ZMP
LOC562782
Ensembl ID:
Human Orthologue:
ANO8
Human Description:
anoctamin 8 [Source:HGNC Symbol;Acc:29329]
Mouse Orthologue:
Ano8
Mouse Description:
anoctamin 8 Gene [Source:MGI Symbol;Acc:MGI:2687327]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41774 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10269 | Nonsense | Available for shipment | Available now |
sa41773 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13612 | Nonsense | Available for shipment | Available now |
sa38823 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41774
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108628 | Essential Splice Site | 138 | 1110 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 6023268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5991451 |
GRCz11 | 11 | 5988706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAAACACACCCGAATGTACGCCTTCTTTGTCACCGCCACATATGAAAA[G/A]TAAGAGGGGATTGGAGGGAAACTGATTTATCTGTCTTTTATGTGTGCTTA
Long Flanking Sequence:
TACCTTAACCAAGTTTAGTGTTGTATCCTCTCACTATAACCTGCTGCTCATGTTTTGATATTTTAATTAAACTTGTAGAGTCAAATATTGTGCGGTGTCCCCTCTGGACATCCCTTTCATCACATACAGTATGTGTGTATAGTGTAATTGATGACAGAAGTGCTGCAGTGCGTGTAGTTAGGAAACGGTGTAAGGAAACCTTTTTTAAAACCTTAAATTGCTAGATAGGATGCTGGTTGAAAGCAGCCTGAAGCAGTATATGTAAGTTCAGGATGATTTTTTGCTGTATTTTTCACGGGTGTATCTGAAAGTATGAATGATGTGTGTTACCTCAAAGACAAAGGTGTTTATATTGGTCTCCATGCAGACACCACAGATGACCACACGCTGCTCTGGCTCCTGAACCACATACGGCTCGGCATCCCAGAACTCATTATCCAGATCCGGCATCACAAACACACCCGAATGTACGCCTTCTTTGTCACCGCCACATATGAAAA[G/A]TAAGAGGGGATTGGAGGGAAACTGATTTATCTGTCTTTTATGTGTGCTTACTTGAGGTCATTTTAAAGGGGGAGTTCATCCAAAAAACCTATCAGATTAACTAGCCAAACCCGTGGAAGATATTTAGAAAAATGCGGAAAACATGCAACCACTGACTTTCAATAGTATTTCTTTGTTTTACTTTGCATGTCAATGGTTGCATGTTTTCAGCTTTCTTTGAAATATCTTTTTTGTGTTCAACAGAATGTGATACAAAACCACTTGAGGCTGAGTAAATAGTGAATGCATTGTCATTTTTGGGTGACCTCTCCCTTTAATGTAATTATCATACAACCCGACTTGGGATAAGACATGAAAGGCAATCAAATGCTAGTTTGATGTTTATTGTTAAGTTCCAAAATGAGCCTCTAAACAAGAAATCGAGGGCCTCATGGGAGCTCAGGGGGCAGAAGTCTGTCACAAGATGCATCTGATTAAAGATACAGTTGAAGTCAGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10269
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 |
---|---|---|---|---|---|
ENSDART00000108628 | Nonsense | 502 | 1110 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 6006309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5974492 |
GRCz11 | 11 | 5971747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATACTCCTGCAGATGCTGGCCACGCTGCTGATTATCCGGCAGTTTGTG[C/T]AGAACATGAAGGAAGTCCTGCAGCCCTACCTGGCRGAGCGGCACCGATTR
Long Flanking Sequence:
TTCGATCCGGTGGTTTTTCGCGCGAGAACGGCGCGGGCGCGAACGCCGCGCGCTCCTGAGAGGCGCCCGCCCGCCTGAGACACAAAAAAGCGCGCACATAGGCCTCTCGCGGATCCGCGAAAACAAAAAAAACGCTCGAATACGTACCTCCCTGGACGTAAATCGCGGTCCGCAGAATGAGCAATGAGCCCGGGTTGTAATATTGCCTTAAAATGGTGTTTAAAAAATAAAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGGAGCAAAAATATTATCAGACATACTGTGAAAAATGTCTTGCTCTGTCAAACGTCATTTGGGAAATATTTAAAAGAGAAAAAAAAATAAAAAACACAGGAGGGCGAATAATTCTGACAACTGAATATCAATTATCAGCCGTTTAGATAGTGAGAATGTAACTTTGTGGTGTCCATACTCCTGCAGATGCTGGCCACGCTGCTGATTATCCGGCAGTTTGTG[C/T]AGAACATGAAGGAAGTCCTGCAGCCCTACCTGGCGGAGCGGCACCGATTGGGTGAGCTGACGCTGAGGGCCGTTTGGGAGCTGCTGGTGTCGGCACTGCTCAAATATGGTCGTCTCGCAGCAGGACGAGCACAGGTCTCACCCAGCGACCCAACAGTGCTCGGGCCAGGTCTGCGAGGTCCACAGATGGGTGAGGAGGGACACCAAGATAGACGAGAACGCAAGTGTCTGAACGGTGGCTGCGGCGTCCCGGATGAAGACATGGAGGAGGAACACGGGGAGAGGCACAGCGAAGAAGAAAACGAATCCGAGAGCCTCATTGACTGCGGCCTGAAGCTACGCAAGGTCAGCTTCATCGAGAAGGTGGAGCGCAAGTCTGCGAGCTGCGTCAGCCCAGTGGACGACAGCTTCCTGGAGGAGGGGAGTCCCACCATGGTGGAGAGGGGCATGGATCCTGCATCGGTTTTCGAGATGTGTGATGATGAGGATGAAAACGGGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41773
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 |
---|---|---|---|---|---|
ENSDART00000108628 | Nonsense | 717 | 1110 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 6005664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5973847 |
GRCz11 | 11 | 5971102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTGACAGCAAGACCAAGAGAGATTCGTGGATGGATCCTCCTGAGGAG[C/T]AAGAAACCAACACACTCACACAGGCAGAGGTTGAGGGCTGCATGCAAACG
Long Flanking Sequence:
GCGACCCAACAGTGCTCGGGCCAGGTCTGCGAGGTCCACAGATGGGTGAGGAGGGACACCAAGATAGACGAGAACGCAAGTGTCTGAACGGTGGCTGCGGCGTCCCGGATGAAGACATGGAGGAGGAACACGGGGAGAGGCACAGCGAAGAAGAAAACGAATCCGAGAGCCTCATTGACTGCGGCCTGAAGCTACGCAAGGTCAGCTTCATCGAGAAGGTGGAGCGCAAGTCTGCGAGCTGCGTCAGCCCAGTGGACGACAGCTTCCTGGAGGAGGGGAGTCCCACCATGGTGGAGAGGGGCATGGATCCTGCATCGGTTTTCGAGATGTGTGATGATGAGGATGAAAACGGGGCTCCGGAGATGAAGGAGCTGGCAGCAGAGCCGCTGCCGACTGGAGTGGAGAACAGCTCCTCGGTAAAGCTCAGGAAGAGGGGACGCAGCTTAGAGAGAGCTGACAGCAAGACCAAGAGAGATTCGTGGATGGATCCTCCTGAGGAG[C/T]AAGAAACCAACACACTCACACAGGCAGAGGTTGAGGGCTGCATGCAAACGTACCAGGTCAGAACACTCTCCATACTGTAGTGAATTAAGCTCATGACATTATTAATATTAATAATTATTAATAACAAGTTATTATTTAATTATGAATATTTGGGTTGACTTCATTGCTAATGGTAACCGAACTAAAATTACATTAAATTGAACAACTCATCTGTTGGTGCCTACAATTTATTTGTCTGTTAATTCATTCATTTTCTTTTTGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGTGTAATGAACCGCCAACTTATCAGCACGTTTTTTATGCTGTGGATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCATACACACTCATTCACACTCATACACTACGGACAATTTAGCCTACCCAATTCACCTGTACCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACGAACGCAGGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13612
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 |
---|---|---|---|---|---|
ENSDART00000108628 | Nonsense | 797 | 1110 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 6004062)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5972245 |
GRCz11 | 11 | 5969500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGCACCAGCCTACAGAGACCGYTCGGCCTGAGGGTGGCGAGCATCGGA[C/T]AATGGCAGGTTCGACAACACTGACTACTCTAAMAAATCCTTAATATACKC
Long Flanking Sequence:
AGGGACTAAGCTGACGGAAAATGAATGAATGAATATTACAGTGCTTTTTTATTATTTTGATTAAATAATTACAGCCTTTTGTGAGGATGAGACTAAAAAAACACATTAAAAATCTTACCAACTCCAAACTTTACAGTGTCTATCAACATTCATAACAAAACACAATGGTTTCCAACTAAACGTTTGATTGTGTGTGTTATCAGAAAAGCAGTCAATGTCTGTGTGATTTAGATTACTGCTATTCTCTCCCTGCAGTCAAACAGACACTTTCAAAATAACGTGAAGCATTTAAAACAGCTCTGTCAACTGCTTTTCAGGACACATTTCAGGACTACCAGGAGATGTTCGTCCAGTTTGGATATGTGGTGCTCTTTTCCTCTGCCTTCCCATTGGCCGCCATGTGTGCCCTCATCAACAATATCATCGAGATCCGGAGTGACGCTTTTAAACTGTGCACCAGCCTACAGAGACCGTTCGGCCTGAGGGTGGCGAGCATCGGA[C/T]AATGGCAGGTTCGACAACACTGACTACTCTAACAAATCCTTAATATACTCTTGAAGAACAAAATGTATTCTTTTGATGCTGTTCCAGGAGTGTCTTTATGTAATACGGTTATGTAAAAGTCCTGTATCATTGCACAGACAGTGATGGAAGCCATGGGTCTGATTGCCATCATAGTGAACTGCTATCTGATTGGTCAGTGTGGGCAGCTTCAGAGACTGTTTCCCTGGCTTAGTCCAGAGATGGCCATAATCTCTATTGTCATCCTAGAGGTACGTGCACACATACACACACACACACACGTTTGTACAGCTATCTTTATGGGGACTTCTCATTGACTTAATGTGTTTTCTACTGTATATACTAAGTGTATATTCTGTTTATCTTCCCCAACCCTAGCCCTAAACCAGTGTTTAATTGAGCCAAATCTTGCCAGATCCTGTTCCGCAAAATGTCAGATATTCCTGCTTTGCATTCCTGTATTTATTTTAATAGATCCGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38823
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108628 | Nonsense | 1093 | 1110 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 11 (position 6000310)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 5968493 |
GRCz11 | 11 | 5965748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGTCTGACCTCAATGGGGTGCCGGACGAAATCCCATCTCCTTGTGGA[G/T]AGAATGGGGAAAATGGATCCTCATCCGATGCTGATCCATCAGGCCCTAAG
Long Flanking Sequence:
ACCACCACCATGAGAAGAGCCAGAGTGGCAAAGCCAGATCAGGGGGCGGAGGAGGCTCTTCTGGCGGAGAGAAACCCAAGCGGCCCAGCTCGCTTCTTGGCAACAACAATGTGATGAAACTGAAGCAGATCATCCCTCTACAGAATAAGTTTTCTTCCGGCACAGCTCGTTCCCCACAGTCACCCACAGGGAACGAACCTAAGCTACCAGGTTTCCTCAGTTTCAAGTTCCTGAAGTCTCCAGAGAACAAGAAGGAAGCGGCGATGGCTTCTGCCAGTGCGTCAGTGGCTCCCCCAGTCCAGGAGAAGGTAGAGAGGTCCCAATCACCCAACAAGTCCTTCAATCCCGGCAAACTTTTTAACTTTGGTAAATCGGAAGGTGGTGCATGTGTGAACGGGGCTCAGCTTTCAAAACTAGGGGATGGGGGACAGATGCAGGACAAGCCCCCAACAAAGTCTGACCTCAATGGGGTGCCGGACGAAATCCCATCTCCTTGTGGA[G/T]AGAATGGGGAAAATGGATCCTCATCCGATGCTGATCCATCAGGCCCTAAGATGTAACATCAAAATAATCGTCAATAAAAAAAAATAAACAGTGTGAGAAACTACTTAGTAAGAACGAGGGTGGGAGAGTGTGGAGAGGAATCTCCTCGCCTGAGGCTGTGCAAGACTCGACCTGGAAGCTGTTGAGTAAAAGACATAAGGGGGAATTCACTAAAGGTATACTTCATTTTCCGTGTTCCGCTCCATCTAGCGCACAACTGAGCACTGAAATCATTTGCACACGCACTGCTGTACATGCACAAGTCCACGTGGACTCAAAAATCGAGCTGCAAACAGACAGTAGGGGTGTGCGATATTTATCATCCAGGGTGATATCATCATTTTGACAATGTACTAGCTGACATTATTGAATGTCGTGCTGTTTGAAGAAAGCAAAAAAACGTTTTAAGAGTCTGATAGCATTTACTGCAAGATGTAGCATATTAGTACAATTAGATTTTT
Associated Phenotype:
Not determined