ZMP
si:dkey-22l11.2
Ensembl ID:
ZFIN ID:
Description:
F-box only protein 18 [Source:RefSeq peptide;Acc:NP_001038614]
Human Orthologue:
FBXO18
Human Description:
F-box protein, helicase, 18 [Source:HGNC Symbol;Acc:13620]
Mouse Orthologue:
Fbxo18
Mouse Description:
F-box protein 18 Gene [Source:MGI Symbol;Acc:MGI:1354699]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33396 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9000 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40228 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33396
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091630 | Nonsense | 532 | 1011 | 10 | 22 |
ENSDART00000133169 | Nonsense | 536 | 992 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 8922277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 9859125 |
GRCz11 | 4 | 9860041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGCGTCCACAGACCAGCGTGTCGACACGCAACACGTCCCGTTCGAGTA[C/A]AAGAATACAAAAGGCTTAAGGGAACAGCCAGATGAAGAGGCCAAAAGGGT
Long Flanking Sequence:
AAAAAATATTTCTTAAGGGGGCTAATAATATTGACATAAAAAAAATTAAAAACTGTTTTCATATTAGCCGAAATAAAACAAAAAAGACTTTCTCCAGAAGAAAAAATATTATAGGAATTACTGCGAAAACTTCCTTGCTCTAATAATTTGGGAAATATTTCAAAAAAACAATTGAATAATTAATTCATAATAATGAATAATTTTGCCTTCAACTGTAGCAGAATAACAAAATATTGCAAATTTTCCAATATCGTGCAGCCCTAATAATAATAATAATGAATGAGCTAAGATTATTTGCATGTCTTTTTTTTTTTTTTTTTGCTTTGCAGGTATAAGAATATCAGGAAACTGTCAAGTAATTTGAAGCCATTTGATGTGGCGTGGGTCTTACCGAAAGGACATGGAGGATTCGTCAATGCTAAAGTCGTGACGCAAACGCTTAACAACTACTGGGCGTCCACAGACCAGCGTGTCGACACGCAACACGTCCCGTTCGAGTA[C/A]AAGAATACAAAAGGCTTAAGGGAACAGCCAGATGAAGAGGCCAAAAGGGTAACATGAAGATGCATTGTTGAATGGGCTGTTTTGTGTCTGCATTCAATTATACTTATTTATATACATATAAATCATGTTTAATATGAGAAAACCATCTGCTTTAATGTAAAAATAATGAATAAAAAAATCCTCATCTCTGAACATGACGGATACATTAAAGTAACAATAAAACAACATGTAACAATAAAACAACATGCTTACATTCATGTAATAATAAAACAACATGCTTCTATTTTGACCCGCACTTAACATATATCAAAGAATGAGCGACAATATTAAATGTGTTATTACTATTTTTAAATTATTAAATTAAAATCATGAGAACATAGAAGGGATATTAACTTGTTGAAGGATAGTGAAAAAGTATAAAATTACAATTACTACACTGTGATTCGTAAATCATCCAGGTCATTTAATTTGTCATTAAAATGTTTTTGTTAAGTTCCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9000
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091630 | Nonsense | 617 | 1011 | 13 | 22 |
ENSDART00000133169 | Nonsense | 621 | 992 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 8920905)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 9857753 |
GRCz11 | 4 | 9858669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGTTATTATTTCATCAGTCATCATGGACATCATGCTCTCCCAGCGCTG[T/A]GGGAAAATCCTGGTWGGAGATCCTCATCAGCAGATCTACACTTTYAGAGG
Long Flanking Sequence:
CGAGTGTACAACATGACCCATGATGGTAAGCTGCAAAAATTCTAATATAATTCTAAATAATAAGAGAAATGTTAAACAAAATTCTAAATAATCAATGGAAAATAATAAACAAAATTGCATTTTATTATTTTTTTAATATTGTTTGTCAATAGGATACCTCAAACTCTGGCAGCTGGAAAATCCAGTCCTGGACCGATATGATGCCATATTTATTGATGAAGCTCAAGACTGTACGCCAGGTAAAAATTAAAACTAACCTATGATTGTTTAGTAAATTCATCCAATTTTAGGCAATTATATGTTTTGTTTAGTATTTGTGTTGTAAATGTAGAAAAAAAAACTATTTAAGAAATTAAAATATTGTAATTTTTAGTGTAATTTAGTAATTTTGCATTTTCATTCTGCACTAAATTCCTAAAAGTTGTGTTTTCAGATACTATAATGTGTTGTTATGTTATTATTTCATCAGTCATCATGGACATCATGCTCTCCCAGCGCTG[T/A]GGGAAAATCCTGGTTGGAGATCCTCATCAGCAGATCTACACTTTCAGAGGAGCAGTCAACGCTTTGTATTTTGTTCAACACACACACATCTACTATCTCACACAGGTAAGAATCAAACCACAAAGTGACTAGAGATATAGCATTCGCTGCCACTGTGAGATTTGATCATATTCATTTTTTTTTTTTTTTTTTTTAACAGAGCTTTAGGTTTGGCTCTGAAATTGCGTATGTTGGTGCTTCAATATTGGACGGCTGTAAAGGAGTGAAACAGATATTGGTTGGCGGCCATCAGGATGGTGAGATTAAGCAATATTATTGGGTCAAAAAAAATCTTTCAGCAAATATAATAATAATAATTCTGCTACTAATATTAATTAAGTATTATTATTATTAGTAGTAGTAGTAGTATTAGTAGTATTGGTAGTATTATTATATTTGCTGAAACAATATTTTTTTCCTTGCATTTAGGGTTTGAACTAGGCAAAATAATCTGTGCCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40228
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091630 | Nonsense | 912 | 1011 | 20 | 22 |
ENSDART00000133169 | Nonsense | 894 | 992 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 4 (position 8917557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 9854405 |
GRCz11 | 4 | 9855321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTATCCATATGTGATGACACTGAAGCATATTTGTCTGTCACAGGAGTA[T/A]TTCCTGAGATCAGAGCAGACCAGCTCTCTGCTGAGTAAAGATCCAGCGCT
Long Flanking Sequence:
ATTCTTCTGCATGGTCTTATTTTAAACCCTAGTCCTACATAATACCTAATACCAATAACTTAACTATTTATAAGTAGCAAATTAAGAGTTTATCAAGCAGAAAGTCAGAGTTAATGGTTTGTTATTAGCAAAAAATATACATTTTAAAATAAAGTGTGACCAAAAATCATACACTTTACACTTTACACTAAAATTCATATGCATAAAAATGCAAATGTAAAAAAATAATCATAATTAAAAAAAGTTTAATAGATTGTTCCCAATTTAGTCATTCATAAACCTAAATCTTTACTCTCTGGCTGCAGATAACGTCCCAGATGACGAGTGGAACCTGATATACGTGGCCATCACTCGAGCCAAGAAAACCCTTTACATCAGTAAGACCATCACCAATCTCATCACATTCACTGGGGTGAGTTACTGCTCTTTGTCTTTGCATTTCATCATTATTTTTATCCATATGTGATGACACTGAAGCATATTTGTCTGTCACAGGAGTA[T/A]TTCCTGAGATCAGAGCAGACCAGCTCTCTGCTGAGTAAAGATCCAGCGCTCACCTGCTCAACTAAGGACTGTGAGAACCAAATCAGCGCAGACTCCGTCCTCAGCATGTGCAAACTCCCCGTCAGATATGTCAGTGTCTTTTTACTCTTTAATTTGTTTATAATATGTCTAAAAACAGGTTTAAGCAGACCATGGAATTTCAAGGATTTTTATTTGTTGCTTTAAATTTGGTTTTCATTTATTAAAATGTAATTTTTAAATACCATATTTTGTACTGCATTGTTTCACCCCTGTTGCTATTTTTCAGCTCCATTTTATTCCTTTCATGGTCCTCAATTAGTAGTCACTCAAGTCAAATGCAGTCACCAGACTGTACCTGATTATGGCTAATATGTCATTTTTTTCAAATAACCAAGACATTTCAACCAAATATGTTTAGAAAATACAGTGAACTACATTAGAGGCCACCAATGACAGAATATAGAAAGATTAAGCAATTT
Associated Phenotype:
Not determined