ZMP
zgc:92763
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC436833 [Source:RefSeq peptide;Acc:NP_001002560]
Human Orthologue:
GSTK1
Human Description:
glutathione S-transferase kappa 1 [Source:HGNC Symbol;Acc:16906]
Mouse Orthologue:
Gstk1
Mouse Description:
glutathione S-transferase kappa 1 Gene [Source:MGI Symbol;Acc:MGI:1923513]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36187 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32099 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36187
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 |
---|---|---|---|---|---|
ENSDART00000030282 | Essential Splice Site | 94 | 229 | 4 | 8 |
ENSDART00000130111 | Essential Splice Site | 94 | 229 | 3 | 14 |
ENSDART00000138701 | Essential Splice Site | 94 | 167 | 4 | 6 |
The following transcripts of ENSDARG00000056510 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 34326027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32057527 |
GRCz11 | 16 | 32011557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTCCTGTGCGTCAACCTTCCAACGTTTTTGAGACAATGTTTGAGAAAG[G/A]TATTTACAGAACAAGTCATACGTTTTATGTATAGAAAATTAACGTTTGAC
Long Flanking Sequence:
GGTATATTTTTGTCAGGCTATTTGTTCCAAACAGTTCCACAGAACCCCTAACACTTCTTTGCAGCCCCTTGGTATGAATACCCCTGAATTACTGGACAAAGTACATCTTAGAGCTGCATTTTACATGTATATTTTACAAATAAATCTATTTTACTAGTCAATAAAGGCCTACACGACACAGTTAAAAAAATCTAGATCATCAAAAATGGTGCATTCTACACAAAATGATCTTGCTCTATATGATTTATAATGTACTAAAAACTTCTCTGCGAAGAATAATCAAACAAAAGCTAAAAGATTAAGGCCTAAAAATTGTATGCAGTTTTTATAGATGATAACCAAAGATAACTTTAAGTGTCTTTTGTTTGTAGGCAATCGGCCTCCTGGAATGATCCCCAACAAGTTTTTGTACATGACCAGTGATCTGAAGCATGTGTCCGAGTACTTTGGGGTTCCTGTGCGTCAACCTTCCAACGTTTTTGAGACAATGTTTGAGAAAG[G/A]TATTTACAGAACAAGTCATACGTTTTATGTATAGAAAATTAACGTTTGACTATTTTTAGAGTACTTTTTTATTTAAAGGCATAGTTCACACAGAAAGGAATATTTGCACATTAACTCCCCCTGAAGTGGTTAAAATCTTGTTTTAGTTCTTCTGTTAAATACAAAAAAAGATATTTGGAAGAAAGCTGAAACCTGTTGACTTTTAAAGAAGAAAAACAAATACTATGGAGGTCAATAGTTAAAGGTTTCCATCTTTCCTCAACATTTTTTTTTTATCAGAATCAGAAAGAAAGTGATGATAGTTTTGGAACGAGTGAGTGATGACAGATTTTTCATTTTTGTGTGAACTCTGCTTTTAAAGAAAAATCTAAATAAGGCATAATCTTGATTTCTTACTAAATTGCTCCTATCCTTTCTTTTCCTTTATCTTCTCATATAGGTTCACTGAAAGCAATGCGCTTTGTGACAGCGGTAGCAGAGAAGGAGAAAGAGGGAGATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32099
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 |
---|---|---|---|---|---|
ENSDART00000030282 | None | None | 229 | None | 8 |
ENSDART00000130111 | Essential Splice Site | None | 229 | 11 | 14 |
ENSDART00000138701 | None | None | 167 | None | 6 |
The following transcripts of ENSDARG00000056510 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 34320031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32051531 |
GRCz11 | 16 | 32005561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGTGGAGCACTCATCAGGACATAGTCCAGCCTGCCTCACTCACAGAG[G/A]TATGCTATGCTCATGATGATTACAAATTTAATCAAGATTAGGCGTGTGGA
Long Flanking Sequence:
TTAGACATGTAATTACAAAAACGTAACCCATCTGTTTGTTTTTTGCTTAAATCATATCTGCAGTTACTATCACCATTCACCTCAATATTTCCTGGTTCTGCTGGGAGGAAAATGATGGCGCACTGGGTTGCTGGAATCAGTTTCCAACTGATCTTTATTTCTATAGCACTTTTACAATGTAGATTGTGCCAGAGTAGATTATAGTGAATTGAAACCGTGTCAGTTCAGTTTTCAGAGTTTAAATTCAGTTCAGTTCAGTGTGGTTTACTCGCTGCTGAGAGTACAAACACTGAAGAGCAAATCCATCGATGCACACATTTCTTATATTCTCCTTTTTTCTCTTTGCTGAATTAGACTCTCTGATTCCGATGCATTTTGTGACCGCTGTAGCAGGGAAGGATAAAGATGGTGGCGATCTGGTAGAGAAGGTGTCTAGGGAGCTCTGGAAACGAATGTGGAGCACTCATCAGGACATAGTCCAGCCTGCCTCACTCACAGAG[G/A]TATGCTATGCTCATGATGATTACAAATTTAATCAAGATTAGGCGTGTGGATATTCCAAAATCTATTTTAGTACTGACATATACTAAACCTATAACAAAGTCAATACTATAAACTATTTTGTTTTGTAAAATCCTTCTGATTTTCACAGGTGGGAATCAAGGCTGGTTTCTCAGCCACTGAGGTGGAAGACATTCTGATCCTTGCTAAATCTCAGCAAATTAAAGACAAGCTGACAAGTATCACAAATGAAGCCCTGGAGTATAAGGTCAGTTGGGGGTTGCTTGCATGTCTGGGGTTAGCAAAATTAGTGTTAATAAAACACACTAACACAATTTTCCCCTCTGTAGTGCTTTGGTTTACCATTCATTGTGGTTCAGGTTGATGGGAAGGCTGAGGTCTTCTTCGGGTCAGATAAATTTGAGCTTATGGCGTATTTCCTTGGTAAGACTTTAAAAATTATCTAATACCCACAGAATCTCCATTGTTCTAAAATGCACCAA
Associated Phenotype:
Not determined