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 |
---|---|---|---|
sa22008 | Nonsense | Available for shipment | Available now |
sa10854 | Essential Splice Site | Available for shipment | Available now |
sa18122 | Essential Splice Site | Available for shipment | Available now |
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:
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