ZMP
gcn1l1
Ensembl ID:
ZFIN ID:
Description:
Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:B5DE37]
Human Orthologue:
GCN1L1
Human Description:
GCN1 general control of amino-acid synthesis 1-like 1 (yeast) [Source:HGNC Symbol;Acc:4199]
Mouse Orthologue:
Gcn1l1
Mouse Description:
GCN1 general control of amino-acid synthesis 1-like 1 (yeast) Gene [Source:MGI Symbol;Acc:MGI:244424
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6092 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21180 | Essential Splice Site | Available for shipment | Available now |
sa34283 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6092
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 |
---|---|---|---|---|---|
ENSDART00000081272 | Essential Splice Site | 851 | 2669 | 23 | 61 |
Genomic Location (Zv9):
Chromosome 8 (position 3766384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 3512867 |
GRCz11 | 8 | 3571616 |
KASP Assay ID:
554-3859.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAGATCCAGCTGGAGAAAGAGTCTACTATCCGCAAGCGTCTGCAGGAG[G/A]TGAGAGCTCATACAGCAGCAGCAGTGATGGTCTGAGCTGCGCTGATCAAA
Long Flanking Sequence:
CAAACACACTTGCCATGCTTGCCATGTGTTGTTGATGTAAGATTGTATTCTGATTGATCGGAATATTCATATTGATTAGAACGAGCAGGCGTGAGAGCTGTCACTGCGCACACACACACACACACACACACACACATTTTGTTATTTAACCTACTATTTTTATGCAACAGTCAAGTTGCATGTTAATTTGCTTTAAAGAAAAGTAGGGTAAAATGGGGTGACGTGGTCATATTTGCAACCATTTTTGAGGATTTCGAGCTCCCTGAGATTTGGCGATGTTATAAAACTAAGACTCTGTAAGTGGGAAGTTATAAAAGCATGGTTTACTGTCTCTCGTAGCTTTTCAGGCCAAACGTGTTTTATTTTGGAAAGTGTTTGTGTTTTAGGAGATCAAGAAGAAGAAGGGCATCAAAGAGGAGATCCAGCTGACTAGCAAACAGAAGGAGATGATGCAGATCCAGCTGGAGAAAGAGTCTACTATCCGCAAGCGTCTGCAGGAG[G/A]TGAGAGCTCATACAGCAGCAGCAGTGATGGTCTGAGCTGCGCTGATCAAAGCGCTGATCTGCTATTTTGTGTGTTTGTGTGTGTGTTCTGTCAGCTGGACATGGAGCTGCTGTGTGCTGTGGGTTTGCTGGAAGCCGCTCTGGCTCGTCGTCCTCCGCTCATCTGGATGCACCTTCCAGCACTGGTGCAGGTTCTCCTGCCGCTCCTGCAGTCTCCTCTGGCCGCTTCGTTGATAAAGCGTGTGTTTCTGCAGATCGGTGTCACTCTAATGCCTAAAGAACTGCACCAGCTGGGTGAGTCGCATTTAATTCAACTTTATTTGTATAGCGCTTTTCTCTATAATTATTGATTCAAAGCAGCTTCGCAAGAGGTGCACATTATTGCATTACAATCAAAATCAGAAAAAGTTAAGGTTATTAGTAGGGATGCACGATATATCGGCGGCCGATAAATGCTATTTTTAAAATTATCATTATCGATGTCTAAATTAGGCTGATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21180
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081272 | Essential Splice Site | 851 | 2669 | 23 | 61 |
Genomic Location (Zv9):
Chromosome 8 (position 3766385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 3512868 |
GRCz11 | 8 | 3571617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATCCAGCTGGAGAAAGAGTCTACTATCCGCAAGCGTCTGCAGGAGG[T/C]GAGAGCTCATACAGCAGCAGCAGTGATGGTCTGAGCTGCGCTGATCAAAG
Long Flanking Sequence:
AAACACACTTGCCATGCTTGCCATGTGTTGTTGATGTAAGATTGTATTCTGATTGATCGGAATATTCATATTGATTAGAACGAGCAGGCGTGAGAGCTGTCACTGCGCACACACACACACACACACACACACACATTTTGTTATTTAACCTACTATTTTTATGCAACAGTCAAGTTGCATGTTAATTTGCTTTAAAGAAAAGTAGGGTAAAATGGGGTGACGTGGTCATATTTGCAACCATTTTTGAGGATTTCGAGCTCCCTGAGATTTGGCGATGTTATAAAACTAAGACTCTGTAAGTGGGAAGTTATAAAAGCATGGTTTACTGTCTCTCGTAGCTTTTCAGGCCAAACGTGTTTTATTTTGGAAAGTGTTTGTGTTTTAGGAGATCAAGAAGAAGAAGGGCATCAAAGAGGAGATCCAGCTGACTAGCAAACAGAAGGAGATGATGCAGATCCAGCTGGAGAAAGAGTCTACTATCCGCAAGCGTCTGCAGGAGG[T/C]GAGAGCTCATACAGCAGCAGCAGTGATGGTCTGAGCTGCGCTGATCAAAGCGCTGATCTGCTATTTTGTGTGTTTGTGTGTGTGTTCTGTCAGCTGGACATGGAGCTGCTGTGTGCTGTGGGTTTGCTGGAAGCCGCTCTGGCTCGTCGTCCTCCGCTCATCTGGATGCACCTTCCAGCACTGGTGCAGGTTCTCCTGCCGCTCCTGCAGTCTCCTCTGGCCGCTTCGTTGATAAAGCGTGTGTTTCTGCAGATCGGTGTCACTCTAATGCCTAAAGAACTGCACCAGCTGGGTGAGTCGCATTTAATTCAACTTTATTTGTATAGCGCTTTTCTCTATAATTATTGATTCAAAGCAGCTTCGCAAGAGGTGCACATTATTGCATTACAATCAAAATCAGAAAAAGTTAAGGTTATTAGTAGGGATGCACGATATATCGGCGGCCGATAAATGCTATTTTTAAAATTATCATTATCGATGTCTAAATTAGGCTGATATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34283
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081272 | Nonsense | 1650 | 2669 | 39 | 61 |
Genomic Location (Zv9):
Chromosome 8 (position 3796715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 3543697 |
GRCz11 | 8 | 3602446 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCATAGATTTACTGTGTGTATGCGTTTTCAGGATCTGTCTCCGTATT[T/A]GCCCAGTGTGATTCCAGGCCTCAAAGCATCTCTGCTGGACCCTGTGCCAG
Long Flanking Sequence:
ACCCCGATCCTGCTGGACGCTCTGACTGACCCGTCTCACAGGACGCAGCACTGCCTGCAGACACTGCTGGACACCAAGTTTGTGCATTTCATCGATGCTCCATCTCTGGCTCTGATCATGCCCATCGTCCAGAGAGCCTTCCAGGACAGATCCACCGACACGCGCAAGATGGCGGCGCAGATCATCGGAAACATGTACTCACTCACTGACCAGAAGGTACATGATGCACAGAACACTGGTTCATTCATGTGTTTTCATCCATAAAAATTATATATATTTATATTATAGTGTTCTTACTGACAAAATACATAGTTTTTACAACTATTTTAAGTATTTTAATTGTCATTGTGATGTAGCTATAAGCAACCTTATGCCAAGTGACACAATAATTCTGGTTAAGAATATGCATTAACCCTGGTAAATCAGTGTAACACATGAATGGCTTTAAATGGCTCATAGATTTACTGTGTGTATGCGTTTTCAGGATCTGTCTCCGTATT[T/A]GCCCAGTGTGATTCCAGGCCTCAAAGCATCTCTGCTGGACCCTGTGCCAGAGGTAATGCTGCCTGTCCTGTGAAGCTGTCTTGATCAGTGCTGTGTGTGCGCGCGCATTCTTTCTGTCTGTGTTGTGTGTCTCATTAGTGTGTGTGCTCTTTTAGGTGCGGACGGTGTCAGCGAAGGCTCTGGGTGCGATGGTGAAGGGAATGGGTGAGTCCTCCTTTGAGGATCTGCTGCCGTGGCTGATGGAGACTCTGGCGTCTGAACAGAGCTCTGTGGATCGATCAGGAGCTGCGCAAGGTGAGAACAGACCAGTAGAGGGCAGCAGACACATGCACACTAACACAGCGCCAATTCATCTTTATTTTTATATCACTTTCACAATGAAGATTGTGTCAAAGCAGGTAAGCATAGAAGTTGAAGTAAATTGAAACATTTGAAGTGCAGTTTAGTTCAGTTCGGTGTGTTTTTTTACTGCTGAAAGTCCAAACACTGAAGAGCAAAAC
Associated Phenotype:
Not determined