ZMP
gstcd
Ensembl ID:
ZFIN ID:
Description:
glutathione S-transferase, C-terminal domain containing [Source:RefSeq peptide;Acc:NP_001019633]
Human Orthologue:
GSTCD
Human Description:
glutathione S-transferase, C-terminal domain containing [Source:HGNC Symbol;Acc:25806]
Mouse Orthologue:
Gstcd
Mouse Description:
glutathione S-transferase, C-terminal domain containing Gene [Source:MGI Symbol;Acc:MGI:1914803]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24856 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa4866 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa24856
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006394 | Nonsense | 304 | 614 | 3 | 11 |
| ENSDART00000053016 | Nonsense | 300 | 610 | 5 | 13 |
| ENSDART00000124185 | None | None | 342 | None | 4 |
| ENSDART00000133255 | None | None | 320 | None | 3 |
| ENSDART00000134661 | Nonsense | 304 | 614 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 50475415)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49324506 |
| GRCz11 | 1 | 49968332 |
KASP Assay ID:
554-7836.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCACGCTATCCCATCTGCCCTTACTGCTGAGATGGTACCAGCGCACA[C/T]AGGAGCTCTCCGGTGTACTGAGAGCCGCAAAGGACTGTGGGATGGTCTTT
Long Flanking Sequence:
CCCCTTTAAGCTATATATTTTTTCATAGTCTGCAGAACAAACCATCATTATACAATAATTTGCCTAATTACCTTAACCTGTCTAGTTAACCTAATTAACCTAGTTAAGCCTTTTAATGTCACTTTAAGCTGTATAGAAGTGTCTTGATAAACATCTAGTCAAATATTATTTACTGTCATGGCAAAAATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTATTATGATTAGAAATGTGTTGAACAAAATCTCTCTGTTAAACAAAAATTCTGGAAAAAAAAATAAACGAGGGGCGAATAATTCAGGGGGGCTAATAATTCTGACTTCAACTGGATCTCATTTACTGTCCTTTTTATACTCAGACTTTCTATTTTAGGCTCTTTAAATTAAAATCTACCACGTCTCTGATTAAACCCTTTTCAGATCTCTCTCCGAACTCACTCTCCCTCCACGCTATCCCATCTGCCCTTACTGCTGAGATGGTACCAGCGCACA[C/T]AGGAGCTCTCCGGTGTACTGAGAGCCGCAAAGGACTGTGGGATGGTCTTTCTTACCCTCAGTGCGGCCGACCCTTGTCTTACCCAGCAGGACGCCCCCCCACAAGCCAGCGAAGAGCCCAAACCAAAGCAAGAGCCCTTCATCGGGGGCCCGAGGCCAACACTCACCAAACTGCAGGTAATTGAATTTCGCTCTCTCCTATTTCTCTCTCATTTGATTCTCTAAATCTTCGCTCTCACGGAAAGGAGATTACACAGAAGCGCTTCTCTTTGCCACTCCACTAAACCTGTCAGTGGCGAACTCGCATAATCCCTAAACAGCGATCCGCTCTCAATACGTTCAGTGCCGCACACCCGTCCCTTTACGGCAGCCCTGTGTGCCACCGCGGGGCCTGAACCGTGATGATAAAGGATTTATGCACTCCAGCGAGGCAGAACAGCAGCCGTTCTGACTCGCTCTTAACTGATGGGACACCCTGCCACTCGATACTTTAAGGAGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4866
Status:
F2 line generated
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006394 | Nonsense | 439 | 614 | 6 | 11 |
| ENSDART00000053016 | Nonsense | 435 | 610 | 8 | 13 |
| ENSDART00000124185 | None | None | 342 | None | 4 |
| ENSDART00000133255 | None | None | 320 | None | 3 |
| ENSDART00000134661 | Nonsense | 439 | 614 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 50540500)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 49389591 |
| GRCz11 | 1 | 50033417 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAATTTTTTTCCCTCTGTTTGTTTTCTCAGGGGCACGTTGGGATTGTTT[T/A]GGCCTACATGCTTCCTAAATGTCAGGTAAGGCTTTCTGATTTGTTCAAGT
Long Flanking Sequence:
CCAGTGAATAAGATGATAAATATAAGTAAATTTTTTGGACTCTGCATATCTCGTTGCAGTGTGTTACATTTCCCCGTCTCCTCCTTAACATCAAATCTTTTCCCCTGAAGGTAAGATGTCAGACAGCCGTGCGCTGCGCAAACAACAACAGCTCGACAACCTGCTGGCGATGGTGTTGAATCAGGCCCAGCCGGGACACACAGTGGTGGATTTCTGCAGCGGAGGGGTACGTCAGATGACATTTCCGAAAAGCCCTGGACTCTTTTTCTGTTTTCTTCAGAGACTCGGCATGCGTGTCAGTAAAGCATCTGCTCTCCTCGTATAATCTGGGGACGAGCTCTTGTTATTCTGTGCATACATATAAGCCCTGATGTTACTGCTCGCGGGCAGCGGGTCAATATTCACAGGGGTTTTTTTGTGAGCACGCTTTGATCCAATGAGCTGTTTTTCCAAATTTTTTTCCCTCTGTTTGTTTTCTCAGGGGCACGTTGGGATTGTTT[T/A]GGCCTACATGCTTCCTAAATGTCAGGTAAGGCTTTCTGATTTGTTCAAGTGTAGCGAGGTTTGAGTTAACGCAGTCAAAGAAAAGAAACTAAATCTGTCTTCATCGCTGCTGACCTCATTTGTAGACACTGGAAAAATGCCACACTTTCTTTCTCTCAAAGACTTGAGGAACCACCGTCATGCATTACTAAATGACTGTTAAGCATCTTTTATTGCACTGAACTGTTTTATTGTACTGTAATTAGACAATGTTTTAATCAGAGGTGTGATAACTGTCACACAATTTTGGCCTTAAAATTTAAAACTGCATATGATATGTATTACTAATCACACAACTTATGTCTTATGTTGAATGGGGAAGATATAGGTTTTTCTTTTATGTCAAAAATCATGAGGATGTTTAGTAAAGATGATTTTTTTTCTAAAATTATTTGTACATTTTCTGCTGTATATCAAAACTTAGCTATGCACAAGCTTTATTTAGACGGATTTAAACAGTT
Associated Phenotype:
Not determined