ZMP
TRPM4 (2 of 3)
Ensembl ID:
Description:
transient receptor potential cation channel, subfamily M, member 4 [Source:HGNC Symbol;Acc:17993]
Human Orthologue:
TRPM4
Human Description:
transient receptor potential cation channel, subfamily M, member 4 [Source:HGNC Symbol;Acc:17993]
Mouse Orthologue:
Trpm4
Mouse Description:
transient receptor potential cation channel, subfamily M, member 4 Gene [Source:MGI Symbol;Acc:MGI:1
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35196 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22008 | Nonsense | Available for shipment | Available now |
sa41947 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10854 | Essential Splice Site | Available for shipment | Available now |
sa18122 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35196
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092492 | Nonsense | 149 | 1109 | 3 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 5151891)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4430946 |
GRCz11 | 12 | 4469022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGGACTACTCGCCATAAAGGTGGAGAGCTGGCGTTCAGAGCCCGTCTG[G/T]AGGATTACATTTCACACCAGCGCCCAGGTACAGCATAAACCTGAAAAAAC
Long Flanking Sequence:
AGACCTTATTGTCGTAATTAAATAATTAAAAATTAAGGCATGATCATATTTTATTTTGGTCAAATAAGCGTAATTTAGAGCCCTTTGCCTTTCATATTTAATAAGTTATTATTTGTTGTTCTTAAAACTTGAATATAGGGGACAAGACTTTTGTCAGGTAGTGTATGTAATATGCCTGCTTACAATATATATCCTTTTATTCCACTATATATGTGATTTATTGTGTATATATTGTTGCCTAATAAAAAAAAACTCCTAATATAAAAATGTTCTCAATTCCTTATGTAATAATCAGTCAACGGGACAAATATGGCGATTAAACTCATTATCACACCCCAATTGACCTCTGTTTATCATAGGGAAGCTTTCCTGCAAGGTATATGGTCAGGAACATATCGCCTGAATACTGCTATCTGGATAACAACCATAAGGCTTTTCTACTGGTGGACGACGGGACTACTCGCCATAAAGGTGGAGAGCTGGCGTTCAGAGCCCGTCTG[G/T]AGGATTACATTTCACACCAGCGCCCAGGTACAGCATAAACCTGAAAAAACAGACTGAACCGTATCCTGGACCATATTAGTGCCCCCACCAGTGCCCATATACAGCCATATCGCACTGCTACGAGTGTGATATTGCGTTTATACAACAGTTTGAGGGCATAATTGTGTATATAAAAACAAAATCAAACATGGAGAGTCTCAAAAACCCTTTTGTATGAGGAACTACTTTCTTCCGCCTTGGATTCAAATCATAAGCTGACAGTTAAACAGCTGAGCAAGCATCTTTTAAACTTTAGACCTGTAGTGTCTGCTTTTGCTATCTGTATGTAGGTGGAGTAATACACAAAGGGTAAAGAGTCTTTACGGGTGCTGACATTACTTAAATATATCATGGCTATCACCAAATGGACTCTGACCAATCAGAGCAGAGCTCTTTGTCAAAAAGCAAACAGAAAAGCCTCTGGAATTGCTTGAAAGCTGACACGCACAATACCTATTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22008
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 |
---|---|---|---|---|---|
ENSDART00000092492 | Nonsense | 442 | 1109 | 9 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 5143103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4422166 |
GRCz11 | 12 | 4460242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGTCTGAACTCTCGTTGTACGCAGGATCGACTAGAAGAAAAGACATA[A/T]AGGTACCAGACCCCATTTTAAAATCTGTGTAGTCTAAAAACACACACTTT
Long Flanking Sequence:
AAGTGTAAAGCTCACAGAATGAATTTAATTCCTGGATGTCTGGATGCTGCCCACACTAATCTTTTATTTTGTTCCTAAATTATTTTCTTCAATCTCTTTTTATTTGATTATTTAGCCACAATATGGCATCAAACAGTCACAAACAGCAGTGTAACAGATTGGCATGTGTGTTTATTTATTTATTTATTTATTTAAGCATGACTGTATGTACAGTAGCATGTATCGCCAAAGTTTACAATCTCTAGTTGTTTTTAATTATTGAACTACTTTAGCGGGTGCTGTTTTTGGATCGCAATTGCAGAGAATTGGTTTTGTGCATTAAATATCCTCACCATGTGCATCCTAAAGTGCCTAACCTGTGAATATATGCAGTTGTAAATGTGCCGGATCTGTGATTGCAGGTGTCTCGGCTGCTGGAAGATCTGCTCGGTGATGTCTGTCATCCTTTCTACTTGTCTGAACTCTCGTTGTACGCAGGATCGACTAGAAGAAAAGACATA[A/T]AGGTACCAGACCCCATTTTAAAATCTGTGTAGTCTAAAAACACACACTTTTTTTCACACTCTCTTTAAAAATGAAATGTGATTGTTTTACCACACAGAAAGCATGCAAGGTCCTGAAGGGGAAATGCAAATATCAGGATGAGATGTGTGAGCACCCATGGTTGTCCCTCTTTATCTGGGCAGTGCTGCAGAACCGCAGTGAGATGGCCATCTTCTGCTGGGAAATGGTAATACTGTGTGTTCCTGAGGCATGCTTGAGATTTAGTTTATTTTGACATCTGCATAACAAGTACATTTAAGACATGCTGTATATCCTCTATTGACCTTAATCTCCAATGTGGAAGTAAGCTCTCTTCAGTGATTGTTTTAGAACTTCCAATTCATTTGTCTATGGGGAAATGATTAGGAATAATAAATGGCAGTAAAAGGTCCAACTTCTTGCTGTACAAACATTTATTTTTATGACAATACATAAAAATAATATAATAAGAAAGTACAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41947
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092492 | Nonsense | 585 | 1109 | 13 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 5136667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4415730 |
GRCz11 | 12 | 4453806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTAACAGTCTTTTTTTTTGTTCAGTCTCTGCTGTCTCAGATCTGGTG[G/A]GGAGATATAGAGAGAGATACTGCGCTTTGGAAAGTGCTGCTGGTGATGAT
Long Flanking Sequence:
TCTTACTCGCCACTGATGTGCAACTAAAGCGATTTTGTGCCTGTAAACACAGCGCCCCCTCTGTTCAATAAATGTATCGCAATTCGTTCAACATTTCTACCGATTTGAATCGCCACATATTTGAATCGATTTTTATCTGGCTCTCTGTGAATTGTTACATCCTTAACAAACTCTCCTTCCAGCTTTGTATGAAACCAGTTGAGCCCCTGTAGTCACACAACGTTTTGACAATGTTTTTGGTCCTTTTCTGGACTTTCTCAGGATAACTGCTGTCTATGCAGGATGAGGGAGCTCTCTGATTTTTATCTAAAGTATCTTAATTTGAGATCTGAAGATGAATAAAGGTCTTGAGGTATTGCAATGATGTAAGGGCCGCAAATAATAACAGAATTTTCATTTTTGTGTGAACTAACACTTTAATAGTTGCCTTTTATTTTGAAATGAGATTTTTTGTTAACAGTCTTTTTTTTTGTTCAGTCTCTGCTGTCTCAGATCTGGTG[G/A]GGAGATATAGAGAGAGATACTGCGCTTTGGAAAGTGCTGCTGGTGATGATCTGTCCTCCTGTCTGCTACAGCAACTTCATTGAATTCAGGTACAGTAGCATTTTTTTTTTTTTTTACTTCCTTTCACAAAATTGCATACAGTGCTCAGCATATATTAGTACACCCCTCACAAATCTCTCTTTTACATTTCATATTCTTAATATGAAGCTAGTCAATATTATATTTGTTTATATACATCAGATTAGTCAGCACTGAAGCCAAATCTGGAGCTGATCCAACAAAATTTACGAGAAAGGTCCAAAAACTAGTACAGCTAAATTTATATGTCATAAAAAATATTAAATGCAAATTTTAAAAAGAGGAAAAATCAAGAAAAGCAAAGAAAATGGGGAAAATTTAGTCAAAAATTTGTAGGATGTTTTTTTTTTTTTTTTTTTTTTTTTGCTTAAATTTAATAGTATTTTTCAATCTCTAATTATGTTTGGTGACTAAAATATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10854
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092492 | Essential Splice Site | 944 | 1109 | 21 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 5084419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4367046 |
GRCz11 | 12 | 4403704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTATAARWGACTGTCAAATCATCTGTGTGTTGCTTTGTGTTTTNCTGC[A/T]GCTAWACGTTTACKAAGGTTCAGGAGCACAGCGACAAATACTGGAAGTTT
Long Flanking Sequence:
TGAATTTTAGATAAAGCATGCGTTCTTCTTCCTGTTCTTCCTGCTGGTGTGGTTAATTGCATATGGAGTAGCCAATCAAGCTCTACTATACCAGTACGATCCGAGCCCTGCTAGAGTGTTTCGGCGAGTGTTGTACAGGCCATATCTGCACATATTCGGAGACATCCCTGTGGAAGAAATAGACAGTATGTTCACTTCTGATTTTGCTGCTTTTAGTTAGCATCCATCCACTGACTGGATCATGTCTGTGTGTGTTAAGCTGGCAAACACTGGGAAAGAGACTGCACAGATAATCTGACGTTGATTAATGAAGGGATAGAGCCGTGCAGGGACACCAGCCACAACTGGCTTGTGGTCATTTTGTTGGTCATCTTCTTACTAGTCACCAACATTTTACTTATTAACCTGCTCATCGCCACATTCAGGTATTTATATATCTGTACATCCATTTTCTATAAATGACTGTCAAATCATCTGTGTGTTGCTTTGTGTTTTTCTGC[A/T]GCTATACGTTTACTAAGGTTCAGGAGCACAGCGACAAATACTGGAAGTTTCAGCGGTACAATCTGATAGTGGAGTATCATTCACGTCCAACGCTCGCGCCGCCATTTATCATCTTCTCTCACATCAACATCCTGATCAAAAGATACCTACGCAAAGTGCCGTCCGCCAAAACCCAACGATTTGGTAAAGTTTAACTAGAAAAGTACAGTTTAAAGGGTTAGTTCACTCAAAAAGGATAATTCTGTTATTAATTAGTCACTCTCATGTCGTTCCAGTCTTTGAACACAAAGTAAGAAATTTTAGATGAAATCTAAGAGCTCCCCCATCCTCCATAGACAGCAAGTCTAGAAAAGGAACCAAAAACAGTTGTTTAATTGGTTCAGCTGTAATCAAACAAAACTCCAAGAACACTTTTGTGTGCCAAAAAAACACACAAAAAAAGGACTTTATTTAACAGTATCCCGCGTAGTCAGGGTGCACGTTTACTACAGACAATACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18122
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092492 | Essential Splice Site | 1104 | 1109 | 24 | 25 |
Genomic Location (Zv9):
Chromosome 12 (position 5078807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4361434 |
GRCz11 | 12 | 4398092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCWCAGAGCAGCACAGCGAASAGCACTAAAGCACATCCTACTCGCAAAG[G/A]TAAAAACTGCWGATACTTATCTCAACACTTACAAATATGATAACAGCATT
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTTGGTGTATTTGAGACTTTCCTGCTAGCACACACCTCCTATATGGGTCACTTGAGCCCTGTAGCCAATAAGATGCGAGCTTACTGTTTAACAAATCACAACCCACTGAGAACCTTTCTTTTTAAAACATTGATGTTTAAAAATTATGTTTAACAGAGCAAGAAAACTTTCACAGTATGTCTGATAATATTATTTCTTCTGGAGGAAGTCTTATTTGTTTTATTTCGGCTGGAATAAAAGCGGCTTAATTCTATGATAACAATCTCCAGGATATATTTTATGCCTAATATTTTCTGCACTCACAGAGACATATCTAATAAAGTGGTCCAGGTTTATCTAATAAGAGTGTATATGGACTATTGCTGATTGATTGATACTCTTGTATATGCAGATAGAGTTCTGTACCTCTTCTCTACAGTGGATTATGGAGACTCTTTCTCAGAGCAGCACAGCGAAGAGCACTAAAGCACATCCTACTCGCAAAG[G/A]TAAAAACTGCTGATACTTATCTCAACACTTACAAATATGATAACAGCATTTCTTCACAATAGAATGTGAAATTCTCATAGTAATCATTTCAAGAATTGGTTCACCCAAAAATGAAAAGTGTGGTATTAATTACTCACCTTCATGACGATTCAATGTCTCTGAGACTGTCGTTTATCTTCAGAACACAAAGATATTAAGATATTTTAAATGAAATTCTTCATAACGTGTCTGCCCAAACCCTTTAAACCTAAATATCTCCCTCATGCTTAAAGTTAATATTAGCATTTTTATATTTTTTATATTTAATATCTTTATTTCTACAATCTTGTAAATGACACCAAAAATTGTAAAAGAAAATCTGTGTAACATGTGCACTCACCAGCCACTTTATTAGGTACACCATGTAGACATGGTCGAGACGATCTGCTGCAGTTCAAACTGAGCATCAGAATGGGGAAGAAAGGTGATTTAAGTGACTTTGAACGTGGCATGATTGTTGG
Associated Phenotype:
Not determined