ZMP
cacna2d3
Ensembl ID:
ZFIN ID:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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 |
|---|---|---|---|---|---|
| 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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
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 |
|---|---|---|---|---|---|
| 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