ZMP
LOC100329789
Ensembl ID:
Human Orthologue:
CNNM4
Human Description:
cyclin M4 [Source:HGNC Symbol;Acc:105]
Mouse Orthologue:
Cnnm4
Mouse Description:
cyclin M4 Gene [Source:MGI Symbol;Acc:MGI:2151060]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21890 | Essential Splice Site | Available for shipment | Available now |
sa21889 | Essential Splice Site | Available for shipment | Available now |
sa44738 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21890
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115310 | Essential Splice Site | 688 | 757 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 21293621)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150361.1 | 22036 |
GRCz11 | KN150361.1 | 22036 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACACACCTGACTTCAACGTGCGCGCGCTCACTGACCTGCAGTACGCC[A/T]AGGTAACACACACACACACACACACACACACACACTCACACGCATGCATC
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAAGTGTGCATGTGTGTATGCAATTGTGTGTGTGTGTGTGTGTGTGGGTGTGTGTGTGGGTGTGTGTGTGGGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACATTCACGCGTGCGTGCATGCATGTGTGTTTAATTGTGAGTGCGTGCGTGCATGTGTGGGGTGTGTGTGTTTGTGTAGTGTGTGTGTATGTATATCCCTCATTAACACAGCTGTGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGAGTTGCGCTCCCCGTCTCATCTGAGTGTGCTGAACCGCTCTGCGTCTCTGAGCTGTACGGAGCGAGTGGACTCCAGCGTCTCCATCAGCGGCAGCAGCTCTCAGATCTACAGCTCCGCCCCCGCGCCCCAGTACACACCTGACTTCAACGTGCGCGCGCTCACTGACCTGCAGTACGCC[A/T]AGGTAACACACACACACACACACACACACACACACTCACACGCATGCATCAAGAGTTTATAAAGTGTGATATTATTCAGTTCACACCGCAGGGCTGTTGAGTGCTCGATGCTGATTGGCTGGTGAGCATTGTAAAGATGTGCCGCTATTGTCAGATAAACACACAGCTAAAGTAGATCCGGCAGGTTTAGAGCACATCACTGCTCCATCACGATTAGAAATATTCCACAGCTACAACAGTCAGACATCACATCAGAACACAGCAGCAACAGGAGGAGGAGGAGGAGATGTGTTAGGGGCTGCTCACACCCAGCACACTCATCTGTTCTGAGAACGCGAGACACACTCATCTGTTTTTTGGAGGCACTATAAACAGCAGCAGCGGCAGGTCATCAGGGTGTGTTACTCTGTTATTGTCTGCTTGCAGATCACTCGCTCTCAGTACCAGAACGGCCTGTTGGCTTCAAGGCTGGACAGCACACCTCAGTCTCCGGAGAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21889
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115310 | Essential Splice Site | 688 | 757 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 21293202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150361.1 | 21617 |
GRCz11 | KN150361.1 | 21617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACAGCAGCAGCGGCAGGTCATCAGGGTGTGTTACTCTGTTATTGTCT[G/T]CTTGCAGATCACTCGCTCTCAGTACCAGAACGGCCTGTTGGCTTCAAGGC
Long Flanking Sequence:
TCTCAGATCTACAGCTCCGCCCCCGCGCCCCAGTACACACCTGACTTCAACGTGCGCGCGCTCACTGACCTGCAGTACGCCAAGGTAACACACACACACACACACACACACACACACTCACACGCATGCATCAAGAGTTTATAAAGTGTGATATTATTCAGTTCACACCGCAGGGCTGTTGAGTGCTCGATGCTGATTGGCTGGTGAGCATTGTAAAGATGTGCCGCTATTGTCAGATAAACACACAGCTAAAGTAGATCCGGCAGGTTTAGAGCACATCACTGCTCCATCACGATTAGAAATATTCCACAGCTACAACAGTCAGACATCACATCAGAACACAGCAGCAACAGGAGGAGGAGGAGGAGATGTGTTAGGGGCTGCTCACACCCAGCACACTCATCTGTTCTGAGAACGCGAGACACACTCATCTGTTTTTTGGAGGCACTATAAACAGCAGCAGCGGCAGGTCATCAGGGTGTGTTACTCTGTTATTGTCT[G/T]CTTGCAGATCACTCGCTCTCAGTACCAGAACGGCCTGTTGGCTTCAAGGCTGGACAGCACACCTCAGTCTCCGGAGAGCAGCCACACCCACCTAGACCATGCCTCTGACTCCGCCCAGCCACCACCTCTGACTCCGCCCACCAGCACCAATCACAGCACAGCGACGCCCCGAGATGGCCGGCTGGACGAGAACACCTCACTGCTGAACGACAGGAACAGCCTGACCAAACGCCGCTCTAGCCACGCCCACCCACACCTCAACACCAATCACAACTGCAGCTCTAGCCCCGCCCCCCGTCCCCACAGCAACAGCAGCCCCACGCCCCGCCCACATGCTCATACGTTTACACACGCACACACCGAGAGCACCATCTGACAACACTGACCTGGGGCCCGGGGCTTCACAGCTGCATATGGGTACAACACTGACCTGGGGCCCGGGGCCTCACAGGCGCATATGGGTACAACACTGACCTGGGGCCTGGAGCCTCACAGCTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44738
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115310 | Essential Splice Site | 713 | 757 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 21293085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN150361.1 | 21500 |
GRCz11 | KN150361.1 | 21500 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTCCGGAGAGCAGCCACACCCACCTAGACCATGCCTCTGACTCCGCCC[A/G]GCCACCACCTCTGACTCCGCCCACCAGCACCAATCACAGCACAGCGACGC
Long Flanking Sequence:
TCACACGCATGCATCAAGAGTTTATAAAGTGTGATATTATTCAGTTCACACCGCAGGGCTGTTGAGTGCTCGATGCTGATTGGCTGGTGAGCATTGTAAAGATGTGCCGCTATTGTCAGATAAACACACAGCTAAAGTAGATCCGGCAGGTTTAGAGCACATCACTGCTCCATCACGATTAGAAATATTCCACAGCTACAACAGTCAGACATCACATCAGAACACAGCAGCAACAGGAGGAGGAGGAGGAGATGTGTTAGGGGCTGCTCACACCCAGCACACTCATCTGTTCTGAGAACGCGAGACACACTCATCTGTTTTTTGGAGGCACTATAAACAGCAGCAGCGGCAGGTCATCAGGGTGTGTTACTCTGTTATTGTCTGCTTGCAGATCACTCGCTCTCAGTACCAGAACGGCCTGTTGGCTTCAAGGCTGGACAGCACACCTCAGTCTCCGGAGAGCAGCCACACCCACCTAGACCATGCCTCTGACTCCGCCC[A/G]GCCACCACCTCTGACTCCGCCCACCAGCACCAATCACAGCACAGCGACGCCCCGAGATGGCCGGCTGGACGAGAACACCTCACTGCTGAACGACAGGAACAGCCTGACCAAACGCCGCTCTAGCCACGCCCACCCACACCTCAACACCAATCACAACTGCAGCTCTAGCCCCGCCCCCCGTCCCCACAGCAACAGCAGCCCCACGCCCCGCCCACATGCTCATACGTTTACACACGCACACACCGAGAGCACCATCTGACAACACTGACCTGGGGCCCGGGGCTTCACAGCTGCATATGGGTACAACACTGACCTGGGGCCCGGGGCCTCACAGGCGCATATGGGTACAACACTGACCTGGGGCCTGGAGCCTCACAGCTGCATATGGGTGCAACACTGACTTGGGGCCCGGGGCTTCACATGTAAACGACTAAAACACTGACCTGGGGCCCGGAGCCTCATGGATGCATACCAACAATAGTGTCTGATGACACTGACCT
Associated Phenotype:
Not determined