ZMP
pgm1
Ensembl ID:
ZFIN ID:
Description:
phosphoglucomutase-1 [Source:RefSeq peptide;Acc:NP_957319]
Human Orthologues:
PGM1, PGM5
Human Descriptions:
phosphoglucomutase 1 [Source:HGNC Symbol;Acc:8905]
phosphoglucomutase 5 [Source:HGNC Symbol;Acc:8908]
phosphoglucomutase 5 [Source:HGNC Symbol;Acc:8908]
Mouse Orthologues:
Pgm2, Pgm5
Mouse Descriptions:
phosphoglucomutase 2 Gene [Source:MGI Symbol;Acc:MGI:97565]
phosphoglucomutase 5 Gene [Source:MGI Symbol;Acc:MGI:1925668]
phosphoglucomutase 5 Gene [Source:MGI Symbol;Acc:MGI:1925668]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31516 | Essential Splice Site | Available for shipment | Available now |
sa15441 | Essential Splice Site | Available for shipment | Available now |
sa20723 | Essential Splice Site | Available for shipment | Available now |
sa45255 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31515 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31516
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 |
---|---|---|---|---|---|
ENSDART00000006417 | Essential Splice Site | 82 | 561 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 31717036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32037952 |
GRCz11 | 6 | 32024866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGAAAGACGCGATTCAGCTCATCATCCAGATTGCTGCTGCTAATGGG[G/A]TTAGTATGGGCCCAATTTAACGAGTAGCTTAAACTTAAAACAAACGTCTT
Long Flanking Sequence:
CTGCCAATTGCTCTGGCATGTGTTTTATGTGGAGGATCATATCATATTATCATACATTAAAAACTTGTTTTGTTCTGTAGACTAAATTATAAATATTGCATTTGGTTTTACTGTCCCTTTAAATGTGGGCGTGTCCGTTGAAGCTCTGAAAGGCCAATGTGTGAGTATATCGAGTCTACGTGTAGACCAGTGAACACACACACAATCCGCTGGGCTCCCGGATAGTGACACATACACCTGACCGCTGCTGCACCATGGTGAAAATCACGGTTATCAAGACCAAACCGTACACCGACCAAAAACCCGGAACCAGCGGCTTAAGAAAGCGGGTAACGGTCTTCCAGCAGAACCAGCATTACGCGGAGAACTTCATCCAGAGTATCATTTCCACGGTTGACCCTGCGCAGAGGCAGGAGGGCGCGCTGGTGGTGGGAGGAGATGGACGCTTTTTCATGAAAGACGCGATTCAGCTCATCATCCAGATTGCTGCTGCTAATGGG[G/A]TTAGTATGGGCCCAATTTAACGAGTAGCTTAAACTTAAAACAAACGTCTTGCAAATGCTATTTCCTTGAATGGGTAGGGGAGGCTCTGACTTCATGACAAATTCAAGTTCATTGCAAAAGAGGCACTTACAACATTAGCAAACAATAGCTTTGCTCCAGACGTGCATGAATAAACAGAATACTTGTTGTCATTTCTTCCTTATAATTTATCATGGTGCCTTTAAATAACATTGCATGCACATGTAGGAATTACATAATAATTGTCCCAGGGGAATTATTTTCAACACTGCGATGTTCTGTTCGGAACGACTCTTTTATATGAGTCGAATCTTTTATATGATTCACTAACCCTTTATGAACCATTCATTAGAGAGCTGTTCATTAGCAACTTGTTATTATTGTCAGATCAGTGATTTTATTAATACATCAATTCGTAATTAATTCTGAATAAAGCTTATATAAAGTGGGTGAGGACTTGTTAATGAAATTTAGTAAACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15441
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 |
---|---|---|---|---|---|
ENSDART00000006417 | Essential Splice Site | 82 | 561 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 31717035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32037951 |
GRCz11 | 6 | 32024865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGAAAGACGCGATTCAGCTCATCATCCAGATTGCTGCTGCTAATGGGG[T/C]TAGTATGGGCCCAATTTAACGAGTRGCTTRAACTTAAAACAAACGTCTTK
Long Flanking Sequence:
TGCCAATTGCTCTGGCATGTGTTTTATGTGGAGGATCATATCATATTATCATACATTAAAAACTTGTTTTGTTCTGTAGACTAAATTATAAATATTGCATTTGGTTTTACTGTCCCTTTAAATGTGGGCGTGTCCGTTGAAGCTCTGAAAGGCCAATGTGTGAGTATATCGAGTCTACGTGTAGACCAGTGAACACACACACAATCCGCTGGGCTCCCGGATAGTGACACATACACCTGACCGCTGCTGCACCATGGTGAAAATCACGGTTATCAAGACCAAACCGTACACCGACCAAAAACCCGGAACCAGCGGCTTAAGAAAGCGGGTAACGGTCTTCCAGCAGAACCAGCATTACGCGGAGAACTTCATCCAGAGTATCATTTCCACGGTTGACCCTGCGCAGAGGCAGGAGGGCGCGCTGGTGGTGGGAGGAGATGGACGCTTTTTCATGAAAGACGCGATTCAGCTCATCATCCAGATTGCTGCTGCTAATGGGG[T/C]TAGTATGGGCCCAATTTAACGAGTAGCTTAAACTTAAAACAAACGTCTTGCAAATGCTATTTCCTTGAATGGGTAGGGGAGGCTCTGACTTCATGACAAATTCAAGTTCATTGCAAAAGAGGCACTTACAACATTAGCAAACAATAGCTTTGCTCCAGACGTGCATGAATAAACAGAATACTTGTTGTCATTTCTTCCTTATAATTTATCATGGTGCCTTTAAATAACATTGCATGCACATGTAGGAATTACATAATAATTGTCCCAGGGGAATTATTTTCAACACTGCGATGTTCTGTTCGGAACGACTCTTTTATATGAGTCGAATCTTTTATATGATTCACTAACCCTTTATGAACCATTCATTAGAGAGCTGTTCATTAGCAACTTGTTATTATTGTCAGATCAGTGATTTTATTAATACATCAATTCGTAATTAATTCTGAATAAAGCTTATATAAAGTGGGTGAGGACTTGTTAATGAAATTTAGTAAACAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20723
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 |
---|---|---|---|---|---|
ENSDART00000006417 | Essential Splice Site | 227 | 561 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 31712244)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32033160 |
GRCz11 | 6 | 32020074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCAGGACCCAATCATATCAATGTGCGACTTGATGCAATGCATGGAGG[T/C]AAGAGCTCAATTCCTGCCAGACAAAAATAAAGTTCAGTGTTTCAGAAATG
Long Flanking Sequence:
CAATTGTGGCATTTTGAGGCAGAATGATTGGCCTGTAGATGTTTGCCAATCTGGATGGCCTGAAGATGAGTAAATTAGAAGTAAAAAAAATGTTGTAAACTTTCTTTAAACACGTGCACTCGGATTCAATAAATCTGTATTGTCTTTCCCAGGTCCTGCACCAGAGGGTATCACAGACAAAATCTTTCAGATCAGCAAGAGCCTCCAGGAATATCACATCTGCCCTGAGCTCAAGGTGGACCTCTCCACAATTGGGAAACAAACCTTTGAGGTGGACACCTTCAAGCCCTTTACTGGTATTTTTTTTTCTGTCTAACCATTTACTTCTATTTTTTAGTCTAACTGTTGCTGATGATCGAGTATCTTTTTTCAGTTGAAATCGTGGACTCTGTGGAATCCTATGCAGAAATGCTCAGAGATATCTTTGATTTTGCTGCTCTGAAGGAATTGCTCTCAGGACCCAATCATATCAATGTGCGACTTGATGCAATGCATGGAGG[T/C]AAGAGCTCAATTCCTGCCAGACAAAAATAAAGTTCAGTGTTTCAGAAATGTTCACACTGGGCAGGTTTGCTTTGAATAAAACAAACTGTGGTGCGATTGCTCTTTTAGACACAGTTCATTTGAATAAGCGTGAATGCTACAACCCAAACCTTACACACCAAGCCAAATGCTGGCTGGAAAAATAGGCCCTAGTCCACTTACAAATGATTTCTTATGCAGGTTGACTGCAGTATGATTGTAAAACAAATGAAAGTCATCTAAATGATTCAAATATATGAAATGGTGTCACAAGATATGACCATAAAGAAATAGAATGCACAATTATGCCAGCAGGACTTTGTTTGACTGTGGTGGAAACATTCCTACTGTTTTGATTCTTTTACATATTTTATAAGTTCCTTACTAGTTCTAAACTAATGCATATACCATTGTACACATGCAATAAGTAAGCCAAGCGCAGAATAGATTTTGGATATTTGCTAAGTTCTGTCGCAAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45255
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 |
---|---|---|---|---|---|
ENSDART00000006417 | Essential Splice Site | 290 | 561 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 31710959)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32031875 |
GRCz11 | 6 | 32018789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGAAGGGAGGGGAATATGACTTTGGAGCAGCATTTGATGGCGATGGT[G/A]TAAGTATAGGAGTATGAAGTGCAACATACAGTAGCATTACGAAGTTTGGG
Long Flanking Sequence:
ATTCCAATTTCAAGCCTAACATTTAAACAAATCAAACAAGTGAAATTAAGAAGCATATAAGGGTTACCAGCAATAATCTTTATTTTGTGGGTGAGCATTTTGGGTATGTGCAAACAGAAACCCATCTCTCACAGTGTGTGTCTTGTTGTGCATGAAGGTTTTAAAATACCTTGAATGTTTGAATTGGCAACAACATTGCAAGTGACAACATTTCATGAGGATCCATGAATAGCTCAATTATATTCTGTTTTAAGTCACTGAGTTATTGCCTGAAACTGAAAACATAGTTTTTTGTGTTCTTTATACTAGTGGTGGGTCCATATGTGAAGAAGATTGTGTGTGAAGAGCTTGGTTCTCCTGCTAACTCTGCCGTGAACTGTGTCCCCTCTGAGGATTTTGGGGGACACCATCCTGACCCCAATTTAACATATGCTGCTGACCTGGTCAACACCATGAAGGGAGGGGAATATGACTTTGGAGCAGCATTTGATGGCGATGGT[G/A]TAAGTATAGGAGTATGAAGTGCAACATACAGTAGCATTACGAAGTTTGGGGATGATGTGTTTTTTTAAGACCAAGGCTGCCATTATTTAATTAAACTACAGTAATCCTTTAAAAAATGTATTTTTTTAATATTATGATTTGATTGTAAGGTAAACTTTTAAATATTATTGTTATAAAACACTTGTTATTATATTGCTTAATATAATAGAAAAGTTACTAACTTTAAATATTGGAACAGTAATTTATGCAATTATTAGTAATTCTCAGGCAAAGCTTCATCAATTTTCCCTGTTTTTGTTCTGTTTGCAGGATCGTAACATGGTTTTGGGTAAGCATGGGTTCTTTGTAAACCCTTCTGACTCTGTGGCAGTCATTGGTGCCAACATTACATCCATCCCGTACTTCCAGAAGACTGGCGTAAAGGGTCTGGCTCGCAGTATGCCCACCAGCGGGGCTTTGGACAAGTATGAGCATCTAAGCATACTTACAATTTGTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31515
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006417 | Essential Splice Site | 342 | 561 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 6 (position 31710493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32031409 |
GRCz11 | 6 | 32018323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTAAAGGGTCTGGCTCGCAGTATGCCCACCAGCGGGGCTTTGGACAAG[T/A]ATGAGCATCTAAGCATACTTACAATTTGTGATTTGGCTCTATATTTGACT
Long Flanking Sequence:
ATATGACTTTGGAGCAGCATTTGATGGCGATGGTGTAAGTATAGGAGTATGAAGTGCAACATACAGTAGCATTACGAAGTTTGGGGATGATGTGTTTTTTTAAGACCAAGGCTGCCATTATTTAATTAAACTACAGTAATCCTTTAAAAAATGTATTTTTTTAATATTATGATTTGATTGTAAGGTAAACTTTTAAATATTATTGTTATAAAACACTTGTTATTATATTGCTTAATATAATAGAAAAGTTACTAACTTTAAATATTGGAACAGTAATTTATGCAATTATTAGTAATTCTCAGGCAAAGCTTCATCAATTTTCCCTGTTTTTGTTCTGTTTGCAGGATCGTAACATGGTTTTGGGTAAGCATGGGTTCTTTGTAAACCCTTCTGACTCTGTGGCAGTCATTGGTGCCAACATTACATCCATCCCGTACTTCCAGAAGACTGGCGTAAAGGGTCTGGCTCGCAGTATGCCCACCAGCGGGGCTTTGGACAAG[T/A]ATGAGCATCTAAGCATACTTACAATTTGTGATTTGGCTCTATATTTGACTATTAGTCATGTAATTCTCACAATAAACTTTTGAGCAATGTATTTATTCCCTCTCTTTCTCCATATAGTGTGGCCAAAGCTCTGAAGATGCCGCTTTATGAAACCCCCACAGGCTGGAAATTCTTTGGAAACTTGATGGATGCTGGCAAGTTATCGCTGTGCGGTGAAGAAAGTTTTGGTACTGGTGAGTAGCTTTGAAACTGTTGGTGATATTCTGTTAAAAAGGACATTTTTATTTTGCTTTAAAGTTGCTAGATTGGATTTGGGCTGAATGACAGTAAATTAAAATACGTGATGATTAAATATATCTAAAAAAAAATCATTGGTTTAGTATTCATGAGTAGAGTGTTCTTATTAGCGATACTGTATATTTCAGCTTGATGTTCCTTTGTCAATGTGACTTGATGAATGATTGATCTCTGTATTTTAATATTTTGTACTATGAAATATT
Associated Phenotype:
Not determined