ZMP
scn8ab
Ensembl ID:
ZFIN ID:
Description:
sodium channel, voltage-gated, type VIII, alpha b [Source:RefSeq peptide;Acc:NP_001038648]
Human Orthologue:
SCN8A
Human Description:
sodium channel, voltage gated, type VIII, alpha subunit [Source:HGNC Symbol;Acc:10596]
Mouse Orthologue:
Scn8a
Mouse Description:
sodium channel, voltage-gated, type VIII, alpha Gene [Source:MGI Symbol;Acc:MGI:103169]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2298 | Nonsense | Available for shipment | Available now |
sa8756 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33913 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33912 | Nonsense | Available for shipment | Available now |
sa20765 | Nonsense | Available for shipment | Available now |
sa9145 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2298
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022761 | Nonsense | 198 | 1958 | 4 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 39389104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39460704 |
GRCz11 | 6 | 39458240 |
KASP Assay ID:
554-2723.1 (used for ordering genotyping assays)
KASP Sequence:
CGAGGTTTCTGTATAGACGACTTCACCTTCCTCAGAGACCCCTGGAACTG[G/A]CTGGATTTCATGGTYATCTCTATGGCGTAAGTATGATAATGTYCTGTAAA
Long Flanking Sequence:
AATAGAGTCAGTAGTGCGTTCACACTGAAAGCTCTAAAAATATAGATTTTTTTATGATTTTTTTTTCACTATATCTTCCTTTCTGTTAAGCAGAAGAAAGAAACTCAAACAGGTTTGATTAAATAGTGGCAAAATTTGGATGTATGGGCGAACTATCCCTTTAATATGTCTGCCCAGTAAGATGCTAGAATAAAATTGTAAGGTAACATCATACTGTATATGTTGTCTTTGCTGTATCCAGTACCACAATACATTTTGACTTTTAGTAAAAAAGGTGGATGAAGCAGAAGAACTATTTAGAATAAACTAGCATTCAATTTAATACAAAAAGTATCTACAAAATATTATAAAATGCACATTACCTGCATGTTTGAACTCATTTTATCGCTCTATGTCAGGTACACCTTCACAGGAATCTACACTTTCGAGTCTCTCACAAAGATTGTGGCTCGAGGTTTCTGTATAGACGACTTCACCTTCCTCAGAGACCCCTGGAACTG[G/A]CTGGATTTCATGGTCATCTCTATGGCGTAAGTATGATAATGTCCTGTAAATTAAACAAGGAAATATTTTGATAATGATACACTTTAAATCTGTTTTTGCATGCAATGGTTGCAGGTTCATAAAACTCTTGTGTGCCGCATTTAACATTAGGCTTTAGTGGCGCTTCAGTTGGTGCCAGCTACTTTAGTAAAATTCTAGATAAAAAATCATCGCTTCAATTTTTGAAGTTACACATGCACTCACATCTCAAACAAGCAAGCTTCTTGTGATTGCTGCATATTTTTACACAGACTTTCAGATTTTTTTTTGGAAAATTGGCAGTGGTGGAAAGAGTAAAATCCTACGCAAGTAAAAGTACCATTAGTAGAATAAAAGTATCTGTTAGTTTCTACTCAAAGTATGAGTAAAAGTAACCCTTCTAAAAGTAGTGAGTATGCTACACTGAGAAAACAATTCCATCTTATAACCTGCAAATTAAAAATGTAGCTTAAATAAATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8756
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 |
---|---|---|---|---|---|
ENSDART00000022761 | Nonsense | 1012 | 1958 | 16 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 39349094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39420694 |
GRCz11 | 6 | 39418230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CYGAAGAAGAAACCTCTGGAAGATGAAGACAAACCGCTYGATGACATRTA[T/A]GACAAAAAACTGAACTTAATGGGCAACCACACCGGYGTGGAAATCAAATG
Long Flanking Sequence:
TCACTCTAAAAAAAGCTGATTCTCTCTATATATTTTCTTTTCTCCAGTCATTTGTTGAAATATTTTTCTATATAATTTTTATTCCCAATATTATGCAGACCTATAATTGGCCCCTATATATTATAATAATTAGTGGATTAAATAATGGCCACTTATTTGGAAATCATCAGAAAATGATCATCCCGGATTCATTGTGGCCATTAAAGTGGACATATTAAACAGAAATGAACAAGTTGCACAGCCAATAAATGTGAAATCTAAAGCGCTCCTGTTTCTCTTGACCAGGTGCTGAACCTGTTCTTAGCCTTGCTGCTGAGCTCCTTCAGTGCTGATAATCTGGCTGCCACAGATGATGACGGTGAGATGAACAACCTGCAGATCTCCGTCATCCGCATTAAGAAAGGCATTGCTTGGTTCAAAATTCATGTACGGCTGCTGGTGGCCCACGTCCTGAAGAAGAAACCTCTGGAAGATGAAGACAAACCGCTTGATGACATGTA[T/A]GACAAAAAACTGAACTTAATGGGCAACCACACCGGCGTGGAAATCAAATGTGGTGATCTGAACTACCCCAAGAACGGGAATGGCACCACAAGTGGCATTGGGAGCAGCGTGGGAAAGTACATGATTGATGAGGAGCCCATGTCCTTCATCCACAACCCCAACCTGACTGTACGGGTTCCCATTGCTGTTGGAGAGTCCGACTTTGAGAATCTGAACACGGAGGACTTCAGCAGCGAATCGGATGTGGAAAATAGCAAAGATGTGAGTATTATTAAAGTTTCTTCAATGAAGTTGGCTTTGTTTGCAACAACTTGCAAAGTTTAATTTGTAGTTGAATGGAAAATTGCTGACATTTGATATTAACTTATATGTACTTGCATAAAAAATAAATATAATATATTTACTGTGTTCATAATGTATTCTGGCAGAACACTTATGGTAGTCTTGAGTTGGGATACGGGTATGGTTAGGGATAGGTTTGGTGGTATGGGTAGGTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33913
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022761 | Nonsense | 1174 | 1958 | 18 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 39340703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39412303 |
GRCz11 | 6 | 39409839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGGTGGTTTCTGAGGAAAACTTGCTACCTCATTGTTGAGCACAACTG[G/A]TTTGAGACGCTCATCATTTTTATGATTCTTCTCAGCTCTGGAGCTTTGGT
Long Flanking Sequence:
AGTACTTTGAAATACTATAAGATTATATACATAATTTATAGAAAAAAATAAGTCCGTAAAACAACAGAAAACGTACTGGCAGCTTATTACAAGGTTTTTGTAACGTAACACACAGCAACAACCCAGGCAATATATGACTTCAAACAATTAAAAATGTTAATAAAAATAACTTTTTTTTCAAACTTTTCAAAGTTAAGTCCCACAATGCAATTTGAAAGCATAAATAAACTGGGAAATATTCAAAATAAATCACAAAATACAGAAAACAGCTAATTTTCAGTTTTTTTTTTTACAGTGTACATCTGTTTTACTTTTAGAACTACTAAAAAACTTACATTTTAAGTCTGGGTATGATGTAAATGTGTATTCAGCTTACATGTTTGATGTTTTTCAGCTTGTGTGGCGCGCTACAAATGTTGTGATGTGCCTATTACTGAGGGCTGGGGGAAGTACTGGTGGTTTCTGAGGAAAACTTGCTACCTCATTGTTGAGCACAACTG[G/A]TTTGAGACGCTCATCATTTTTATGATTCTTCTCAGCTCTGGAGCTTTGGTGAGGACACACACATTGCATAACTTTCTAAGAGACAAAAAAAACAGCAGCTGAAATTATTTGTTACTAATTTCTAAAAAGTGTGAAGACGTACACATTGGTGTTCAAATCAGCTTTGTATACAACTGAAGTCAGATTTATCAGAACCCTTTGAATTTCTCTTTCTTTGTAAAATATTTCCTAAATAATGTTTAACAGAGCGAGGACATTTTCACAGTATGTCTGATAATATTTTTTCTCCTGAAGAAAGTCTTGTTTGTTTTATTTCAGCTAGAATAAAATCCGCTTTTAATTTTTTAAAAATCATTTTAATGTCAAAACTATTAGCCCCTTTAAGCAATATTTTTTTCGATAGTCTACAAAACAAACCTTCGTTTTACAATAAGTTGCCTAATTATCCTAACCTGTCTAGTTAACCTAATTAAGCCATTAAATGTCACTTCAAGCTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33912
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 |
---|---|---|---|---|---|
ENSDART00000022761 | Nonsense | 1310 | 1958 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 39329028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39400628 |
GRCz11 | 6 | 39398164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTTTGGTGGGTGCCATTCCCTCCATCATGAATGTGCTGTTGGTGTGTT[T/A]GATCTTTTGGCTGATCTTCAGTATTATGGGTGTCAACCTGTTTGCTGGAA
Long Flanking Sequence:
AACTTAAAAGTTGACAATTGTATTTTTATGTATATATTAAAATATAATAATATATTATTACAGTATATAATTATAATATACTATAATTATAAAAGTTTGTAGAATATTATATTATATAATTATAATATATTATAATGAAAAACTTTTGTAGATTTAAATTCATGTAGATACCAAAATGTGATGAAGAATTCTATATATAGCTTATTTGTCATTATTAAACAACTGACAACAAAAACTAAATACTGTTGTCATGGAGATAAATTTTTCTTTGTCAAAGTATGTCATGTGAAAATGCGATTAAAATGAGCTTGGAGATATATACATTAAATGCTGGTCATTGGCATATCAAAATAGCTCAGTTTTGGTACATTACTCTAATACTTTTTCTGTCTTTTCTTGCCCACTTCCCCCGATTCTGTTGTTGTTTTTTACCCTGTAGGTTGTGGTGAACGCTTTGGTGGGTGCCATTCCCTCCATCATGAATGTGCTGTTGGTGTGTT[T/A]GATCTTTTGGCTGATCTTCAGTATTATGGGTGTCAACCTGTTTGCTGGAAAGTACTATTACTGCTTCAACCAGACTGCAGAGGAGTATTTTCAAGTCGACGTTGTCAATAACAAGACCGAATGCTTTGCACTCATCAATGCAAACTACACAGAAGTTCGCTGGAAGAACGTAAAGATCAATTTCGATAATGTGGGCGCAGGTTACCTGGCACTCTTGCAAGTGGTAAGACATTGTCCCTGTGTAAAAATTCTCTGAATACCCACTAACATCCCAGTTCTTAATGCTTGATGAGTAAACCAGTCTCTTCATGAATTCACAAATTATAAACACAAACATACAATTAAATATTAATGACTACCACTGTGGATTGAGCTAGTTGTTTTTCCATGACATAGGCTACATTCAAAGGCTGGATGGACATCATGTATGCTGCTGTGGATTCCAGAAAGGTATTTTTCTACTGTACATATTATATTTCTTTGCAAATGGAGACCCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20765
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022761 | Nonsense | 1554 | 1958 | 25 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 39325891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39397491 |
GRCz11 | 6 | 39395027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCCTTCACTGGCGAGTTCGTCCTGAAACTCTTTGCGCTGCGACACTA[T/G]TATTTCACCAATGGCTGGAATGTCTTTGACTGCGTCGTTGTCATTCTGTC
Long Flanking Sequence:
ATGTCGATTTCGATTACTTTTTAATTAATCGTCCAGCCCTATTTACATTTGAATACATTTTAAAATATTAATTCAACAGTTTTACATTTTCATTTGTCAATTGACTAAATTTATTTATTATATTACATTTAGCTACATTTATAAAAGTTTAAAATGGTATTTTAACTATTGATTTGTAATGTCATTTTTTATTTTATGAATTTCTTTAGCTTTTTTTATTATTAGATGAAGTCGCACTTCTAGTCCACTGTTGTAATTGTGCGCCAATGTGTGTTTTCTTTCTCATAGAACAAAATCCAGGGGATGGTATTTGACTTTGTCACTCAGCAGGCCTTTGATATTTCCATCATGATGCTCATCTGTCTTAACATGGTAACCATGATGGTGGAAACAGATGATCAGTCAGACGAGACAGAGAACATCTTGTATTGGATAAACTTCGTATTCATCGTGGCCTTCACTGGCGAGTTCGTCCTGAAACTCTTTGCGCTGCGACACTA[T/G]TATTTCACCAATGGCTGGAATGTCTTTGACTGCGTCGTTGTCATTCTGTCCATTGTGGGTAAGTGCTGTGTCTAAATGTTTTTTTCTGTTTTCTAAAGTACCCAGCATGAACTAGTACATCCTGACAGATTTTTCCTTTAAATTACCTTTCTATGGGATCTTATACAAAAAGATATTTGTGCAGATCTGTTTTTAAGTTCTGTTTTAAGTCAATTAGTTAGTCTTACTATTCTATCAAATTAAGTTAAGATCGTGGTGCAAAAAAATGAGTACACCCCAATTAGGAGAACTCAGAACATAACATTTGAATTCACCAGCAGATGAGTCAGATCAACTCCCACTTACTGCAATGCTGACACAATGACATCAAATGGAAAAATGCCACAATACAAGTGTCACTTTGATAAGGAAGGACAAAGCTATAGGAAAGCTTTGCTAGTAAGTATGAAAAATGTTGCTGTATGATAAAAAATAGAATTTTGGGACGATTGCTGGGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9145
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022761 | Nonsense | 1682 | 1958 | 26 | 26 |
Genomic Location (Zv9):
Chromosome 6 (position 39324138)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 39395738 |
GRCz11 | 6 | 39393274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGGCAACAGCATGATCTGTCTATTCATGATCACCACATCAGCTGGCT[G/A]GGATGGCCTGTTGGCTCCTATCTTGAACTATCCGCCTGACTGCGACCCTA
Long Flanking Sequence:
GTTATCAGTTGTAAACATTTTTGTAACAACTTGTTTGAACTCCATGTATAATTTTCACAAGATCATATTCTTGTGTTAATAAAAATAAACCAAAATTTTAAAGGGGGTGTACTCATTTATGCTGGGCACTGTACATTTTGTAAGGTTTTGTAATGTGTTTTCGCTTGGTTTTTCAGGTATGTTCCTGGCAGACCTCATCGAGAAATACTTTGTCTCACCAACTTTATTCAGAGTAATCCGTCTGGCTCGAATCGGCCGAATCCTGCGTCTGATTAAAGGAGCCAAGGGCATCCGGACATTACTGTTTGCTTTGATGATGTCACTTCCTGCTCTGTTCAACATTGGCTTATTGCTTTTCCTAGTCATGTTCATCTTCTCTATCTTTGGCATGTCCAACTTTGCCTACGTGAAGAGAGAAATAGGAATTGACGACATGTATAACTTTGAAACCTTTGGCAACAGCATGATCTGTCTATTCATGATCACCACATCAGCTGGCT[G/A]GGATGGCCTGTTGGCTCCTATCTTGAACTATCCGCCTGACTGCGACCCTAATAAAGAGAACCCAGGAACCACAGTTAAGGGCAACTGTGGCAATCCTTCAGTGGGAATCTTCTTCTTTGTAATGTACATTATCGTGTCTTTCCTGATTGTGGTGAACATGTACATCGCTATCATCTTGGAGAACTTCAGCGTTGCCACCGAAGAGAGTGCGGATCCACTGTGCGAAGACGACTTTGAGTCCTTCTATGAAATCTGGGAAAAGTTTGACCCCGACGCTTCCCAGTTCATCACCTTCGCCAAGCTGCCAGACTTTGCGGATACATTAGAGCATCCCCTCCGTGTGCCAAAGCCAAACATCATCGAGCTGATCGCCATGGACCTGCCCATGGTGAGCGGCGACCGCATTCATTGCTTGGACATTCTGTTTGCCTTTACCAAGCGCGTGCTGGGTGACAGCGGTGACCTGGACATGATGCGACAGCAAATGGAGGAGCGCTTTG
Associated Phenotype:
Not determined