ZMP
si:ch1073-404h7.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
ARMC9
Human Description:
armadillo repeat containing 9 [Source:HGNC Symbol;Acc:20730]
Mouse Orthologue:
Armc9
Mouse Description:
armadillo repeat containing 9 Gene [Source:MGI Symbol;Acc:MGI:1926045]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24216 | Nonsense | Available for shipment | Available now |
sa43882 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29834 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24217 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24216
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 |
---|---|---|---|---|---|
ENSDART00000125991 | Nonsense | 144 | 532 | 6 | 17 |
ENSDART00000132181 | Nonsense | 128 | 516 | 5 | 16 |
The following transcripts of ENSDARG00000087299 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 39475209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 36621982 |
GRCz11 | 22 | 36590991 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCTGTACCTGTCTCAGATTCCAGCTTTACTGCCATTTCTGCTGGACTG[T/A]CTGAAGACTGAAGAGAAAGAGTCTGTCACTCGAGAGAATGTGCTGGCAGC
Long Flanking Sequence:
AGATATGACTTGCTATATGAGTGTAACACGACTACATATAAGAGCCCATATGCTGTATTTGTGCTCATAAACACACCCACGTTGGCTTTTCTACATTAAAATGTTAATATATTGTATTTTGAAACTACATAAAAATCAGTGCTTTGTACAATAGACTTTATTATTTTTAGATTAATTGCCACAGTTTAAATTAAGTACTTTAAAAAGTGTTTACACAACGGCAGAATATATTCTAAAGAGTTAAAGTTCATCACACACATTCATTGTGTCGTACACCGTTGACAGTAAACATCTGACTATGTCGCCTGAAACTTTTGTAATCGTTGTAATGTTTTGAGCAAATTCATTATTGTTTCTCTATTTTCTCTTTCCTAGTTCAACTCTGTTGCAAAAAAAGTGTTGCGTGACTAGTGTTTTCATCAGGTTAATGTGTGTATTTCACACTCAGGGCGCCTGTACCTGTCTCAGATTCCAGCTTTACTGCCATTTCTGCTGGACTG[T/A]CTGAAGACTGAAGAGAAAGAGTCTGTCACTCGAGAGAATGTGCTGGCAGCGCTGCAGAAGCTCAGCCTCAGGTATGCCCTTTCTTAAGCGGTAATCAAACCTTACACAGACATTTCTTGTAAGAATTTGATTTATTTGTTTTCTCTCTCTCCACCATTTGAAGGTGAGTTATTCCCTGATTTCTAAGCTGAAAGTGGCCAAGTGCTTAGGACACAGACTCCTGTATATGGTTATATGCTGTCATGGCTTTGCGATCAAATAAATGTGCTTATAATGCAAGTCACACACCAGCAACATAACAAAAGGATAGTCAATTTAAACAACACACAAGAACTAAACACCATAAAACACACTGGGCTCTATTTTGACGGTCTATGCTCAGAGCGCAAAACGCAGGGCGCAAACGCTTTTTTGCTAATTTAAGGACGGGAAATCTGCCTTGTGCCGCGGCCCATGGTCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTATAGGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43882
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125991 | Nonsense | 249 | 532 | 9 | 17 |
ENSDART00000132181 | Nonsense | 233 | 516 | 8 | 16 |
The following transcripts of ENSDARG00000087299 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 39479008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 36625781 |
GRCz11 | 22 | 36594790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGTTTTTTGTGGGTTTTTTAGATTCGGTATTATGTGAATGGAGCTT[T/A]ATACAGCATCCTGTCTGTGCCAGAGATACGAGAGGAAGCCAAACAGATGG
Long Flanking Sequence:
TATATTTATTTATATTTACTTTTTACCTTTTCACTTTTTTTTTAATCTTCAGAAAATTTTTTTTTTTCAAATAAGTTTTGTTTGTTTTTATAAATGTTTTTATGAGTTTTAATTAAAATCAGGGTTATTTTACTAAATATTGATTTCATTATAGTTGTGAAGGTAAAGCATTACCTTGCTGTTGTCTAAAAAATGACATTTTCCAGATTTTTTGGCCGTTTTTATTGTAATTTTACTGTAAATATACATTTTAAATACACACACACACACACACTTTTTTTTAAATATTTCCCAAATGATGTTTAATAGAGAAAGAAAATTTTCACAGTTTGTCTGATAATATTTTTTCTTCTAGAGAAGACTTATTTGTTTTATTTCGGCTGGAATAAAAGCAGTCTTGAATTTTTTAAAGATTCATGACACATTTATAATGGCCTTGTGGAATTCATGTTTGTGTTTTTTGTGGGTTTTTTAGATTCGGTATTATGTGAATGGAGCTT[T/A]ATACAGCATCCTGTCTGTGCCAGAGATACGAGAGGAAGCCAAACAGATGGTACGTGTTTAACAGCTTCATTCACAGTTACAGTTACGCAACATCAGCATTAATGCCTGGACTCCAGTCTTCTGATAGCAATAAAACTACAAGATGTGAAATGAGCGATAAGATTCAAACCTTTCAAGGCTAATCGCTGATAAGTGACCAAGCAAAGGGAGCAGATTCAAAAAGTTCAACCACTTAACTATTATTTATTTGTTTAATAATAATTTAATTTTAATTTAATTTGTTTACTTTATTTAATTAATTTATTTTATATTTAATTTTATTTTATTTTATTTAAATGTCTTAATTTTGTTTTATTATTTTTTTAACTTATTTTAATTTATTTTTTACCATTTAATATTTTATAGATTTTTATTTATTTATTTATTCATTCATGAAGTTTTATTAACAATATATATATATATATATATATATATATATATATATATATATAATTATAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29834
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000125991 | Nonsense | 264 | 532 | 9 | 17 |
ENSDART00000132181 | Nonsense | 248 | 516 | 8 | 16 |
The following transcripts of ENSDARG00000087299 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 39479052)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 36625825 |
GRCz11 | 22 | 36594834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTTTATACAGCATCCTGTCTGTGCCAGAGATACGAGAGGAAGCCAAA[C/T]AGATGGTACGTGTTTAACAGCTTCATTCACAGTTACAGTTACGCAACATC
Long Flanking Sequence:
ATCTTCAGAAAATTTTTTTTTTTCAAATAAGTTTTGTTTGTTTTTATAAATGTTTTTATGAGTTTTAATTAAAATCAGGGTTATTTTACTAAATATTGATTTCATTATAGTTGTGAAGGTAAAGCATTACCTTGCTGTTGTCTAAAAAATGACATTTTCCAGATTTTTTGGCCGTTTTTATTGTAATTTTACTGTAAATATACATTTTAAATACACACACACACACACACTTTTTTTTAAATATTTCCCAAATGATGTTTAATAGAGAAAGAAAATTTTCACAGTTTGTCTGATAATATTTTTTCTTCTAGAGAAGACTTATTTGTTTTATTTCGGCTGGAATAAAAGCAGTCTTGAATTTTTTAAAGATTCATGACACATTTATAATGGCCTTGTGGAATTCATGTTTGTGTTTTTTGTGGGTTTTTTAGATTCGGTATTATGTGAATGGAGCTTTATACAGCATCCTGTCTGTGCCAGAGATACGAGAGGAAGCCAAA[C/T]AGATGGTACGTGTTTAACAGCTTCATTCACAGTTACAGTTACGCAACATCAGCATTAATGCCTGGACTCCAGTCTTCTGATAGCAATAAAACTACAAGATGTGAAATGAGCGATAAGATTCAAACCTTTCAAGGCTAATCGCTGATAAGTGACCAAGCAAAGGGAGCAGATTCAAAAAGTTCAACCACTTAACTATTATTTATTTGTTTAATAATAATTTAATTTTAATTTAATTTGTTTACTTTATTTAATTAATTTATTTTATATTTAATTTTATTTTATTTTATTTAAATGTCTTAATTTTGTTTTATTATTTTTTTAACTTATTTTAATTTATTTTTTACCATTTAATATTTTATAGATTTTTATTTATTTATTTATTCATTCATGAAGTTTTATTAACAATATATATATATATATATATATATATATATATATATATATATAATTATAATATATATATAATATGCATTTATCATTTTAAGTGTGAACTGAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24217
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 |
---|---|---|---|---|---|
ENSDART00000125991 | Nonsense | 525 | 532 | 16 | 17 |
ENSDART00000132181 | Nonsense | 509 | 516 | 15 | 16 |
The following transcripts of ENSDARG00000087299 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 39506936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 36653709 |
GRCz11 | 22 | 36622718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCAGCCGGCCCGGATCAGCAGGGGGCTCCAGTGGGCGACCGAGCCAA[C/T]AGAGTGAGTATTTCACCCAGCCTTCCCTCACAAACGGATACTCTTAAAGG
Long Flanking Sequence:
GGCATTATATAATAAGTGGCATACAACTGGTCTTAAAAATGTCGATAAAATTGTTTATCGCAATATATATTTTGGTTCAATAAATTGTACAACAAAATAGATATCATGACAGGCCTAAATATATTGTGCATCACTACTAACTTTACAAAAGAAAACATCCTTTAATCATCCCAAAATTGTATCTTGTTTAAAAGTGAAGCATCCTTGACTTGAAAAACTCGAATGCAAACGTATTGAAATGAGTTTGCTAGTCACTCACTGCAGCTCTGGCTGAAGGCAAATCCTAAACTTAGTGGCATCACTGTCGTTCTCTTCTTTCTAGTGGCCACATGGTGGGCTTTGCGAGCCGGCCAAAGATTCCTCGCACCCCTGACAGTGACGCAGGCAGTGCTGGCAGGTCTCGTTTGCCCCCGTTGGCCCCCCAGTTCTCCAACAGCGAGCCCCAGCAGAGCGGCAGCCGGCCCGGATCAGCAGGGGGCTCCAGTGGGCGACCGAGCCAA[C/T]AGAGTGAGTATTTCACCCAGCCTTCCCTCACAAACGGATACTCTTAAAGGTTCAATGAAGTGATTTGAAATGTGCATTTTTTTTATGAGATGTTTGACAATCTCAATCAAAACATAAAGAGGGGCGGGGAAATAGAGTAGCTCCTCCCCTTTTTAATAACAGCCAATAGTGTTTTGTTTTAGCACTAGTGGGAGTGGTTGAGCTCAAGTGCATCAAACAAAAAGTGTCTTGAAGGGGGCGGGGCTTGTCAGATACTAGCGAGCATTTGATTGGTCAGAAGATTTAATAGTAAAGCTGTATAGAAGTGTCTTGAAGAATATCTACTCAAATATTATTTACTGTCATCATGACAAAGAGAAAATTAATCAGTTATTAAAAATAATTTATTAAAACTATTATGTTTAGAAATATGTTGAAGAAATCTTCTCTCCTCTGCTCTGCAGTTTTCATGTATCTCTTTATTTTTTTAATAAAATAAAGTTTTAATTAAAGTCGTCCAT
Associated Phenotype:
Not determined