Busch Lab

ZMP

CACNA2D3 (2 of 2)

Ensembl ID:
ENSDARG00000045204
Description:
calcium channel, voltage-dependent, alpha 2/delta subunit 3 [Source:HGNC Symbol;Acc:15460]
Human Orthologue:
CACNA2D3
Human Description:
calcium channel, voltage-dependent, alpha 2/delta subunit 3 [Source:HGNC Symbol;Acc:15460]
Mouse Orthologue:
Cacna2d3
Mouse Description:
calcium channel, voltage-dependent, alpha2/delta subunit 3 Gene [Source:MGI Symbol;Acc:MGI:1338890]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa10825 Essential Splice Site Available for shipment Available now
sa21406 Essential Splice Site Available for shipment Available now
sa41320 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa41319 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10825
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066454 Essential Splice Site 118 1022 4 38
Genomic Location (Zv9):
Chromosome 8 (position 55998029)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53770458
GRCz11 8 53600188
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAGTCTRTAGTGATTTTGTCATGTACTCTATTAATTAACTTGTGTTTC[A/T]GACTCAGACATCGTGAACGGGGTTTACTGGTCAGAGGCTCTCAAMACAGT
Long Flanking Sequence:
AGTGTGTTAACATAGCAACTGTTGAATCATTACAGCAGATCAATTACTATAGTTGTTGTGTTACCATAGCAACTGTAGAATCACAACAACAGATCAATTACTATAGTTGTGTTACTATAGCAACTGTAGAATCACCACAACAGATCAGTTACTATAGTTGTTGTGTTACCATAGCAACTGTAGAATCACCAAAACAGATCAGTTACTATAGTCGTTGTGTTACCATAGCAACTGTAGAATCACCACACCAGATTAATAAATTAATTAATAACAATTTCTTTCATGTGTGGTTCAAAAACACTGTAGTTTACTTGATTGAATTTACTGAAGTGATTCTACATCGTGATATATATCGTTGTCAGAATATGACAGTATATGTAATATCGCCCAGCACTAGTAATCTATATGTATCTCTGGTCTGAAAAATACAGATTACACACAGATCAGCATGTAAGTCTGTAGTGATTTTGTCATGTACTCTATTAATTAACTTGTGTTTC[A/T]GACTCAGACATCGTGAACGGGGTTTACTGGTCAGAGGCTCTCAACACAGTGTTTGTGGACAACTTTAAAAGAGACCCTTCTCTCCTATGGCAGTATTTTGGCAGCGCTCAAGGTTTCTTCAGACAGTATCCAGGTGAGTTTATATAGTGTCAAGGCAATCACATTACTGATGCAGCATTTTTAGTGTTTGAATGATTATAAAAGGGAAAGACTGTGACTGTGCTTTATTAGAGATACAGTAAATCATCAACAAAGTATGAGACGGTCAGCGCTGCTTACTCAAAAACTTGGACATTGTGTATTGCTATGAAAATATATTTTAATATCTTACATTTCAGCTACTTTTTATTTTATTTTAGATTAACGTTTGACTTATTTGTTTGTTTTTTTCTTCTTGTTTAGACAATCAAAAAATTATAATTTCTTAACAGGGCCCATAATTTTTTGCTACAGTTGCTTTTACATTTAAACAAAAAATCCAGCCAAACTAAAAGAAATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21406
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066454 Essential Splice Site 183 1022 5 38
Genomic Location (Zv9):
Chromosome 8 (position 55995625)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53772862
GRCz11 8 53602592
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCTGATGAACACGGAGTTCTAGAGTTTGACTGTCGAAATCGGAAATGG[T/C]AAGACATTTTGTTTGCTTCTCAATCCTCTTCGCATCCAGCTGAGGAGAAA
Long Flanking Sequence:
AGGAAATGAATGAATATAAATATATATGATATATAAAAAATACTATAATATGACTGAAATCATGATTAAACAAACTAAAATAAATGATAGTTAATAGTATTGTATATTTCCCGCATCAATAGTGCAGGTATCAGCCACAAAAGGCAGCAGTAGAGAGTTGTAGATTTAATATTTTTTGACCGCGTTAGCTGATTGGCTAACATCATATGACAGTTGGGTTTAGGGGTGGAGTCAGGTAAAGGGAATCAATTCATTGGATGACTTAAAAAACACCCACAAATCCAGAAACACCCACTTTTGCTCTGCAGAGACGTCATTTTTTATTAATGAAGCCTTCCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTATTCTGTATCTTGACAGGAATGAAGTGGACGCCTGATGAACACGGAGTTCTAGAGTTTGACTGTCGAAATCGGAAATGG[T/C]AAGACATTTTGTTTGCTTCTCAATCCTCTTCGCATCCAGCTGAGGAGAAATGCAGCTTTCTTCACTCATAAGAACGCTGCAGCCATTTTGTTGTGTTTTATTTATGTTTAAAAATGAGTTGCTTGTGTTTTATTTAGTTGTACCATATTAAAATTCCAGAGGAAAGTCCTTACCCCAGGTGGAGGAGTTCACGTATCTTGAGGTTTTGTTGTGGAGTGAGGGAAGGATGGAGGTGAGATTGACAGGTGGATCTGTGCAGCAGCAGCAGTAATGCGGCTGATGTATCGGTCCATTGTGGTAAAGAAGGATCAATCTACTTTCCTACGTTCACCTACGGTCATGAGGTTTGGGTCAAGACTGAAAGGACAAGATCTCGGATACAAGCAGCCGGAATGAGTTTCCTTCACAGGGTGGCAGGGTGCACCATTCTAGATAGGGTGAGCAGCTCTGACAACTGCGAGGAGCTCTGAGTCAGGGCCGGCGCATCAATAGAGGCAACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41320
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066454 Essential Splice Site 258 1022 7 38
Genomic Location (Zv9):
Chromosome 8 (position 55993736)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53774751
GRCz11 8 53604481
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCGTGTCTGAACGGAACATTAGTTCAGGCTGACATTACCAACAAAGAT[G/A]TAAGTGTGTTTACTAATATAAATATCTATTAACCGTAAATTACAATCAAA
Long Flanking Sequence:
TTATTAACCCCCTTATATGTTTTTCCCAATTTCTGTTTGACGGAGAGCAGATTTCTAAACATTACAGTTTTAATAACTCATCTCTAATCACTGATTTATTTTCTCTTTGTCATGATGACAGTAAATAATATTAGATTTGATATTCTTCAAGACACTAGTGTTCAGCTTAAAGTGACATGTAAAGGCTTCACTAGGGTAATTAGGGTAAAGTTAGGGTAATTAGGCAAGTCTTTGTATAACAGTGGTTTATTCTGGAGACAATCCAACACTAATATTGCTGAAGGGGCGAATAATATTGAGCTTAAAATGGCTTTAAAACAATTAAAAACAAAAATACTTTCTCCAGAAGAACAAATATTCTCATGAAATTCACAGGAGGGCGAATAATTTTAACCTTGACTCTATATATATTGTGTGTTTTGCAGTACAACGAGGATCTGCATTACGTGGAGCCGTGTCTGAACGGAACATTAGTTCAGGCTGACATTACCAACAAAGAT[G/A]TAAGTGTGTTTACTAATATAAATATCTATTAACCGTAAATTACAATCAAAACTCAGCAAATGTAAATAACAGTATATAGCAGTCTGTGGGAACTGGAAGTTGCTGAGAGGTTTTCTATAGTTTGCTGATGTGCTTCCAACTGAAACTGAATATTGATTAGGGGGCGGGGCATTATTTCAGTATGTTAATGTACTTCTAACTGAAACTGAATATTGAGTAGGGGGCAGGGCTTTATTTCAGTATGTTGATATACTTCCAACTGAATTTGAATATTAAGTAGGGGGCGGGGCTTTATTTAAATATGGTAATGTGCTTCTAACTGAACCTGAATATTGATTAGGAGTGGGGCTTTATTTCAGTATGTTAATGTACTTCTAACTGAAACTAAATATTGAGTAGGGGCGGGGCTTTATTTCAGTATGTTAATGTACTTCTAACTGAAACTGAATATTGAGTAGGGGCGGGGCTTTATTTCAGTATGTTAATGTACTTCTAACTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41319
Status:
Mutation detected in F1 DNA
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
ENSDART00000066454 Essential Splice Site 424 1022 13 38
Genomic Location (Zv9):
Chromosome 8 (position 55981256)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53786869
GRCz11 8 53616599
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCATGACTACCGTGGCCATGCCTGTGTTCAGCACCAAAAACGAGACCG[T/C]GAGTGATCATAAGCTCTCACTGCTGGGGTGGTAATTGTTAATATTGTTGA
Long Flanking Sequence:
GTAGTTTAGTCTACCTGTTTCCTGTCCTGCTTTCGCCATGTGCCCCTTTGTGTGTGTGTGTGTGTGTGTGTGTTCATTGGCTGAGTTAGTCTAATGTCTTGTTCTTCATTGGTCATGTGTCTGGTTTCTCTTTGGTTGAATCATGTCATGTGATCTTTAGTGTTTCATACGTGTACCCTCATGTTTCCTTGCTCTTGGTTTAGCTTTGTTTGTGTAACCTCTCTCTCTCTCTCTCATTAACTAATACTACCTTATTGTAAAGTGTTACCTACAGAAGCTTGATGTTTCTGTAGTTTTGATTTGTTTGCACTGGGAGTAAAAGCTGCAGGCTTTTCTTCAGTTTAGGTCACGTTTAGAAAAGCACTTGTAGCAGGCAATGAATGTCACTGATGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTGTAGCTGGAAGACGCTCAGGGTCCAGTGCTCATGACTACCGTGGCCATGCCTGTGTTCAGCACCAAAAACGAGACCG[T/C]GAGTGATCATAAGCTCTCACTGCTGGGGTGGTAATTGTTAATATTGTTGAGAATCCTCTGAAATGTCTCATTCTGTCTATCAGTTCTGGTTCTGTTCAAATTAATAAACAACTTTGTAACGTAGGAGATTGGAAAACAATGACTAAATCACTTCCAGTCGGTGGTTGATCGATTATTTTAATCATTTATTCAAGTTATTCGTTCAAAATAGATGATTCATTTAGAAATGAGGCACATGACTGTCTTTATGAATGGATCATTGAGTCATTGACTCAAATGATTTGTTCAATATAGCGGATTTATTTAGAAATAAAGCATGTGATGGATCTTATGAATAGATAATTAAATCATTGATTAAATCATTCATTCAGAAACCGACTCATTCAAACTATTTGTTCAAAATAGCTGATTCATTTAGAAATGAGGCAAGTGACTCTTTAATGAATGAATCATTTAATCATTTAATTGTTGACTCAAATGATTCAATTCAGAAACAAAAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5515
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066454 Essential Splice Site 549 1022 18 38
Genomic Location (Zv9):
Chromosome 8 (position 55973117)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53794155
GRCz11 8 53623885
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCACAATGATTACTACTACACAGACATTAAAGGAACGCCCTTCAGG[T/C]GATATATGTTGGTTTCTGTTTCTTTACATTYAAAGTATAGTGTAAAACAA
Long Flanking Sequence:
TTTATTTACTTGCTTGTTTATTTGTTTGTTTTCTTTGTTTGTTTACTTACATGTTTGTTTGTTTGTTTGCTTGCTTGTTTGTTTGTTTGTTTGTTTGCTTGCTTGCTTGTTTGTTACATACTGATTTACTTGTTTGTTTGCTTGTTTGTTTACTTGTTTGTTTGTTTACATGTCTGTTTGTTTGCTTGCTTGTTTGTTACCTACTGATTCACTTGTTTGTTTGTTTGTTTGTGTGCTTGATTGTTTGTTTACTTGTTTGTTTATTTCAACCTAACTAAAAGAAATAAAACTTTCTTCAGAAGAAAAATATAGGAAATATTCTGAGAAATGTCCTCGCTATGTTAAACAGCACTTATAATATTATTATGAATAAAGACACTACCATACAGAGTTTTTCTTTCATTCTCTTATAGTGTTTGTGTGTGTTTGTGTTTCAGAAGCGGGTGCTTGTTCTTCACAATGATTACTACTACACAGACATTAAAGGAACGCCCTTCAGG[T/C]GATATATGTTGGTTTCTGTTTCTTTACATTCAAAGTATAGTGTAAAACAACAAGAAAACTGGAGATTAAAGAGTTGTTACCATAACAACTGCAGAATCACCACAACAGATCCATTACTATAGTTGTTGAGTAACCTTAGCAACAATAGAGTCGCATCACCGCAACAGATCAATTACTGCAGTTGCTGTGTTACCATAGCAACTGTAGAATGCCACGAAAGATCAATTACAGCCGTTGTTGTGTTACCATAGCAACTGTAGAATCACCACAACAGATCAATTACAGCCGTTGTTGTGTTACCATAGCAACTGTAGAATCACCACAACAGATTAAGTCTAGTAAATATAAGTATAACTACACAATGTTTCTCTGGTTTTCAGCTTAGGAGTGGCTCTGTCTGGAGGTCACGGCAAATATGTCTTCAGAGGAAATATCTCTGTTGAAGAAGGTAACTATACGTGGAACTACAATTCTGCCTGTGTTGGGCACGTTACTTCAAA
Associated Phenotype:
Not determined