Busch Lab

ZMP

TRPM7

Ensembl ID:
ENSDARG00000036232
Description:
transient receptor potential cation channel, subfamily M, member 7 [Source:HGNC Symbol;Acc:17994]
Human Orthologue:
TRPM7
Human Description:
transient receptor potential cation channel, subfamily M, member 7 [Source:HGNC Symbol;Acc:17994]
Mouse Orthologue:
Trpm7
Mouse Description:
transient receptor potential cation channel, subfamily M, member 7 Gene [Source:MGI Symbol;Acc:MGI:1

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa36550 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa39184 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28944
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052617 Essential Splice Site 674 1771 16 47
ENSDART00000098433 Essential Splice Site 674 1786 16 48
Genomic Location (Zv9):
Chromosome 18 (position 127613)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 137531
GRCz11 18 137531
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCA[G/A]TGAGTTCGGCACGCTGGCGGTGGACCTGCTGGAGCAGTCGTTCCGTCAGG
Long Flanking Sequence:
ACTCGGTGTCAGAGCTGCAGAAGAAGAAGAGTAAGGAGGAGGTGGTGGACGTGGACGACCCGGAGACGCGGCGCTTCCCGTACCCGTTCAACGAGCTGCTGGTGTGGGCGGTGCTGATGAAGCGGCAGAAGATGAGTCTGTTCTTCTGGCAGCACGGGGAGGAGTCCATGGCCAAAGCGCTGGTGGCCTGCAGACTGCTGCGCTCGCTCGGGGACGAGGCCAAGAAGAGCGACGTGGTGGACGACACCTCTGAGGAGCTCAAGGAGTACTCCAGGTCAGAGCGCAGACGCAGAACCAGCGACAGGCGTCACTAGTACAGTACAGAGCTGATCCCAGAACAGCCTGAACACTGCTGGAGCACACCGACACAACACAACACTCAGCTGAGCACCGCCACCACATGCACTCCTGTCCCTCTGTCTATGTGTGTGTGTGTGTCTGTACTATCTTTAACCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCA[G/A]TGAGTTCGGCACGCTGGCGGTGGACCTGCTGGAGCAGTCGTTCCGTCAGGACGAGACGATGGCGATGAAGCTGCTGACGTACGAGCTGAAGAACTGGAGCAACTCCACCTGTCTAAAGCTGGCGGTGTCGTCACGGTTACGGCCCTTCGTGGCACACACCTGCACACAGATGCTGCTGTCCGACATGTGGATGGGCAGACTCAACATGCGCAAGAACTCCTGGTACAAGGTATAGCACAACACACACACACATACACACCTGCACACACATCCCATGATGCACTGCTTCAGCTATGTCACACCCGGCCAATAGATCGCCCCCTGCAGGACGAGTCATACATCAGTCATTTAATGCTATTGAAACAAGGCGTGTCCTCATGATTGACAGCTGTGATTGACAGCTTCTCAGAGCAGACTGTGGGAGCTTCAGGAGGAGGTTGCAGCAGCAGGGTTTGAGTTCTGTGTGATTAAATGAGCTGAGCAGTGAACTGTTCTGTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36550
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052617 Essential Splice Site 1407 1771 37 47
ENSDART00000098433 Essential Splice Site 1407 1786 37 48
Genomic Location (Zv9):
Chromosome 18 (position 142051)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 123487
GRCz11 18 123487
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTC[A/T]GCACTCAGTAAGCAGGAGAGGACGCGCGTGTCGCTGGAGGACGTCTCTCG
Long Flanking Sequence:
GTGTGCGCACGCTCCTGCAGGGTAACATGCGGACGGTGAACTCTTACGCCGGCTTCACAGAGTTGGACAGAAACCCTTCGCTCCTGCATCCAGAGTCCAGTGAGTGTAAACCTTGAGCAACACCAGTGAATGCTGTAAACATTAACTGATGAGCACACACACACACACACACACACACACACACACACACACACACACACACACATCTGAAGAGCATCTCACACACTGATGGAGTCACTCTCTGTGTTTGTGTGCTTGTGCATGTTTGTCTATCTGTGCGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGCGCGTGTGTGTGCGCGTGTGTGTGCGCGTGTGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTC[A/T]GCACTCAGTAAGCAGGAGAGGACGCGCGTGTCGCTGGAGGACGTCTCTCGATATGAGGATCTGCTGCTGGTCAGTCAAACACACGTTCAGAATGTTTAGTGTGGTGTGAGCTGTGTGTGAACGGGTTTCCCTCAGGGACGGCTGCTAGATGACAGATAGAGCTGCTGTGTGTGTGTGTGAGTGTGTGTGAGTTTCTGACTCTAGATTGAAGACATCATCCTGTGTGTTCAGAGATCTGACAGTGATGCTGATGAGTGTGTGTTTAAAAGTTCTCAAATCAAGAAGCGTTTTCTAGACAAGCAAAATATGTTGTCTTGTTTTAAGAAATAATCTGCCAAAATAAAGTGAGTCTTTCCTTAAATCAAGCTAAATAATCTGTCAATGGGGTCAGCAAAATAATCTTGCTTTTCCTTTTGACGTAAGATTGTTTTGCTGACCCCATTGACAGATTATTTAGCTTGATTTAAGGAAAAATTCACTACATTTTGGTTTATTATTTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28945
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052617 Essential Splice Site 1484 1771 41 47
ENSDART00000098433 Essential Splice Site 1499 1786 42 48
Genomic Location (Zv9):
Chromosome 18 (position 145278)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 120260
GRCz11 18 120260
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGATGCGGTTGTCTCAGAGCATCCCCTTCACCCCGGTGCCCCCTAGAG[G/T]TAAGACACACTCCTGCCCTCCTGTCTCTCGTTCCCATCATGCTTTGCTGC
Long Flanking Sequence:
CAGAGGAATTCATATATGGATTTAACCCTCACTTCAGGACTTATTCTCTAACACTCTTGTGCATTGTGTTGCTTATGTTCACTTGTTGTTGTTGTTGTTGTGTGTGTGTGTGTGTGTGTGTAGCGATCGGTTCTCCATTCAAGCCCATGGAGAGTTATCAGTACTCGGGTGAGTGTTTGTGTGGTTCCTCATGGTAATCTCAGTGTCCTGGAAGCAGAAATATGTCCTGGTTTAAACCCGACCCACAATGCATCAGTCACACACACACACGCGCGCTGTAATGTGTGTGAACAGTCATTATTGTGGAAAGCGCTGTACAGAGATGAATGTGAGCTGAAGGTGTGTGGTTTGGGTTTAAATCAGGCGTGTGGCAGCAGCTCCTGTGATGTGTACTGACATCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTAGCGGTGGAGCGTAATAACCTGATGCGGTTGTCTCAGAGCATCCCCTTCACCCCGGTGCCCCCTAGAG[G/T]TAAGACACACTCCTGCCCTCCTGTCTCTCGTTCCCATCATGCTTTGCTGCTGTAGTTGTGGGCGGCTCAATAGGGTTGAGGTCAGGGCTGGGGTTGTCCCCTACAGCAGAGGGAGATACCGCAGGAAATGTTGGAGAGTGCAGCTGGGCCTGACTCAGCCTGTGTGTTGAGCTCATCCTGCAGCGCCCAGCTGAAGACCTGTATAGACCCCGCCCACAACTACAGAGAGCTGCTGGTACTGTGTGCTCACGCGTGTGTGTGTGCGCATGCGTGAGTCTGTGCGTGCGTGCGTATGTGTGAGTGAGTGAGTGAGTGAGTCTGTACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGCTAGTCTATCTGTCTGTGTGTCTGAGTGTGTGCGCGGGTCTGTGTGTGTGTGTGTATGCTAGTTTATGTGTGCACACAAGTCTGTGTGTTTGTGTGGGTGCCCATGCATGTGTGTGTTTATGCAAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39184
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052617 Essential Splice Site 1675 1771 44 47
ENSDART00000098433 Essential Splice Site 1690 1786 45 48
Genomic Location (Zv9):
Chromosome 18 (position 147920)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 117618
GRCz11 18 117618
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGACGTATGAATACACACGAGGAGAGCTGCTGGTGCTGGACCTGCAGG[G/A]TTTGTGTCTAAACACACACGTCAGCAGGTTACACATATGGGGTAATGCAC
Long Flanking Sequence:
GGGAAACACCCATACACATTCATTCACTCATACACTACGGCCAGTGTAGTTGATCAGTTCCCCTATAGCGCATGTGTTTGGGAAACCGGAGCACCCGGAGGAAACCCACACCAACACGGGCAGAACATGCGATCGTGCTACCCACTGCGCCATCATGACACCCTCCTGCCAGTGCTTTTACAGGTTTATTGCAGTTCAGCATTTTAAATGAGGTGCTGTCCTGATACTCTACATGTGAGCTGTAGTTTAGTCTTGGTTTCCTGAACTCTCCTGGTTCTCCGCTGTGGGCTGCAGGTTCCTGGAGGTCTTCCTGCTGTACTGTCATTCTGCCGGTCAGTGGTTCGCCATCGAGGAGTGCATCACTGGAGATTTCCGCAAGTTTAACAACAACAACGGAGATGAAATAGTGCCGACCAACCTTCTGGAGGAAACCATGCTGGCCTTCAGCCACTGGACGTATGAATACACACGAGGAGAGCTGCTGGTGCTGGACCTGCAGG[G/A]TTTGTGTCTAAACACACACGTCAGCAGGTTACACATATGGGGTAATGCACATCCAGCGCTGCTCGCGGAGTCTTACCGTATTAAAAGATGATGAATCAATTAATAGAGATTTGAGAGCCGCACCGTCTCAAATGAGTGTCACTTTAACTATCAGTCTACTGTACAATGAGTTTGATCTGCTAATGTTGGGGTGCTGCGTTGTTTTTGAACACTAATCATCTAAAACTAGACTGGACACCACGCTGCCAAGGCAACACTGCAGTTCTGTAGGCGCCCCCTGCTGGATTAGCGTTTCTATTCAGCTTATGAATTATGTTTTAGTTTCATGTTTCGTACAGTTAGTATTTAGTAAATATACTGTTAGTTAAAGTGTTGCCAATGTTACCTACAGTGGTGGTGGGGTCTGAATGTATTAAAGGGCACATAGGTCACCCCTTTTTTCAGATTAAAATAAGTATTTTGTGTCCCCAGAATGTGTTTGTAAAGTTTCAGCTCGAAAC
Associated Phenotype:
Not determined