ZMP
si:ch73-79d13.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens FBXL20, F-box and leucine-rich repeat protein 20 (FBXL20) [Source
Human Orthologue:
FBXL20
Human Description:
F-box and leucine-rich repeat protein 20 [Source:HGNC Symbol;Acc:24679]
Mouse Orthologue:
Fbxl20
Mouse Description:
F-box and leucine-rich repeat protein 20 Gene [Source:MGI Symbol;Acc:MGI:1919444]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15339 | Nonsense | Available for shipment | Available now |
sa36765 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15339
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 |
---|---|---|---|---|---|
ENSDART00000110398 | Nonsense | 34 | 436 | 2 | 15 |
The following transcripts of ENSDARG00000075567 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 5464833)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 4924144 |
GRCz11 | 19 | 4840630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATAATGATGAGGCTGTTATTAACAAGAAGCTGCCGAAGGAACTGCTGT[T/A]ACGGTTGGTGTGAAACCCTTKTAGTACTTYTCTGCTTCATTTCCACATTG
Long Flanking Sequence:
CTACTGCCAGTTCTAAATAAGGAATGAAAAACACCAAATTTTTGAACAAATCCCACACTATATAAAAATACATTTAATAATTTGGCTATTTTCCCAAAGAGGCATGCAAATGAGCATGTTTTCTCAATGCAGCAGAAAAACAACAGTAGAGATTTGCAAAAGTTGATCAGTTAGCTGTATGTGTGGCCATAATGGTGATACTACATAATATAAATAAAATATATATTATAAAATGTCAATTTAATTCAAACCTGTTTTTTTTTTGTCAGTTTAAACCACAGCATCTTTTCTCAAACATGAATATGAAAGACATTTAATTACCAAAGGAATTCATTGTTTTTTAAAATGGTGTGTGATTCGGACCGTGTAAACAAAGCTGTATTAACGTTTGACTATGGAAATGCTTACTTTTTGAAAACTGTGTCTTTGTTTTCCTCCTCAGATGTTCTCCAATAATGATGAGGCTGTTATTAACAAGAAGCTGCCGAAGGAACTGCTGT[T/A]ACGGTTGGTGTGAAACCCTTGTAGTACTTTTCTGCTTCATTTCCACATTGAATAATCTCTTATTTAAAACAATCATCCGTACTCTGCACCTTTTCTGTTTTTGCACTTCTTTCTTGATAAGTTGTTAATGATGTTTACTGTGATTCTCTCCGTCTGCAGAATTTTCTCATTTCTGGATGTAGTCACACTTTGCCGCTGTGCTCAAGTCTCACGAGTAAGTGCCTTTTAAAAAAAAGTACATTTAAAGATTAGATTAACCCCACCACTTTTTTGGGGAAAATGGGTTTTGTGAAACCATCTACCCTAGTGTGGTGGAATATACAGTTGAAAGCAGAAGTTTACATGCACTGTATAAAAAGGCACATAACCATTAAAAAAAAAAGTCAGATGGTAATGTGACTAAACTTTTTCTCTCTTAGGTAAGTTAGGATTATCACATTTGTTTTTGTTATGCTTAATAGATGAATAATGACAGAGATATTTTTTGAGAAATTGTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36765
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 |
---|---|---|---|---|---|
ENSDART00000110398 | Nonsense | 48 | 436 | 3 | 15 |
The following transcripts of ENSDARG00000075567 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 5464634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 4923945 |
GRCz11 | 19 | 4840431 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTCTGCAGAATTTTCTCATTTCTGGATGTAGTCACACTTTGCCGCTG[T/A]GCTCAAGTCTCACGAGTAAGTGCCTTTTAAAAAAAAGTACATTTAAAGAT
Long Flanking Sequence:
ACTACATAATATAAATAAAATATATATTATAAAATGTCAATTTAATTCAAACCTGTTTTTTTTTTGTCAGTTTAAACCACAGCATCTTTTCTCAAACATGAATATGAAAGACATTTAATTACCAAAGGAATTCATTGTTTTTTAAAATGGTGTGTGATTCGGACCGTGTAAACAAAGCTGTATTAACGTTTGACTATGGAAATGCTTACTTTTTGAAAACTGTGTCTTTGTTTTCCTCCTCAGATGTTCTCCAATAATGATGAGGCTGTTATTAACAAGAAGCTGCCGAAGGAACTGCTGTTACGGTTGGTGTGAAACCCTTGTAGTACTTTTCTGCTTCATTTCCACATTGAATAATCTCTTATTTAAAACAATCATCCGTACTCTGCACCTTTTCTGTTTTTGCACTTCTTTCTTGATAAGTTGTTAATGATGTTTACTGTGATTCTCTCCGTCTGCAGAATTTTCTCATTTCTGGATGTAGTCACACTTTGCCGCTG[T/A]GCTCAAGTCTCACGAGTAAGTGCCTTTTAAAAAAAAGTACATTTAAAGATTAGATTAACCCCACCACTTTTTTGGGGAAAATGGGTTTTGTGAAACCATCTACCCTAGTGTGGTGGAATATACAGTTGAAAGCAGAAGTTTACATGCACTGTATAAAAAGGCACATAACCATTAAAAAAAAAAGTCAGATGGTAATGTGACTAAACTTTTTCTCTCTTAGGTAAGTTAGGATTATCACATTTGTTTTTGTTATGCTTAATAGATGAATAATGACAGAGATATTTTTTGAGAAATTGTTATAACTTATCTTGAAAGTCAAGTTTAAATACAGTAAGATTATTCTGCCTCTGAAAAAGCTCAGATGATGATGTCAAGGTTTTGGAAGTTTCTGATTGGCTAATTGACAACATTTGAGTTAATTGGAGGGCACAACTGTAGAATAGTATTTAAGGAAATCCTCGCACACACTGCTTCCTTGTGTGAAAACATGGGAAAATCAA
Associated Phenotype:
Not determined