ZMP
si:dkeyp-81e1.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
TRPC5
Human Description:
transient receptor potential cation channel, subfamily C, member 5 [Source:HGNC Symbol;Acc:12337]
Mouse Orthologue:
Trpc5
Mouse Description:
transient receptor potential cation channel, subfamily C, member 5 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13112 | Nonsense | Available for shipment | Available now |
sa10159 | Nonsense | Available for shipment | Available now |
sa23990 | Nonsense | Available for shipment | Available now |
sa23991 | Missense, Nonsense | Available for shipment | Available now |
sa23992 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13112
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086115 | Nonsense | 59 | 781 | 1 | 12 |
ENSDART00000141770 | Nonsense | 74 | 428 | 1 | 5 |
ENSDART00000148115 | Nonsense | 91 | 1012 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 33133180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34132873 |
GRCz11 | 21 | 34167363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGATTATGCCGGAGTTAAACAGGCCCTTGAGGAGGCARATATMTATTA[C/A]AACATTAATGTGAACTGCCTAGACCCGTTAGGCCGCAGTGCGCTCCTCAT
Long Flanking Sequence:
TTTAAGGTACAATTCTGTTCCATAAAAAGGTACTGCCCCAGTGACAAGGGTTTGCACCTTCTTTGGTTCGACATTGTACCCTTTTTATCTGAGAGTGTATTGTATTTTGTATGCTCATGTGAAATATAAATTTCTGCTCACAATCGCTGTGCAGACAATAAAGTAAACATTCACACTAATAGAACGTTTTGTACTACTTTTGTATTTGTTTTAATTCAACATCCTAAAAGAAACATAGAGTAAACTTGAAAAAAGCAATCTGATTTGTTCTCTTGCAGCATTCTCTGGACTTGTGCCGTCTCATTCAAAGTCCACATGAACCTCATGGCGCAGCTGTACTACAACAAGGCCAGTAACTCTCCATACCTGGACCGTATCCCTCTGCAGATCGTGAGGGCAGAAGTTGAGCTGTCTGCCAAGGAACGAGCATATCTGACGGCAGTGGAGAAGGGTGATTATGCCGGAGTTAAACAGGCCCTTGAGGAGGCAGATATATATTA[C/A]AACATTAATGTGAACTGCCTAGACCCGTTAGGCCGCAGTGCGCTCCTCATTGCTATCGAGAATGAGAACCTGGAGGTGATGGAGCTGCTATTGAGTCATGGCGTGCATACTGGTGATGCGCTCCTCTATGCTATCCGCAAGGAAGTGGTGGGAGCTGTTGAGTTACTGCTATCCTACAGGAAGCCCTGTGGCGAGAAACAAGTGAGTGAAGCTGTAGCTTTATCTGAAAGGACAGTGTATGTGATATTTATATGTGCAAGTTACTTCCAAACTGTAATACATTACAGATTACTTGTTACTGTTATTTAAAAGTAATCCCTTACCTTACAATATTACTGTATCAGAATTGTAATATGTTACATGACTCTTATATTACTTTTTAGTTATTTTCACCAAAATAACTACAGAATAAGAACATTACATTCAAAAATGACAAAATGTAAACTGCAGAGCATTTTACATCTAGAAGAAAGCGATATGATGTAGCAGAATGACTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10159
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086115 | Nonsense | 348 | 781 | 3 | 12 |
ENSDART00000141770 | Nonsense | 363 | 428 | 3 | 5 |
ENSDART00000148115 | Nonsense | 380 | 1012 | 4 | 10 |
ENSDART00000086115 | Nonsense | 348 | 781 | 3 | 12 |
ENSDART00000141770 | Nonsense | 363 | 428 | 3 | 5 |
ENSDART00000148115 | Nonsense | 380 | 1012 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 33141715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34141408 |
GRCz11 | 21 | 34175898 |
KASP Assay ID:
2261-5870.1 (used for ordering genotyping assays)
KASP Sequence:
GTCACATGCTTCATCATTGGTCTGCTCTTCCCTGTATTCTCCATCATAYA[C/A]CTTCTGGCTCCAAAGAGCACACTGGGAACCTTTATTAAGAAACCATTCAT
Long Flanking Sequence:
GTTCCTAAAGGTGTCAGGACTTTTCATCTTGATGACACTGATACTTTTATTGACATCACTACTTGCTTTTGAGGAATGAGCTCTCCATTTTGAGCAAGTGACACACTTGTGCAGGTTATCAACTAGGTTTTGCAGTTTGTACAGATTGTTTTGAGAAATGCATTAACTGTTGTGCAAATGTAAATAGTGTTGTGAGAAATGCACTAAAGCAACTGAGAAAAACTGTAATGTCTTTTACACTAATGGGTACATGTACGTCAGAAAAAAAATAACATGCCAAGTAACCAATAGCAACTTTATATGTATTTGTCAAGAATTTTTACTCTTTTATTAATACAAAATATTATATAATTTCAGTTTGTTGCTCAGCCCAACTGCCAACAACTCCTGGCAACACTGTGGTATGATGGTTTCCCGGGCTGGAGGCGACGTCATTGGGCAGTGAAGCTTGTCACATGCTTCATCATTGGTCTGCTCTTCCCTGTATTCTCCATCATATA[C/A]CTTCTGGCTCCAAAGAGCACACTGGGAACCTTTATTAAGAAACCATTCATCAAGTTCATCTGCCACACAGCCTCCTATCTGACCTTCCTCTTCCTCCTCCTCCTCGCTTCACAGCATATTGTTCAGACTGATCTGCATGTACAGGGACCTCCACCAACATTTGTTGAGTGGATGATCTTACCTTGGGTTCTAGGTAAGTCTTTTTGGTATACATTGAGTTCAAAAACAGGATAGATAGGTGGATGGATTGATGGATGGATGGATGGATGGATGGATGATTGGTAGGTAGATAGATAGATAGATAGATAGATAGCTTACTTTGATCACTTTAAATGACTCAATTGCATGAGTCATTACAATTATTTAATTATTAGAGTATTAATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTCAGTAATATGCTGAAAAAAATCTTCTCTCCATGAAACAGACAATGGGGAAAAAATAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23990
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 |
---|---|---|---|---|---|
ENSDART00000086115 | Nonsense | 418 | 781 | 3 | 12 |
ENSDART00000141770 | None | None | 428 | None | 5 |
ENSDART00000148115 | None | None | 1012 | None | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 33141925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34141618 |
GRCz11 | 21 | 34176108 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTGAGTGGATGATCTTACCTTGGGTTCTAGGTAAGTCTTTTTGGTA[T/A]ACATTGAGTTCAAAAACAGGATAGATAGGTGGATGGATTGATGGATGGAT
Long Flanking Sequence:
AACTGAGAAAAACTGTAATGTCTTTTACACTAATGGGTACATGTACGTCAGAAAAAAAATAACATGCCAAGTAACCAATAGCAACTTTATATGTATTTGTCAAGAATTTTTACTCTTTTATTAATACAAAATATTATATAATTTCAGTTTGTTGCTCAGCCCAACTGCCAACAACTCCTGGCAACACTGTGGTATGATGGTTTCCCGGGCTGGAGGCGACGTCATTGGGCAGTGAAGCTTGTCACATGCTTCATCATTGGTCTGCTCTTCCCTGTATTCTCCATCATATACCTTCTGGCTCCAAAGAGCACACTGGGAACCTTTATTAAGAAACCATTCATCAAGTTCATCTGCCACACAGCCTCCTATCTGACCTTCCTCTTCCTCCTCCTCCTCGCTTCACAGCATATTGTTCAGACTGATCTGCATGTACAGGGACCTCCACCAACATTTGTTGAGTGGATGATCTTACCTTGGGTTCTAGGTAAGTCTTTTTGGTA[T/A]ACATTGAGTTCAAAAACAGGATAGATAGGTGGATGGATTGATGGATGGATGGATGGATGGATGGATGATTGGTAGGTAGATAGATAGATAGATAGATAGATAGCTTACTTTGATCACTTTAAATGACTCAATTGCATGAGTCATTACAATTATTTAATTATTAGAGTATTAATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTCAGTAATATGCTGAAAAAAATCTTCTCTCCATGAAACAGACAATGGGGAAAAAATAAAACAGTGGGGCTAATAAATCAGGGGGGCTAATACTGTAATTCTGACTTTAACTGTATATCATTTAGCCACTACTGTAAATGTGTTGTAGAAAAAAGGTTTTTACAGTACTGAATTATTTCATTTGTATCCATTAGTACAACAGCTCTCGTCCTCGTGTGGAGTGGGAAATGTGGCACCCAACACTCATCGCTGAGGCTCTATTTGCTATTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23991
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086115 | Missense | 470 | 781 | 6 | 12 |
ENSDART00000141770 | None | None | 428 | 5 | 5 |
ENSDART00000148115 | Nonsense | 468 | 1012 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 33142416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34142109 |
GRCz10 | KN150502.1 | 10813 |
GRCz11 | 21 | 34176599 |
GRCz11 | KN150502.1 | 10813 |
KASP Assay ID:
2261-5872.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGTGGAGTGGGAAATGTGGCACCCAACACTCATCGCTGAGGCTCTATT[T/A]GCTATTGCCAACATCTTCAGCTCCCTGCGTCTCATCTCTTTGTTCACTGC
Long Flanking Sequence:
TTTTTGGTATACATTGAGTTCAAAAACAGGATAGATAGGTGGATGGATTGATGGATGGATGGATGGATGGATGGATGATTGGTAGGTAGATAGATAGATAGATAGATAGATAGCTTACTTTGATCACTTTAAATGACTCAATTGCATGAGTCATTACAATTATTTAATTATTAGAGTATTAATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTCAGTAATATGCTGAAAAAAATCTTCTCTCCATGAAACAGACAATGGGGAAAAAATAAAACAGTGGGGCTAATAAATCAGGGGGGCTAATACTGTAATTCTGACTTTAACTGTATATCATTTAGCCACTACTGTAAATGTGTTGTAGAAAAAAGGTTTTTACAGTACTGAATTATTTCATTTGTATCCATTAGTACAACAGCTCTCGTCCTCGTGTGGAGTGGGAAATGTGGCACCCAACACTCATCGCTGAGGCTCTATT[T/A]GCTATTGCCAACATCTTCAGCTCCCTGCGTCTCATCTCTTTGTTCACTGCCAACTCTCACTTGGGCCCACTGCAAATCTCTCTCGGTCGCATGTTGCTGGACATTCTCAAGTTCCTTTTCATCTACTGTTTGGTGCTTCTGGCCTTTGCCAATGGCCTCAACCAACTCTATTTCTACTATGAGACAAAGGCATCTGAAGAGCCCAACAACTGCAAAGGGATTCGTTGTGAAAAGCAGAATAACGCCTTTTCCACGTGAGTGAAAAAGCATTTAGTCATCTAGTAGAATATTTAGGCTACTGAAAAAATAAACTTTTAAGAACCTATTATGGAAATATTATACTTTGCATACGAGCAATCTCCCACATGTGGTCATTCAATAAATCAGTAAGTAGATTTTCACATTTGGGCATGCAGTATTAGCTCAAGAGAAATATTAGCAATTAATTATATTTAGCTGTAATTTTTAGATTTTACTTAACAATTTTTACTACATGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23992
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 |
---|---|---|---|---|---|
ENSDART00000086115 | Nonsense | 507 | 781 | 6 | 12 |
ENSDART00000141770 | None | None | 428 | 5 | 5 |
ENSDART00000148115 | None | 504 | 1012 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 21 (position 33142525)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34142218 |
GRCz10 | KN150502.1 | 10704 |
GRCz11 | 21 | 34176708 |
GRCz11 | KN150502.1 | 10704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGGGCCCACTGCAAATCTCTCTCGGTCGCATGTTGCTGGACATTCTC[A/T]AGTTCCTTTTCATCTACTGTTTGGTGCTTCTGGCCTTTGCCAATGGCCTC
Long Flanking Sequence:
ATAGCTTACTTTGATCACTTTAAATGACTCAATTGCATGAGTCATTACAATTATTTAATTATTAGAGTATTAATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTCAGTAATATGCTGAAAAAAATCTTCTCTCCATGAAACAGACAATGGGGAAAAAATAAAACAGTGGGGCTAATAAATCAGGGGGGCTAATACTGTAATTCTGACTTTAACTGTATATCATTTAGCCACTACTGTAAATGTGTTGTAGAAAAAAGGTTTTTACAGTACTGAATTATTTCATTTGTATCCATTAGTACAACAGCTCTCGTCCTCGTGTGGAGTGGGAAATGTGGCACCCAACACTCATCGCTGAGGCTCTATTTGCTATTGCCAACATCTTCAGCTCCCTGCGTCTCATCTCTTTGTTCACTGCCAACTCTCACTTGGGCCCACTGCAAATCTCTCTCGGTCGCATGTTGCTGGACATTCTC[A/T]AGTTCCTTTTCATCTACTGTTTGGTGCTTCTGGCCTTTGCCAATGGCCTCAACCAACTCTATTTCTACTATGAGACAAAGGCATCTGAAGAGCCCAACAACTGCAAAGGGATTCGTTGTGAAAAGCAGAATAACGCCTTTTCCACGTGAGTGAAAAAGCATTTAGTCATCTAGTAGAATATTTAGGCTACTGAAAAAATAAACTTTTAAGAACCTATTATGGAAATATTATACTTTGCATACGAGCAATCTCCCACATGTGGTCATTCAATAAATCAGTAAGTAGATTTTCACATTTGGGCATGCAGTATTAGCTCAAGAGAAATATTAGCAATTAATTATATTTAGCTGTAATTTTTAGATTTTACTTAACAATTTTTACTACATGCTTTTACTTGACGATGTCCCTGGATAAAGTGTTTATTCCTTTAAAGAATGTTAATTTCCAGCTCATAAGAAATAACTTTCCATTTATTCCCATTCTGATGCTGTTTTTGAGGC
Associated Phenotype:
Not determined