ZMP
LOC559809
Ensembl ID:
Human Orthologue:
ANO9
Human Description:
anoctamin 9 [Source:HGNC Symbol;Acc:20679]
Mouse Orthologue:
Ano9
Mouse Description:
anoctamin 9 Gene [Source:MGI Symbol;Acc:MGI:1918595]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20985 | Nonsense | Available for shipment | Available now |
sa34107 | Essential Splice Site | Available for shipment | Available now |
sa38622 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17446 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20985
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 |
---|---|---|---|---|---|
ENSDART00000115420 | Nonsense | 103 | 788 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 34240885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32635225 |
GRCz11 | 7 | 32906375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGATTTTTACAAAGTACAAGTACCTGCTGAAGGTGTCCGATGGCTG[T/A]AACTGGAGTGCAGAGGAAAGCCGTGAATCATCTGTCTCCTTCTGCACCCG
Long Flanking Sequence:
ATATCTAACCACAATATGGTCATAATGTCACACATCAGCATTGCCCCTGCATGACCTAAATCTCCTGAAATAAACAGACGATAGTCACAAACACTGAAAGGAAGAGAGCCAGCAGTAATACAGCCAAACATCTGATCAATCATTTAAAAAAAACAATCAATTTCTTTTGTTTCTGCTTTTGTGTCATTCAGCATAACACCTATGTTCCTCGATTATATGACTATGTCCTGGTGGCTAATAAAGTGGAGGACATGGAGGATCAACTCTTCAAGAAGCAGGATGCCTTTATCCTGGAACTGAAGCGGAAGAACATTAGAGTGACTGTATGTTATGTCACCGCCACTTGTTTGTGTTTTTCATTTATTTTTAATGATCTTCCTCAACAGTTTTATTATTGCTCAACAGAGAGTTGAAAATGACGGAAAGTTGTTTTTCGGTGTCCGCGCACCTGAGGAGATTTTTACAAAGTACAAGTACCTGCTGAAGGTGTCCGATGGCTG[T/A]AACTGGAGTGCAGAGGAAAGCCGTGAATCATCTGTCTCCTTCTGCACCCGGTACCCTATTTCCCTCTGATTCAAATGCTTTTACAATCTGCTATAGATGAAATCCCTTACCACAAACATTCCTTTTGTTTTACAGAATCAGGATTGTTCACTTTGTCTTAAACAATACGTTCATAGGATCAGGAGGTACCTGTCACTTTCTTTTTCACTTCATCTTTCTTCACATTGTTATCACTCTTTTCTTCTACCTGAAACTAAAAATGTACTATTCAAAAGTCTGCTGTCAGTAAGAAATTGAAAGTTTTTTTTTTAGAAATTTGGTGCAGATAACCTAGTGCTGTGGTTACTTACCTTTTTTTTGCCCAAGACCCCCTTTTCCCCTGGAAAATATTGTAAGGCCCCTGTCCACATATAAGTTTGCAGTAAGAATGACAAAAAATGCATGTGGCTGGGTCAAGGACTCGTTGCCTCGAGAAAAAGGTATAAAATTATAGTTCAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34107
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 |
---|---|---|---|---|---|
ENSDART00000115420 | Essential Splice Site | 185 | 788 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 34243410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32637750 |
GRCz11 | 7 | 32908900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGTATTCAGTTTTGAGGCTTTTTCAACAGCCTGTTACTGATGTAAAG[T/C]AAGTTCTCCCTGGTTTTATTTTGTTATATCTTTTTTTGCTTATTTATTTA
Long Flanking Sequence:
CTATACAGCTTAAAGTGACATTTAAAGACTTAACTAGACAGGTTAGGGTAATTAGGCAAGTTATTGTAAAAATTATGATTTGTGAAAATTTCCTTGCTCTGTTTTTGAAAATATTTTTTAAAAGAAATAAAATTCAAAGGGCCTAATAATTCTGACTTCAACTGTATATTCATGTAAATTTTTTAAAAATAAATATTTCTGAAAGGATTGTCCTAACTGACATAAGCATCAATGTCTCTCTTCACTTTTTTTTGCACTTCAAGAGGGTCTTCAAGATCTGCTGCGTCAAGGTGCTTTCGAGACCATGTTCTGTCTGCATGAGGTAAAATACCTTATTGTCATTGCTTATTCATCAGTAGCCAAAGACAATCAATCTCTGGGTCGTGCTGAATTTCATTGATTTCTCTTGTCAGAAAAAAGAGCAGAAAAAGCTAAAGAAGAAGTGGGCAAGCTGGTATTCAGTTTTGAGGCTTTTTCAACAGCCTGTTACTGATGTAAAG[T/C]AAGTTCTCCCTGGTTTTATTTTGTTATATCTTTTTTTGCTTATTTATTTATGTTTCCATATGTCTTTTTCAGGGACTATTTTGGGGAGAAAGTGGCACTGTATTACCTGTGGCTCGGCTGGTACACTCGAATGCTCGTCCCGGCCGCTGTAATTGGTATAGTTGTGTTCTTGTACGGTCTTGCCTTCTTCAACACCAGCCCGCTCATGTGAGTATATTTATAGTATTGAAGTATAGAAAACTAGGAATGACTGATCTGTTGCAGATTGCAGACTAATTTGTTTTTAATTTACACTATTAAATCTCATTTGTGATGCCGTTACAGTCATGAAGTATGTGACTCTGACATCATCATGTGTCCAAGATGTGACATAAAATGCAAGGCGTGGAACCTGTCTGACACATGTATATATGCCAAGGTCAGTCAATAAACATCTTAATATAACTGATAATTCTAGATGTTATACAGTAATCCACAAGACTCTTGTTTGCCCGGTCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38622
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 |
---|---|---|---|---|---|
ENSDART00000115420 | Essential Splice Site | 282 | 788 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 34247747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32642087 |
GRCz11 | 7 | 32913237 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGACAATGAAGGCACCGTGGCTTTTGCGATGTTCATGGCAATTTGGGG[T/G]GAGTTTTTCCACTTGAACTTAAGCAAAACTGTTTCTTGTGTGATAAATAA
Long Flanking Sequence:
CTAAATATTGTAATGATTGTATTGTTCATGGGTCAGTTGGTGTTATTGTGTGGAGTTTGCAAGTTCTCCCTGCGTTCGCGTGGGTTTTGTCCCCAAAGACAAATGGTACAGGTGAATTGGGTAGGCTAAATTGTCTGTAGTGTATGAGTGTGAATGAGTGTGTATAGATGTTTCCCAGAAATGGGTTACAGCTGGAAGGGCATCTGCTGCGTAAAAACATGTGCTGAATAAGTTGACACTGTGGCAACCCCGGATTAATAAAGGGACTAAGTCGAAAAGAAAATGAATAAATGAATGTATTGTTCGTTGTTTGTTCATGTTAGTAAATGCATTAACTAATATTAACTTATACAACCTTATTGTAAAGTGTTACCAATATATGCATGTGTGTGTTGGGTTCTTAAAATTTGTATAAACTCTGTAAATCCTTACAAACAGGTGAGCCAACTATTTGACAATGAAGGCACCGTGGCTTTTGCGATGTTCATGGCAATTTGGGG[T/G]GAGTTTTTCCACTTGAACTTAAGCAAAACTGTTTCTTGTGTGATAAATAACATTGATGTTAAAGTGCTGTCTTGTTGTTTAACTAGCAACCCTGTTTTTTGAGGTGTGGAAGAGACATCGATCTCTGTATGTGTCAAAGTGGAATGTGTTTGACTGGTGCGATGATGAGGTAGAATCATACATTCTTTACATTATTATTTTGTGTTTAATGTGAATCTTCTGATTGAGCCGAATGACTTCGTCTGCCAACAGGAAGAATTGATTTTGGAGATTGTCAATGACCCTCAGTGTAAGCCAAAAGAGTACAGACATTCTTACCTGCGCAGCACCTTGGTGCTTCTTTTGGTCACGTTAGTGGTAAGAAATGCTTTTTACGCACACACGCACGCACGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTTTGTTGGTTTATGAGGACTCTCTATTGGCGTAATTTATTTTATACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17446
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 |
---|---|---|---|---|---|
ENSDART00000115420 | Essential Splice Site | 567 | 788 | 18 | 24 |
Genomic Location (Zv9):
Chromosome 7 (position 34252203)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32646543 |
GRCz11 | 7 | 32917693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAGTGATGTCAATGCTTTCTCCTTGTTTAATGAGTTTTTGGAAATGGG[T/C]ATGTATMTCCTTTGTCATTACATAGTGCATCTTCATRGTGCTAAYTTTAT
Long Flanking Sequence:
GTAGCCAAAGTGTGAATCAAATCTTTTTTTCTCTCTCTCTCTCTCTGATTTAGTGTCATCCAAGCGGATGCCTTACAGATCTCTTCATCCAGATGGCTGTTATTCTAGTGCTCAAACAAACTATAAACAACATATTTGAGTTCACAGTGCCGTAAGTGTTGTCAAAAATTGCACTAAAACCTTAAACATTCAGTTTTTACTGTTCAACTTTATATTTTACCAGATAAAAATATTAAAATAAAAATGTTACCCGTTCTACTTGGGTTTCTCACTTAAAATCTTCTTCTGTGGTTTCTCTGTAGCTGGTTAAAGATGCTTTTTAAGCGCTCAAAAACTAAGAAAAAAAGCAGGAAGTGCGGTAACTGTTACCGAAAGGCATGTCGAGAAAAGGATGGAAACATTGAGCAATGTGACCTCTGCAAGCTTCGTGATTGGATGACAAACTACGACCTGAGTGATGTCAATGCTTTCTCCTTGTTTAATGAGTTTTTGGAAATGGG[T/C]ATGTATCTCCTTTGTCATTACATAGTGCATCTTCATAGTGCTAACTTTATAGTTTACTAGAAATGTATTTTTGTTATACCCTCATCAAACACTATTGGGACACTTCACTTTAGTTGATTCATAAAGTTCAGTTTCTTTCAAAAGTGGCCGTTTTGGAGAGACAATGACCTGTGTCTGATGATATTTCTCTTTGTTGTTTACTTTGATGGAGTAATGTGTTTTTTTAACCTGATGAAAAAGTTTCATGTTTAAATTACCCAGTGAAGTAACTTATATTTTACATTTATGAAAGTAGTAGAATTTATTTGTTGCTTTTATATTTACTCATTTTCTTTTCGTTTAGTCCCTTTATTAATCAGGGGTTGCAACAGCAGAATGAACCGCCAACTTATCCAGCATATGTTTTATGCAGCGGATGCCCTTCCAGAAGCAACACAGCACTGGAAAACACCCATACACTCTTGCATTCACACACATAAACTACGGTCAATTTAGCTTAC
Associated Phenotype:
Not determined