ZMP
si:ch73-177h5.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate transmembrane protein 16F (TMEM16F) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
ANO6
Human Description:
anoctamin 6 [Source:HGNC Symbol;Acc:25240]
Mouse Orthologue:
Ano6
Mouse Description:
anoctamin 6 Gene [Source:MGI Symbol;Acc:MGI:2145890]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16196 | Nonsense | Available for shipment | Available now |
sa40199 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30845 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33353 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40198 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20176 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16196
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087835 | Nonsense | 401 | 910 | 11 | 20 |
ENSDART00000139586 | Nonsense | 356 | 764 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1753604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 2043659 |
GRCz11 | 4 | 1892972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGACTCTGTTCTTGGAGTTCTGGAAACGTTACCARGCCAAACTGGAGTA[C/A]AAGTGGGACACAGTGGAGTTTCAGCAGCAGGAGGAGCAGCCCAGGYCTGA
Long Flanking Sequence:
TCAGAGGGGGAAAGCCCCGCCCATCAGTGATGTATAACTAGCCCTGAGTGAGAGGCAGCCATTCTCCATTAGAGTTTTGATCTGCCTTAAGATAATGTCAGCGACTTAGAGGATTATAAATGTTACGTTTTTTAATCTACCATTTTGCTGACACAAAGGCATTTGTAGCTCCGTCCTTTTCGAAAAGAGCACCATCTCATTTGCATTTAAAGCGACAGTCACCAAATCTACATAATTTGAATCAAAGCCTAACAGGGTCAGTTAGGGTCAGAGAGTTATAAAGCATTATTTGTGTGGTATTGTGTGCTGAAACTTCACACACACACACACACACACACACACACACACACACACACACACACACACACACACTCTAGGGACATCACAGACACTTTACATCTTGTAAAAAGCTCCTGAGGTTTTAATATACAGTATGTTTTATCTTTTACAGTGACTCTGTTCTTGGAGTTCTGGAAACGTTACCAGGCCAAACTGGAGTA[C/A]AAGTGGGACACAGTGGAGTTTCAGCAGCAGGAGGAGCAGCCCAGGCCTGAATATGAGGCTAGATGCACCTATGAACGATTTAGTCCTATCACACAGGTACCTGTACTGGAAACTCTGGTTTTCACATTGTTTTTACATCAACAATGTGCACATAAACACCTCAGATCTAACCTGTAGCGGGCTTTTGTGTTTCTTTACACAGTCCAATGAGAAGGTGCCGTATACAGCCTGTGGAAAGTGCATGAGAGTGTCGTGTGGCATTGGCACTGTGCTTTTCTGGGTAATGACTGTCCATTATACATTTAATTATGATGATAATTACATCTAAATATAATGATCATCATCTTAAAGTCTGCATTAAATCAAAATGTACAATGTTTATTTTGTTAGTGAAATTGTTAGTCTTAAGGTTAATAATTAATCACTGTTTGTCATAGCTTGTTTTGGTAATCTTTAAATAAAATCTGCCCGTCTGCTTCCGCTTTGAAGTGGCAGTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40199
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 |
---|---|---|---|---|---|
ENSDART00000087835 | Nonsense | 482 | 910 | 13 | 20 |
ENSDART00000139586 | Nonsense | 437 | 764 | 11 | 16 |
ENSDART00000087835 | Nonsense | 482 | 910 | 13 | 20 |
ENSDART00000139586 | Nonsense | 437 | 764 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1749891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 2039946 |
GRCz11 | 4 | 1889259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTGGTCGGGGTGATTGTGTATCGTTTGGCGATGTTTATGGTGTTCT[C/A]GATGCAGCTGCGCTCTGACCTCAATAGAAAAGAGCTGGAGCCGTTCAGAG
Long Flanking Sequence:
TGAAATTAAGCTCCACCCTCTAATCAATATTAAATTTTATTTGTGAATACATCATCATAATGAAATTAAACCCCACCCCCTAATCAATACTCAATTTCAATTAGAAATACATCATCATACTAAACTCTGCCCCCCACTCAATATTCAGTTTCAGACTGAAATACATCATCATACTGAAATTAAACTCCGCCCCCTACTTAATATTCAGGTTCAGTCAGAAATACATCATTGTAATGAAATAAATCCCACCCCTACTCAATGCTTGGTTTAAATTGGAAATACATCATCATACCAGTCAGAAATACATCATCATACTGTAATTTAACCCCGCCCCCTACTCAATATTCAGATTCAGTTGGAAATACATATTCATACTGCATTGTTGTTGGAAATGTTAACTGGTATGTACATGCTTCTTTATCATCTTGTGTAGATTCTGTTGATCGTAGCGTCAGTGGTCGGGGTGATTGTGTATCGTTTGGCGATGTTTATGGTGTTCT[C/A]GATGCAGCTGCGCTCTGACCTCAATAGAAAAGAGCTGGAGCCGTTCAGAGAGTACATCACGCCTCAGATGGCCACATCCATCACCGCCTCCATCATCAACGTCATCATCATCATGATCCTCAATATTGTCTACGAGAAAGTGGCCGTCTGGATCACAGACTTCGGTCAGTCTCTGGTTTCATCTGATGTTTTTGTGCCAGCCGAACTCCTCTCATATTATATACAGTGGTTAGCACTGTCGCCTCACAGTAAAAAGATCGCTGATTCGAGTCCCGGCCTGGCCAGTTGACATTTCTCCCCGTTTTGGCGTGGGTTTTCTCCGGGTGCTCTGGTTTCCCTTCACGGTTCAAACACATGCGCTAGAGGGGAATTGGATGAACTAAATTGGCCGTAGTGTATGAATCCTTGTGAAAATGCGAGAGTGTATAGGTGTTTCCCAGTTCTGGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAAAATTTGCTGGAATAGTTGGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30845
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 |
---|---|---|---|---|---|
ENSDART00000087835 | Nonsense | 482 | 910 | 13 | 20 |
ENSDART00000139586 | Nonsense | 437 | 764 | 11 | 16 |
ENSDART00000087835 | Nonsense | 482 | 910 | 13 | 20 |
ENSDART00000139586 | Nonsense | 437 | 764 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1749891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 2039946 |
GRCz11 | 4 | 1889259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTGGTCGGGGTGATTGTGTATCGTTTGGCGATGTTTATGGTGTTCT[C/A]GATGCAGCTGCGCTCTGACCTCAATAGAAAAGAGCTGGAGCCGTTCAGAG
Long Flanking Sequence:
TGAAATTAAGCTCCACCCTCTAATCAATATTAAATTTTATTTGTGAATACATCATCATAATGAAATTAAACCCCACCCCCTAATCAATACTCAATTTCAATTAGAAATACATCATCATACTAAACTCTGCCCCCCACTCAATATTCAGTTTCAGACTGAAATACATCATCATACTGAAATTAAACTCCGCCCCCTACTTAATATTCAGGTTCAGTCAGAAATACATCATTGTAATGAAATAAATCCCACCCCTACTCAATGCTTGGTTTAAATTGGAAATACATCATCATACCAGTCAGAAATACATCATCATACTGTAATTTAACCCCGCCCCCTACTCAATATTCAGATTCAGTTGGAAATACATATTCATACTGCATTGTTGTTGGAAATGTTAACTGGTATGTACATGCTTCTTTATCATCTTGTGTAGATTCTGTTGATCGTAGCGTCAGTGGTCGGGGTGATTGTGTATCGTTTGGCGATGTTTATGGTGTTCT[C/A]GATGCAGCTGCGCTCTGACCTCAATAGAAAAGAGCTGGAGCCGTTCAGAGAGTACATCACGCCTCAGATGGCCACATCCATCACCGCCTCCATCATCAACGTCATCATCATCATGATCCTCAATATTGTCTACGAGAAAGTGGCCGTCTGGATCACAGACTTCGGTCAGTCTCTGGTTTCATCTGATGTTTTTGTGCCAGCCGAACTCCTCTCATATTATATACAGTGGTTAGCACTGTCGCCTCACAGTAAAAAGATCGCTGATTCGAGTCCCGGCCTGGCCAGTTGACATTTCTCCCCGTTTTGGCGTGGGTTTTCTCCGGGTGCTCTGGTTTCCCTTCACGGTTCAAACACATGCGCTAGAGGGGAATTGGATGAACTAAATTGGCCGTAGTGTATGAATCCTTGTGAAAATGCGAGAGTGTATAGGTGTTTCCCAGTTCTGGGTTGCAGCTGGAAGGGCATCCGCTGTGTAAAAAATTTGCTGGAATAGTTGGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33353
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 |
---|---|---|---|---|---|
ENSDART00000087835 | Nonsense | 672 | 910 | 17 | 20 |
ENSDART00000139586 | Nonsense | 627 | 764 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1746037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 2036092 |
GRCz11 | 4 | 1885405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGCTGTGAGTTTCAGGATTATCTGAATGTCTGCTGCGTTCCAGTGATC[C/T]AGTTTGGCTTTGTGACTCTGTTTGTGGCGTCTTTCCCGCTGGCTCCTCTT
Long Flanking Sequence:
TTAGTTCTAAAATACATACATAGTATATTAAAATACATGCATAGACACCGGCTTATCCCAAAAGATAATATGATGATGCACAAGAGGCATCATTATGCAAAATTATATTTCTCCGCTTTTATTTACATTTGAACAAAAACTTTGTCGAAATTTTCCAGGGGTATGAATAAATTCAGGCTTCATTATATATCAACATTTACAGTAAAAGTAATATTTTCTCTTCAAATTGTAATATAAAATGTAGTGTTTGCCATCAGTAAAAAGCGCTTCATTAATAAGCGATGGTGTTTCTAGGTGGCTGAAGAATCTGATGTTTCGTCATTGCACCCAGGTGGGATCAGAAAAAGCGATTCCTCGCTGGGAACAAGACTATCAGCTCCAGCCGATGGGAACACTCGGCCTGTTTTATGAATATCTGGAGATGGGTAAGATGTCAAAATCAAACATGTTATCGCTGTGAGTTTCAGGATTATCTGAATGTCTGCTGCGTTCCAGTGATC[C/T]AGTTTGGCTTTGTGACTCTGTTTGTGGCGTCTTTCCCGCTGGCTCCTCTTCTGGCGCTGGTCAATAACCTGTTTGAGATCCGTGTGGACGCCTGGAAGTTCACCACTCAGTTTCGTAGGATTGTCCCAGAGAAAGCTCAGGACATCGGAGCCTGGCAGCCCATCCTGCAGGGGGTGACCATTCTGGCGGTGGTCACTAATGTAAGTCCAGAACATGGATTTCTTCATTTGAATTTGCTGGTGTTGATTCTTAAATATTGAACATTTTTATTTTAGTCACTGCTGTTTTCTAAACTGCACTGAACATTAGTTGTATGCATGCCTAGCTTCTAGCTTTTAATATTAAAATAACGTTTATGAACTGAAAATGTACTTTACCTTATATAAATGTACATGAATGGAGTTAACTTGTTAACAAAGGTTCTGCGGTAGAACCACGCCTCACTTTGTCTCCTTAACCAATCACCCACTCCCTAAAACTTATTTAAGGCAGACTAGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40198
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087835 | Essential Splice Site | 738 | 910 | 17 | 20 |
ENSDART00000139586 | Essential Splice Site | 693 | 764 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1745835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 2035890 |
GRCz11 | 4 | 1885203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCAGCCCATCCTGCAGGGGGTGACCATTCTGGCGGTGGTCACTAATG[T/C]AAGTCCAGAACATGGATTTCTTCATTTGAATTTGCTGGTGTTGATTCTTA
Long Flanking Sequence:
TAAAAGTAATATTTTCTCTTCAAATTGTAATATAAAATGTAGTGTTTGCCATCAGTAAAAAGCGCTTCATTAATAAGCGATGGTGTTTCTAGGTGGCTGAAGAATCTGATGTTTCGTCATTGCACCCAGGTGGGATCAGAAAAAGCGATTCCTCGCTGGGAACAAGACTATCAGCTCCAGCCGATGGGAACACTCGGCCTGTTTTATGAATATCTGGAGATGGGTAAGATGTCAAAATCAAACATGTTATCGCTGTGAGTTTCAGGATTATCTGAATGTCTGCTGCGTTCCAGTGATCCAGTTTGGCTTTGTGACTCTGTTTGTGGCGTCTTTCCCGCTGGCTCCTCTTCTGGCGCTGGTCAATAACCTGTTTGAGATCCGTGTGGACGCCTGGAAGTTCACCACTCAGTTTCGTAGGATTGTCCCAGAGAAAGCTCAGGACATCGGAGCCTGGCAGCCCATCCTGCAGGGGGTGACCATTCTGGCGGTGGTCACTAATG[T/C]AAGTCCAGAACATGGATTTCTTCATTTGAATTTGCTGGTGTTGATTCTTAAATATTGAACATTTTTATTTTAGTCACTGCTGTTTTCTAAACTGCACTGAACATTAGTTGTATGCATGCCTAGCTTCTAGCTTTTAATATTAAAATAACGTTTATGAACTGAAAATGTACTTTACCTTATATAAATGTACATGAATGGAGTTAACTTGTTAACAAAGGTTCTGCGGTAGAACCACGCCTCACTTTGTCTCCTTAACCAATCACCCACTCCCTAAAACTTATTTAAGGCAGACTAGCCATCTAGCACTGTTTTGAACCTTCCCTTTCTCCCTATGTTTCCTCACTTTCCATTCACGATCCTATAACTCTTTTTACTCTTAGGTTGAATCAGGGGGTCCAGTCACTCTACCAAAATATTACAGAGACAGTACCCCCACTCTGAGTCTCTGGGCATCATCATAGGATACCAAATCAACCTACCTACCTGTTCACTGTTTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20176
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 |
---|---|---|---|---|---|
ENSDART00000087835 | Nonsense | 810 | 910 | 19 | 20 |
ENSDART00000139586 | None | None | 764 | None | 16 |
Genomic Location (Zv9):
Chromosome 4 (position 1741837)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 2031892 |
GRCz11 | 4 | 1881205 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCGATCCTGTGAATAAAAATATTCTGTATTCTGTTTTCTTCTCAGGTA[T/A]CGAGATTACAGGAATCCCCCTGATCATCAGAACCCATATCAGTTCAATGT
Long Flanking Sequence:
GAAACAACTTTTCTTTTATAAATTGATGTGTATATGTGTTGGTTTAGTTATGTTTAATTATGTTTAGCTTTAATAAAACTGGTTTATTTATATGTTTATGTGGCTATATAATAATTTTAATCGTAATAATTATAACAGCATTTTTTTTAAATACATAAACATATATAATTGCATTAATTAGCATAAATAATTTGGCATTATTTCTATTTTTACTTTATTTAATGCTTGCTATAGTTGTATATAAATATTACTGAATGTACATAAATTGTTCTAATTTTACAATATAATATAATTTATTAAATGTTGCTTAATTTATAATGTTTAAATATCCATAGCTCCAAACAAATCAAGAGCCAATCTTTATTGAATTGGCATCCTTTTACTTTTATTTTACAGAGAAATATCCAGATGAATCGATATTAAATCAAACTGATTCAGCTACGAACTCAATTGCGATCCTGTGAATAAAAATATTCTGTATTCTGTTTTCTTCTCAGGTA[T/A]CGAGATTACAGGAATCCCCCTGATCATCAGAACCCATATCAGTTCAATGTTTATTACTGGCATGTCATCGCCGCCAAACTGGCTTTCATGATCGTGGTGGAGGTACGTGACTTAAGATCATCTTATGATTTATTTGACATTTTTGACAGTAAAAAAATCAGTCTTTAATCAAGTGTTGAACTGCGAGAGTGTGTCTGAGCCTCGGACATTATCAGGAAGGCTATTCCAGAGTTTAGGAGCCATAAATAAGAAGGCTCGACCTCCTTTAATTGACTTTGCTGTTCTAGGTACTACCAGAAGCCCTGAGTTTTGAGATCTTAAAGAGCGAGTTGGATTGAAGTGAGACAGAAGCTTGGTTAGATAAACAGGAGCTAGATTATTTAAAGCTTCATACGTAAGAAGCAATATTAAAAAAATTAACAGGCAGCCGGTGTAAGGAGGATAAAATTGTAAAGTTTTTTTTTTCTTTTGTTTTGATCATTGAGCTGACAGAAGCCTGT
Associated Phenotype:
Not determined