ZMP
gss
Ensembl ID:
ZFIN ID:
Description:
glutathione synthetase [Source:RefSeq peptide;Acc:NP_001006104]
Human Orthologue:
GSS
Human Description:
glutathione synthetase [Source:HGNC Symbol;Acc:4624]
Mouse Orthologue:
Gss
Mouse Description:
glutathione synthetase Gene [Source:MGI Symbol;Acc:MGI:95852]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43926 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12631 | Essential Splice Site | Available for shipment | Available now |
sa12621 | Essential Splice Site | Available for shipment | Available now |
sa29894 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa688 | Nonsense | Available for shipment | Available now |
sa37644 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43926
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054909 | Nonsense | 12 | 475 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 14878844)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15010777 |
GRCz11 | 23 | 14766854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCAGATTTAGTACTATGTCTGTCAAACTGGAGGACACCCTGAAAGAT[G/T]AAAACCTGATCAAACGTTTAGAGGAGATAGCAAAAGACACGGCGCTGTTA
Long Flanking Sequence:
ATTTTATATTTTCCATGATGATAATACATAATATTTTGCTGAATATTTTTCAAGATGCTAATATTCAGATTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGCAAACCATTGTATAACAATGGTTTGTTCTGTAGACAATTGAAATAATCTATTGCTGAAGGGAGGTAATAATATTAACCTTAAAATGTAAAAAAAAAAATTGCTTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAACATATTATGGAAATACTGTGAAAAATTCCTTGTTCTGTTCAACTTCATTTGGGAAATATTTGGAAAAGAAAAAAAAAATCACAGAAGCGGTAATAATCTTGACTTGTATATGAAAATGTCTAGCTCCCTGAAAATCAGACTCCGACAAGTGAAGCATTTGCTTATAAAATGAATCAAATGTGTTTTATTCTGACTGCAGATTTAGTACTATGTCTGTCAAACTGGAGGACACCCTGAAAGAT[G/T]AAAACCTGATCAAACGTTTAGAGGAGATAGCAAAAGACACGGCGCTGTTACATGGAGTGTTGATGCGGACCAAAGACACGCCAAACTCTCCTGAAGTAAGAGAACGTCTTTATCTACTTAGAAATATAATAAAGAAATGCATGTTTACTTGTGGTAAAATGTATGCAAAATATTTATTATGTTTATTGGTAAAAACTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTTATAATGCTGAACCATGATTAATAAATGCTGTTCAAGTATTGTTCATTTAGAATTCATGTTAACTAACCACAAAACCTTAATGCAAAGCATGACAATTCATTGTTTAATGTGTGATATTATAACGTGTATTATTGTATTAAATGTATTATTATTTTCTGATGTATAGTACTTTTTGTTTATCTGCATAGGTTTTGAGCTAAATTTGTGGTTTTCATTTTATCTTAATACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12631
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 |
---|---|---|---|---|---|
ENSDART00000054909 | Essential Splice Site | 43 | 475 | 2 | 13 |
ENSDART00000054909 | Essential Splice Site | 43 | 475 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 14878748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15010681 |
GRCz11 | 23 | 14766758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTACATGGAGTGTTGATGCGGACCRAAGAYACGCCAAACTCTCCTGAA[G/A]TAAGAGAAYGTCTTTATCTACTTAGAAATATAATAAAGAAATGCATGTTT
Long Flanking Sequence:
GGTTAATTAGGCAAACCATTGTATAACAATGGTTTGTTCTGTAGACAATTGAAATAATCTATTGCTGAAGGGAGGTAATAATATTAACCTTAAAATGTAAAAAAAAAAATTGCTTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAACATATTATGGAAATACTGTGAAAAATTCCTTGTTCTGTTCAACTTCATTTGGGAAATATTTGGAAAAGAAAAAAAAAATCACAGAAGCGGTAATAATCTTGACTTGTATATGAAAATGTCTAGCTCCCTGAAAATCAGACTCCGACAAGTGAAGCATTTGCTTATAAAATGAATCAAATGTGTTTTATTCTGACTGCAGATTTAGTACTATGTCTGTCAAACTGGAGGACACCCTGAAAGATGAAAACCTGATCAAACGTTTAGAGGAGATAGCAAAAGACACGGCGCTGTTACATGGAGTGTTGATGCGGACCAAAGACACGCCAAACTCTCCTGAA[G/A]TAAGAGAACGTCTTTATCTACTTAGAAATATAATAAAGAAATGCATGTTTACTTGTGGTAAAATGTATGCAAAATATTTATTATGTTTATTGGTAAAAACTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTTATAATGCTGAACCATGATTAATAAATGCTGTTCAAGTATTGTTCATTTAGAATTCATGTTAACTAACCACAAAACCTTAATGCAAAGCATGACAATTCATTGTTTAATGTGTGATATTATAACGTGTATTATTGTATTAAATGTATTATTATTTTCTGATGTATAGTACTTTTTGTTTATCTGCATAGGTTTTGAGCTAAATTTGTGGTTTTCATTTTATCTTAATACAAATAAAGCTTTCCCTTGTAGCATTTCAGAGCTAAAATGTCTAGTCCAGACTCATAGGTGGCAATTATTTTGTGAGTGTTTTGACTGAAGCACTGAGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12621
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 |
---|---|---|---|---|---|
ENSDART00000054909 | Essential Splice Site | 43 | 475 | 2 | 13 |
ENSDART00000054909 | Essential Splice Site | 43 | 475 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 14878748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15010681 |
GRCz11 | 23 | 14766758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTACATGGAGTGTTGATGCGGACCRAAGAYACGCCAAACTCTCCTGAA[G/A]TAAGAGAAYGTCTTTATCTACTTAGAAATATAATAAAGAAATGCATGTTT
Long Flanking Sequence:
GGTTAATTAGGCAAACCATTGTATAACAATGGTTTGTTCTGTAGACAATTGAAATAATCTATTGCTGAAGGGAGGTAATAATATTAACCTTAAAATGTAAAAAAAAAAATTGCTTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAACATATTATGGAAATACTGTGAAAAATTCCTTGTTCTGTTCAACTTCATTTGGGAAATATTTGGAAAAGAAAAAAAAAATCACAGAAGCGGTAATAATCTTGACTTGTATATGAAAATGTCTAGCTCCCTGAAAATCAGACTCCGACAAGTGAAGCATTTGCTTATAAAATGAATCAAATGTGTTTTATTCTGACTGCAGATTTAGTACTATGTCTGTCAAACTGGAGGACACCCTGAAAGATGAAAACCTGATCAAACGTTTAGAGGAGATAGCAAAAGACACGGCGCTGTTACATGGAGTGTTGATGCGGACCAAAGACACGCCAAACTCTCCTGAA[G/A]TAAGAGAACGTCTTTATCTACTTAGAAATATAATAAAGAAATGCATGTTTACTTGTGGTAAAATGTATGCAAAATATTTATTATGTTTATTGGTAAAAACTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTTATAATGCTGAACCATGATTAATAAATGCTGTTCAAGTATTGTTCATTTAGAATTCATGTTAACTAACCACAAAACCTTAATGCAAAGCATGACAATTCATTGTTTAATGTGTGATATTATAACGTGTATTATTGTATTAAATGTATTATTATTTTCTGATGTATAGTACTTTTTGTTTATCTGCATAGGTTTTGAGCTAAATTTGTGGTTTTCATTTTATCTTAATACAAATAAAGCTTTCCCTTGTAGCATTTCAGAGCTAAAATGTCTAGTCCAGACTCATAGGTGGCAATTATTTTGTGAGTGTTTTGACTGAAGCACTGAGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29894
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 |
---|---|---|---|---|---|
ENSDART00000054909 | Essential Splice Site | 118 | 475 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 14875375)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15007308 |
GRCz11 | 23 | 14763385 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTATATAGATGTAAATCTTAATTTATTTAACTCCTCTTTCATTCAA[G/A]AAAATAGTAGTGGGTCTGAATCGCTCAGACTACATGTTAGACCACAGTCC
Long Flanking Sequence:
AGCCAGACTTTTCAACATCTACAAACAAGTTCAGCAGGAGGGCCATGCTCAGGTATACCGGTAATTGTTTACCACTCATTTGCTGATTCATTTAAAGAGATAGTTCACCCAAAAATCAACAAACCCACTTTTTACTCATCCTCAAATGCTTTCAAACATTGACAAGTTTCTTTTTTCTGCTGAACACAAAAGAAGATACTGTGAAGAATGTTAGAAACTGGTAATCATTGACATCCAGCAGGAAAAACAAATACCATGGAAGTCAATGTTTACTAGTTTCCGGCATTTTTTTCTAAATATTTTCTTTTGTGTTAAACTGAATAAAAAAAAAAACAGGTTTGTGAATGATGAGTAGAATTTTGTTTTGTTTTGTGTAAATCAAATCCCTTTAAATTTCACGTAAAAAAGTTACATCACTGTTTAAATTCATAAAAAAAGAAAAGTAATCAATTTGTTATATAGATGTAAATCTTAATTTATTTAACTCCTCTTTCATTCAA[G/A]AAAATAGTAGTGGGTCTGAATCGCTCAGACTACATGTTAGACCACAGTCCAGACGGTCGAACATCTCTGAAGCAGATTGAAATCAACACTATTGCTGCGAGTTTTGGTGGTCTTGCTTCACGAACACCAGATGTCCATCGGTAAGTCTGACCATACATTTTAAGTGGACCTATTATGCAAAAAAAAAATCACTTTTATGAGTTGTTTAAACACAGTTGTGTGGCAACAATGTACTGCTATATCTGCTGTCTAATGGTAAAAAGTAATTAATTCTATTGTTGTAATCACACTTCATAAAAAACAATGTGATTCTCCCTTTGTACGTGTCATCAGACGGGGAAAACCCCACCCATTAGTGTCCCCACTCCATTAATCTCTTCCTTGTTGGCATAGACACCCCTGAGTGAGAAGCGGCCGTTAAGTTTTCAACCCCTACCTGCTGAAGATAATGCCAGCGACAAAGAGGCATTATAAATGTGGAGTTTTAGAATGCACAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa688
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 |
---|---|---|---|---|---|
ENSDART00000054909 | Nonsense | 158 | 475 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 14875254)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15007187 |
GRCz11 | 23 | 14763264 |
KASP Assay ID:
554-0596.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGATTGAAATCAACACTATTGCTGCGAGTTTTGGTGGTCTTGCTTCA[C/T]GAACACCAGATGTCCATCGGTAAGTCTGACCATACATTTTAAGTGGACCT
Long Flanking Sequence:
AACCCACTTTTTACTCATCCTCAAATGCTTTCAAACATTGACAAGTTTCTTTTTTCTGCTGAACACAAAAGAAGATACTGTGAAGAATGTTAGAAACTGGTAATCATTGACATCCAGCAGGAAAAACAAATACCATGGAAGTCAATGTTTACTAGTTTCCGGCATTTTTTTCTAAATATTTTCTTTTGTGTTAAACTGAATAAAAAAAAAAACAGGTTTGTGAATGATGAGTAGAATTTTGTTTTGTTTTGTGTAAATCAAATCCCTTTAAATTTCACGTAAAAAAGTTACATCACTGTTTAAATTCATAAAAAAAGAAAAGTAATCAATTTGTTATATAGATGTAAATCTTAATTTATTTAACTCCTCTTTCATTCAAGAAAATAGTAGTGGGTCTGAATCGCTCAGACTACATGTTAGACCACAGTCCAGACGGTCGAACATCTCTGAAGCAGATTGAAATCAACACTATTGCTGCGAGTTTTGGTGGTCTTGCTTCA[C/T]GAACACCAGATGTCCATCGGTAAGTCTGACCATACATTTTAAGTGGACCTATTATGCAAAAAAAAAATCACTTTTATGAGTTGTTTAAACACAGTTGTGTGGCAACAATGTACTGCTATATCTGCTGTCTAATGGTAAAAAGTAATTAATTCTATTGTTGTAATCACACTTCATAAAAAACAATGTGATTCTCCCTTTGTACGTGTCATCAGACGGGGAAAACCCCACCCATTAGTGTCCCCACTCCATTAATCTCTTCCTTGTTGGCATAGACACCCCTGAGTGAGAAGCGGCCGTTAAGTTTTCAACCCCTACCTGCTGAAGATAATGCCAGCGACAAAGAGGCATTATAAATGTGGAGTTTTAGAATGCACAAATGAACACCGTAATCTCTTTAGACTACCTTTTTCTTAACCATTTTGTTGATATTTTCAGTTTTCATAGACATATGCTGATGCACAGACATGTGTAGCTCTGCCCTCTTTTGAAAAGAGCACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37644
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054909 | Essential Splice Site | 164 | 475 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 23 (position 14875233)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 15007166 |
GRCz11 | 23 | 14763243 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGCGAGTTTTGGTGGTCTTGCTTCACGAACACCAGATGTCCATCGG[T/G]AAGTCTGACCATACATTTTAAGTGGACCTATTATGCAAAAAAAAAATCAC
Long Flanking Sequence:
CAAATGCTTTCAAACATTGACAAGTTTCTTTTTTCTGCTGAACACAAAAGAAGATACTGTGAAGAATGTTAGAAACTGGTAATCATTGACATCCAGCAGGAAAAACAAATACCATGGAAGTCAATGTTTACTAGTTTCCGGCATTTTTTTCTAAATATTTTCTTTTGTGTTAAACTGAATAAAAAAAAAAACAGGTTTGTGAATGATGAGTAGAATTTTGTTTTGTTTTGTGTAAATCAAATCCCTTTAAATTTCACGTAAAAAAGTTACATCACTGTTTAAATTCATAAAAAAAGAAAAGTAATCAATTTGTTATATAGATGTAAATCTTAATTTATTTAACTCCTCTTTCATTCAAGAAAATAGTAGTGGGTCTGAATCGCTCAGACTACATGTTAGACCACAGTCCAGACGGTCGAACATCTCTGAAGCAGATTGAAATCAACACTATTGCTGCGAGTTTTGGTGGTCTTGCTTCACGAACACCAGATGTCCATCGG[T/G]AAGTCTGACCATACATTTTAAGTGGACCTATTATGCAAAAAAAAAATCACTTTTATGAGTTGTTTAAACACAGTTGTGTGGCAACAATGTACTGCTATATCTGCTGTCTAATGGTAAAAAGTAATTAATTCTATTGTTGTAATCACACTTCATAAAAAACAATGTGATTCTCCCTTTGTACGTGTCATCAGACGGGGAAAACCCCACCCATTAGTGTCCCCACTCCATTAATCTCTTCCTTGTTGGCATAGACACCCCTGAGTGAGAAGCGGCCGTTAAGTTTTCAACCCCTACCTGCTGAAGATAATGCCAGCGACAAAGAGGCATTATAAATGTGGAGTTTTAGAATGCACAAATGAACACCGTAATCTCTTTAGACTACCTTTTTCTTAACCATTTTGTTGATATTTTCAGTTTTCATAGACATATGCTGATGCACAGACATGTGTAGCTCTGCCCTCTTTTGAAAAGAGCACAATATTGAAAGCGACAGTCGCCAA
Associated Phenotype:
Not determined