ZMP
msh6
Ensembl ID:
ZFIN ID:
Description:
DNA mismatch repair protein Msh6 [Source:RefSeq peptide;Acc:NP_878280]
Human Orthologue:
MSH6
Human Description:
mutS homolog 6 (E. coli) [Source:HGNC Symbol;Acc:7329]
Mouse Orthologue:
Msh6
Mouse Description:
mutS homolog 6 (E. coli) Gene [Source:MGI Symbol;Acc:MGI:1343961]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu1811 | Nonsense | Available for shipment | Available now |
sa12638 | Nonsense | Available for shipment | Available now |
sa22382 | Nonsense | Available for shipment | Available now |
sa15374 | Nonsense | Available for shipment | Available now |
sa15299 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
hu1811
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 |
---|---|---|---|---|---|
ENSDART00000018840 | Nonsense | 474 | 1369 | 4 | 10 |
ENSDART00000143175 | None | None | 109 | None | 3 |
ENSDART00000143315 | None | None | 234 | None | 3 |
ENSDART00000146105 | None | None | 129 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 49394373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 48075665 |
GRCz11 | 13 | 48366695 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTGGCTTCCCTGAAATCGGCTTCGGCCGCTTCTCAGACGTACTTGTG[C/T]AAAAAGGCTACAAAGTAGCTCGCGTAGAACAGACTGAAACTCCAGATATG
Long Flanking Sequence:
CCACAGAAAAGCCTACTAAATCAAAGAGCAAACCAGAAACTCCAAAGCGAGCGCCTGCAGCTCTGCCATCAGTGTCGACTGATGCCAAATCTCGACTTTCTGCTTTCTCTGCACCAGATAACTTTGATAGTCAGAATAGTGCAAATGGGACCGAGGGCGGATCGACCGTATGGGACCACGAGAAACTGGAGTGGCTGCAGGACGGCAAGAGAAAAGACGCACAGCGTAAACGTCAGTCTGACGAAAACTACGATCCCACAACTCTATATGTGCCCGAAGACTTCCTTAACAGGACGACGCCTGGAATGCGCCGCTGGTGGCAACTTAAATCTGAGATGTTTGATACTGTTCTGTTTTACAAAGTTGGTAAGTTTTATGAACTCTACCACATGGATGCAGTCATTGGCGTCAATGAACTTAATCTTACCTTCATGAAAGGTACCTGGGCCCACTCTGGCTTCCCTGAAATCGGCTTCGGCCGCTTCTCAGACGTACTTGTG[C/T]AAAAAGGCTACAAAGTAGCTCGCGTAGAACAGACTGAAACTCCAGATATGATGGAGGCACGATGCAAGAAACTGGCACGTCCCACTAAATTTGATAAAGTTGTCAAAAGAGAGGTTTGCCGAATTATCACGCGAGGCACTCAAACGTATAGCGTGCTTGATGGCGCCCCTTCTGAAACTCAAAGCAAGTATCTGTTGAGCATTAAAGAAAAGAGTGAAGAGGATAGCACAGGTCATGGTCATATCTACGGAGTTTGTTTCATTGACACATCAGTGGGGCGTTTTCACATCGGTCAATTCCAGGATGACCGACATTGCTCCCGTTTGCGTACTTTAGTGGCACACTATTCCCCTGCTCAAGTTATTTTTGAGAAAGGAAACCCTTCAATTGAGACATTAAAAATCTTTAAGGCCATCGTGGCATCATCTCTACAAGAAGGCCTGAATGCTGGTTCCCAATTTTGGGATGCCCAGAAAACCCTCAAGGTACTTGCAGAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12638
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018840 | Nonsense | 911 | 1369 | 4 | 10 |
ENSDART00000143175 | None | None | 109 | None | 3 |
ENSDART00000143315 | None | None | 234 | None | 3 |
ENSDART00000146105 | None | None | 129 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 49393062)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 48076976 |
GRCz11 | 13 | 48368006 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAGACTGAAAACGAAGATGGTCTTTTCCCTGACCTTTCTCCAGAGCTC[A/T]AACGTTGGGATACTGCTTTCGACCATCAGAAAGCTCGCACTACAGGTGTC
Long Flanking Sequence:
TCGAAATCCTTCAGAATAGCTCGACTGGAGGTCCTGAGGGAACACTACTTGAACGACTGGACACATGTTGCACTCCTTTTGGCAAGAGGCTGTTGAAACAATGGATTTGTGCCCCTCTTTGTAATCCATCCTCCATTGGTGATCGCTTGGATGCTCTGGAGGACCTAATGGGCGCTCCATCCCAAACATCCGAAGTCACAGACCTGCTCAAGAAGCTTCCAGATTTGGAAAGGCTACTTAGTAAGATCCACAGCATGGGTACTCCTTTAAAAGGACAAGACCATCCGGACTCCAGAGCCATTCTGTACGAAGAGGTAGTTTACAGCAAACGTAAGATTGCAGATTTTCTCGCAGCACTTGAGGGATTTAAAGTTATGAAAGAAATCGTGTCGATCATGGAGCCTGTCGGCGAAGACCTCAAATCCAAACTACTGCGCCAAGTGGTGCTCCTCAAGACTGAAAACGAAGATGGTCTTTTCCCTGACCTTTCTCCAGAGCTC[A/T]AACGTTGGGATACTGCTTTCGACCATCAGAAAGCTCGCACTACAGGTGTCATCACACCAAAAGCTGGCTTCGATCCAGAATACGACCAGGCCTTAAATGGAATAAAAGAGTGCGAGAGAGACCTGCAGGACTACTTGGATCGACAGAAAAAGCGATTGGGCTGTAAGAATCTATCCTACTGGGGAACGGGAAGAAACCGATACCAACTGGAAGTTCCAGAGAGTGTTTCTGAAAGAAGCCTACCGGAGGAGTACGAGGTCAGGTCTACTAAAAAGGGCTGGAAGCGATACTCCACCAAGGATATCGAGCGAATGTTTTCAGAGCTACAGAGCTGGGAAGACAAGAGAGATGCAGCGCTGAAGGACTGCATGAGGAGACTCTTCTACAACTTTGACAAGAATTACAAGGACTGGCAGACGGCTGTGGAGTGCATGGCAGTGCTCGGTAAGAAAAATTGACTACATCTACTTTCAGCTATGTTGCTTGTTTGAAGTTCACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22382
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018840 | Nonsense | 938 | 1369 | 4 | 10 |
ENSDART00000143175 | None | None | 109 | None | 3 |
ENSDART00000143315 | None | None | 234 | None | 3 |
ENSDART00000146105 | None | None | 129 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 49392979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 48077059 |
GRCz11 | 13 | 48368089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCGCACTACAGGTGTCATCACACCAAAAGCTGGCTTCGATCCAGAATA[C/A]GACCAGGCCTTAAATGGAATAAAAGAGTGCGAGAGAGACCTGCAGGACTA
Long Flanking Sequence:
AAGAGGCTGTTGAAACAATGGATTTGTGCCCCTCTTTGTAATCCATCCTCCATTGGTGATCGCTTGGATGCTCTGGAGGACCTAATGGGCGCTCCATCCCAAACATCCGAAGTCACAGACCTGCTCAAGAAGCTTCCAGATTTGGAAAGGCTACTTAGTAAGATCCACAGCATGGGTACTCCTTTAAAAGGACAAGACCATCCGGACTCCAGAGCCATTCTGTACGAAGAGGTAGTTTACAGCAAACGTAAGATTGCAGATTTTCTCGCAGCACTTGAGGGATTTAAAGTTATGAAAGAAATCGTGTCGATCATGGAGCCTGTCGGCGAAGACCTCAAATCCAAACTACTGCGCCAAGTGGTGCTCCTCAAGACTGAAAACGAAGATGGTCTTTTCCCTGACCTTTCTCCAGAGCTCAAACGTTGGGATACTGCTTTCGACCATCAGAAAGCTCGCACTACAGGTGTCATCACACCAAAAGCTGGCTTCGATCCAGAATA[C/A]GACCAGGCCTTAAATGGAATAAAAGAGTGCGAGAGAGACCTGCAGGACTACTTGGATCGACAGAAAAAGCGATTGGGCTGTAAGAATCTATCCTACTGGGGAACGGGAAGAAACCGATACCAACTGGAAGTTCCAGAGAGTGTTTCTGAAAGAAGCCTACCGGAGGAGTACGAGGTCAGGTCTACTAAAAAGGGCTGGAAGCGATACTCCACCAAGGATATCGAGCGAATGTTTTCAGAGCTACAGAGCTGGGAAGACAAGAGAGATGCAGCGCTGAAGGACTGCATGAGGAGACTCTTCTACAACTTTGACAAGAATTACAAGGACTGGCAGACGGCTGTGGAGTGCATGGCAGTGCTCGGTAAGAAAAATTGACTACATCTACTTTCAGCTATGTTGCTTGTTTGAAGTTCACCCTCAAATGACTAGTTTGATTTATGCTTGATTTTTGATTTTGCGCATGATTTATGCTTAAAGCATCTTAGGTAGGCATGGGCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15374
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018840 | Nonsense | 1004 | 1369 | 4 | 10 |
ENSDART00000143175 | None | None | 109 | None | 3 |
ENSDART00000143315 | None | None | 234 | None | 3 |
ENSDART00000146105 | None | None | 129 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 49392782)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 48077256 |
GRCz11 | 13 | 48368286 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAAGAAGCCTACCGGARGAGTAYGAGGTCAGGTCTACTAAAAAGGGCT[G/A]GAAGCGATACTCYACCAAGGATATCGAGCGAWTGTTTTCAGAGCTACAGA
Long Flanking Sequence:
CCATCCGGACTCCAGAGCCATTCTGTACGAAGAGGTAGTTTACAGCAAACGTAAGATTGCAGATTTTCTCGCAGCACTTGAGGGATTTAAAGTTATGAAAGAAATCGTGTCGATCATGGAGCCTGTCGGCGAAGACCTCAAATCCAAACTACTGCGCCAAGTGGTGCTCCTCAAGACTGAAAACGAAGATGGTCTTTTCCCTGACCTTTCTCCAGAGCTCAAACGTTGGGATACTGCTTTCGACCATCAGAAAGCTCGCACTACAGGTGTCATCACACCAAAAGCTGGCTTCGATCCAGAATACGACCAGGCCTTAAATGGAATAAAAGAGTGCGAGAGAGACCTGCAGGACTACTTGGATCGACAGAAAAAGCGATTGGGCTGTAAGAATCTATCCTACTGGGGAACGGGAAGAAACCGATACCAACTGGAAGTTCCAGAGAGTGTTTCTGAAAGAAGCCTACCGGAGGAGTACGAGGTCAGGTCTACTAAAAAGGGCT[G/A]GAAGCGATACTCCACCAAGGATATCGAGCGAATGTTTTCAGAGCTACAGAGCTGGGAAGACAAGAGAGATGCAGCGCTGAAGGACTGCATGAGGAGACTCTTCTACAACTTTGACAAGAATTACAAGGACTGGCAGACGGCTGTGGAGTGCATGGCAGTGCTCGGTAAGAAAAATTGACTACATCTACTTTCAGCTATGTTGCTTGTTTGAAGTTCACCCTCAAATGACTAGTTTGATTTATGCTTGATTTTTGATTTTGCGCATGATTTATGCTTAAAGCATCTTAGGTAGGCATGGGCCAGTATAAAATTCTTACGGTATGATAACCTTGGATAAAAATATCACGATATTGTGCTCACTGCTCTAAAATATATTATTTTTAAATGTCCGTGTAAAAAAATAATAAAAATAAAAAGTTTTCCTTTAAACACAATATATTTTATTTTTTGAAAGATTTTAAATATTTTGGAACAGTAAACATGTCAGGCAGAATCATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15299
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018840 | Essential Splice Site | 1343 | 1369 | 9 | 10 |
ENSDART00000143175 | None | None | 109 | None | 3 |
ENSDART00000143315 | None | None | 234 | None | 3 |
ENSDART00000146105 | None | None | 129 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 49385372)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 48084666 |
GRCz11 | 13 | 48375696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGGCCCGCGACTTCGAAAGGAGCACCGTATCTCTCCGCATATTCAAG[T/A]ACGTCTCTTYATCAACATGTTTTACATCGTGATCWTTTYATTGCCTTAAA
Long Flanking Sequence:
TAACCGAAAGCGGGGAGTGTCATGGCCCTTTAATAAACATTTACCAGACGCCATATATTAACATAAACGTTGGGGCTGCATCTCACATCACAATACAATCTCATATCCTGATAACATAGTATATTATGGTATAATACCTTGCTGTAAACTCAATCAAATTACAGTTTCACACATTTATAAAAAAATGTACTCAAAAATGATTTAATATGTGATTTAAAACACAGGTCACCAACCTTTTTCCATCCCTGACCTCAGCCTTGCCTATTTATTAAAGCGATGTCCGTGTGTTTTGTTGTCAGGCCTGTATGGTGGAGAATGAGTGTGAAGACCCCAGTCAGGAGACCATCACCTTCCTCTACAAGTTCATCAGAGGAGCGTGTCCTAAAAGCTACGGCTTTAATGCGGCTCGCTTGGCAAACATCCCGGAGGACGTGATCCAGAGCGGACACAAGAAGGCCCGCGACTTCGAAAGGAGCACCGTATCTCTCCGCATATTCAAG[T/A]ACGTCTCTTCATCAACATGTTTTACATCGTGATCATTTTATTGCCTTAAAAAAGACAGCTCACGCCAAAATCTGTAAAACATGTAGGAGTTTCTTCTGTTGAACACTAAAGGAGATATTTTGAGGAATGTTGGAAAGCGATACCCATTGACATCCATAGTAGACAGGAAGAAAATACTATGGGAGTGAATAGGTGCATCCCAAATCGCATACTTATGCACTATTCTACGCCATTTTGTAGTATTAATAGTGTAAGTAAGTAGTGCATTCACACTGAAAATGCTATAAATAATAAGTGCACTTTAATTAAGCTGATGATGCTCCTATTCAACCGTTAAAAAGAAGTGTGTAATGTCGGACACTTCACACACTCAACAGCTAAGGGTGTCACGATCCTCCAAATCCTCGATTCGATTACATTTTCGATTCTAAAGTCACGATTCGATTCGATTATGAATAATTAATTAATTAATGACCAATTAATTATTTGTAGCCTACCGT
Associated Phenotype:
Not determined