ZMP
trpc6
Ensembl ID:
ZFIN IDs:
Description:
short transient receptor potential channel 6 [Source:RefSeq peptide;Acc:NP_001025453]
Human Orthologue:
TRPC6
Human Description:
transient receptor potential cation channel, subfamily C, member 6 [Source:HGNC Symbol;Acc:12338]
Mouse Orthologue:
Trpc6
Mouse Description:
transient receptor potential cation channel, subfamily C, member 6 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23930 | Nonsense | Available for shipment | Available now |
sa37301 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15581 | Essential Splice Site | Available for shipment | Available now |
sa10188 | Essential Splice Site | Available for shipment | Available now |
sa37300 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37299 | Nonsense | Available for shipment | Available now |
sa23929 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23930
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 |
---|---|---|---|---|---|
ENSDART00000079151 | Nonsense | 213 | 855 | 2 | 11 |
ENSDART00000112175 | Nonsense | 213 | 874 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21925673)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22774086 |
GRCz11 | 21 | 22810691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGCTTTTCTCATGACGTCACTCCAGTCATTCTAGCCTCTCACTGTCAC[G/T]AGTACGAGATCGTGCACATACTTTTGGGAAAGGGTGCGCGCATTGAGCAG
Long Flanking Sequence:
TTCGCAGTGAGAACGTGGCCCGTCAGGTGCTGCCCAAGAGCCGCAGGCAGGCGGTGCGAGGAGCGGCTTACATGTTCAACGGCCATCCCAATAGCTTGACCCCGCTGGAGGAGCGCTTCCTCGATGCTGCTGAGTATGGGAACATCCCAGTGGTGCGTAGGATGCTGGAGGAGCTGCCGGAGCTGGACGTCAACTGTGTGGACTACATGGGCCAGAATGCACTGCAGCTCGCGGTGGCCAACGAGCACCTGGAGGTGACAGAGCTCTTGTTAAAAAAAGACAACCTGTCACGTATCGGGGATGCTCTTTTGTTGGCCATCAGCAAAGGTTACACCAGGATTGTGGAAGCCATTTTAAGCCACAAAGCTTTCGCGGACTCAAGGAGACTCACCGCGAGCCCCAGCCAGGCCCCGATGCACGATGACTTCTTCGCCTACGACGAAGATGGCACGCGCTTTTCTCATGACGTCACTCCAGTCATTCTAGCCTCTCACTGTCAC[G/T]AGTACGAGATCGTGCACATACTTTTGGGAAAGGGTGCGCGCATTGAGCAGCCTCATGATTACTTCTGTACCTGCGACACCTGTAATTATCATCAAAAGTACGATTCCTTCTGTCACTCCCGCTCGAGGATCAACGCTTACAGAGGATTGGCCAGTCCGGCTTACCTCTCTCTGTCCAATGAGGATCCAGTGTTGGCGGCCCTGGAGCTCAGCAATGAGCTCGCATCCTTGGCCAATATTGAAAAGGAATTTAAGGTATACCAGCAAGCACTTATTTTACTAAAAATTTAACTCTCGTGGTTACTTGCTCATCTTCAGCAAACACAGAGTTTCCTCTAAAACTTTCAAAGTCTCTAAAGGGTTGTTTGGCTGAAAGGCTGTAACTGAAAGAGAACCTAAAAGAGAGAATCAGAGCAATGTTCTCCTTACTTGAGGGAACATGTAATGTGTTTAAACATACATAAGCTGACTTATAGATCTTGACATACTGTATAGAACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37301
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079151 | Essential Splice Site | 485 | 855 | 6 | 11 |
ENSDART00000112175 | Essential Splice Site | 485 | 874 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21923359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22771772 |
GRCz11 | 21 | 22808377 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCTGATGCAACATTCATGTATTTGTTTTCATGTCAATCTCTCTCTCA[G/A]GGATGATTTGGGCAGAGTGCAAGGAGATCTGGTCCCAAGGACCAAGAGAA
Long Flanking Sequence:
TTGTAAATTATAGCAGTGCTTAAAATATCCACCGTATCATATGAGTCATAATAATGTTGATAAACATATCAGGCTGATAATGTACGAATACACAATAGAAGAATGCAGTATTTTGTTAATCACACCACAATCAGTCTAAAATGCTGTTACCAACAGATGGGAAAGATCATGCGTGGCCCTTTCCTTAAGTTTGTGGCACATGCGGCCTCCTTTACTATTTTCCTTGGCCTTTTGGTCATGAACGCTGCCGACCGCTTTGATGGGACAAAGCTTCTTCCAAATATGACCATCCATGACTATCCGACACAGCTGTTTCGTATGAAAACAACTCCCTTCACGTGGATGGAAATGCTCATCATTTCCTGGGTCATAGGTTTGTTTCTTACTTGTTAAAGATTACTACTTAACTACAGTCTGTATTCACAGAACAAAGTGTGCAGTTCATTTGCATGTCCTGATGCAACATTCATGTATTTGTTTTCATGTCAATCTCTCTCTCA[G/A]GGATGATTTGGGCAGAGTGCAAGGAGATCTGGTCCCAAGGACCAAGAGAATATCTGCTTGAGCCTTGGAACTTGCTAGACTTTGGAATGTTGGCCATTTTTGTGGCATCCTTCATCTCAAGGATAATGGCTTTCTGGCATGCAAGTTCAGCACAACGCTATGTTGATGAGCATTACACAGATCTAACCAATGTAGTATTACCTTTTGAGGTGGGATACTTCCAGCGGGGTGAGTGAATGTCCTGACAAGTCACAAATCACACTCCAAATCAACAACAAAGCAAAATATTTTTTTTTATTTTTGTTCCAGCTCGGATTGACTGGCTTCCATCAGATCCTCAGTTAGTCTCAGAGGGCTTGTATGCCATTGCAGTGGTGCTGAGTTTTTCTCGAATTGCCTATATTCTGCCAGCTAATGAGAGCTTTGGACCACTGCAAATATCTTTGGGACGAACTGTGAAGGACATCTTCAAGTTCATGGTTATCTTCATCCTAGTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15581
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079151 | Essential Splice Site | 561 | 855 | 7 | 11 |
ENSDART00000112175 | Essential Splice Site | 561 | 874 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21923051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22771464 |
GRCz11 | 21 | 22808069 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACACTCCAAATCAACAACAAAGCAAAATATTTTTTTTNATTTTTGTTCC[A/C]GCTCGGATTGACTGGCTTCCATCAGATCCTCAGTTAGTCTCAGAGGGCTT
Long Flanking Sequence:
GCTGTTTCGTATGAAAACAACTCCCTTCACGTGGATGGAAATGCTCATCATTTCCTGGGTCATAGGTTTGTTTCTTACTTGTTAAAGATTACTACTTAACTACAGTCTGTATTCACAGAACAAAGTGTGCAGTTCATTTGCATGTCCTGATGCAACATTCATGTATTTGTTTTCATGTCAATCTCTCTCTCAGGGATGATTTGGGCAGAGTGCAAGGAGATCTGGTCCCAAGGACCAAGAGAATATCTGCTTGAGCCTTGGAACTTGCTAGACTTTGGAATGTTGGCCATTTTTGTGGCATCCTTCATCTCAAGGATAATGGCTTTCTGGCATGCAAGTTCAGCACAACGCTATGTTGATGAGCATTACACAGATCTAACCAATGTAGTATTACCTTTTGAGGTGGGATACTTCCAGCGGGGTGAGTGAATGTCCTGACAAGTCACAAATCACACTCCAAATCAACAACAAAGCAAAATATTTTTTTTTATTTTTGTTCC[A/C]GCTCGGATTGACTGGCTTCCATCAGATCCTCAGTTAGTCTCAGAGGGCTTGTATGCCATTGCAGTGGTGCTGAGTTTTTCTCGAATTGCCTATATTCTGCCAGCTAATGAGAGCTTTGGACCACTGCAAATATCTTTGGGACGAACTGTGAAGGACATCTTCAAGTTCATGGTTATCTTCATCCTAGTCTTTCTGGCCTTCATGATTGGAATGTTCAACCTCTACTCATATTATCGGGGTGCAAAACAGAATGAAGCTTTCACAACGTGAGTTGAAATTATGATCTATTAGAAGTGTCTATAGTGGCAAGGGTAAAGAAGGTGAGTGGACCTTGGTGAAACAGGGTAGACCTTAGTACTTGATCTGAATCTACAGAACATTATTTTACTAAATTTAGCTAGAAGTGGTTTTGCTGAGTTTTTTTTTTTGTTGAAAGAGAAAAATATAAGGCAGAAACATGTGCCTAAAGTTAAATAAAATGTGTGGCTTTACTTGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10188
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 |
---|---|---|---|---|---|
ENSDART00000079151 | Essential Splice Site | 781 | 855 | 9 | 11 |
ENSDART00000112175 | Essential Splice Site | 781 | 874 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21918881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22767294 |
GRCz11 | 21 | 22803899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTTTCTGTCAGGCAAAAAGCCATTATGAAGGGGTCTGAACTCAGTGAG[G/A]TGAGGCAAATCCAYTCTTTTRCATTAAGTTRTAGTGACATTARCMATATT
Long Flanking Sequence:
CTCAACATGCTCATTGCCATGATCAACAACTCATTTCAGGAGATTGAGGTTCATCTCAGTTTCATTTCTTTAGATTTCTCTCTGAGAACTGCTGACATGATAAATCTTGAGGGTTTAGTGAGTCTTTGTGCTGATGAAGCACCCTATTGTAGTGGTTTTTGCAGACTACAAAAAAACAACCTTATCTCTTCAAAATGGGATAATTAGTTTGACTGCTTAGCAAGTTTCAAATCATCTTTTTACTGATTAAGTTGTTGCTTTATAAATTTAAAGCATCAGCACTTTCTATCATTTTCCAGGATGACGCAGATGTGGAGTGGAAGTTTGCCCGTGCCAAGCTCTGGTTCACCTACTTTGAGGAGGGCAGGACTCTCCCTGTGCCTTTTAACCTGATTCCCAGTCCCAAATCAGTACTTAGTCTGGTTATGGGGGTCAAGGGTCTCCTGCGAGAGCTTTCTGTCAGGCAAAAAGCCATTATGAAGGGGTCTGAACTCAGTGAG[G/A]TGAGGCAAATCCACTCTTTTACATTAAGTTATAGTGACATTAGCCATATTAAAGCAGAGATGTATGAAGCACACACAGAAATCACTTTCATAACAAGCAGCTTTCCTTTGGTACAATGGACAAAGTATAAACAGCTTGTTTTAGTCCCATTTCCCGCAACACACACCATAACAATCCCATTTTCGATTACCTCTGCAAGTTGTTGAACGTGGAAAAGGTCAAAATATGACTAGACTAGACAAGATTGTATTAGCAAAACTGCAGCGATAAAAAGATCTGTATTGTCCAATCATGTCAATAGCCTGCATATATATGTAGTACAGCCCACACATGAGTCAATGCCGCAAATGTGGTAGATTTATGGGCGTAGACCCATTTCAAAATGACTGAGTTTCACACACTTGCAAAGCTGCCAATCATGAAGTTTAGTGGTTTTCACCCACAATTTTTGTCAGTGATGGTAAATGTCACCAAACATTTAAAGTACACATGAAATCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37300
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079151 | None | None | 855 | None | 11 |
ENSDART00000112175 | Essential Splice Site | 782 | 874 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21916868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22765281 |
GRCz11 | 21 | 22801886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCATTCATATGTGTCCTGTGGTTTGTTGGGTCATTTGTTTACAATTCA[G/A]TTGGGACAGAGCAAAACTTGCCAGGCCAAGACTCTTCCACGTTCCAGTCG
Long Flanking Sequence:
TGAACTGAAGCCTAGGAGGATGCTCTTAAAGAGATTGTGATGTTGTTTGATGCCTAATATGCTTTTAATTGTTTAAATTAAACTTACTGAGTGATATTAAATTGAGGTTTACACCATATCTGCATTTTGACATCGCGGCAACAGCTGAAAGTTTGTAGTCCACAGCATGTTGTTGCAATGTTTACAGTGCTGATCCTATCCTTCTGGGTTTCTTCCCACCGCAGCCTCGCTTTCGTGTTTTATAATGGCGGCCGCATGAAACAAGAGTATGCAATGCCTACTGTACTACATTCAATCAGTTCATAGTAAAAAAAAAGTCACGTCTACTGTTTTCTCATTTAATATGCCGTTTCTCTAGGAACTGCGTCACAATAGGAAAAAAAACTGTTGCAGCTTGGAAGTTAATGTGGAAGTTAAAGTAATTAATTCATTTACGATCACAATAAACTAACCCATTCATATGTGTCCTGTGGTTTGTTGGGTCATTTGTTTACAATTCA[G/A]TTGGGACAGAGCAAAACTTGCCAGGCCAAGACTCTTCCACGTTCCAGTCGATATCAGGCATGTTTATTTCCGTTTTAATTTGCTACACTGCATATATTTAATAGATGTGAATATGGTTCATATTTCCTATTTGAATTTGAAGTCAGTTTGTAATCTGTACAGAAAATTATGAAGCGTCTTGTGAAGCGATACATCATCAAGGCTCAAAATGACAAGGAATGTGATGAAGTCAACGAGGGTGAGTGTCTGAATTTGAGGAATAATTCACAAATTTTACACACGTTCTATAACGACAGCCATCAATAGATAGAGCAATATAAAATATATTATTCCTATTTATGTATCCCACTGAATCAAAATCCCAAAGAGGATCAGCAGCAAAAGGATTCTTAGGGGAAATTTCTCTGTTAACATAATGTAAATATTTCACAATACTTGTTGCAGGTGAACTGAAGGAGATCAAACAGGACATTTCAAGCCTTCGCTATGAACTGCTGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37299
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 |
---|---|---|---|---|---|
ENSDART00000079151 | Nonsense | 796 | 855 | 10 | 11 |
ENSDART00000112175 | Nonsense | 815 | 874 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21916663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22765076 |
GRCz11 | 21 | 22801681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTACAGAAAATTATGAAGCGTCTTGTGAAGCGATACATCATCAAGGCT[C/T]AAAATGACAAGGAATGTGATGAAGTCAACGAGGGTGAGTGTCTGAATTTG
Long Flanking Sequence:
GGGTTTCTTCCCACCGCAGCCTCGCTTTCGTGTTTTATAATGGCGGCCGCATGAAACAAGAGTATGCAATGCCTACTGTACTACATTCAATCAGTTCATAGTAAAAAAAAAGTCACGTCTACTGTTTTCTCATTTAATATGCCGTTTCTCTAGGAACTGCGTCACAATAGGAAAAAAAACTGTTGCAGCTTGGAAGTTAATGTGGAAGTTAAAGTAATTAATTCATTTACGATCACAATAAACTAACCCATTCATATGTGTCCTGTGGTTTGTTGGGTCATTTGTTTACAATTCAGTTGGGACAGAGCAAAACTTGCCAGGCCAAGACTCTTCCACGTTCCAGTCGATATCAGGCATGTTTATTTCCGTTTTAATTTGCTACACTGCATATATTTAATAGATGTGAATATGGTTCATATTTCCTATTTGAATTTGAAGTCAGTTTGTAATCTGTACAGAAAATTATGAAGCGTCTTGTGAAGCGATACATCATCAAGGCT[C/T]AAAATGACAAGGAATGTGATGAAGTCAACGAGGGTGAGTGTCTGAATTTGAGGAATAATTCACAAATTTTACACACGTTCTATAACGACAGCCATCAATAGATAGAGCAATATAAAATATATTATTCCTATTTATGTATCCCACTGAATCAAAATCCCAAAGAGGATCAGCAGCAAAAGGATTCTTAGGGGAAATTTCTCTGTTAACATAATGTAAATATTTCACAATACTTGTTGCAGGTGAACTGAAGGAGATCAAACAGGACATTTCAAGCCTTCGCTATGAACTGCTGGAGGAAAAGTCACACAACATGGAGGAGCTGGCGAAGCTAGTCAGGACACTTGAAAAAAACCTCTCTCAGGACTGCTTGGTTATGAAGTCTCACTGAGAAAGTCAGACAGCTGTGTTTTGATTCTATGAGGCATAGAATCAACTATTTATCAAGCAAGATATTTTGCACAAAGACTATGTGGCTTCACATGATTCTCTGCCTTGGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23929
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079151 | Nonsense | 799 | 855 | 10 | 11 |
ENSDART00000112175 | Nonsense | 818 | 874 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 21916654)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 22765067 |
GRCz11 | 21 | 22801672 |
KASP Assay ID:
2261-5587.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTATGAAGCGTCTTGTGAAGCGATACATCATCAAGGCTCAAAATGAC[A/T]AGGAATGTGATGAAGTCAACGAGGGTGAGTGTCTGAATTTGAGGAATAAT
Long Flanking Sequence:
CCCACCGCAGCCTCGCTTTCGTGTTTTATAATGGCGGCCGCATGAAACAAGAGTATGCAATGCCTACTGTACTACATTCAATCAGTTCATAGTAAAAAAAAAGTCACGTCTACTGTTTTCTCATTTAATATGCCGTTTCTCTAGGAACTGCGTCACAATAGGAAAAAAAACTGTTGCAGCTTGGAAGTTAATGTGGAAGTTAAAGTAATTAATTCATTTACGATCACAATAAACTAACCCATTCATATGTGTCCTGTGGTTTGTTGGGTCATTTGTTTACAATTCAGTTGGGACAGAGCAAAACTTGCCAGGCCAAGACTCTTCCACGTTCCAGTCGATATCAGGCATGTTTATTTCCGTTTTAATTTGCTACACTGCATATATTTAATAGATGTGAATATGGTTCATATTTCCTATTTGAATTTGAAGTCAGTTTGTAATCTGTACAGAAAATTATGAAGCGTCTTGTGAAGCGATACATCATCAAGGCTCAAAATGAC[A/T]AGGAATGTGATGAAGTCAACGAGGGTGAGTGTCTGAATTTGAGGAATAATTCACAAATTTTACACACGTTCTATAACGACAGCCATCAATAGATAGAGCAATATAAAATATATTATTCCTATTTATGTATCCCACTGAATCAAAATCCCAAAGAGGATCAGCAGCAAAAGGATTCTTAGGGGAAATTTCTCTGTTAACATAATGTAAATATTTCACAATACTTGTTGCAGGTGAACTGAAGGAGATCAAACAGGACATTTCAAGCCTTCGCTATGAACTGCTGGAGGAAAAGTCACACAACATGGAGGAGCTGGCGAAGCTAGTCAGGACACTTGAAAAAAACCTCTCTCAGGACTGCTTGGTTATGAAGTCTCACTGAGAAAGTCAGACAGCTGTGTTTTGATTCTATGAGGCATAGAATCAACTATTTATCAAGCAAGATATTTTGCACAAAGACTATGTGGCTTCACATGATTCTCTGCCTTGGCCTGCTGGTTTGA
Associated Phenotype:
Not determined