTG[G/A]CCAGTTGATCTGATGGAGAAACTCTTACCGCGACACCTGCAGATCATATACAAGATCAACCTAATACACCTGAATGTGAGTACACTTACTTGTCCAACTTAAAGCAGCTATAAAGTTCCCACTGTCAGCTTTAGTTTTACAAAAGTGCTGTTTTTTATTTATTTTTTCTTAAATAATAGCCATGTTAATAATGGATTTTAAATTTTTTCACTTTTCATGTGCCTTAGACTTCTGTTGTTTCTTTATGAATTCCATGTCCAAAGAGCACCCCTTAATTACCCATATTTATCAGGTTTAGTTTACTTTGACCCCAAAGTGCACATAAATCCACATACTGTACACTAGAAAACCTAGTAGACCCCAATATTGTATGCATGTTTTTTGTGTTTGCCTGAGTGTTTGAATGTGTATTTTCTTGTCTGTGTGTGTAGCATATAGCGTCTCTGTTTCCAGAGGATATGGACCGAATCCGCAGGATGTCTCTGATCGAGGAAGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38964
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 > A
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023449 | Missense | 542 | 965 | 16 | 31 |
Genomic Location (Zv9):
Chromosome 13 (position 37253760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36726062 |
GRCz11 | 13 | 36851894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGAATACAAACGGCAGCTGCTCAACTGCCTCCACGTCATCACCATGTA[C/A]AACCGTATGTATGCTACACAAACATAAACACACACTTGCGTTTTTATGCT
Long Flanking Sequence:
CTTGCTGATCTAATTGCCGAGGTCCAAACACACTCGCACACATGCATACTTTTTTTTTCTCTTCATAACAGATTTCTTTTAGCAATTTTGTGTTTGTTTGTAGGCTATCGGTGAGGAGTATGTGAAAGATCTGACTCAGCTGCAGAAGCTGAATGATCTGGTTGATGACGAAGCCTTCATCCGAGATGTAGCCAAAGTCAAACAGGTTATAAATTGTTTTTGAATGGCTTACCCCTTTTTTTATTTGCAAATTATGCATATTAGTACCTTAAATTAATTGGTATACTTTTTTTTTCCAAGTATTTTTTTCAAAGATATTAATTCATTTTGCATTAATTCATTTCTTTGTATGAACAGGACAACAAGCTGAAGTTTGCACATTATTTAGAGAAGATCTACAAAGTGGACATAAATCCTGCCTCCATGTTTGATGTCCATGTTAAAAGAATCCACGAATACAAACGGCAGCTGCTCAACTGCCTCCACGTCATCACCATGTA[C/A]AACCGTATGTATGCTACACAAACATAAACACACACTTGCGTTTTTATGCTGAAGTATGTTGTTGTTGTTTCTAAATACGTTTTTCCATGTGGAGACGCATGAAATGGGAATTGTTAACATTTACTGTATTTATTCTTTCTGGGGGGTTTTTCTTCTGTCAAACACAAAGTAATAAATGGAAAATGTTTCAACTATTTGACACACAGGCATCAAGAGCCATCCTACTAAACCATTTATACCCCGGACTGTGATCATTGGAGGCAAGGTAAAACAAACACGCCCACATGCACTTATTTGCAATAAATGCACAATACTGTTAAAAAGTATGACTGATCTGGGATTTCAAGATTTTACAATATATCGATAAATATAATAAACGTTGGGATTTGTGTGAGACTAAACGGTTTAGATAGTTTGATATCAGTCTATAAATTAGCTGAGGACACAGAGTAAGCTGTTGTGTGGAAAGTACATAATCAAATTTGACCTAAAACCCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38963
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023449 | Nonsense | 956 | 965 | 31 | 31 |
Genomic Location (Zv9):
Chromosome 13 (position 37248820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36721122 |
GRCz11 | 13 | 36846954 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCACTGACCTGAAGATTCCTCCACCAGGCGAACCTCGTGAAGCTCTA[G/T]AGGAAACTGCACGCTCCCTGCGCAAGACCTGAAGACAAGATCATCAGATC
Long Flanking Sequence:
TGAGTTTAAGGATAGTTTTAACTAATCAAAATAAAAAATTGAAATGAAAATCAGTTCAAGCATAGTTTAACTAACTGAAAATGAAAAATCAAATCATAATTTAGTAGACTCTTGCGCATGCACATGGCTCTGCAAGCCCATATGAAATCTGTTGATATTTGGAACATAAATGAACATATCTCATAGATTTCTGAAAGTGAATGCACCCAAAAAACTCTGATAATTGAATGTTAAATTATTAAATGCCTCACTCATTAAGATATAATTATTTCTGTTGAGTCTCTTGAAACAAATAATTCAGTGATGATGAGTCAATTGCAGTGGTGTTTATCTGTGTTGGACAGGATCAGAGAGAGTGGACTCGGGTGGTGATTAAGAACATCGCCGCATCTGGAAAGTTCTCCAGCGACCGCACTATTACAGAGTACGCCACTGAGATCTGGGGTGTGGAGCCCACTGACCTGAAGATTCCTCCACCAGGCGAACCTCGTGAAGCTCTA[G/T]AGGAAACTGCACGCTCCCTGCGCAAGACCTGAAGACAAGATCATCAGATCACCTCCAACAGTAGTTATAACGCTAAATAAATAAATCTCACTATCAATTTGTTTCAATTTTTCATGCAGTACTCTTTAAATGAATGAATTGTACTGCAAAACGCCTGAATAAATGTGTTGTCTTCAAATGTTTAAAACAAGTCTTTCTTTAATGTTTAATTTATTTATATAGTATCAGCCAATGTTGTGAAATAAGAAATGTTATCAGACCTTCACAGAATAAAACAAAAAAACACAATTACACTTAAACACATACTTTTTAACAAAAAATATCAATAATTTTCAAGTCGTCTTGATATATATATATTTTTTTTTTAGAAAACAAATATCTGTAGAAGAAGAAATGAAAGAAATTAGCCTTCTAAATGTGTTAAACCAAGTCAGGACCCTTTTAAATGTAAAGAAACAACTGTTTAAGAAAATAAATCGTAAGAAGAAAATAAAATGTCA
Associated Phenotype:
Not determined