ZMP
actl6a
Ensembl ID:
ZFIN ID:
Description:
actin-like protein 6A [Source:RefSeq peptide;Acc:NP_775347]
Human Orthologue:
ACTL6A
Human Description:
actin-like 6A [Source:HGNC Symbol;Acc:24124]
Mouse Orthologue:
Actl6a
Mouse Description:
actin-like 6A Gene [Source:MGI Symbol;Acc:MGI:1861453]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8548 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40709 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8548
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 |
---|---|---|---|---|---|
ENSDART00000104303 | Nonsense | 130 | 429 | 5 | 14 |
ENSDART00000130813 | Nonsense | 130 | 428 | 5 | 17 |
The following transcripts of ENSDARG00000070828 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 29104071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 29399714 |
GRCz11 | 6 | 29390275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCATTTGACTCACGCRATCTTGATTTGTTCATCCKGCAGTGGAACACA[C/T]GAGCGAARAGAGAGAAGCTGACGGAGCTGATGTTTGAGCATTACAAMATT
Long Flanking Sequence:
GTAACTCATTTGTTTTTGTTTATTTTAATCTAAAAAAACAAAAACAAATCACCTTTCACTGCCATTATATGAATCACCAAGGACCACAGATTTAGCCAAAAGTCTTCATGTTCTACTGAAGAAAAAGTCACCTACATCATTAAAGACCTGTGTATAAGTAAATTAACAGGAAATTTGTGTGAACTATCCGTTTAAGCAAATCACTTTTGAAAAAAAGTGATGTGACATCTTTCACTGACTCAAATACCCATCTATTTCATGTGTTTTTTTCCCTTTCTAAAGTTGAGGACTGGGACAGTTTTCAAGCCATTTTAGATCATACCTACAAAATGCACTTCAAGTCACAGCCCGGTCTGCATCCAGTCCTGATGTCAGAGGCCTCGGTATGTAAATATCATGGCATAGAACTCGAACCTGCAGAAAACATCACGTGTGTAATCTGCTAGGATGCTTCATTTGACTCACGCGATCTTGATTTGTTCATCCTGCAGTGGAACACA[C/T]GAGCGAAAAGAGAGAAGCTGACGGAGCTGATGTTTGAGCATTACAACATTCCCGCTTTCTTCTTGTGTAAATCAGCTGTGCTGTCAGCGTATCCTTCATTGAAAATGTTGCATACATCTTTGTGAAAGGCATTGTCATGTTTAAAGGTGGCTAAAGCTTGCACTGAAGCAGAGGAATGATTAAAGATGATTTCTATTTGATGTACAGCCATGTTATGCATATTGAAAGTTCAGAATGTTAAATCCTTTACTCAGCATTTCAGGTTTGCCAATGGACGATCCACAGGCTTAGTGTTAGATAGCGGAGCAACACATACTACTGCTATTCCAGTGCATGATGGTTATGTCCTACAACAAGGTAATTCAATTCAACACATTAAGACTTCAATATTAATATGCTAGAATTTAATTTGTAAAATAAATTATTAATTTTTAAAGCGTTATACAAAATATTACACCAAATTAAGATGTTATACAGTGAATCTGTGGACTTAATATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40709
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 |
---|---|---|---|---|---|
ENSDART00000104303 | Essential Splice Site | 277 | 429 | 9 | 14 |
ENSDART00000130813 | Essential Splice Site | 276 | 428 | 12 | 17 |
The following transcripts of ENSDARG00000070828 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 29105545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 29401188 |
GRCz11 | 6 | 29391749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTCAGGCCTCTGTGCTTCAGGTGTCAGATTCACCCTATGATGAACAG[T/C]AAGCTCAGTTTCTTTCCTTTCACTAATACAGCTTAAATAGCTTGTGGTCA
Long Flanking Sequence:
ATTCATATTTAAAATGGGGTGTACTCATTAATGCTGAGCATATATATTTAACTTTTATTTTGTTTCTGCAATCTGTTTTATAATTTTCCAGGCATCGTAAAGTCTCCTCTTGCTGGTGACTTCATGAGTATGCAATGTAGAGAGCTGTTTCAAGAGTTAGGTGTTGAAATAGTGCCTCCTTATATGATTGCATCAAAGGTAAGGCCTTTTGAAGGTTATGATTCTCAGTTGATAAAAATGTTTGAATCAAATAATTTCATTATGTTTTCATTAAAGGATTCAGTTCGTGAAGGCACTCCTGCTAGTTGGAAGAAAAAGGAGAAACTACCTCAAGTTACCCGATCATGGCATAACTATATGTGTAATGTAAGTTATCAAAGCTATCATTAATGGAGATATGTGAAGAAAATCTTAAATGTTGCAATTTGTGATTTCAGACCGTCATCCAGGATTTTCAGGCCTCTGTGCTTCAGGTGTCAGATTCACCCTATGATGAACAG[T/C]AAGCTCAGTTTCTTTCCTTTCACTAATACAGCTTAAATAGCTTGTGGTCAATATCAGTGATTTATTTAGTCATAAATCAATGTTTTAATACAGCACTTTTAATAAATTTATTTAAATGACATAATGCCTTTAACATTTGTATTCAAAGAAACAAGTGAAACCTGAAAGGCATAATGACTGTCTTCATGGAAATATTAAAGGGATAGTTCACCCAAATTGAACTTTTGGAAACCGATAACTTCCATAGTAAGAAAAATAAATACTGTGGAAATAATTTCTAAATTTTTCTTAATCCTAGAACTACCGAGGTGGTCATTTTGACCATTTTTTATTTGTTTAATTGAATAACTTTGTTGAAATAAGAACCCCATATCTATAATACCCTGACTTTTCCTAAATATCTTTATATTTCTTTCTAACATTGCTATTTTATTAAAATGACAAAACACTCTTGAGTATTTTTACCTGTAATTATATATTATATAGCAACTCTTTGCTAA
Associated Phenotype:
Not determined