ZMP
si:ch73-263b18.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
TRPM2
Human Description:
transient receptor potential cation channel, subfamily M, member 2 [Source:HGNC Symbol;Acc:12339]
Mouse Orthologue:
Trpm2
Mouse Description:
transient receptor potential cation channel, subfamily M, member 2 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34783 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38766 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21609 | Nonsense | Available for shipment | Available now |
sa34781 | Nonsense | Available for shipment | Available now |
sa34780 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14804 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34783
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085351 | Nonsense | 8 | 1421 | 1 | 39 |
ENSDART00000136940 | Nonsense | 4 | 290 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 54745621)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53380699 |
GRCz11 | 9 | 52920206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGACCCTTGTGCAAACACTCGCGGTGAGCACTGCTAAAGGCGGCCGATA[T/A]CTGTCTCTGTCTCCCTCTTTCCAGCGCTGCTCACTCGCCTCCTGGATTAA
Long Flanking Sequence:
CTAAATAAAACAAATAGAACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTGAAAAATTATTCGCTCTGTTAAACAAAATTTTGGAAATATTTGAAAAAATCCACAAGAATGCAAATAATTTGGACTTTAACTATACATGAAATAGCATTTAATAAAATCCACACACAAACACACAAGCAAACATTTTAGCATACTGTGCGGTATGTTTCCATAGCGCAGCTCCTCATTAAGTAAATGAAGCTTTGGGCTGTATTCCAGCAATTCCTCCGTCTGTGTGTCTGACATCACTGGTGCAGCAGTGCAGTTTTTCAGTGCAGCAGCAAATGCATTGTAGGCCGTCCCGCTCACACACACACACACACACACCCTCCCCCTCCTGTATCTCTGCGCTTCTCATTCACGCTCACTGTGTCTGACCTGAGCATGGATGAGGCAGCGCTGGAGCCGACCCTTGTGCAAACACTCGCGGTGAGCACTGCTAAAGGCGGCCGATA[T/A]CTGTCTCTGTCTCCCTCTTTCCAGCGCTGCTCACTCGCCTCCTGGATTAAAGAAAACATCAAGAAGAAAGAGTGCTGCTTCTATGTGGAGGATGGCAGGTATGGAGCCTTCAGTGACCTTGTTTATATACAGTTAAAGTCAGAATTATTAGCCCCCCCCCCCTCTATATTTTTCCCCTAATTTCGGTTTAACTGAGAGAAGTTTTTTTTTTAACACATTTCTAAACATAACAGTTTTAATAGCTCATTTATTTTATCTTTGCCATGATGACAGTGCATAATATTTGGCTGTATGATTTTCAAGATACTAGTATTCAGCTTAAAGTGACATTTAAAGGCTTAACTAGCGTAATTAATTAAGTCATTGTATAACGATGGTTTGTTCTGTAGACCTACGAAAAAATAATATTGCCTAAGGGGGCAAATAATTTTGAGGAATCAAGCCTATGAATAAACAATGTGAGCAAAACTTTGCTGTTAAACCTGTGGTACACAATCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38766
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085351 | Essential Splice Site | 302 | 1421 | None | 39 |
ENSDART00000136940 | None | 290 | 290 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 54728895)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53363973 |
GRCz11 | 9 | 52903480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACCAGTGGTCTGTGTGGTTCTGGACGGCGGTCCGGGAACTCTAAATG[T/A]GAGTTTTTCAAGTCATCAGCTTTTTTTAAAACAGTATTTCTAGATTGTTT
Long Flanking Sequence:
TTCTCTTGTTCAGACCATTCTCTGTAAACCCTAGATATGGTTGTGCGTGACAATCCCAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCCATCTTGCATCAACAACTATGCCACATTCAAAGTCACTTAAATCCCCTTTCTTCCCCATTCTGATGCTCGGTTTGAACTGCAGCAGATCGTCTTGACCATGTCTACATGCCTAAATGTGTTGAGCTGCTGCCATGTGATTGGCTGATTCGAAATTTGCGTTAGCAAGCAGTTGGACGTGTACCTAATAAAGTGGCCAGTGAGTGTGTATCAGTCAAAGGATCATTTTTAGCAATGCAGATCTCAAAACTGTTGGTAAAAGCCACATGTTTGATTGCATGGCTCTTTAACACTGTTTGCTGATCACTTAATTACTTGTGGTTTATGTTTGTCTGTTTTCCATCAGAGAGTGGAGTGACGATACCAGTGGTCTGTGTGGTTCTGGACGGCGGTCCGGGAACTCTAAATG[T/A]GAGTTTTTCAAGTCATCAGCTTTTTTTAAAACAGTATTTCTAGATTGTTTAATCTCTAGATTGTTTCATTTATTTCTAGAATAACAGCGTTAAAATATTTATTGCAGACATTTAAAGTGAGGGAATTTAATATTTTTTTGTCCAGATCATGAAGTATCATGGGCCCAAGTCATTTTAAATTAGACAAAAAAATCCATCTTTTTAAAAAAAGTTTTATTCATAAGTATAGACTTAATTTAAGATTTACATTTTTAAATCATGAAGCTTATTTTTGGAAAAGCAAAACATAGAGTCTTGCTTTAACAAAAAAAAATGTTAAAGAGAGTTTTTTTCTTAAAACAAGCAAAATAGTCATGTGTCAAAAGGAAAAGCATGGTTATTTTGCTTGTTTTAAGGAAAAACTTGCTTAATTTTGGCATAGTAATTCCTAATGCAAGACTTTGTTTTGCTCAACTTTTGCTTTGTTTTGTTCAACAAGTTTTGCTTGTCCAGAAGCAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21609
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 |
---|---|---|---|---|---|
ENSDART00000085351 | Nonsense | 391 | 1421 | 8 | 39 |
ENSDART00000136940 | None | None | 290 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 54616096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53357307 |
GRCz11 | 9 | 52896814 |
KASP Assay ID:
2260-2600.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGATGCCTCATTTGCTCACAGTATTCCGCATCGATGAGGATAAAAACTA[T/A]GACGTGGATGTGGCCATTCTGCAGGCGCTGCTAAAAGGTATTGCTTTTCA
Long Flanking Sequence:
TATTATTTATGTTTGTTTATTTATTTATTTTTCAAATTTATTTAGTCATTTTATTTATTTATTTATTTTTTTGCTTATTTATTTTTCATACAAATAAATTAGTAAAAATATATTAAAAAATTAATGAACTAAAAATACAATAAATAAAATAAACAAATATAAATAATAACAAAAATAGCTAGAAATGTTGAAATAAAATATTATATGGTATCATCACTTATTATTTTTTAAGAATAATTCTAGCAGCTTTTTGTTTGTTTATTGTAATTTTTAAATTTATTTTATTTTATTTATATATATATAATCATTTTGGGGGGGGGTTAATAATTTTGTCTACAACTCTATATACTACTATTACTATTACTATTACTATATGTAGTAATGGTGGATAATAAGTGGTGAATTCGCTCAGCATTTATTGTTTCCTCTCTGCAGATTCAGGACATCTTGCGGATGCCTCATTTGCTCACAGTATTCCGCATCGATGAGGATAAAAACTA[T/A]GACGTGGATGTGGCCATTCTGCAGGCGCTGCTAAAAGGTATTGCTTTTCAGACATGCTCCAATTTCTCCTAATCTGGAAACTGAATTTACAGTAAATGATGGCTAATGTTCTCATTTCCAGGCAGACGGTAATGGGATCGTGCTGTAAATGGGTTGCACTGTATCTAATGCCAGCGCTGTTTGTCTTTAACCGTAATCAAGGTTAAAGAGCCTGTCAGCATTTCTCTTTATGCAGTTTCTGTTGAAGCCGTTTGTTACATTGAAGCCTAATGGTTTCTAAGGAATGAATCATGTAACTGCACTGACCACCAGGGGTTTGTCTCTTTTCCCTGGAAAGTCAGAGAGCTATTTGTGTTCATTTTACAGTGATGCATGGCACACGTCTCCATTGCTAAAGAGAATTGTTGTATTTAATCATGATTAATATTGCAATGCTCAATGCAACTGTTAGATGCTGGTAGCCAATACAGTTTTTCAGTGCTTACAAAAGGAGATAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34781
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085351 | Nonsense | 896 | 1421 | 22 | 39 |
ENSDART00000136940 | None | None | 290 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 54489618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53332605 |
GRCz11 | 9 | 52872112 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGACTTCATCATATTCTGCCTGCGATTAATGGCCATCTTCTCCATCAGT[C/T]GAACTCTGGGTCCCAAAATAATCATCGTCAGGAGAATGGTGGGTTTGCAA
Long Flanking Sequence:
ACCTTACTGTCCCAATGAAATCATTCAAATTAAGGCGTGATCATATTTTATTGTGGTCAAATAAGTGTAATCTAAAGGTCTTTGCCTTTCATATGAGCCACTTCTAATACCAAATGATCAACTAGAAGTGAAGTTATTATTGTTGTTCCTTTTGTCAGGTAGTGTATATGCATTAACACAACAACGAACAATACTGAAAAGCAACATTTAGCTGCAGATGTTTGTATTAGTACTTTAATACTTTAACAGTTTTAATGAAAACCGAAAGCAATGAAAAATCTGTTTATTAAAAAAGATTGAATCATGTTTAAAGTCTTTCAAATTTAATTGAGTAGTTGCATATAATGAGCCTCAGATCAGCATGCTTCACAGTTAACTAGTCTCTGTGTTTGTCCTGCAGACTTCAGGCCTCGGACACTGTGTTTTACATTGGTAAAGTCATCCTCTGCATCGACTTCATCATATTCTGCCTGCGATTAATGGCCATCTTCTCCATCAGT[C/T]GAACTCTGGGTCCCAAAATAATCATCGTCAGGAGAATGGTGGGTTTGCAATTAAAGTTAAAATACTGTTTAAAAAACTTAAAAAAAACAAAAAAAAAACAATCTTTTTTTTTTTGCGTGTATTTCAAGAGTCCACACTTAGCTGGTGACTGATAATAAAGCTTGTTTGGCATGCTGTCCTGGGAGAGAGCCCTGAGCTCAGAAAATCCTCGAGCCCTGGGCTCCCTCTCGTTTGCAGGGCGAGAGGGGAGTTTGAGCTTAGGTAGGTCTCGAAAACTCCCTTGCTTGTTAAGGCAAATGGCGGATTAAGCATTGCTATGAATATGAACTGCTGACCTCACCTATTGTGTCGACCTATTGGTTTAGTCGATTTACCTATGTTGCGTGTCTTTTGACTGTGGGATGAAACCAGAGAACCCGGGGGAAACCCACACGAGCACTGGGAGAACATGTAACTCTGCACAGAAATGTCACCTGGCCAGGTCAAGACCTGAACCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34780
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085351 | Nonsense | 931 | 1421 | 23 | 39 |
ENSDART00000136940 | None | None | 290 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 54488337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53331324 |
GRCz11 | 9 | 52870831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCATGTTTCTGCTCAGTATCTGGGTTGTGGCGTACGGAGTAGCCAAA[C/T]AGGGCATTCTGATCGAAAACGAAGAGAGACTAAACTGGATCATCCGTGGA
Long Flanking Sequence:
CTTTAAAGAATTAATAATTATTAATTATTTAGAAAGATAAACAAACAACTTGTTTTCAAACTATTAAAATAAATAAATTATTTTTTTCTTTTGGATAAAATTTTAACTTTGGAATCTGTGAGTGTAGTGTGATCTGTCTCCCCCTTTTTTGCACCATTTGAAACTAAAATAAACATAGATTTAGGATTAGAAATACAAGAAGACACGTGTGAGAAAATTGATGTAAGAAAAATTAATAAAAAAAGTCAAATGAATCATTTTAAATTAAGTAATGCACCTGAAAAAAAATGCACCTGCTTAAATCTAACTTTGGAAAAGGAGTAATAACTATATGAATAGTCAATGATATGAGGAATATTAGTGCACATAAAATTGGTTTAGCATGACAGCAGTTGTGAATGTGCATTTCTGACTCTCTGCCTTTGTCTCCGCAGATGTTGGATTTGTTTTTCTTCATGTTTCTGCTCAGTATCTGGGTTGTGGCGTACGGAGTAGCCAAA[C/T]AGGGCATTCTGATCGAAAACGAAGAGAGACTAAACTGGATCATCCGTGGAGCTGTTTATGAGCCCTACATCACTATATTTGGCAACTTCCCTACTAATATAGACAGTGAGAAGTTTATATTTTACTTTGAATAATTCAAATAAACCCAGACTCATTGGAAATATGTCCCCTGGGCTACATTTTTGAGAACCGAGAAATATGTTCCCTGGTCTACGGTTTCTTGCCATTTTTGTTTTCACAAATCCACTAGAGTGCACTGTGTACACTTCTGATGATCTTAAATGCGTTACTGGGGCACATTTTCTCATATGTTTTACACACAAAGGACTCTATTTTACTGATCTAGGTGTAAAGACTTAAGCGCATGGCACAAACGCATAAGGGGCGTGTCCGAATTCACTTTTGCTATTTTAAGGACGGACCCCGGCACATGGTCTAACAGGGTTGTGTTTATTCTCTTAATGAGTTTTGGGTGTGTTTAGAGCAGGGGCGTCAAACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14804
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 |
---|---|---|---|---|---|
ENSDART00000085351 | Nonsense | 1388 | 1421 | 38 | 39 |
ENSDART00000136940 | None | None | 290 | None | 6 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 54460882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 53304048 |
GRCz11 | 9 | 52843555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGCGCAGGTGCTGGAGAGGATTCTGGGTAAAAAGTTAAATGAAAAGACC[A/T]AGACTCTTCTAAAAGCTGGAGAAGAGGTGAGCATGGYAAACGCAAAASAT
Long Flanking Sequence:
TATTTCCTATTATATTTTTCTTCTGGAGAAAGTATTAATTCTTTTAATTTGATAATATAAAACTAATTGATTTTTTGTTTCAAGATTGAAACTAATCTTGTCCATTTGCTTACCAAAATTAACATAATTAATCCAGCCTTTGAATTGCGCTAAATATCTTGCAAAATAACTAGTAAAATATTATGTGCTGTCATCATTGCACAGACAAAAAATAATTTATTATTAGTTAATAAAACTATTGTTGAAAAATGTGTTGGAAAAAACTGTTAAACAACATTTGAAAAATAGTTTAAGTTTCACAGGAGAATTTCACATCAAGAAAATAATTGCATTTGATTTCGATCCAGTCTTAAAATGATCAAATATATATTTTTTGTATTAGCCATGTTTGAACTAGATATTTTATGCCTGTTGTTTTTTTATAGGGTCCAGCCCAACCCGATGAGCCTCTAGCGCAGGTGCTGGAGAGGATTCTGGGTAAAAAGTTAAATGAAAAGACC[A/T]AGACTCTTCTAAAAGCTGGAGAAGAGGTGAGCATGGCAAACGCAAAAGATTTGAAACATTAAAATTTGAATTTTAGATTACATTTACATATCATCTTATCTTGTGTTGTACTGAAAAATTAAGCATGCAAGTTCAGATATTTAGTTATAGAATTAACATTTTCAACCCCTCCTTATTGTACTCTAGGTGTTTTGAATGTACTACAAAACGTTACTGATTTATTTATTTTATTTTTTGATGAAAAAAATACATCCTTTACTGATAAAAAAAAGTTATGTGCTATGAGTATACTTTGTTTAAACAATAAACTTTCAGTAAACTTTTTATGTACTTATCTGAAATTTCTCAGAAATATGATGATGATGATGATGAAGCCTTTATTTGTCACATACACTTTTACATGTAGTGAAATTGGACCCCCTCGACCATACACAAACATCACACATTTCAGGGGAAGACGGGTCAGACGAGAAGTAGCTTTTAGAAAGAGAAAATAGGAT
Associated Phenotype:
Not determined