ZMP
gpia
Ensembl ID:
ZFIN ID:
Description:
glucose phosphate isomerase a [Source:RefSeq peptide;Acc:NP_658909]
Human Orthologue:
GPI
Human Description:
glucose-6-phosphate isomerase [Source:HGNC Symbol;Acc:4458]
Mouse Orthologues:
Gm1840, Gpi1
Mouse Descriptions:
glucose phosphate isomerase 1 Gene [Source:MGI Symbol;Acc:MGI:95797]
predicted gene 1840 Pseudogene [Source:MGI Symbol;Acc:MGI:3037698]
predicted gene 1840 Pseudogene [Source:MGI Symbol;Acc:MGI:3037698]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31115 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44355 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44356 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31115
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022437 | Essential Splice Site | 161 | 553 | 5 | 18 |
| ENSDART00000022437 | Essential Splice Site | 161 | 553 | 5 | 18 |
The following transcripts of ENSDARG00000012987 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 37011234)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 35418850 |
| GRCz11 | 25 | 35923789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGCATCACTGATGTGGTGAACATCGGCATCGGAGGATCAGACCTGG[T/A]GAGTTTCCTAAAGCACCCCAGAACTGATTGTAAAGAAATCTGATCAGAGA
Long Flanking Sequence:
ATTTGATTGATTTATTTAATATTTTATTTATTTATTTTATTTATTTATTTAATTATTTATTTTATTTATTTATTAAATTATTTATTTTATTATTTGTTTATTTATTTTATTATTTTATTTATTCTTTTGTGCGTGCCCCAGTAGAGCTTTTATGTCTAACAACGCCCCTGGGTGGTTTTGGTTTCTTCTGTAAATCATAATAAAAATCTTGTATGATCATTTTTATTGCTGTTGAGGGAACTCTATCATGTACACTGTCCCCTGGCTATTATTTAAGCTTCTCCATAAACATTTTAGAGCAATACAACAATGATTTAACTAATTTATCAGATTATGTTTTATATTTGATTTGTTTATTTTATAACCAATTATGAAAAGTCCTGAACATAGATGTTGTGTGTCTGTTATTGTGCAGAAAGTGCGCAGCGGCGCTTGGAAAGGCTTCAGTGGGAAAAGCATCACTGATGTGGTGAACATCGGCATCGGAGGATCAGACCTGG[T/A]GAGTTTCCTAAAGCACCCCAGAACTGATTGTAAAGAAATCTGATCAGAGATGTCCGGCTGTCGAAATGAATGTTGAAAGGGATTAGTTTCGTGTAGGTGTAGACATTAATGGAATACAGTTTACTGGGTAATTTAATAAGTTAAAGAATAAAAATCTTCCAGTTCCTTCTAGACACAACCAAACCTGCCGGAACTACTTGCGGTGTGCTTATCTGACAATAGTTGCATGCCTTAATGTTCGTCAGCCAATCAGAATGGGGCACTTAACAGCCCTGCAGTTTACTTGTCAGTTTTTAGTTTACACATAATATTAGAGCTTCTTTTGATTTACATTTAGATATATCATATCGCAATACTGAAAGCAAAATTCATTTACCACTTGACTGCTTCATTTTGTGTGTATAAACTTTCCCAATTTAAGCATTAGTTGAACAACCCCTTTACCGTTAGTTTGCTATAAGGGTAAGATGTGCAAAAATAAAGCCCCACCTCCTACTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44355
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000022437 | Essential Splice Site | 161 | 553 | 5 | 18 |
| ENSDART00000022437 | Essential Splice Site | 161 | 553 | 5 | 18 |
The following transcripts of ENSDARG00000012987 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 37011234)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 35418850 |
| GRCz11 | 25 | 35923789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAGCATCACTGATGTGGTGAACATCGGCATCGGAGGATCAGACCTGG[T/A]GAGTTTCCTAAAGCACCCCAGAACTGATTGTAAAGAAATCTGATCAGAGA
Long Flanking Sequence:
ATTTGATTGATTTATTTAATATTTTATTTATTTATTTTATTTATTTATTTAATTATTTATTTTATTTATTTATTAAATTATTTATTTTATTATTTGTTTATTTATTTTATTATTTTATTTATTCTTTTGTGCGTGCCCCAGTAGAGCTTTTATGTCTAACAACGCCCCTGGGTGGTTTTGGTTTCTTCTGTAAATCATAATAAAAATCTTGTATGATCATTTTTATTGCTGTTGAGGGAACTCTATCATGTACACTGTCCCCTGGCTATTATTTAAGCTTCTCCATAAACATTTTAGAGCAATACAACAATGATTTAACTAATTTATCAGATTATGTTTTATATTTGATTTGTTTATTTTATAACCAATTATGAAAAGTCCTGAACATAGATGTTGTGTGTCTGTTATTGTGCAGAAAGTGCGCAGCGGCGCTTGGAAAGGCTTCAGTGGGAAAAGCATCACTGATGTGGTGAACATCGGCATCGGAGGATCAGACCTGG[T/A]GAGTTTCCTAAAGCACCCCAGAACTGATTGTAAAGAAATCTGATCAGAGATGTCCGGCTGTCGAAATGAATGTTGAAAGGGATTAGTTTCGTGTAGGTGTAGACATTAATGGAATACAGTTTACTGGGTAATTTAATAAGTTAAAGAATAAAAATCTTCCAGTTCCTTCTAGACACAACCAAACCTGCCGGAACTACTTGCGGTGTGCTTATCTGACAATAGTTGCATGCCTTAATGTTCGTCAGCCAATCAGAATGGGGCACTTAACAGCCCTGCAGTTTACTTGTCAGTTTTTAGTTTACACATAATATTAGAGCTTCTTTTGATTTACATTTAGATATATCATATCGCAATACTGAAAGCAAAATTCATTTACCACTTGACTGCTTCATTTTGTGTGTATAAACTTTCCCAATTTAAGCATTAGTTGAACAACCCCTTTACCGTTAGTTTGCTATAAGGGTAAGATGTGCAAAAATAAAGCCCCACCTCCTACTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44356
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 |
|---|---|---|---|---|---|
| ENSDART00000022437 | Essential Splice Site | 267 | 553 | 9 | 18 |
The following transcripts of ENSDARG00000012987 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 37013624)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 35421240 |
| GRCz11 | 25 | 35926179 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGAAGGAGTTCGGCATCGACACCAACAACATGTTTGAGTTTTGGGAT[G/A]TGAGTATGTGCTACAGAGCAATTTCCAGGACAGACTGAATGCATGATTGC
Long Flanking Sequence:
TTAATTTATTTAGTTTATTTATTTATTTCAGCCAAACAAAAAGAAATTACTTTCTCCAGAAGAAAAATATAGTGGAAAATCCTGTGAAAAATGTCCTTGCTCTGTTAAACAGCACTTTTATATAGATATTTAAAAAACTATTATCATTTTACAAGAGAGCTAATCATTTTGTCTTAAACTGTATAACATTAATACCAAAGTCAATCCTCCTGTAAAGAGCTTAATCATTTAAAGTATGAGATGTCAGAACTCTTATTATCGTCAGCACATTATAATCTGTTAATATACGGACACTAATAATTTATATTTGTATTTCAGAAATCTGCTGTGGCCAAACATTTCGTGGCTCTTTCCACAAACGCGGTGAGTACAGCAGCATAACTTCATGTATTCTCTTTTAAGTACAGTTTAATCAACGTGTATTTATTTCTGTCTCCCATTATCAGCCAAAAGTGAAGGAGTTCGGCATCGACACCAACAACATGTTTGAGTTTTGGGAT[G/A]TGAGTATGTGCTACAGAGCAATTTCCAGGACAGACTGAATGCATGATTGCCTGAAATATTGACTGCTCTGCCATATTGCTGAATCCACTTCTAAGTTAGTGTTGATTTGATGCTGATGTTTCAGTGGGTCGGCGGCCGCTATTCTCTGTGGTCTGCTATCGGCTTGTCCATCGCTCTGCACATCGGTACGTCTGCTGTGGGGAAAAGTCCCCAAATATGCTGTAATGTTTTTCAGGAGTGACAATTGACATGCAGCTAAGTCTGAAATTATTCAAATCTTTGGCAAACTCTGACTTGAGAGTTATTTTATTTAACCAGCAGTTTCTGTTGTTGTTGTTGCTATTATTTATTTTTGACCGGAAATGACTCCGACTTCTTCCAAAAGATAATAATATGATGTTCAAGAGGGATTATTGTGGGAAAAAATATATATGTTTTAGCTTTAATTTACATTTGAACAAAAATGTAAGTCCGAATTTGCAAGGGGTATGAATACGTTT
Associated Phenotype:
Not determined