ZMP
zgc:153683
Ensembl ID:
ZFIN ID:
Description:
Armadillo repeat-containing protein 8 [Source:UniProtKB/Swiss-Prot;Acc:Q05AL1]
Human Orthologue:
ARMC8
Human Description:
armadillo repeat containing 8 [Source:HGNC Symbol;Acc:24999]
Mouse Orthologue:
Armc8
Mouse Description:
armadillo repeat containing 8 Gene [Source:MGI Symbol;Acc:MGI:1921375]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21497 | Essential Splice Site | Available for shipment | Available now |
| sa41433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21498 | Essential Splice Site | Available for shipment | Available now |
| sa9128 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31717 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21497
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 |
|---|---|---|---|---|---|
| ENSDART00000089761 | Essential Splice Site | 112 | 673 | 4 | 22 |
| ENSDART00000133997 | Essential Splice Site | 113 | 674 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 9 (position 28917660)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 28073356 |
| GRCz11 | 9 | 27884102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACATCAAGTCCCTGGTGGACTGTCACATCATCCCAGCCCTGCTGCAAG[G/A]TTCTCAATCTATTATTTTTTCTTGAAATCTATGGACATTTCTACTTTATA
Long Flanking Sequence:
GAGTTTTTTATATTATATATAAATTTGAGTTAGAATCTTTCTTTTATTTGTATCTTTACATTTTAACTTCTGTATCAGAACCATCAATAAATAAACTTAATCTTTAGAGATAAAAAGTCAAGTGTGAGGTAATAATCTAATAACTTCATGACTTGAAATGGTAAAATTCAAACTATTCTGAAAAAAGCCATCCAATTGATTCAGGCAAACAAACTCAAGCCCTCCTTATGTTTTTTTCCTGTTTCTCTTCAATCAGCATTGACTATTTTTGAAATTGACATTTTAAATGATTTCTCAAGTTGAATATACACATTAGATATGTTCATTGCTGATCAGAAAGTGTGTTTGGGTTTGTAGACTCCTGTATCTCCTCCAGCAGAGCTCCTCCACTCTGGAGCTGAGGACTGAATGTGCGGTTGTGTTGGGCAGTCTATCCATGGGCACCGAGAACAACATCAAGTCCCTGGTGGACTGTCACATCATCCCAGCCCTGCTGCAAG[G/A]TTCTCAATCTATTATTTTTTCTTGAAATCTATGGACATTTCTACTTTATATGTCCTAAGAAAAGTGCTCAAGTCTCCAATGTTTGTGCGCAGGTCTCTTGTGTTCTGATCTGATCTTTATTGAGGCATGTCTGCGCTGTTTAAGAACTGTTTTCATCAGCCCAGTCACACCAGTCCAGCTGCTCTACACAGTAAGCACATGTCCAGTTCTTTTATATAGTTACATATGTATAAGCGAAAGAGTGATCAACGTGTTTTTATTTTCATCAGGATCCCACCGTGATCCCCCACCTCATGTCTTTGTTGAGTCGGTCACAGCACACGCAGGAATACATCACGCAAATCTTCGCCCACTGCTGCAAGGTAGTTTAGTTTAAACCTTTATTATTCCCTTTGGGGCAATTCATTTCTACATGGTGGTACTTTACATATAGTATTACAAGAATGACACACTTAACGCAATAAACATCAACACTTAACGGCAAGTTCAAAAAACAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41433
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089761 | Nonsense | 175 | 673 | 6 | 22 |
| ENSDART00000133997 | Nonsense | 176 | 674 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 9 (position 28918019)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 28073715 |
| GRCz11 | 9 | 27884461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTCACAGCACACGCAGGAATACATCACGCAAATCTTCGCCCACTGCTG[C/A]AAGGTAGTTTAGTTTAAACCTTTATTATTCCCTTTGGGGCAATTCATTTC
Long Flanking Sequence:
TCCTGTATCTCCTCCAGCAGAGCTCCTCCACTCTGGAGCTGAGGACTGAATGTGCGGTTGTGTTGGGCAGTCTATCCATGGGCACCGAGAACAACATCAAGTCCCTGGTGGACTGTCACATCATCCCAGCCCTGCTGCAAGGTTCTCAATCTATTATTTTTTCTTGAAATCTATGGACATTTCTACTTTATATGTCCTAAGAAAAGTGCTCAAGTCTCCAATGTTTGTGCGCAGGTCTCTTGTGTTCTGATCTGATCTTTATTGAGGCATGTCTGCGCTGTTTAAGAACTGTTTTCATCAGCCCAGTCACACCAGTCCAGCTGCTCTACACAGTAAGCACATGTCCAGTTCTTTTATATAGTTACATATGTATAAGCGAAAGAGTGATCAACGTGTTTTTATTTTCATCAGGATCCCACCGTGATCCCCCACCTCATGTCTTTGTTGAGTCGGTCACAGCACACGCAGGAATACATCACGCAAATCTTCGCCCACTGCTG[C/A]AAGGTAGTTTAGTTTAAACCTTTATTATTCCCTTTGGGGCAATTCATTTCTACATGGTGGTACTTTACATATAGTATTACAAGAATGACACACTTAACGCAATAAACATCAACACTTAACGGCAAGTTCAAAAAACAAATAATAGTCTATCGATTAACTACATTTATTACATAACCTAATTGCTTCAGGCACAAAATTAAATTTATAACGATTTGTGGAACATCTTATTGTCCTTAGACGTCGACCAAGGGGTGTGTGTGCTGTCTCCTAGTATTTTATGTGCCATCCTCAACACTTGCTGTTCGTAATAGTATGCAAGACTTCGCAGGGGAACTCCCAAAATCTTTGAACACAAATTAACGACGCCTTGAAGATGATTCTTGTTTTTTATGGACAGTGAAGAAAACCAACAAATAAAGGAAAAGTACAAAATACTTTCAATAAATGAATTGCAAAAGGTCTTAAGAATAACTTTCTCTACATTAAAAGAGTTGAGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21498
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089761 | Essential Splice Site | 279 | 673 | 10 | 22 |
| ENSDART00000133997 | Essential Splice Site | 280 | 674 | 10 | 22 |
Genomic Location (Zv9):
Chromosome 9 (position 28922024)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 28077720 |
| GRCz11 | 9 | 27888466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCGAGCAGGAGCCATCAGGACAGAAGACAACTGCATTGTACTGAAGG[T/C]AGCAACAACACCTATTCATATTGTGACTAATTTAAAAGCTGACAGCACAC
Long Flanking Sequence:
GTATTAACCTCATTCTTCAATGTGGAAGTGCTCTCGTTTTTTGCGATTGTTTTAGAACTTCCAATTTAGTTGACTATTGGAGAAATGACTAGAACAAAAATAATGTCAGAAAACAGTCAAACTACTTGTGTTTGCATGACTATACAGACCAAGAAGAATATTATAATAAGAAAATTTACAACATCAAGAAGCTTAACAAGCTGTTTTTAACATATAAAAATGAATGGAAGTGAATGAGACCGGAAGTCTCAAGCCAAAGACATTCAAATGGCTGCATTCGCGCTTATGTGAAGACTAAGGTGAATAGATATTGACAAGAATTAAAGTTTGAAAAAGAGCAGGAGGAATGATTTGCCACTAGATTATCTGTGCCACTAATTTAAAGTAAATTTACCTGTGTGAACTCTTCAATTTATATACTCCTACTCTTCCTCCTAGTTTAACATACATGTGTCGAGCAGGAGCCATCAGGACAGAAGACAACTGCATTGTACTGAAGG[T/C]AGCAACAACACCTATTCATATTGTGACTAATTTAAAAGCTGACAGCACACATAAACAAGTTGGGTGTGTGTGTGTGTTTGTTTGGACAGACTCTGCCATGCCTGGTCCGGATGTGCAGTAAAGAGCGGTTACTGGAGGAGAGAGTGGAGGGTGCAGAGACGCTGGCCTACCTAATGGAGCCAGATATTGAACTGCAACGCATTGCCAGTGTCACAGACCATCTTGTATCCATGTTAGCTGACTACTTTAAATACCCAAGCTCTGTCAGCGCCATCACTGATATTAAAAGGGTAACTGCATACATGTACATGGGTCAAAGGGAAATCAATAGGGATTTCATAAACAGTTGAAATAAATATCATTAGCCCTCCTGTGAAATTAGCACTCTTTTTCAAATATTTTAAACATAATAGTTTTAATATTTGCTTTCTAAAACTCATTTATTTTGCCTTTTCCATGGTGGCTGCACATACTATTTTTCTGGCTATATATTCTCACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9128
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089761 | Essential Splice Site | 433 | 673 | 14 | 22 |
| ENSDART00000133997 | Essential Splice Site | 434 | 674 | 14 | 22 |
Genomic Location (Zv9):
Chromosome 9 (position 28925166)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 28080862 |
| GRCz11 | 9 | 27891608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTAAGAACGAGTTTCCATGATCATGCCGTATGGAAACCACTAATGAAGG[T/G]ATGACATCTCRATGATGCTAAGCTRAATATCAAMGCTAATCTAAGCTRAA
Long Flanking Sequence:
AAATGTCAGTTGTCAGTCAGGAAAAAGATTCACAATGAACATCCCTAAGTAAAGATATTGGGTTGATGTAATGAAAGATCCAATTTCTCCCCTACAGATTACAGAGACGGAAAACATGATGGACAGAATTGTTAGCGGCTTATCAGAATCTAGTATCAAAGTACGGTTAGCAGCAGTCAGGTATGAGGCATCTCTTTTCACAGTACTTCTGTAATTAATTTTTATAATATGAATGCACTGTTGATGAGCTTAAAAACATTCAAGACCTCTTACTGACCTCAAACTATTGATCAGTGGAGCAAATATGAAATGTGTTTGTTGAAATGCCACAGCAATTGGATGTTGAAAGAGTTTCAAGAATTTAAAAAATGTTGCTTTTGTATTTCAGATGATTTCTTTTTATTTGTTTTCCTCTAGATGTCTCCACAGTTTATCACGATCAGTACAACAGCTAAGAACGAGTTTCCATGATCATGCCGTATGGAAACCACTAATGAAGG[T/G]ATGACATCTCGATGATGCTAAGCTGAATATCAACGCTAATCTAAGCTAAACAGAATAAACGTTTGTTTTGTTTGTTTTGGTAGTTATTACAGAACGCACCAGATGAGGTGCTGGTCATGGCCTCTTCAACACTATGCAACCTTCTTCTGGAATTTTCACCCAGTAAAGAGGTAAAGTATTTACACTTTGTTGGGCTTAGCATTATTAACACATATCTACAAAGCGAAAAACTGTCAGCACACCTTAACTTTAGTGCTTAATCTCTTCCTATCAGTCAACAAAAATAGTTTTGGATTTATAAGATTTGATTTGTGTGCTTTCTGTATAGCAAAGTTTTTTTTTTAAATTGACGATGGACTAAGTTTGTCATTCATGTTGTGCTATTATACAGTATGATGTGCTTTTGAAAATGCAAAATGAGCCTCCTGGATAATTTTTAATAATTAAATAAAAAATAACATCTATTCATTTGAAGAATTTGAACAGAAGACACATATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31717
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089761 | Essential Splice Site | 663 | 673 | 21 | 22 |
| ENSDART00000133997 | Essential Splice Site | 664 | 674 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 9 (position 28933497)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTCTACACAAACTTACCCAGGCATCAGATCCCAACCTCTGTGACAGG[T/G]GAAGGACACACACACACACACACACACACACACACACACACACACACACA
Long Flanking Sequence:
AGGACGGTGAGAAAATCAGCGTTCAAAACACTGATAGACAGGCTGACAGTTTTGCTCTGTTTTTCTGACATTTTGGCATATGAAACAATGCAAAGTTTAATACGACAATAAAATGTAACCATTTATGTTTGATTATTAAACAAATGATTTTAATTTAATACGACTTTTTCATTCATTTAATGGTCAATGCAAATGATTTATTTACTGTTCAATGTTTCTCTTTAAACCCCCTTCAAAAATTTCACTCATCAAATCCTTTTTTAGATACCATAAACAATACAGGGCTGAGAATAATGAAACAAAAAATAAGAGTTATGCAATGTTGTTTATTGTTATCTGATGCTGTAAATTGGATTCTTTGTGTGCAGTCCAGAATACACGGCTCTGTTTTCCTTCTTCCTCCAGGCTCACAAGAGAGACAAGATAAGCTGAGGGAGATGGGCTTTGTTGATATTCTACACAAACTTACCCAGGCATCAGATCCCAACCTCTGTGACAGG[T/G]GAAGGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAACACAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTTACACACTCATCTCCAGCTAGCCATTTTATTAAAAAGGTTGCATCCTTATTAATGAGACTTTAACATTACACTGTGTGTAACTGAATTCATTTAAAATCTTCTTGTTCCCTGCATACCGACATTGTATGTGTGTGTAGTATATTTCCAGTAGGTTTAAAAACGAATAAGGAGTTCTGATCAACACATTTTGGCTGTCATTTTTAATTTTTTTTAACATTTGCAAGTGTTTAGGTGACCTTTGTTTAAGCGCTCCTAGACGTGAATAAATGACTGAATTCAGCATCAGCAACAGTGTCTTGAAGGGGGCGGTACATCTTAAATACTTGAGAGCATTTGATTGGTCAGAAGATTTGATGAGAAATT
Associated Phenotype:
Not determined