ZMP
mcm6l
Ensembl ID:
ZFIN ID:
Description:
MCM6 minichromosome maintenance deficient 6, like [Source:RefSeq peptide;Acc:NP_001020704]
Human Orthologue:
MCM6
Human Description:
minichromosome maintenance complex component 6 [Source:HGNC Symbol;Acc:6949]
Mouse Orthologue:
Mcm6
Mouse Description:
minichromosome maintenance deficient 6 (MIS5 homolog, S. pombe) (S. cerevisiae) Gene [Source:MGI Sym
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18268 | Essential Splice Site | Available for shipment | Available now |
sa10448 | Nonsense | Available for shipment | Available now |
sa19897 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18268
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 |
---|---|---|---|---|---|
ENSDART00000000042 | Essential Splice Site | 116 | 824 | 3 | 17 |
ENSDART00000147117 | None | None | 238 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50792832)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50488364 |
GRCz11 | 2 | 50222594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCCAAAGAGTTTTATGTGGCTTTTTCGGAGTTTCCATCAAGGCAAAAG[T/C]AACYATTTCTGTGCTTAGACACTTTTTGYAGACWCTCTTTAAAACAGAGG
Long Flanking Sequence:
TATACAGTTAAATGGGACACAAATACACGTAAATTAAAGAAGTTAAATCAGCAAAACAAGTGAGTGTACTGAGGGTATGCGCAATGATCGATCCTCAGAAGTTGTAATACTCAAACAGCTTGTGGAAAAAAAAAAGTAGGCATATGCAGTATACATGTGTATAGCCCCAACTACACCACTGGCTGATAGTATGGAAAAAGCTTTCATTTAATTTCATACATTTATTTGAATAGCTGTGAAAACAGCTTTCTTAATGTAAATCAAATATGTAATAACCTTTAAATTGATTATTTTGGGAAAATACCTTTCATAAAGTTTCATATAGTGTATAATCTTATACTCTAATTTGTACTGTCATCTTTCATAATTATGTTTCTTCTTTTTTCAGGGTTTATCCGTTTCTCTGCAGAGCAGTTCGTCACTTTGCCAGAGATCATGGAAATATTCCACCTTCCAAAGAGTTTTATGTGGCTTTTTCGGAGTTTCCATCAAGGCAAAAG[T/C]AACCATTTCTGTGCTTAGACACTTTTTGTAGACTCTCTTTAAAACAGAGGTGCCCAAATTTTTCAAATGAATGGCCAAAATTCAAAAATCGTTGCAAGCCATGGGCCAAAGTTAAATATACTAAACTGTACTACCTTAAAGTTGTCATTGGAAATGTCCTAATTTATTTCCTAATATTTCCAAATAAATAGAAAGTTAATATGATTTAAAGTAATGCTAATGCAGTACAACTTTTTAAATGATAACTTATTGCCATAAAAACATGAACAGTCACATTCATAACATGCTGGAGTTCAATACTGAATACACAGGTCAAGCAGAATTTGCCTTTGACTTGATTTGCTCACCAAAGCCTCTGCATTGTTGGGTAACAGTACGTACCTTTGAACAAAATCATTAAAAATAACAAAACATAATTTACGCCATTTAACTGAAACATTTAATTTGTTAGCTTTTAGCCATAAAACAAACAAAAAGATGAATTAATCCCGAGACACGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10448
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 |
---|---|---|---|---|---|
ENSDART00000000042 | Nonsense | 558 | 824 | 12 | 17 |
ENSDART00000147117 | None | None | 238 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50784054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50479586 |
GRCz11 | 2 | 50213816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATTGCCCGGCGTATTGTTGATCTTCATGCCAGGAAYGTTGAATCYGTA[G/T]AAAGAGTTTACAGTACTGATGAAATCCAGCGATACATCTTGTTTGCCCGC
Long Flanking Sequence:
GTATATAAAATATATTTGTTCATTTATATAAATTTTTAAACGATTGTTTTAAATGATAGTTTTTATTATTTATTTCATTTGTATTTATTTTTGTTTATACATTTTTTTATTTATTTTTATTTTTATTTTTTTATTTATTTAAATTTATGTATTTTAGTAATTTTTTTGTTTTCATTTATACATTTTTATTTTGAATTTGTTTAAATATTTTTTTTGTGTGTTCATATTTTTATTTAATGTATTTTTTTATTTTTATTTAAAATTGTTTATTTTTAATTTATTTGTGTTTCACCCTCTTTTATTTGTATTTCACATTATTACACTTTTGACTTTATTAATAATCAAATAAATTAACCCTATTTTATTAACCCTAATAAAGTATATGTCAAAGTTTAAAAAAAAAAAACCATTTAACCAATACTTTGCTTTTCTACCAGGTAACAGACTATGCCATTGCCCGGCGTATTGTTGATCTTCATGCCAGGAATGTTGAATCTGTA[G/T]AAAGAGTTTACAGTACTGATGAAATCCAGCGATACATCTTGTTTGCCCGCCAGTTTCAGCCAAAGGCAAGATGCATTCATTAAACTGTGGATATGGATAGTATTCAGACTTCCTTAAATTTTTCACTCTGTTATATTGCAGCCATTTGCTAAAATCATTTTCCCAAATCCAGTTGTGAAAACTTGCATCTCTCCCAAAAAGACTCATGGCTATATTAGATCAAAGGGGAGCTTCTACTAAATACTGAGCAAAGGGTCTGAATGCTTGGGACCGACCATGTAATATTTCAGTTATTCTCTTTAATAAATTTGCAAAAAAATCTGCAATTCTATGTCTTTTTCAAGTTGAGATGCTGTATATACATTGAAGGAAAAATGATTTAGTAAATGGTGGCAATATAACAAAGAGTTGAAAATTTAAGGGGGTCTGAATACTTTCCGTACCCAAAGTATTAAGTTTAATTCAAAATTAGACAGCCCGGGTAATGTCTTGCAGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19897
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 |
---|---|---|---|---|---|
ENSDART00000000042 | Nonsense | 672 | 824 | 15 | 17 |
ENSDART00000147117 | None | None | 238 | None | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 50780577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 50476109 |
GRCz11 | 2 | 50210339 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGGTCACACATATTTTAATGTGAAGCAAAAATGTTTGTTCCACAGAT[C/T]AGAATGAGCTGTTTGGTAAGGAGACTGAAGGTCAGAATGGAGGTGATGTG
Long Flanking Sequence:
CAGATTACAGATATTAAAATATTTTTCATCATAAAGATTAATCAGTGGAAAGCTCATTCATTCAGCTATCAGAGGAAACGAAGTTGAAAAGTGTGGATTTTTGTGGTTCAGGGTCACATTTTAATGTAAAGCAAAAACCTTTGTTCTACAGATCAGAATGAGTTGCTTGGACATTACTGGCATTAGCCCCAAAAAAAGCATTGTATGTGTCAATGTAATCTATTTTTTTCCTTTTATGGCAAAAAAAATGTATATTAAATAAAGATCACGATTATTTTGTAAATTTATTACTGTAATTATTTTCAGCAGCAAGTTTTTCCTATTTTTTATTTTATTTTATTTTATTTTTACCTCAGGTTGCAGAAATATTGTCCCATCATAGTTTGATCAGTTGAAAGCTCGTTTATTCAGCTGTCAGATTTTTTGAAAAACTGACACTCATGACTGGTTTTGTGGTCACACATATTTTAATGTGAAGCAAAAATGTTTGTTCCACAGAT[C/T]AGAATGAGCTGTTTGGTAAGGAGACTGAAGGTCAGAATGGAGGTGATGTGAACGGTCATGCAGTGGAGGACATGGAGACTGATCAGACTGAAAAACCAGAGAAACCAGCCGCAGCCAAACCTGCTCTCAGGATGTCTTTTGCAGAGTACAAGAGAGTCTCCAACCTGCTGGTGCTGCACATGCAGAAGATGGAGCAGCGTGAGTCTCAATATCATTTTTTTTTATATATCTAATTTAAAATACCAATTTTCAATTCATCTTAATTTATATAGCACTTTTACAATGTATATTGTCAAAGCAGCTTAACATAGATGTTCTAGTACAGTGGTTCTCAAACTGTGGTACGTGTACCACTAGTGTTATGCAGGCTTCCTTCTAGTGGTATGCGGATGAATCAAATATGTCATATGTACATGCTATATATATTTAAATAAATTATCAAATGATTTATATATGAATATGATGACAGTCTATATTTATGAGGTCCAGGCAACATTTCC
Associated Phenotype:
Not determined