Busch Lab

ZMP

trpv1

Ensembl ID:
ENSDARG00000059883
ZFIN ID:
ZDB-GENE-030912-8
Description:
transient receptor potential cation channel subfamily V member 1 [Source:RefSeq peptide;Acc:NP_0011
Human Orthologues:
TRPV1, TRPV2
Human Descriptions:
transient receptor potential cation channel, subfamily V, member 1 [Source:HGNC Symbol;Acc:12716]
transient receptor potential cation channel, subfamily V, member 2 [Source:HGNC Symbol;Acc:18082]
Mouse Orthologues:
Trpv1, Trpv2
Mouse Descriptions:
transient receptor potential cation channel, subfamily V, member 1 Gene [Source:MGI Symbol;Acc:MGI:1
transient receptor potential cation channel, subfamily V, member 2 Gene [Source:MGI Symbol;Acc:MGI:1

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa11782 Nonsense Available for shipment Available now
sa12465 Nonsense Available for shipment Available now
sa33682 Nonsense Mutation detected in F1 DNA Not yet available
sa33683 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa11782
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
ENSDART00000083731 Nonsense 335 819 7 17
ENSDART00000140743 Nonsense 331 813 6 15
ENSDART00000083731 Nonsense 335 819 7 17
ENSDART00000140743 Nonsense 331 813 6 15
Genomic Location (Zv9):
Chromosome 5 (position 43766575)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 41547840
GRCz11 5 42147993
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCGGGAGCTTATGGGCTGCAGACATCTGTCCCGAAAGATCACGGARTG[G/A]GCCTAYGGTCCAGTGTGCTCSTCTTTGTATGACCTCTCCTCCCTCGACAC
Long Flanking Sequence:
CCATATTTGAAAAACATTATCTGAGAAGGTTCCAGTTGACCTGCTACATGCTAAAGCGTGCATCTAATGGACACTTTACTATCCCCTGAGGCCAAAAGAGAGAATTTATGGATGTGAGTGACAATATGTGGAATGAAGTATGTCTGGGGCAAAATATATATAGAAACGAGCTTCCTTATACCTTACTCTCTATGAGGGGCTTTGAAGGGTGTAGGGCACATCATGTAATGTTCCTTTAATTAATGGACACATGAAAGGGCCTTTCAGGAAGTGATTCAGATGTTTAAAAGTGTAAAAAAAGAATTATACTACTCACATTCATATTATATACCACATACTATACTATATTTGAAGTCTTAGCCAATGTTTGAAAATATTATTAATAAGCATATGTTGTTTGAAAAAATCATTCTGGTTTTTTTTTTTTACTAGCTGTTTAAGCACATTGTGCAGCGGGAGCTTATGGGCTGCAGACATCTGTCCCGAAAGATCACGGAGTG[G/A]GCCTACGGTCCAGTGTGCTCGTCTTTGTATGACCTCTCCTCCCTCGACACCTATGAGAAAAACTCCGCTCTCGAGATCGTTGTCTATGGCAGTGAGATTCCTGTGAGATTCTCATGCTGCTTGTTTGATACTAATTAACTTTAGTTAGATATTTTACTACTTCAAATCATTGAAGTAAACATTCAATTTCTAAGCATTTGTACAGATCGAGATAGCAACATATGTTTGTTTTTGCTTTTCCATTACATTTCAGAATCGCCTCGAGATGCTCCAAATTGAGCCACTTAACAGACTAATAGAAGAGAAGTGGGATCAATTTGCGCATCGGATGTTCTTGTTTAACTTCATTGTTTATGTTATCTACCTTTTCATCTTCACTGCTTCAGCTTTTTACCACGAAGAAGGGAAGGATTACGCGAATCAAGTAGGTGCACTGTAAAAAAATGCTGCGCTCCACACAATTCCTTCATGTTGAAGGAAGGGGACTTCAAGGAGGGTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12465
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
ENSDART00000083731 Nonsense 335 819 7 17
ENSDART00000140743 Nonsense 331 813 6 15
ENSDART00000083731 Nonsense 335 819 7 17
ENSDART00000140743 Nonsense 331 813 6 15
Genomic Location (Zv9):
Chromosome 5 (position 43766575)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 41547840
GRCz11 5 42147993
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCGGGAGCTTATGGGCTGCAGACATCTGTCCCGAAAGATCACGGARTG[G/A]GCCTAYGGTCCAGTGTGCTCSTCTTTGTATGACCTCTCCTCCCTCGACAC
Long Flanking Sequence:
CCATATTTGAAAAACATTATCTGAGAAGGTTCCAGTTGACCTGCTACATGCTAAAGCGTGCATCTAATGGACACTTTACTATCCCCTGAGGCCAAAAGAGAGAATTTATGGATGTGAGTGACAATATGTGGAATGAAGTATGTCTGGGGCAAAATATATATAGAAACGAGCTTCCTTATACCTTACTCTCTATGAGGGGCTTTGAAGGGTGTAGGGCACATCATGTAATGTTCCTTTAATTAATGGACACATGAAAGGGCCTTTCAGGAAGTGATTCAGATGTTTAAAAGTGTAAAAAAAGAATTATACTACTCACATTCATATTATATACCACATACTATACTATATTTGAAGTCTTAGCCAATGTTTGAAAATATTATTAATAAGCATATGTTGTTTGAAAAAATCATTCTGGTTTTTTTTTTTTACTAGCTGTTTAAGCACATTGTGCAGCGGGAGCTTATGGGCTGCAGACATCTGTCCCGAAAGATCACGGAGTG[G/A]GCCTACGGTCCAGTGTGCTCGTCTTTGTATGACCTCTCCTCCCTCGACACCTATGAGAAAAACTCCGCTCTCGAGATCGTTGTCTATGGCAGTGAGATTCCTGTGAGATTCTCATGCTGCTTGTTTGATACTAATTAACTTTAGTTAGATATTTTACTACTTCAAATCATTGAAGTAAACATTCAATTTCTAAGCATTTGTACAGATCGAGATAGCAACATATGTTTGTTTTTGCTTTTCCATTACATTTCAGAATCGCCTCGAGATGCTCCAAATTGAGCCACTTAACAGACTAATAGAAGAGAAGTGGGATCAATTTGCGCATCGGATGTTCTTGTTTAACTTCATTGTTTATGTTATCTACCTTTTCATCTTCACTGCTTCAGCTTTTTACCACGAAGAAGGGAAGGATTACGCGAATCAAGTAGGTGCACTGTAAAAAAATGCTGCGCTCCACACAATTCCTTCATGTTGAAGGAAGGGGACTTCAAGGAGGGTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33682
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
ENSDART00000083731 Nonsense 452 819 9 17
ENSDART00000140743 Nonsense 446 813 8 15
Genomic Location (Zv9):
Chromosome 5 (position 43767965)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 41549230
GRCz11 5 42149383
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGTAGGGAAGGCTACCTGCTTCTGACAGGACACATCATATCTATCACT[G/T]GAGCATTTTACTTCTTTATTAGAGGGGTGTGTATCTGACGCTCTTGCTTT
Long Flanking Sequence:
TGTCTTCTGCATTGTCCTCTCTGTTAAGTGACAGTATTTATATTTTTAAAAATCTGATTCATTTAACAATGCATTTAATTGAATTTTTTTTTTTATTTTTATTTTTTTGTAGCTCAGGAAATAAACAAAGAAATAAAAAAGTTAAGTTAAATTAGAAATTACAATCTCTGTTAAAGGCCCTCATCATCATTCTTACTCTCTTTCCATGTGGGGACTCAACTCAAAGGTTACCATGGGCCAACTTTGGTCTACACTTTGTCCAAAAAAAAAAAAAAAACTTACAAGGAAAAAATCATGACTAATAACACTCACTGACCTTATTTCAGTTCACTATCTATAATCTTATGTTGTGTATGAACTGTAAAATGTTTTTTTTTTTTCACTATTTAATGCCATGTCTCAACCCTACTGTTTCTTATTTTCAGACAAAGCCTCCATATCTTTATGCAAAGAGTAGGGAAGGCTACCTGCTTCTGACAGGACACATCATATCTATCACT[G/T]GAGCATTTTACTTCTTTATTAGAGGGGTGTGTATCTGACGCTCTTGCTTTAAAACTAATTCATAATTAACTTTCAATAATTACATTTTTTTAATAAATTCCTGTTTCTTAAGTTAATAGATATGGTAAGGAAGCGTCCAAGATTTCAATCCCTGATTATAGATGGATACACAGATCAGCTTTTGTGAGTCCTTTTACTCTCTATTTTTTATTTTCATCATTAATTGACCACTGTAGATTAATATGATTGAGTCCTTTGCTGATCATTCAACTGATTTAAACTGCATGTTTAATTTGAAAACAGTTTTATGTACTATATATGAAGATAATGAAATAAAACTACTCTTATTTAAGTTGTATTTGTGCCCTGATGAAGTTTTTAGTTTCATGGCTTGATCCTTGATGTTGGATGTGTGCAGATTATTTTGAACTTATAAATGCACAGCACCCAGCTAAACTGCACCGTCTGCTTTATCTGTAGTACAGAAAATGTCATCAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33683
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083731 Essential Splice Site 540 819 12 17
ENSDART00000140743 Essential Splice Site 534 813 11 15
Genomic Location (Zv9):
Chromosome 5 (position 43768791)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 41550056
GRCz11 5 42150209
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTTACAACCTACTTGTGCATACACTCTTACGCTCTTTAATTATTATC[A/T]GATGGTTCTTGGAGAAATTCGCAGATTCCTTGTTGTGTACATGGTGTTTC
Long Flanking Sequence:
TAATGAAATAAAACTACTCTTATTTAAGTTGTATTTGTGCCCTGATGAAGTTTTTAGTTTCATGGCTTGATCCTTGATGTTGGATGTGTGCAGATTATTTTGAACTTATAAATGCACAGCACCCAGCTAAACTGCACCGTCTGCTTTATCTGTAGTACAGAAAATGTCATCAGTAAGTACATGCATTGTTTTATAATGCTATTTTTCTTTTTATGCATTAGTTTTGTGCAGGGCTTGCTCTTCTTGGCAAGTGTTGTACTGTACTGTTATGGCCAGTATGAATATCTGGCCTTTCTAGTGCTCTGTCTTGCCTTGAGCTGGATAAACTTACTCTACTTCTCCAGGGGGTCCAAAAATTTGGGAATCTACAATGTGATGATACAGAAGGTAAGGCCATTTCCTTTCCTGTATACTTGACTACATATTTAAAGCATCCTTGTACAGTAAAGTAGTCTTACAACCTACTTGTGCATACACTCTTACGCTCTTTAATTATTATC[A/T]GATGGTTCTTGGAGAAATTCGCAGATTCCTTGTTGTGTACATGGTGTTTCTAATTGGATTCTCAGCAGGTATCATCCTTCATTTCATATATTCATGAATGTTATTTGACTTTTATTTTGATTTCACTTCATCTAGGAACAAAATATCAGTTGAAAATTTTGTGTAAAGTCCGAAGTTGCAGAGACTTTGATTTTAGTATGCTGATGTGCTTATTGAAATGGTATAATGAGTAGGGGACGGAGCTTTCTTTCACAATATTCCCTCATAGCTGTGCCTCAAAGCAAACTAATGGTAACAGGGGTGTGGCTAAGAATATCAGTATACTGTTGCTACTGAAGCCCTCCACTGACGTCAGCAGAAAGACCACCACTCCAAACATGGAAGCAGATAGTCAGACTTTGATTGAACATTAAAAACAAAACATTTTTACACTTAATTGACTTTAAATTTATTTAGCAAGTATACATTAAGTTCATTAATAGTGAAGACTCCTAGTCTTT
Associated Phenotype:
Not determined