ZMP
si:dkey-117n22.2
Ensembl ID:
ZFIN ID:
Description:
LOC100003278 protein [Source:UniProtKB/TrEMBL;Acc:A2VCY5]
Human Orthologue:
CACNG7
Human Description:
calcium channel, voltage-dependent, gamma subunit 7 [Source:HGNC Symbol;Acc:13626]
Mouse Orthologue:
Cacng7
Mouse Description:
calcium channel, voltage-dependent, gamma subunit 7 Gene [Source:MGI Symbol;Acc:MGI:1932374]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22780 | Nonsense | Available for shipment | Available now |
sa36063 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22779 | Nonsense | Available for shipment | Available now |
sa11809 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22780
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 |
---|---|---|---|---|---|
ENSDART00000103891 | Nonsense | 198 | 346 | 5 | 5 |
ENSDART00000133735 | Nonsense | 225 | 373 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 14715477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13073936 |
GRCz11 | 16 | 12964056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTTGTTGTCTCGATGTTGTCCAGGGCGCTGGTGTGATGTCAGTGTA[T/A]CTTTTCATGAAGCGTTATGCAGAGGAGGAGATGTATCGGCCTCACCCCAC
Long Flanking Sequence:
TTAGGTTGGACGTTGGACATTGACATTGGCCTGACATTGCGTTTTGACGTCAACCCAATTTGCATTTCCAAACAAAATGCAACGTCTCCATGACATTGGGATACAACGTCATTTTGGCATCCTGTGCCTGCTGGGTAGATTTAAATAAAGTCCCTTTAAGGCAAGTCATTTCAGCAGCCATCTTTAAACACATCTCGGGCAGTATGCTCAGGTATTTTGTCTGAATTGGGAAACATCAAACTCTCCAAAACTGCCTGCCAAACTTACCATTGAGTTTCATATTAAAAATCACCAATAAAATTAATCAACAACAGTGTCTTTACAAACTTTTGCCCGATCAAAAAGATAACAGTGACATGTCTTGTGTATTCTATAGTCTTTGATTTAAAACCGATTTTTTTTCCTGGACATGTAGAATGTGGCAGTTATGGATCATCATAGAATTAATCTCTCTCTTGTTGTCTCGATGTTGTCCAGGGCGCTGGTGTGATGTCAGTGTA[T/A]CTTTTCATGAAGCGTTATGCAGAGGAGGAGATGTATCGGCCTCACCCCACTCTCTATCGCCCCCGTCTTTCCGAGGGCAGTGACTACAGCGGTCAGTATCTTCACCCAGAGACCTGGCCTCCACCTCAGCGAGCACGCAGCGCCTCTGAGATCTCCAGCGACATCTCCATCCAACTCACCCAGAACCCACAGCACCCATCCAAGGCCAGTGGGCAGCAGGGCACGTCCTCTCCAGGAATCACCGCCGCCTCCAGTCCCGCCTCAGGAACTGGATACCAGCTGCCATCTCCAGGTTCTGCCGCTCCATACCCACACAACCACCCCCTCCACCCCGGGGCGCACGGCCCAGCTGCGGCATCACAGGCCATGCCCATGTCCGCTCCGCCCGCTGCTGTGCCACCGCCACACTACCACACACACATGCGCATGAGCGCCTCGCCATGCTAAAGAGAAAGTTTATAGCGCACTCGTTTTTCATTGAGATGATGCATAGTACATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36063
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103891 | Nonsense | 210 | 346 | 5 | 5 |
ENSDART00000133735 | Nonsense | 237 | 373 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 14715441)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13073900 |
GRCz11 | 16 | 12964020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATGTCAGTGTATCTTTTCATGAAGCGTTATGCAGAGGAGGAGATGTA[T/A]CGGCCTCACCCCACTCTCTATCGCCCCCGTCTTTCCGAGGGCAGTGACTA
Long Flanking Sequence:
TTGCGTTTTGACGTCAACCCAATTTGCATTTCCAAACAAAATGCAACGTCTCCATGACATTGGGATACAACGTCATTTTGGCATCCTGTGCCTGCTGGGTAGATTTAAATAAAGTCCCTTTAAGGCAAGTCATTTCAGCAGCCATCTTTAAACACATCTCGGGCAGTATGCTCAGGTATTTTGTCTGAATTGGGAAACATCAAACTCTCCAAAACTGCCTGCCAAACTTACCATTGAGTTTCATATTAAAAATCACCAATAAAATTAATCAACAACAGTGTCTTTACAAACTTTTGCCCGATCAAAAAGATAACAGTGACATGTCTTGTGTATTCTATAGTCTTTGATTTAAAACCGATTTTTTTTCCTGGACATGTAGAATGTGGCAGTTATGGATCATCATAGAATTAATCTCTCTCTTGTTGTCTCGATGTTGTCCAGGGCGCTGGTGTGATGTCAGTGTATCTTTTCATGAAGCGTTATGCAGAGGAGGAGATGTA[T/A]CGGCCTCACCCCACTCTCTATCGCCCCCGTCTTTCCGAGGGCAGTGACTACAGCGGTCAGTATCTTCACCCAGAGACCTGGCCTCCACCTCAGCGAGCACGCAGCGCCTCTGAGATCTCCAGCGACATCTCCATCCAACTCACCCAGAACCCACAGCACCCATCCAAGGCCAGTGGGCAGCAGGGCACGTCCTCTCCAGGAATCACCGCCGCCTCCAGTCCCGCCTCAGGAACTGGATACCAGCTGCCATCTCCAGGTTCTGCCGCTCCATACCCACACAACCACCCCCTCCACCCCGGGGCGCACGGCCCAGCTGCGGCATCACAGGCCATGCCCATGTCCGCTCCGCCCGCTGCTGTGCCACCGCCACACTACCACACACACATGCGCATGAGCGCCTCGCCATGCTAAAGAGAAAGTTTATAGCGCACTCGTTTTTCATTGAGATGATGCATAGTACATAAAAAGAAACAAAAACTACAGTGTAAGGCAAGATATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22779
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103891 | Nonsense | 217 | 346 | 5 | 5 |
ENSDART00000133735 | Nonsense | 244 | 373 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 14715420)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13073879 |
GRCz11 | 16 | 12963999 |
KASP Assay ID:
2260-9347.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAGCGTTATGCAGAGGAGGAGATGTATCGGCCTCACCCCACTCTCTA[T/G]CGCCCCCGTCTTTCCGAGGGCAGTGACTACAGCGGTCAGTATCTTCACCC
Long Flanking Sequence:
ATTTGCATTTCCAAACAAAATGCAACGTCTCCATGACATTGGGATACAACGTCATTTTGGCATCCTGTGCCTGCTGGGTAGATTTAAATAAAGTCCCTTTAAGGCAAGTCATTTCAGCAGCCATCTTTAAACACATCTCGGGCAGTATGCTCAGGTATTTTGTCTGAATTGGGAAACATCAAACTCTCCAAAACTGCCTGCCAAACTTACCATTGAGTTTCATATTAAAAATCACCAATAAAATTAATCAACAACAGTGTCTTTACAAACTTTTGCCCGATCAAAAAGATAACAGTGACATGTCTTGTGTATTCTATAGTCTTTGATTTAAAACCGATTTTTTTTCCTGGACATGTAGAATGTGGCAGTTATGGATCATCATAGAATTAATCTCTCTCTTGTTGTCTCGATGTTGTCCAGGGCGCTGGTGTGATGTCAGTGTATCTTTTCATGAAGCGTTATGCAGAGGAGGAGATGTATCGGCCTCACCCCACTCTCTA[T/G]CGCCCCCGTCTTTCCGAGGGCAGTGACTACAGCGGTCAGTATCTTCACCCAGAGACCTGGCCTCCACCTCAGCGAGCACGCAGCGCCTCTGAGATCTCCAGCGACATCTCCATCCAACTCACCCAGAACCCACAGCACCCATCCAAGGCCAGTGGGCAGCAGGGCACGTCCTCTCCAGGAATCACCGCCGCCTCCAGTCCCGCCTCAGGAACTGGATACCAGCTGCCATCTCCAGGTTCTGCCGCTCCATACCCACACAACCACCCCCTCCACCCCGGGGCGCACGGCCCAGCTGCGGCATCACAGGCCATGCCCATGTCCGCTCCGCCCGCTGCTGTGCCACCGCCACACTACCACACACACATGCGCATGAGCGCCTCGCCATGCTAAAGAGAAAGTTTATAGCGCACTCGTTTTTCATTGAGATGATGCATAGTACATAAAAAGAAACAAAAACTACAGTGTAAGGCAAGATATAGTTTTTTATATGAGGAAAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11809
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 |
---|---|---|---|---|---|
ENSDART00000103891 | Nonsense | 231 | 346 | 5 | 5 |
ENSDART00000133735 | Nonsense | 258 | 373 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 14715378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 13073837 |
GRCz11 | 16 | 12963957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCTCTATYGCCCCCGTCTTTCCGAGGGCAGYGACTACAGCGGTCAGTA[T/A]CTTCACCCAGAGACCTGGCCTCCACCTCAGCGAGCACGCAGCGCCTCTGA
Long Flanking Sequence:
GATACAACGTCATTTTGGCATCCTGTGCCTGCTGGGTAGATTTAAATAAAGTCCCTTTAAGGCAAGTCATTTCAGCAGCCATCTTTAAACACATCTCGGGCAGTATGCTCAGGTATTTTGTCTGAATTGGGAAACATCAAACTCTCCAAAACTGCCTGCCAAACTTACCATTGAGTTTCATATTAAAAATCACCAATAAAATTAATCAACAACAGTGTCTTTACAAACTTTTGCCCGATCAAAAAGATAACAGTGACATGTCTTGTGTATTCTATAGTCTTTGATTTAAAACCGATTTTTTTTCCTGGACATGTAGAATGTGGCAGTTATGGATCATCATAGAATTAATCTCTCTCTTGTTGTCTCGATGTTGTCCAGGGCGCTGGTGTGATGTCAGTGTATCTTTTCATGAAGCGTTATGCAGAGGAGGAGATGTATCGGCCTCACCCCACTCTCTATCGCCCCCGTCTTTCCGAGGGCAGTGACTACAGCGGTCAGTA[T/A]CTTCACCCAGAGACCTGGCCTCCACCTCAGCGAGCACGCAGCGCCTCTGAGATCTCCAGCGACATCTCCATCCAACTCACCCAGAACCCACAGCACCCATCCAAGGCCAGTGGGCAGCAGGGCACGTCCTCTCCAGGAATCACCGCCGCCTCCAGTCCCGCCTCAGGAACTGGATACCAGCTGCCATCTCCAGGTTCTGCCGCTCCATACCCACACAACCACCCCCTCCACCCCGGGGCGCACGGCCCAGCTGCGGCATCACAGGCCATGCCCATGTCCGCTCCGCCCGCTGCTGTGCCACCGCCACACTACCACACACACATGCGCATGAGCGCCTCGCCATGCTAAAGAGAAAGTTTATAGCGCACTCGTTTTTCATTGAGATGATGCATAGTACATAAAAAGAAACAAAAACTACAGTGTAAGGCAAGATATAGTTTTTTATATGAGGAAAGGAAGTAAAATACTGTTTGTAACAAAGGCCTCTTTTTAAGACTGAA
Associated Phenotype:
Not determined