ZMP
cacna1i
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate calcium channel, voltage-dependent, alpha 1 family subunit (CANN
Human Orthologue:
CACNA1I
Human Description:
calcium channel, voltage-dependent, T type, alpha 1I subunit [Source:HGNC Symbol;Acc:1396]
Mouse Orthologue:
Cacna1i
Mouse Description:
calcium channel, voltage-dependent, alpha 1I subunit Gene [Source:MGI Symbol;Acc:MGI:2178051]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15653 | Nonsense | Available for shipment | Available now |
sa31334 | Nonsense | Available for shipment | Available now |
sa20022 | Nonsense | Available for shipment | Available now |
sa10549 | Nonsense | Available for shipment | Available now |
sa6897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20023 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15653
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 |
---|---|---|---|---|---|
ENSDART00000085216 | Nonsense | 260 | 1547 | 6 | 27 |
ENSDART00000145615 | Nonsense | 181 | 1106 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 3 (position 29386724)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29104763 |
GRCz11 | 3 | 29235605 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCATCTTGTCCTCAGCACATCTGGCCTCRCCCTTCCCACACCATATTAT[C/T]AGCCTGAGGAGGATGACGAGCGGCCCTTCATCTGCTCGTTGGCTCAAGAT
Long Flanking Sequence:
TTTTTTTTTTAATTAAAACAAATATAAATATAAATATAAATATGCATATAATAAATAATACTGCTAATAATATTAACATTATACAAACACAAATTGTCATGAATAAACTGAAAAAAAAACCTTTAGACCTGCTTTTAGATGGTCAATGGAACAGTCTATTTCAGTTCCTCAAATAGCAATGCACCAACAATGAGCCTTAACAAACCACCTTTTTTTAAGTCGGCACACCCATGAGTCCACAAAGTAGCACTAATGCATTTTTTATTTAAACAACGATGCGCAAAACTTGAAAATTAGGGCTGTGCTGGTCTAAAAATTGCAACAAATTGTTCCATACACGTCTTGCGCCTGATATGATAGGGTGTATGATAGTGCCCTTAGTGTTTTTCACTTGCAAGAAATATTTGTTTAGTGTTAACCTGCATATTTTCAAAAGCCTTGACTTATTCCCTCATCTTGTCCTCAGCACATCTGGCCTCACCCTTCCCACACCATATTAT[C/T]AGCCTGAGGAGGATGACGAGCGGCCCTTCATCTGCTCGTTGGCTCAAGATAACGGCATCATGTCCTGCAGCGATGTGCCTGCTCGGAGAGAGGGCGGACGGGAGTGCTGTCTGGATAAAGAGGACGCTCTTCACCGGCAGGCTCTGGGTCTGAGCGCCGAGCCGCTGGTCAACGGCAGCGCATCTGCCATGGGCCTCTGTGTGAACTGGAATCAGTACTACACCCGCTGCCACACTGGACACACCAATCCTCATAAAGGAGCAATTAATTTCGACAACATAGGATACGCATGGATCGTCATATTTCAGGTATGAGATCAAAGTCACGTGGCATTTTCTGGAACGAAGCATCTGTTCTCTTTGATCGTCTTTTTCGGGTGATCTTGTCATAAATCAACAGTGTTAAGTAAATCAGAAGCGTTTTGTGATGCAGTCACTCAAAGGACATTTAGAAATACATGTGTCCACATTGCTTGTGTGGTGTGCTGCAAGTGCTAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31334
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 |
---|---|---|---|---|---|
ENSDART00000085216 | Nonsense | 275 | 1547 | 6 | 27 |
ENSDART00000145615 | Nonsense | 196 | 1106 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 3 (position 29386769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29104808 |
GRCz11 | 3 | 29235650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATCAGCCTGAGGAGGATGACGAGCGGCCCTTCATCTGCTCGTTGGCT[C/T]AAGATAACGGCATCATGTCCTGCAGCGATGTGCCTGCTCGGAGAGAGGGC
Long Flanking Sequence:
ATATAATAAATAATACTGCTAATAATATTAACATTATACAAACACAAATTGTCATGAATAAACTGAAAAAAAAACCTTTAGACCTGCTTTTAGATGGTCAATGGAACAGTCTATTTCAGTTCCTCAAATAGCAATGCACCAACAATGAGCCTTAACAAACCACCTTTTTTTAAGTCGGCACACCCATGAGTCCACAAAGTAGCACTAATGCATTTTTTATTTAAACAACGATGCGCAAAACTTGAAAATTAGGGCTGTGCTGGTCTAAAAATTGCAACAAATTGTTCCATACACGTCTTGCGCCTGATATGATAGGGTGTATGATAGTGCCCTTAGTGTTTTTCACTTGCAAGAAATATTTGTTTAGTGTTAACCTGCATATTTTCAAAAGCCTTGACTTATTCCCTCATCTTGTCCTCAGCACATCTGGCCTCACCCTTCCCACACCATATTATCAGCCTGAGGAGGATGACGAGCGGCCCTTCATCTGCTCGTTGGCT[C/T]AAGATAACGGCATCATGTCCTGCAGCGATGTGCCTGCTCGGAGAGAGGGCGGACGGGAGTGCTGTCTGGATAAAGAGGACGCTCTTCACCGGCAGGCTCTGGGTCTGAGCGCCGAGCCGCTGGTCAACGGCAGCGCATCTGCCATGGGCCTCTGTGTGAACTGGAATCAGTACTACACCCGCTGCCACACTGGACACACCAATCCTCATAAAGGAGCAATTAATTTCGACAACATAGGATACGCATGGATCGTCATATTTCAGGTATGAGATCAAAGTCACGTGGCATTTTCTGGAACGAAGCATCTGTTCTCTTTGATCGTCTTTTTCGGGTGATCTTGTCATAAATCAACAGTGTTAAGTAAATCAGAAGCGTTTTGTGATGCAGTCACTCAAAGGACATTTAGAAATACATGTGTCCACATTGCTTGTGTGGTGTGCTGCAAGTGCTAATCCATCTTGATGTGTCTTGGGCAACAGTGAAAGGCCGCCTACACACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20022
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085216 | Nonsense | 296 | 1547 | 6 | 27 |
ENSDART00000145615 | Nonsense | 217 | 1106 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 3 (position 29386834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29104873 |
GRCz11 | 3 | 29235715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTCCTGCAGCGATGTGCCTGCTCGGAGAGAGGGCGGACGGGAGTGCTG[T/A]CTGGATAAAGAGGACGCTCTTCACCGGCAGGCTCTGGGTCTGAGCGCCGA
Long Flanking Sequence:
AAAAAAAAACCTTTAGACCTGCTTTTAGATGGTCAATGGAACAGTCTATTTCAGTTCCTCAAATAGCAATGCACCAACAATGAGCCTTAACAAACCACCTTTTTTTAAGTCGGCACACCCATGAGTCCACAAAGTAGCACTAATGCATTTTTTATTTAAACAACGATGCGCAAAACTTGAAAATTAGGGCTGTGCTGGTCTAAAAATTGCAACAAATTGTTCCATACACGTCTTGCGCCTGATATGATAGGGTGTATGATAGTGCCCTTAGTGTTTTTCACTTGCAAGAAATATTTGTTTAGTGTTAACCTGCATATTTTCAAAAGCCTTGACTTATTCCCTCATCTTGTCCTCAGCACATCTGGCCTCACCCTTCCCACACCATATTATCAGCCTGAGGAGGATGACGAGCGGCCCTTCATCTGCTCGTTGGCTCAAGATAACGGCATCATGTCCTGCAGCGATGTGCCTGCTCGGAGAGAGGGCGGACGGGAGTGCTG[T/A]CTGGATAAAGAGGACGCTCTTCACCGGCAGGCTCTGGGTCTGAGCGCCGAGCCGCTGGTCAACGGCAGCGCATCTGCCATGGGCCTCTGTGTGAACTGGAATCAGTACTACACCCGCTGCCACACTGGACACACCAATCCTCATAAAGGAGCAATTAATTTCGACAACATAGGATACGCATGGATCGTCATATTTCAGGTATGAGATCAAAGTCACGTGGCATTTTCTGGAACGAAGCATCTGTTCTCTTTGATCGTCTTTTTCGGGTGATCTTGTCATAAATCAACAGTGTTAAGTAAATCAGAAGCGTTTTGTGATGCAGTCACTCAAAGGACATTTAGAAATACATGTGTCCACATTGCTTGTGTGGTGTGCTGCAAGTGCTAATCCATCTTGATGTGTCTTGGGCAACAGTGAAAGGCCGCCTACACACCTGTCAATCAAACACTATGCTATAACAAAGCTTTAAACAAATCAAATTGCAAATGAAGTTAGATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10549
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085216 | Nonsense | 395 | 1547 | 8 | 27 |
ENSDART00000145615 | Nonsense | 316 | 1106 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 3 (position 29400207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29118246 |
GRCz11 | 3 | 29249088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATGGATTTCATTATTTTCAAGCTGTATCTCTCCTTCCTGTTCCAGATT[G/T]GATCTTTCTTCATGATTAATCTGTGCCTGGTGGTCATTGCCACTCAGTTT
Long Flanking Sequence:
AGTGAATGCACTACACCTTTAAAGGAGGCATGTGTATAAGACTCTGACGGTATGATAACCTTGGATATAATTATCACTGTTTCACGGTATTGTGATTAATACTCTAAAATCTGTTTTTTTTATGTCTAGGTAGAATACTAAAACTTTTTCACCCTTTGAACAAAATATATTTTATTATAAGAAACATTTAAGATATTTTGTAACAGTAGACAAATGAATCATGATTCAAATGAATCATGTACTTTTTCTGTCATCATTAGTTACAAAAACACCAATTTCTTTAGAAAACAAATGTATCTTTTTCTGCTGGAATCTTGCATATACCTTAGAAATGGTATAGCAGAACGTTTTGGTGAATACTTTGACTTTTCCAAACCGTGGTATACCTTAAAAATGGTTATCATCTAATGCCTACTTCAAAGGTCAAGGAACAGTGTAGGAAGAAGTAAATGATGGATTTCATTATTTTCAAGCTGTATCTCTCCTTCCTGTTCCAGATT[G/T]GATCTTTCTTCATGATTAATCTGTGCCTGGTGGTCATTGCCACTCAGTTTTCGGAGACCAAACAGCGAGAGCACCAGCTGATGCAAGAGCAACGTGCTCGCTACCTGTCCTCCAGCACGCTGGCTTCACTCGCTGAGCCCGGAGACTGTTACGAGGAGCTCTTCCAACTGGTCTGCCATATCCTACGCAAAGCCCGCCGCCGCTCTGCTGCCCTTTATTACATGCTCCGTGGCAAAGCCCCTCCCCCTGGAGGTGGGAGGGGGCGTGGCAAAGGAGGAGCAGGATCGATAGGAGGAGGAGCCAATGTTAATGGAGGAGAGAAACATCACTGCCATTCAGCTCAGAGTGAGTAACGAGGCAGAGAAATGACAGTGGATCATAGAGAAGTTGTGACTAACAATAAATTGTTAAAAGTAAAAACTCTTTAAAATAGTAGCTAGAATTGTATGTCCTCTTAAGCCCTTTTTCTGCCTGCTTTACCAAACAGTTGACCTTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6897
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085216 | Nonsense | 416 | 1547 | 8 | 27 |
ENSDART00000145615 | Nonsense | 337 | 1106 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 3 (position 29400270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29118309 |
GRCz11 | 3 | 29249151 |
KASP Assay ID:
554-4831.1 (used for ordering genotyping assays)
KASP Sequence:
TGATTAATCTGTGCCTGGTGGTCATTGCCACTCAGTTTTCGGAGACCAAA[C/T]AGCGAGAGCACCAGCTGATGCAAGAGCAACGTGCTCGCTACCTGTCCTCC
Long Flanking Sequence:
GATATAATTATCACTGTTTCACGGTATTGTGATTAATACTCTAAAATCTGTTTTTTTTATGTCTAGGTAGAATACTAAAACTTTTTCACCCTTTGAACAAAATATATTTTATTATAAGAAACATTTAAGATATTTTGTAACAGTAGACAAATGAATCATGATTCAAATGAATCATGTACTTTTTCTGTCATCATTAGTTACAAAAACACCAATTTCTTTAGAAAACAAATGTATCTTTTTCTGCTGGAATCTTGCATATACCTTAGAAATGGTATAGCAGAACGTTTTGGTGAATACTTTGACTTTTCCAAACCGTGGTATACCTTAAAAATGGTTATCATCTAATGCCTACTTCAAAGGTCAAGGAACAGTGTAGGAAGAAGTAAATGATGGATTTCATTATTTTCAAGCTGTATCTCTCCTTCCTGTTCCAGATTGGATCTTTCTTCATGATTAATCTGTGCCTGGTGGTCATTGCCACTCAGTTTTCGGAGACCAAA[C/T]AGCGAGAGCACCAGCTGATGCAAGAGCAACGTGCTCGCTACCTGTCCTCCAGCACGCTGGCTTCACTCGCTGAGCCCGGAGACTGTTACGAGGAGCTCTTCCAACTGGTCTGCCATATCCTACGCAAAGCCCGCCGCCGCTCTGCTGCCCTTTATTACATGCTCCGTGGCAAAGCCCCTCCCCCTGGAGGTGGGAGGGGGCGTGGCAAAGGAGGAGCAGGATCGATAGGAGGAGGAGCCAATGTTAATGGAGGAGAGAAACATCACTGCCATTCAGCTCAGAGTGAGTAACGAGGCAGAGAAATGACAGTGGATCATAGAGAAGTTGTGACTAACAATAAATTGTTAAAAGTAAAAACTCTTTAAAATAGTAGCTAGAATTGTATGTCCTCTTAAGCCCTTTTTCTGCCTGCTTTACCAAACAGTTGACCTTGATTTGACTGTTTTAAATAATGACTGGTAAAGTCATTTAAAGAATGACTGTTTTTAATAATGGCTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20023
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085216 | Nonsense | 1431 | 1547 | 25 | 27 |
ENSDART00000145615 | None | None | 1106 | None | 18 |
Genomic Location (Zv9):
Chromosome 3 (position 29462695)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29180734 |
GRCz11 | 3 | 29311576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTAATCCGATGTGCTGATTTCTCTCAGAGGCCCAGAAGTTGCCCTACTA[T/A]GCCAGTTATAGTCATGTACGGCTGATGATCCACACCCTGTGCACCAGTCA
Long Flanking Sequence:
GAAAATGTACTCAATATCTACTCAAACTCAAATGGTTTTAAGCCTTGATGAGTTTATTGTTTTCTGCTGATCCCAAAAGAAGTTATTTGGAAAATCAAAAACTGTTATTTGGATGAAACCTGTAACCATTTACTTCTACAGTTCCATAGGAAGTCAATGGTTACCAGTTTTTTAGCATTTTCCTTATTTTACATTTTTCCTTTATTTTACATTCACCGGAAGAACAAAACTCAAACAAGTTTATGACAAGTGAAGGGTGAGTAAATCATAACTGAATGTTCAGTTTTTGGTGAACTATCCCTTTAAATGATTTCCAGACTAGTATAAACACTGTGTCTCTGTAAGGCTATCAAAAGTTGAGCTGCCAATTGTGAATGAAGCATGTTTGATATACATTTGTTGAATTGACAGAATTCAGCTTTGTGAATTATAGTCAAAATGTGCGCATGCTCTAATCCGATGTGCTGATTTCTCTCAGAGGCCCAGAAGTTGCCCTACTA[T/A]GCCAGTTATAGTCATGTACGGCTGATGATCCACACCCTGTGCACCAGTCACTACCTGGATATCTTCATCACCTTCATCATCTGTGTGAATGTAGTCACCATGTCACTGGAGCACTACAGCCAGCCTCATGTAAGACTTTTTTTGGAATCAATCATTGTTTTGGATTTTTAAATTAATTTTTGTTTTGAGACTATTTTTAAATCTGCTCTGCATTTCAGTTTGATTTTAGTTTGCATAATTATGATTATAATTATTATTTTTTTTAATTTATCAATGTATTAATTTATTCATTTATTATTATTATTATTATTATTAATATTATTATTACTATCATTGTATTATGTTATTTTAGGTTAAGTTTTTATATACTTAGTTTTAGTAATTCCAAAGTTGAATGTTTACATAGCTAACGTAGACTATGTTCCGTATACTATGTTCCGTACACATATTCCATACACTTTTTGCTATTCAGCGCACTAAAAGGATCACTCCTCCATTAT
Associated Phenotype:
Not determined