ZMP
LOC100149353
Ensembl ID:
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 |
sa6976 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7276 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31437 | Nonsense | Available for shipment | Available now |
sa44606 | Nonsense | Mutation detected in F1 DNA | Not yet available |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa6976
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123535 | Nonsense | 387 | 1200 | 9 | 29 |
Genomic Location (Zv9):
Chromosome 5 (position 26938367)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150339.1 | 18727 |
GRCz11 | 5 | 25332093 |
KASP Assay ID:
554-5157.1 (used for ordering genotyping assays)
KASP Sequence:
AAATAGTGTTTGTTAYTCAAAATGAAAATACAGGGACGAGAGCTTCCCCC[G/T]AGGARCAGCTGAGTCTCACTCTGGCYTGGGACAGAGCTGATATTGCAAAA
Long Flanking Sequence:
CGCTTGTAGCTTCTCCCTTTATTGAAAAGAGCTTGAATTTAAAGTGACAGTCACCAAAAAAGCACCCTTTGGATCAAAACCTAAAAGGGGCAGTTTCAAAGAGTTATAAAACATTATTTGTGGGGTATTTAAGCTGAAACTTCACAGACACACTCTTGGGACATCAGTGACTTATTTTACATCTTGTAAAAAGTGGCATAATAGGTTTGAAAGTGTAAACCAGGGGTCACCAATCTCAGTCCTGGAGGGCCGGTGTCCCTGCAGGGTTTAGCTCCAACTTTCCTCAACACACCTGCCTGGGTGTTTCAAGCAAACCTAGTTGGACGTTGGTTAGCTTGTTCAGATGTGTTGATTAGGGTTGGAGCTAAAATCTGCAGGATACCAGTCCTCCAGGAACAAGTTTGGTGACCCCTGGTGTAAACAATAATTCAACCTCTTTAAAAGTTGTATAAATAGTGTTTGTTACTCAAAATGAAAATACAGGGACGAGAGCTTCCCCC[G/T]AGGAACAGCTGAGTCTCACTCTGGCTTGGGACAGAGCTGATATTGCAAAAGACCACATTCTGGTCTATGGGCAACAATGGCAGGTATAGTAAACAGCTAATTTGACAATCAGGGTTGAGATGTTTTATGTGTTAAACCAGCCCATGTCTAATTCAGCACTGGATTTTGTAGGTAGGATCTCTGGAGCAGATCATGCTGGATGCGCTGATAATGGATCGCGTCAATTTTGTAAAGCTGCTAATTGAGAATGGCATGACCATGAGTCACTTCTTGACAATCTCTCGTCTGGAGCAGCTCTACAACATAGTAATGCACATGTACTGCTTGCATTGATCTTAAGCGTGTAATTCAAGTGAGTATCTCTGATCCTCATTTGTGTTTCTTTTTTCCCAGCAAACAGGCTCCTCACATCATTTCCTTCGACATGTTATTGCAGATGCCAAACAGGTTTGTGTAGAGTAAAACCCTAAATGCTTGTGTAGAGTACTTTTGTAAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7276
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123535 | Nonsense | 646 | 1200 | 15 | 29 |
Genomic Location (Zv9):
Chromosome 5 (position 26934594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150339.1 | 14954 |
GRCz11 | 5 | 25335866 |
KASP Assay ID:
554-5179.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGTTGGTCTATYAGAGAGTTTGGACAGTTGGCTGTGGATGTCCTGGAT[C/T]AGGCTTTCAGAGAGAATGAGCGCATGGCKATGAAGCTGCTGACCTGGGAG
Long Flanking Sequence:
TTTAACTGGGCTAGGCTTACTTGTTTGTAATAGTATAACGAACAAGTATAATTTGACAAATATAAGTCCATTTTATACCAAAAGTGCAAGTGACTTGAAAAACCTCAGGCTGCAGACCGATACAGGCTGTATCATCTAAACAATCTTCCGATTTCTGACAATGTGGGTACAGAAGAATAAATGTCAGGCAATAAATATGGAAAATAAAGTTAAATCATTACTTTTTGTGAAACAATAGCTCAGATATTGTCTTGAAATTTTAAAAGTAATGCATTACTAGTTACGTAAAGTAATCTGATTACATTACTCATGCTACTTGTAATGCTTTACCTTGAAAAATGGTTAATTTTACCTAATAGAAGTTGCACTTTTTAAGTAAATATGAGATTGAACATTTGACCGAAATTCTACTGTATTGATAAGGATGTCACCAATGTAATGCAATGTAAATGTGTTGGTCTATCAGAGAGTTTGGACAGTTGGCTGTGGATGTCCTGGAT[C/T]AGGCTTTCAGAGAGAATGAGCGCATGGCGATGAAGCTGCTGACCTGGGAGATGAAGGATTGGAGTAACTTCACCTGTCTGCAAATGGCCGTCTCCTCAGGACTCAGGCCCTTTGTGGCTCACAACTGCACTCAAATGCTGCTCACAGACCTGTGGATGGGCCGTCTAAACTTGAGCAAGAACTCCTGGTTTAAGGTGTGTTTAGTGTGACTTAAAGGTGCAGTAGGTGATCTACGACAATGCTAACCGGCTAACGTAAATCTCTGAAACACAGTCCCACCCATGCCGTCCAAAGCCATGCCTCCTGAAATACAAGTGAGCGAGTAGTGCTTGGCAGGCGGCATGCAGGAATTACACTTATTACTAAGCCATACTTGCATGCTATTTCAGACCGAGTATTTAGAATAGCAGTAAACAATATAGGGAGCACATCACAGGTTTACAGTGTTAAAAAATGAACTAATGTGATGTGAATATAAAAGCAACTTCACCTCAGTTAAG
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa44606
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123535 | Nonsense | 826 | 1200 | 20 | 29 |
Genomic Location (Zv9):
Chromosome 5 (position 26930327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150339.1 | 10687 |
GRCz11 | 5 | 25340133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGGCTGAACGAGACACCCAACATTCAGGAGTGCTTGGTCATGACTTA[C/A]ATCCTGGCCATGGCGGTGGAGAAAGCTAGAGAGGTGGGACATCTCAAAAT
Long Flanking Sequence:
TCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTGTGCGTAAATGTGTGTGTGTGGGTGTTTTCCAGAGATGGGTTGCGTCTGGAAGGGCATCCGCTGTGTAAAAGCTTGCTGGATAAGTTGGCGGTTCATTCTGCTGTGGCGACCCCAGATTAATAAAGGGACTAATCCGACAACAAAATGAATGAATGAATGTATCCATAGTACAAGTTTTTTCTTACTGTGGAGATCAAATTAATTACTGGTTGCCAAATTCTTAAATTTTTTTGTTGTTGTACAAAAACAAGCTCAAGAACTATATCCCTGTAATCAACCTTTGTTTTCATGACACCCCTTTGCTCCATCTTCCATCTGTATTTCTGTCCAAACAGATGGCGTTTTTGGGATTCCTCATGATGTTTGCTTATACTTGTTTGGTGAGGCTGAACGAGACACCCAACATTCAGGAGTGCTTGGTCATGACTTA[C/A]ATCCTGGCCATGGCGGTGGAGAAAGCTAGAGAGGTGGGACATCTCAAAATTACTCTCTCCTCAGCAGATAAGAGAAGTATACAGTATGACATATAAATTGATGTCATTGAGATGTTGGCCTGGTGCTCTTTGCAGCTGTTCAGAGCAATTAAAGAATAAAATGCATCTTTGAAAAGTCTTATCTTAATCAAGCTGGATTCCAAAGGTCCACTGTAAGGTGTTATCTCTTTCTGGTTATGGAGTTGACCCTGAGAATGTCTCTGTCTGACTCCCCCTTTCCTCTATTATCTATGAACTCAACAGCAGTGCACTAGTGGGAATTATTAACCAGTTCTGTCATAGACTACACATTTGAGTGATTGTTTATTGTATTTCGGTTAGATAAACTCCAAGAGCCTCTTTCAATCCCAAGGAAAATAGTGATTTTTTTTTAAAAATGGATTTTGTCTTCTGGTCTGTCAGGCTTCTGGATCTATAAGCTGTCAATCAGCATGCAGGAC
Associated Phenotype:
Not determined