ZMP

osbpl6

Ensembl ID:

ENSDARG00000063730

ZFIN ID:

ZDB-GENE-070912-206

Description:

oxysterol-binding protein-related protein 6 [Source:RefSeq peptide;Acc:NP_001120877]

Human Orthologue:

OSBPL6

Human Description:

oxysterol binding protein-like 6 [Source:HGNC Symbol;Acc:16388]

Mouse Orthologue:

Osbpl6

Mouse Description:

oxysterol binding protein-like 6 Gene [Source:MGI Symbol;Acc:MGI:2139014]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21414	Essential Splice Site	Available for shipment	Available now
sa41333	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21414

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000093412	Essential Splice Site	108	903	4	23
ENSDART00000124777	Essential Splice Site	108	910	4	23

Genomic Location (Zv9):

Chromosome 9 (position 1418008)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	1427061
GRCz11	9	1429349

KASP Assay ID:

2260-1355.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTCGTCCTGGATAACGGCATCCTGAAGTACTCCAAATCTCCAGTCGAT[G/A]TGAGTGAAAATGTGTAGTTGTCCACAAACATATTCAGCTGTTTGTTTAGT

Long Flanking Sequence:

TGCACACACTCACAGGCACTACGGCCAATTTAGTTTCTCCAGTTCCCCTATAGCGCATGTGTTTAGACTGTGGAGGAAACCCACACCAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCGGCCGGGACTTGAACCAGCAAACTTCTTGTTGTACGGCCACAATGGTAACCACTGAGCCACCCTGTGCATTCATTCATTTTATTGTCGGCTTAGTCCCTTTATTAATCAGGGGTCTCCACAGCGGAATGAACCGCCAACTTATCCAGCACGTGTTTTGCAGCGGATGCCCTTCCAGTGCTGGGAATCACCCTGTGCACATTCACATAACTGAAATATTCATGGGCTTGCTTTTCCTCCGTTTTCCTCTTTGTGATCTGCTTGTTTATTGTGAATATTGATTGTAATATTTCCTCCTCTCTTCTTCTCCGCAGCGTTTCTTCGTCCTGGATAACGGCATCCTGAAGTACTCCAAATCTCCAGTCGAT[G/A]TGAGTGAAAATGTGTAGTTGTCCACAAACATATTCAGCTGTTTGTTTAGTAGTTCTGCCAATGAAACCCTTCATTTAAATAGGAATAATTACAAATAATTATGAATAAAATGACAGAACTTTACAACATCAGCATGTAGTTAATGCATTTATTAACGTGAAAAATACAATGGAGAACACCTTTATTACAGTGTTTATTCATCTTTGTTGATGATAGATGAATGATGCTGTCAGTGATGTTTAGTCATGATTTGTGTTTTAATAATGCATTAGTTAATGTTGAATTATGATTAACAAATGTTTGTTCATGTTAACTAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGATTCAGAAAGGAAAGCTTCATGGCAGTATAGATGTGGGTCTGTCTGTGATGTCCATCAAGAAACGAGCTCGCCGCATCGACCTGGACACAGAGGAGCACATTTACCATCTGAAGGTGTGTGTGTGTGTGTGTGTGTGTGTGAGGCCGCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41333

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000093412	Nonsense	599	903	15	23
ENSDART00000124777	Nonsense	598	910	15	23

Genomic Location (Zv9):

Chromosome 9 (position 1393393)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	1402446
GRCz11	9	1404734

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGGAGTACACCGAGCTCCTGGATAAAGCAGCTCAGACTGACGACCCCTA[C/A]GAGCGCATGGTACGGTCGAGCTCTTAAAGGCACGGTGCACCCTGAAACTA

Long Flanking Sequence:

GCCGTTTAAAGCTCATTTGTGGTGAATGATGTCAGAATTTACCGGTATTTTGGAATGGATGTGTGAATGCTCTTTTCCGGAAAATTTCCGTAACGTCCTCGCCTGTGTGAACAGCGCTTTTTTCAATATACCGGTAAAGTTGTTCCGGAAATTTTCCAGATATTTACCGGTATCACTGTGTGAAAGGGGCTTATAACTAACCCTGACTGCAGATATTCAGTATCATGTAGTGTGTAAGCTTGTGTTTCTCCCTCAGTGCCTAATGGTGAGCTGGCCAGCAGTATGTTTCGTAACGGCAGACGTCCGTGTCTCCCGGCTCCTGCTCCCGACACCTCCAACATCAACCTGTGGAACATCCTGAAAAACAACATCGGCAAAGATCTGTCCAAAGTGTCCATGCCGGTGGAGCTGAACGAGCCGCTGAACACGCTGCAGCACATGTGTGAAGAACTGGAGTACACCGAGCTCCTGGATAAAGCAGCTCAGACTGACGACCCCTA[C/A]GAGCGCATGGTACGGTCGAGCTCTTAAAGGCACGGTGCACCCTGAAACTAAAACTCTGTCATTTACTCACAGGGTTTCAAACCCTTAATGTGTCCTCCAAAGTGCTTTCTTTTAAATATGAGATGTGATTTAAACTGAAACCGGAAGACAAGTTGGGTCATATTCAGTAGCTCCTCCCCTTTTCTAAAATAGCCAATAGCGTTGAGTCATGCAATCCCTTAAAATGCTACAGACCTGATAGATTACTGTTAAAATATGCTGTCAGTGTGATAAATGCTAGCAGCATACTAAAACATGCTTTTAATGCACTAAAACAAGTTAGCACTGTGCTAAAACATGCTAACAGCATGCTAAAGTGTGTTAACAATGTCCTAAAACATGTCCGCAATGCACAAGAACACACAAAGGCTGCCATAAAGCGTTTAAACAAGATGATTTAATATTAACAACATGTGCAGAGACATTAACAATGTTGCTAATACATTATAAACATATTAGCA

Associated Phenotype:

Not determined