ZMP
msh2
Ensembl ID:
ZFIN ID:
Description:
DNA mismatch repair protein Msh2 [Source:RefSeq peptide;Acc:NP_998689]
Human Orthologue:
MSH2
Human Description:
mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli) [Source:HGNC Symbol;Acc:7325]
Mouse Orthologue:
Msh2
Mouse Description:
mutS homolog 2 (E. coli) Gene [Source:MGI Symbol;Acc:MGI:101816]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31876 | Nonsense | Available for shipment | Available now |
sa22101 | Essential Splice Site | Available for shipment | Available now |
sa11438 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31876
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 |
---|---|---|---|---|---|
ENSDART00000002465 | Nonsense | 218 | 936 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 26428168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24800609 |
GRCz11 | 12 | 24921828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATAATCATGCTTAATAAATACTTGTGGTTGTTGATGATTCAGGTGGTG[C/T]AGCGTGGTGGCATTCTCCTCACAGACAGGAAGAAGTCAGAGTTCACAACT
Long Flanking Sequence:
TTTGTGTAAACCATGATACACTACAATCTAAATCTATGTTAATAAAAAATAAACATGACTTGAAAAAAAAAAGATTCTTTAAAGTAGAAAGCATTCAATACTAAAAGTGAAGACTATTTTTTATAATGTAATAATGCTACAAGTAATTCAAAAGCTATTTCAAATTTAAAAGTGTTATTTTAAATGTATTGTTTTAAACTGTAGAATGCTGAAAAATATATGAGATTCCCACTGAGCACCAATTTAACATATTACAAGGATTTCTGAGAAATAACTGCTAAGAAAATAGTGTATTAGCGATACCTTACTTATAAGAGGTGAATACTTAGTTTTAATTTAACGATAGAACATTTTACAATGTTTTTAATCAAACAAATAAATACCATTGGCAAGCATAAAAAATAAACATCATAAATCTGAATGTTTTGCATCCTTTGACATGTAGTATATCTATAATCATGCTTAATAAATACTTGTGGTTGTTGATGATTCAGGTGGTG[C/T]AGCGTGGTGGCATTCTCCTCACAGACAGGAAGAAGTCAGAGTTCACAACTAAAGACATTGTGCAGGATCTGAATCGGCTACTGAAGGCCCGTAAAGGAGAGACTGTGTCCAGCGCTGCCCTGCCTGAGATGGAGAAAAAGGTTTGGGGATCTGCCACTAGTGATAGGAGAAACTATGCTTTTCAAAGCTTCAAAACAATTGAATGAAAAGATTTCTTTTTTGAAGCTTTTGAAACATCGTGTCCAAGGGACACCTTGTGGTCATAACATTTAAATGCAGAAAACCCTCAGGCAAAACTTGTTAGTTGACTTTTTCAAACATTGCAAGCTTTTAAATTAAAAGTATAATATATAAATGCACTTAGCCTAAATTTCCCTAATTTCTCTAATTTCATCAAATATTAAGTGTCCTTAATAGTATGTGTACAACCCAACCCGACTATTAACCATTCCTTTTCATTTTACAAATGTCGCATCAAAACATCTACAGAATAATAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22101
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002465 | Essential Splice Site | 426 | 936 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 26426117)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24798558 |
GRCz11 | 12 | 24919777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTGGGGCAACTGCCCAATGTGGTGCTGGCACTGGAGAGATACAGTGG[T/C]AAGCAAAACAACAACTTTATCAATAATCGATAACATTAAGCCTGAGAATC
Long Flanking Sequence:
CTCACTGATTCTGACTGGACAACTTTTGTTGCTATTGTTATGCTCAATATACTTGTATATCAGTACGATAATAGTTATATAATTAGTACAATACAATTAGTATAATAATGATTGCAGTGATTTTGATTGTTTACATTTACAATTTCACATTATGGATAGTTTTCTGATCAAACCTCTGAATTGCAATCATAATGAAATCTTTACTTCAGTTTCACAGCATAATTTAAGATATCGTTTTCTCTTTGAATCGAACTTTTGTAACATGCAATGAGACTATACCTTTGCTTGTACATGCTTAGACTGGACCTTGTGGAGACATTTGTGGAGGACTCGGAGCTAAGGAAAAGTTGTCAAGAGGATCTACTTCGTCGCTTTCCTGACTTAAATCGGATGGCAAAGAAGTTCCAGCGTCAGAGCTCCAATTTACAGGACTGTTACCGGGTCTATCAATCTGTGGGGCAACTGCCCAATGTGGTGCTGGCACTGGAGAGATACAGTGG[T/C]AAGCAAAACAACAACTTTATCAATAATCGATAACATTAAGCCTGAGAATCCTTATAGTTTTAAGGTTTAATTCACTCATCAAGGATTCTTTCTTGACTTGTTTGACTTTCTTTCGTTTATTGAACTGAAAGAAAGATATTCTGAAGAATGTTGGAAACAAGCAGCCAATGACGTCCATTGTATCTTTTGTTCCTACTATGAATGTCAATGGCTGTTTTTATCCGATATTCTTCAGAATATCTTGAGGTTGTTTGGTCAGTAGTAAAAAGTAATCTATAAGTTTAAAAAAACGAGTTAACTATTTCCTTTTTGGGTGAACTATCCTTTAAAGCCGGGGTCCAAACTCAGTGTGCGGGAGAGTTTAGCTCCAACTTGCTTCAACACAGCTGCCAGGAAGTTTCTTGTATATCTAGTAAGAGCTTGATTAGCTGGTTGTAGCTAAACTCTCCAGGGCCGAGTGTAAAAAACCCCTGCCTTAAAGAACGATGCTTTTTATGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11438
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 |
---|---|---|---|---|---|
ENSDART00000002465 | Nonsense | 451 | 936 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 26425110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 24797551 |
GRCz11 | 12 | 24918770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCATTCATCTCTCCACTAAACGACCTCATCTCAGACTTCTCCAAATTT[C/T]AGGAGATGATTGAAACCACACTKGACATGAACCAGGTCTGCTCTTGTCTT
Long Flanking Sequence:
GAGTGATTTTAATGTGTTAACAGCAATGTAAAGTTACAAATACTCAAATGACTGTAATTGAGTATTTATTTTTCCTCAGGAATTGAAGTTTTAAAAATGTAAAGCGTTAAAAGGGTCCAAGATGATGTCAAATCTTTATGCTCAATGACCCATGATGACTGAAGTTGCCAAATGACCTTAAACAAAAACTACATGCACTACAGAATATTACTTTTTCACACACATGCAAACACATGCATGTAAACACATAAGCCATTCACAGCGTAACACTCACTACTCTTGAGTACTTTTAAAATGGTTACGTTTTACTCATACTTGCGGTATAATTTAAAACAGATAATTTACTTGCGCTACATTTTTGGGCAAGTTATGTTACTTTTACTTGAGTGATTTTTCAGTACTCTTTCCACCACTCTGTGTTAACAGGAAAACATCAGGTCCTCCTGCATGCAGCATTCATCTCTCCACTAAACGACCTCATCTCAGACTTCTCCAAATTT[C/T]AGGAGATGATTGAAACCACACTGGACATGAACCAGGTCTGCTCTTGTCTTCTATCTTAGGGTTTTGCTTCTGTTTACATTTTATTCACTTATACAACAACCATTTGCTTTTATAAAACAAAGAAAACTAGTGTATTGCACTTTCATCTCAGTCTGCATTTCAGTAGAAATGTCATTGAAATACAAACTAAGTCAGAACGAAAAAAGTATTCTGTTTTGTTGGCAGATCATTTAGGGTATTGATAAGGTGTTCCTAAAATTTGCACAACGGACTGACATTTCCACATCCCTAAATAGGACACTGCACAAAATGAAAAGTGATTGGTTCGTTAAACTGTCACTCATGTAGCATCATGGGTGGTCCTTGACCATACATAGCAGACAAATTGTCCAGACTCCAGACCTGATGGCTATAGAAGACTTAAGTGCAGCGTGATAAACAGGCTTTGAGAACAATCTGTTGTCTAATCTTTCTAATACTGTTGTGTTATTGTCCAGGTT
Associated Phenotype:
Not determined