ZMP
fbxo30
Ensembl ID:
ZFIN ID:
Description:
F-box only protein 30 [Source:RefSeq peptide;Acc:NP_957445]
Human Orthologue:
FBXO30
Human Description:
F-box protein 30 [Source:HGNC Symbol;Acc:15600]
Mouse Orthologue:
Fbxo30
Mouse Description:
F-box protein 30 Gene [Source:MGI Symbol;Acc:MGI:1919115]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36316 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8723 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36316
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 |
---|---|---|---|---|---|
ENSDART00000081447 | Nonsense | 645 | 740 | 2 | 3 |
ENSDART00000123838 | Nonsense | 645 | 740 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 7464939)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 7467713 |
GRCz11 | 17 | 7624891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCAACTCTCTCGAGTGTCTCGCACTATGAGGGATGTGTGTGCCAGTT[T/A]ACTTCAATCCCGTGGCATGGTGGTCCTGATCTGGGAAAAGATAAAGCAAG
Long Flanking Sequence:
CCATGCAAGTCCGCAGCTGTCCAACCCAAGTCCATTTCACACACTCAGGTTAGACCTCGTTCTGGAGTGTGTGGCTCGCTATCAAACTAAACAGCGCTCGATGTTCACTTTCGTGTGTGGACAGCTGTTTCGCAGGGATGAATTCTCCTCTCATTTCAAGAACGTCCATGGGGACATCCATGCTGGTCTTAATGGGTGGATGGAGCAAAGGTGCCCTTTGGCGTATTACGGCTGCACCTACTCACAAAGAAGGTTCTGTCCATCAGTACAAGGTTTCAGAATTATTCATGACAGACACTTAGGCTCTTTTGGAGTACAACCTGGGTTAGCAGAAGGTGAACCTTTATCCAAAATCAACATTTGTCAATCTAAGTCCCACTGTGACCACCTTAGCGACTTGCCCTTTGAGTTACTTCAGCACATTGCAAGCTTCTTGGATGGCTTCAGCCTTTGTCAACTCTCTCGAGTGTCTCGCACTATGAGGGATGTGTGTGCCAGTT[T/A]ACTTCAATCCCGTGGCATGGTGGTCCTGATCTGGGAAAAGATAAAGCAAGCTGATGGAAACTCATCCTGGCAGATACAAGACAAGGTAAATCAGAGAGTATTCATCTTTTCTGTTCAGATACCCTCATTCACTATTCCCAACATTAGTTCACTAATATAGTTCACTTAAAGGAGTGAATGAAAGCGAGAGTGATTTGGAGCACCAGAAGGGATGCCTTTTGTTTGTGCTTTGCTGGTTGATAAATTTTCAACTACTTTGTCAGACCGTGTGACAGTTATTTAATAATTAGCAGGACTCGAAATTAACTTTTTTACTTGGTAGCACCGGTGCTCCCAACTTCAAAAATTTAGGAGCACCAGAAAAAATTTAGGAGCACCAGAAAAAAATTAGTAGCACCAGAAAAGATTTAGGAGCACCCTCCAAAAATGAATTGAGTACCGCTGCAAATTGTATATTAAGGGATTTTATGTATTTTAATACAACATCAATTAGGACTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8723
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 |
---|---|---|---|---|---|
ENSDART00000081447 | Nonsense | 702 | 740 | 3 | 3 |
ENSDART00000123838 | Nonsense | 702 | 740 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 17 (position 7468259)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 7471033 |
GRCz11 | 17 | 7628211 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTGGAAGTTTGCCAACATTTCCAGCATGGCCGACCACCTCAAGACATG[C/A]AAGTTTAACACAATAGCGCGGCGAGAAGAGGCAATCCCGCTCCCATGCAT
Long Flanking Sequence:
GTGGCATCTCTCTGCCGTCTCAACATCGTAACAGGTAAAAACAGTCTACGAAGCTATATCATGCATATAAGGAACTTGCACATCATACACAACAAAGCGCGCTGATTGGTTCGAACCAAGTCTATCTCTTGAATTAATGATGAAAAATCAAAGACGTCATGTTGTACCTGTTAGTACAGACAGCCAATCTACACGCTGGAATTTACACAATGGTCAAATCACTGTGCTTCTAATTTTCTTTTCAAACTGGAAGAACGAATTTGCCGGAAATAACTTAAAAAAACAATTTTCACTTTTTTTGTGAAATATATGTGTCCTAATAGTTTTTATAGCAACATGTGACACATATATGACTGTCAACATCTCAAAAAAAGTGCTTTGGTGTTTCATAATGTTGTTTGTTGTTTGTTTTAGGTGTGGAGGTTCAGTACAGCGTTTGACACTGTGAACGAGTGGAAGTTTGCCAACATTTCCAGCATGGCCGACCACCTCAAGACATG[C/A]AAGTTTAACACAATAGCGCGGCGAGAAGAGGCAATCCCGCTCCCATGCATGAGTTTCACAAGAGAACTTACGAAAGAGGGACGCTCACTACGTTCTGTTCTTAAACCAGTGATATAGACTATAGTCGGATTTTGTTTTATAATACAACATGCCTTATGTGTTTGAGTGAGTGGTAGGATTTTTTTGTTTCAACAGTCATTAACACAAGCCTCAACTTAATAAACTACTTTTGGAAGATGTTTTTTTATGAACGATATCAACCTGTTGACGTGTTATCTACCTGTACTCATTGATGAAGGTTGTGCTGAGTTTTTTGATACAGTATATTCAGTTATATTCATTAGTTGCGATATGTAGCTTCAAAATTGAAACATTGAATTGTTAAATGGCGATGACCAAATGGAAAACCATTGTCTATTTTGGTAATGCACGAAGACACGATGGATGTGTTTCTTGTAGATCAGTGGTTCTCAACTAGATTTACTTTTGGACCTTAATTT
Associated Phenotype:
Not determined