Mutagenetix > Incidental Mutation

Incidental Mutation 'R3735:Olr1'

270066

Institutional Source

Beutler Lab

Gene Symbol

Olr1

Ensembl Gene

ENSMUSG00000030162

Gene Name

oxidized low density lipoprotein (lectin-like) receptor 1

Synonyms

Scare1, SR-EI, LOX-1

MMRRC Submission

040722-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3735 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

129462207-129484128 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to A at 129476838 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032265] [ENSMUST00000162815] [ENSMUST00000182784] [ENSMUST00000183258]

AlphaFold

Q9EQ09

Predicted Effect

probably benign
Transcript: ENSMUST00000032265

SMART Domains

Protein: ENSMUSP00000032265
Gene: ENSMUSG00000030162

Domain	Start	End	E-Value	Type
Blast:CLECT	45	186	4e-13	BLAST
low complexity region	202	226	N/A	INTRINSIC
CLECT	235	355	3.83e-21	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000162815

SMART Domains

Protein: ENSMUSP00000124660
Gene: ENSMUSG00000030162

Domain	Start	End	E-Value	Type
Blast:CLECT	24	75	1e-8	BLAST
low complexity region	76	97	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000182784

SMART Domains

Protein: ENSMUSP00000138588
Gene: ENSMUSG00000030162

Domain	Start	End	E-Value	Type
CLECT	61	181	3.83e-21	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183258

SMART Domains

Protein: ENSMUSP00000138228
Gene: ENSMUSG00000030162

Domain	Start	End	E-Value	Type
CLECT	27	147	3.83e-21	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000203564

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.1%
20x: 94.3%

Validation Efficiency

100% (71/71)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a low density lipoprotein receptor that belongs to the C-type lectin superfamily. This gene is regulated through the cyclic AMP signaling pathway. The encoded protein binds, internalizes and degrades oxidized low-density lipoprotein. This protein may be involved in the regulation of Fas-induced apoptosis. This protein may play a role as a scavenger receptor. Mutations of this gene have been associated with atherosclerosis, risk of myocardial infarction, and may modify the risk of Alzheimer's disease. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]
PHENOTYPE: Homozygous mutation of this gene results in no obvious phenotype. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921539E11Rik	C	G	4: 103,123,603 (GRCm39)	E90Q	probably damaging	Het
Acadl	G	A	1: 66,892,448 (GRCm39)	A125V	probably benign	Het
Acot12	T	A	13: 91,932,465 (GRCm39)	I487N	probably benign	Het
Acox3	A	G	5: 35,768,497 (GRCm39)	K686R	probably benign	Het
Adam17	T	C	12: 21,375,413 (GRCm39)	D802G	probably benign	Het
Aoc3	A	T	11: 101,223,045 (GRCm39)	D427V	probably damaging	Het
Bivm	C	T	1: 44,165,594 (GRCm39)	H15Y	probably benign	Het
C8a	T	C	4: 104,674,812 (GRCm39)	E509G	probably benign	Het
Ccdc158	A	C	5: 92,780,283 (GRCm39)	L930R	possibly damaging	Het
Cdca7	T	A	2: 72,314,209 (GRCm39)		probably null	Het
Cep170b	A	T	12: 112,707,438 (GRCm39)	I395F	probably damaging	Het
Champ1	T	C	8: 13,928,735 (GRCm39)	S298P	probably damaging	Het
Cimip2c	A	T	5: 30,639,442 (GRCm39)	Y123F	probably benign	Het
Cyp2j8	T	A	4: 96,332,836 (GRCm39)	R503S	probably damaging	Het
Dcaf10	C	T	4: 45,348,117 (GRCm39)	T191I	probably benign	Het
Dido1	A	G	2: 180,325,829 (GRCm39)		probably benign	Het
Dnah7b	C	T	1: 46,339,035 (GRCm39)	T3361I	probably benign	Het
Dync1h1	G	A	12: 110,598,109 (GRCm39)	V1767I	probably benign	Het
Eml5	G	A	12: 98,822,248 (GRCm39)	T721I	possibly damaging	Het
F8	G	A	X: 74,254,981 (GRCm39)	P2138S	probably damaging	Het
Fam169b	G	T	7: 68,000,049 (GRCm39)	R198S	probably damaging	Het
Gm7694	A	G	1: 170,130,330 (GRCm39)	S23P	probably damaging	Het
Grk3	T	A	5: 113,101,697 (GRCm39)	T248S	probably benign	Het
Helq	T	G	5: 100,938,054 (GRCm39)	D464A	possibly damaging	Het
Ido2	C	T	8: 25,025,209 (GRCm39)	V273M	probably damaging	Het
Il12rb1	T	C	8: 71,269,862 (GRCm39)	L518P	probably damaging	Het
Irag2	G	A	6: 145,106,596 (GRCm39)		probably benign	Het
Kansl1l	A	G	1: 66,840,409 (GRCm39)	V297A	possibly damaging	Het
Kcnj10	A	G	1: 172,197,533 (GRCm39)	Y349C	possibly damaging	Het
Krt18	A	G	15: 101,936,936 (GRCm39)	T75A	probably benign	Het
Lrp4	A	T	2: 91,328,716 (GRCm39)	I1539F	probably damaging	Het
Map3k6	T	C	4: 132,973,683 (GRCm39)	V458A	probably benign	Het
Med12l	T	A	3: 58,998,916 (GRCm39)	H614Q	probably damaging	Het
Med13	A	C	11: 86,170,484 (GRCm39)	M1850R	probably benign	Het
Mfsd13a	A	G	19: 46,356,767 (GRCm39)	Y256C	probably damaging	Het
Mogs	C	A	6: 83,093,757 (GRCm39)	T242K	possibly damaging	Het
Myo9b	T	C	8: 71,801,241 (GRCm39)	V1133A	probably benign	Het
Myom2	A	T	8: 15,119,676 (GRCm39)	H144L	probably benign	Het
Ncapg	A	T	5: 45,853,469 (GRCm39)	Q906L	probably benign	Het
Nkx1-1	C	T	5: 33,591,074 (GRCm39)	V83I	unknown	Het
Npy4r	T	A	14: 33,869,226 (GRCm39)	T21S	probably benign	Het
Nup88	A	G	11: 70,847,018 (GRCm39)	S331P	probably damaging	Het
Or4k44	T	A	2: 111,368,241 (GRCm39)	H131L	probably damaging	Het
Osmr	A	T	15: 6,851,561 (GRCm39)	Y656N	probably damaging	Het
Otogl	A	T	10: 107,735,390 (GRCm39)	Y131*	probably null	Het
Pgr	G	A	9: 8,901,534 (GRCm39)	G356S	probably damaging	Het
Prdm2	T	C	4: 142,860,929 (GRCm39)	E787G	probably damaging	Het
Prpf18	A	G	2: 4,648,484 (GRCm39)	I114T	probably benign	Het
R3hdm2	T	A	10: 127,300,879 (GRCm39)	I280N	probably benign	Het
Rims4	T	C	2: 163,705,905 (GRCm39)	D243G	possibly damaging	Het
Rmnd5a	T	C	6: 71,373,846 (GRCm39)	D316G	possibly damaging	Het
Rpap2	T	C	5: 107,803,017 (GRCm39)		probably benign	Het
Sdr16c5	G	A	4: 4,005,614 (GRCm39)	T240I	probably benign	Het
Shroom3	T	C	5: 93,112,303 (GRCm39)	V1888A	possibly damaging	Het
Slc36a4	T	A	9: 15,649,569 (GRCm39)	Y466*	probably null	Het
Slco3a1	A	G	7: 74,154,245 (GRCm39)	I80T	probably damaging	Het
Sptlc2	G	A	12: 87,388,339 (GRCm39)	A381V	probably benign	Het
Stam	A	T	2: 14,133,823 (GRCm39)	Q190L	probably damaging	Het
Suclg2	T	A	6: 95,474,677 (GRCm39)	I363F	probably damaging	Het
Tacstd2	A	G	6: 67,511,843 (GRCm39)	V283A	probably damaging	Het
Tln1	G	T	4: 43,549,370 (GRCm39)	A616E	probably damaging	Het
Trdmt1	A	T	2: 13,524,684 (GRCm39)	F257Y	possibly damaging	Het
Trip12	TATACATACATACATACATACATACATACATAC	TATACATACATACATACATACATACATACATACATAC	1: 84,792,511 (GRCm39)		probably null	Het
Trps1	A	G	15: 50,709,456 (GRCm39)	I298T	possibly damaging	Het
Tti2	T	C	8: 31,645,925 (GRCm39)	L413P	probably damaging	Het
Utrn	A	G	10: 12,354,228 (GRCm39)	V343A	probably damaging	Het
Vwf	G	T	6: 125,565,576 (GRCm39)	W288L	probably damaging	Het
Zfp629	T	A	7: 127,211,950 (GRCm39)		probably benign	Het
Zfp873	G	A	10: 81,897,015 (GRCm39)	S582N	probably benign	Het
Zfp979	A	G	4: 147,697,939 (GRCm39)	Y257H	possibly damaging	Het
Zfpm1	G	A	8: 123,050,475 (GRCm39)	C117Y	possibly damaging	Het

Other mutations in Olr1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00579:Olr1	APN	6	129,470,486 (GRCm39)	missense	probably benign	0.02
IGL01751:Olr1	APN	6	129,465,811 (GRCm39)	missense	possibly damaging	0.62
IGL02308:Olr1	APN	6	129,476,860 (GRCm39)	missense	possibly damaging	0.70
IGL03120:Olr1	APN	6	129,465,898 (GRCm39)	missense	probably damaging	0.97
IGL03237:Olr1	APN	6	129,479,117 (GRCm39)	missense	probably damaging	1.00
ANU74:Olr1	UTSW	6	129,477,032 (GRCm39)	missense	possibly damaging	0.91
PIT4618001:Olr1	UTSW	6	129,476,869 (GRCm39)	missense	probably damaging	0.99
R0112:Olr1	UTSW	6	129,465,869 (GRCm39)	missense	possibly damaging	0.77
R1375:Olr1	UTSW	6	129,484,039 (GRCm39)	missense	possibly damaging	0.94
R1650:Olr1	UTSW	6	129,484,052 (GRCm39)	missense	probably benign	0.29
R1828:Olr1	UTSW	6	129,465,895 (GRCm39)	missense	possibly damaging	0.94
R1971:Olr1	UTSW	6	129,470,498 (GRCm39)	missense	probably benign	0.06
R2074:Olr1	UTSW	6	129,479,057 (GRCm39)	missense	probably benign	0.23
R3110:Olr1	UTSW	6	129,476,881 (GRCm39)	missense	possibly damaging	0.91
R3112:Olr1	UTSW	6	129,476,881 (GRCm39)	missense	possibly damaging	0.91
R3736:Olr1	UTSW	6	129,476,838 (GRCm39)	unclassified	probably benign
R4200:Olr1	UTSW	6	129,479,068 (GRCm39)	missense	probably damaging	0.98
R4780:Olr1	UTSW	6	129,465,839 (GRCm39)	missense	probably damaging	0.99
R4801:Olr1	UTSW	6	129,465,053 (GRCm39)	missense	possibly damaging	0.71
R4802:Olr1	UTSW	6	129,465,053 (GRCm39)	missense	possibly damaging	0.71
R4856:Olr1	UTSW	6	129,470,559 (GRCm39)	nonsense	probably null
R4929:Olr1	UTSW	6	129,477,044 (GRCm39)	missense	probably damaging	1.00
R5148:Olr1	UTSW	6	129,470,572 (GRCm39)	missense	probably benign	0.02
R5659:Olr1	UTSW	6	129,476,992 (GRCm39)	missense	probably damaging	0.96
R6037:Olr1	UTSW	6	129,470,504 (GRCm39)	missense	probably damaging	1.00
R6037:Olr1	UTSW	6	129,470,504 (GRCm39)	missense	probably damaging	1.00
R6116:Olr1	UTSW	6	129,476,947 (GRCm39)	missense	probably damaging	1.00
R6356:Olr1	UTSW	6	129,470,522 (GRCm39)	missense	probably benign	0.22
R6676:Olr1	UTSW	6	129,477,040 (GRCm39)	splice site	probably null
R7001:Olr1	UTSW	6	129,465,074 (GRCm39)	missense	probably damaging	1.00
R7056:Olr1	UTSW	6	129,465,904 (GRCm39)	missense	probably damaging	1.00
R9169:Olr1	UTSW	6	129,470,528 (GRCm39)	missense	probably damaging	1.00
R9288:Olr1	UTSW	6	129,470,202 (GRCm39)	intron	probably benign

Predicted Primers

PCR Primer
(F):5'- AAACCTTACGCCCATGAGAAGG -3'
(R):5'- CGAACCTTACTCAGCAGGATC -3'

Sequencing Primer
(F):5'- AGGGAGCTTGAGCAATTCTG -3'
(R):5'- GAACCTTACTCAGCAGGATCGTATC -3'

Posted On

2015-03-18