ZMP
cacna1da
Ensembl ID:
ZFIN ID:
Description:
voltage-dependent L-type calcium channel subunit alpha-1D [Source:RefSeq peptide;Acc:NP_982351]
Human Orthologue:
CACNA1D
Human Description:
calcium channel, voltage-dependent, L type, alpha 1D subunit [Source:HGNC Symbol;Acc:1391]
Mouse Orthologue:
Cacna1d
Mouse Description:
calcium channel, voltage-dependent, L type, alpha 1D subunit Gene [Source:MGI Symbol;Acc:MGI:88293]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1422 | Essential Splice Site | Available for shipment | Available now |
sa17298 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1422
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058276 | Essential Splice Site | 494 | 1716 | 13 | 40 |
ENSDART00000089956 | Essential Splice Site | 860 | 2083 | 22 | 50 |
ENSDART00000100118 | Essential Splice Site | 835 | 2069 | 21 | 50 |
Genomic Location (Zv9):
Chromosome 11 (position 37699880)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36597108 |
GRCz11 | 11 | 36859091 |
KASP Assay ID:
554-1343.1 (used for ordering genotyping assays)
KASP Sequence:
GTCATTGGCTGCTGAGGATCCAATCAGAAACTTCTCTGCTAGGAAYATTG[T/A]GAGTATTACCACAGTAATGCCAAGATTATACAGTAAAGTYCAAACCATTT
Long Flanking Sequence:
TTCATTGATTCATTTGAAAATGTATTGATGTTGAAGCAATTTGTAAGTTAATATTTTAATTTAGGATTGGCATTTTATGATATATTTTTGTTATGGTTATAGAAGCATGATCTAAGAATATTAAAAATTACACAATTGCTAAAAATGCATTATTTCTTTAAAATGAATATGCTGTAATATTATAATAAATGGTAAATTATTTAGATGTTTGGACAGAACATGTGACAAAAAATGGATTAGAATTAACATTTTTATTTTTTAAAAGTCAGCAGTCAACCTATTCTATTGTTATTCTTTTTTGACACATTAAAGGTTTCTAAACCCTGAAAATATTTAAGTCATTCTCTGTCTCTCTTTGTTTCTCTCTAGAGTTCGAGTCGCCTGCCACAAGCTGATAAACCACCACATCTTCACCAACCTCATCCTTGTGTTCATTATGCTAAGCTCAGCGTCATTGGCTGCTGAGGATCCAATCAGAAACTTCTCTGCTAGGAATATTG[T/A]GAGTATTACCACAGTAATGCCAAGATTATACAGTAAAGTCCAAACCATTTCATAGATAGTTGAACTAAAACAATATTTTAGTTAAATATTGCCATCATGAAATGTTTTATTTATTTATTTATTTATTTAACTAACTTTTACTTATTTATTTATTTATTTTTATTTTACTTTTATACTTTTTATTTATTTATTAGCTTACTTTTAGACTTTTATTTATTTATACTTTTATATTTTTACTTATTTTATTTTTATTTATTTACTTTTACTTTTAACTTTTTTATTTATTTACACATTTATATTTTCATTTATTTTTATTTATACTTATATTTAGTTGTATATATGTTTTACTTTTAAACTTTAATTTATTTATTTATACTTTTATCCTTTGATATGTTTGTTTTATTTATTTATTTATACTTTTATTAATTTATTTATACTTTTATCCTTTATTTGTTTATACTTTTATTTTTATTTATTTATTTATTTATACATTTATTATA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa17298
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 |
---|---|---|---|---|---|
ENSDART00000058276 | None | None | 1716 | None | 40 |
ENSDART00000089956 | None | None | 2083 | None | 50 |
ENSDART00000100118 | Essential Splice Site | 855 | 2069 | 22 | 50 |
Genomic Location (Zv9):
Chromosome 11 (position 37698393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36595621 |
GRCz11 | 11 | 36857604 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCAGATTATGTCYTCACTAGTATGTTTACATTTGAGATCGTGTTAAAG[G/A]TAACCTTTCGGCACACAGGCCTGGCTGCATTATCYCCATRTGTGTCACCT
Long Flanking Sequence:
TGAAAAAAAACTGTAATTATTTCAACAATATGATTTTATTGAGGCAAATTTTTCAGAAAATCTGGTAATATTTTTTCTGTGCTTCTGTTATTCCTTCCTGTCATTATGTTTTCTAACCTATTTCTTTCAAACTAAGGAATCTACCTTTACTGAAACACTTGTTTTTGTGGTGTTACCAAAAAAGACACACTGGTACACCCTGGATTAATTAATCAAAGATAAACCTACACATCTAAATCTATATAATCTGATGATAAACAATGATGTATTTTCTTTTTGTTAAACATGTATATTGCTCTTTGCAGATACTTGGTTACTTTGACTATGCTTTCACGGCTATCTTTACTGTAGAGATCGTGTTAAAGGTAAATGTCCTTGCCTGTGCTGGTGTTGTGTGTGGTGTATGTGCAGTAACGCTGTAACCGTCTGGTTTATTCCAGGTCCTAGGCTATGCAGATTATGTCTTCACTAGTATGTTTACATTTGAGATCGTGTTAAAG[G/A]TAACCTTTCGGCACACAGGCCTGGCTGCATTATCTCCATGTGTGTCACCTGCTACTTCAGTACTTCCTGGCTTGATCAATCTCTTTTCTTTCTATTATTTAAACCATAGCACCTCTTTTACTAAATGACTCAAAGAAAAAGTCTCCGAACATCCTCATCAAAGCACAAGAGTTGTCAGGTTTTCACTTTTGTTTTGGGGAGAACGACAGGGCTTGAAGTCAACCCTGATTGGTTAAAGTGGGGTTAAGAAAAGAGATCTGGAGAAATCACACAGGAAGTGTCTGTGAAACTAAAACGTTGTTGAAAAAAATACGAAAAGATAAAACTATGCAACTCTTTGTGAAATGAAAAACAGCATTGCCTCTCTCATGCCTTCATAACTGATTGGCCCGTTTCCAGTCCATAAAAGAGGGGGCAAATACAACCATGCTTGGACAGAACATGGTTCAAACCCCTTGGCTGAGTGCATATCAATGCAATGTGACCTCAAGCGCCGTGTG
Associated Phenotype:
Not determined