ZMP
mcm7
Ensembl ID:
ZFIN ID:
Description:
DNA replication licensing factor MCM7 [Source:RefSeq peptide;Acc:NP_997734]
Human Orthologue:
MCM7
Human Description:
minichromosome maintenance complex component 7 [Source:HGNC Symbol;Acc:6950]
Mouse Orthologue:
Mcm7
Mouse Description:
minichromosome maintenance deficient 7 (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1298398]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42318 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44797 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11737 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42318
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 |
---|---|---|---|---|---|
ENSDART00000051890 | Nonsense | 72 | 721 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 211030)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCGGAAGAAGACCCGGATCTGGTGGAGAGTGTGTGTGAGAACGCCAAA[C/T]GATACACAGCGCTGTTTGCAGACGCCATTCATGAGCTGCTGCCGGAGTAC
Long Flanking Sequence:
TTTGTTTACGAACACGATCAGTATCACGTGACTACTGTTTATCAGCGGGCCCGCGCCTCTGCAACTTTTCTCAAACACACACCACATAACCCTAACTAACAATACTGAACGGTTAGCGTTTTCTGTAGGAGTTTTAACTGAGGATGGTGTGTGTGTGTGGTGTTTCTGACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGAGAAATGTAAGCGGTTCCTGCAGGAGTTCTACACTGAGGATGACTCCGGGAAGAAGATCTTCAAGTATGGTGCTCAGCTGGTGAGTGCTGGCCGGTGCTGCACATCTGTCTGTGTGTGTGGAGGTGTCGCTCGCTCACAGGTGTGTGTTTGTGTGCAGGTATCTCTGGCACATCGGGAGCAGGTGGCGCTGCTGGTGGATCTAGACGACGTGGCGGAAGAAGACCCGGATCTGGTGGAGAGTGTGTGTGAGAACGCCAAA[C/T]GATACACAGCGCTGTTTGCAGACGCCATTCATGAGCTGCTGCCGGAGTACAGGGAGCGGGAGGTGATGAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGGGTGCTGCAGTGAAGAAGGGTTCTTAAAGGGTCAGTGTTGAGCTGTTGTCAGTGGTATATGTGTCCCACACTGCTATAAACACTATTAAGACACCTATATTTCACTAAAAAGTGTAAATTGGTTGTTTTTGCGTTATTTCAAGCAAATTCGTACTTCTGGTTTGAAACCAATTTTTGAAGCTTTGTCACGGTCATGACATAATAGCGTGTATTCCAGCGTGCAGACTGAGCGTCTGTGCCAGAGTGTGTCTTATTACGTCTTACAGTGTGCTGCATTAATGCATGAGTAAAGCTTGGTTCAAACCAATCAGCGCGCTCTATTGTGCAACTTCATTAATATTCATTACTGTCACAGTGTTTAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44797
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 |
---|---|---|---|---|---|
ENSDART00000051890 | Nonsense | 580 | 721 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 205904)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 156541 |
GRCz11 | 14 | 100306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAAGTGTAAGCAGAAGCAGCCGGTGGTGCCGGAGTCTCTGTCGGACTA[C/A]ATCACTGCGGCGTATGTGGAGATGCGGAAGGAGGCGCGGGTCAGTAAAGA
Long Flanking Sequence:
GACTTGCGGCTGGCGCAGCACATCACATACGTGCACCAGCACTGCCGGCAGCCGCCCACACACTTCACCCCCATCGACATGAAGCTCATGAGGTGACTAGCGCTCCGCCACCGTTAGCCATAACACTGTGTGTGTGTGTGGGGGGGGGGGGGGGGGTCTCCCCTAAACCTTATTGTCTTCAGTTGGTCTTCAAGTTCTCCATCTTTCATTCACACACACCGACCTGCAGAACAACACACACCTGAGCTGAAGACCACACTGCTGCTGCACACCAGAACACCTGTGTGAGGGTTATCATACCACACACACACACACACACACACACACACACACACACACTCCAGCTTTACCTGTACTCTGCACACCTGTAGACCAGAGACTGACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGACGCTACATCAGCAAGTGTAAGCAGAAGCAGCCGGTGGTGCCGGAGTCTCTGTCGGACTA[C/A]ATCACTGCGGCGTATGTGGAGATGCGGAAGGAGGCGCGGGTCAGTAAAGACACCACCTTCACCTCCGCCAGAACACTGCTGTCCATCCTGCGGCTGTCCACTGCACTGGTGAGACTCACACACACACACACACACACACCCTACTGTCCGTCGTGCTGATCAGACACACACACACACACACTCTCTCTCGTGGCTGTGTGTGTTAAAAGTGCTGTTTGTGCAGGTAGTGTGTTTCCTCTACTGTAGGAGCAGCACTTCACAACACACACACTGCTGCTAACACCGTCTGATCTGTTGTTGCCGTGACAACTGTTGTCTTGTGCCTCCGCCTTGGTTTTGTCGCCGTGACGACTGTTGTGTGGCGGTCAGCTTTGCGGGGTGGGCAGTCAGCCTCCGTGTGGCCGCTGTGCAAACCCATGCAAAACTGAGCGCTGCGCTACGCTACACTGATGCTACGCTAGCCGGCGCTGAGAGGCGGAGACTTGGGCAGCTGCCGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11737
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 |
---|---|---|---|---|---|
ENSDART00000051890 | Nonsense | 709 | 721 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 201590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 158218 |
GRCz11 | 14 | 101983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGGCGCAGTTCCAGGCGGCGCTGCAGGAGTACGAGGAGCTGAACGTGTG[G/A]CAGATCAACCAGGCCCGYACACGCATCACATTCGTCTAACACGTATGCAC
Long Flanking Sequence:
GCCGCTCTACTGAACACCAGCACTGACGGACACACACAGGGAGGGGGACGACCACGCTCCGGCACAGTCCAACACAAGCTGACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGCTCGTCTGCGTATGGTGTCGGTGGTGGAGAAGGAGGATGTGAACGAGGCGATGCGTCTGATGGAGATGAGCAAAGACTCTCTGCAGGCGGACCGGAGCAGCAGCAGCAGGTGTGGATCAGCGGGTCACTGCACTGCGGTCACTGTGATGATGATGATGATGATGATGATGATGCTGATGCTGAGTGTGTGTGTGTGTGTCCCGCAGAGCTCAGCGGCCGGCTGACGTGATCTTCTCTCTGCTGCGGGAGCTGTGTGGAGAGTCCGCGGGCCGCAGCGTGCGCGTGTCTGCAGCGGAGCAGAGGTGTGTGTCGCGCGGGTTCACCCCGGCGCAGTTCCAGGCGGCGCTGCAGGAGTACGAGGAGCTGAACGTGTG[G/A]CAGATCAACCAGGCCCGTACACGCATCACATTCGTCTAACACGTATGCACACCCACACACACACACACACACACACTCGCACACTCTTGTGCTGTTGTTGGTTCTGTTCTGGAGTGTGTGCTGTAAATAGAGCTGGCACTGACACTGTTTTAATAATAAAGCTCCTCCTCCTGCTCCTCCTCCTGCTCCTCCTCCTGCTCTGCTGTTCTGACTCTGCTCCTGTGTGAGGGTCCGCTGTTGCCTGTATATTTGCGCTTGTTTGTTGTTGTTTATTTTCTGCAATAAAGATGATGACCGTCTCTGTCTGAGCCTCGGCTTTATCACTGTACTGAGATCAGCCTGTGCTCCACTGTTCACAGTAGTAGTAGAGGCTCGTTTCCTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAATCAGTCAGTACAGCACCTCAAAGTCTCTAATTCT
Associated Phenotype:
Not determined