Busch Lab

ZMP

LOC100149353

Ensembl ID:
ENSDARG00000087272
Human Orthologue:
TRPM6
Human Description:
transient receptor potential cation channel, subfamily M, member 6 [Source:HGNC Symbol;Acc:17995]
Mouse Orthologue:
Trpm6
Mouse Description:
transient receptor potential cation channel, subfamily M, member 6 Gene [Source:MGI Symbol;Acc:MGI:2

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa14386 Nonsense Available for shipment Available now
sa31437 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa14386
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123535 Nonsense 369 1200 8 29
Genomic Location (Zv9):
Chromosome 5 (position 26941449)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150339.1 21809
GRCz11 5 25329011
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTTTCATTTCAGATCAGCATTTTTGACTCTGAATCTGAAGACCTTCAA[G/T]AGGCAGAWGTTGMAATCCTGTCCACATCGCTGAGAGGTATGTCATGTTGT
Long Flanking Sequence:
TGCTAAGCCTCCATCAAACAGAATGTTGTAGTTCACCACACCCATCCCGCATTTCTGAGCTTCTAAATTGAGAGGGAACAGAATAATTGGAATGATGGCGCATGAAACGTATTTCCATATTAATCGAGTAGAAGGGATTAATTTGGTCCCCAGGCGCACAGATTCTTTGATTGGGTATGAATCACTCATGTGGAGATGAAGTGCCAAAGGCATGTTAAGAGAAGAACATCTCCTCTGGGTGTCTTGTAGAGTTACATGCATTTATATATTGGCATGGGATATGATGGTAGTTTCATATTAATACCAAACAAAATAAATAACCGCTGGCTATATTGAAAGCAACACAACAGCAGTGGCACTAGTTTACAAATCTGTTTTAATGCTGGCCATCTGTGCTAATTAATTGTTTTAAAGGTGCAACTATTTTTTTAATGAGGTCAAACTTTAACAATGTTTCATTTCAGATCAGCATTTTTGACTCTGAATCTGAAGACCTTCAA[G/T]AGGCAGATGTTGCAATCCTGTCCACATCGCTGAGAGGTATGTCATGTTGTTATTATATTATTCAAATAAGTCTTGTTGTGCTTTTTTACACAATGCTCTTTAGGTCTTAGGTGTCCCCAGAAAACATATGTGAAGTTTTTGTTTATGTCTCTTTAAAAGTGAACAAAGTGCATCTTCCCATCCCTAAAACAAAACACTGCCTTCATATCATGTGGAGTTTATTGGGCTTATAAAAGATTTGGTTATTTGTTGATGAGAATATGACTAGCAGCTTTGTTTTTGGGTTGTTATTATATCTATTTTTATGGTCACTGTGATTGACAGAGTTAGTTTACAGTTTTTGGTAATCAATGTAATAATTTAAATATTGTTGATTTACAGGATTTTAATTCAGTTTGATGATTTATTTTAAAGGGGATGTATCATGCTCATTCTGACCAATCTCATAATCTTGAATCATAAAGTAAACCCAAAACAAAAGTGTCCACCTGGATCTCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31437
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123535 Nonsense 673 1200 15 29
Genomic Location (Zv9):
Chromosome 5 (position 26934513)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150339.1 14873
GRCz11 5 25335947
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCTGCTGACCTGGGAGATGAAGGATTGGAGTAACTTCACCTGTCTG[C/T]AAATGGCCGTCTCCTCAGGACTCAGGCCCTTTGTGGCTCACAACTGCACT
Long Flanking Sequence:
AAGTGCAAGTGACTTGAAAAACCTCAGGCTGCAGACCGATACAGGCTGTATCATCTAAACAATCTTCCGATTTCTGACAATGTGGGTACAGAAGAATAAATGTCAGGCAATAAATATGGAAAATAAAGTTAAATCATTACTTTTTGTGAAACAATAGCTCAGATATTGTCTTGAAATTTTAAAAGTAATGCATTACTAGTTACGTAAAGTAATCTGATTACATTACTCATGCTACTTGTAATGCTTTACCTTGAAAAATGGTTAATTTTACCTAATAGAAGTTGCACTTTTTAAGTAAATATGAGATTGAACATTTGACCGAAATTCTACTGTATTGATAAGGATGTCACCAATGTAATGCAATGTAAATGTGTTGGTCTATCAGAGAGTTTGGACAGTTGGCTGTGGATGTCCTGGATCAGGCTTTCAGAGAGAATGAGCGCATGGCGATGAAGCTGCTGACCTGGGAGATGAAGGATTGGAGTAACTTCACCTGTCTG[C/T]AAATGGCCGTCTCCTCAGGACTCAGGCCCTTTGTGGCTCACAACTGCACTCAAATGCTGCTCACAGACCTGTGGATGGGCCGTCTAAACTTGAGCAAGAACTCCTGGTTTAAGGTGTGTTTAGTGTGACTTAAAGGTGCAGTAGGTGATCTACGACAATGCTAACCGGCTAACGTAAATCTCTGAAACACAGTCCCACCCATGCCGTCCAAAGCCATGCCTCCTGAAATACAAGTGAGCGAGTAGTGCTTGGCAGGCGGCATGCAGGAATTACACTTATTACTAAGCCATACTTGCATGCTATTTCAGACCGAGTATTTAGAATAGCAGTAAACAATATAGGGAGCACATCACAGGTTTACAGTGTTAAAAAATGAACTAATGTGATGTGAATATAAAAGCAACTTCACCTCAGTTAAGCAGGCTAGGCAGAATAGCGCTGTTTACTGATGTTTTGTTGTTAAACTAAATACAAATCAAGCAACAACAACATCTGCATCA
Associated Phenotype:
Not determined