ZMP
zgc:172265
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100141346 [Source:RefSeq peptide;Acc:NP_001108383]
Human Orthologue:
ITGA8
Human Description:
integrin, alpha 8 [Source:HGNC Symbol;Acc:6144]
Mouse Orthologue:
Itga8
Mouse Description:
integrin alpha 8 Gene [Source:MGI Symbol;Acc:MGI:109442]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17254 | Splice Site, Nonsense | Available for shipment | Available now |
| sa22861 | Nonsense | Available for shipment | Available now |
| sa14004 | Nonsense | Available for shipment | Available now |
| sa15736 | Nonsense | Available for shipment | Available now |
| sa22862 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17254
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059038 | Splice Site, Nonsense | 297 | 1059 | 9 | 30 |
| ENSDART00000059044 | Splice Site, Nonsense | 286 | 397 | 9 | 13 |
| ENSDART00000141061 | Splice Site, Nonsense | 297 | 517 | 9 | 15 |
| ENSDART00000059038 | Splice Site, Nonsense | 297 | 1059 | 9 | 30 |
| ENSDART00000059044 | Splice Site, Nonsense | 286 | 397 | 9 | 13 |
| ENSDART00000141061 | Splice Site, Nonsense | 297 | 517 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 30639409)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28476547 |
| GRCz11 | 16 | 28411170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGCAGAATTRGTAGCAGGGGTTCCTCGAGGGGCACACAACTTTGGYTA[T/A]GTAAGTATACAGACYTTGTTTCCTGTGTTTTTGTTGTGYTAAGATCAGGA
Long Flanking Sequence:
GAAATTTGAGGTTGTGGGGGGAAGGGTTGAGGACGAACAGGCTCCTTGGAAGTCTGGGAGATTTCAAGTTCGAAACGAGTCAACCATCCCTCTCTCCAATCTCAGTGTGTGGGACAGATCTGACAGACAGCCGCAAACCCCCCCACCACATCACTATCTCCACCATCATCCATCAGTGTCTGTCTCCTTCACTATGACTCTTTCCCTCTCTCTCTTCTAAATATTTATAACTAATGAGTGACTGGCGTGCTGTTGACAGAGACGAGATTTACAGCACTCACAGGTCTCACCTCACTGTTTACCCTGAGATGCACTTGATAAGTGGTTGGAAAAGTGTGTTTTATTATTGTTCCTTGTTGAAGCACATCATTTGTTTTTTTAGACTCTGCTACTTTAAAACATATAAACCTGCTGATATGTTTGTGTACTGTATGACTTTCTCATGTTGTCTATGCAGAATTGGTAGCAGGGGTTCCTCGAGGGGCACACAACTTTGGTTA[T/A]GTAAGTATACAGACTTTGTTTCCTGTGTTTTTGTTGTGCTAAGATCAGGATTTAAAGGTCAGAGGTAAAGGTCAAAAGGAAGGAAGAACGTAAGAAATGTTTGAGAGGTTAAACACTGCTTTTGTACTAAAATTGGCACAAACATGAAAATAGTGTTACAAATTACACAACCCAAATGGTAAAAAAGGTATATACTATTGTTCCTTTTTTGACCACAAAAGGAGATGGCTAGTAGCTAGCATTTGGTTTAAAAAAATAAATGTAAAAGTGTTATAGAATGATCCAATGTGCTGTTTGTTGTGTATTCTAAGAATATCGAAAGAGCAAAACACTACATATGGAAAATACAGAACATGTAAACAGCAGGAATGGAAATAAAAGGAATGTGTAAAAACAATTAATTAGAATAATATTGGTAGTATTTAAATAGCATTTAACATCTTAATAACAATTATAATGATAATAATAAAGTTGGTGATGATAAAAGTGATATTTTGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22861
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 |
|---|---|---|---|---|---|
| ENSDART00000059038 | Nonsense | 669 | 1059 | 20 | 30 |
| ENSDART00000059044 | None | None | 397 | None | 13 |
| ENSDART00000141061 | None | None | 517 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 30691770)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28528908 |
| GRCz11 | 16 | 28463531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTTTCTGTATAGGGACCGGACTGAGCTTATAATCGGGGATGACAACT[T/A]GCTGATGTTGACTATTAATGCAGCCAATGAGGGTGAGGGGGCGTATGAGG
Long Flanking Sequence:
ACAAATTGATAATGTGACAAAAGTATCACTTAAAATGCTTTCCTGACATTAGACTTCATGAAAAAACACTGTGAAAATCTCAAAATCGACAGGTGCATGTGCTTTTATTCTTACAGTGTCTCACCTGAGGTATAAAAAAAACATACAGTATGTTAAATTCCTTGAACAAGCATAAAAAACAGAAAGAGAAAATCTATTTTTCCATTCCTCTTAGGCAAACATCCTGTTGGACTGTGGAGAAGACAACATGTGCATCCCAGATCTCAAACTCTCTGCTAAAATGTGAGTCTGAGAGTCTGTTGTGTTCATATATGTGCCACTGAGCATTGTTTACATACTTGTTGTAATTTATGTCCTGTGTTGTATCATGCATCCTTTGTTTATGTTTTAACCACATGCTGTTCTCTCATCTGTATCTAAACGTCAAGTGATTTTAAATACAGCTTTCCTTATGTTTCTGTATAGGGACCGGACTGAGCTTATAATCGGGGATGACAACT[T/A]GCTGATGTTGACTATTAATGCAGCCAATGAGGGTGAGGGGGCGTATGAGGCGGAGCTTCACGTGACCCTCCCACCAGAGGCAGATTATATAGGTGTGGAGCGTAGGCGTGAGGTAAACAACTACACTCTGTCCTTATTTACATGTATGTGTGTCTTGCCATCACTGTGTTTTGCAGATATGTTTGCAGATGTGGCTCTGGGTGGGCGAAGTTAATAAATAGTCAGTGAAATTTTTTTGCATGATGTCTTTCATTTATAGTGAATCTGATTGTGAGAGGTTTATTTTAGTCTCAGACTTGATCACTGCTGTGTTTAGAATAGATTGTGACTCACTCACTGGATCCTCTATCCAGGAAAACTGATTATGCAGAAGTTTATTTTGCTGAACTGGTTTACCCTTTAGTTTATACATTGTATATAAACACTGCACATGTGTTAAATATAGTTATTAGAAGCTAGATCTGTCGGTCTGTCTATCTATTGTTCTATCATTTGATCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14004
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 |
|---|---|---|---|---|---|
| ENSDART00000059038 | Nonsense | 904 | 1059 | 26 | 30 |
| ENSDART00000059044 | None | None | 397 | None | 13 |
| ENSDART00000141061 | None | None | 517 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 30726109)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28563247 |
| GRCz11 | 16 | 28497870 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGTTACTGGGCTTCCTGAGGAACAGCAGCGGAGTGACCCGCCGAAGA[C/T]GATCTGTTTCTATAGGCCAAAGCTACARYAGCAAAACACTGGTACAAACA
Long Flanking Sequence:
TTGGCGCAGTGGGTAGCACAATCGCCTCGCAGCAAGAAGGTTGCTGGTTCGAGCCCTGGCTAGGTCAGTTGGCATTCCTGTGTGGAGTTTGCATGTTCTTCCTGTGTTCGCGTGGGTTTCCTCCGGGTGCTCTGGTTTCCCCCACAGTCCAAAGAATTGGGTACAGGTGTGTGAAGGAGTGTTTCCCAGTGCTGGGTTGTGTATAAAACATATGCTGGAGAAGTTGGCGGTTCATTCCGCTTTGGTGACCCCAGATTAATAAAGGGACTAAGCCAAAAAGAAAATGAATGAATGAATGAATGAATGAATGAATGAATGAATTAGCATTACTAAATAATACTAAAATATTACAGATTTTATTATTTTCTACACACACTGTTTTTGTATGATATTAATTGCATCTCTGTATTTCTTCTGCATGCTTGTAGACCTCGACTCTTCAGGACACTCCAGAGTTACTGGGCTTCCTGAGGAACAGCAGCGGAGTGACCCGCCGAAGA[C/T]GATCTGTTTCTATAGGCCAAAGCTACAACAGCAAAACACTGGTACAAACACAAACAACCCATCTGAACACACAAAACCATCTCCTACATGTGACAGATTGACTCATATGTTGAACTTGACTTGTATTGGGGACCTGTGTTGACCTCAGAGGGCGAGTTCACCTGTAAATCTCCTAACAGCTCATCCATATTATGCTTATTGTCTCTTTAGGGGATTTGTGTGTGCTCATGGGACAGATGGTTTTCATAATCATAGTCCATCTCGCCACAGGTTATAAGATAAGTTGGAGCACAGGTCAAGTCAAAACTGATGGCATTCATATTACATGCACATCAGCACTCAAAAATGAAAATGTAAATACTTTAAATCGCTCACAATCAAGTGTGAGGCTTTAACACACAGCATATCTGGTACAATGAGGTCAAGATGCTTATACTGTATATGAATTTTAGATTTTTTAACTTGCCCTCCAATTTTTGGGAAGTGTAATATTGTGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15736
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059038 | Nonsense | 979 | 1059 | 28 | 30 |
| ENSDART00000059044 | None | None | 397 | None | 13 |
| ENSDART00000141061 | None | None | 517 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 30732696)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28569834 |
| GRCz11 | 16 | 28504457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTAAACTCCACAGTGTCCTTTCAAGTGACRGCCATGCCTTATCGCATC[A/T]AAGCTGAGASACTCCCACGCCAGAGCAAATCAGTGAGTAATACAATTGTG
Long Flanking Sequence:
CAAATGTTCTCCTGGTGTCACAGGACATGACATCACCGGTACAGTTAGACACCTTAAACACCTCAGTCATGTGACATTGTTAACCATGACATCATCTGAACAAAATGCCTTTCATCTCACCTCCAGAGGAACGTCCACAGAAAGCAGACACATGTATAAAAGCACGTTCGCTGACGTGTGTATGTGCGAGAGTGATCCTAGTTTAAAGGAAGTGCTTTAAGTTTTTGTTTTGCTGCTCTTTTGACCATTGCTTCTCACTAAGCCTCATTCATGCTGAAGCCATTACAACCCAGCGCACTGTCAGACACCCGCCATGTGCGTCCTGTTAATGCTAATCTGACATTTTCCTCTCCGGCGAGGGGGTCGGAGTCTATTCTGAGATGTTTCCATGTGTGTTGTATTTGCGCTAATCCATTGCTTTCCTCTGGCAGAGAAGGAATGACCACTACACGCTAAACTCCACAGTGTCCTTTCAAGTGACGGCCATGCCTTATCGCATC[A/T]AAGCTGAGACACTCCCACGCCAGAGCAAATCAGTGAGTAATACAATTGTGATTGTGTGGGCACAGATTAATGAAGAAAACAACAGACGATGTGGCTGAAAGACAAGATTTTTTTTACTTAAACCCAAAGCATACTTAGTTTTTTTATGTACGCTTACAAAAACAATGATCGACAAACTTTGTCCCCTTACTCATGCACTCATCAACTTGGGTGTCTGTTGTTTTTATCATTTTCAGTAGTTTGTTGTTGTTTCTTTTATTCCGATTGTATAAATACAGCTTGGTTCAGTGTTGCCACCTGGTGGATAAACTAAATAGTGCAAAATATGTAATAATAAAGTATATTCTGACCATACCCAGCAAACAATTTTTGTGTTTAAAAGTTATCTAAAAATAGACAGCTTGGCTAAAACAAAGCTAAACTTGGGCTGTCAGTGAAACCTAATACACGTTTAAGATTAGACCAAAACTAGACTAGTCGTCAAATAGACAAATTAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22862
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 |
|---|---|---|---|---|---|
| ENSDART00000059038 | Essential Splice Site | 1030 | 1059 | 29 | 30 |
| ENSDART00000059044 | None | None | 397 | None | 13 |
| ENSDART00000141061 | None | None | 517 | None | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 30735530)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 28572668 |
| GRCz11 | 16 | 28507291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGCTGGGACTGCTGGTGCTGGCAGTGCTTAGCCTAGCAATGTGGAAG[G/A]TAGGTCATAAAAAAGACTGAAAATACATGTTTATGATACTGTTGGTTATT
Long Flanking Sequence:
CTAAACATATCTTATTATTCTTAAAAGTGTAACGGATAGCTATATCCTTTTAGTGCCACAGTACTTTTTTAAAAACCCTCTTGATGTCTATTAACAGCATTGTCAGCATTTCTTAGCTAAGTGCTGTAAGCAAATCATTAAGACTCCCAATTTCTACTCTATGTACCATGTAAAACTGTCAAAAAAGGAGGGAAAAAGCAATAAACAAAACTTTCTGAAGGAGCTTCTGTTACATTTAGTCGTAAGATGATTCAGAGATGAGAGATGATAACGGAAAATGAGCTGCCAGTCTGATTTACGTGTGCTAATATCGTAGCTACATCAGTTCTAGTGAAATATTAATGACCTCTGTGTTTGTGTTCGCTTGTGTTTTTAAGATCGGCACGTTTGTGGTGTGGGCCATTCCTGACGTCTCCTTTGCCATTCCCCTGTGGGTCATAATTCTGGCTATACTGCTGGGACTGCTGGTGCTGGCAGTGCTTAGCCTAGCAATGTGGAAG[G/A]TAGGTCATAAAAAAGACTGAAAATACATGTTTATGATACTGTTGGTTATTTATTTGTTTATTTTATTTTTTTTATTTTTTTTCAAATAAATGCTGTTTGAACCTTCTATCAATCAAATGATTCTAAAATGCATCATGTTTTCCACAAAGTATTAAAGCAAGACAAGTAAAACTTTTTTATGCACCTGTCAATTTTATGGTTTTAAGGTTGTTTGGCTTTAATTAAATGTTAGTCTAATGTAAAGAATAGATCCACAACACACTTTTAAGTGTTTCTTTTGTCACAATATATCTTATATATCAATATATCTATATAACACATTGTGTCTATGTCTATGCTTATATGTTAGTTTTCTCCAACAATGAGCCGTAACCATCTCTCTCGTTACAAAGTTCACGCGAACGCACACACACACACGTGGATGCACATTAATATCCTCTGCTGTATGGATATTTGTTATGTTATTAATCAGGTATGGTAAACAAACCAGGATTGAATGG
Associated Phenotype:
Not determined