ZMP
LOC100333016
Ensembl ID:
Human Orthologue:
ATG7
Human Description:
ATG7 autophagy related 7 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:16935]
Mouse Orthologue:
Atg7
Mouse Description:
autophagy-related 7 (yeast) Gene [Source:MGI Symbol;Acc:MGI:1921494]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10973 | Essential Splice Site | Available for shipment | Available now |
sa14768 | Nonsense | Available for shipment | Available now |
sa14235 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10973
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 |
---|---|---|---|---|---|
ENSDART00000111987 | Essential Splice Site | 132 | 697 | 4 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 875450)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 858451 |
GRCz11 | 11 | 884949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTCGAAGACTCTTCAATCCTCAACAAGTTCATCCTCTTGACATTTGCGG[T/C]TTGTGTGCCAACATTTTAGAAAATGTCCCWGTAAAATTAATGTCCTTTCA
Long Flanking Sequence:
TTAAAGGGAATGAGAGACGAGACTCTTATTGGTTTAATGCTTGTTATGGTCAAAACACACCCAAAACTCATTAAGAGAATAAGCACAACCCTGTTAGACCATTCGTCGGGCACAGAGAGTATTTGTCCATTCTTAAAACAGCAGATTCGGACATGCCCTTAATGCTTTTGCATCATGAGCTTTAGACTTTGAGCCTAGATCAGTAAAATAGAGCTCTTTGTCTTATCGTTTTTGTTTTTTCATTTATTTATTTATTTATTTTTATTTTTTTTGTTTTTGAATTAACAAATTTAAAAAAAAAAACTACAATTACAGCCAGGACTGTTACATTTTCACTTTTGCATTTGCGTAAACCATATCATTAATATCCCCTGCTGTACTGTCCCTTTAATTAATCCTGATAATGTTGTCTTCTTCACAGATCTGGAGCGCTATTCAGTCCGGCGCTGCTCTCGAAGACTCTTCAATCCTCAACAAGTTCATCCTCTTGACATTTGCGG[T/C]TTGTGTGCCAACATTTTAGAAAATGTCCCAGTAAAATTAATGTCCTTTCATCCATTTGTTTCTGACTGGGGCTTTTGTTTGTGCAGGATCTGAAGAAATATCACTTCTATTATTGGTTCTGCTTTCCTGCGCTCTGCTTTGTGGAGGGCATCCAGCTGCTGCGCGCGCCGCTGTCATTAGAGCAGCATTTCTCTGACAAACAGGTGTGCAGGAGAGCCCAAACTGATGCCCACACGGAGGATTCGTGCGAAGGATAATGAGTCATTAGGCGCTGCTTTATGGAAAGCATGTGCTGATTAGAAATATTTATTCAGCAGTAATTATTGGAAGGCATAATCTCAGATAGGCTGTGAGAAACATGATGTGTCTTAAGGTCAGCGTGTATTGGAAGATAAGATTTTTCCTGTATTGCAACGTACAGTACATCCAGTTAAAGTAGAATAGGCTTAATTGCTCCACCCTAAATGGCTGATAGCTCCACCCAAAAAGACTGCTTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14768
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 |
---|---|---|---|---|---|
ENSDART00000111987 | Nonsense | 448 | 697 | 15 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 854601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 837262 |
GRCz11 | 11 | 863760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCCCKATGCCCGGACACCCTGTCAACTTCYCAGATCTGACCGTAGCT[C/T]AAGCGCAGCAGGACGTGGAGCAGCTGAAAAAACTCATTTCWGAACRYGAT
Long Flanking Sequence:
TACTGGGTTGCGACTGGAAAGGCATCCACTGTGTAAAACATATCCTAAAATAGTTTGTGGTTCTTTCCACTGTGGCGTTCTCTGATGAAAAAAGGGGCTAAGCCAAGGGAATTGATGAATGTGTTTAACATGAAGAAACAATCACCAACACTTGTATTACAGTATTTGTTCATGTCAGTTGTAAACACAGTTGCTGATTGTTAGTTCATGTTAACTCAGTGCATTTGCTAATTTTAACTACTTTAATAATGCATTAGTGAATGTTGGTTGTTATTTATAATGCTGTTTGAGTACTGTTCAGAATAAATTCATGCTAGTAAATACATTTTTAGATGAAATCTTATTGTAAAGTGACCAAAATATTTGCTGTCTTTTTGTCATTGCGTGTTTTACAGTGTATGGATGTATTGTTGTTTTCTGTTGTTCAGAATGCAGAAGGCTTCAACATGAGCATCCCGATGCCCGGACACCCTGTCAACTTCTCAGATCTGACCGTAGCT[C/T]AAGCGCAGCAGGACGTGGAGCAGCTGAAAAAACTCATTTCTGAACACGATGTGGTTTTTCTGCTGATGGACACCAGAGAGAGCCGCTGGCTGCCCACCGTCATCGCTGCCAGCCAGAGAAAGGTACAGCAGCACCATACCTTGCAAAAAATATGACAGCGTAATACTGTGTTTTTCTGCGATATGAGTACAAGTCCAAGTTTTGTAGTTATGTTTTAGTTAAGTGATTTAATAAGTAAATAAGTAATTATGTAAATAAGTGAATAATAAAAAATTAATAGGTAAATAAATAAATAAACATAAATAAGTAAATGATTAAGTAAATATGTAAATAAATAAAAAAAATAAATAAGTAAATGATTAGGTAAATAAGTAAATAAATAGGGAAATATGTAAGTAAATAAAAATATAAACAAATGAATAAGTAAATGAATAAAAAACAAATATGTAAGTAAATAAATAAAAATAAGTAAATAAATAAATAAATAAGTAAATATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14235
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 |
---|---|---|---|---|---|
ENSDART00000111987 | Essential Splice Site | 554 | 697 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 846616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 829277 |
GRCz11 | 11 | 855775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCACCGTCTCGGCTGTTACTTCTGCAATGAWGTGGTGGCTCCTGGAGAC[G/A]TGAGTTTAATCAAGCACTTTTACATCTGTGGTCAAATCAGATTTTCCTCA
Long Flanking Sequence:
TGCTCTGTGATATAAGATCCACTCAAGCGAAATCTGATGAATGTTGAATATGTTTAATGTTTCTTATAGGCTTGAGATGTCATTGATCCTTATTCATGTTAAAATATGTGTATTTTACAAAGTCCTTCGCCATCTCAAACATCGACAGATCTGAATTCAGATAATGCTAATTACACTGATCTTTTGTCCTCAGTAGGCTTATGTTCTAAATGTTTAATTACATAAAAAGTAAACATCTGAAGTTAATTTAAAGTTCTTTTTCTGTGAAACTGTGAAGTTTAAGTAACAGAGATCTGAATTTTCCTGCCTGACAGAATTCACTGGACTGAAGTGTGTGAGCTGATGTTGTAAATCTGCAGAGTTGTAACTCATGCTTAGTTGTTGTTGTTCTGCTGTAAACTTGACGTATGTGTTTATTCCCAGGATCCTCTCTGTTCTCCAACATCCCCGGTCACCGTCTCGGCTGTTACTTCTGCAATGATGTGGTGGCTCCTGGAGAC[G/A]TGAGTTTAATCAAGCACTTTTACATCTGTGGTCAAATCAGATTTTCCTCAGGACACTTATTATATTAGGAAATCAATATTGCTGAAACTGATCAGTCATGTGTTTAAGTGACTGGACGCCTGGAAATCATATCCAGAGGCAAATTATTAGCACTGGGAAAATAAATAGATGCGTTAAATTATTCTGAGACCTTCTGAATGCATTGCGGAACAGAATCTGCTGTTAAACACTATCCTAGAGCGCCATCTGCTGTTAAACTCTATCCTAGAGCGCCATCTGCTGTTAAACACTATCCTAGAGCGCCATCTGCTGTTAAACTCTAGCCTAGAGCGCCATCTGCTGTTAAACACTATCCTAGAGCGCCATCTGCTGTTAAACTCTATCCTAGAGCGCCATCTGCTGTTAAACTCTAGCCTAGAGCGCCATCTGCTGTTAAACACTAACCTAGAGCGCCATCTGCTGTTAAACTCTAGCCTAGAGCGCCATCTGCTGTTAAACAC
Associated Phenotype:
Not determined