Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02867:Osbpl6'

362382

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Osbpl6

Ensembl Gene

ENSMUSG00000042359

Gene Name

oxysterol binding protein-like 6

Synonyms

1110062M20Rik, ORP-6

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.520) question?

Stock #

IGL02867

Quality Score

Status

Chromosome

Chromosomal Location

76236852-76430991 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 76426214 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000139363 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077972] [ENSMUST00000111929] [ENSMUST00000111930] [ENSMUST00000184442]

AlphaFold

Q8BXR9

Predicted Effect

probably benign
Transcript: ENSMUST00000077972

SMART Domains

Protein: ENSMUSP00000077123
Gene: ENSMUSG00000042359

Domain	Start	End	E-Value	Type
low complexity region	14	35	N/A	INTRINSIC
PH	87	183	3.65e-7	SMART
low complexity region	200	211	N/A	INTRINSIC
coiled coil region	255	285	N/A	INTRINSIC
low complexity region	537	550	N/A	INTRINSIC
Pfam:Oxysterol_BP	603	951	1.4e-135	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000111929

SMART Domains

Protein: ENSMUSP00000107560
Gene: ENSMUSG00000042359

Domain	Start	End	E-Value	Type
low complexity region	14	35	N/A	INTRINSIC
PH	87	183	3.65e-7	SMART
low complexity region	200	211	N/A	INTRINSIC
coiled coil region	255	285	N/A	INTRINSIC
coiled coil region	441	472	N/A	INTRINSIC
low complexity region	529	542	N/A	INTRINSIC
Pfam:Oxysterol_BP	595	944	1.1e-139	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000111930

SMART Domains

Protein: ENSMUSP00000107561
Gene: ENSMUSG00000042359

Domain	Start	End	E-Value	Type
low complexity region	14	35	N/A	INTRINSIC
PH	87	183	3.65e-7	SMART
low complexity region	200	211	N/A	INTRINSIC
coiled coil region	255	285	N/A	INTRINSIC
coiled coil region	410	441	N/A	INTRINSIC
low complexity region	498	511	N/A	INTRINSIC
Pfam:Oxysterol_BP	564	913	1e-139	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000184442

SMART Domains

Protein: ENSMUSP00000139363
Gene: ENSMUSG00000042359

Domain	Start	End	E-Value	Type
Blast:PH	1	70	8e-41	BLAST
low complexity region	87	98	N/A	INTRINSIC
coiled coil region	142	172	N/A	INTRINSIC
coiled coil region	303	334	N/A	INTRINSIC
low complexity region	391	404	N/A	INTRINSIC
Pfam:Oxysterol_BP	457	794	2.6e-135	PFAM

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. Transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Allele List at MGI

All alleles(2) : Gene trapped(2)

Other mutations in this stock

Total: 34 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcf2	T	A	5: 24,776,149 (GRCm39)	Y310F	probably benign	Het
Adarb1	C	T	10: 77,149,375 (GRCm39)	V371I	probably benign	Het
Antxr2	G	T	5: 98,125,509 (GRCm39)	H249Q	probably benign	Het
Arel1	A	T	12: 84,981,097 (GRCm39)	N303K	probably benign	Het
Bloc1s6	T	C	2: 122,584,604 (GRCm39)	Y60H	probably damaging	Het
Ccdc125	A	T	13: 100,820,790 (GRCm39)		probably benign	Het
Cxcl16	A	T	11: 70,349,892 (GRCm39)	Y45N	possibly damaging	Het
Dnajb3	T	A	1: 88,133,249 (GRCm39)	Q51L	probably benign	Het
Ear10	A	G	14: 44,160,726 (GRCm39)	F34L	probably damaging	Het
Fgf11	A	G	11: 69,690,498 (GRCm39)	S100P	possibly damaging	Het
Fpgs	G	A	2: 32,575,891 (GRCm39)		probably benign	Het
Fyb1	A	T	15: 6,609,527 (GRCm39)	Q33H	probably damaging	Het
Ints3	G	T	3: 90,300,143 (GRCm39)	H925N	probably damaging	Het
Krt16	T	C	11: 100,138,402 (GRCm39)	K249E	probably damaging	Het
Lrp2	A	T	2: 69,382,794 (GRCm39)	S30R	possibly damaging	Het
Naa35	T	C	13: 59,756,668 (GRCm39)		probably benign	Het
Or11g27	A	G	14: 50,770,970 (GRCm39)	I34V	probably benign	Het
Or1e22	A	G	11: 73,376,817 (GRCm39)	Y278H	probably damaging	Het
Or8g2b	A	G	9: 39,751,533 (GRCm39)	M268V	probably benign	Het
Pramel6	A	T	2: 87,340,736 (GRCm39)	Q356L	probably damaging	Het
Prima1	A	G	12: 103,163,575 (GRCm39)	V132A	probably benign	Het
Psme1	A	G	14: 55,817,383 (GRCm39)		probably benign	Het
Rdh11	A	G	12: 79,235,828 (GRCm39)	V40A	possibly damaging	Het
Rin1	C	T	19: 5,103,198 (GRCm39)	R485C	probably damaging	Het
Rnf40	C	A	7: 127,190,601 (GRCm39)	S255*	probably null	Het
Spata24	C	A	18: 35,789,805 (GRCm39)	R194L	probably benign	Het
Spata31h1	C	T	10: 82,119,654 (GRCm39)	S482N	probably damaging	Het
Tas1r1	A	T	4: 152,112,735 (GRCm39)	S773T	probably damaging	Het
Trdv5	G	T	14: 54,386,429 (GRCm39)		probably benign	Het
Trpc3	A	C	3: 36,694,850 (GRCm39)	D701E	probably benign	Het
Vim	A	G	2: 13,585,491 (GRCm39)	R424G	probably damaging	Het
Vmn1r216	A	C	13: 23,283,649 (GRCm39)	T111P	probably damaging	Het
Zbtb26	A	C	2: 37,326,261 (GRCm39)	N247K	probably benign	Het
Zfp629	T	G	7: 127,209,203 (GRCm39)		probably benign	Het

Other mutations in Osbpl6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00391:Osbpl6	APN	2	76,420,783 (GRCm39)	missense	probably damaging	1.00
IGL01109:Osbpl6	APN	2	76,379,871 (GRCm39)	missense	probably damaging	1.00
IGL01288:Osbpl6	APN	2	76,395,167 (GRCm39)	missense	probably damaging	0.98
IGL01717:Osbpl6	APN	2	76,418,938 (GRCm39)	missense	probably damaging	1.00
IGL02146:Osbpl6	APN	2	76,380,094 (GRCm39)	missense	possibly damaging	0.90
IGL02597:Osbpl6	APN	2	76,386,318 (GRCm39)	nonsense	probably null
IGL02652:Osbpl6	APN	2	76,423,798 (GRCm39)	missense	probably damaging	1.00
IGL03143:Osbpl6	APN	2	76,378,716 (GRCm39)	missense	probably damaging	1.00
3-1:Osbpl6	UTSW	2	76,416,495 (GRCm39)	missense	probably damaging	1.00
R0085:Osbpl6	UTSW	2	76,423,758 (GRCm39)	missense	probably benign	0.30
R0201:Osbpl6	UTSW	2	76,376,386 (GRCm39)	missense	possibly damaging	0.92
R0573:Osbpl6	UTSW	2	76,420,735 (GRCm39)	missense	probably damaging	1.00
R0644:Osbpl6	UTSW	2	76,425,184 (GRCm39)	missense	probably damaging	1.00
R0855:Osbpl6	UTSW	2	76,422,183 (GRCm39)	missense	probably damaging	1.00
R0855:Osbpl6	UTSW	2	76,415,477 (GRCm39)	missense	probably damaging	1.00
R1017:Osbpl6	UTSW	2	76,380,063 (GRCm39)	missense	probably damaging	1.00
R1459:Osbpl6	UTSW	2	76,385,409 (GRCm39)	missense	probably benign	0.01
R1505:Osbpl6	UTSW	2	76,409,586 (GRCm39)	missense	probably damaging	1.00
R1588:Osbpl6	UTSW	2	76,409,560 (GRCm39)	missense	probably benign
R1786:Osbpl6	UTSW	2	76,416,558 (GRCm39)	missense	probably damaging	1.00
R1863:Osbpl6	UTSW	2	76,415,402 (GRCm39)	missense	probably damaging	1.00
R2131:Osbpl6	UTSW	2	76,416,558 (GRCm39)	missense	probably damaging	1.00
R2132:Osbpl6	UTSW	2	76,416,558 (GRCm39)	missense	probably damaging	1.00
R2133:Osbpl6	UTSW	2	76,416,558 (GRCm39)	missense	probably damaging	1.00
R2233:Osbpl6	UTSW	2	76,417,113 (GRCm39)	missense	probably damaging	0.99
R2235:Osbpl6	UTSW	2	76,417,113 (GRCm39)	missense	probably damaging	0.99
R2256:Osbpl6	UTSW	2	76,414,818 (GRCm39)	missense	probably damaging	1.00
R2294:Osbpl6	UTSW	2	76,407,423 (GRCm39)	missense	possibly damaging	0.81
R3023:Osbpl6	UTSW	2	76,417,077 (GRCm39)	missense	probably damaging	1.00
R4192:Osbpl6	UTSW	2	76,415,573 (GRCm39)	missense	probably damaging	1.00
R4544:Osbpl6	UTSW	2	76,414,836 (GRCm39)	missense	possibly damaging	0.84
R4546:Osbpl6	UTSW	2	76,414,836 (GRCm39)	missense	possibly damaging	0.84
R4664:Osbpl6	UTSW	2	76,398,552 (GRCm39)	missense	probably benign	0.02
R4764:Osbpl6	UTSW	2	76,376,344 (GRCm39)	missense	probably damaging	1.00
R4884:Osbpl6	UTSW	2	76,379,883 (GRCm39)	missense	probably damaging	1.00
R5080:Osbpl6	UTSW	2	76,354,429 (GRCm39)	missense	probably benign	0.31
R5430:Osbpl6	UTSW	2	76,416,482 (GRCm39)	missense	probably damaging	1.00
R5614:Osbpl6	UTSW	2	76,398,453 (GRCm39)	missense	probably damaging	1.00
R5807:Osbpl6	UTSW	2	76,414,857 (GRCm39)	missense	probably damaging	0.98
R5956:Osbpl6	UTSW	2	76,379,856 (GRCm39)	missense	probably damaging	1.00
R6394:Osbpl6	UTSW	2	76,386,298 (GRCm39)	missense	probably benign	0.00
R6430:Osbpl6	UTSW	2	76,409,620 (GRCm39)	missense	probably damaging	1.00
R6450:Osbpl6	UTSW	2	76,395,174 (GRCm39)	missense	possibly damaging	0.90
R7116:Osbpl6	UTSW	2	76,426,225 (GRCm39)	missense	probably benign	0.06
R7385:Osbpl6	UTSW	2	76,379,794 (GRCm39)	missense	probably damaging	1.00
R7422:Osbpl6	UTSW	2	76,423,730 (GRCm39)	missense	probably damaging	1.00
R7561:Osbpl6	UTSW	2	76,416,498 (GRCm39)	missense	probably damaging	1.00
R7829:Osbpl6	UTSW	2	76,423,731 (GRCm39)	missense	probably damaging	1.00
R7921:Osbpl6	UTSW	2	76,415,441 (GRCm39)	missense	probably damaging	1.00
R8183:Osbpl6	UTSW	2	76,415,404 (GRCm39)	missense	probably damaging	1.00
R8219:Osbpl6	UTSW	2	76,386,247 (GRCm39)	missense	probably damaging	0.98
R8548:Osbpl6	UTSW	2	76,409,566 (GRCm39)	missense	possibly damaging	0.88
R8682:Osbpl6	UTSW	2	76,407,425 (GRCm39)	missense	probably benign	0.00
R8935:Osbpl6	UTSW	2	76,379,800 (GRCm39)	missense	possibly damaging	0.60
R9157:Osbpl6	UTSW	2	76,382,468 (GRCm39)	missense	probably benign	0.00
R9303:Osbpl6	UTSW	2	76,378,716 (GRCm39)	missense	probably damaging	1.00
R9305:Osbpl6	UTSW	2	76,378,716 (GRCm39)	missense	probably damaging	1.00
R9526:Osbpl6	UTSW	2	76,415,603 (GRCm39)	missense	probably damaging	0.98
R9536:Osbpl6	UTSW	2	76,416,554 (GRCm39)	missense	probably benign	0.00
R9564:Osbpl6	UTSW	2	76,426,321 (GRCm39)	missense	probably damaging	1.00
R9571:Osbpl6	UTSW	2	76,425,191 (GRCm39)	missense	probably benign	0.03
R9585:Osbpl6	UTSW	2	76,354,438 (GRCm39)	missense	probably benign
R9771:Osbpl6	UTSW	2	76,423,771 (GRCm39)	missense	possibly damaging	0.89
R9790:Osbpl6	UTSW	2	76,385,361 (GRCm39)	missense	probably damaging	1.00
R9791:Osbpl6	UTSW	2	76,385,361 (GRCm39)	missense	probably damaging	1.00
Z1177:Osbpl6	UTSW	2	76,370,523 (GRCm39)	missense	probably benign	0.01
Z31818:Osbpl6	UTSW	2	76,385,426 (GRCm39)	missense	probably damaging	1.00

Posted On

2015-12-18