Busch Lab

ZMP

LOC100329789

Ensembl ID:
ENSDARG00000077508
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

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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