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

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

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