ZMP
ano7
Ensembl ID:
Human Orthologue:
ANO7
Human Description:
anoctamin 7 [Source:HGNC Symbol;Acc:31677]
Mouse Orthologue:
Ano7
Mouse Description:
anoctamin 7 Gene [Source:MGI Symbol;Acc:MGI:3052714]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12503 | Essential Splice Site | Available for shipment | Available now |
sa35794 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9119 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22580 | Essential Splice Site | Available for shipment | Available now |
sa15317 | Essential Splice Site | Available for shipment | Available now |
sa35793 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12503
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045474 | Essential Splice Site | 323 | 883 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 4006072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3941624 |
GRCz11 | 15 | 4143653 |
KASP Assay ID:
2260-8091.1 (used for ordering genotyping assays)
KASP Sequence:
TTATTATATTTCTGTTTGGTATCTGGCTGATGGTCACTGATGTGCCAGCG[T/A]AAGTATYATCACAGGCTTGCMAATAATGGCATAATATTGATGACCCTGCA
Long Flanking Sequence:
TCGCTTTTAATTTTTGGATTCTGTTTTTCATCTTACCTGATTTCTGGAACCGCTCTTCCCCAGACTCGAACCCAGTCGTCGCCGCGGCCGGCTCCTCCTCCTACGGGCCTCTGCTCCGCGACGTAACACTGTGAGCTAAGCGGACAAACTGGTTGCGGCGGGACAGCCCTCCACACAGAGGTGAGTGAGCCGTCTCAGCCGGCGAGCAAGCGCGAAGAAGAGCAGCGGCGTCACACCGGCCCGTAGCGTTCACTCGAAAAAACCAAATGCGGCCATACGTACCTCCAGCCATGTAAATTGCAGCCTCCAGAAACGTCCGCGGGGCTACGTTTTCAGAATGAGCTTGGGTTGATAAGAAAATGTGGATTAAAACTTGTGAGTATCATTACTTCTTTCTGTTGTCTGCAGGTTTCTACACTGGTTGGTTATTACCAGCAGCAGTAGTGGGTTTTATTATATTTCTGTTTGGTATCTGGCTGATGGTCACTGATGTGCCAGCG[T/A]AAGTATTATCACAGGCTTGCCAATAATGGCATAATATTGATGACCCTGCACCAGTTGTAACCCTGTGATTCATGCTGGTATCTTCTCCACAGGGAAGAGTTGTGCTCCAGTGGAAATGCCTTCATCATGTGTCCACTATGCAACATCTGCAGCCACTGGAACCTCTCGAGTATCTGCTATACTTATAAGGTGACTCTTCTACAGGTTTTTGAACAGTGTAATTAGTAAGCCAAAAATAAAATTACTTAAAATAAGTGTTCATAAATTTGCAATAGGCAGGCTTGCTATTTGACAATGGAGGAACTGTGTTCTTCAGTATATTCATGTCTCTGTGGGCCGTCACTTTCCTGGAGTACTGGAAGCGGACAAGTTCTATACTTTCACACCGATGGGACTGCTCCGAATTCGAAGAAATAGAGGTTAGAAAGTTGGTTAGAGAGTGTCAAAAGCTTAAATACTTAGTTGTCCTCAAGTTTGAGGAATGCAACACATACTTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35794
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 |
---|---|---|---|---|---|
ENSDART00000045474 | Nonsense | 336 | 883 | 10 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 4005940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3941492 |
GRCz11 | 15 | 4143521 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTCCACAGGGAAGAGTTGTGCTCCAGTGGAAATGCCTTCATCATGTG[T/A]CCACTATGCAACATCTGCAGCCACTGGAACCTCTCGAGTATCTGCTATAC
Long Flanking Sequence:
GAGCTAAGCGGACAAACTGGTTGCGGCGGGACAGCCCTCCACACAGAGGTGAGTGAGCCGTCTCAGCCGGCGAGCAAGCGCGAAGAAGAGCAGCGGCGTCACACCGGCCCGTAGCGTTCACTCGAAAAAACCAAATGCGGCCATACGTACCTCCAGCCATGTAAATTGCAGCCTCCAGAAACGTCCGCGGGGCTACGTTTTCAGAATGAGCTTGGGTTGATAAGAAAATGTGGATTAAAACTTGTGAGTATCATTACTTCTTTCTGTTGTCTGCAGGTTTCTACACTGGTTGGTTATTACCAGCAGCAGTAGTGGGTTTTATTATATTTCTGTTTGGTATCTGGCTGATGGTCACTGATGTGCCAGCGTAAGTATTATCACAGGCTTGCCAATAATGGCATAATATTGATGACCCTGCACCAGTTGTAACCCTGTGATTCATGCTGGTATCTTCTCCACAGGGAAGAGTTGTGCTCCAGTGGAAATGCCTTCATCATGTG[T/A]CCACTATGCAACATCTGCAGCCACTGGAACCTCTCGAGTATCTGCTATACTTATAAGGTGACTCTTCTACAGGTTTTTGAACAGTGTAATTAGTAAGCCAAAAATAAAATTACTTAAAATAAGTGTTCATAAATTTGCAATAGGCAGGCTTGCTATTTGACAATGGAGGAACTGTGTTCTTCAGTATATTCATGTCTCTGTGGGCCGTCACTTTCCTGGAGTACTGGAAGCGGACAAGTTCTATACTTTCACACCGATGGGACTGCTCCGAATTCGAAGAAATAGAGGTTAGAAAGTTGGTTAGAGAGTGTCAAAAGCTTAAATACTTAGTTGTCCTCAAGTTTGAGGAATGCAACACATACTTTGGCTAATAGAAAGGCTATAATATAATGTACATCGATTGCTTTCCACATTTCCATTATAATATTAGGAAAGGCCAAGACCAGAATTCACAGCACTGGCACCTATGACAGTTCGTAATCCTGTGACTGGGGCTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9119
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 |
---|---|---|---|---|---|
ENSDART00000045474 | Nonsense | 435 | 883 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 4005416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3940968 |
GRCz11 | 15 | 4142997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCGTAATCCWGTGACTGGGGCTGAGGAGCCTTATTTCCCAGAGGCCCGT[C/T]GACTGAGYCGTACTCTAACCGGCAACATRGTCATCATTCTAATGGTAGGT
Long Flanking Sequence:
CTGGAACCTCTCGAGTATCTGCTATACTTATAAGGTGACTCTTCTACAGGTTTTTGAACAGTGTAATTAGTAAGCCAAAAATAAAATTACTTAAAATAAGTGTTCATAAATTTGCAATAGGCAGGCTTGCTATTTGACAATGGAGGAACTGTGTTCTTCAGTATATTCATGTCTCTGTGGGCCGTCACTTTCCTGGAGTACTGGAAGCGGACAAGTTCTATACTTTCACACCGATGGGACTGCTCCGAATTCGAAGAAATAGAGGTTAGAAAGTTGGTTAGAGAGTGTCAAAAGCTTAAATACTTAGTTGTCCTCAAGTTTGAGGAATGCAACACATACTTTGGCTAATAGAAAGGCTATAATATAATGTACATCGATTGCTTTCCACATTTCCATTATAATATTAGGAAAGGCCAAGACCAGAATTCACAGCACTGGCACCTATGACAGTTCGTAATCCTGTGACTGGGGCTGAGGAGCCTTATTTCCCAGAGGCCCGT[C/T]GACTGAGTCGTACTCTAACCGGCAACATGGTCATCATTCTAATGGTAGGTCCACTCCATTTTTTTCAATCTATAATGATTGAACTCCACAGATTCGCAGCTTCACTAGTCCAAACCAAGCAAACCAAATATGACAATGACTGAAGTGAAAAAAAAAAAGCCTTAAGAGAGAAGCCTGGCTCAGCTTGGCAAGCTCTGGCCAAGCGTTTTGTGCAGAGCTTCAGGCTGGACGTCAGAGGCTTGAGAATAATGACCTTTGGTTGGGGAAAAGGTACAAGTCCAAGTAGGTCACCAGTTTTGTGTTTTGTGTTTTTGTGCAAAGACTATTTTGTCTCTGGGATCTTATGGTCTTGACTTATTGATAATCATAACAGTTATCTGCTCAGGATATGGGCCAAATCGACAATTAAGTAGACCTAAGAAGAAACAATCAACTAACATAAGCATGCTTACATACCTTTAGAGTTACAGTGCTCTTTGAGAAATGTTCCTAGCTTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22580
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 |
---|---|---|---|---|---|
ENSDART00000045474 | Essential Splice Site | 449 | 883 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 4005370)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3940922 |
GRCz11 | 15 | 4142951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCGACTGAGTCGTACTCTAACCGGCAACATGGTCATCATTCTAATGG[T/G]AGGTCCACTCCATTTTTTTCAATCTATAATGATTGAACTCCACAGATTCG
Long Flanking Sequence:
CAGGTTTTTGAACAGTGTAATTAGTAAGCCAAAAATAAAATTACTTAAAATAAGTGTTCATAAATTTGCAATAGGCAGGCTTGCTATTTGACAATGGAGGAACTGTGTTCTTCAGTATATTCATGTCTCTGTGGGCCGTCACTTTCCTGGAGTACTGGAAGCGGACAAGTTCTATACTTTCACACCGATGGGACTGCTCCGAATTCGAAGAAATAGAGGTTAGAAAGTTGGTTAGAGAGTGTCAAAAGCTTAAATACTTAGTTGTCCTCAAGTTTGAGGAATGCAACACATACTTTGGCTAATAGAAAGGCTATAATATAATGTACATCGATTGCTTTCCACATTTCCATTATAATATTAGGAAAGGCCAAGACCAGAATTCACAGCACTGGCACCTATGACAGTTCGTAATCCTGTGACTGGGGCTGAGGAGCCTTATTTCCCAGAGGCCCGTCGACTGAGTCGTACTCTAACCGGCAACATGGTCATCATTCTAATGG[T/G]AGGTCCACTCCATTTTTTTCAATCTATAATGATTGAACTCCACAGATTCGCAGCTTCACTAGTCCAAACCAAGCAAACCAAATATGACAATGACTGAAGTGAAAAAAAAAAAGCCTTAAGAGAGAAGCCTGGCTCAGCTTGGCAAGCTCTGGCCAAGCGTTTTGTGCAGAGCTTCAGGCTGGACGTCAGAGGCTTGAGAATAATGACCTTTGGTTGGGGAAAAGGTACAAGTCCAAGTAGGTCACCAGTTTTGTGTTTTGTGTTTTTGTGCAAAGACTATTTTGTCTCTGGGATCTTATGGTCTTGACTTATTGATAATCATAACAGTTATCTGCTCAGGATATGGGCCAAATCGACAATTAAGTAGACCTAAGAAGAAACAATCAACTAACATAAGCATGCTTACATACCTTTAGAGTTACAGTGCTCTTTGAGAAATGTTCCTAGCTTTAATTACCTTGATTATTGCAGCCTAACAAACCTTTAGAAGATTTGGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15317
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 |
---|---|---|---|---|---|
ENSDART00000045474 | Essential Splice Site | 605 | 883 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 4002270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3937822 |
GRCz11 | 15 | 4139851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCATGGTRGGCAAGCARGTCATCAGCAACATCCAGGAATTTGTATTACC[G/A]TAAGTCTGTATGCTCACTGCATCTTCTTACAGGTTTTGTTTATACAATTT
Long Flanking Sequence:
CTATTTCCTAATGACCAAGTATTATCAACTTTCCTATATTAGAAATGCACCGCACCCAGACGGAATATGAGAATGCATTCATCCTCAAGGTCTTCATCTTCCAGTTTGTCAACTTCTACTCATCTCCTGTTTACATTGCGTTTTTCAAGGGCAGGCATGTATCTAAGCACCACAAATGAATGAATATTTATGAGGACTCAATATTTATATAATATTTGATCTGTTCTACAGGTTTGTTGGATACCCTGGAAGCTATAACACATTGCTAGGAATCCGAAATGAGGATGTTAGTGTTTACTCTGTTACAAAGCTAATGTTCTCACTAAATTACACAATTGCACAATCGGGGAAAATAATTTGAATAACTCATTAATGTGTGCTTTCTGTTCTTGTTTTATGTAGTGTGGTGCATCTGGATGTCTCATTGAGCTTGCACAAGAGTTGTTGGTAATCATGGTAGGCAAGCAAGTCATCAGCAACATCCAGGAATTTGTATTACC[G/A]TAAGTCTGTATGCTCACTGCATCTTCTTACAGGTTTTGTTTATACAATTTAGTATATTGTATTACATTTTGTATGCAAAATTGGACCCAAGAAGTATCCCTTCTCTTTTAAACAGTAAATTAAAAACATGGTGGCACAAGAGGAAGTTAAAGCCAGCTCGCAGTCAGGAGGTCATAGATGAACCAGACACCAATTCACAGATCAACCCATGGGAAAATGACTATCAGTTGCTGGTGTGTGAGGGACTATTTGATGAGTATCTGGAAATGGGTGAGTTCTCCGGTATCCTGCAGTATTGTTGATGGTTGAATTTTAGAAGCTAGATAAGGTGGAGACCTTGCCAGATTTGAGGGCATGAAGAACAAGGGCAACACTGCTTGTCGAAAGACCAATGTGTCACTGTAGTCAGGGTTTGACCACCATGAAGCTGGTGTGAGTCCAGAGGTAGAGGGCTGAAGCAGTGTCTAGAATCCATGATGTAATCAGTGTGATAATGTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35793
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 |
---|---|---|---|---|---|
ENSDART00000045474 | Nonsense | 854 | 883 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 15 (position 3991071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 3926623 |
GRCz11 | 15 | 4128652 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCTTTCTTTAGTCGTTGAGTAAATCTGTCCTGGAAGAGATGGGGAGG[C/T]AAAACTTTGAGCTGCGGCAAAGGATAAGAACACAGAGTCCAACAAACAAC
Long Flanking Sequence:
GCCTATAGCACTCATTCATTGTTGCTCTTAGTTGTGTAAGTTGCTTCCTTGTCCTCATTTGTAAGTCGCTTTGGTTAAAAGCGTCTGCTAAATGACTTAATGTAAATGTGTGTGATGTGCCAAACTATTTATGGGTCTTACCAGCATAGTTACCAGTCATAAGTCTGACTGCTGTGATTTTTTGTGTTCGGTAACACATTAGTTTATCAGTTCATACAATTTACTACTGGCTTTTACCTGCTTTTTATTAAGATATTAATTAGCACTTACTGTATAAAGTATGATCTTATTTTACATCCTTAATCCTACCAAATACCTAAACACAACTACTCCCTTACTACCTATTAAATAGCAGCTAATATAATTACTCCCATAAACCTCTTAGGTAATGGTTTATTAATATGAGTTAAAATAAAGTGTGACCATGGTTTCTCTTACATATTTTTCATCTTGTCTTTCTTTAGTCGTTGAGTAAATCTGTCCTGGAAGAGATGGGGAGG[C/T]AAAACTTTGAGCTGCGGCAAAGGATAAGAACACAGAGTCCAACAAACAACATGTCACCAACATCTGAAGATGAGGCCATGCCTGCGCTCTGAAACGATATATCTTAGGATTTTAATACACTTCACAGATCACTCTACAGATGAATACATGTTTTGGAAACTGCTTACTGATTTTCGTGGCATTACACTGATCATTTTAGGATAAACTCGTAAGGCATTAAAACAATAATGGTTCCGAGAACCATCCCTGTGTCCTGATTTTAAAGTTATCATGAATTAAGCATGGGCGACGCAGTGGCACAGTAGGTAGTGCTGTCGTCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTCGGGTGGGTCAGTTGGCGTTTCTGTGTGGAGTTTGTATGTTGTCCCTGCGTTTGTGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAAAACATGCGGTCCAGGTGAATTGGGTCGGCTAAATTGTCCATATGAGTGTGAATG
Associated Phenotype:
Not determined