ZMP
ENSDARG00000078758
Ensembl ID:
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10223 | Essential Splice Site | Available for shipment | Available now |
sa10300 | Nonsense | Available for shipment | Available now |
sa32502 | Essential Splice Site | Available for shipment | Available now |
sa32503 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10223
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097722 | Essential Splice Site | 578 | 1841 | 15 | 51 |
Genomic Location (Zv9):
Chromosome 24 (position 42796401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40757498 |
GRCz11 | 24 | 41033763 |
KASP Assay ID:
2261-9158.1 (used for ordering genotyping assays)
KASP Sequence:
CCGAGACCGAGCCCTGAGCGCAACCAGCTACATCACTGACGCCATGGAGG[G/A]TGAGAGAGACACACAACACAACACARCACARCACAACACARCACARCATA
Long Flanking Sequence:
CACATTTTTACACAGCGGATGCCCTTCCAGCCGCAACCCATCACTGGGAAACTTATAATGTTTATATTTGAACTAAATATTAACATTGTACTTAAGCTCTTAACTAAAATTGTGACAATAGCCAGTCTACCATATAGCAACCCAAGCAACAACAACGAACAAACAGAATTAACTACATAGCTATTTGCTTAAATGATATATTTAAAGAGCACAGCACTGAAGTGTCCTTGCAATCTCACACAATGCTTCAATACATAGCTGGCTGGTTTATTTTATTCTTGTATTCATGAATTTGTTGGTCTAAAACTGTACTGGAGTGATGCATGTCTTATGAAAAGTTGTGTGTTTGGTCCTGAAGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTGCAGGGCCAGAACTCCTCCAATGAGCTGAGCAGTATGCTGCTGCCCCAGCTGCCCCCAGAGGGCCGAGACCGAGCCCTGAGCGCAACCAGCTACATCACTGACGCCATGGAGG[G/A]TGAGAGAGACACACAACACAACACAACACAGCACAACACAGCACAACATACACTAATACAGCAGCAACAATACTCAGGTAGGCTGTGGCGTTGACACGATGCTCAATGGGTACTAATGGACCCAAAGTGTGCCAAGAAAATCTCCCCCACACCATTACACCACCACCACCAGCCTGAACCGCTGATACAAGGCAGGATGATCCATGCTTTCATGTTGTTGAGGCCAAATTGTGAGCCGAGCATCCGAATGTGTCAGCAGAAATGGAGACTCATCAGAGCAGCAACGTTTCTCCAATCTTCTATTGTCCAGTTTTGGTGAGTCTGTGTGAATTGTAGCCTCAGTTTCCTGTTCTTAGCTGACAGGAGCGGCACCCGGTGTGCTCTTCTGCTGCTGTAGCCCATCCGCCTCAAGGTTGGACGTGTTGTGTGTTCAGAGATGCTCTTCTGCAGAGCTCGGTTGTAACGAGTGCTTATTTGAGTTGCTATCAGCTGGAACCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10300
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 |
---|---|---|---|---|---|
ENSDART00000097722 | Nonsense | 681 | 1841 | 17 | 51 |
Genomic Location (Zv9):
Chromosome 24 (position 42819247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40780344 |
GRCz11 | 24 | 41056609 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCACGGCTGAGATGGTKCTGAAAATCATCGCTCTGGACCCGTATTATTA[C/A]TTTMAGCAGGGCTGGAACATTTTCGACAGTCTGATCGTCAGTCTGAGTCT
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATAATCGCAATGCAGTAAAATATGATTCAATATTCAGTATTATGGAGTGTAATTATGTTTTCTCCTTCCCTGTGTGGTTGTCAGGTGTTCACGGGGATCTTCACGGCTGAGATGGTGCTGAAAATCATCGCTCTGGACCCGTATTATTA[C/A]TTTCAGCAGGGCTGGAACATTTTCGACAGTCTGATCGTCAGTCTGAGTCTGATGGAGCTCGGTTTGTCCAACGTGGAGGGTCTGTCTGTCCTGCGCTCATTCAGACTGGTAAATAAACAAACACGTAATGCAGCGTAAACACCTGCTGACAGCAGCGCACATCATCTGCTGCCAGATTATTGTTAAGATAAAACACTTCATTTTATTACTTCTGAAAACAAGACTATATTTGTTGGACCACATTGACGATAGAGTTTAGTTTGACTTGCTATTAAAACCGTCTCCTGATCTTCTCCTGCAGCTGAGAGTCTTTAAGCTGGCCAAATCCTGGCCGACTCTGAACACACTGATCAAGATCATCGGGAACTCGGTAGGCGCTCTGGGAAACCTGACGCTGGTTCTGGCCATCATCGTCTTCATCTTCGCTGTGGTCGGCATGCAGTTGTTCGGGAAGAACTACGATCTGTGCGTCTGTAAGATCTCCAAGGACTGCACTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32502
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097722 | Essential Splice Site | 970 | 1841 | 29 | 51 |
Genomic Location (Zv9):
Chromosome 24 (position 42838493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40799590 |
GRCz11 | 24 | 41075855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATACATCCTTTCATCAATCCATCTATCGCTTAATCTATTGTTCTTTCC[A/T]TCATTTCATCATTTTATCCATCAATCCATCCACGATTTGTTCTATCTATC
Long Flanking Sequence:
CCACTGAGAACACTTTAGCAACCTCCTAACAATTCCCTGAACACCCTAGCAACAACCTTAAAAAATACAGAAAACTTTAGCAACCCCCTAGCAACCACAGAAAACACCTACACAACAGCATCATCAAATAACACCTAATCCCTAACCACATTTGTCACTTAGCAACCACACAGAAGACTAGGACAACCACCTAGCAACCTTCAAGAACACCTTATAAAATAAAAACCACCTAATAACCAATGAGAACACCTTAGCAACCTCATAACCACCATCCTAAATACCCTAGCAACAACCTAAGCAATTCCAAAACACTTTAGCACCCCCCAGCAACATTAAATCTATTGTTCTATCCATCCATCCATCCATCTATCCATCCATCATTATATCTTTTGGTCTATCCATCGCCCCATCCATTGATCAATCCTTCATTCCATCCATGCATCCTTCCAACCATACATCCTTTCATCAATCCATCTATCGCTTAATCTATTGTTCTTTCC[A/T]TCATTTCATCATTTTATCCATCAATCCATCCACGATTTGTTCTATCTATCTATCTATCTATCTATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTTGCTATATTTCAATCCATCCATCTATACATTTTGCCACCTTTCCATCCATCTTGACATCCATCCATCCATCCATCCATCCATCCATATACTATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCACCTGCCACCCCAAAACCACAACAAACCAGTCAGTCTAGCTCTGGCCTTTAAAGCACACGCCACACTTAACAGCATACAGAGATATGAGAGGTTATTGTTTTCTGTCCCTGAGGTGCTGAGAATGTGCTGTTAGCATTTATGGAGTCAGATGAACTCTGCTGTGTTCATTTACTAATCAAATATACAATATAGACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32503
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097722 | Nonsense | 1741 | 1841 | 51 | 51 |
Genomic Location (Zv9):
Chromosome 24 (position 42889380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 41226160 |
GRCz11 | 24 | 41142577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCGTTTACGAAACGCGTGTTGGGCGAATCGGGAGAAATGGATGCGCTC[A/T]AGCAACAAATGGAGGAGAAGTTTATGATGGCAAATCCGTCAAAGATTTCC
Long Flanking Sequence:
AGATCACCACATCCGCCGGCTGGGATAATCTGCTGAGTCCCATCCTGAACACGCCTCCGGAAGAGTGCGATCCCGAAATTCCCCACACTGGCACTAATGCACGAGGAAACTGCGGAAACCCTTCGGTTGGAATTACGTTTTTCGTAACGTACATCATCATCTCATTTCTCATCGTGGTCAACATGTACATCGCCATCATCCTGGAGAACTTCAGTGTGGCGACGGAAGAGAGCACCGAACCGTTGAGCGAAGATGACTTTGAGATGTTTTACGAAGTTTGGGAGAAGTTCGATCCTGAAGCGACGCAGTTTATCGAATATTTAAAATTATCGGATTTCGCAGATACGCTTTCGGAACCTCTCCGCATTGGGAAACCCAATAAAATCAAACTGATCTCCATGGACTTGCCGATGGTGAGCGGAGATAAAATCCACTGTTTGGATATTTTATTCGCGTTTACGAAACGCGTGTTGGGCGAATCGGGAGAAATGGATGCGCTC[A/T]AGCAACAAATGGAGGAGAAGTTTATGATGGCAAATCCGTCAAAGATTTCCTACGAACCCATCACTACGACACTCCGTCGGAAGCAAGAGGAGGTTTCCGCCATTATGATTCAACGTTCGTATAGGAGACATTTAATTCGTAGACAGTTAAAACAAGCGTCGCTTTTGTATCGTCAGATGACCATGCCGGACGCTGATAAAGCTGGCGACAGCTCGCCGGAGAGCCAAGGACTCATCGTTTCGATGATTATGGAAAACTACGCAACTGAAGCTGAAATTACGATATCTGCGACGTCGTCTCCTCCATCGTACGATAGCGTTACAAGAGCGACGAGTGAGATTTTCCATGCTCTGATTCCCGAAGAGACGAATGAAATCCTCAGCGAACATTTGGCTGATGCAGAAAAAGAGAGCGAAACTTTTCTGTGACGCAAAAACATTTTTTTTTGTTTACCGAATGTAACATAGTCTGCGAAGGTTTTTGTAGACTTCTCTTGAGGA
Associated Phenotype:
Not determined