ZMP
atg12
Ensembl ID:
ZFIN ID:
Description:
Atg12 protein [Source:UniProtKB/TrEMBL;Acc:A8KBB4]
Human Orthologue:
ATG12
Human Description:
ATG12 autophagy related 12 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:588]
Mouse Orthologue:
Atg12
Mouse Description:
autophagy-related 12 (yeast) Gene [Source:MGI Symbol;Acc:MGI:1914776]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31002 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42684 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31002
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 |
---|---|---|---|---|---|
ENSDART00000101304 | Nonsense | 79 | 120 | 2 | 4 |
ENSDART00000136005 | Nonsense | 32 | 73 | 2 | 4 |
ENSDART00000101304 | Nonsense | 79 | 120 | 2 | 4 |
ENSDART00000136005 | Nonsense | 32 | 73 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 15637037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13995496 |
GRCz11 | 16 | 13885616 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCACTCGCCCAGTTCATCTCACGCTTCCTCAAGCTGGAGCCCAGCGAA[C/T]AGTTGGTAAGTTGTTTCATTAAAGAGTAGTGGAAAGACCACAGAAAGTAT
Long Flanking Sequence:
AACTTGAGAGAACACAAAGCAATATGGAATAAAATAAACAAAACACAGTAAATTATTTCCACTTTTCCACTTTACAAACTTATATTGTATGTAATTTGTAATAGTTTTTATCTGCATAAAACACACAGACCATTTCAATGTGGTGATGTCATTGGCCCATGAACATTACCTGCTTGTTATCAAACTATTTCATTACTGTAACAAGAGACAATTCAATCATAACCTTGTGTTAAAACAGCTGTCATAAGATTATTTATCAAAAGCGAAGTACGTTGCGACCTTTGTTTTTTTTTTACATCCCTCAAAATGGTCTATAGTCCACATCATCTGCTTTACTTGATTTTATTGTCCCCCCTCTCCATTTTTTAGTTGATGTGCTTTTAAAGGCGGTCGGTGACACACCCATCATGAAGACCAAAAAATGGTCTGTGGAGAGAAGGAGGACGATACAGTCACTCGCCCAGTTCATCTCACGCTTCCTCAAGCTGGAGCCCAGCGAA[C/T]AGTTGGTAAGTTGTTTCATTAAAGAGTAGTGGAAAGACCACAGAAAGTATACTTTGTTTTTAAATTTGTTCTCATGTTTACATCACATTTAATAAAACTGATGGTTGCTTCTATACGCTTTCAACAAAAATATGCAATCTGTATTCTTGTAAGCTTCCCTCAAACTATTAAGTGAGAGAATAATTTCTGCAGAATACACTTAAAGCTAAATAGAGATGTGATTATTATGTTATGTGTTCTGTTGGTTTCTCTTGTTTTTTATGTTTATGTTTAACAGTCAATTATAAACCACACCAAATGCCAAAATGTCTGCCTGGTTTGTGCAAAAACAGGAATATTCTCATTAATCGTAATATCTAATATTAATTAATCCAATTATAGCACTAATATATGTACCAAAGATGATCAGTGGTTTTGTGTTTATTGGTGATTAACACATCACAAAATGCACTTAATTGTTTTTTATATATTCAGTACAAAAATTTAGACTGACAGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42684
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 |
---|---|---|---|---|---|
ENSDART00000101304 | Nonsense | 79 | 120 | 2 | 4 |
ENSDART00000136005 | Nonsense | 32 | 73 | 2 | 4 |
ENSDART00000101304 | Nonsense | 79 | 120 | 2 | 4 |
ENSDART00000136005 | Nonsense | 32 | 73 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 15637037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13995496 |
GRCz11 | 16 | 13885616 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCACTCGCCCAGTTCATCTCACGCTTCCTCAAGCTGGAGCCCAGCGAA[C/T]AGTTGGTAAGTTGTTTCATTAAAGAGTAGTGGAAAGACCACAGAAAGTAT
Long Flanking Sequence:
AACTTGAGAGAACACAAAGCAATATGGAATAAAATAAACAAAACACAGTAAATTATTTCCACTTTTCCACTTTACAAACTTATATTGTATGTAATTTGTAATAGTTTTTATCTGCATAAAACACACAGACCATTTCAATGTGGTGATGTCATTGGCCCATGAACATTACCTGCTTGTTATCAAACTATTTCATTACTGTAACAAGAGACAATTCAATCATAACCTTGTGTTAAAACAGCTGTCATAAGATTATTTATCAAAAGCGAAGTACGTTGCGACCTTTGTTTTTTTTTTACATCCCTCAAAATGGTCTATAGTCCACATCATCTGCTTTACTTGATTTTATTGTCCCCCCTCTCCATTTTTTAGTTGATGTGCTTTTAAAGGCGGTCGGTGACACACCCATCATGAAGACCAAAAAATGGTCTGTGGAGAGAAGGAGGACGATACAGTCACTCGCCCAGTTCATCTCACGCTTCCTCAAGCTGGAGCCCAGCGAA[C/T]AGTTGGTAAGTTGTTTCATTAAAGAGTAGTGGAAAGACCACAGAAAGTATACTTTGTTTTTAAATTTGTTCTCATGTTTACATCACATTTAATAAAACTGATGGTTGCTTCTATACGCTTTCAACAAAAATATGCAATCTGTATTCTTGTAAGCTTCCCTCAAACTATTAAGTGAGAGAATAATTTCTGCAGAATACACTTAAAGCTAAATAGAGATGTGATTATTATGTTATGTGTTCTGTTGGTTTCTCTTGTTTTTTATGTTTATGTTTAACAGTCAATTATAAACCACACCAAATGCCAAAATGTCTGCCTGGTTTGTGCAAAAACAGGAATATTCTCATTAATCGTAATATCTAATATTAATTAATCCAATTATAGCACTAATATATGTACCAAAGATGATCAGTGGTTTTGTGTTTATTGGTGATTAACACATCACAAAATGCACTTAATTGTTTTTTATATATTCAGTACAAAAATTTAGACTGACAGTTTTT
Associated Phenotype:
Not determined