Busch Lab

ZMP

ENSDARG00000078758

Ensembl ID:
ENSDARG00000078758
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]
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]

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.
Availability:
Order Allele From ZIRC
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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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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