Busch Lab

ZMP

ENSDARG00000090153

Ensembl ID:
ENSDARG00000090153
Human Orthologue:
CYLD
Human Description:
cylindromatosis (turban tumor syndrome) [Source:HGNC Symbol;Acc:2584]
Mouse Orthologue:
Cyld
Mouse Description:
cylindromatosis (turban tumor syndrome) Gene [Source:MGI Symbol;Acc:MGI:1921506]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa20732 Nonsense Available for shipment Available now
sa33887 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20732
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000121562 Nonsense 725 761 14 14
Genomic Location (Zv9):
Chromosome 6 (position 32542203)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 32859868
GRCz11 6 32844558
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAAGTGCGTGCTTGTCCTGAGGTTGGCCAGTATTTACACATGCCTT[T/A]GGCTCAGCTGGCAAATCAAGTGCCTCGAGAAATGGATGGTGTGGCCAAAC
Long Flanking Sequence:
TTAATCATACTCATTGGTCTGTGAATGTAGCAGTGATATTAATTACCAATAAATATCAGAATAATCAATTAATTTTCCTACTACATTTTTCAGTATCATATCCTAAACCATCTTGGAATTGATATTTCTGTGTAGGTTCACTCTCACCAGCAGCGTCGACACCACACTCCCAGCAGTCTTCATCTTCCTCAGGGCTTCTCTTACTCTGATTCACTCACGCCTCCACCAGAGAAACTGGAGCTGTTTGCTGTGCTGTGCATAGAGACCAGCCACTACGTCTCTTTCGTCAAACATGGACCTCGGGATACTGACTGGATTTTCTTTGATAGCATGGCTGACCGTGTTGGTAAGTAAATGTGTTTACAGTGTGAGTTCACACACATTTAGTGGAGTAGAACATTCAGTGCACTTACAGAACCTGTTTGCAGGTGAAAGCAATGGTTATAATATCCCAGAAGTGCGTGCTTGTCCTGAGGTTGGCCAGTATTTACACATGCCTT[T/A]GGCTCAGCTGGCAAATCAAGTGCCTCGAGAAATGGATGGTGTGGCCAAACGACTCTTCTGCGATGGTTACATGTACCTTTACCAGAGTAAGAGCATGTCTCTATATCGATGAGTGAATCTACTGAACATGTACAATAAACGAGAGTGTGCAATCAGATTACATTAGACTACATCTGTTCAAGGGAAATTATGAAACTCTATGGTTCTTTGCTTCATATTTGAGCATTTTAAATATTTGAAATGAAATATTAACACTGTTTTGGTATAAGTTTCCTGTATTGCATTGCCAGGGTGGTATATACTCTTTAAGCATTTGGTATATACTTTTTTAATGGAAGCTTTTAGCGATTAGGCTGAGATAAAAGTGCTAAAAGTGCCTTGTATGTATAAGAAATAATAATATAATAATTTTCTTCTCTTTAATGTCTTTGCAATTTTTCCCCCCCTTTTTTTATTATTTGGGTGCACAGAACATTCTTTAAACATCTTATATATATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33887
Status:
Mutation detected in F1 DNA
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
ENSDART00000121562 Nonsense 734 761 14 14
Genomic Location (Zv9):
Chromosome 6 (position 32542229)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 32859894
GRCz11 6 32844584
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGCCAGTATTTACACATGCCTTTGGCTCAGCTGGCAAATCAAGTGCCT[C/T]GAGAAATGGATGGTGTGGCCAAACGACTCTTCTGCGATGGTTACATGTAC
Long Flanking Sequence:
GTAGCAGTGATATTAATTACCAATAAATATCAGAATAATCAATTAATTTTCCTACTACATTTTTCAGTATCATATCCTAAACCATCTTGGAATTGATATTTCTGTGTAGGTTCACTCTCACCAGCAGCGTCGACACCACACTCCCAGCAGTCTTCATCTTCCTCAGGGCTTCTCTTACTCTGATTCACTCACGCCTCCACCAGAGAAACTGGAGCTGTTTGCTGTGCTGTGCATAGAGACCAGCCACTACGTCTCTTTCGTCAAACATGGACCTCGGGATACTGACTGGATTTTCTTTGATAGCATGGCTGACCGTGTTGGTAAGTAAATGTGTTTACAGTGTGAGTTCACACACATTTAGTGGAGTAGAACATTCAGTGCACTTACAGAACCTGTTTGCAGGTGAAAGCAATGGTTATAATATCCCAGAAGTGCGTGCTTGTCCTGAGGTTGGCCAGTATTTACACATGCCTTTGGCTCAGCTGGCAAATCAAGTGCCT[C/T]GAGAAATGGATGGTGTGGCCAAACGACTCTTCTGCGATGGTTACATGTACCTTTACCAGAGTAAGAGCATGTCTCTATATCGATGAGTGAATCTACTGAACATGTACAATAAACGAGAGTGTGCAATCAGATTACATTAGACTACATCTGTTCAAGGGAAATTATGAAACTCTATGGTTCTTTGCTTCATATTTGAGCATTTTAAATATTTGAAATGAAATATTAACACTGTTTTGGTATAAGTTTCCTGTATTGCATTGCCAGGGTGGTATATACTCTTTAAGCATTTGGTATATACTTTTTTAATGGAAGCTTTTAGCGATTAGGCTGAGATAAAAGTGCTAAAAGTGCCTTGTATGTATAAGAAATAATAATATAATAATTTTCTTCTCTTTAATGTCTTTGCAATTTTTCCCCCCCTTTTTTTATTATTTGGGTGCACAGAACATTCTTTAAACATCTTATATATATTTAAAAGATTTTGGCTTAAAAGTCATTTC
Associated Phenotype:
Not determined