ZMP
zgc:110143
Ensembl ID:
ZFIN ID:
Description:
fas apoptotic inhibitory molecule 2 [Source:RefSeq peptide;Acc:NP_001013536]
Human Orthologue:
FAIM2
Human Description:
Fas apoptotic inhibitory molecule 2 [Source:HGNC Symbol;Acc:17067]
Mouse Orthologue:
Faim2
Mouse Description:
Fas apoptotic inhibitory molecule 2 Gene [Source:MGI Symbol;Acc:MGI:1919643]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15600 | Essential Splice Site | Available for shipment | Available now |
sa19800 | Nonsense | Available for shipment | Available now |
sa14757 | Nonsense | Available for shipment | Available now |
sa25840 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15600
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056639 | Essential Splice Site | None | 306 | None | 12 |
ENSDART00000141884 | Essential Splice Site | None | 204 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 32222938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32521845 |
GRCz11 | 2 | 32505063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATTGTTTTTGCTTGGGAATAGCGACTAACGTTCGCCGTTACAGTAAGG[T/A]AAGTTAAAATGTATWACTCTGTCTGCAGTTCAYTAGCTAYAGCCTGCATT
Long Flanking Sequence:
CAATTATTGATTTGGCCTGTGCTTTGTTTTGCTTTATTAAGTATCTTATACTTTAAATCTACTGAATAATTTAAGACTAACCATGTTTCCAGTAACCTAAAGTTTTATCACATTGGGCTTAATGTATATTATGAAATTGCGTTTTTGCTTAATATTAACATCAAAAGTATTAGTTGGCGTTTAAGTTGCATTTATTAAATGCACAATTAAAGGACACCAATAGCTTGTGACGGTTTCAAAGTTACAGTGAGTATGACACTAAGGGATATGAAATATGGTGACCAGATATACGTGTCGTTTTATCTGGCTTGCGTGGTTACACCGTGATATACATTGCTGAAGATATCATTTTACATTAAAAATTCTTCCATCATCGCTTCTCGCCGTCTAGTCAGTGTCGTTTTCGTTTCGTCATTTCCGGAAACACCGGATGTACGTCATTGGTTGAGTTCATTGTTTTTGCTTGGGAATAGCGACTAACGTTCGCCGTTACAGTAAGG[T/A]AAGTTAAAATGTATAACTCTGTCTGCAGTTCATTAGCTACAGCCTGCATTTGAACTTGTCGTATAACGTTATTCCCGAATGCATAACGTTAGTCCTCTCCTTCGCGACTGCCCAACAGGCTTGGAGACTATCATGGATGTGCGAGCTAAGCTAAGCGCTGTCAAAATACATTGCAGAGCTGTTAATAAAACTGGCTTCCGTTTAACGGCAGCCCTCTAACTTATCAGGTAACGCTAATAGTTTACGATAAGGACAGTTGTGCTGTGTGTTAGACAGCTCTGCAGACTCTAGCTAACGTTAGCCAGATTAATATGTCTAATGTTTTCTGTTTACTTCTGATATTACGTGGTAAATATAGCACAATTTTCACCGTAACATTAAGAATATAAAACCTACTGTATCATATTTGATAAACGTTTTTGTCATGCATTTGATTCACCAGTATAGTTATGAAAATGATCATGTTTTACTCATTTTCTGTTATATTTCTATTTGGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19800
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 |
---|---|---|---|---|---|
ENSDART00000056639 | Nonsense | 104 | 306 | 4 | 12 |
ENSDART00000141884 | Nonsense | 104 | 204 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 32215982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32514889 |
GRCz11 | 2 | 32498107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGAAAGGCATCCGTCTTGTTTGCAGGTCTTCTGTATTCTCATGGTA[C/T]AGCTCATGGTTACGTTTAGTGTGGTGTCGCTCTTCACATTTTGGTAATTG
Long Flanking Sequence:
CTTATGTCTGACTCGAGTCAAGTCATGTGACTCAAGTCCCCCACCTCTGGTAAATGTAATCTTTAAACTGATTAACTAAAGATCAACTGATTAACTAAAAGATCACCATTAAGACATTTTGTAAATTTCTTACTGTAAATAAATGAAAACATTTTTTTAAAATTTGTAATATTACGCTATCCATGGGTCAGGAATTTCTGCAATATCGTGAAATGTTAAAAGGTTTTGCTGATTGTTATGGTTTGACTTTTTTTTATTGCGATTTTTATTCTTTTCCAATTTGCAAATACGCAATCAAATGCATTCAGCAAGCTGGACCTGTTAAAATACATTTGTTTGGTCAGTGGGCCAGTGCTCTTGAGTCCCTTATAGATTTTGTGGGGAAAAATGGCATAATTATTACTGTCACATGATTGATTTAAACAAGAGTGTCACACACTGAAGATTGTGTTTCTGAAAGGCATCCGTCTTGTTTGCAGGTCTTCTGTATTCTCATGGTA[C/T]AGCTCATGGTTACGTTTAGTGTGGTGTCGCTCTTCACATTTTGGTAATTGACACACACATCAGATTACATGACATAACCCCATTTTTATTTGCTTATTCTACTTTTTAAAAAGGCAACTGTCGCTGATGACCCCTTGTTTTTCTACAGTGAGCCGGTCCGCAAGTTTGTACAGTATAATCGGGTTTTCTATCTGACCTCATAGTAAGTGCTGCTCTCTTTCATCTTTACATGTTTAATGCTTGAATGATTATATTTACAATGTTGTCATTATATGTTATTTGCTAATTTGATCACATTTACAATTGCTATATTGTCCTCCGAGTGACACTGATTTGTTTTGTCCAGCATGACTTTCATGGGAACATACCTGATGCTTGTATGCAGCACAAACGCAAGGTAAACAAATAGTGTTTGTTATACCTTATTGCTACCTTCTGGATTAGTTCTCAACTGTTCTTTGATATCTAGTACTTATCAATGAGTGTTTATGTTTCATCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14757
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056639 | Nonsense | 132 | 306 | 5 | 12 |
ENSDART00000141884 | Nonsense | 132 | 204 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 32215791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32514698 |
GRCz11 | 2 | 32497916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTACAGTGAGCCGGTCCGCAAGTTTGTACAGTATAATCGGGTTTTCTA[T/A]CTGACCTCATAGTAAGTGCTGCTCTCTTTCATCTTTACATGTTTAATGCT
Long Flanking Sequence:
GAATTTCTGCAATATCGTGAAATGTTAAAAGGTTTTGCTGATTGTTATGGTTTGACTTTTTTTTATTGCGATTTTTATTCTTTTCCAATTTGCAAATACGCAATCAAATGCATTCAGCAAGCTGGACCTGTTAAAATACATTTGTTTGGTCAGTGGGCCAGTGCTCTTGAGTCCCTTATAGATTTTGTGGGGAAAAATGGCATAATTATTACTGTCACATGATTGATTTAAACAAGAGTGTCACACACTGAAGATTGTGTTTCTGAAAGGCATCCGTCTTGTTTGCAGGTCTTCTGTATTCTCATGGTACAGCTCATGGTTACGTTTAGTGTGGTGTCGCTCTTCACATTTTGGTAATTGACACACACATCAGATTACATGACATAACCCCATTTTTATTTGCTTATTCTACTTTTTAAAAAGGCAACTGTCGCTGATGACCCCTTGTTTTTCTACAGTGAGCCGGTCCGCAAGTTTGTACAGTATAATCGGGTTTTCTA[T/A]CTGACCTCATAGTAAGTGCTGCTCTCTTTCATCTTTACATGTTTAATGCTTGAATGATTATATTTACAATGTTGTCATTATATGTTATTTGCTAATTTGATCACATTTACAATTGCTATATTGTCCTCCGAGTGACACTGATTTGTTTTGTCCAGCATGACTTTCATGGGAACATACCTGATGCTTGTATGCAGCACAAACGCAAGGTAAACAAATAGTGTTTGTTATACCTTATTGCTACCTTCTGGATTAGTTCTCAACTGTTCTTTGATATCTAGTACTTATCAATGAGTGTTTATGTTTCATCTGCAGGCGAAGATATCCTACCAATATGATCCTTCTAGCCATTTTTGTAAGCAATCTCATTGTCTCATTAATATGTTGGTTTATATTAATAAGTATTAACTATCATTTCTATAAATGTTGTATAATTATAAACAAATTAAAAAAAATTTTTTTGCTCTTTTTTCAGACTTTGGCAATGTCCTATATGGCAGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25840
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056639 | Essential Splice Site | 208 | 306 | 9 | 12 |
ENSDART00000141884 | None | None | 204 | None | 9 |
Genomic Location (Zv9):
Chromosome 2 (position 32214700)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32513607 |
GRCz11 | 2 | 32496825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGCTCTGGTGTGTCTGGCCATCACTCTCTTCTGTTTCCAGTCCAGGG[T/C]GAGCAATTATTTTTTGTAAATCAGTCTTTTCGAGTGCTTTCTTTATGTGT
Long Flanking Sequence:
TTATATTATATTATATTATATTATATTATATTATATTATATATCATATCATATCATATCATTTTATATCATATTATATTATATTACATTATATTAAAATATATTAGTAATAAAGGTAAGACATTCTTTATAGTTATTTAGAAAATATATTATTAATATTCTATGCTCTCTGGATACCATATAATTTTATGAAATTATATATTTATATATTAATATATTGTTTTAAATATGAATCAATTGAATTATCAATTAGAAGACTTAGAAATTAAGACTATAGTTCTTTTTAACTAAATGTAAATTTTAATAAATTGAAATAATTGCAGGACAACTTTCAGTTTTTAATCTCTCTCTCTCTCTCTCTCTCTCTCACTCTCTCCTCTCTCTCTCTCTTTCTCTCTCTCTCTATCTTCAGCTATCATAATACCAAAGTGGTGATGCTGAGTGTGGGCATCACAGCTCTGGTGTGTCTGGCCATCACTCTCTTCTGTTTCCAGTCCAGGG[T/C]GAGCAATTATTTTTTGTAAATCAGTCTTTTCGAGTGCTTTCTTTATGTGTCATTTGACCAAATATTGTGTTCAGGTTGACTTCACCACCTGTCATGGGCTGCTGTTCTCTCTTATGATGGTGCTGATGATCACTGGGCTTCTGCTGTTCTTCACTGCTCCATTCGGATATGTAAGCCGCTGACATTTGAATGCTGTAAATTGTGTTGAAGCTGCTATTTGTGCTCTGTGTTAGAATCTTTTAAAATTGAAACACCACAATTACTGTTGATTTTTTAAAAATGTATTTTCTTTTTATGTTTTTAAAAAACATTACTTATCCAGCAAGTTTTTACGCAGCGGATGCCTCTCTCTGGGAAACACACACATTCACACACACTCATACACTACGGTCAATTTAGCCTACCCAATTCACCTGTAACGCCTGTCTTTGGACTGTGGGGGAAACCGGAGCAACCGGAGGAAACCCACGCGAACACAGGGAGAACATGCAAACTCCACA
Associated Phenotype:
Not determined