ZMP
si:dkey-106m10.4
Ensembl ID:
ZFIN ID:
Human Orthologues:
AC008661.1, TRPC7
Human Descriptions:
short transient receptor potential channel 7 isoform 1 [Source:RefSeq peptide;Acc:NP_065122]
transient receptor potential cation channel, subfamily C, member 7 [Source:HGNC Symbol;Acc:20754]
transient receptor potential cation channel, subfamily C, member 7 [Source:HGNC Symbol;Acc:20754]
Mouse Orthologue:
Trpc7
Mouse Description:
transient receptor potential cation channel, subfamily C, member 7 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15708 | Essential Splice Site | Available for shipment | Available now |
sa34889 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15708
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063619 | Essential Splice Site | 780 | 861 | 9 | 12 |
ENSDART00000138703 | Essential Splice Site | 771 | 842 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 21504258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 21465672 |
GRCz11 | 10 | 21423053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGGGATTCACGGTTAGAAATMCCATCAAACACCCTACACGATATCAG[G/T]KAATGATTGGATTTTGATCCAGAGACACTTCTCTGTAGGCCATTTYAAAT
Long Flanking Sequence:
TAACATGCTCATAGCCATGATTAACCACTCATACCAGGAAATTGAGGTGAGCCCATGCACATTTACAATAATAAACTCAAGTATTTTGCTCTTATTGACACAGTGATGTTTGTGTGTGTGAGCACAGGAGGATGCTGATGTGGAATGGAAGTTTGCTCGTGCAAAGCTCTGGCTCTCGTATTTTGATGAAGGCAGCACTCTTCCAGCCCCCTTTAATCTAATACCCAGCCCCAAATCCTTCTATTACATGGCTCAGCGCACCAAAGCATGCCTAGTGAGTTTATGCAAGGCCAGGGTCCGCAGCAACAGCAGCCAGCAGGACATGGGAATGGCCAATTCTCGCTCTAAGGTCAGAGATCAGCGTGGGTTTTCTAACTGTTCAAATCAACAAATGGCCGTCCTTAATTTTGATATCTTTACAGCTTTATCGATTTCGACCTTACCATTCGCAAGAGGGATTCACGGTTAGAAATCCCATCAAACACCCTACACGATATCAG[G/T]TAATGATTGGATTTTGATCCAGAGACACTTCTCTGTAGGCCATTTTAAATTAAAATCCTATTCACAATCTTTTTATCGTTGTAGAAACTCATGAAGCGACTCATCAAGCGATATGTCCTGAAAGCCCAAATTGACAGTGAAAGTAATGAGATCAATGAAGGTAAGATTTATCCAAAACAATCTTTTTACAATAGCTATTTTACAATTTTATCATATTCTGTGGCTAATTTGTAGTTCACGCAAAATTAAACTTCGTTATGAATATTCTATAAGGGCAGGTTATGTGGGAATAATGCTGTCATTGGTACAGAGCAAAGGGTTCAAGAGTTCTGAAATGTTTTGAAGAAACTGGACTCATTAGAAGATGTGTCCAATAGACACAATGCTCAAGCATACAGTGCATCCAGAAAGTATTCAAAGTGCTTTACTTTTTCCACATTTGTTCTAGTTACAACCTCATTCCAAAATGGGTTAAATTCATTTATTTCCTCAAAATTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34889
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 |
---|---|---|---|---|---|
ENSDART00000063619 | Nonsense | 841 | 861 | 11 | 12 |
ENSDART00000138703 | Nonsense | 832 | 842 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 10 (position 21510168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 21471582 |
GRCz11 | 10 | 21428963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAAAATCCCAGGCCACAGAGGAGCTGGCTGAACTGATCCAGGAGCTT[G/T]GAGACAAACTCAGCAAAGGAAACAAGAGACCGTGACAAACGAACTGGTGT
Long Flanking Sequence:
AAAGCTCAAGCTCGTTCAAGCAGGGTGGATTCTTATTAGTTTATTTTTATTATTCATGAGCTTGAAAAAAAATGTTATGAAAGGGATTCCAACGGTATCATTCCTCTGTCACCATACTTTTGATGCTGACTTTATACATTGCAAACAATTTGCAGAACTTTATTTGCATGAAAGAAGCACATCTTTTAGAGATATGTGATTCTGGAGAATATGATTCTAAATAGCATTGTGCAAATAACTAATTTTTAGAGTTCAAAAAGTGTCAAGCTATTAAGTGTTGAAAAAAACACTTATAAAAATAAGTAAACATATAAAAATTTATATATGACTATAACTCTGTTTTTGAGGATGTATTTTCATTGAAAGAGATCAAACTGTTGTGCTTTTTCTCTTCAGGTGAGTTGAAGGAAATCAAGCAGGACATTTCCAGCCTGCGTTATGAGCTCCTGGAGGAAAAATCCCAGGCCACAGAGGAGCTGGCTGAACTGATCCAGGAGCTT[G/T]GAGACAAACTCAGCAAAGGAAACAAGAGACCGTGACAAACGAACTGGTGTGAAAGTAGCTGAAAGTGTCCTAGAGCTTATTAAATTCCGAAATATTTAGTTTAGATACAAACTTTAAAGTCTTTTTATACTCTCAAGACACCAGTTTGTGAAATAGGTATGATTTGTGGTTGCCATTTGGGTGTAGGGTGCAATTTAATAAAGTAATTATAGAGCAAACTCAGGAAAACCAATAAATTCAGAAGACTCTGTTTCCTCAGAACGTATATTATTAAGACAAAAACAGCAGAACTAAGTGTGTTAGTATTAAATATTATGATAGTTCTGGAGTCCCAGCACTGTGCATTATGGTTTAGAAGGTTGGACTAATGAGATCATGTTTTAAATAAATGTTTGTTGAATAACAATCTAAAATGTGCAAGGGGAGCTCAAAGACCTGGACAAAAATGCAATAACAGTTTAATGTTTCCTATATTTAAATTATGTATGAAGAGTACAACA
Associated Phenotype:
Not determined