ZMP
NP_001038387.1
Ensembl ID:
Description:
sodium channel, voltage gated, type XII, alpha a [Source:RefSeq peptide;Acc:NP_001038387]
Human Orthologues:
SCN10A, SCN11A, SCN5A
Human Descriptions:
sodium channel, voltage-gated, type V, alpha subunit [Source:HGNC Symbol;Acc:10593]
sodium channel, voltage-gated, type X, alpha subunit [Source:HGNC Symbol;Acc:10582]
sodium channel, voltage-gated, type XI, alpha subunit [Source:HGNC Symbol;Acc:10583]
sodium channel, voltage-gated, type X, alpha subunit [Source:HGNC Symbol;Acc:10582]
sodium channel, voltage-gated, type XI, alpha subunit [Source:HGNC Symbol;Acc:10583]
Mouse Orthologues:
Scn10a, Scn11a, Scn5a
Mouse Descriptions:
sodium channel, voltage-gated, type V, alpha Gene [Source:MGI Symbol;Acc:MGI:98251]
sodium channel, voltage-gated, type X, alpha Gene [Source:MGI Symbol;Acc:MGI:108029]
sodium channel, voltage-gated, type XI, alpha Gene [Source:MGI Symbol;Acc:MGI:1345149]
sodium channel, voltage-gated, type X, alpha Gene [Source:MGI Symbol;Acc:MGI:108029]
sodium channel, voltage-gated, type XI, alpha Gene [Source:MGI Symbol;Acc:MGI:1345149]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15768 | Nonsense | Available for shipment | Available now |
sa12942 | Nonsense | Available for shipment | Available now |
sa19899 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15768
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083256 | Nonsense | 563 | 1027 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 51504826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 52296978 |
GRCz11 | 2 | 51889740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATAACCATYATGATGCTCATTATCCTCAATATGATAACCATGATGGTT[G/T]AGACTGATGAACAATCTGCTCGCATGGAGACCATCCTCAATAACATCAAC
Long Flanking Sequence:
GATAAACCTCTACATGTACCTCTACTTTGTCATCTTCATCATCTTTGGATCATTCTTTACCCTGAATTTGTTCATCGGTGTCATTATCGACAATTTCAATCAACAAAAAAGAATGATAGGTGTTTAAGATTGGCTTCTTTTCTAAACACATTTTGTTTGACATGTAATGTGTTCCATGAAAATAATACCAACCGTTGTTCTTTGTACTAAAGGTGGCCAAGACATATTCATGACCGAAGAGCAGAAAAAGTACTACAACGCAATGAAGAAACTTGGATCTAAAAAGCCACAGAAGCCAATTCCAAGACCAATGGTAATTTAACATTATTGTAACTGAAAACTAGTAATTACTTTCATAAGTACTCTTTCAAAAATCTCACTACAAATACATTTCCATCTAGAATATTCTACAAGGATTCTTCTTCGACTTGGTGTCCAAGCAAGCCTTTGATATAACCATCATGATGCTCATTATCCTCAATATGATAACCATGATGGTT[G/T]AGACTGATGAACAATCTGCTCGCATGGAGACCATCCTCAATAACATCAACTTGGCCTTCATTGTCATCTTCACTACTGAATGCCTCATCAAGATTTTTGCCCTCCGCTGTTATTTCTTCACCATTAGTTGGAACATATTTGATTTTGTAGTCGTCATTCTGTCCATCGTTGGTAAGTGCACGACTTTCCAGTCTGGTAAGTGGTATGTATGGAAAGATACTTTCCTTGCTGAAAAGACCAACTTGGTTTAAAAGTAATTAATGCTTTGGTACTGGTCTATCTGGTCACCATTACGACAAAACCAAGCAAGTTTGGTTTAGTTAGTTAAGAAACATGGAGGCGACACCAGCTGGTCTTTTCAACTGGGATGTTGTAGTCTTAAGATTTTCATACTATTGTTGCATTTCTCAATTCTTCAAGAGATTTTTTTTAAGAGTCTACCTTCATTGCATGTGTTGATCATGTGCCTTTTTTCACAGGAATTGTCCTGGCGGATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12942
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 |
---|---|---|---|---|---|
ENSDART00000083256 | Nonsense | 728 | 1027 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 51505630)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 52296172 |
GRCz11 | 2 | 51888934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCGGGAACAGCATGATCTGYCTTTTCCAGATCACCACATCGGCCGGTT[G/A]GAATAACCTGCTGGATCCTATCCTGAACAACTCTCCGGAAGAGTGTAGCT
Long Flanking Sequence:
AAGCAAGTTTGGTTTAGTTAGTTAAGAAACATGGAGGCGACACCAGCTGGTCTTTTCAACTGGGATGTTGTAGTCTTAAGATTTTCATACTATTGTTGCATTTCTCAATTCTTCAAGAGATTTTTTTTAAGAGTCTACCTTCATTGCATGTGTTGATCATGTGCCTTTTTTCACAGGAATTGTCCTGGCGGATATAATTGAAAAGTACTTTGTCTCCCCAACTCTTTTTCGAGTCATCCGGTTGGCAAGAATAGGACGAGTTCTTCGACTGATACGAGCAGCTAAGGGAATAAGGACTTTACTTTTTGCCTTAATGATGTCATTGCCGGCATTGTTCAACATCGGTCTCCTACTGTTTCTGGTCATGTTCATCTATGCCATTTTTGGCATGGCAAACTTCGCTTATGTGAAGAAGCAGGGTGGGATTGATGACATGTTCAACTTTGAGACCTTCGGGAACAGCATGATCTGCCTTTTCCAGATCACCACATCGGCCGGTT[G/A]GAATAACCTGCTGGATCCTATCCTGAACAACTCTCCGGAAGAGTGTAGCTCCAGTTTTGCGAACACCGGAACAAATACTAAGGGCAACTGTGGTCACCCCTCAGTAGGGATCACTTTCTTTGTCAGCTACATCATCATTTCCTTCTTGATCGTCGTCAACATGTACATCGCCATTATTTTGGAGAACTTCAGCGTGGCCACTGAGGAGAGCACTGAACCTTTGAGCGAGGACGACTTTGAGATGTTCTACGAAGTTTGGGAGAAGTTCGATGTCGAGGCTACGCACTTCATCGAATACGCCAAACTCTCCAATTTCGCTGACAGCCTTTCCGAACCCCTAAGGATTGCCAAACCCAACAAGATCAAACTCATCCACATGGATCTACCCATGGTCAATGGTGACAGGATCCATTGCCTGGACATCCTGTTCGCTTTCACCAAACGCGTCCTTGGGGAGACTGGAGAAATGGATGCTTTGAAGCAACAAATGGAGGAGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19899
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083256 | Nonsense | 1023 | 1027 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 51506514)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 52295288 |
GRCz11 | 2 | 51888050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATATCTGACTCTAGATCCAATGAGCCTCATAAATCAGAAGAGACATAC[G/T]AAGAGACCTTTCTTTAGGAACTCTTTTCATAGTAGGCAGTCATTATTTGC
Long Flanking Sequence:
TACCCATGGTCAATGGTGACAGGATCCATTGCCTGGACATCCTGTTCGCTTTCACCAAACGCGTCCTTGGGGAGACTGGAGAAATGGATGCTTTGAAGCAACAAATGGAGGAGAAGTTCATGGTGACGAACCCTTCTAAGATATCTCACGAACCCATCACCACTACACTGCGGCGCAAGCAGGAGGAGATTTCAGCAACTCTGATCCAGCGTGCCTATAGAGCACACCTAATTAGACGGCAAATGAAGCAAGCTTCTTACTTGTACAGGCACATTAACCAAGAGACGCCCTGGTCGGAAGAGGACAGCGCTCCAGAGCAGGAAGGTCTTATAGCGTCTATGATTAAAGAGAACTATGGCCCTGAGAAAATGGTGGGTACACTGTGCTATGCATCCTCTCCACCATCCTATGAGGCAGTAACAAGGAGTCCTAGGGACCATTTCAAGTTGTTAATATCTGACTCTAGATCCAATGAGCCTCATAAATCAGAAGAGACATAC[G/T]AAGAGACCTTTCTTTAGGAACTCTTTTCATAGTAGGCAGTCATTATTTGCTTTTTTTAACCACATTTGGATGTGTGTAAACAAACCTAATCAGGATAAGTCCACATGCAAACAAGATTGCACTTTTTTAATCTGTAAAAATATTGAAAGCCTGTTGTTTCTGTCATAAAATATGGCACGGTATTATGATAAATAGATGACATGCATGGATATATCATAGCGAGGATGTACATGTAGAGAATGTACTACAGCACAGATGTGTTGAACATATCAAAACTGTAATATATTGCACAGATATTATGTTGATTGTTTCCTATAAAGGTTTTTCCCAGGATTACAAACATCTAAACAGAGTTTTCTATTGCTCAGGATTACGTGGGTAATGTTATCACTTTTCTTTTTTATAACACTTGATGAGAGTGACTGATTTTGAGTGACGGGTGCAAGAAAAAGGCCCATAAAATGAAGATTGAATGACAGCAGTGAAACTTTTTGAGTTTT
Associated Phenotype:
Not determined