ZMP
TRPM4 (1 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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25252 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33216 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25252
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 |
---|---|---|---|---|---|
ENSDART00000083969 | Nonsense | 11 | 1194 | 3 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 32631562)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32362872 |
GRCz11 | 3 | 32494586 |
KASP Assay ID:
554-7636.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCGAAAATGACTCATACTTCACTGTGTAATGTCTGCATTGTAGAGTTG[G/A]ATCCCAAAGATGATTAAAAAGAGAGTGTGCACCACCTTTGTGGAGGATTC
Long Flanking Sequence:
TGTCTGTAGTTGTAGGAAAAATCAGAAAGTAAGTCTATTTGTGTACAGTGCTCATAAATGATCACTTGTGTGTTTCATCCTTTATCTCATCTATTTTTTGTAATAACATATAATTATAACATATAATTATTATAATTTTATAATAATAGTTATTTTCATGTTTTTATCAATGTTTCTAAATACATCAATTTGCTAGAACATTATGTACTTTCATGCAGACAAAAGCCTTAAATTTTATTATCCATTTAAAATTGCAGTAGTTCGGTTGTGTGATTAAGGTTTTGTTGTTCCATGTTTTTAGCTAAATTAATTTTTGAGGCAACTAAAAATAGGCAAATGAATAAAATGTGTTTCCGTGATTAGGATTACATTTCCTTGTAAGCTCTTTTGCTATTCAACAAAATAGTTTGCTCTTCTCGGCTGCTGACTTTGAAAAGAAACCGGACCTGCATGCGAAAATGACTCATACTTCACTGTGTAATGTCTGCATTGTAGAGTTG[G/A]ATCCCAAAGATGATTAAAAAGAGAGTGTGCACCACCTTTGTGGAGGATTCATGCAGGTACAGCAGTTTTTTTCATTTCTCATGCATTTAGATTTACTAGAATATGCAGGAAACTATTCAGTCCTTTCTGTCATTTAAAACAGTCATTCAGCCTCTTGTAATATGAGCTGAGCCGTTAAATCTCGGATTTGGCAATGTAGGGTGGGTCAACAAACATGTCATTTTGTCTTGAATACAGGTGAACTCCTAACCATTTGTCAACTCATTATAATCCGTGTCCTTTTCCTCTCTTTATTTCAAGCTATTGTTAAATGTAATGGGCTTGATTCATAATGGGATTTGGGCAGGTACAGTTTTAATCTAATTTATTTATTCAATCAATGATGTGTACATTACGTGACATTCTTGAGTTTGATTTAGGTTACTACCATTTTGATGTATTACATTAAAATGAACAGGTCACATATTACAGTGTCAGTGATACACACATATAAACAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33216
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 |
---|---|---|---|---|---|
ENSDART00000083969 | Nonsense | 150 | 1194 | 7 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 32639307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32370617 |
GRCz11 | 3 | 32502331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAACTTTTTTTGTTGTTTTTTTCCCCCTTGTCTTTTAATGCAGGGGCTT[G/A]GATCATGACGTCAGGTCTGAAGGAGGGTGTTAGCCGTTGTGTAGGTGAGG
Long Flanking Sequence:
CTTAATGAGTTTCTTTATTCTGTTGAATATAAAAGAATATATTTTGAAGAAAGTTGAAAACTGGTATTCATCCATAGTAGGAAACACAAGTATGAATATTAATAGTTACAGGTTTGTAGCTTTCTTGAAAACATTTGTGTATTATATAAGAAAGAAAGTCAAATGGGTTTTAAACAAGTAAACAGTGAGTAAATGATGACGGAATTTTCTGTTTTGGAAATATTGTACTATCCCTTTAAGGTCAGTAATAGACAGTTTAGCATGAATTTCTCAACAGTGGCATTCCTGCTGTTTGTAGTCTTGTTTGCCAGATAAGGTTTATTATCATTTAAATGCTAGGCTTGGCTTGAACTACGAACGTTTGTGCTGCATTATTTGAATTCTTTGTCTGTCAATGATAGTGTTTTGTGAGCCCTGATGTATTTCTGTGCAGTACGGTTTTGTAATTTAGTAACTTTTTTTGTTGTTTTTTTCCCCCTTGTCTTTTAATGCAGGGGCTT[G/A]GATCATGACGTCAGGTCTGAAGGAGGGTGTTAGCCGTTGTGTAGGTGAGGCCGTCAGGCATCATTGTGCAATGGCTTCATCTCTTTCTCAGGCTAAAGTTATTGCCGTTGGTGTTGCACCATGGGGGTTAATTTACCAACGTCATCAACTTGTAAACCCACAGGTACTGCAGTGTCAATTCTGTTAAATAATGAACAGTTCACATAAACGCCATGCTTAGAATGAATATTTGAGTAGTTCTATTTATATAATCACCTGAGGTAAAGGTTAATAATTGATTATTAGTTTGAATATTAGTTCAAATTGATTATTAGTTAAATGAAGTTGTCAATAATAGGTATGTTGAGAGTTAAAAAAAATAATTATATATATATATGTATATAAAAATCGAGCAAAATAGTTCTAGGCCGGGACAACCTGTCAATCATAGGAGAACCACAGATATCGTTTATGAAGTAACAATCCAATCAATTTCCCAATGACAAGATCAAGTCGTGTCC
Associated Phenotype:
Not determined