ZMP
mcm10
Ensembl ID:
ZFIN ID:
Description:
Protein MCM10 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q5RHY1]
Human Orthologue:
MCM10
Human Description:
minichromosome maintenance complex component 10 [Source:HGNC Symbol;Acc:18043]
Mouse Orthologue:
Mcm10
Mouse Description:
minichromosome maintenance deficient 10 (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1917274]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31374 | Nonsense | Available for shipment | Available now |
sa16502 | Nonsense | Available for shipment | Available now |
sa14779 | Nonsense | Available for shipment | Available now |
sa8675 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31374
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 |
---|---|---|---|---|---|
ENSDART00000067339 | Nonsense | 96 | 833 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 7046445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 7857664 |
GRCz11 | 4 | 7866293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTTTTCCAGCTGAGCTGAAATTAATGCAGGAGAAAATGCAAAAACTA[C/T]AACAGCAGCTGGAGGCCTCACAGAAGACCACACCAGCTCAAAACAAACCC
Long Flanking Sequence:
GATGAGACTCTAATTGGTTTATTCTCAAAACACACCTATAACTCATTAAGAAAATGAACTCAACCCTTTTCGCCCATGCGCCACGGCGCAAAGCAGGTTTTCCCGTCCTTAAATTAGCAAAAATGCGTTCTGACACGCCCTGAAAGCGTTTGCGTCCTGCCTTTTGCGCTCTGCGCATGCACCGTCAAAATAGATCCCATAGACTCCTACGCAGTGTGTAAACCAATAGATTGAAGCTTTCATTTCTTCCTTCCTCTATAATGTACCTGTACATATTAGTACCCGTGTTCTGTGTTTTAAATATTTCATATTTATATGTGGTCTTACATTGTAAACAATGTATCTTTTTAATTGTTTTGTTTTAATTATTTTACTGTCTGCAAGCGTTGTTGCACTTATTTGCCAAAGACAAAAATCCTCTCTGGGACAAATAAAGTTTATCCAATCCTATATGTTTTCCAGCTGAGCTGAAATTAATGCAGGAGAAAATGCAAAAACTA[C/T]AACAGCAGCTGGAGGCCTCACAGAAGACCACACCAGCTCAAAACAAACCCGCCGTCCAGAGACAAAGCACTAAATCCTTAACTTCACCTCAAGCGGGTGTGAAAACTACCCCACCAACAGTACGAGATAGCGATGGCTCTCCATCAAACATCACGGCAAAGCTGAAAAACAAGCAGAGGACGGCCCACCAACCCAAAGCAGGTGAATATCAAGTTACAAGCCTTAGTTTTTAACCTTATGAATTTATTTATTGCAGTTGATGTCTTATCTTTATTTTGTTTTAATTATCACAGACAGGGTTCATACGCATTTTTACTACTAAAATTCAATGACGTTTCCATGACTTTTCCAGGACTTTCAAATCAATTTTCATGACCTAATGTTTCATGTAATGTCTATGTATGTGTGAATAATAATAAGCAAAAAACAGTGCACGTTCAAAGTTATTACAGCATATCATAAATATTTACTTTGAATGAATCTTAATATCTATGTAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16502
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 |
---|---|---|---|---|---|
ENSDART00000067339 | Nonsense | 421 | 833 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 7040810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 7852029 |
GRCz11 | 4 | 7860658 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTTTACAGGCTCCGCCCCTGGTAAAGGAAGGGGGCGGGGCAGTTTGAAG[G/T]AGCGCCTGTGCCAGTCTGATTTCCACTATGGCGGCATGTCAKCACTCGCT
Long Flanking Sequence:
GTAATAAATCAATAAATAAAAGGGAAATATATTACTTATTTTTGATAGACATCACTTTTGCACATTTATATGAATAAACACTTGTGATTTTCAAAATGTTAAATCACTCGAGTAAAACAGTTTGCGTCGTGTGTTCATTTCTAACATCAGTAATGTAGTATTTGTCTCTCTCCAGCTCAGCCTGACAGTGGATCACCCACAGAAAGTCCTCATAATAGGAGAAGCCATGGACTTTGGCACCTGCAAGGCTAAAAAGAAGAACGGGGATTCTTGCACTCAACTTGTCAACTTGGTGAGTCTCCAAACATCAAGCTTTTCTGGGAAAAAGAAAATCCCTGATCAGTTTATTCATTATTTGTTTGTTTGAACAGTATGAATGCCAGTTCTGTCAGTACCATGTTAAAGCCCAATACAAGAAAATGAGCTCCAAGAGGGCGGAGCTTCAGTCCAGCTTTACAGGCTCCGCCCCTGGTAAAGGAAGGGGGCGGGGCAGTTTGAAG[G/T]AGCGCCTGTGCCAGTCTGATTTCCACTATGGCGGCATGTCATCACTCGCTTGTGCGCCCTCAATGTGAGTTTACGGCATCCCATAAACATCACCTCCATCGAAATTCACCCCACAATTAATGCATGAATCTTTTGTTTTTGACAGGTCTGCCCCACAGCCAAAGAAACAACCCACTATACAGTCTGCTTTGGCATCCATCCCAACTAAGAAACTCGGTAAACTCTCTTTCCACCTATATGATGTTTTATACATGTGTTTATGGTTTCTAATCAAGTGTTACGTCTTGTAGTTCTGAACTCAGGTCAGGTGTCAGGCTGTTCAGATGATTTCAGAGGTCTGATGTCTATGCCCACGCCTGGAGCACTTAACATCAAGAGACATTTAGGACAATCCAAGAGTTCAGGTAAGTTTATTCAGTTACAATTCAATTCATGTTTATTTGTATAGCGCTTTTACAATGTTCTCTTAGTAAAGTTCTAGTAAGTTGAGACTACGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14779
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067339 | Nonsense | 438 | 833 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 7040757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 7851976 |
GRCz11 | 4 | 7860605 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCCTGTGCCAGTCTGATTTCCACTATGGCGGCATGTCAKCACTCGCTTG[T/A]GCGCCCTCAATGYGAGTTTACGGCATCMCATAAACATCACCTCCATCGAA
Long Flanking Sequence:
ACTTTTGCACATTTATATGAATAAACACTTGTGATTTTCAAAATGTTAAATCACTCGAGTAAAACAGTTTGCGTCGTGTGTTCATTTCTAACATCAGTAATGTAGTATTTGTCTCTCTCCAGCTCAGCCTGACAGTGGATCACCCACAGAAAGTCCTCATAATAGGAGAAGCCATGGACTTTGGCACCTGCAAGGCTAAAAAGAAGAACGGGGATTCTTGCACTCAACTTGTCAACTTGGTGAGTCTCCAAACATCAAGCTTTTCTGGGAAAAAGAAAATCCCTGATCAGTTTATTCATTATTTGTTTGTTTGAACAGTATGAATGCCAGTTCTGTCAGTACCATGTTAAAGCCCAATACAAGAAAATGAGCTCCAAGAGGGCGGAGCTTCAGTCCAGCTTTACAGGCTCCGCCCCTGGTAAAGGAAGGGGGCGGGGCAGTTTGAAGGAGCGCCTGTGCCAGTCTGATTTCCACTATGGCGGCATGTCATCACTCGCTTG[T/A]GCGCCCTCAATGTGAGTTTACGGCATCCCATAAACATCACCTCCATCGAAATTCACCCCACAATTAATGCATGAATCTTTTGTTTTTGACAGGTCTGCCCCACAGCCAAAGAAACAACCCACTATACAGTCTGCTTTGGCATCCATCCCAACTAAGAAACTCGGTAAACTCTCTTTCCACCTATATGATGTTTTATACATGTGTTTATGGTTTCTAATCAAGTGTTACGTCTTGTAGTTCTGAACTCAGGTCAGGTGTCAGGCTGTTCAGATGATTTCAGAGGTCTGATGTCTATGCCCACGCCTGGAGCACTTAACATCAAGAGACATTTAGGACAATCCAAGAGTTCAGGTAAGTTTATTCAGTTACAATTCAATTCATGTTTATTTGTATAGCGCTTTTACAATGTTCTCTTAGTAAAGTTCTAGTAAGTTGAGACTACGTCAGTCCAGTTTTCAGAGTTGAAGTTCAGTGTGGTTTAACTTTCACTGCTAAAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8675
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067339 | Essential Splice Site | 442 | 833 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 7040744)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 7851963 |
GRCz11 | 4 | 7860592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGATTTCCACTATGGCGGCATGTCAKCACTCGCTTGTGCGCCCTCAATG[T/C]GAGTTTACGGCATCMCATAAACATCACCTCCATCGAAATTCACCCCACAA
Long Flanking Sequence:
TATATGAATAAACACTTGTGATTTTCAAAATGTTAAATCACTCGAGTAAAACAGTTTGCGTCGTGTGTTCATTTCTAACATCAGTAATGTAGTATTTGTCTCTCTCCAGCTCAGCCTGACAGTGGATCACCCACAGAAAGTCCTCATAATAGGAGAAGCCATGGACTTTGGCACCTGCAAGGCTAAAAAGAAGAACGGGGATTCTTGCACTCAACTTGTCAACTTGGTGAGTCTCCAAACATCAAGCTTTTCTGGGAAAAAGAAAATCCCTGATCAGTTTATTCATTATTTGTTTGTTTGAACAGTATGAATGCCAGTTCTGTCAGTACCATGTTAAAGCCCAATACAAGAAAATGAGCTCCAAGAGGGCGGAGCTTCAGTCCAGCTTTACAGGCTCCGCCCCTGGTAAAGGAAGGGGGCGGGGCAGTTTGAAGGAGCGCCTGTGCCAGTCTGATTTCCACTATGGCGGCATGTCATCACTCGCTTGTGCGCCCTCAATG[T/C]GAGTTTACGGCATCCCATAAACATCACCTCCATCGAAATTCACCCCACAATTAATGCATGAATCTTTTGTTTTTGACAGGTCTGCCCCACAGCCAAAGAAACAACCCACTATACAGTCTGCTTTGGCATCCATCCCAACTAAGAAACTCGGTAAACTCTCTTTCCACCTATATGATGTTTTATACATGTGTTTATGGTTTCTAATCAAGTGTTACGTCTTGTAGTTCTGAACTCAGGTCAGGTGTCAGGCTGTTCAGATGATTTCAGAGGTCTGATGTCTATGCCCACGCCTGGAGCACTTAACATCAAGAGACATTTAGGACAATCCAAGAGTTCAGGTAAGTTTATTCAGTTACAATTCAATTCATGTTTATTTGTATAGCGCTTTTACAATGTTCTCTTAGTAAAGTTCTAGTAAGTTGAGACTACGTCAGTCCAGTTTTCAGAGTTGAAGTTCAGTGTGGTTTAACTTTCACTGCTAAAACACTGAAGAGTAAATC
Associated Phenotype:
Not determined