Busch Lab

ZMP

cacna2d3

Ensembl ID:
ENSDARG00000078760
ZFIN ID:
ZDB-GENE-030616-133
Description:
Novel protein similar to calcium channel proteins [Source:UniProtKB/TrEMBL;Acc:Q8JFR4]
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 7 alleles of this gene:

Allele Name Consequence Status Availability
sa21959 Nonsense Available for shipment Available now
sa16189 Nonsense Available for shipment Available now
sa41890 Nonsense Mutation detected in F1 DNA Not yet available
sa16051 Nonsense Available for shipment Available now
sa35140 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17764 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa21959
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002055 Nonsense 225 1095 6 38
Genomic Location (Zv9):
Chromosome 11 (position 37584204)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36481432
GRCz11 11 36743415
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCAACCCTCATCTGGCAGTACTTTGGAAGCGCTAAAGGTTTTTTCCGA[C/T]AATACCCAGGTGCGTAACGTGGCATTATGTCAGCGCAGGAATTGATGAAG
Long Flanking Sequence:
GCTTCTAAAAGAAACAAAAATAGCGAAGTTCGAATTAAAAGAGACCAGGCTATCTGACCAATCAGAAGAGGGGAGATTCTTGGAAAGGAAGGGTTTAGTAAGATTTGATCCTTGAGTAAACCATTTCAGACACTGTGATACATTAGGTAATGCTGCAGTGTATGTTATGAGAAAATTAAAGTGTTTTTTAACCTTGTGTGGGTGTAGGAGACCTCCAAAACTAAATTAGGAAAGTACCATAAAAAGGTCACTTCAGCTGCTCCACTTGAGGCTTGTACGATTAACAAAATTAGGGTTAAAGGTCAAGTTTGAACTATGTTTTTGTATGATTTTTAAATAAATGTTGCCATTTTCTCACTCTACTCTTTGTCCTTTTAGATCCTGACATAGTCAATGGAGTTTACTGGTCGGAAGCCTTGAACAAAGTTTTCGTGGATAACTTCAGGAGAGACCCAACCCTCATCTGGCAGTACTTTGGAAGCGCTAAAGGTTTTTTCCGA[C/T]AATACCCAGGTGCGTAACGTGGCATTATGTCAGCGCAGGAATTGATGAAGATCAAACTGGCTGATTTCACTAATGTTTTAATTTTACAGACCACCAGAGAGGACATTGAGAAAATTCATTCCATTAATCAAAGCCTGTGGCGGACTAAATCACATCTTGCGTCTTATAGCATTGTGCCAAATGTACACATATTAGCTATTTGTGCTAAACAGATGTATTTAAAAAGCTGAGCTGGAGATAACTTAAGCATCTGCAAGCTTAATGATTTTAGTTGGAATAGTTCTGAGACAGTAATGGGAAATATATCACTAGAGTGTCAACCTGTGAATTACTATAAATTCTTTACATTATGTGTGTTTTCAGGCGTGAAATGGTATCCTGACGAACACGGCGTCATTGCATTTGATTGCAGAAACAGAAAATGGTATGAATGACTTTTTTTGTTCAAATTATTCTCTTTTGTTGGCTTATTTGTTATTAGGTGATGAGTGTATTAGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16189
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002055 Nonsense 231 1095 7 38
Genomic Location (Zv9):
Chromosome 11 (position 37583830)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36481058
GRCz11 11 36743041
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAATTACTATAAATYCTTTACATKATGTGTGTTTTCAGGCGTGAAATG[G/A]TATCCTGACGAACACGGCGTCATTGCATTTGATTGCAGAAACAGAAAATG
Long Flanking Sequence:
TTAGATCCTGACATAGTCAATGGAGTTTACTGGTCGGAAGCCTTGAACAAAGTTTTCGTGGATAACTTCAGGAGAGACCCAACCCTCATCTGGCAGTACTTTGGAAGCGCTAAAGGTTTTTTCCGACAATACCCAGGTGCGTAACGTGGCATTATGTCAGCGCAGGAATTGATGAAGATCAAACTGGCTGATTTCACTAATGTTTTAATTTTACAGACCACCAGAGAGGACATTGAGAAAATTCATTCCATTAATCAAAGCCTGTGGCGGACTAAATCACATCTTGCGTCTTATAGCATTGTGCCAAATGTACACATATTAGCTATTTGTGCTAAACAGATGTATTTAAAAAGCTGAGCTGGAGATAACTTAAGCATCTGCAAGCTTAATGATTTTAGTTGGAATAGTTCTGAGACAGTAATGGGAAATATATCACTAGAGTGTCAACCTGTGAATTACTATAAATTCTTTACATTATGTGTGTTTTCAGGCGTGAAATG[G/A]TATCCTGACGAACACGGCGTCATTGCATTTGATTGCAGAAACAGAAAATGGTATGAATGACTTTTTTTGTTCAAATTATTCTCTTTTGTTGGCTTATTTGTTATTAGGTGATGAGTGTATTAGTGTATTCATTTTTAAATTCAATAAGCTTTTGTCTAATTTTAAGCATAGAATCAAGATTAGCCTGTGAATAATCTTGATTAAACATGAACTCTTGTCGTCTTAGGTATATCCAAGCAGCCACTTCACCTAAAGATGTTGTGATTCTAGTGGACGTCAGTGGCAGTATGAAGGGTTTAAGACTGACTATAGCCAGACAGACGGTTGCTTCAATACTGGACACACTCGGCGATGATGACTTCTTCAACATTATTGCAGTGAGTTTAAGTTACACTAAAAAAAATACATTTGCTGTTTGTTTAACCTTTTTTATAAAATGAGCAATAACATAGTTCTTGTCTTTTGGGACAACTTGATTGTGTTAAGTTCAGTCAACTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41890
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002055 Nonsense 402 1095 12 38
Genomic Location (Zv9):
Chromosome 11 (position 37570251)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36467479
GRCz11 11 36729462
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTCTTTTTCTCCATAGGTCCGTATATTCCCATACCTGATTGGCCGT[G/T]AATCTGCATTTGCTGATAACCTAAAATGGATGGCGTGTGCCAATAAAGGT
Long Flanking Sequence:
AATCATTATATTTAACTATGTGAATTGTACTATTCTATTTTTAAGCATACATTTGTGTAATGTTTTGGGCAAGTGAGATTCATATAAATATAATTTAGCTTGTTCACCAAGGCATTTATTGATTTATTAAACCAATAGTCATATTTTGAATGTTATTTCAGTTTAACTAACTAATTTTAAAATATAATTTTAAAACTTTTGCGTTTTAATCCACTTAAAAGGAGGGAAAAATTTTTCACTTTCATAATTATTATGATAAAAATGGTATGATCAAAGTATTTTTATTACGATGATTTTTTTCTTAAGTGTAGTTGTTGTTGCATTTTTTTGTTTAAATTATTCTATTTTAACAACTCTAATTATTCTATTCTATTTTAACCCTTATCTTGAACATTAACTTAAACTTTTAAAATAGAAAAGAATTGCACAAACATTCAGCACAAATCAAACTCTCTTCTTTTTCTCCATAGGTCCGTATATTCCCATACCTGATTGGCCGT[G/T]AATCTGCATTTGCTGATAACCTAAAATGGATGGCGTGTGCCAATAAAGGTTGGCTTTTCTTTTTTTTTTTCTTGTTTTTTTTGGGGGATGATTTTCTAAATGACATGCTGAATTTGATTTACATTCCATTTTAATGTTTGCTAATTGGTTAATTAATTATCCTGGCCGGGCTTTCTTGGAGCACGGACGCATCCGTTCGTCTTCCAGAGCTGAGCTGTGCTGTGCTGGAGGGGGTTTTGAGTGCTTGATGGCAGAAACTGTGACGGAAACTGGCTCAACTGGCAGAGCTGACATGCAGAGGTCGAAGGTCAACTGAGCCTAAATCACTCTTCCTGTCAGCTCGGCTCCTGTGGCTGCACAGCACTGATCACTCCCATGTGCCCACGCCACGCATGACTGACCGCGGGATGAGAAGCGCTCACACACACACACACAGCATGCTGAGGATTTGTAGCTCTGCACCTGGAGCCTCTGCAGTATATGCACATTTTCAACACAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16051
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002055 Nonsense 697 1095 24 38
Genomic Location (Zv9):
Chromosome 11 (position 37550324)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36447552
GRCz11 11 36709535
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTAANTGTCCTCTCCTGCTTGTTGTAGGTGACAGAGAGCTGATTCAG[C/T]AGGTTCTGTTTGATGCTGTGGTCACCGCTCCTGTAGAAGCCTACTGGACT
Long Flanking Sequence:
TTCCCCATTTTATTTATGCTTTGTTTGGGACTTTACTCTTTCTTCCAACAACTTTTAAACATGAAAAACCTTTGAAAAAGTGACCTTTATTAACATTTTTAATAGTTTAATATATTGTCTGGGTTGGTGATGAATATTACGTTACAAAAACCTTATAATAAACTAAGTATATTTTCTGATATTTTACATGTATTTCTCTATGTATTATTTCTTATATACTATATGATTTCACACTACTAAAATGTCCATAAAAGTCACTTTGTTGAACTCTCCTTCTCACAAAGCTTTTTTATTGGCCTGAAAAGTCTCTGACCTGCACTGTTTTTCAGTGTTTTGTTGTAGTTGTTCCTGCGAAGTTTGGCCACAATGTCCTTTAACTATCTTACAAAATTACCTCAGTGGTTTAAAGACTGTCCTCATTAAAGTCGCTGTCCGACACGTATTCTGGAGTGTGTAAATGTCCTCTCCTGCTTGTTGTAGGTGACAGAGAGCTGATTCAG[C/T]AGGTTCTGTTTGATGCTGTGGTCACCGCTCCTGTAGAAGCCTACTGGACTGGACTGGCCCTCAATAAATCTGAGTGAGTTTGGACTTTCACTTAACCTTGAAGATGCCACATTTTTATTTCATGTAATGTTTCGTAAACAAATTTCGGGAGGAGCACGCGCAGAAGTTTTGGTATCAAATACGTCATTGACAATTATTCAATTATCCAATCAATTCTTGACCAAACCCCTATATATACCAAAGCTGTCTTACCGGCAGTATCTCACGACTTTAGCATCCCTCCACCCCCCGACCCCTTACCTCTAAGCATTACATTCCCGGAGGGAGTGTTCTGGGGCCGGGCTAGATACTATGCTCGAATCCCAACTCCTCTTTGTTCCCTATTAAGGGGAATAACATGAGTTGGGGTGTCTTCCCCTAGCTCAGAGCCCTCTCCCCGGGCAGCACGCCAAATACCCCTGAAACGCTTGCAAGTGTGAATTCGTGAATTGTGTTACAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35140
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
ENSDART00000002055 Essential Splice Site 794 1095 26 38
Genomic Location (Zv9):
Chromosome 11 (position 37549174)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36446402
GRCz11 11 36708385
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGCAGGTGCCCGGCACATTTGTGTACTCCATTCCCTTCAGTTCAGG[T/C]AGGATTCTCAAGCACATCAACAAACACAGCTGTTACTCTAGTGTCACTGA
Long Flanking Sequence:
GTTGAATGGGAGTAAATGTACTCAATCCAATTAGAGCAGTCTTTAGAGAGTCTTCCAGATATTTAAGAACTTTTTTAATGATTTAATGGTTGTCTGGGAAGATAACTGAGAGCTTTTGTGCAGCAAATTGTCTCAGTTAATACGGTTTTTATTTGTTTTTATCTGCAGGAACTCAGATAAAGGGGTTGAGATTGCTTTTCTCGGCACCCGGACTGGCCTTTCACGTACCAACTTGTTTGTAGTTCCTGAGCAACTGACCAATCGGTGAGCTGTATTGATAATGCCTGACTAATGACAAATTCTGATCCCATTGCACTGGTTGAATAAAATGTCTGTTAATGATGAAATGAACTATCAGTGTTTGTGTATGACTGCAGAGATTTCCTCACTGCTGAAGATAAGGAGGGCGTCTTTAACGCTGATCACTTTCCTCTGTGGTATAAAAGAGCAGCAGAGCAGGTGCCCGGCACATTTGTGTACTCCATTCCCTTCAGTTCAGG[T/C]AGGATTCTCAAGCACATCAACAAACACAGCTGTTACTCTAGTGTCACTGAGATAATATTACAGGTTTTAGATTTGTTTTAAAAAATGTAAAAAATGATCATACACAAACACACACACAAACACATATATATATACAGTATATATATATATATGTATATATATATATAATTTTTTATTATTTTTTAAAATTGTTTAGTTTTTCAGTTGTTGTTTTTGTTTTCTTAGAGCTATGTCTGTCTGTCTGTCTAAAATAGAAGTATAATACTGAAAATGTAAATGAGAAATTATTTCTAGATGACTAGCTGAAAACAAAAAAATAAAAGTGTTATTATAACATTATACATATTATATCGTAATACTATACACAGTTTTATAAAACATTTATTATAAATAAGGTTTTAGTTTTAGTTTACTCTGACAAACATCCAAAGTTTTCATGGGATGCAAAATATTCCAAGCATTAATAACTCAAATAGTTTGGATTATATTCATATTTCATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17764
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002055 Essential Splice Site 902 1095 31 38
Genomic Location (Zv9):
Chromosome 11 (position 37543117)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 36440345
GRCz11 11 36702328
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGAAGGAGCCGTCATGAATAAACTGCTTCTGATGGGCTCGTTTAAAAA[G/A]TGAGAGACGCACTGCTCRTATATTAACCTCTTTTTAATGAATTAACCTGC
Long Flanking Sequence:
TTTAAAGAGTTATAAAACATTATTTGAATTGTTTTGAGCTGAAACTTCACATACACACTCTAGGGACATCAGACTTATTTTTCATCTTGTAAAAAGGAACATAATAAGTACTCTCTTTAAATTCTGTGTCCTATTAATGTTTGTAAAAGTTATCAAATGTGTGTTATATTACCGTCTTGTTGAATTTGGGCTCAAAATGTATGTTCAGTAGATGTTTGAAGTTATTAAAGTTGATCAGAAATTATCAAATGAGAAGTTTCTTTATCTTTCCCTCTTATATTAGGACATTAAATGCTATCTCATAGACAACAATGGCTTCATCCTGGTCTCTGAAGACACTTCTCAGGTATGACACAAAAAAACATATACGGTATCGATATTGTTATGAAATGGAGATTTGTATAACTGTACATATTGTGTTTTCCACAGACAAACCTCTTCTTTGGAAAAGTGGAAGGAGCCGTCATGAATAAACTGCTTCTGATGGGCTCGTTTAAAAA[G/A]TGAGAGACGCACTGCTCATATATTAACCTCTTTTTAATGAATTAACCTGCACTGTCAGCCTTCAAGATTTTACACTACATCTGTAAGCCCAGAGTAAACACTAATATTTGCATATTTATGAGGTAATTTGCATACTAATCATTGATTGAGCATTACAACATGCAACAAGTATGCAGCACGTTTAATTATAACTATCATTTCTATCTATTTGTTCCTTTAGAGTACTGCAAAATAGTTATCAAAAAGATCAAAAGATCCTTAAAAATTGTCTAATTAAAGCTATTTTTCTTGTTCTATTAGTAAATAGTTTTCCTATTTGAACATCAGTCTCTTTCAATTCGTGGTATTTTAAATTCAAAGTGTTTTGTTGTTGTTGGTCAATCACAGCCTTTTAAATACTCTCCAAATAACCACACGTATGATCTTTGCACTTGTATTCTTACATGTATTTCCTTCTTTGAGTGGGCTTAAAGACCACAAGTGTGCATAGTGTTTTTGAC
Associated Phenotype:
Not determined