ZMP
cacnb2b
Ensembl ID:
ZFIN ID:
Description:
calcium channel, voltage-dependent, beta 2b isoform 2 [Source:RefSeq peptide;Acc:NP_001159796]
Human Orthologues:
CACNB1, CACNB2, CACNB3, CACNB4
Human Descriptions:
calcium channel, voltage-dependent, beta 1 subunit [Source:HGNC Symbol;Acc:1401]
calcium channel, voltage-dependent, beta 2 subunit [Source:HGNC Symbol;Acc:1402]
calcium channel, voltage-dependent, beta 3 subunit [Source:HGNC Symbol;Acc:1403]
calcium channel, voltage-dependent, beta 4 subunit [Source:HGNC Symbol;Acc:1404]
calcium channel, voltage-dependent, beta 2 subunit [Source:HGNC Symbol;Acc:1402]
calcium channel, voltage-dependent, beta 3 subunit [Source:HGNC Symbol;Acc:1403]
calcium channel, voltage-dependent, beta 4 subunit [Source:HGNC Symbol;Acc:1404]
Mouse Orthologues:
Cacnb1, Cacnb2, Cacnb3, Cacnb4
Mouse Descriptions:
calcium channel, voltage-dependent, beta 1 subunit Gene [Source:MGI Symbol;Acc:MGI:102522]
calcium channel, voltage-dependent, beta 2 subunit Gene [Source:MGI Symbol;Acc:MGI:894644]
calcium channel, voltage-dependent, beta 3 subunit Gene [Source:MGI Symbol;Acc:MGI:103307]
calcium channel, voltage-dependent, beta 4 subunit Gene [Source:MGI Symbol;Acc:MGI:103301]
calcium channel, voltage-dependent, beta 2 subunit Gene [Source:MGI Symbol;Acc:MGI:894644]
calcium channel, voltage-dependent, beta 3 subunit Gene [Source:MGI Symbol;Acc:MGI:103307]
calcium channel, voltage-dependent, beta 4 subunit Gene [Source:MGI Symbol;Acc:MGI:103301]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10313 | Essential Splice Site | Available for shipment | Available now |
sa16129 | Essential Splice Site | Available for shipment | Available now |
sa31283 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10313
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 |
---|---|---|---|---|---|
ENSDART00000049219 | Essential Splice Site | 282 | 374 | 10 | 14 |
ENSDART00000123495 | Essential Splice Site | 282 | 600 | 10 | 13 |
ENSDART00000126594 | Essential Splice Site | 285 | 377 | 11 | 14 |
ENSDART00000130722 | Essential Splice Site | 285 | 377 | 11 | 15 |
The following transcripts of ENSDARG00000055565 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31219352)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31520412 |
GRCz11 | 2 | 31503630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCTCCTTGGCCCCGATCCTGGTGTATGTCAAGATTTCATCCCCCAAG[G/A]TCAGAAACATTGTYCACAGAACTCACAGACATAACCATCATTTATTACGT
Long Flanking Sequence:
TAAACCTTCATTGTTCTGTTACTTCCTGTAGACAAGGAACTGTCCGTCAGCATATTTTGATCATCACTATTTTCAATGACATATTGCATGACCTCGCTATGGAATGTGTTTAGTACTGAGAACGGGACTTTCATTTTATGCTTTTTTAATTGTATCATGTTGAGAAAAAGAGCAAAAACACATTTGTTTCTTTATTGTTGTATTGGATTTGGATTGGACATAAAAAAGCTTTCCATTTTGTTTTAAAAACATATATTTTACTTTGATAGAATTTTATTTTAAGATGCTGCCTGGAAACCTGGATAATAGGTTGACTAGCCTCACTTATTTCTTTATCTGCCCTTACAGCTCAAATCCAAGGAGAGGTTGAGAGGATTTTTGAGTTAGCACGCAGTCTACAGCTTGTGGTTCTGGATGCTGACACTATTAACCACCCTCTTCAACTAAGCAAGACCTCCTTGGCCCCGATCCTGGTGTATGTCAAGATTTCATCCCCCAAG[G/A]TCAGAAACATTGTTCACAGAACTCACAGACATAACCATCATTTATTACGTTGAAGAATTAATGAGACTGATGCTTACATAGGATTTATTCTTTAATATCATAAATACAGTAAAAAAAGTAAGATTCTAATTCCAGAAAGCTTGTTTTTATCTTAGATTTAACCCTGATACAGTTTAAAGGTGGACTGTATTACCTTTATTCATTCATTAATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATTCGGGGTCGCCACAGCGGAATGAACCGCCAGCTTATCCAGCACGTTTTTACGCAGCGGATGCCCTTCCAGCCACAACCCATCTCTGGGAAAATCATCTTTATTGCTTTTATCATATTTTTACATACTGTATATGCGCACATTTTTTTTTAGGATTCTTTAATATATATAGAAATTCTTTGTAACATTTAAAAATTCCTTTGCTGTCATTATTATAGGATCTACACTAATTAACATTGTAACCCTTGTGTATTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16129
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049219 | Essential Splice Site | 282 | 374 | None | 14 |
ENSDART00000123495 | Essential Splice Site | 282 | 600 | None | 13 |
ENSDART00000126594 | Essential Splice Site | 285 | 377 | None | 14 |
ENSDART00000130722 | Essential Splice Site | 285 | 377 | None | 15 |
The following transcripts of ENSDARG00000055565 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31219353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31520413 |
GRCz11 | 2 | 31503631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACCTCCTTGGCCCCGATCCTGGTGTATGTCAAGATTTCATCCCCCAAGR[T/G]CAGAAACATTGTTCACAGAACTCACAGACATAACCATCATTTATTACGTT
Long Flanking Sequence:
AAACCTTCATTGTTCTGTTACTTCCTGTAGACAAGGAACTGTCCGTCAGCATATTTTGATCATCACTATTTTCAATGACATATTGCATGACCTCGCTATGGAATGTGTTTAGTACTGAGAACGGGACTTTCATTTTATGCTTTTTTAATTGTATCATGTTGAGAAAAAGAGCAAAAACACATTTGTTTCTTTATTGTTGTATTGGATTTGGATTGGACATAAAAAAGCTTTCCATTTTGTTTTAAAAACATATATTTTACTTTGATAGAATTTTATTTTAAGATGCTGCCTGGAAACCTGGATAATAGGTTGACTAGCCTCACTTATTTCTTTATCTGCCCTTACAGCTCAAATCCAAGGAGAGGTTGAGAGGATTTTTGAGTTAGCACGCAGTCTACAGCTTGTGGTTCTGGATGCTGACACTATTAACCACCCTCTTCAACTAAGCAAGACCTCCTTGGCCCCGATCCTGGTGTATGTCAAGATTTCATCCCCCAAGG[T/G]CAGAAACATTGTTCACAGAACTCACAGACATAACCATCATTTATTACGTTGAAGAATTAATGAGACTGATGCTTACATAGGATTTATTCTTTAATATCATAAATACAGTAAAAAAAGTAAGATTCTAATTCCAGAAAGCTTGTTTTTATCTTAGATTTAACCCTGATACAGTTTAAAGGTGGACTGTATTACCTTTATTCATTCATTAATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATTCGGGGTCGCCACAGCGGAATGAACCGCCAGCTTATCCAGCACGTTTTTACGCAGCGGATGCCCTTCCAGCCACAACCCATCTCTGGGAAAATCATCTTTATTGCTTTTATCATATTTTTACATACTGTATATGCGCACATTTTTTTTTAGGATTCTTTAATATATATAGAAATTCTTTGTAACATTTAAAAATTCCTTTGCTGTCATTATTATAGGATCTACACTAATTAACATTGTAACCCTTGTGTATTGACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31283
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049219 | Essential Splice Site | None | 374 | None | 14 |
ENSDART00000123495 | None | None | 600 | None | 13 |
ENSDART00000126594 | None | None | 377 | None | 14 |
ENSDART00000130722 | Essential Splice Site | None | 377 | None | 15 |
The following transcripts of ENSDARG00000055565 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31224480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31525540 |
GRCz11 | 2 | 31508758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAACTCTCTTGGACATTTAAAGAAGACTTGAACTTAAAGGACCTCTGG[T/C]AAGTGGGAAGATGGTGGTTCCTGAGGTAAAATACCTATAGTGTTAGTACC
Long Flanking Sequence:
TTTTGACATTGTAAGTGTCTACTTATTATACATTTTTATTTCCACCACATCTCCTATTATGTATTGTTTTTAATAGCATTCTGTGGTTGGAAATGACAATGTAACTTTGCTTTTGATATTAAATAGTGACTCTTTTGCTTAAACTCATTTTAAGACTCATTGCTAGCTTCATAAAAGCACTCAATAAAATAATCTTTCCATACTTTTCACATAATTTAACAATAACTGTTTGCTGCCCATTTTTCCATTCCATTTTTCTTAGAAATATTGCTTCACTGAAACAGTTTTTATCTTAGTAACCTAGTGTTTTCAAAACTTTTTTTTAAAGGTTTTGTCTTCTTATATAAGCAAGTCTTAAATTATGACTGCTTGGAAACATCTGCAGGCTCTATAAATTGTGGGTAGTGGTGTGTCATTTTGTGACCTTTTCAATTTCCTCCCCAACTCTTACTAAACTCTCTTGGACATTTAAAGAAGACTTGAACTTAAAGGACCTCTGG[T/C]AAGTGGGAAGATGGTGGTTCCTGAGGTAAAATACCTATAGTGTTAGTACCTACTAGTTTGTACTACTTCTTCATACCCATAGTATTAGCTATAATATATTAGATGTTGTAAATGAACCGTATAGTATGACAATAACCCATCTGTAGTGTAGCTTCATAAAAGGAATTACTTAGGGATTTGTGATAGTTGGTGTATTTAACGATTGGTGACTGGCTCTTTTATTTTGAACGTGGACAATATCCTTTCTATAGTAATCTTCAATTAGTCCACATTTTGTTCATTCTTAAGTAATACAGTACAGTAAAACAAAAAAGTAACCCTAAAATGTATTATTTTTTATAAGCCAAAAGAGATCGTTTGAGTATCAATATACATTTTATGCTAAAAATTAAAGATCATGTTCTATGATGACTTTGTTTGAATTTCTTCTCATAGTTCTAAAAAACTTCATATTGGATTTGTTACTTTGAACACCTTAAAGGCATTTTTCTTAATATTTA
Associated Phenotype:
Not determined