Busch Lab

ZMP

ENSDARG00000089724

Ensembl ID:
ENSDARG00000089724
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa16979 Nonsense Available for shipment Available now
sa41840 Nonsense Mutation detected in F1 DNA Not yet available
sa41841 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa16979
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126211 Nonsense 455 594 11 13
Genomic Location (Zv9):
Chromosome 11 (position 26220739)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 25049564
GRCz11 11 25287180
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTRAATATGAATGTGTGCAATGCCTGAYGGACCGCAAGCTTCAGCCAGGC[A/T]AAATTAAGCWGTWTTGCTCCACCTGCAACACACAGGTAGTRCAYCTGAAC
Long Flanking Sequence:
CTTATACGCATCAGATCATTGTAGAGAAGAATCAGGTCGCAGCCGTGCCTTCAGTTCAACAGCTGCTTGAGATGTCTTTTGTAACAAGCAATCTAAAGTTTGAAGAGGTTGGTTCATTTCCTAAATGTTTAGCATGCGCTTCCATACAAAAGTATGCATCATTAATCAAACCTTTTTCTTTTAGATTCCATCCTGCCTCATAGTTCAGATGCCACGTTTTGGAAAGAAGTTCAAGATGTTCCCTAAAATCATTCCCTCAACAGAGCTGGACATCACAGACGTATTGCATTGCTGTGAGTGTGTAACAAACATGCTTGTAAATGAAATCTGCTCCCGATAACATTTGTTTTGTGGAAATAGATATTGGAGTGTTGCCGGTTGCAATACCTCTTATGCTTCCTCTATTTTCTTTGGCAGCTCCTCGGGAGTGTTTTCTGTGTGGTCATCTGGCTAAATATGAATGTGTGCAATGCCTGATGGACCGCAAGCTTCAGCCAGGC[A/T]AAATTAAGCAGTATTGCTCCACCTGCAACACACAGGTAGTACACCTGAACCTAAAATCCAGTGATATTTGTATTCTTATAAAATCTTTATTCCTATGTGGGAATTTGATACATGGAAATATATGAAAAATACATGCAAGTTTATATTCGAATTTCACATATACAAAATGTCACATATGCAACATATATTTTGACATATTGCATTTTTAAAACATTGGTATTACAAATATGTAGATAGATATATGTTCATATAGATTATATATAGATATTTATATTTGATCAAACACATAAAATTATAGCTAAAATATTTAGTCATGTATTTGCATATATGTATTTTTAATGGTTGAAAAATATATAGGTAGGCAGCCCTTTTTTAAATATATGTTGCATAAATTTCATATATTATAAACAGTTGTAGTCAAAATAATTCGCCCTCCTGTAATTTTTCTTTTTTTTTTCAAATATTTCCCAAATGATTTTTAACAGAGCAAGGTATTTTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41840
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126211 Nonsense 587 594 13 13
Genomic Location (Zv9):
Chromosome 11 (position 26224858)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 25053683
GRCz11 11 25291299
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTGAGGCGGTGCGCCGACTGATGGTTGATTCATACATGTGTCTTTA[T/G]CAGACAACAGACTGTCAACAATAATCACACACACACACACTTACACACAC
Long Flanking Sequence:
TTTAGTGGATGTTTTCATCCCAAACATAAAAAAGGGTAGTAAATTTGAACAGTGCACAAGGGTTAAATCTTTTAGTTTCTATTTTCTGTTGAACACAGAATCAGCATTTATCAAAATATCTACTTTTGTGTTCAACAGAAGGAAGAAGTTCAAATGGGTTTGGAACAAGTGAAGGGGAGAAAATTAAAACAGAATTGTCATTTTTGGGTGAACTATCCCTTTAAATTTAAACAATTATTTAAACAATTAGCATTGAGATTATACAAACCTTTCTGAAATTCCTTTATTATTGCGTAAGAAAATGTTTGATTCATCATGTTTGATTTTTGTTTTGTATTCTTAGGTGATGACAACAAGGGCTACAGCATTCCTGTGATCAGGTCTTGTCCTGAGGTTGGAGATTTTCTGTCGCAGTCTGAAGAGGAGATCAGCTCAGCCGATCTGAGTCAGTGCAGTGAGGCGGTGCGCCGACTGATGGTTGATTCATACATGTGTCTTTA[T/G]CAGACAACAGACTGTCAACAATAATCACACACACACACACTTACACACACACACACACATTTCTGATGCCCATACTGTAACTCTTATGTCATTACATCATGAGGGCTGACACAAATGAAGGACTGCTCAGACACTCTGTTCTTATGATTTCTGATGGAAGTTTATGTCTGCTTGAAAGTGCCCTGATTTATACGGACATTAGGATCATAGGACGTTAGGGCATTTGATCAAGGACAAGTATGAGTTTGCACACAAGCAACATTTTCTCTATTTTGATATGAGAAACGTTCTAGTATATCATGTAAGGTTTTTGTAGGATTTTTTTTGTCATTTTTATTAGATTATTTATTTTGTACATTATCGTCTATTCAAATTATATATATTATATTTTATTAAAGTTAAATCATCATAAATTTGTCTCTGTTATGCTTCATGTCTGAGAAAATGTAAAGAAGTATGACCAAAATTTTGGAATTCATAAGATGGGAGGGATTTATTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41841
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
ENSDART00000126211 Nonsense 593 594 13 13
Genomic Location (Zv9):
Chromosome 11 (position 26224874)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 25053699
GRCz11 11 25291315
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGACTGATGGTTGATTCATACATGTGTCTTTATCAGACAACAGACTGT[C/T]AACAATAATCACACACACACACACTTACACACACACACACACATTTCTGA
Long Flanking Sequence:
ATCCCAAACATAAAAAAGGGTAGTAAATTTGAACAGTGCACAAGGGTTAAATCTTTTAGTTTCTATTTTCTGTTGAACACAGAATCAGCATTTATCAAAATATCTACTTTTGTGTTCAACAGAAGGAAGAAGTTCAAATGGGTTTGGAACAAGTGAAGGGGAGAAAATTAAAACAGAATTGTCATTTTTGGGTGAACTATCCCTTTAAATTTAAACAATTATTTAAACAATTAGCATTGAGATTATACAAACCTTTCTGAAATTCCTTTATTATTGCGTAAGAAAATGTTTGATTCATCATGTTTGATTTTTGTTTTGTATTCTTAGGTGATGACAACAAGGGCTACAGCATTCCTGTGATCAGGTCTTGTCCTGAGGTTGGAGATTTTCTGTCGCAGTCTGAAGAGGAGATCAGCTCAGCCGATCTGAGTCAGTGCAGTGAGGCGGTGCGCCGACTGATGGTTGATTCATACATGTGTCTTTATCAGACAACAGACTGT[C/T]AACAATAATCACACACACACACACTTACACACACACACACACATTTCTGATGCCCATACTGTAACTCTTATGTCATTACATCATGAGGGCTGACACAAATGAAGGACTGCTCAGACACTCTGTTCTTATGATTTCTGATGGAAGTTTATGTCTGCTTGAAAGTGCCCTGATTTATACGGACATTAGGATCATAGGACGTTAGGGCATTTGATCAAGGACAAGTATGAGTTTGCACACAAGCAACATTTTCTCTATTTTGATATGAGAAACGTTCTAGTATATCATGTAAGGTTTTTGTAGGATTTTTTTTGTCATTTTTATTAGATTATTTATTTTGTACATTATCGTCTATTCAAATTATATATATTATATTTTATTAAAGTTAAATCATCATAAATTTGTCTCTGTTATGCTTCATGTCTGAGAAAATGTAAAGAAGTATGACCAAAATTTTGGAATTCATAAGATGGGAGGGATTTATTGTGAAGTAAAACAGATAT
Associated Phenotype:
Not determined