Busch Lab

ZMP

osbpl5

Ensembl ID:
ENSDARG00000076002
Human Orthologue:
OSBPL5
Human Description:
oxysterol binding protein-like 5 [Source:HGNC Symbol;Acc:16392]
Mouse Orthologue:
Osbpl5
Mouse Description:
oxysterol binding protein-like 5 Gene [Source:MGI Symbol;Acc:MGI:1930265]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa44310 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa30264 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:
sa30263
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109843 Nonsense 103 865 4 21
Genomic Location (Zv9):
Chromosome 25 (position 24136999)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 23316112
GRCz11 25 23413660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCGCATAAAACCTTGACTTTTGATGTTGTAGGTTCAGAAAAAGAACTA[T/A]CGGCAGGAGAAGAAGAGGGTTGCCAAAGAACTCTTTAGTGCACTTAAGGA
Long Flanking Sequence:
TGATTAATAATAATAATAATAATAATAATAATAATAATAATAACAATAATAATAATAATAATGAAAAAAGTACATAATGCAATTTCTCAAAACATGGGTTCATAATTAAAAACCTATAAATATTATAATAGTACATACAAATTCTAAAAAATAAAAAAAACCAGATCCAGTGACAAATAATATTTCATCTCTGGTCATGAATATGCTCAATTTAAATAATAATGTAAAAAAAATATTTTTGTGAGAATTTAAAATAAGCTCTCCATGATCTACAATAATACCATAAAATGTGAGATTTAAAGATGCAGCAGTCGTTCAGTAGTTTCTTTCTTCTCGCATCTGTTTCATTTGCTGATCTGTAGCACTCGTGAATAGCGCGCTCTAGTGTTTAACTAGGATTATAAATATTTTTCATATCTTGCAACCCACATGCGCCCCCTAGCTGCTTTAAATCGCATAAAACCTTGACTTTTGATGTTGTAGGTTCAGAAAAAGAACTA[T/A]CGGCAGGAGAAGAAGAGGGTTGCCAAAGAACTCTTTAGTGCACTTAAGGATCCAAGTGTGGTTATTATGTCCAACTGGCTAAAGGTTGGTCAGATTCATTGTTTTTTATTTGAACAAGCTAAAATCCTTTCATAGTAGTTTTAAAGATGTGTTTTTTTTTTTGTTTTTTTTTTTTGGATGTTTTAGATTCGGGGAACATTGAAGAGTTGGACAAAGTTATGGTGCGTCCTGAGGCCTGGCATCCTCATTATTTACAAAACACCTGGTTCAGATCACTGGGTCGGGACGATTCTTCTCAATGCCTGCAAACTTATTGAAAGACCATCAAAGAAGGACGGGTTCTGCTTCAAACTCTACCATCCAATGGACAAGTCAATTTGGGCCATGAAGGTTAGACAGGAGCACCTCTGGAATGATTTATGGCATGCAGTATAATAAGTTTTTAAATCTTTTTCATGATGACACTACGTAATATTTTTCTAGATATTTTTAAAGATACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44310
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109843 Essential Splice Site 645 865 16 21
Genomic Location (Zv9):
Chromosome 25 (position 24159293)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 23338406
GRCz11 25 23435954
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACGAGTGGTGCCGATTGACCAGCAGGAGGCGTTCGAGTCCGAGAGG[T/G]GCGGAAACACTTAGTCATTATAAAAATAGAGCAAAGCAAATAACAAAAGA
Long Flanking Sequence:
TAACCAGATTTCTGGAAAGATCCGGATTGGGGAGGATATTCTGGCTACAGTAGAAGGACACTGGGTAATAATAATTACACATTTTCACATATAAAAAAAATCATCAAAATTCAAAATCAAAATTATTATTATTATTATTATTATTACAATACTGATGATGATAAAATAATAATAATAAGAATAAGAATAATAAGAATAGTAATAATAATAATAATAATAATAATAATAATATGAAATCCTTCAAATGTCTTAAAGATTATAGACAAAACAATTAACTTTACAACAGACTACAAGATTTTTTATGACATTGCTTGGCGGCACATAATCTCACAGTTGTGTTTGAAATCCAAATTATTCCCCAGGACAGCAAAGTGCACCTGATAGAGAAGAAGACGGGCCACCAGGAGGTGCTGTGGAACCCTGGTCCAGACATACGCAGACAGAGGCTGAAGAAACGAGTGGTGCCGATTGACCAGCAGGAGGCGTTCGAGTCCGAGAGG[T/G]GCGGAAACACTTAGTCATTATAAAAATAGAGCAAAGCAAATAACAAAAGAAAGGAGTTGATTTTCATATCTTATTTTGCTTGTGATTTACCATATTACAATTAGTCGTTCTGCACTGTAAAACCTAACAAAGTACTGTAGATTTTACCCCAATATTTGTTCATTTTACTTATTGGAAGAAGTTGCTTTACTCTTCAAATTAAAGAGATAGTTTGCTCACTAATGAAAACTATAACATCATTTTTCACACTCCCTCATGTGGTTTTAAACTTTTATGAATTTCTTTCTTCTTTAGAACATAAAAGAAGATATTTTGAAGAATGCTGGTTGCTGGCACCCACTGACTTCCATAGTAGGAAAAAGAAATATCTTGGAAGTCATTGGGTGCCTGCGACCAGCACTCTTCAAAATACCTCCTTTTGTATTTAAAAGAATAAAGTCAAATAGGTTTTAAACAATAAATGATATCAGATCTTTCATTTTTGAGTCAACTATCTCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30264
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109843 Essential Splice Site 748 865 18 21
Genomic Location (Zv9):
Chromosome 25 (position 24163693)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 23342806
GRCz11 25 23440354
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGACGCAACCGTTACTCCTACAGCCAGGACTGGGCTGGACAGCAGAAG[G/A]TGAGTCATATAGAAACTCCCACAAAGAAAATAAAAAATTCTAACCACCTT
Long Flanking Sequence:
TGTTTGACGAAAATGTTTTTTGACCAATAGATTTAGTAAACAAACATTTAATTAAATCCTTCAACACTTCATCTCTTAATGAATTGTTTGAAATGTCTTTTAGTACAACAGTTTTAGCTTAATAGACTGTCAGTGACAGTAATCTCTCAGATCTGATTAAAAAATATATTCAGTGTTGTTCCAATGATAAATTAATTATGGGTTTAAAAAGACACATAGGTGATTTGAATTATGACTCACTTTTAATTTTGTGGTGAACTAACCCTTTGAAGTGTAATTCACAGCTACCATAATTTCCTTTGGTTACAAATCCAACAATCTGTCAGCATTTCAATAACTAATTATTTCCTCATCCTAATTACATTCTCAGCACTAAGCCATGGGATCCGGAGCGCTGTCTGGTGCAGTTTGAGAAAGACGGCATCATCCAAACTAAAGAGAAGTCGCAGCGCCGACGCAACCGTTACTCCTACAGCCAGGACTGGGCTGGACAGCAGAAG[G/A]TGAGTCATATAGAAACTCCCACAAAGAAAATAAAAAATTCTAACCACCTTCTTCCTACACTCCATGATGCTTGGCATGATGGCAGTAACATCTATCTTGGCATCGTGGGAGTAACATCTTTCAAACTGTAAAATCTAATACACTCACAGTAAAACAACTTGTTGGAATAAACTACTTTCAGCAGATCACCAATAATGTCAAAAACTTAATTTGAGGCTTTTTTCAGCAATATTATGGTTTTATATTGAAGTACTTTACTGTAGGGAATACATAGAGAGTGTAATTTGGTGGAATTTAACACGGTGAACTCAAAAGAGCTTCGGTCAGTGACATGCTTGTGATACTAGTGTCATAGTGAAGCACAAATCCAAGTGTACTTCCTACTCACACTGTAAAACAATCAAACATAAACACATTGAAAAAAAACTTAAAACCTTCTGTCCATAAAAAATACCACTAACTTTAAATGTTAAGAATCAACCTGGATTATCAAATAGTCC
Associated Phenotype:
Not determined