ZMP
si:ch73-374a13.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
AIM1
Human Description:
absent in melanoma 1 [Source:HGNC Symbol;Acc:356]
Mouse Orthologue:
Aim1
Mouse Description:
absent in melanoma 1 Gene [Source:MGI Symbol;Acc:MGI:109544]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15726 | Essential Splice Site | Available for shipment | Available now |
sa23087 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15726
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041721 | Essential Splice Site | 247 | 1001 | None | 23 |
ENSDART00000139451 | None | 204 | 947 | 1 | 19 |
The following transcripts of ENSDARG00000031782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 25370114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25510033 |
GRCz11 | 17 | 25528424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTTGAATCTGACTTCCAACACGTCTAAWTCAAASATTGTGCTGCAAGG[C/G]ATATCAGGATTAACATCTCCATCAGACATCACTCAGCAGATTCCATTGTC
Long Flanking Sequence:
GTCACAGTCACTGAGGAGAATAATGATGGAGAAAAACAAACCGCAGAAGGCTCTGGAAAAATGTCCTCGAGGTTAGAAAGAATGTCAATCATCTCAAACCTTGTGAACTCTCCTAACACCTCACGAAAAGTAAGAACTGAACCAAGCAATCTTATCAATGGGATTCAGTCACCCATAACACCACCAGCAGAGGTGATGCCAACCTCAGGAAAGACTAAAGACATGCCGCTGTCCCAGGTCGCCAAAGCACCAAAAGAGAGGCTTGGCGACTTTCCTGATCCTGGCATTGTAAAAGGAGGACCTGGTGATTTAGTAATAAGCCCAACCACATGTCCTCCTCTTCCAACTTTCACAGACGTCAAGTTGCCTGACTTTTTGGAGAAATACATGAGTAAAGGCAAAGAACCAAGCACAGTGAGCCAGCAAAAGCCTGACACTGTCACTGCACTGGATTTGAATCTGACTTCCAACACGTCTAAATCAAACATTGTGCTGCAAGG[C/G]ATATCAGGATTAACATCTCCATCAGACATCACTCAGCAGATTCCATTGTCCACACCCACCAGCCTCTCTCCAACATATGCACAGGTAAGAGAATGCTGATAATCTCTGCAGTTTTAAAAGATTACTCTTTTAAGTTGAAAAAAAAAGGCTAACAATATTTGCCTTTAAAATATATATTTTAAAATGTTTTCGTATTTTATTTTGACATAATTTGTGTCCATTTATGCTGCCAGATATTTTAGAAAGAAGTATCTTATGCTCAGCAAGGCTGCATTTATTTACGAATATAGTAAAACAGTAACAACGACTGAATTTTATTAGTTGTTAATTTAATAAAAACAATGACAACTTTTGATGTTGCATTATTAGGCTTTAACTAAGATTAATAAATGCTTTTGTAGTTTTCATTTTTAAATTAACTTGTTAATAAATGGAACCTTACTGTACAGAGTTAACGAAGAAAAGGCCTATAAATAGTCAAAGAATTTTCAGAATTTAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23087
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 |
---|---|---|---|---|---|
ENSDART00000041721 | Nonsense | 413 | 1001 | 9 | 23 |
ENSDART00000139451 | Nonsense | 361 | 947 | 5 | 19 |
The following transcripts of ENSDARG00000031782 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 25372630)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 25512549 |
GRCz11 | 17 | 25530940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTACAGCACACCACAAATTGACCTGTTCACAGAGCTCAATGGGATGGGC[C/T]GAATATCTTCATACTGCGATGACACAATAGAAACCTGTTCTTTTGGCCTT
Long Flanking Sequence:
CTCTCTCCACTCATCTCCATAAAGGTCGTCAGAGGATGGTAAGAACAATCACATTCATCTGACTAGTCATGTAATACTTAAAATGCTGAGTTTGCTATTTTTTTGTCCTGTTAGCTGGCTTTTATATGAAAAGCCAGGCTTCCAGGGTCGATCCATCGCTCTGGAGGAGGGGCCAGCGGACATAGCAAATGAGTGGGCGGACACAGAGCCCAGTGAGGAGGTGGAGCAAAATGACTCAGCACTCCCATCCACACCCATGGTTATTGGATCTATTAGGCTTGCATTAAGGGTGAGTCTAAAATCACGAGTCCACACTTGACCTCAATTTTCTGATTAATTAGTCTTATTAGCCACAGAATCTCTTAAATACAAAATATATTTCATGTTCTGACAAATGCATATGAACCATAAGCTTGTTTTGATTACTTGATACTATATCTTTTTCTCAGGACTACAGCACACCACAAATTGACCTGTTCACAGAGCTCAATGGGATGGGC[C/T]GAATATCTTCATACTGCGATGACACAATAGAAACCTGTTCTTTTGGCCTTCCTCAGAGTACTGGATCGATTAAGGTCCACAGTGGAGTGTAAGTGAGCTTCTGGGCTTAAATAAATGCTCACATTAAAATAATAAATGCATAACATTAAAATAATGTGTTTAGAAATTCTTCAGCTTTGTTTTTTTACATTTTTATCTTGGTGATATTTTGATACACACTATTGTTTACTAGAGATGTATTGATTTATTGTGAACCTGTTGAAAATTGATTCAAATATGTGACAATTCAAACCGGCAGAAATGTTAAATGAATGGTGATACATATTTTAAACAGAGGGGGTGCTGTGTGTTTGTTATTTAAATTTGTGACTAAATCGTATTGTAAGATTAGTGATCATGAATTGTATTAAATCGTGAGTCAGGCGAATCGTTACATCCCTACAATTTACAAATTTTGGGATGGTACATTTTTAAAAATTCTTTTTTAAAGTCTCTTAAGG
Associated Phenotype:
Not determined