ZMP
zgc:110010
Ensembl ID:
ZFIN ID:
Description:
glutathione reductase, mitochondrial [Source:RefSeq peptide;Acc:NP_001018390]
Human Orthologue:
GSR
Human Description:
glutathione reductase [Source:HGNC Symbol;Acc:4623]
Mouse Orthologue:
Gsr
Mouse Description:
glutathione reductase Gene [Source:MGI Symbol;Acc:MGI:95804]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15125 | Nonsense | Available for shipment | Available now |
| sa39011 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15125
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000047050 | None | None | 425 | None | 13 |
| ENSDART00000127479 | Nonsense | 379 | 500 | 11 | 13 |
| ENSDART00000147521 | None | None | 273 | None | 8 |
The following transcripts of ENSDARG00000019236 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 40353495)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 38516729 |
| GRCz11 | 14 | 38857043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTTGCTATTGCTGCTGGCAGAAAGCTTGCTCACCGACTGTTTGAGGGC[A/T]AAGCAGACTCCAAAGTCGATTATAATAACATCCCTACAGTAGTGTTCAGC
Long Flanking Sequence:
GTTAGATTTCTGTGTGAGGATTATTTTGTTGGACAAAACGTGTAAGTATAATGAATTGTGTTTGAACACAGAGCTTATTATTTGCAATCTTCGAAAAGCCTGTGGGAAAATCCTATAGGGATTTTATTGAGGGAACTGGTTTTATGCTAGCAGCCGATTGGCCTACAAGGTGACGTCATAGTTCCTCCACTCAATGGACTTCCATAGTAGGAAAAATATGGATGTCAATAGTGACAGGTTTCTGCCATTTTCAGAGTAAAGTCTTTTGTGTTCATCAGAAAAAATAAACTCATAGAGGTTTGAATCCACCAGTGTAAATGAGTGAGTCAATAGTGTGTGCATTTTTATTTTTGGTTGAACTATCCCTTTCATTTTTCAGCATTTGTTTATTGTGTATGTGTATTTAGTTTATGATGAGCTGTTGTTGTGTCCTGTTTTTGTTTGTGTGTACAGTTGCTATTGCTGCTGGCAGAAAGCTTGCTCACCGACTGTTTGAGGGC[A/T]AAGCAGACTCCAAAGTCGATTATAATAACATCCCTACAGTAGTGTTCAGCCACCCGCCTATTGGCACCGTGGGACTAACTGAAGGTGAGCTCATGCTTGCTTCAAGTTTTCATCACACTCGGTATGCAGCTTTATCTATCTGTCTATTCATCCAACTGTAGTTTCTTCTTTTTTTATATTTGTCAATCACTCCATCTATTTGTCTGTCATCTACTCATCCATTCATCTATCTGTCTATTCTTTGTCTGTCTTACCATTGGACCATCCATCTGTCATTTTATCTGCCTATCAGTCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCATCCATCCATCTATCTTTCCTATCTTCCTATCTATCTGTCTGTATGTCTGTCCATCCGTCTATCTTATCCATCCATCCATCCATCCATCCTCATTTATGCATCCCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39011
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 |
|---|---|---|---|---|---|
| ENSDART00000047050 | Nonsense | 355 | 425 | 12 | 13 |
| ENSDART00000127479 | Nonsense | 430 | 500 | 12 | 13 |
| ENSDART00000147521 | None | None | 273 | None | 8 |
The following transcripts of ENSDARG00000019236 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 40350240)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 38513474 |
| GRCz11 | 14 | 38853788 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAAGACAAGGTGAAGGTTTACACCACTTCTTTCACCCCCATGTATTA[C/A]GCCATTACCACTCGAAAGAGTCAGTGCATCATGAAGTTGGTGTGCGCTGG
Long Flanking Sequence:
ACAACTCTACATGCCTCCATTAATTATTGTTTATTTTCAGGGTTCTGGAATATTACAGAATTTCTAAAGGTCTATTTCAGACACTGAAAGACAGAGAATTTTATTTTATTGTTTATTTTGTCCAAGTAATGGAATACCAGGAGTTTTGTGTAATTTAAAATTTAACTTTCCATTTTTGAAGAGATGAATTTTCACATTTTTCAGTGCTCAATACAACAACTGTCAGTTTTTCTGTTCATTATAGGTCATGGAAAGCTTTTCAGTCAGTGACGTTTGTTTTCGATTGGGAACCCAGTGTTTAATTTCAGATTAATTTAACACTAAAAACTACTGTAATAGATTTAGTTCCAGCAATAGCAACTCTTAATGTGAGTGGTACTTGATATACTAACATCCTGAATGTATTTTTATTTTAAATTACTTTTTGTAGATGAAGCAGTTAAGACGTATGGAAAAGACAAGGTGAAGGTTTACACCACTTCTTTCACCCCCATGTATTA[C/A]GCCATTACCACTCGAAAGAGTCAGTGCATCATGAAGTTGGTGTGCGCTGGTGAAAATGAAAAGGTGAGAGCATAATCTGATCATAAAAGAGCCTCAAAACTGAGAACATCTATATTTGGTTGTATTCATTGTTAGTCAAACCCCGTCTGGGCCTCTTTTCTTCTATTAGGTGGTCGGTCTCCACATGCAGGGTTTTGGCTGTGATGAGATGCTTCAGGGTTTTGCCGTAGCCGTTAACATGGGGGCGACTAAAGCAGACTTTGACAGAACCATTGCCATCCACCCAACGTCCTCAGAGGAGCTAGTAACACTGCGCTAATCAGTGCCTTTTCATTACATCTCCACTGCAATCCAAAGAGTGTAAATGTAAACAAATGTAATTCCCTGGACTATTGTTCCATCTACAGAACTAACAGTGTAACACCACAAGCATATGTTTGATATTGGTTGTGTAGAAGTTGCACACAGTACAACCATTTATCAGGCTGCGTCTCTTGTAC
Associated Phenotype:
Not determined