ZMP
cylda
Ensembl ID:
ZFIN ID:
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21010 | Nonsense | Available for shipment | Available now |
sa7600 | Missense | Mutation detected in F1 DNA | Not yet available |
sa18879 | Nonsense | Available for shipment | Available now |
sa16446 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21010
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 |
---|---|---|---|---|---|
ENSDART00000084249 | Nonsense | 199 | 951 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 38934446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37271086 |
GRCz11 | 7 | 37542344 |
KASP Assay ID:
2259-9171.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCGTTGTGAAGATGAATGTGGGGTCTTTGTTGCACTGGATAAACTT[G/T]AGCTCTGGGAAGATGAGGAGTTGGAGGTGGATCGTGTGACGCTGGAGGAT
Long Flanking Sequence:
GAACACCGGAGTGTCGACACACAAACCACTACACTATTGGCGGCTATACACTAAATTTTTTATATATTGTATATGTAAAAAAAATAGGTTCTACTAACTTTAAAAAATATGTTTGGTTACTAAAATGTTTGAAGACTATAGGCTTCCACAAATGTATTGCGTTATTCAAGTTTTCCATTCTACATGCCCGTGTTTAACTCGAGGGCTTAGCTGAGAGTTTTGAATGGGCATAACTTAAGCCAGTGGGTTGGTTGTGTGGGTGAAGGCCAGTCTCAGATTTACCATCACAAGTCACAGTGTCTTTTGTTCAAATGCCAAATGTGTGACATATTTATGTGAGATCTGATGCCTGTGCTGGTGTGTGTAATGTCTTTTTATCCTCTGCGAACCTCTTGCAGGAGGAGGGTCGGGGTCAAGGTTTCACGGAGGGCTCTTATCAGGGTCAGCAGCTGTTTCGTTGTGAAGATGAATGTGGGGTCTTTGTTGCACTGGATAAACTT[G/T]AGCTCTGGGAAGATGAGGAGTTGGAGGTGGATCGTGTGACGCTGGAGGATAATGACCCGGAAGAGGAAGGTGAAGCACCGCCACTGGAGATCAACTCTCGAGTCTTGGTACAGACTCGGGAAGGACCAGAAAGGGGCACTGTAATTTTCTGTGACCTACTGCCTGGCAATGAAAGTCTGGGATACTACGTTGGCGTTGATATGGTAAATTCATCTGTTCATTAATAATGCTGTCATTGCATGTTTTAAAGGTGACCTATTATGCCCTGCTTTACAACATGTAAAATAAGTATTTGAAGTCCCTAGAGTGTGTATGCAAACTTTCAGCTTAAAATACCAAACAAATAATATTTTTTAACTCTTTGAAACTGCCCCTTTTAGTCTTTGATCCAAATTGTGCCGTTTTTTTGACTGACGGTTTAAATTCAAATGAGATTTTGTTGCCAGTTCTTTTTTTCAAAATTGGTGGAGCTATAAATGATTGTGTCAGCATAGTGGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7600
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 > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084249 | Missense | 679 | 951 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 38913065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37249705 |
GRCz11 | 7 | 37520963 |
KASP Assay ID:
554-4257.1 (used for ordering genotyping assays)
KASP Sequence:
KGAGTGATGTGTTTGACCTGAGGCATTTACTCTCTTTTTAGATCCAGAGG[A/T]GTTCCTCAACATCCTGTTTCATCACATCCTGAGAGTTGATCCTCTTCTCA
Long Flanking Sequence:
CTCTGGATGCGGGATCGTGACAGTGTACTTGACAGGGTTTTTGTTGTTACAATAGTACCATGTACACCATAAAATGATAATTATACATTTTTATTATTATTTATGCCTTTTTACCTTGTGCTTATTAAATAAATACTCTATGTAATTACAGACAGTTAATTTCTGTGAAAAAAATGTGTATGTTGTTAACGCTACTCCTACTCCTACTGAACTCATCACAAAATGTACATTGTTCCTATCAATTACTTTCTTTGAATGCAAGTGCTAATTAAGTAGTAGTTAAAGAAAACTAATGGATCCCCTGCAACCTTATAAATTAAAATGAGAAACAAACATTTTGTTTGTAAATGTGATCAGTCTATTATGACATGATTTGCATTGATTATTTGATTTGGTTTATTGACAGAGTTCAAATATTTATCTGAATGTTTTATATCCAATGTTTTGTGTGGAGTGATGTGTTTGACCTGAGGCATTTACTCTCTTTTTAGATCCAGAGG[A/T]GTTCCTCAACATCCTGTTTCATCACATCCTGAGAGTTGATCCTCTTCTCAGACTTCGGTGGGCATGTCCTTCAAATCCATGCAAAAATCTGCCTTTTCTGATATGATGAAGTTGGTATTGAAAAGTGCTGTGTGTCTTTTGCAGGTCTGCAGGGCAGAAGGTTCAGGACTGTTACTTCTATCAAATCTTTATGGATAAGAAAGATAAAGTGATGGTGCCGACCAGCCAGCAGCTTCTGGAGTGGTCTTTTATCAACAGTGATCTCAAATTTGCAGAGGTACGATGTACATGTGCATCTGGAGCCTTGTGAACCATACAATTAGCAGAGAGGCCTGTTTCACTTTCCAAACTTTATTGTTTAATAATGTCATCTTTATTGTTTTTATGTTGAAACTAAACATTACAAACCTTACAAACAAAAGATGACATGAACAAACCATTAGGCATGGGATTATAACCGTTTTCAAGGTATACCGCAGTTTGAAAAAGTCAAGGTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18879
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084249 | Nonsense | 798 | 951 | 14 | 16 |
ENSDART00000084249 | Nonsense | 798 | 951 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 38910699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37247339 |
GRCz11 | 7 | 37518597 |
KASP Assay ID:
554-6142.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGTCGAATCTGTGGAGGTTTAGCTCTATATGAGTGCAGAGAGTGCTA[T/A]GAAGATTATGACATCACACCAGGAAAGATCAAGCAGTTCTGTGAAAAGTG
Long Flanking Sequence:
TTAAAAAGGTCTAGAAACCACTCAGACTACTCCTATATTTACTACTGTTTCACGAATGAGTCCCATTAAACACTTAATATTTATAAGAGACAGATGTGTTCAAATGAGAATTGATGCATCTAAATATTGTTGTTCACTGTGATAAATGAGTGAATAAGGGGAAATGTCATGTTCTGGTCTGTTTATTTCTCTCCAGGCCCCTTCTTGCCTTATCATTCAGATGCCTCGGTTTGGGAAGGACTTCAAAATGTTTAATAAGATCTTCCCATCTCTGGAGCTTGACATCACAGATCTATTAGACGACAGTAAGTCACTTCAGTAACTAAATAGGCTTTGAAAAAAAACAAAAAAAAAACACATAATGTATTTTATCTGTGTTGGGATGAAGAATATAAGAAAAAAGTGCATTATATTTAAAGGAATTGACGAAGGTTTGTTTTAGCCCCTAGAGAATGTCGAATCTGTGGAGGTTTAGCTCTATATGAGTGCAGAGAGTGCTA[T/A]GAAGATTATGACATCACACCAGGAAAGATCAAGCAGTTCTGTGAAAAGTGCAATACGCAGGTATTACAAACACACACACATAATCGTCTCATGAACATGCTCTACTGCAGCGATGTCAAACTCAATTCCTGGAGGGCCGCAGCCCTGCACAGTTTAGTCCCAACCCCAATTAAACACACCTGATCAAACTAATTGAGTCCTTTAGGCTTGTTTCAAAAATACAGGTAAGTGTGTTGGTGCAGGGTTGGAACTAAACTGTGCAGGGCTGTGGCCCTCCAGAAATTGAGTTTGACATCCCTGCTTTACTGGCTACTTAACTGAATTATCTCGCAGTTGTACCTTTCATATCCACTAGGTGGAGACCTTTTCTTATGAATAGCCGTTCAAATAAGCAGGTAGACAAGTGTAAGAGTTTAGTGCCACTGTATATAGACCATTTCAATGTTGTCATGTCATTGGCCCATGAACATTTCCTGCTTGTTATCAAACTATTTCATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16446
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084249 | Nonsense | 798 | 951 | 14 | 16 |
ENSDART00000084249 | Nonsense | 798 | 951 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 7 (position 38910699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37247339 |
GRCz11 | 7 | 37518597 |
KASP Assay ID:
554-6142.1 (used for ordering genotyping assays)
KASP Sequence:
GAATGTCGAATCTGTGGAGGTTTAGCTCTATATGAGTGCAGAGAGTGCTA[T/A]GAAGATTATGACATCACACCAGGAAAGATCAAGCAGTTCTGTGAAAAGTG
Long Flanking Sequence:
TTAAAAAGGTCTAGAAACCACTCAGACTACTCCTATATTTACTACTGTTTCACGAATGAGTCCCATTAAACACTTAATATTTATAAGAGACAGATGTGTTCAAATGAGAATTGATGCATCTAAATATTGTTGTTCACTGTGATAAATGAGTGAATAAGGGGAAATGTCATGTTCTGGTCTGTTTATTTCTCTCCAGGCCCCTTCTTGCCTTATCATTCAGATGCCTCGGTTTGGGAAGGACTTCAAAATGTTTAATAAGATCTTCCCATCTCTGGAGCTTGACATCACAGATCTATTAGACGACAGTAAGTCACTTCAGTAACTAAATAGGCTTTGAAAAAAAACAAAAAAAAAACACATAATGTATTTTATCTGTGTTGGGATGAAGAATATAAGAAAAAAGTGCATTATATTTAAAGGAATTGACGAAGGTTTGTTTTAGCCCCTAGAGAATGTCGAATCTGTGGAGGTTTAGCTCTATATGAGTGCAGAGAGTGCTA[T/A]GAAGATTATGACATCACACCAGGAAAGATCAAGCAGTTCTGTGAAAAGTGCAATACGCAGGTATTACAAACACACACACATAATCGTCTCATGAACATGCTCTACTGCAGCGATGTCAAACTCAATTCCTGGAGGGCCGCAGCCCTGCACAGTTTAGTCCCAACCCCAATTAAACACACCTGATCAAACTAATTGAGTCCTTTAGGCTTGTTTCAAAAATACAGGTAAGTGTGTTGGTGCAGGGTTGGAACTAAACTGTGCAGGGCTGTGGCCCTCCAGAAATTGAGTTTGACATCCCTGCTTTACTGGCTACTTAACTGAATTATCTCGCAGTTGTACCTTTCATATCCACTAGGTGGAGACCTTTTCTTATGAATAGCCGTTCAAATAAGCAGGTAGACAAGTGTAAGAGTTTAGTGCCACTGTATATAGACCATTTCAATGTTGTCATGTCATTGGCCCATGAACATTTCCTGCTTGTTATCAAACTATTTCATAAC
Associated Phenotype:
Not determined