ZMP
aif1l
Ensembl ID:
ZFIN ID:
Description:
allograft inflammatory factor 1-like [Source:RefSeq peptide;Acc:NP_942571]
Human Orthologue:
AIF1L
Human Description:
allograft inflammatory factor 1-like [Source:HGNC Symbol;Acc:28904]
Mouse Orthologue:
Aif1l
Mouse Description:
allograft inflammatory factor 1-like Gene [Source:MGI Symbol;Acc:MGI:1919598]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11473 | Essential Splice Site | Available for shipment | Available now |
sa6989 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11473
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009500 | Essential Splice Site | 9 | 148 | None | 6 |
ENSDART00000139317 | None | None | 122 | None | 5 |
The following transcripts of ENSDARG00000009336 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 36167652)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 33949601 |
GRCz11 | 5 | 34549754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGTGAAGCCTCCAGACCGCTGAATAATTGCTCCCATGTCTCATTTTTCT[A/G]GGCGGAAAAGCCTTCGGGTTGCTCAAAGCTCAGCAGAGGGACAAGCTGGA
Long Flanking Sequence:
TATATAACTTAAAAGGGCTAATAATATTGAATAAAAAAACAAAAACGGGGCTTTCCTGTTCAGCTCGTACGGTCTGCATTCCCTCTCTTCACCGCGCGATGGCGCTTACAGCTGCATTCCTGGCGGCCAGTGAGCGCATCACAGGGAGACCTGCGCCTCTAAATAACAGCGTGAGATTCATTCCCTCTCTCTGTCTCTCTCCCGCATAACCGACGCAAGCGGCCAGCAGACGCCAGCGTCTCTCCTCTCTCCACCACCGCCTCTCGACCTTCCCAGCATGCCTTCCAACATGGACTTACAAGGTATGTTGTTGTTTCCAGTCTGTGTTTTGGGAATGATGCTTTAGCCACCGTTAAACGCGCGAAGGCTGTTTTTGTTCTGTTGGCGCGCTTGTTTGCCGTTAGCGGCCGACCGTCCTTATCTCATGCCTGCAAGTGCACCAGACAGCCTGGGTGAAGCCTCCAGACCGCTGAATAATTGCTCCCATGTCTCATTTTTCT[A/G]GGCGGAAAAGCCTTCGGGTTGCTCAAAGCTCAGCAGAGGGACAAGCTGGAGGAAATCAATAAGGTAAATGAGCGACCGCTGATGGATTATTATTGTCTCGATCTGGAGGCGAGTTTGTCACGTTGGTCTGTTCACTCTCGTGGTGCTGCTAGACGCATTGTCTGGAAATATGAGTGAGGTAAAAGGTGGTCTCTTTGGCTGATATATGTTATTTTGGACTGCAGCGCAATTGTTAAGCTCGATTTTACAGCAGCATGACCTAATTTAGTTAGACAGCTCGACCACATTAAGCCGCAGTTCATTTCACAATCCAGAGCAGGGCTGCGTCTCGGTCTCTATTGAGCTGTAGGATTTTCACCTTATATTGCTGATTCACGAGACTGGAGCGTTTAAAAATCGCTGTGTCGATTGGCAGCTTGGCTGAGTTTTTTGACCCGACCATGAGTCATTCACAGCTGCTTTGTAAAGTCCCCATGAAGTCACACTTTTGTTTTTAGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6989
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009500 | Essential Splice Site | 29 | 148 | 2 | 6 |
ENSDART00000139317 | None | None | 122 | None | 5 |
The following transcripts of ENSDARG00000009336 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 36167716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 33949665 |
GRCz11 | 5 | 34549818 |
KASP Assay ID:
554-4480.1 (used for ordering genotyping assays)
KASP Sequence:
TCGGGTTGCTCAAAGCTCAGCAGAGGGACAAGCTGGAGGAAATCAATAAG[G/T]NNNNNTAAATGAGCGACCGCTGATGGATTATTATTGTCTCGATCTGGAGGCGAGT
Long Flanking Sequence:
TCGTACGGTCTGCATTCCCTCTCTTCACCGCGCGATGGCGCTTACAGCTGCATTCCTGGCGGCCAGTGAGCGCATCACAGGGAGACCTGCGCCTCTAAATAACAGCGTGAGATTCATTCCCTCTCTCTGTCTCTCTCCCGCATAACCGACGCAAGCGGCCAGCAGACGCCAGCGTCTCTCCTCTCTCCACCACCGCCTCTCGACCTTCCCAGCATGCCTTCCAACATGGACTTACAAGGTATGTTGTTGTTTCCAGTCTGTGTTTTGGGAATGATGCTTTAGCCACCGTTAAACGCGCGAAGGCTGTTTTTGTTCTGTTGGCGCGCTTGTTTGCCGTTAGCGGCCGACCGTCCTTATCTCATGCCTGCAAGTGCACCAGACAGCCTGGGTGAAGCCTCCAGACCGCTGAATAATTGCTCCCATGTCTCATTTTTCTAGGCGGAAAAGCCTTCGGGTTGCTCAAAGCTCAGCAGAGGGACAAGCTGGAGGAAATCAATAAG[G/T]TAAATGAGCGACCGCTGATGGATTATTATTGTCTCGATCTGGAGGCGAGTTTGTCACGTTGGTCTGTTCACTCTCGTGGTGCTGCTAGACGCATTGTCTGGAAATATGAGTGAGGTAAAAGGTGGTCTCTTTGGCTGATATATGTTATTTTGGACTGCAGCGCAATTGTTAAGCTCGATTTTACAGCAGCATGACCTAATTTAGTTAGACAGCTCGACCACATTAAGCCGCAGTTCATTTCACAATCCAGAGCAGGGCTGCGTCTCGGTCTCTATTGAGCTGTAGGATTTTCACCTTATATTGCTGATTCACGAGACTGGAGCGTTTAAAAATCGCTGTGTCGATTGGCAGCTTGGCTGAGTTTTTTGACCCGACCATGAGTCATTCACAGCTGCTTTGTAAAGTCCCCATGAAGTCACACTTTTGTTTTTAGGTATCAAGTTAACGTTAGACTTAAAAGTAGCGTTCAGGTTAAAAACAAAAAGCTAAATTCCTATTTA
Associated Phenotype:
Not determined