ZMP
inadl
Ensembl ID:
ZFIN ID:
Description:
InaD-like [Source:RefSeq peptide;Acc:NP_001120657]
Human Orthologue:
INADL
Human Description:
InaD-like (Drosophila) [Source:HGNC Symbol;Acc:28881]
Mouse Orthologue:
Inadl
Mouse Description:
InaD-like (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1277960]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24137 | Nonsense | Available for shipment | Available now |
| sa24136 | Nonsense | Available for shipment | Available now |
| sa32397 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa24135 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24137
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 |
|---|---|---|---|---|---|
| ENSDART00000036467 | Nonsense | 111 | 1180 | 3 | 41 |
| ENSDART00000132829 | Nonsense | 115 | 1831 | 4 | 45 |
| ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16971854)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16723612 |
| GRCz11 | 22 | 16749882 |
KASP Assay ID:
2261-6669.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGATCAGTTCTGTCCAATGGCACGGCTTTAACTAACGCCTCTTCTGAG[C/T]AGCTTCAGAGGTGGATACAGGCAGCTGCAAAGGTGAGGAGTTATTTCATG
Long Flanking Sequence:
AAAAGCACAATTAGGCCATTATTAATAAAATTAGTTGTAGTATTAATTGAAGTAGTGTTGTAATTTTGTCTTTTTGTTTTATATATTTAAAACCAATTTGTGATTTGTGTTGGTTTGGGTTTTTTTTATTTTTTTTTTAGTTGAAGCTGTTTGTTTTGTAGCTTGTCTTTTTTATTATTTATTTAACCATTTTTATTATTTTCCATTATTATTATTTGTTCTTTTTAATGTTAGAATTTATTTAAATCCATATTTATTGCAAGTAATATAAAGAGCTCCAGGTTTAAGTTTTGCTTGTAGTCATCGATGGATTTTTCTACATGTCTTTTAAAAATGTCTTTGTCTTCTTCTATCTGCAGTTGAACAGTTTGCCTCCGGACACATGCAGCGAGTTCAGTTTCTCCAGGAAGGGTCAGCTGATCGTCAGTGCCAGTCGGCCGTCCAGTAGTCTGGGATCAGTTCTGTCCAATGGCACGGCTTTAACTAACGCCTCTTCTGAG[C/T]AGCTTCAGAGGTGGATACAGGCAGCTGCAAAGGTGAGGAGTTATTTCATGTCAGCTTTTATTTCACAAATGCAGTTTCTACCATGCTTTGGCCTAGTTTGCATTAGTTAAGTCATTCTACAGGAATTACTTCCTTCGATAAAATACCTAAAAAATGTCTTTGCAAAAACCTTAAAGTCTTTGCAGCCATTAACCACTTTTAGCTACCTTTAGTCACACTTAACTGCACCACTCTTATTGCTGGTCTTGACTTGTGGTGCTCTTCAAGTTATGCTTGCGTCTCCATATTATACCGGCAATGTCCTTTCCTTCTGATATTGTTGAACCATGTATAATTTCCCTTCGTTGCCTTGGACAACAGAACACTTGACTGAGTTCATTGGTTAAATTGTCCTGGTTCTTCTTTCATACTTGTATTGAGCCTTGTTCTTACTGTAGCTCCCTTCAGCAACAAACGAGCAAGAGTCTTTTTTTTTTTTTTTACTGACTGGTTTATTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24136
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 |
|---|---|---|---|---|---|
| ENSDART00000036467 | Nonsense | 648 | 1180 | 21 | 41 |
| ENSDART00000132829 | Nonsense | 631 | 1831 | 16 | 45 |
| ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16940425)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16692183 |
| GRCz11 | 22 | 16718453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCTTTCCTTAGAGAAGTTCCTACTCCATTTACTTTGGTTTGCTGCAGA[C/T]GACTTGCTAAAGAGGACAACGAATATCACCCTGAATCTGAAGACTGGCAC
Long Flanking Sequence:
CTTTCAATATAACCAATATTCTTATGTACTCCTTTTGGCCTCATTTGATGCTTAAAAGCCTAATGATGCATGATGATGATGATGATGATGATGATGATGTGTGTGTGTGTGTATGGGAAAGGGTTATGTGATGACCATGGCTTCCCCTTGATTTGGGCAGATGGCACAGTGCCGCCCCCACTCACCATAGCAGCTCCAGGCTTGACCGCTCCTGGAAATGCCAATCAAAAATGGTCATTAGATGCCACAGAGACTATGGAATATAGTTACTTGCCTAATAAGCACTAAATGCGCATGTCCAAAATGTGCAAAAAAATAGGTGGATGGAAATGTAGCTATTGAGAAAATCCATATTCTGAGTTTTTGCATAATTTTCTATCAAACAATTCTGAATTTTAATTTTGCAGGTGAATGGTGTGCAGCTGTATGGGAAGTCTAGACGAGAGTCTGTAGCTTTCCTTAGAGAAGTTCCTACTCCATTTACTTTGGTTTGCTGCAGA[C/T]GACTTGCTAAAGAGGACAACGAATATCACCCTGAATCTGAAGACTGGCACTCATCCAGCTTACAGGAGCAGGTAACCGAGGAGTAATGAGTAAAAGCTGGCTTCGGCAAGTATTGGCTGATACTTTAAAGAGTACTACAAAACAATACATTCTCATTTAGTAATTATTCCACAGATTGAGCATAACCTCTCCATGTTGGCCAGAGATACAAGTCTACGCGACAGCATTAGGGAAGAGTTTCAGGTTTGTTCATGTTTTCTAATATAAAATTACTATTATATTGACAGTTATAGTGTTTATGATGGTGTTGCTTCAGGTTTTAAGTCAAACATATTTTTATTTTTTACTTCAATATGTTCAATTAAATGAAATGTAACATGACATAGATTTGTCCTATATGTGTGTTCACTGTTGGTTAACAAGAAAGTCGTCACTTCCTGATTAACTGGTGGCAAATTTTGAGATATTAAGCTTCAAAGTTTTTGCATTTCATAGCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32397
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, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000036467 | Essential Splice Site | 650 | 1180 | 22 | 41 |
| ENSDART00000132829 | Missense | 684 | 1831 | 18 | 45 |
| ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16939032)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16690790 |
| GRCz11 | 22 | 16717060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCA[G/A]TAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCT
Long Flanking Sequence:
TCAATATTTTTTTATGTGCTTACCAAAAATGTGCATAAAAATAGGTTGATAGAAACGTAGCTAGTGAAATCAAAGTAATGTCTGTATTTCCACTTAAAGAAGCGACCACTTTCGACAGCAGCTATTTCAGCTCATGCTTATTAACTGACGTTTCAGTGGAAGACGTGATTTAAAAGAAGTATTTTTTTCCTTCTAAAAACTATCATTGTAATGTACAGTAAGTAACGCAATTACTTGACGCAATTAACTTGACTTAAGTGACTGTAATCGAATTACACAAATTTAAAATGTAATTCGTTACATTACTGCATTCCTCAGAAATGTAATTAGAATACAGTAATGGGTTACTGTGAAACGCCTTACTCCCAACTGTGTCTGATTGATTGATTAAGTGACCCCATCATAATAGACCCATTTTTGGGCCACAACCCACCAATTTAGAGCCACTCCTTGCTCACCATGATTTGTACATTTCTTTTCAGGCCCGTCAGGCTTCGGCA[G/A]TAGAGCGGGAGGTTGACGATGAAGGAGAGCCCCTAGAGCCAATCAGCCCTGAGAAAGAGCAGATGGACCAGGAGAATGATGATGACGACGAAGAGGAAGAGGAGGAGGATGAAGGAGAACTAGCTCTATGGTCTCCAAATGTGCAAGTGTTAGAACTAGAGAAAGCAGAGCGAGGTCTTGGCTTCAGTATACTAGACTATCAGGTAGGCAGTAATTTTTTTGCACTTTATATGCATCATTAAATTACTAAATGTATGCAGTAAAGCAATTTAGAAAAAGTCTTTAAGGAATACAGCTTTATTGCAAAAAAAAAAACTATAAATAGACAAAATAACAAACTTCAGAGCATAAACATAAGATTTGTTCTAAACGTCATCATTAAACTACGTTTACTGTAAAAAGTCAAGACAAGGAATCTGTTCACACATAATCTAGCTGAGGGGAAGGGGACCAGACTCAGTTAATCCCCATTGACTTTCCCAAAGTGCGATCACAGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24135
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 |
|---|---|---|---|---|---|
| ENSDART00000036467 | Essential Splice Site | 977 | 1180 | 33 | 41 |
| ENSDART00000132829 | Essential Splice Site | 979 | 1831 | 22 | 45 |
| ENSDART00000145208 | None | None | 98 | None | 5 |
Genomic Location (Zv9):
Chromosome 22 (position 16923730)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 16675488 |
| GRCz11 | 22 | 16701758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCG[G/A]TAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTG
Long Flanking Sequence:
TAAAATGCTAATCATACAAAGTGAAGCTAAGTCACTTTCTTTGTTTATAGGACTTTGTAAACGGCTCCATTTTATCTGACGACCTGGATGAGGAGCCAGAGCTGATCCTGGACGCAGAGCCGCGCTACGCCTCTCCCCTCACCACTGTTGACCTCCAGCCTGACGTAGAGAAAGAGATGGCTGTGGATGAGGAGGAGGAAGATGTAGACGTGAATGTCATGGAGGACCAGCAGAGCTCTAAGGTCAATGACACCAGTCTGCCTTCATATCTCAGTGAGAAGAGTCGCTCCTGGGAAGAACCAGCAACATCCAGCCGCTACCATCTCAACACAGAGCCTGATTTACAAGAACAGGTGAAACTCCAATGATTTGACGGCTTTCCTAAAGTAATGTATACAGTTTTACAACTGTTGTGTTTCTGCTGTGGTTTGCAAAGGTGGACGACGATCTTTCCATGAATTTGGAGAAGATTCAACTGCAGCCATTGAAAATTCCTCTCG[G/A]TAAGTGTCTGTTAAAGCTTTTTAACACTTTCCAGGCTGTTGATAAGATTGAGTTTGTCAATTAAGAAGACTACACTTCCCCGCCATTGGGTTTTTACAGCAACACAAATTTCTGGTGTGTTATGGTAAGGAAAAACCCTAATGCATGGCAAGAACAGAACGCTAATCCATTGGTTCATATGAGCTGTCAATCACTCTGTTCCGATGACAGGGTGCCACAGCCGCAAAAATATAAAGGTCTGGATCTGAGAGAATAACAATAACACTGACAGATTTAGTTTAAGAAACCAGCTAGAGTTACAATTATGACACATCTGATTAGTGATCATGTGCTGAATGTCAGTCCAGCATTTACACTTTTCGAAGAGTGGATAAAAGACTTCCCGCGTTTAAAGTCCGCTATGAATAAAGCATTCACTGTAAAGCCAGTAGGGCGGAGTTTTCAGGTAAGTGTTTGCCTCATCTACACATTTTAAGCACAGGATGTTCTAACGTTATTTA
Associated Phenotype:
Not determined