Incidental Mutation 'IGL00826:Osbpl8'
ID 12875
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Osbpl8
Ensembl Gene ENSMUSG00000020189
Gene Name oxysterol binding protein-like 8
Synonyms ORP-8, D330025H14Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.155) question?
Stock # IGL00826
Quality Score
Status
Chromosome 10
Chromosomal Location 111000663-111133110 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 111108181 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100911 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095310] [ENSMUST00000105275]
AlphaFold B9EJ86
Predicted Effect probably benign
Transcript: ENSMUST00000095310
SMART Domains Protein: ENSMUSP00000092948
Gene: ENSMUSG00000020189

DomainStartEndE-ValueType
low complexity region 43 59 N/A INTRINSIC
coiled coil region 71 102 N/A INTRINSIC
PH 107 225 3.65e-16 SMART
Pfam:Oxysterol_BP 364 715 6.4e-91 PFAM
coiled coil region 789 811 N/A INTRINSIC
transmembrane domain 829 846 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000105275
SMART Domains Protein: ENSMUSP00000100911
Gene: ENSMUSG00000020189

DomainStartEndE-ValueType
low complexity region 85 101 N/A INTRINSIC
coiled coil region 113 144 N/A INTRINSIC
PH 149 267 3.65e-16 SMART
Pfam:Oxysterol_BP 406 752 4.6e-91 PFAM
coiled coil region 831 853 N/A INTRINSIC
transmembrane domain 871 888 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a member of the oxysterol-binding protein (Osbp) family, a group of intracellular lipid receptors. Like most members, the encoded protein contains an N-terminal pleckstrin homology domain and a highly conserved C-terminal Osbp-like sterol-binding domain. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit elevated of HDL and gender-specific alterations in lipid metabolism. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars1 T G 8: 111,766,932 (GRCm39) S105A probably damaging Het
Adamtsl1 C T 4: 86,075,041 (GRCm39) P136L probably damaging Het
Akap13 C A 7: 75,327,195 (GRCm39) N376K probably damaging Het
Casp2 T A 6: 42,246,219 (GRCm39) Y192* probably null Het
Cfap206 C T 4: 34,721,562 (GRCm39) S162N probably damaging Het
Cyp2c68 A G 19: 39,727,949 (GRCm39) Y68H possibly damaging Het
Cyp2j9 A T 4: 96,474,167 (GRCm39) I91K possibly damaging Het
Diablo T C 5: 123,650,751 (GRCm39) I179M probably benign Het
Dnah9 C T 11: 65,880,768 (GRCm39) V2610M probably damaging Het
Dsc2 C T 18: 20,168,372 (GRCm39) A696T probably damaging Het
Eaf2 A T 16: 36,621,038 (GRCm39) M218K probably benign Het
Emc9 G T 14: 55,822,377 (GRCm39) L64I possibly damaging Het
Epb41l2 T C 10: 25,317,620 (GRCm39) S46P probably benign Het
Galnt7 A T 8: 57,993,105 (GRCm39) Y405* probably null Het
Gnl3 A G 14: 30,734,753 (GRCm39) probably benign Het
Map1a A G 2: 121,132,757 (GRCm39) Q1191R possibly damaging Het
Map2k2 G A 10: 80,954,052 (GRCm39) V173I probably benign Het
Nbeal2 A G 9: 110,455,971 (GRCm39) V2408A probably benign Het
Npepps T C 11: 97,126,884 (GRCm39) probably benign Het
Phf12 G T 11: 77,906,332 (GRCm39) R282L probably damaging Het
Phf21a T G 2: 92,174,881 (GRCm39) probably benign Het
Plin2 T C 4: 86,582,683 (GRCm39) N98D possibly damaging Het
Prl7a1 A G 13: 27,824,778 (GRCm39) V19A probably damaging Het
Slfn10-ps T C 11: 82,926,085 (GRCm39) noncoding transcript Het
Spag11b T G 8: 19,191,423 (GRCm39) V33G possibly damaging Het
Trappc13 A T 13: 104,281,016 (GRCm39) S349T probably benign Het
Trim34a T C 7: 103,910,140 (GRCm39) probably null Het
Other mutations in Osbpl8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00785:Osbpl8 APN 10 111,108,905 (GRCm39) missense probably benign 0.30
IGL00839:Osbpl8 APN 10 111,127,371 (GRCm39) missense probably benign 0.01
IGL01148:Osbpl8 APN 10 111,112,424 (GRCm39) splice site probably benign
IGL01338:Osbpl8 APN 10 111,103,608 (GRCm39) missense probably damaging 0.99
IGL01927:Osbpl8 APN 10 111,106,477 (GRCm39) missense probably benign 0.00
IGL02378:Osbpl8 APN 10 111,118,006 (GRCm39) missense possibly damaging 0.94
IGL02863:Osbpl8 APN 10 111,120,286 (GRCm39) splice site probably benign
IGL02933:Osbpl8 APN 10 111,117,991 (GRCm39) missense probably damaging 1.00
IGL03075:Osbpl8 APN 10 111,127,417 (GRCm39) missense probably benign 0.01
R0388:Osbpl8 UTSW 10 111,108,143 (GRCm39) missense probably benign
R0725:Osbpl8 UTSW 10 111,122,101 (GRCm39) missense possibly damaging 0.64
R1353:Osbpl8 UTSW 10 111,112,340 (GRCm39) missense probably damaging 0.97
R1434:Osbpl8 UTSW 10 111,127,442 (GRCm39) missense probably benign 0.01
R1803:Osbpl8 UTSW 10 111,110,910 (GRCm39) missense probably damaging 1.00
R1939:Osbpl8 UTSW 10 111,125,672 (GRCm39) missense probably benign 0.19
R2847:Osbpl8 UTSW 10 111,105,297 (GRCm39) missense probably benign 0.27
R2848:Osbpl8 UTSW 10 111,105,297 (GRCm39) missense probably benign 0.27
R2849:Osbpl8 UTSW 10 111,105,297 (GRCm39) missense probably benign 0.27
R2879:Osbpl8 UTSW 10 111,105,297 (GRCm39) missense probably benign 0.27
R2935:Osbpl8 UTSW 10 111,105,297 (GRCm39) missense probably benign 0.27
R3693:Osbpl8 UTSW 10 111,105,297 (GRCm39) missense probably benign 0.27
R4088:Osbpl8 UTSW 10 111,125,651 (GRCm39) missense possibly damaging 0.52
R4374:Osbpl8 UTSW 10 111,105,280 (GRCm39) missense possibly damaging 0.93
R4376:Osbpl8 UTSW 10 111,105,280 (GRCm39) missense possibly damaging 0.93
R4377:Osbpl8 UTSW 10 111,105,280 (GRCm39) missense possibly damaging 0.93
R4621:Osbpl8 UTSW 10 111,105,279 (GRCm39) missense probably benign 0.01
R4622:Osbpl8 UTSW 10 111,127,357 (GRCm39) missense probably benign 0.00
R4851:Osbpl8 UTSW 10 111,040,661 (GRCm39) start codon destroyed probably null 0.00
R5134:Osbpl8 UTSW 10 111,124,554 (GRCm39) missense probably benign 0.28
R5179:Osbpl8 UTSW 10 111,108,025 (GRCm39) missense probably benign 0.01
R5309:Osbpl8 UTSW 10 111,106,418 (GRCm39) missense probably benign 0.00
R5590:Osbpl8 UTSW 10 111,108,029 (GRCm39) missense probably damaging 0.98
R5783:Osbpl8 UTSW 10 111,103,644 (GRCm39) nonsense probably null
R6293:Osbpl8 UTSW 10 111,108,099 (GRCm39) missense possibly damaging 0.96
R6362:Osbpl8 UTSW 10 111,108,929 (GRCm39) nonsense probably null
R6527:Osbpl8 UTSW 10 111,129,066 (GRCm39) missense probably benign 0.23
R6751:Osbpl8 UTSW 10 111,110,874 (GRCm39) missense possibly damaging 0.67
R6851:Osbpl8 UTSW 10 111,106,479 (GRCm39) nonsense probably null
R6955:Osbpl8 UTSW 10 111,105,305 (GRCm39) critical splice donor site probably null
R7224:Osbpl8 UTSW 10 111,110,872 (GRCm39) missense possibly damaging 0.94
R7235:Osbpl8 UTSW 10 111,105,288 (GRCm39) missense probably benign
R7685:Osbpl8 UTSW 10 111,112,370 (GRCm39) nonsense probably null
R7988:Osbpl8 UTSW 10 111,107,941 (GRCm39) missense possibly damaging 0.67
R8055:Osbpl8 UTSW 10 111,120,255 (GRCm39) missense possibly damaging 0.68
R8458:Osbpl8 UTSW 10 111,113,177 (GRCm39) missense possibly damaging 0.81
R8777:Osbpl8 UTSW 10 111,128,974 (GRCm39) missense probably benign 0.01
R8777-TAIL:Osbpl8 UTSW 10 111,128,974 (GRCm39) missense probably benign 0.01
R8844:Osbpl8 UTSW 10 111,112,336 (GRCm39) missense probably damaging 1.00
R8948:Osbpl8 UTSW 10 111,103,530 (GRCm39) missense probably damaging 0.97
R8954:Osbpl8 UTSW 10 111,108,053 (GRCm39) missense probably benign 0.02
R8997:Osbpl8 UTSW 10 111,091,575 (GRCm39) missense probably benign 0.01
R9236:Osbpl8 UTSW 10 111,106,496 (GRCm39) missense probably benign 0.01
R9249:Osbpl8 UTSW 10 111,122,012 (GRCm39) missense probably benign 0.02
R9380:Osbpl8 UTSW 10 111,108,980 (GRCm39) missense probably damaging 0.99
R9394:Osbpl8 UTSW 10 111,127,375 (GRCm39) nonsense probably null
R9595:Osbpl8 UTSW 10 111,108,909 (GRCm39) missense probably damaging 0.99
RF007:Osbpl8 UTSW 10 111,112,328 (GRCm39) missense possibly damaging 0.94
Posted On 2012-12-06