ZMP
ano5b
Ensembl ID:
ZFIN ID:
Description:
anoctamin 5b [Source:RefSeq peptide;Acc:NP_001073452]
Human Orthologue:
ANO5
Human Description:
anoctamin 5 [Source:HGNC Symbol;Acc:27337]
Mouse Orthologue:
Ano5
Mouse Description:
anoctamin 5 Gene [Source:MGI Symbol;Acc:MGI:3576659]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40934 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40934
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 |
---|---|---|---|---|---|
ENSDART00000099919 | Essential Splice Site | 355 | 890 | 8 | 18 |
ENSDART00000132504 | None | None | 167 | None | 4 |
ENSDART00000141828 | Essential Splice Site | 380 | 915 | 9 | 19 |
The following transcripts of ENSDARG00000036147 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 34192316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32586656 |
GRCz11 | 7 | 32857806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGATAATGAAGGAACTGTGTTTTTTGCCATGTTCATGGGCATTTGGGG[T/G]GAGTATACTGCCTTTTTTTTCTAGCTTAGTAGCGCCATCTAGTGCATGGC
Long Flanking Sequence:
CATTGTCTCATAACTTAATTTAAAAGTGAAGGCATGAACTCTAGAGGCCTCTTGATATTTTTGTTGGTTTTTCCCTATAGCTCTCACTAATGATTGTTTTGGATCATGCTTAACAGTAGTTGATTTGTTCCAAATTCTCCATGGTGTCTTTGCACTGTTTTTTTTCCCCAGCATGCATAATGAAGATCTGTTGATATTCCCTTCTGCAACATTTCTCCCCTGTCACTTTTTCTCTTTGTGTTTTCAGTAAGGAAATCTGTGACCCAAAAATAGGAGGCATGATTGTCATGTGTCCGCTCTGTGACAAAAAGTGCAGCTACTGGAAACTCAACTCAACATGTCTGTCCTCCTGGGTGAAAACAAGCACTGTTTAAATTGTAAATAACTATTTATTAATCGTATACAGTTTCCTAATTTCTGATCCCTTTTTTTTCTTAGCAATCCCATCTCTTTGATAATGAAGGAACTGTGTTTTTTGCCATGTTCATGGGCATTTGGGG[T/G]GAGTATACTGCCTTTTTTTTCTAGCTTAGTAGCGCCATCTAGTGCATGGCTGGACATTTGTAGTAGCCCCACTCAGAATCTAATGAGAATGAGATCATAATAGCCATGCATGAAGCATTTTAGCGTATTCTTAATGTCAAATAATTGGCCACAGGATTTGTTCACTATATAAATCTACAATAGAGGAGCATAATTTGTGTATGCTTTTTGAAAATGAAATCTGTAATGACTAATGATGCTCACTGATTATCCATTACTGAACACTGAATTAATTTCTCACATGGCTCAAAATGAGCTCTGCTTATGCAGGGATTTGATTAATCAGCACTGTGGATATTCTTTTATCCAGTGTCCTCATTAATTAAAACTGTTTATGTTGCTGCTGAATCTTTGGACTTGAGTACTGTAATGTTAATGAAAGAAAAACAGAGTGTGACTGAAGAGATAAACCTGGTTGGATTTGAATAGAACTAATATTTAGGGTTTGTTCACGCAAAGCA
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa5425
Status:
Allele not cryopreserved
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:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099919 | Nonsense | 572 | 890 | 13 | 18 |
ENSDART00000132504 | None | None | 167 | None | 4 |
ENSDART00000141828 | Nonsense | 597 | 915 | 14 | 19 |
The following transcripts of ENSDARG00000036147 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 34183184)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32577524 |
GRCz11 | 7 | 32848674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTAAAGATTTGGATGTTTTTCATGTTTAGTGTGCTCCTGGAGGTTG[T/A]CTGATTGAGCTGACCACTCAGCTRCTTATTGTCATGGCTGGGAAACAAAT
Long Flanking Sequence:
AAAATGTATGTGCAATCTCTAAGTTTAGTTAGTCATTATTATTACTAAAGAACACTGGGTGCTTTTTTTAATATAACTGACTGTACATTCCCCCCTGACATGTTTATCTTAAACAGTATGAAAAACATTTGCCATTATCTCTCATCTATTTTTAACCCTCAGAAATCCCCAAGACCCATCTGGAGTATGAGAACAAGCTGACCATGAAGATGTTCATGTTCCAGTTTGTGAACTACTACTCTTCCTGTTTCTATGTGGCCTTCTTTAAGGGAAAGTTTGTGGGTTATCCGGGAAACTACAGTTATATGTTTGGAAAGTGGAGCACTTTGAGAAATGAGGAGGTGAGACTCCATGAAATATTACTGTGCTTCACAACCTAATGTTCTTCAGCTGAATTTCACAATATTTTTTGACCTTGTATTTGTTAACTCTTCACTTTTTGAGGGAACCTTTTTTAAAGATTTGGATGTTTTTCATGTTTAGTGTGCTCCTGGAGGTTG[T/A]CTGATTGAGCTGACCACTCAGCTGCTTATTGTCATGGCTGGGAAACAAATGGTCGGGAACGTCCAAGAGGCTCTTTTGCCGTAAGCTTTACAATTTGACATCTATAATTGAGCTAGTGTCTGTTTTAATGCTTGAATATTTGGTTGCATGCATTTTAAGGAGGTCAGAATGTAGTTGTCCTCTAGACAGTTTTCAAATCCCATGTAACCGAGTGAGTAATGGTCCCTTGTGTCACAGACTTGTCCGAAACTGGTGGAGCAGCAGGAAAGGCCGCAGTCATCCAGAAAGCACGTATAGTAGATGGGAGCAGGACCATGACCTCCAGAACTTCAGCCAGTTTGGACTCTTCTATGAGTATCTGGAGATGGGTACGAGTTTACTCTGATATCCATTTTATTTTTTTGCGTTTCTTTTAAATAGTGAATAATAGTTTGTAGATTCACAAAATATATATTTTTTTTACAATACAGTACTCTTCAAAACCTACATTCATAAGTATT
Associated Phenotype:
Not determined
Mutation Details
This allele has been removed from public view.
Allele Name:
sa26984
Status:
Less stringent filtering
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:
n/a
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099919 | Nonsense | 871 | 890 | 18 | 18 |
ENSDART00000132504 | None | None | 167 | None | 4 |
ENSDART00000141828 | Nonsense | 896 | 915 | 19 | 19 |
The following transcripts of ENSDARG00000036147 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 34170855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 32565195 |
GRCz11 | 7 | 32836345 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGGAGAAACTGAAGATGCAGCTAAGCCAGAGTTTCTGCCTATCCACA[G/T]AAACGGCCTCACTGCTGCCCTCTAGTCCAAACAAACACCAGGTGATTTCT
Long Flanking Sequence:
CTAGTAATTTAGTCCTCCAAACAATTTAACAATGTACTTTTATGTATTAAGTCGGGACATGATAAATAGAGCTGAGGTATGGGACTGTCCTGGGAAAAGTTGAATGTCAGGTCACCCTACTCTCATTTTTGGTCAGCCACATAAATCCCTCTTTCTTTGCCTTTTTACCACAGTTTTTTTCTCTGTGCCTTCAGTCTGTCCTGACAGTGAGTGTAAAATCACTAGAGGATTTGCGCTGATCAAGCCGATTGTAAATACGGCCTGAAACATGCACTTTTGGTTTTCTGCACACATGAATGATGGATGTTCCTCTGTTTCTTCTGCTTTCTCAGCATGTTGTGTTTGTGGTAAAGTTCTTCGTGGCGTGGCTCATCCCAGATGTGCCTTCAGAAGTGAAAGCCCGTATAAAGCGTGAGCGCTTTCTGGTCCAGGAATACCTGCACAACTATGAAGTGGAGAAACTGAAGATGCAGCTAAGCCAGAGTTTCTGCCTATCCACA[G/T]AAACGGCCTCACTGCTGCCCTCTAGTCCAAACAAACACCAGGTGATTTCTGAATGTGTCTGAACATCCTCAGGAGGACTACACTTAGATGTACTGTACACTGCAAAGCATGAAGGACTCCTTCATACTGTACATTCAGTGCTAAAAAATAACTCGCCCTCACTCAGACAACTGCCAGAAGTTTTACAAACAGCTCTAAATGTGAAACAACTATACGGTCTGCTTTCATTTTGCTCAAGGTTTATCAGAGAACGTCAGCTTTTGCAATGGATAAAAATGGCAGTGAATTCAACAGCAAACCTTCTGGAATGCAACCCGATGCTCCTCCAGGTGCTGTGAAGGCAACTCGTAAACAATCAGGAAAATCACCATTAAAAAAAGACATTCGGAAATGTTTTAAGAAGGCATTAAGTGTTTCTCTGTCCAGCTTGTTGCCATCTTTGATTTGAAGACATAATCTGCATGCTTTGCTCTGTATGTCTGACTGTGAAAGAGCTCCTC
Associated Phenotype:
Not determined