ZMP
wu:fj78b06
Ensembl ID:
Human Orthologue:
G6PD
Human Description:
glucose-6-phosphate dehydrogenase [Source:HGNC Symbol;Acc:4057]
Mouse Orthologues:
G6pd2, G6pdx
Mouse Descriptions:
glucose-6-phosphate dehydrogenase 2 Gene [Source:MGI Symbol;Acc:MGI:105977]
glucose-6-phosphate dehydrogenase X-linked Gene [Source:MGI Symbol;Acc:MGI:105979]
glucose-6-phosphate dehydrogenase X-linked Gene [Source:MGI Symbol;Acc:MGI:105979]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24272 | Nonsense | Available for shipment | Available now |
sa11949 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24272
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 |
---|---|---|---|---|---|
ENSDART00000104834 | Nonsense | 217 | 523 | 6 | 13 |
ENSDART00000138696 | Nonsense | 217 | 523 | 7 | 14 |
The following transcripts of ENSDARG00000071065 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 13969356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 14101289 |
GRCz11 | 23 | 13857366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGGAGCAAATCTACCGTATAGACCATTACCTGGGCAAAGAGATGGTG[C/T]AGAACCTGATGGTCCTCAGGTGTGCCACTCTTATTTCTCTCTCGCTGTGT
Long Flanking Sequence:
ATAGAACTAAAAATGTTAGAATTGTGTCGATGTCCGAATATTTATGGACCTAACTGTATAAATGGTTCTCAAGGTCCAAAATTAGTAAAGAGATAAGATGTGTAAATTTGTGTATATGCATGGTAAAAAAAAAACCTTTTGAGTTTAGCAAAAATAGCCACAAAATAGGTAATTTTATTTGCAAAATCTGAAGTATTATTATTATTATTTTTTTATTATTATTTTGCAAAATCCTGGAGGGACTAATTTACTATATTCACAATGTTACAGTGTTCACTTGGGTTAAATTTAATATGGGTTTGTTCTTGTAAAAAAAGTCATTTTTTAAAACACTGCATATGCTGTAATTGTGTTTGCGCAGAGGCTGGAACAGGGTGATTGTGGAGAAGCCGTTTGGCCGTGATCTGCAGAGCTCAGAGGAGTTATCCAGTCATCTATCCTCTCTCTTCACTGAGGAGCAAATCTACCGTATAGACCATTACCTGGGCAAAGAGATGGTG[C/T]AGAACCTGATGGTCCTCAGGTGTGCCACTCTTATTTCTCTCTCGCTGTGTGTGTTTATCCCTGTCTGCCTTCTGCTTTTCACTGGCTGTCATACACAGTTGTCATTTTTGCATAATTAAGGATTAAAAAGCATTAGGAAGCTCTTCTTCTGTATCCCATGGTTTCTCTCCTCTCTTTCCTTAAAGGTTTGGAAATCGGATTTTTGGTCCCATATGGAACCGAGACAGCGTGGCGTGTGTGGTTCTGACCTTCAAAGAGCCGTTTGGTACCCAGGGCCGCGGAGGATATTTTGACGATTTTGGTATCATTCGGTTAGTTATGGTTTCTTTTGCTTTAAGATGTTTTTGCACATGAGAATGTTTAATCATGTGGTATGAAAGGAAGGTCATAATTTTCTTCGGTGTAATGTGAATAAATAAAAGCAGTAGGAAAAAAAGAATGCTTAATTGGATTAAATGGCCACAATTTCTTTCCACAAGAATTCTCTAAAAAAAAAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11949
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 |
---|---|---|---|---|---|
ENSDART00000104834 | Essential Splice Site | 494 | 523 | 12 | 13 |
ENSDART00000138696 | Essential Splice Site | 494 | 523 | 13 | 14 |
ENSDART00000104834 | Essential Splice Site | 494 | 523 | 12 | 13 |
ENSDART00000138696 | Essential Splice Site | 494 | 523 | 13 | 14 |
The following transcripts of ENSDARG00000071065 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 13959478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 14091411 |
GRCz11 | 23 | 13847488 |
KASP Assay ID:
554-6186.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAGATAGAGTCTGAGAAAACACCACCCATCAAATACAAATACGGGAGG[T/C]AATATAAACCAGCTCACCATCGACAGACTKTTTCCAGGAAAYKATGTGTA
Long Flanking Sequence:
GTGATGTCCAAGCAGGTCCATGCACGCAAGATGAGAAATACTATTTTTTTTTTCAGAAAAAAAGTTTATATTAAAAAGCAATTTCTATTTATAAATGAGTAATAAAAATTATTATTTTTTTAAATGTCTCAACATTTCCCTTCGAATCTTTTAGCAGTCTATGAGTTTCTAGTATTCATTATTTAATTCATTTAACCATGGTGAATGAACAGAGTATAAAGGCTCTGGCTTTAGCACTCCTTTATTTCGGACAACGCGAGAATCAGCTTCTCTCCCATGGTGCACAACAAAACTAAAAGTTCTGTGTGACTGCCACAAAAGAGCGTATTCCGACAGTCGTGTCCAAATGTCGTGTGCGGTGGAAAAGTGGCTTAATGTAAACGCAATCTGTCTTCTACTGTCACAGTGATGAGTTGAGGGAAGCCTGGAGGATCTTCACTCCTCTCCTTCATCAGATAGAGTCTGAGAAAACACCACCCATCAAATACAAATACGGGAGG[T/C]AATATAAACCAGCTCACCATCGACAGACTTTTTCCAGGAAACGATGTGTAATGTATCTCACATTCTCTCTGTCTGTGTTAAAGTCGTGGTCCCGCTGAGGCTGATGAGCTGGTGCAGAAAGTGGGCTTCCGCTACGAGGGAACATACAAATGGGTGAATCCACACAAACTGTGAAAGCAGCAGATGCGGAAGCTGAAGCCTGTTTAAAAACAAAAAATCAGCAGTCGAGTGCCTGAAACGAGCACTTTAAACAAACTAAATATTGAAAATTCGTTCTGTTTAAGCACTGCATTTACAGAAAGACCAACGTGATTGGAAAACCTTTTTTTTTAGCATGTTATGAATCATAACCAGCTCCTTGTGGTATATGATTTAGAACAGTGTTTGTTAACCAAGTTCCTGGAGGACCACCAGCTCTGCACATTTTCCATGTCGTTTTAACTAAACACACCTGATTAAGATGATCAGCTCATTAGCAGAGACTGAAAGACCTGTAACGG
Associated Phenotype:
Not determined