Busch Lab

ZMP

TRPM4 (3 of 3)

Ensembl ID:
ENSDARG00000063435
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
sa31852 Nonsense Available for shipment Available now
sa27870 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10730 Nonsense Available for shipment Available now
sa10961 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa31852
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
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092687 Nonsense 600 1176 16 29
Genomic Location (Zv9):
Chromosome 12 (position 5474539)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4469825
GRCz11 12 4504837
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGTGGCGAGTCGGTTCTGACGGCTCTGGCTGGATGTAAACTGTTGT[T/A]GGAGCTCTCTAAACAGGAGATCGAGACCGAGGCCAAGCTCTCCATGAAGG
Long Flanking Sequence:
CCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACTCATTAATACGCACACTCATACAATTTAGCCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCGAACGCAAGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGCCGAGGTTCAAACCAGCGACCCTGCGACCTTCTTGCTGTGAGGCGACAGCAGCCCATTGCATCACCTTATGCATATTTAACATAGAATTTTTTTTTAACTTGCTTTGACTCTCAAAGAGTAAAAACAACATTTTCCCCAATTTGGACAGTTAAAAATAGAGTTTGGGACATTTAATATGCTGCAAAAGAGTTACAGGATGGCACTGTATGTCTGTAACAAAAGTGTAGTTTCACACTCATCGCTCTCGCTCTTCTGTCTCAGTGTGGCGAGTCGGTTCTGACGGCTCTGGCTGGATGTAAACTGTTGT[T/A]GGAGCTCTCTAAACAGGAGATCGAGACCGAGGCCAAGCTCTCCATGAAGGAGCTGGCGCTGAAGTTTGAGCAGATGGCTCATGGTAGGATGTGTGTTTGGTCTTTTTTGTTATCTTATAAAACCAATACGATTTCAAGCTTCTATGGCACTAACATTACTTTACAGATGTGTTTGGCACATGCTACCAAACCAAAGCAAGTCATTCCTACAAGCTGTTGATCCGCAAGTCAAAACTGTGGGGTGACGCCACCTGTCTGAAGATGGCCATAGCTGCGGATGCCCGGATCTTCTTCAGCCATGATGGAGTGCAGGTCTGGCAGCACACAAACCATTGTTAATAGTGTCATGTGATTTAAAACAAGGTTGGTGTTTTTCCTAAAAACCCCCTTTCTTTTTTTAAGTCTCTGCTGTCTCAGATCTGGTGGGGGGATATAGAAAGAGGAACTGCGTTCTGGAGACTCCTGCTGGTGATGATCTGTCCTCCTCTCTGCTACACCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27870
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092687 Essential Splice Site 759 1176 20 29
Genomic Location (Zv9):
Chromosome 12 (position 5477310)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4467054
GRCz11 12 4502066
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCGTCTACTCCTTCAAAGACATCAAACACCAGTACATCAGCTTTTA[T/C]TCAGTACTTCATGCATACTTATGTCTGTCAACATCTACAAAACAGCATCT
Long Flanking Sequence:
CAGTGTTGATGTATGAGACCCCTGGTTTTCGTTCTTCTGACTCTTATTTTAACGGAGAGAAAGTTTTATTGCAACAGCCATTGATTGCCTTTCAGTGAACATGTCAAATTACCAATTAAAGACCACAAATTTTAGCCTAGGATTATTGGAAGATTTTCCGATTTTCCAATTTAATCTCGTTTAGCCAAATCAAGGCCAAAATTGCAGTGTGAGCCAGGCTTTACTTCACTAGTCTGCATATGTGTTTTTGGGTCAGTGTCCTATTTTGGCACACTAGCACCTAGAAATAAAATCTTAAAACCAAAATTTCACTCAATATATTACAAACTGAAAATGTGCTGCATCAGGGGAAAGACATAAGTTGTGTTTCCTCCTAGGAAAACAGATCCAGCAAAAGAAGAGAAATCGATGACGGCACCTCCATCTTCACCGACAGACAGCCATTACGAAAAGACCGTCTACTCCTTCAAAGACATCAAACACCAGTACATCAGCTTTTA[T/C]TCAGTACTTCATGCATACTTATGTCTGTCAACATCTACAAAACAGCATCTGTTATCTTATGATCTTTAGAAATGAAGGCGAGAATGAGGACTCAAATCATATCAGACAGAACACAAAAGGTTTGACTTTGATTTTGAAGCTTTTGCTGAAGAATTTAATAAAACTAGTTCATCATTGCTCTACAATTTCAGCCATTCTGCTCAAAATCAATAAGTCTTTCTGTCATCAGGAGAACCTGCATTCATCGAATCAATGAAGAGTAGCTTTGTGGTCTCCCGCTGGAAGCAGTTCTGGTACGCTCCTGTCACCTCATTCATCGGCAACCTTCTGATGTACTTCCTCTTCCTGTTTCTGTATGCCTACGTGCTATTGGTGGACTTCAAGCCGCCTCCCCCTGATGGCCCGGCGGTTTCGGAGTATGTGCTGTATTTCTGGGTCTTCACTTTAGTGTGCGAGGAGATTCGAGAGGTACGGTAGATGCTTTTTTCCTACTTGCATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10730
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092687 Nonsense 813 1176 21 29
Genomic Location (Zv9):
Chromosome 12 (position 5477730)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4466634
GRCz11 12 4501646
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGTSGACTTCAAGCCRCCTCCCCCTGAWGGCCCGGCGGTTTCGGAGTA[T/A]GTGCTGTAYTTCTGGGTCTTCACTTTAGTGTGCGAGGAGATTCGAGARGT
Long Flanking Sequence:
CCATCTTCACCGACAGACAGCCATTACGAAAAGACCGTCTACTCCTTCAAAGACATCAAACACCAGTACATCAGCTTTTATTCAGTACTTCATGCATACTTATGTCTGTCAACATCTACAAAACAGCATCTGTTATCTTATGATCTTTAGAAATGAAGGCGAGAATGAGGACTCAAATCATATCAGACAGAACACAAAAGGTTTGACTTTGATTTTGAAGCTTTTGCTGAAGAATTTAATAAAACTAGTTCATCATTGCTCTACAATTTCAGCCATTCTGCTCAAAATCAATAAGTCTTTCTGTCATCAGGAGAACCTGCATTCATCGAATCAATGAAGAGTAGCTTTGTGGTCTCCCGCTGGAAGCAGTTCTGGTACGCTCCTGTCACCTCATTCATCGGCAACCTTCTGATGTACTTCCTCTTCCTGTTTCTGTATGCCTACGTGCTATTGGTGGACTTCAAGCCGCCTCCCCCTGATGGCCCGGCGGTTTCGGAGTA[T/A]GTGCTGTATTTCTGGGTCTTCACTTTAGTGTGCGAGGAGATTCGAGAGGTACGGTAGATGCTTTTTTCCTACTTGCATTCTTGTACAAATATGCATTTATACCACTTTGTTTTCTTTCTCTTCCAGGCGTCCATTGCAGGCAATAAGAAGTTTCCTCAGATGTTGTTCGTGTATGCTCAGGATATGTGGAATAAGTTTGATGTTCTTGCCATTTCCCTCTTCATTACTGGTTTGTGCTGCAGGTAAACACGCCTTGATGGTTTACTATCATAAATATATTATAAGGTTTGGCTATTAAATAGAAATAAATTAAATATTCACCACAGGTGCCACCCAATATCCCAATGTCACAATCTAATGGCATGGGTGAAGGTTCAATTCATGATAGTCTTACAAATGCATGTGTGAAGATAAAGTTGAACACTCAGTTGAACTTGTGGGGTAATAAATTTGGAGGAGGGAGGGTGGTTTGCGACGAAATAGTTGGAGGGAGGTTTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10961
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092687 Nonsense 1117 1176 27 29
Genomic Location (Zv9):
Chromosome 12 (position 5487144)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 4457220
GRCz11 12 4492232
KASP Assay ID:
2260-4894.1 (used for ordering genotyping assays)
KASP Sequence:
AATGGGAGAAYCTGCAGAAGGAGAACTATCTGGCCCTTGAGATCAAAAAA[C/T]AGAGAGGAACTGACKCTGAGAGGCTCAAACGCATAACTTCTAAGTGAGTT
Long Flanking Sequence:
TTATTAGTTTCAAAAACACAGACTTATTAATGATTTAAAAAGGCATCTATAGCTTTTCATTGTTCTTTTCTGCTGGGGATACTGTTGCTCTAATAAAATGCCCAAAAATTTATTAAACATTAATTAATGTTCTTCTGCAGCTATACGTTTTCCAAGGTTCAGGAGCGCAGTGACACATACTGGAAATTTCAGCGGTATAATCTGATCGTGGAGTATCATTCACGTCCGACGCTCGCTCCACCATTCATCATCCTGTCTCACATCAACCTCCTGATCAAAAGAAAAATACGCAAAGTGCAGTCCGCCAAAGTCCAACGATTTGGTAAAGTTTAAAAAATGTATAGCTCAACAAGAACATTTGTTAGAGCTAAACGACTGATAAATAAATGTCTGTGTTTGCCTTTAATATAGCCCTGAAGATAAAGGGTCAAGAGAAGAAGGAGCTGGTGAAATGGGAGAACCTGCAGAAGGAGAACTATCTGGCCCTTGAGATCAAAAAA[C/T]AGAGAGGAACTGACTCTGAGAGGCTCAAACGCATAACTTCTAAGTGAGTTAAACTTAAATTGAACATTTTTATATTAGGACATGCTGATACAACTTTCCAATGAGCATTGGACAAAGAGATTAGACAAAAATAATTGTGATAAACCAAAACTGACCAAATATGATAAACTATCACTTGACTACTACTGCTTCATCGCAGCGGTAACTAAACCAGAACAAAATGTGATTTAAACTGTTTTTCCTCAGATTAACATTGATGTGGATGGTGTTTTGTTTCAGAGTGGATAGTGTGATCAAACAGGTTGCAGAGATCAGAGATGTAGACCGCAGACTGAGAGCGGTCGAGTCAGAGGTGAGAAAACATGATGTTTTACCAGTGTTATATTGTGCACTCAATGGCCACCTTATCAGGTACACTAATGGCCCGTTTCCACTGACTGGTACAGTACGGTACGGTATAGGTCACCTTAATCAGGCTGGTGTTTCCAATAGCAAGGGTA
Associated Phenotype:
Not determined