ZMP

FBXL16

Ensembl ID:

ENSDARG00000060915

Description:

F-box and leucine-rich repeat protein 16 [Source:HGNC Symbol;Acc:14150]

Human Orthologue:

FBXL16

Human Description:

F-box and leucine-rich repeat protein 16 [Source:HGNC Symbol;Acc:14150]

Mouse Orthologue:

Fbxl16

Mouse Description:

F-box and leucine-rich repeat protein 16 Gene [Source:MGI Symbol;Acc:MGI:2448488]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa33183	Nonsense	Mutation detected in F1 DNA	Not yet available
sa1026	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa33183

Status:

Mutation detected in F1 DNA
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
ENSDART00000086324	Nonsense	262	505	2	5

Genomic Location (Zv9):

Chromosome 3 (position 28792124)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	28510163
GRCz11	3	28641005

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTAATGCACCTTGAACTCTCCGGCTGCAATGACTTCACAGAAGCCGGCT[T/A]GTGGTCCAGCCTGAACGCGCGGCTTACCTCGCTCAGCGTCAGCGACTGCA

Long Flanking Sequence:

ATAAAAGGGATTGTTTATGTTTTTCTAGTTTTCTATGTTTTCTAGTATTTTTTATATAATAACTATATATATATATATATATATATATATATATACAATGATTTTGTATATATTTGGCCCACAGCCCTCAATTAAGGTTGGTTTTTGGCAAAGTTTATGAACCCCTGGTCTAATGTATCTGAAAAAACTTGCAAAATTTTGTTCCAGAAACTCTGTAATTTAGTACACATATAGGAATGAGACAGTTTAGAATGTAAAAACTGACATTTGTCACACAATGGAAAAAGGAAACAGTCTACTAATACTCAAAAGAGAAGTAGTCGGCATGTTATTGCAATGCAACTTTTAGTCAACAAAATGTGCAAAAGGGACCATCAAAATGAAGTGTTAATAAAATAACATTGCTCCTCCGTCTTGGTCTGTTCAGGTGATGCTGGAGCAGATGCAGGGCCTAATGCACCTTGAACTCTCCGGCTGCAATGACTTCACAGAAGCCGGCT[T/A]GTGGTCCAGCCTGAACGCGCGGCTTACCTCGCTCAGCGTCAGCGACTGCATCAACGTGGCAGACGATGCCATCGCTGCCATTTCTCAGCTCCTTCCTAACCTATCAGAGCTCAGCCTGCAGGCCTACCATGTGACCGACACGGCCATGGCCTACTTCACGGCCAAGCAAGGCTACACCACCCACACGCTGCGTCTGAACTCCTGCTGGGAGATCACTAACCATGGCGTAGTCAACATGGTGCACAGCCTGCCCAACCTCACCTCCCTCAGCCTGTCGGGGTGCTCGAAGATCACAGACGATGGTGTGGAATTGGTTGCTGAGAATCTAAGGAAGCTCCGGAGTCTGGATCTGTCATGGTGTCCTCGCATCACCGACATGGCCCTGGAGTACATCGCGTGCGACCTGCACAAGCTGGAGGAGCTGGTTCTGGACCGGTGAGTGTGCTGAGTTTGCAGAACAGAGCAGAAAGGAAATCTTGCTGAGATTTCCTCTTACAAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1026

Status:

F2 line generated
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
ENSDART00000086324	Nonsense	496	505	5	5

Genomic Location (Zv9):

Chromosome 3 (position 28786200)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	28504239
GRCz11	3	28635081

KASP Assay ID:

554-0930.1 (used for ordering genotyping assays)

KASP Sequence:

AACTGACCAACTGCCCGGGCGCCACYGCCGAACTCTTCAAATACTACTCC[C/T]AACATCTGCCACGCTGCATGGTCATCGAGTAGAGCAAAACGAGTTTTACG

Long Flanking Sequence:

ATAAATAGTCCCAAAATTGTCATTGTTCTGTCATAGGCTAGATTAACGTGAAAAGGATCGTGTTTTAACTATTAAGCGAACCAATTAAGTCTTTAAGCTGTTAAAACCTTCGATCAACGCTGTAATGAACACCACTGTAAATACAATGTGAATATTATTAAAAAATCTCACCAATAATAAATAATTTATCATGGTATTTTGCAGGGTTCACAATAACGACATTGTGCATATTGGTTATCGTGATATATCGAACACCAGCATATGTCTATTATACACACCTATGATGAAAATAACAGTGTTGTTGTCACACCACAATAACAACAGGAAATGAGCTGTTGAGGTCAGATGGCTGTGTTTTTGACGTGTTCTCATTTACTGTCTCAGGCTGCCCTCTGCTGACTACTACTGGTCTATCAGGCTTGATTCAACTACAGGACCTGGAGGAGCTGGAACTGACCAACTGCCCGGGCGCCACCGCCGAACTCTTCAAATACTACTCC[C/T]AACATCTGCCACGCTGCATGGTCATCGAGTAGAGCAAAACGAGTTTTACGGGCACCAGCACCCAACACATCACCAAAACCTCCTCCTTCAGACTGATGATAAACCCTATTTCATCCTGGACCCACAGGGAGAGAAATTGAAAAGGAAGGTTTTTTTTTTTTTTCTTGTTTTTTTCCGGAGGGGTGAAAATTGAAAGTGGGAAGATAAAAAGGAAATCTGAAAGAAAAATCCTGTCGGAATGGGTCAGGACTGGCAAGAGAGAGGGAAAATGTTCAAAGCGCAGTGGGTCAGAGGCTAGATCTTTCATTAAATAACATGACACATGAGTCAGCCCCTACACATACATGAAACATGTTCCTCCACTGAACTGTGAGACTAGCTTCCGTGTCTCATCCAAAAACTGTTTATCTTGAAGTGACAAAGGTGTGTGCCGACTGTTTGAGCTGTCTCTCATATCCAGGGAAAGATTGAGAGGACGTTTAAGGAAAGGAAAGAGGTTA

Associated Phenotype:

Not determined