si:dkey-106m10.4

Ensembl ID:
ENSDARG00000027523
ZFIN ID:
ZDB-GENE-091113-40
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]
Mouse Orthologue:
Trpc7
Mouse Description:
transient receptor potential cation channel, subfamily C, member 7 Gene [Source:MGI Symbol;Acc:MGI:1

Alleles

There are 7 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa2570 Essential Splice Site F2 line generated During 2017
sa5584 Essential Splice Site F2 line generated During 2017
sa34888 Nonsense Mutation detected in F1 DNA During 2017
sa15708 Essential Splice Site Available for shipment Available now
sa9272 Essential Splice Site Mutation detected in F1 DNA During 2017
sa30937 Essential Splice Site Mutation detected in F1 DNA During 2017
sa34889 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa2570
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063619 Essential Splice Site 321 861 2 12
ENSDART00000138703 Essential Splice Site 312 842 2 11
ENSDART00000063619 Essential Splice Site 321 861 2 12
ENSDART00000138703 Essential Splice Site 312 842 2 11
Genomic Location (Zv9):
Chromosome 10 (position 21491122)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21452536
KASP Assay ID:
554-3394.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCCCTGCCTTAGCCGTGTTAAACTGGCCATTAAGTATGAAGTCAAAAAGG[T/C]ACTGGGAAATRAAACATRCACTATAAAGCCCAAAANTTAAGGTAACTCMAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5584
Current Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063619 Essential Splice Site 321 861 2 12
ENSDART00000138703 Essential Splice Site 312 842 2 11
ENSDART00000063619 Essential Splice Site 321 861 2 12
ENSDART00000138703 Essential Splice Site 312 842 2 11
Genomic Location (Zv9):
Chromosome 10 (position 21491122)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21452536
KASP Assay ID:
554-3394.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GCCCTGCCTTAGCCGTGTTAAACTGGCCATTAAGTATGAAGTCAAAAAGG[T/C]ACTGGGAAATRAAACATRCACTATAAAGCCCAAAANTTAAGGTAACTCMAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34888
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
G > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063619 Nonsense 701 861 8 12
ENSDART00000138703 Nonsense 692 842 8 11
Genomic Location (Zv9):
Chromosome 10 (position 21503945)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21465359
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATGTGGAATGGAAGTTTGCTCGTGCAAAGCTCTGGCTCTCGTATTTTGAT[G/T]AAGGCAGCACTCTTCCAGCCCCCTTTAATCTAATACCCAGCCCCAAATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15708
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Essential Splice Site
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AAGAGGGATTCACGGTTAGAAATMCCATCAAACACCCTACACGATATCAG[G/T]KAATGATTGGATTTTGATCCAGAGACACTTCTCTGTAGGCCATTTYAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9272
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > G
Consequence:
Essential Splice Site
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 21504259)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21465673
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AGAGGGATTCACGGTTAGAAATMCCATCAAACACCCTACACGATATCAGG[T/G]AATGATTGGATTTTGATCCAGAGACACTTCTCTGTAGGCCATTTYAAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30937
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
A > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063619 Essential Splice Site 806 861 None 12
ENSDART00000138703 Essential Splice Site 797 842 None 11
Genomic Location (Zv9):
Chromosome 10 (position 21510062)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 21471476
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GAGGATGTATTTTCATTGAAAGAGATCAAACTGTTGTGCTTTTTCTCTTC[A/C]GGTGAGTTGAAGGAAATCAAGCAGGACATTTCCAGCCTGCGTTATGAGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34889
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > T
Consequence:
Nonsense
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
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGGAAAAATCCCAGGCCACAGAGGAGCTGGCTGAACTGATCCAGGAGCTT[G/T]GAGACAAACTCAGCAAAGGAAACAAGAGACCGTGACAAACGAACTGGTGT
Associated Phenotype:
Not determined

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