Busch Lab

ZMP

pgm2

Ensembl ID:
ENSDARG00000018178
ZFIN ID:
ZDB-GENE-040426-2218
Description:
phosphoglucomutase-2 [Source:RefSeq peptide;Acc:NP_998051]
Human Orthologue:
PGM2
Human Description:
phosphoglucomutase 2 [Source:HGNC Symbol;Acc:8906]
Mouse Orthologue:
Pgm1
Mouse Description:
phosphoglucomutase 1 Gene [Source:MGI Symbol;Acc:MGI:97564]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa13033 Essential Splice Site Available for shipment Available now
sa25557 Nonsense Mutation detected in F1 DNA Not yet available
sa39589 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30800 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13033
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000020970 Essential Splice Site 173 611 4 13
Genomic Location (Zv9):
Chromosome 1 (position 17533672)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 18098840
GRCz11 1 18791777
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTATCATGGTAACAGCCTCCCATAATCCCAAACAAGATAACGGATACAAG[G/T]TAGCATCCAACCCTCAMTTAAATCTGATGTTTAATWTGGAAGACTAGATT
Long Flanking Sequence:
ACAAAATAAAGAAAATAATAAGAAAAATATAATAGTAAATACTGGGGAAAATTCCCATTTTCCACACATTCCACACATCATTTGGGAAATGTTAGCAAAAGGAAAAAAATTATTTTGATAATTTTGACTTGAACTGTATGTTGGTTACATGATTTTTAACCGATATGTGAAAATATAGTATTGCATATTGAATATTGCATTATTTAGCATGCATACTATGTATCACATTTACTTCAATCTCAACAACCTAATAAAACAGATAACAGCTTCAATTGCAGTAATATTTTAATATATAATACTATTTTACTGTAATTTTTACCAAAGACATAAACATACAGACCCCAAAACCTTACCCCTAAAATCAAACTGTAATGCAAAAAATGACCACGTCTTCTCTTTTCCTCTATTTCTTTTAGCCTTTTGCTGTGTCGCATCTTGGACTGTGTGCTGGTATCATGGTAACAGCCTCCCATAATCCCAAACAAGATAACGGATACAAG[G/T]TAGCATCCAACCCTCAATTAAATCTGATGTTTAATTTGGAAGACTAGATTTTCTAACATTTTATTTGGAGAAATTTGACATTTATCGGGTGTTTATGTGTTTAAGGTGTACTGGGCAAACGGAGCTCAGATCATTCCTCCTCATGATAAGGGCATCGCTGCAGCTATAGAACAAAACCTTGAGCCCTGGCCTGAATCCTGGGACACAGATGAGGGTCTTCGGAGTTCACTGCTTAATGACCCATATCAGGACATACACAGAGAATACTGTCAAACCATCCAGCAGCACTGCTTTCACAGGTACACTCATTGCATGTAAACAAGTCAAACAAGCCACTTGGGAAAAAAAAAATTATAAAAAAAAATATATATATATAATTAAATATATATATATATATATATATATATATATATATATATATATATAGAGGTGGGCATAGACAAATTTTTTTATCTAGATTAATCTCGGAACTAATCTAGATTAAAATGGCTCATTTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25557
Status:
Mutation detected in F1 DNA
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
ENSDART00000020970 Nonsense 196 611 5 13
Genomic Location (Zv9):
Chromosome 1 (position 17533500)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 18098668
GRCz11 1 18791605
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTCAGATCATTCCTCCTCATGATAAGGGCATCGCTGCAGCTATAGAA[C/T]AAAACCTTGAGCCCTGGCCTGAATCCTGGGACACAGATGAGGGTCTTCGG
Long Flanking Sequence:
ATATAGTATTGCATATTGAATATTGCATTATTTAGCATGCATACTATGTATCACATTTACTTCAATCTCAACAACCTAATAAAACAGATAACAGCTTCAATTGCAGTAATATTTTAATATATAATACTATTTTACTGTAATTTTTACCAAAGACATAAACATACAGACCCCAAAACCTTACCCCTAAAATCAAACTGTAATGCAAAAAATGACCACGTCTTCTCTTTTCCTCTATTTCTTTTAGCCTTTTGCTGTGTCGCATCTTGGACTGTGTGCTGGTATCATGGTAACAGCCTCCCATAATCCCAAACAAGATAACGGATACAAGGTAGCATCCAACCCTCAATTAAATCTGATGTTTAATTTGGAAGACTAGATTTTCTAACATTTTATTTGGAGAAATTTGACATTTATCGGGTGTTTATGTGTTTAAGGTGTACTGGGCAAACGGAGCTCAGATCATTCCTCCTCATGATAAGGGCATCGCTGCAGCTATAGAA[C/T]AAAACCTTGAGCCCTGGCCTGAATCCTGGGACACAGATGAGGGTCTTCGGAGTTCACTGCTTAATGACCCATATCAGGACATACACAGAGAATACTGTCAAACCATCCAGCAGCACTGCTTTCACAGGTACACTCATTGCATGTAAACAAGTCAAACAAGCCACTTGGGAAAAAAAAAATTATAAAAAAAAATATATATATATAATTAAATATATATATATATATATATATATATATATATATATATATATATAGAGGTGGGCATAGACAAATTTTTTTATCTAGATTAATCTCGGAACTAATCTAGATTAAAATGGCTCATTTAAAATCTGTCGAAGACATTCAGATTATGTTTGCTACTCAAATTATAAGTCTTTGGGAACTGGTTTCTTAAGCCAGGTGGCGCATCAGACAAGGGCTCATCTCCTGTTTCCAAAATGCTTCAGAGACAGCTTGAGAAACTGTTCTACTATGATAATTGATGATGAAAATATATTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39589
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000020970 Essential Splice Site 334 611 8 13
ENSDART00000020970 Essential Splice Site 334 611 8 13
Genomic Location (Zv9):
Chromosome 1 (position 17530424)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 18095592
GRCz11 1 18788529
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCTTTTCATTCAGCATGTCAGATTATAAACGACTGTAATTCTCTGT[A/T]GTGGGAAGTGGAGAGTTTTCTCTGGGAATGAATTAGGTGCTTTACTCGGC
Long Flanking Sequence:
ACCACAATAAATTAAGTGGAAACTATTTCATTCATGCTGTTGTATCAAGCTGAAATAATTGGTTTAAATTTTCACTTTTTACAGTGTATGTAAGTGATCACCAAACTTGTTCCTGGAGGGCCGGTGTCCTGCAGAGTTTAGCTCCAACCCTAATCAAACACACCTGAACAAGCTAATCAAGGTCTTACTAGGTATACTTAAAACATCCAGGCAGGTGTGTTGAGGCAAGTTGGAGCTAAACCCTGCAGGGACACCGGCCCTCCAGGACCAGGATTGGTGAACCCTGGTGTATGTAATGGCAAATGAATCTATATTTGTTTGTGTATGTAGACGCTGTCCTTCGCGCTTGCAGATAAAGAAGGAGCAAGTGTTATTCTGGCGAATGACCCTGACGCTGACAGACTAGCTATTGCAGAGAAACAGGAGAGGTCAGTGTTGTTTAGCATTTTGTGTTGCTTTTCATTCAGCATGTCAGATTATAAACGACTGTAATTCTCTGT[A/T]GTGGGAAGTGGAGAGTTTTCTCTGGGAATGAATTAGGTGCTTTACTCGGCTGGTGGATTTTCCAATGCTGGAAGCAGCAGAAAGTGGAAGGAAAAGGCTCCATTAAGGACGTCTACATGCTATCCAGCACAGTCTCCTCAAAAATCCTCAGAGCCATTGCAGTGAAAGAAGGCTTTCACTTTGAGGTAGGTTTCATTGTTTGCCTGTGAAAAGTAATAAAATGAATGATTCTTCAGTTGTGTGGGTTTTCTAACTCAGTGGTGTCCATCGTTTTTTAAACTCAAGGCACCTCTTTGTTCAGGAGAATATTAAATTTAGACTAATAAAATATATGATGCCATTTTTATGTTTTAAGCATGGCATTTAAATGGGCTCTATTAATTCTTTAATACTGAACTCTTTCAAATGCCTTGATTGTAGTTTTTAGACTGTAGTTTTACACTTCAAATTAGCCTGATTCCTAAGCAGCAGACACAAAAATAGGTTGTTTTTGCTTCCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30800
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000020970 Essential Splice Site 334 611 8 13
ENSDART00000020970 Essential Splice Site 334 611 8 13
Genomic Location (Zv9):
Chromosome 1 (position 17530424)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 18095592
GRCz11 1 18788529
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCTTTTCATTCAGCATGTCAGATTATAAACGACTGTAATTCTCTGT[A/T]GTGGGAAGTGGAGAGTTTTCTCTGGGAATGAATTAGGTGCTTTACTCGGC
Long Flanking Sequence:
ACCACAATAAATTAAGTGGAAACTATTTCATTCATGCTGTTGTATCAAGCTGAAATAATTGGTTTAAATTTTCACTTTTTACAGTGTATGTAAGTGATCACCAAACTTGTTCCTGGAGGGCCGGTGTCCTGCAGAGTTTAGCTCCAACCCTAATCAAACACACCTGAACAAGCTAATCAAGGTCTTACTAGGTATACTTAAAACATCCAGGCAGGTGTGTTGAGGCAAGTTGGAGCTAAACCCTGCAGGGACACCGGCCCTCCAGGACCAGGATTGGTGAACCCTGGTGTATGTAATGGCAAATGAATCTATATTTGTTTGTGTATGTAGACGCTGTCCTTCGCGCTTGCAGATAAAGAAGGAGCAAGTGTTATTCTGGCGAATGACCCTGACGCTGACAGACTAGCTATTGCAGAGAAACAGGAGAGGTCAGTGTTGTTTAGCATTTTGTGTTGCTTTTCATTCAGCATGTCAGATTATAAACGACTGTAATTCTCTGT[A/T]GTGGGAAGTGGAGAGTTTTCTCTGGGAATGAATTAGGTGCTTTACTCGGCTGGTGGATTTTCCAATGCTGGAAGCAGCAGAAAGTGGAAGGAAAAGGCTCCATTAAGGACGTCTACATGCTATCCAGCACAGTCTCCTCAAAAATCCTCAGAGCCATTGCAGTGAAAGAAGGCTTTCACTTTGAGGTAGGTTTCATTGTTTGCCTGTGAAAAGTAATAAAATGAATGATTCTTCAGTTGTGTGGGTTTTCTAACTCAGTGGTGTCCATCGTTTTTTAAACTCAAGGCACCTCTTTGTTCAGGAGAATATTAAATTTAGACTAATAAAATATATGATGCCATTTTTATGTTTTAAGCATGGCATTTAAATGGGCTCTATTAATTCTTTAATACTGAACTCTTTCAAATGCCTTGATTGTAGTTTTTAGACTGTAGTTTTACACTTCAAATTAGCCTGATTCCTAAGCAGCAGACACAAAAATAGGTTGTTTTTGCTTCCAC
Associated Phenotype:
Not determined