ZMP
trpv6
Ensembl ID:
ZFIN ID:
Description:
transient receptor potential cation channel subfamily V member 6 [Source:RefSeq peptide;Acc:NP_0010
Human Orthologues:
TRPV5, TRPV6
Human Descriptions:
transient receptor potential cation channel, subfamily V, member 5 [Source:HGNC Symbol;Acc:3145]
transient receptor potential cation channel, subfamily V, member 6 [Source:HGNC Symbol;Acc:14006]
transient receptor potential cation channel, subfamily V, member 6 [Source:HGNC Symbol;Acc:14006]
Mouse Orthologues:
Trpv5, Trpv6
Mouse Descriptions:
transient receptor potential cation channel, subfamily V, member 5 Gene [Source:MGI Symbol;Acc:MGI:2
transient receptor potential cation channel, subfamily V, member 6 Gene [Source:MGI Symbol;Acc:MGI:1
transient receptor potential cation channel, subfamily V, member 6 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17082 | Essential Splice Site | Available for shipment | Available now |
sa1510 | Essential Splice Site | Available for shipment | Available now |
sa16780 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17082
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 |
---|---|---|---|---|---|
ENSDART00000123927 | Essential Splice Site | 485 | 711 | 13 | 17 |
ENSDART00000127453 | Essential Splice Site | 483 | 709 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 14052417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12411508 |
GRCz11 | 16 | 12302410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGCCCGGGGTTTYGAGATGCTGGGACCCTACGTCATTGTGATACAGAAG[G/T]TGGGGTGATTCYCTGGTTTGAAGATCARCCATAAATATAATATGCATTTT
Long Flanking Sequence:
GTCTGGCTATGCAAGATTTATCCACCCCCTTACACCTTATCCCACTTATCCATACCCTCAAACCTATTCCACCTCATTAGCACCGCAAGTGTTTTGCAATACAATATGAACACAATAAGTGCATTGTACTTGTTTTTGCTGCAAGTGAAATAAAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAATTCAATCAGTTTGACTGCATGCATTCACTCAAACTTTCATTTCATTTCAGGATCAGCTACGCTTTGCTGGTTTTGCTTTTGTGTGGGCTGCGAGTCACTGGAATACAAGGAGAATTAATTCCGATGGCTTTTTCTCTGATTCTTGGCTGGTTCAGTCTTGTGTACTTTGCCCGGGGTTTCGAGATGCTGGGACCCTACGTCATTGTGATACAGAAG[G/T]TGGGGTGATTCTCTGGTTTGAAGATCAACCATAAATATAATATGCATTTTTTTTAATATGGATGTTGTTTTGCAGTCAATATTTGGAGATATAACAAAGTTCATGTGGTTGTCCATCATCTTCCTCATTGGATCTTCTGCTGGTTAGTTCAAATACATTTACACTGTATTCATGTGAAGTGCTGGGTAGATTAATAAAAAGTTGTAGTTAGTTTCTGATTCTAAATTGCTTGCCAAAATTGCCAACAAAGTTGATTTTGTTTCTTTATGCTGATTGATCAACAGCTTTATTCACAGCACAGAGACATTAAAGGGTTAATTCACCCAAAAAAGAAAATTATGATATTATGTATCCTTGTGTTGTTTCAACCCCATGAGACCTTTGCTCATCTTTAAAACACAAATTAAGATATTGTAAAATAACTCTGAGGCCTCTCTGATCCTCCATAGACTGCAATAGTCCCAACACCTTTAAAGTCCAAAAAAGTAACAAAAACGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1510
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 |
---|---|---|---|---|---|
ENSDART00000123927 | Essential Splice Site | 508 | 711 | 15 | 17 |
ENSDART00000127453 | Essential Splice Site | 506 | 709 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 14048093)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12407184 |
GRCz11 | 16 | 12298086 |
KASP Assay ID:
554-1434.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTAAGCCTTTGAATCTGTAACCTTAATAACTTACTTGTTTTCCTGTGC[A/C]GCCTTGTGGATTTTCTACATGACTCAGGAACCCTTAGCACTTCCGCAGTA
Long Flanking Sequence:
ACTGAGATAGATACATTTGAATTAAATCACTCAATTATTTCAAACCAGTGCAATATGCATTGCAATATATTGATCGTTTTTATGTATTGTGCAGCCCGACAATGATCTGCTGCAAGGAGATGTGTTTTCAATCATCGTAGTAAGCTGTAATTGTGTGATCTGACTGGGGCTCACGAAGAAAAAAAGTGGTTATACTTGATCATTCAGTCCTTTTTAAAGGTCACATCTTCAGATGTCTTTGGCTTATGTTGCATTTATATTTTAGAACCGTACCAGACTTTTTTGGGAAGTGCACCAAAACCCATTTTTCAGTGGTCTGTCTGTATAGTGCACATTGAGGTTTAGGTGCCAATGTTCAATCACATCAGGCTTTGTTTTAATTCAACCAAAACTGCCGAGTGTTTTTCTGAATTTTCAAATATGAATTATATATAATCATACTACCCAGCACTGTAAGCCTTTGAATCTGTAACCTTAATAACTTACTTGTTTTCCTGTGC[A/C]GCCTTGTGGATTTTCTACATGACTCAGGAACCCTTAGCACTTCCGCAGTACCGCTCCTTTCCCATCACCCTCTTCTCTCAGTTTGAGGTGAGCGTCGGTCAGATTGATTTGCCAGTGGACCACACACTCTTTACCCATCCAGTGGTGTATTGGACCCACGTCTGCTTCAGCTTGATCTCTAACGTCCTCCTGTTTAATCTCCTGGTCGCCATGATGAGTGACACTCAGTGGAGAGTAACTCAAGAACGTGACGAGCTCTGGAGGACGCAGGTCAGTACTTTAGCTACTTCAGTCACAGAGCAACTATGCTGGAAGAAGGAAGAGGTTACAGTTGGTTTCTCTTTTCATAGGTGGTGGCCACTACTCTGATGCTTGAACGAAAGTTGCCACAGTGCCTGTGGCCAAGATTGGGTGTCTGTGGTCTGATGTTTGGGCTTGGAGAGCGCTGGTATCTTCGGTAAGATCACAATCACAATTATAAAAAGTACATTTCAAATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16780
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123927 | Nonsense | 584 | 711 | 15 | 17 |
ENSDART00000127453 | Nonsense | 582 | 709 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 16 (position 14047862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12406953 |
GRCz11 | 16 | 12297855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAYGTCCTCCTGTTTAATCTCCTGGTCGCCATGATGAGTGACACTCAGTG[G/A]AGAGTAACTCAAGAACGTGRYGAGCTCTGGAGGACGCAGGTYAGTACTTT
Long Flanking Sequence:
GATGTCTTTGGCTTATGTTGCATTTATATTTTAGAACCGTACCAGACTTTTTTGGGAAGTGCACCAAAACCCATTTTTCAGTGGTCTGTCTGTATAGTGCACATTGAGGTTTAGGTGCCAATGTTCAATCACATCAGGCTTTGTTTTAATTCAACCAAAACTGCCGAGTGTTTTTCTGAATTTTCAAATATGAATTATATATAATCATACTACCCAGCACTGTAAGCCTTTGAATCTGTAACCTTAATAACTTACTTGTTTTCCTGTGCAGCCTTGTGGATTTTCTACATGACTCAGGAACCCTTAGCACTTCCGCAGTACCGCTCCTTTCCCATCACCCTCTTCTCTCAGTTTGAGGTGAGCGTCGGTCAGATTGATTTGCCAGTGGACCACACACTCTTTACCCATCCAGTGGTGTATTGGACCCACGTCTGCTTCAGCTTGATCTCTAACGTCCTCCTGTTTAATCTCCTGGTCGCCATGATGAGTGACACTCAGTG[G/A]AGAGTAACTCAAGAACGTGACGAGCTCTGGAGGACGCAGGTCAGTACTTTAGCTACTTCAGTCACAGAGCAACTATGCTGGAAGAAGGAAGAGGTTACAGTTGGTTTCTCTTTTCATAGGTGGTGGCCACTACTCTGATGCTTGAACGAAAGTTGCCACAGTGCCTGTGGCCAAGATTGGGTGTCTGTGGTCTGATGTTTGGGCTTGGAGAGCGCTGGTATCTTCGGTAAGATCACAATCACAATTATAAAAAGTACATTTCAAATTAATTTTACATTTAAAAGAACAGTGACAATGTTACCATTGGCTTCAATTAAAGAACAAGTTTTGCTAATTTATGAATACTAAAAAGAGCTTAAGCATTTAAAGCAAAAGATGACTAAATGTGGTATTAGAAGTATACCCGGAATACGCCCCCTTGTGGCTGTCGCACAGCATTTTCAGTTTTGTTGTGCACCATGGGAGAGAAGCTGGATTCTCTCTGTCAGAAATAAATGAAT
Associated Phenotype:
Not determined