ZMP
zgc:114174
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC574002 [Source:RefSeq peptide;Acc:NP_001020352]
Human Orthologues:
FBXO44, FBXO6
Human Descriptions:
F-box protein 44 [Source:HGNC Symbol;Acc:24847]
F-box protein 6 [Source:HGNC Symbol;Acc:13585]
F-box protein 6 [Source:HGNC Symbol;Acc:13585]
Mouse Orthologues:
Fbxo44, Fbxo6
Mouse Descriptions:
F-box protein 44 Gene [Source:MGI Symbol;Acc:MGI:1354744]
F-box protein 6 Gene [Source:MGI Symbol;Acc:MGI:1354743]
F-box protein 6 Gene [Source:MGI Symbol;Acc:MGI:1354743]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31085 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13469 | Nonsense | Available for shipment | Available now |
sa13381 | Nonsense | Available for shipment | Available now |
sa8609 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39402 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31085
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060181 | Nonsense | 103 | 282 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 17052223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16955162 |
GRCz11 | 23 | 16881505 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCAGACCGCCAGAGGACTGGTGTCAGTTTTACTTTATAACTAAAAAA[C/T]GACGGAACCTGATCAAGAATCCCAAAGCTGAAGGTGAGCCATGTATTTAA
Long Flanking Sequence:
CAGCGCCTCTGGCCACGGCCTATAGCTGTGCAGTGTGGGGTGCGCAGTAAACAAACCTTTGTGATCTCACAGGCAGCGGAAGTAATTTTTTGTAGTCCCCAAAATTCGTTCATTGTAGGCTTTGCCAAGCTAACTCTGTAAAAAACAAGGTCTCCCTTTGCATTCAACTTAGAACCTTTTACATTCAGAGATGTTGTTTATGTTCACACAGCTACATTACACATCAACTAAAGTTTACAATAGGATATCATATCATCTTTCTGTTTTTTCAGTTCACATGCGTGGTGCCAGACGCTCCTCTAGCTGTGGTTGAGGAGATCTTGCTGTACCTGCCCGCTTATCAGGTGGTGCGAGTGTGTCGTCTGGTGTGTCATGAGTGGAAAGAGCTGGTGGACAGTGCTGCACACTGGAGAGAGCGCTGTAGGAGAGAGGGGATTCAGCTATGTGATGCTTCCAGACCGCCAGAGGACTGGTGTCAGTTTTACTTTATAACTAAAAAA[C/T]GACGGAACCTGATCAAGAATCCCAAAGCTGAAGGTGAGCCATGTATTTAATATTGTGCAATAAATGGATGCACATTAATCATTTTTTTATTATTTGGTTACTTTTTACTAGCTGGATTGCAAGGATGGGGGATAAAAGTAGATAATAAAAAGGCCTGCTGGCTGGTGGAAGAAAATAGAAAACCATTCCCGGACAACACAGTCACCAGATGTTATGTAGCATCTGATGGGTATGTTTGATATATAGATCTTTTGAGAAAGTTCTGCACTCTTTCCATTTCAGTCAGTGATACAAAATGTAAACAAAGCATGAATTAACCAATATCATTGTCCCCAGGTTGTGTTTGAAGCGACAGCTGATTGATTTGCAGAAAGAAGGCTACAGTGCTGCTTTCATGGATCAACTGCAACCTCACATCAAAATCTCAGACTGGTGAGCATTCACACAACTCACAACTCATGCTACAGCATCTGAATTTTGCTTTTATTGCGATTAATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13469
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 |
---|---|---|---|---|---|
ENSDART00000060181 | Nonsense | 116 | 282 | 3 | 6 |
ENSDART00000060181 | Nonsense | 116 | 282 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 17052341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16955280 |
GRCz11 | 23 | 16881623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCACATWAATCANNTTTTTTTATTATTTGGTTRCTTTTTACTAGCTGGAT[T/A]GCAAGGATGGGGGATAAAAGTAGATAATAAAAAGGCCTGCTGGCTGGTGG
Long Flanking Sequence:
GCTTTGCCAAGCTAACTCTGTAAAAAACAAGGTCTCCCTTTGCATTCAACTTAGAACCTTTTACATTCAGAGATGTTGTTTATGTTCACACAGCTACATTACACATCAACTAAAGTTTACAATAGGATATCATATCATCTTTCTGTTTTTTCAGTTCACATGCGTGGTGCCAGACGCTCCTCTAGCTGTGGTTGAGGAGATCTTGCTGTACCTGCCCGCTTATCAGGTGGTGCGAGTGTGTCGTCTGGTGTGTCATGAGTGGAAAGAGCTGGTGGACAGTGCTGCACACTGGAGAGAGCGCTGTAGGAGAGAGGGGATTCAGCTATGTGATGCTTCCAGACCGCCAGAGGACTGGTGTCAGTTTTACTTTATAACTAAAAAACGACGGAACCTGATCAAGAATCCCAAAGCTGAAGGTGAGCCATGTATTTAATATTGTGCAATAAATGGATGCACATTAATCATTTTTTTATTATTTGGTTACTTTTTACTAGCTGGAT[T/A]GCAAGGATGGGGGATAAAAGTAGATAATAAAAAGGCCTGCTGGCTGGTGGAAGAAAATAGAAAACCATTCCCGGACAACACAGTCACCAGATGTTATGTAGCATCTGATGGGTATGTTTGATATATAGATCTTTTGAGAAAGTTCTGCACTCTTTCCATTTCAGTCAGTGATACAAAATGTAAACAAAGCATGAATTAACCAATATCATTGTCCCCAGGTTGTGTTTGAAGCGACAGCTGATTGATTTGCAGAAAGAAGGCTACAGTGCTGCTTTCATGGATCAACTGCAACCTCACATCAAAATCTCAGACTGGTGAGCATTCACACAACTCACAACTCATGCTACAGCATCTGAATTTTGCTTTTATTGCGATTAATTCTTGTGAACAACCTGTGCCTTACACTCTGGTAAAACGATAGACTGTAAAAGATATGGACGTTGTATCCTTGACATCACCCATAGTTTTCTGAAGAGCACAATTGTAGCTACAAGTAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13381
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 |
---|---|---|---|---|---|
ENSDART00000060181 | Nonsense | 116 | 282 | 3 | 6 |
ENSDART00000060181 | Nonsense | 116 | 282 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 17052341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16955280 |
GRCz11 | 23 | 16881623 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCACATWAATCANNTTTTTTTATTATTTGGTTRCTTTTTACTAGCTGGAT[T/A]GCAAGGATGGGGGATAAAAGTAGATAATAAAAAGGCCTGCTGGCTGGTGG
Long Flanking Sequence:
GCTTTGCCAAGCTAACTCTGTAAAAAACAAGGTCTCCCTTTGCATTCAACTTAGAACCTTTTACATTCAGAGATGTTGTTTATGTTCACACAGCTACATTACACATCAACTAAAGTTTACAATAGGATATCATATCATCTTTCTGTTTTTTCAGTTCACATGCGTGGTGCCAGACGCTCCTCTAGCTGTGGTTGAGGAGATCTTGCTGTACCTGCCCGCTTATCAGGTGGTGCGAGTGTGTCGTCTGGTGTGTCATGAGTGGAAAGAGCTGGTGGACAGTGCTGCACACTGGAGAGAGCGCTGTAGGAGAGAGGGGATTCAGCTATGTGATGCTTCCAGACCGCCAGAGGACTGGTGTCAGTTTTACTTTATAACTAAAAAACGACGGAACCTGATCAAGAATCCCAAAGCTGAAGGTGAGCCATGTATTTAATATTGTGCAATAAATGGATGCACATTAATCATTTTTTTATTATTTGGTTACTTTTTACTAGCTGGAT[T/A]GCAAGGATGGGGGATAAAAGTAGATAATAAAAAGGCCTGCTGGCTGGTGGAAGAAAATAGAAAACCATTCCCGGACAACACAGTCACCAGATGTTATGTAGCATCTGATGGGTATGTTTGATATATAGATCTTTTGAGAAAGTTCTGCACTCTTTCCATTTCAGTCAGTGATACAAAATGTAAACAAAGCATGAATTAACCAATATCATTGTCCCCAGGTTGTGTTTGAAGCGACAGCTGATTGATTTGCAGAAAGAAGGCTACAGTGCTGCTTTCATGGATCAACTGCAACCTCACATCAAAATCTCAGACTGGTGAGCATTCACACAACTCACAACTCATGCTACAGCATCTGAATTTTGCTTTTATTGCGATTAATTCTTGTGAACAACCTGTGCCTTACACTCTGGTAAAACGATAGACTGTAAAAGATATGGACGTTGTATCCTTGACATCACCCATAGTTTTCTGAAGAGCACAATTGTAGCTACAAGTAGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8609
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 |
---|---|---|---|---|---|
ENSDART00000060181 | Nonsense | 148 | 282 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 17052438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16955377 |
GRCz11 | 23 | 16881720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGAAGRAAATAGAAAACCATTCCCGGACAACACAGTCACCAGATGTTA[T/A]GTAGCATCTRATGGGTATGTTTGATATATAGATCTTTYGAGAAAGTTCWG
Long Flanking Sequence:
ATTACACATCAACTAAAGTTTACAATAGGATATCATATCATCTTTCTGTTTTTTCAGTTCACATGCGTGGTGCCAGACGCTCCTCTAGCTGTGGTTGAGGAGATCTTGCTGTACCTGCCCGCTTATCAGGTGGTGCGAGTGTGTCGTCTGGTGTGTCATGAGTGGAAAGAGCTGGTGGACAGTGCTGCACACTGGAGAGAGCGCTGTAGGAGAGAGGGGATTCAGCTATGTGATGCTTCCAGACCGCCAGAGGACTGGTGTCAGTTTTACTTTATAACTAAAAAACGACGGAACCTGATCAAGAATCCCAAAGCTGAAGGTGAGCCATGTATTTAATATTGTGCAATAAATGGATGCACATTAATCATTTTTTTATTATTTGGTTACTTTTTACTAGCTGGATTGCAAGGATGGGGGATAAAAGTAGATAATAAAAAGGCCTGCTGGCTGGTGGAAGAAAATAGAAAACCATTCCCGGACAACACAGTCACCAGATGTTA[T/A]GTAGCATCTGATGGGTATGTTTGATATATAGATCTTTTGAGAAAGTTCTGCACTCTTTCCATTTCAGTCAGTGATACAAAATGTAAACAAAGCATGAATTAACCAATATCATTGTCCCCAGGTTGTGTTTGAAGCGACAGCTGATTGATTTGCAGAAAGAAGGCTACAGTGCTGCTTTCATGGATCAACTGCAACCTCACATCAAAATCTCAGACTGGTGAGCATTCACACAACTCACAACTCATGCTACAGCATCTGAATTTTGCTTTTATTGCGATTAATTCTTGTGAACAACCTGTGCCTTACACTCTGGTAAAACGATAGACTGTAAAAGATATGGACGTTGTATCCTTGACATCACCCATAGTTTTCTGAAGAGCACAATTGTAGCTACAAGTAGGTGTGGCCAACTGTTGCCATTTTGTTCGCACATTACTGCACCAACCGGGCGTTACCAAAAAAGGGAGCGTAGAGGCGGAGCGTCAATGGTGCTACAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39402
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060181 | Nonsense | 197 | 282 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 23 (position 17053942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 16956881 |
GRCz11 | 23 | 16883224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTCTTATCTGCAGGTATACCACAAACCTTGCTTATGGAAGTAGCTAT[C/T]AGGTCTGTATGGAACTGCTTAATGAGGAGATGCAACCCATTAGTAGCAAT
Long Flanking Sequence:
GACAGTGTAAAGCCACATAAAACAAAACAAAAATATGATTTATATGCTTTATGATTTATGAATTAAGTGGCTGATCAGCCGCAATCATGTGAGGTGACTTGAGTGACAGCTAGGTCTCGCTGGTTGTCACTTTTGTGGCCCCATCCTTAATTATGCAGACTTATCATAAATTAATATAAACTTACCAGACGAGTTATAACCCCAACCAATCCTTTTTTGTACCAGACTGTAAACACCTTTTTCTTCTGCTGTAAAGTTGGCCATTTTAACATTGGGATCATTAGAAATGTGCTCAATTATGGAGTCAGGACTAGCGGAATTTTGATAAATTGCAGTTTCATGTTACTTCTGTATTAACTTCATGAGGGAGAGCAAGATGTTGCCGCTTGGGTAAAACACAGTACCTGTTTTTAATCAGGCTCTATTATGAAAAGAGCAACACATTTGTTTGTTGTCTTATCTGCAGGTATACCACAAACCTTGCTTATGGAAGTAGCTAT[C/T]AGGTCTGTATGGAACTGCTTAATGAGGAGATGCAACCCATTAGTAGCAATAATCCGCATAGATTGGTTCTAGATGGGGAGAATTATCCATGGTGTGAGGTGAGCAGAAAAATACTGACGGTTCAGTTAATCAAACTAATAGTCAAAGCTTAACCATCCCGTGTTTGTTTTGCTTTATTTCAGATAACACGTGTCTTTCAAAATTATGGACCTGGTGTTCGGTTTATCCGTTTCACTCATGGTGGGTCGGAAAATCAGTTCTGGAAATGCCGGTATGAAGTAAGAGTCACTAACAGCAGTGTGGAGATCTGCCCAGCTGCAGAGAGAGAGTCATTATCAGTTTGAGTATTTCCTCTTTTGTAAGAAACACTATGAAATGATGAACCCGCAAAAATTCATCTTCATAGATGAGACTGGGCTCTATTGAAAGCATCAGGAGGATTTCTGGTGGCCTGGGCATTTTAAATTGTCCTGCTGCCAGTCAGACTTATTATTAGTATT
Associated Phenotype:
Not determined