Busch Lab

ZMP

trpv6

Ensembl ID:
ENSDARG00000014496
ZFIN ID:
ZDB-GENE-040624-12
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]
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

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa17082 Essential Splice Site Available for shipment Available now
sa42674 Nonsense Mutation detected in F1 DNA Not yet available
sa1510 Essential Splice Site Available for shipment Available now
sa16780 Nonsense Available for shipment Available now
sa25007 Nonsense Mutation detected in F1 DNA Not yet available
sa42673 Essential Splice Site Mutation detected in F1 DNA Not yet available

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa42674
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123927 Nonsense 504 711 14 17
ENSDART00000127453 Nonsense 502 709 14 17
Genomic Location (Zv9):
Chromosome 16 (position 14052287)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 12411378
GRCz11 16 12302280
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTGGAGATATAACAAAGTTCATGTGGTTGTCCATCATCTTCCTCATT[G/T]GATCTTCTGCTGGTTAGTTCAAATACATTTACACTGTATTCATGTGAAGT
Long Flanking Sequence:
TGTTTTTGCTGCAAGTGAAATAAAATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAATTCAATCAGTTTGACTGCATGCATTCACTCAAACTTTCATTTCATTTCAGGATCAGCTACGCTTTGCTGGTTTTGCTTTTGTGTGGGCTGCGAGTCACTGGAATACAAGGAGAATTAATTCCGATGGCTTTTTCTCTGATTCTTGGCTGGTTCAGTCTTGTGTACTTTGCCCGGGGTTTCGAGATGCTGGGACCCTACGTCATTGTGATACAGAAGGTGGGGTGATTCTCTGGTTTGAAGATCAACCATAAATATAATATGCATTTTTTTTAATATGGATGTTGTTTTGCAGTCAATATTTGGAGATATAACAAAGTTCATGTGGTTGTCCATCATCTTCCTCATT[G/T]GATCTTCTGCTGGTTAGTTCAAATACATTTACACTGTATTCATGTGAAGTGCTGGGTAGATTAATAAAAAGTTGTAGTTAGTTTCTGATTCTAAATTGCTTGCCAAAATTGCCAACAAAGTTGATTTTGTTTCTTTATGCTGATTGATCAACAGCTTTATTCACAGCACAGAGACATTAAAGGGTTAATTCACCCAAAAAAGAAAATTATGATATTATGTATCCTTGTGTTGTTTCAACCCCATGAGACCTTTGCTCATCTTTAAAACACAAATTAAGATATTGTAAAATAACTCTGAGGCCTCTCTGATCCTCCATAGACTGCAATAGTCCCAACACCTTTAAAGTCCAAAAAAGTAACAAAAACGCTGCGTCCCAAATCGCATACTTATGCACTATTCTACGCCATTTTGTAGTATAAATAGTGTAAGTAGTGCGTTCACACTGAAAACTCTAAAAATAATAAGTGCACTTTAATTACCCGGATGATGCACTCATTCA
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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

Mutation Details

Allele Name:
sa25007
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123927 Nonsense 607 711 16 17
ENSDART00000127453 Nonsense 605 709 16 17
Genomic Location (Zv9):
Chromosome 16 (position 14047715)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 12406806
GRCz11 16 12297708
KASP Assay ID:
554-7498.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTTGGTTTCTCTTTTCATAGGTGGTGGCCACTACTCTGATGCTTGAA[C/T]GAAAGTTGCCACAGTGCCTGTGGCCAAGATTGGGTGTCTGTGGTCTGATG
Long Flanking Sequence:
AATTCAACCAAAACTGCCGAGTGTTTTTCTGAATTTTCAAATATGAATTATATATAATCATACTACCCAGCACTGTAAGCCTTTGAATCTGTAACCTTAATAACTTACTTGTTTTCCTGTGCAGCCTTGTGGATTTTCTACATGACTCAGGAACCCTTAGCACTTCCGCAGTACCGCTCCTTTCCCATCACCCTCTTCTCTCAGTTTGAGGTGAGCGTCGGTCAGATTGATTTGCCAGTGGACCACACACTCTTTACCCATCCAGTGGTGTATTGGACCCACGTCTGCTTCAGCTTGATCTCTAACGTCCTCCTGTTTAATCTCCTGGTCGCCATGATGAGTGACACTCAGTGGAGAGTAACTCAAGAACGTGACGAGCTCTGGAGGACGCAGGTCAGTACTTTAGCTACTTCAGTCACAGAGCAACTATGCTGGAAGAAGGAAGAGGTTACAGTTGGTTTCTCTTTTCATAGGTGGTGGCCACTACTCTGATGCTTGAA[C/T]GAAAGTTGCCACAGTGCCTGTGGCCAAGATTGGGTGTCTGTGGTCTGATGTTTGGGCTTGGAGAGCGCTGGTATCTTCGGTAAGATCACAATCACAATTATAAAAAGTACATTTCAAATTAATTTTACATTTAAAAGAACAGTGACAATGTTACCATTGGCTTCAATTAAAGAACAAGTTTTGCTAATTTATGAATACTAAAAAGAGCTTAAGCATTTAAAGCAAAAGATGACTAAATGTGGTATTAGAAGTATACCCGGAATACGCCCCCTTGTGGCTGTCGCACAGCATTTTCAGTTTTGTTGTGCACCATGGGAGAGAAGCTGGATTCTCTCTGTCAGAAATAAATGAATACTGAATACTAATAATGAATACTAGAAACTCATAGACCGCTAAAACTTTTGAAGGGAATGTGGAGACAATATAAAAAATATTTTTTTATTACTCATTTGATTATAAATGTTTTTTAATATAAACCTATTTTTGATTCAAAAAACCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42673
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123927 Essential Splice Site 633 711 16 17
ENSDART00000127453 Essential Splice Site 631 709 16 17
Genomic Location (Zv9):
Chromosome 16 (position 14047634)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 12406725
GRCz11 16 12297627
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTGTCTGTGGTCTGATGTTTGGGCTTGGAGAGCGCTGGTATCTTCGG[T/C]AAGATCACAATCACAATTATAAAAAGTACATTTCAAATTAATTTTACATT
Long Flanking Sequence:
TTTGAATCTGTAACCTTAATAACTTACTTGTTTTCCTGTGCAGCCTTGTGGATTTTCTACATGACTCAGGAACCCTTAGCACTTCCGCAGTACCGCTCCTTTCCCATCACCCTCTTCTCTCAGTTTGAGGTGAGCGTCGGTCAGATTGATTTGCCAGTGGACCACACACTCTTTACCCATCCAGTGGTGTATTGGACCCACGTCTGCTTCAGCTTGATCTCTAACGTCCTCCTGTTTAATCTCCTGGTCGCCATGATGAGTGACACTCAGTGGAGAGTAACTCAAGAACGTGACGAGCTCTGGAGGACGCAGGTCAGTACTTTAGCTACTTCAGTCACAGAGCAACTATGCTGGAAGAAGGAAGAGGTTACAGTTGGTTTCTCTTTTCATAGGTGGTGGCCACTACTCTGATGCTTGAACGAAAGTTGCCACAGTGCCTGTGGCCAAGATTGGGTGTCTGTGGTCTGATGTTTGGGCTTGGAGAGCGCTGGTATCTTCGG[T/C]AAGATCACAATCACAATTATAAAAAGTACATTTCAAATTAATTTTACATTTAAAAGAACAGTGACAATGTTACCATTGGCTTCAATTAAAGAACAAGTTTTGCTAATTTATGAATACTAAAAAGAGCTTAAGCATTTAAAGCAAAAGATGACTAAATGTGGTATTAGAAGTATACCCGGAATACGCCCCCTTGTGGCTGTCGCACAGCATTTTCAGTTTTGTTGTGCACCATGGGAGAGAAGCTGGATTCTCTCTGTCAGAAATAAATGAATACTGAATACTAATAATGAATACTAGAAACTCATAGACCGCTAAAACTTTTGAAGGGAATGTGGAGACAATATAAAAAATATTTTTTTATTACTCATTTGATTATAAATGTTTTTTAATATAAACCTATTTTTGATTCAAAAAACCTACTATTTCTCACCTCGCACGCATGGATCTGCTTGAACAACACTGAAATACATCACATCTGGTCGACCGGTCACACACGGTCT
Associated Phenotype:
Not determined