Mutagenetix > Incidental Mutation

Incidental Mutation 'R2117:Lrp2'

231032

Institutional Source

Beutler Lab

Gene Symbol

Lrp2

Ensembl Gene

ENSMUSG00000027070

Gene Name

low density lipoprotein receptor-related protein 2

Synonyms

D230004K18Rik, b2b1625.2Clo, Megalin, Gp330

MMRRC Submission

040121-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R2117 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

69254679-69416373 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 69313729 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 2334 (V2334G)

Ref Sequence

ENSEMBL: ENSMUSP00000079752 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080953]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000080953
AA Change: V2334G

PolyPhen 2 Score 0.049 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000079752
Gene: ENSMUSG00000027070
AA Change: V2334G

Domain	Start	End	E-Value	Type
low complexity region	5	21	N/A	INTRINSIC
LDLa	27	64	5.63e-13	SMART
LDLa	66	105	2.25e-12	SMART
EGF	107	143	2.59e1	SMART
LDLa	107	144	9.29e-14	SMART
LDLa	146	181	6.18e-10	SMART
LDLa	182	219	1.08e-14	SMART
LDLa	221	258	1.05e-12	SMART
LDLa	264	302	1.66e-10	SMART
EGF	310	346	3.23e0	SMART
EGF	350	385	2.32e-1	SMART
LY	414	457	3.88e-3	SMART
LY	458	500	1.17e-6	SMART
LY	501	547	5.96e-13	SMART
LY	548	590	1.94e-12	SMART
LY	591	634	2.66e0	SMART
EGF	661	704	7.76e-3	SMART
LY	732	774	1.76e0	SMART
LY	775	817	3.64e-8	SMART
LY	818	860	1.11e-3	SMART
LY	861	903	2.11e-13	SMART
LY	905	946	9.33e-1	SMART
EGF	972	1013	1.73e0	SMART
LDLa	1024	1061	1.05e-12	SMART
LDLa	1065	1103	4.65e-14	SMART
LDLa	1109	1146	3.63e-16	SMART
LDLa	1149	1186	5.5e-16	SMART
LDLa	1187	1225	1.43e-14	SMART
LDLa	1230	1269	2.1e-12	SMART
LDLa	1271	1308	3.63e-16	SMART
LDLa	1312	1351	4.69e-10	SMART
EGF	1353	1390	9.7e-4	SMART
EGF_CA	1391	1430	6.54e-10	SMART
LY	1457	1501	1.43e-1	SMART
LY	1502	1544	2e-14	SMART
LY	1545	1590	3.03e-14	SMART
LY	1591	1633	5.48e-12	SMART
LY	1635	1677	1.18e-2	SMART
EGF	1704	1742	5.2e-4	SMART
LY	1771	1812	1.68e1	SMART
LY	1813	1856	1.91e-2	SMART
LY	1859	1911	1.88e-10	SMART
LY	1912	1954	7.69e-7	SMART
LY	1955	1994	3e1	SMART
EGF	2022	2060	1.18e-2	SMART
LY	2088	2135	1.14e1	SMART
LY	2136	2182	2.11e-4	SMART
LY	2183	2226	2.22e-12	SMART
LY	2227	2269	1.24e-10	SMART
EGF	2346	2384	2.07e1	SMART
LY	2459	2501	9.91e-10	SMART
LY	2503	2543	1.48e-8	SMART
LY	2544	2586	6.85e-13	SMART
LY	2587	2627	8.13e-1	SMART
EGF_like	2655	2694	3.5e1	SMART
LDLa	2700	2739	2.86e-14	SMART
LDLa	2741	2778	8.09e-14	SMART
LDLa	2780	2820	3.19e-12	SMART
LDLa	2822	2862	6.94e-13	SMART
LDLa	2864	2903	9.29e-14	SMART
LDLa	2907	2947	4.79e-16	SMART
LDLa	2949	2992	8.41e-12	SMART
LDLa	2994	3031	1.08e-14	SMART
LDLa	3033	3072	1.83e-12	SMART
LDLa	3076	3113	1.16e-14	SMART
EGF	3115	3153	8.57e-5	SMART
EGF_CA	3154	3194	3.56e-11	SMART
LY	3221	3263	9.77e-9	SMART
LY	3264	3306	1.22e-9	SMART
LY	3312	3358	5.44e-7	SMART
LY	3359	3401	1.83e-13	SMART
LY	3402	3443	1.41e-5	SMART
EGF	3470	3511	8.91e-3	SMART
LDLa	3513	3552	1.79e-15	SMART
LDLa	3554	3593	9.89e-9	SMART
LDLa	3595	3634	3.07e-14	SMART
LDLa	3636	3675	3.34e-15	SMART
LDLa	3679	3718	1.39e-12	SMART
LDLa	3720	3758	3.83e-15	SMART
LDLa	3760	3797	7.15e-15	SMART
LDLa	3799	3836	2.86e-14	SMART
LDLa	3843	3882	2.38e-11	SMART
LDLa	3884	3924	3.66e-12	SMART
LDLa	3929	3966	1.93e-11	SMART
EGF	3971	4008	6.3e-3	SMART
EGF_CA	4009	4050	1.36e-7	SMART
low complexity region	4072	4084	N/A	INTRINSIC
LY	4136	4178	6.2e-11	SMART
LY	4179	4222	4.32e-10	SMART
LY	4223	4266	3.78e-15	SMART
LY	4267	4306	4.53e1	SMART
EGF	4335	4367	3.46e0	SMART
EGF	4368	4413	1.53e-1	SMART
transmembrane domain	4425	4447	N/A	INTRINSIC
low complexity region	4454	4472	N/A	INTRINSIC
low complexity region	4616	4636	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.2%
20x: 95.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene, low density lipoprotein-related protein 2 (LRP2) or megalin, is a multi-ligand endocytic receptor that is expressed in many different tissues but primarily in absorptive epithilial tissues such as the kidney. This glycoprotein has a large amino-terminal extracellular domain, a single transmembrane domain, and a short carboxy-terminal cytoplasmic tail. The extracellular ligand-binding-domains bind diverse macromolecules including albumin, apolipoproteins B and E, and lipoprotein lipase. The LRP2 protein is critical for the reuptake of numerous ligands, including lipoproteins, sterols, vitamin-binding proteins, and hormones. This protein also has a role in cell-signaling; extracellular ligands include parathyroid horomones and the morphogen sonic hedgehog while cytosolic ligands include MAP kinase scaffold proteins and JNK interacting proteins. Recycling of this membrane receptor is regulated by phosphorylation of its cytoplasmic domain. Mutations in this gene cause Donnai-Barrow syndrome (DBS) and facio-oculoacoustico-renal syndrome (FOAR).[provided by RefSeq, Aug 2009]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit lung and kidney epithelial defects, impaired B12 uptake, reduced proliferation of the neuroepithelium resulting in lack of olfactory bulbs, forebrain fusions, ventricular defects, and perinatal lethality. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 101 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrv1	A	T	13: 81,640,656 (GRCm39)	C3357S	probably benign	Het
Ago1	T	A	4: 126,357,650 (GRCm39)		probably null	Het
Akap10	A	T	11: 61,781,129 (GRCm39)	D562E	possibly damaging	Het
Akr1b7	G	A	6: 34,395,929 (GRCm39)	A144T	possibly damaging	Het
Ankle1	A	G	8: 71,860,562 (GRCm39)	T340A	probably benign	Het
Arf5	C	T	6: 28,424,783 (GRCm39)	Q71*	probably null	Het
Arl15	C	T	13: 114,104,196 (GRCm39)	S111F	probably damaging	Het
Asph	G	A	4: 9,517,671 (GRCm39)	Q468*	probably null	Het
Bcam	G	T	7: 19,492,352 (GRCm39)	A581E	possibly damaging	Het
Blvra	G	T	2: 126,927,989 (GRCm39)	E80*	probably null	Het
Ccr6	T	C	17: 8,474,914 (GRCm39)	F40L	possibly damaging	Het
Cfap161	A	T	7: 83,425,184 (GRCm39)	N302K	possibly damaging	Het
Ckmt2	T	A	13: 92,003,964 (GRCm39)	I345F	probably benign	Het
Cpsf6	A	G	10: 117,202,025 (GRCm39)		probably benign	Het
Ctnna1	A	G	18: 35,285,678 (GRCm39)	N8S	possibly damaging	Het
Cyp2d11	A	G	15: 82,275,954 (GRCm39)	L209P	probably damaging	Het
Dab2	T	C	15: 6,465,096 (GRCm39)	V628A	probably damaging	Het
Dcstamp	C	T	15: 39,618,571 (GRCm39)	Q327*	probably null	Het
Defb38	A	T	8: 19,073,483 (GRCm39)	Y63*	probably null	Het
Dlg5	A	T	14: 24,227,826 (GRCm39)	L365*	probably null	Het
Dnai7	C	T	6: 145,150,967 (GRCm39)		probably null	Het
Dnmt3l	C	A	10: 77,899,130 (GRCm39)	L110I	probably damaging	Het
Exoc3l2	G	T	7: 19,228,907 (GRCm39)	L108F	possibly damaging	Het
Exoc4	T	A	6: 33,324,760 (GRCm39)	N351K	possibly damaging	Het
Fam83h	C	A	15: 75,876,582 (GRCm39)	E252*	probably null	Het
Fancm	A	G	12: 65,123,948 (GRCm39)	D202G	probably damaging	Het
Fat1	T	A	8: 45,490,500 (GRCm39)	V3804E	probably benign	Het
Fbxw28	T	C	9: 109,159,985 (GRCm39)	T190A	probably benign	Het
Fer1l4	T	C	2: 155,881,038 (GRCm39)	T843A	probably benign	Het
Fnip1	A	T	11: 54,391,450 (GRCm39)	H461L	probably damaging	Het
Gcn1	A	T	5: 115,736,884 (GRCm39)	M1276L	probably benign	Het
Gemin4	A	G	11: 76,101,827 (GRCm39)	V978A	possibly damaging	Het
Gm7247	A	T	14: 51,602,792 (GRCm39)	I43F	probably damaging	Het
Gm9978	C	T	10: 78,322,731 (GRCm39)		noncoding transcript	Het
Gpr4	T	C	7: 18,957,070 (GRCm39)	S331P	probably damaging	Het
Hspa1a	T	A	17: 35,189,455 (GRCm39)	N483Y	probably damaging	Het
Ift74	A	G	4: 94,515,496 (GRCm39)	T138A	probably benign	Het
Ints14	T	G	9: 64,887,077 (GRCm39)	L336R	probably damaging	Het
Irak1	G	T	X: 73,066,218 (GRCm39)	P197Q	possibly damaging	Het
Kif4	A	G	X: 99,709,323 (GRCm39)	S315G	probably benign	Het
L3mbtl1	T	A	2: 162,801,990 (GRCm39)		probably null	Het
Lamb3	A	G	1: 193,016,489 (GRCm39)	R657G	probably benign	Het
Ldc1	C	A	4: 130,109,156 (GRCm39)	V295L	possibly damaging	Het
Lrwd1	T	A	5: 136,159,332 (GRCm39)	Y431F	probably damaging	Het
Map3k21	A	T	8: 126,650,781 (GRCm39)	H261L	probably benign	Het
Meis1	G	T	11: 18,831,679 (GRCm39)	P453Q	probably damaging	Het
Mettl16	G	T	11: 74,693,755 (GRCm39)	M255I	probably benign	Het
Mllt10	A	G	2: 18,167,380 (GRCm39)	N435S	probably benign	Het
Mta2	T	C	19: 8,920,880 (GRCm39)	I27T	probably damaging	Het
Nav2	A	G	7: 49,114,328 (GRCm39)	I771V	probably benign	Het
Nisch	A	T	14: 30,899,242 (GRCm39)		probably benign	Het
Npc1	G	A	18: 12,329,613 (GRCm39)	P990L	probably damaging	Het
Nrxn1	A	T	17: 91,011,705 (GRCm39)	I308K	probably damaging	Het
Or13l2	C	A	3: 97,317,765 (GRCm39)	C244F	probably damaging	Het
Or1ad6	A	T	11: 50,860,147 (GRCm39)	I101F	probably damaging	Het
Or5h17	T	C	16: 58,820,783 (GRCm39)	L245P	possibly damaging	Het
Otogl	T	C	10: 107,694,779 (GRCm39)	D823G	probably benign	Het
P2rx7	A	G	5: 122,819,329 (GRCm39)	T584A	probably benign	Het
Pals1	T	C	12: 78,856,696 (GRCm39)	F180L	possibly damaging	Het
Pank1	T	A	19: 34,818,486 (GRCm39)	I18F	probably damaging	Het
Pgap3	A	G	11: 98,281,933 (GRCm39)	L126P	probably damaging	Het
Pgap6	C	T	17: 26,336,858 (GRCm39)	L259F	possibly damaging	Het
Phka1	C	T	X: 101,653,807 (GRCm39)	R290H	probably damaging	Het
Pkd2	G	A	5: 104,631,042 (GRCm39)	E489K	probably damaging	Het
Prdm16	T	A	4: 154,432,382 (GRCm39)	S296C	probably null	Het
Prex2	T	A	1: 11,256,937 (GRCm39)	N1216K	probably damaging	Het
Prmt7	A	G	8: 106,953,930 (GRCm39)	T124A	probably damaging	Het
Ptpra	G	T	2: 130,381,655 (GRCm39)	R372L	probably damaging	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Rap2b	G	T	3: 61,272,512 (GRCm39)	G12V	probably damaging	Het
Rapgef5	T	A	12: 117,677,799 (GRCm39)		probably null	Het
Rassf4	A	G	6: 116,622,088 (GRCm39)	F168S	possibly damaging	Het
Rtf1	T	A	2: 119,535,999 (GRCm39)	H184Q	probably benign	Het
Sacs	A	G	14: 61,451,220 (GRCm39)	K4422R	probably benign	Het
Sec11c	A	T	18: 65,933,720 (GRCm39)	T9S	probably benign	Het
Sema3d	C	T	5: 12,613,240 (GRCm39)	T439I	probably benign	Het
Sephs1	A	G	2: 4,904,351 (GRCm39)	N243S	probably benign	Het
Setd2	TTGGGA	T	9: 110,433,212 (GRCm39)		probably null	Het
Setx	A	G	2: 29,020,313 (GRCm39)	D100G	probably benign	Het
Slc22a7	C	A	17: 46,744,898 (GRCm39)	V383L	possibly damaging	Het
Slc25a40	T	C	5: 8,480,417 (GRCm39)	C56R	probably damaging	Het
Stk38l	T	A	6: 146,670,344 (GRCm39)	L229I	probably damaging	Het
Sult2a5	T	C	7: 13,359,359 (GRCm39)	S112P	probably damaging	Het
Syt4	A	G	18: 31,573,520 (GRCm39)	Y332H	probably damaging	Het
Tcof1	T	C	18: 60,965,857 (GRCm39)	E415G	possibly damaging	Het
Tenm2	A	G	11: 35,915,681 (GRCm39)	L1951P	probably damaging	Het
Tlr9	A	G	9: 106,102,536 (GRCm39)	N609S	probably damaging	Het
Tmem120a	A	T	5: 135,764,977 (GRCm39)	S266T	possibly damaging	Het
Tmem132b	A	G	5: 125,699,615 (GRCm39)	E92G	probably damaging	Het
Tnfrsf18	T	A	4: 156,112,973 (GRCm39)	V196E	probably damaging	Het
Trpc1	A	T	9: 95,599,637 (GRCm39)	L474H	probably damaging	Het
Trpm6	T	C	19: 18,807,316 (GRCm39)	V1020A	probably damaging	Het
Usp20	T	A	2: 30,906,317 (GRCm39)	C562S	probably damaging	Het
Usp47	T	A	7: 111,666,443 (GRCm39)		probably null	Het
Vgll1	A	C	X: 56,137,790 (GRCm39)	K53T	probably damaging	Het
Vmn1r26	T	C	6: 57,985,335 (GRCm39)	N285D	possibly damaging	Het
Zfp445	T	A	9: 122,682,502 (GRCm39)	K480*	probably null	Het
Zfp786	A	G	6: 47,803,931 (GRCm39)	V37A	probably damaging	Het
Zfp821	A	G	8: 110,447,851 (GRCm39)	E64G	probably damaging	Het
Zfp994	T	A	17: 22,419,962 (GRCm39)	D329V	probably damaging	Het
Zkscan8	T	C	13: 21,704,488 (GRCm39)	S484G	probably damaging	Het

Other mutations in Lrp2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00094:Lrp2	APN	2	69,338,123 (GRCm39)	missense	probably damaging	1.00
IGL00594:Lrp2	APN	2	69,316,624 (GRCm39)	missense	probably benign	0.00
IGL00782:Lrp2	APN	2	69,331,989 (GRCm39)	missense	probably benign	0.14
IGL00821:Lrp2	APN	2	69,289,860 (GRCm39)	missense	probably damaging	1.00
IGL00897:Lrp2	APN	2	69,352,225 (GRCm39)	missense	possibly damaging	0.86
IGL01065:Lrp2	APN	2	69,299,780 (GRCm39)	missense	possibly damaging	0.94
IGL01087:Lrp2	APN	2	69,354,417 (GRCm39)	missense	probably damaging	1.00
IGL01095:Lrp2	APN	2	69,322,776 (GRCm39)	nonsense	probably null
IGL01131:Lrp2	APN	2	69,329,583 (GRCm39)	missense	probably damaging	1.00
IGL01350:Lrp2	APN	2	69,341,328 (GRCm39)	missense	probably damaging	0.96
IGL01352:Lrp2	APN	2	69,333,870 (GRCm39)	missense	possibly damaging	0.77
IGL01358:Lrp2	APN	2	69,382,814 (GRCm39)	splice site	probably benign
IGL01375:Lrp2	APN	2	69,308,910 (GRCm39)	splice site	probably benign
IGL01384:Lrp2	APN	2	69,313,846 (GRCm39)	missense	probably damaging	1.00
IGL01384:Lrp2	APN	2	69,284,156 (GRCm39)	missense	probably null	1.00
IGL01411:Lrp2	APN	2	69,312,611 (GRCm39)	missense	probably damaging	1.00
IGL01418:Lrp2	APN	2	69,355,630 (GRCm39)	missense	probably benign
IGL01444:Lrp2	APN	2	69,274,060 (GRCm39)	missense	possibly damaging	0.94
IGL01464:Lrp2	APN	2	69,302,783 (GRCm39)	missense	probably damaging	0.98
IGL01528:Lrp2	APN	2	69,322,804 (GRCm39)	missense	probably damaging	1.00
IGL01663:Lrp2	APN	2	69,259,050 (GRCm39)	missense	probably benign
IGL01761:Lrp2	APN	2	69,311,579 (GRCm39)	missense	possibly damaging	0.85
IGL01780:Lrp2	APN	2	69,316,528 (GRCm39)	missense	possibly damaging	0.66
IGL01994:Lrp2	APN	2	69,313,945 (GRCm39)	missense	probably benign	0.08
IGL02015:Lrp2	APN	2	69,357,922 (GRCm39)	missense	probably benign	0.00
IGL02104:Lrp2	APN	2	69,340,762 (GRCm39)	missense	probably damaging	1.00
IGL02132:Lrp2	APN	2	69,367,960 (GRCm39)	missense	probably benign	0.01
IGL02134:Lrp2	APN	2	69,343,723 (GRCm39)	critical splice acceptor site	probably null
IGL02197:Lrp2	APN	2	69,297,224 (GRCm39)	missense	probably benign	0.01
IGL02212:Lrp2	APN	2	69,281,608 (GRCm39)	missense	probably benign	0.00
IGL02240:Lrp2	APN	2	69,365,390 (GRCm39)	missense	probably benign
IGL02248:Lrp2	APN	2	69,313,152 (GRCm39)	missense	probably damaging	1.00
IGL02369:Lrp2	APN	2	69,294,980 (GRCm39)	missense	probably damaging	1.00
IGL02416:Lrp2	APN	2	69,299,977 (GRCm39)	missense	probably damaging	1.00
IGL02417:Lrp2	APN	2	69,291,649 (GRCm39)	missense	probably damaging	1.00
IGL02458:Lrp2	APN	2	69,352,117 (GRCm39)	missense	probably damaging	0.97
IGL02479:Lrp2	APN	2	69,295,145 (GRCm39)	splice site	probably benign
IGL02508:Lrp2	APN	2	69,333,774 (GRCm39)	missense	probably benign	0.04
IGL02751:Lrp2	APN	2	69,363,806 (GRCm39)	missense	possibly damaging	0.56
IGL02814:Lrp2	APN	2	69,337,080 (GRCm39)	missense	probably damaging	1.00
IGL02867:Lrp2	APN	2	69,382,794 (GRCm39)	missense	possibly damaging	0.67
IGL02889:Lrp2	APN	2	69,382,794 (GRCm39)	missense	possibly damaging	0.67
IGL02943:Lrp2	APN	2	69,285,854 (GRCm39)	missense	possibly damaging	0.86
IGL02948:Lrp2	APN	2	69,318,181 (GRCm39)	missense	probably damaging	1.00
IGL02960:Lrp2	APN	2	69,285,797 (GRCm39)	splice site	probably benign
IGL02990:Lrp2	APN	2	69,271,740 (GRCm39)	missense	possibly damaging	0.56
IGL03027:Lrp2	APN	2	69,367,897 (GRCm39)	missense	probably benign	0.43
IGL03038:Lrp2	APN	2	69,305,808 (GRCm39)	missense	probably damaging	0.99
IGL03064:Lrp2	APN	2	69,313,477 (GRCm39)	missense	probably damaging	0.98
IGL03107:Lrp2	APN	2	69,285,177 (GRCm39)	missense	probably damaging	1.00
IGL03141:Lrp2	APN	2	69,307,370 (GRCm39)	missense	probably damaging	0.99
IGL03154:Lrp2	APN	2	69,379,386 (GRCm39)	missense	probably damaging	1.00
IGL03155:Lrp2	APN	2	69,285,796 (GRCm39)	splice site	probably benign
IGL03163:Lrp2	APN	2	69,331,870 (GRCm39)	nonsense	probably null
IGL03164:Lrp2	APN	2	69,295,043 (GRCm39)	missense	probably damaging	1.00
IGL03169:Lrp2	APN	2	69,353,538 (GRCm39)	missense	probably damaging	1.00
IGL03174:Lrp2	APN	2	69,296,609 (GRCm39)	missense	probably damaging	1.00
IGL03189:Lrp2	APN	2	69,268,822 (GRCm39)	splice site	probably benign
IGL03288:Lrp2	APN	2	69,256,383 (GRCm39)	missense	probably benign	0.02
IGL03350:Lrp2	APN	2	69,268,797 (GRCm39)	missense	probably damaging	1.00
IGL03378:Lrp2	APN	2	69,261,496 (GRCm39)	missense	probably damaging	1.00
casual	UTSW	2	69,329,607 (GRCm39)	missense	probably benign
nonchalant	UTSW	2	69,319,673 (GRCm39)	missense	probably damaging	1.00
Presto	UTSW	2	69,289,875 (GRCm39)	nonsense	probably null
relaxed	UTSW	2	69,365,349 (GRCm39)	missense	probably damaging	1.00
unguarded	UTSW	2	69,296,102 (GRCm39)	missense	probably benign	0.00
Unintended	UTSW	2	69,348,787 (GRCm39)	missense	probably damaging	1.00
BB009:Lrp2	UTSW	2	69,256,371 (GRCm39)	missense	probably benign	0.00
BB019:Lrp2	UTSW	2	69,256,371 (GRCm39)	missense	probably benign	0.00
IGL02835:Lrp2	UTSW	2	69,335,648 (GRCm39)	missense	probably damaging	1.00
IGL03055:Lrp2	UTSW	2	69,288,792 (GRCm39)	missense	probably damaging	1.00
PIT4362001:Lrp2	UTSW	2	69,367,882 (GRCm39)	missense	probably damaging	1.00
PIT4504001:Lrp2	UTSW	2	69,305,747 (GRCm39)	missense	probably damaging	1.00
R0008:Lrp2	UTSW	2	69,346,895 (GRCm39)	missense	probably benign	0.42
R0008:Lrp2	UTSW	2	69,346,895 (GRCm39)	missense	probably benign	0.42
R0044:Lrp2	UTSW	2	69,357,899 (GRCm39)	missense	probably benign	0.01
R0044:Lrp2	UTSW	2	69,357,899 (GRCm39)	missense	probably damaging	0.96
R0048:Lrp2	UTSW	2	69,295,971 (GRCm39)	missense	probably damaging	1.00
R0098:Lrp2	UTSW	2	69,305,756 (GRCm39)	missense	probably damaging	1.00
R0098:Lrp2	UTSW	2	69,305,756 (GRCm39)	missense	probably damaging	1.00
R0103:Lrp2	UTSW	2	69,307,384 (GRCm39)	missense	probably benign
R0167:Lrp2	UTSW	2	69,256,002 (GRCm39)	missense	possibly damaging	0.95
R0226:Lrp2	UTSW	2	69,367,907 (GRCm39)	missense	probably null	1.00
R0243:Lrp2	UTSW	2	69,258,974 (GRCm39)	missense	probably benign	0.00
R0308:Lrp2	UTSW	2	69,313,326 (GRCm39)	splice site	probably benign
R0323:Lrp2	UTSW	2	69,299,983 (GRCm39)	missense	probably damaging	1.00
R0372:Lrp2	UTSW	2	69,365,387 (GRCm39)	missense	probably benign	0.10
R0374:Lrp2	UTSW	2	69,260,651 (GRCm39)	missense	probably damaging	1.00
R0391:Lrp2	UTSW	2	69,290,681 (GRCm39)	splice site	probably benign
R0391:Lrp2	UTSW	2	69,287,202 (GRCm39)	missense	probably damaging	0.99
R0395:Lrp2	UTSW	2	69,263,421 (GRCm39)	missense	possibly damaging	0.89
R0401:Lrp2	UTSW	2	69,309,492 (GRCm39)	missense	probably damaging	0.98
R0471:Lrp2	UTSW	2	69,355,578 (GRCm39)	missense	probably damaging	0.97
R0483:Lrp2	UTSW	2	69,338,145 (GRCm39)	missense	probably damaging	0.99
R0502:Lrp2	UTSW	2	69,341,361 (GRCm39)	missense	probably damaging	1.00
R0542:Lrp2	UTSW	2	69,258,998 (GRCm39)	missense	probably benign	0.00
R0544:Lrp2	UTSW	2	69,322,275 (GRCm39)	missense	probably benign	0.18
R0548:Lrp2	UTSW	2	69,367,982 (GRCm39)	splice site	probably benign
R0593:Lrp2	UTSW	2	69,297,350 (GRCm39)	missense	probably benign
R0608:Lrp2	UTSW	2	69,316,587 (GRCm39)	missense	probably benign	0.02
R0633:Lrp2	UTSW	2	69,278,464 (GRCm39)	missense	probably damaging	1.00
R0691:Lrp2	UTSW	2	69,281,724 (GRCm39)	missense	probably benign	0.19
R0718:Lrp2	UTSW	2	69,341,292 (GRCm39)	missense	probably damaging	1.00
R0737:Lrp2	UTSW	2	69,278,513 (GRCm39)	missense	probably damaging	0.96
R0771:Lrp2	UTSW	2	69,338,334 (GRCm39)	missense	probably damaging	1.00
R0784:Lrp2	UTSW	2	69,348,709 (GRCm39)	missense	probably benign	0.32
R0885:Lrp2	UTSW	2	69,312,697 (GRCm39)	missense	possibly damaging	0.75
R0947:Lrp2	UTSW	2	69,318,182 (GRCm39)	missense	probably damaging	1.00
R1235:Lrp2	UTSW	2	69,354,380 (GRCm39)	missense	probably damaging	1.00
R1293:Lrp2	UTSW	2	69,353,646 (GRCm39)	splice site	probably null
R1301:Lrp2	UTSW	2	69,258,948 (GRCm39)	missense	probably damaging	0.98
R1387:Lrp2	UTSW	2	69,287,262 (GRCm39)	missense	probably damaging	1.00
R1459:Lrp2	UTSW	2	69,313,738 (GRCm39)	missense	probably damaging	0.99
R1459:Lrp2	UTSW	2	69,290,821 (GRCm39)	missense	probably damaging	1.00
R1529:Lrp2	UTSW	2	69,353,526 (GRCm39)	missense	probably damaging	1.00
R1543:Lrp2	UTSW	2	69,331,074 (GRCm39)	missense	probably damaging	1.00
R1546:Lrp2	UTSW	2	69,332,954 (GRCm39)	missense	probably damaging	1.00
R1550:Lrp2	UTSW	2	69,333,005 (GRCm39)	missense	possibly damaging	0.74
R1590:Lrp2	UTSW	2	69,297,107 (GRCm39)	critical splice donor site	probably null
R1689:Lrp2	UTSW	2	69,333,873 (GRCm39)	missense	probably benign	0.09
R1693:Lrp2	UTSW	2	69,340,762 (GRCm39)	missense	probably damaging	1.00
R1753:Lrp2	UTSW	2	69,326,833 (GRCm39)	missense	possibly damaging	0.87
R1799:Lrp2	UTSW	2	69,333,874 (GRCm39)	missense	probably benign	0.04
R1834:Lrp2	UTSW	2	69,297,224 (GRCm39)	missense	probably benign	0.01
R1921:Lrp2	UTSW	2	69,353,631 (GRCm39)	missense	probably damaging	1.00
R2000:Lrp2	UTSW	2	69,297,434 (GRCm39)	missense	probably damaging	1.00
R2077:Lrp2	UTSW	2	69,338,187 (GRCm39)	missense	probably damaging	1.00
R2092:Lrp2	UTSW	2	69,366,365 (GRCm39)	missense	probably benign	0.25
R2093:Lrp2	UTSW	2	69,366,365 (GRCm39)	missense	probably benign	0.25
R2108:Lrp2	UTSW	2	69,336,968 (GRCm39)	missense	possibly damaging	0.75
R2122:Lrp2	UTSW	2	69,314,051 (GRCm39)	missense	probably damaging	1.00
R2134:Lrp2	UTSW	2	69,341,411 (GRCm39)	missense	probably damaging	1.00
R2207:Lrp2	UTSW	2	69,297,372 (GRCm39)	missense	possibly damaging	0.94
R2248:Lrp2	UTSW	2	69,341,354 (GRCm39)	missense	probably damaging	1.00
R2264:Lrp2	UTSW	2	69,312,710 (GRCm39)	missense	possibly damaging	0.88
R2316:Lrp2	UTSW	2	69,322,191 (GRCm39)	missense	possibly damaging	0.75
R2513:Lrp2	UTSW	2	69,336,718 (GRCm39)	splice site	probably null
R2984:Lrp2	UTSW	2	69,256,158 (GRCm39)	splice site	probably null
R3085:Lrp2	UTSW	2	69,297,479 (GRCm39)	missense	probably benign	0.05
R3103:Lrp2	UTSW	2	69,262,328 (GRCm39)	missense	probably benign	0.00
R3727:Lrp2	UTSW	2	69,340,773 (GRCm39)	missense	probably damaging	1.00
R3730:Lrp2	UTSW	2	69,294,923 (GRCm39)	missense	probably damaging	0.99
R3730:Lrp2	UTSW	2	69,365,251 (GRCm39)	critical splice donor site	probably null
R3731:Lrp2	UTSW	2	69,294,923 (GRCm39)	missense	probably damaging	0.99
R3731:Lrp2	UTSW	2	69,365,251 (GRCm39)	critical splice donor site	probably null
R3764:Lrp2	UTSW	2	69,326,680 (GRCm39)	missense	probably damaging	1.00
R3768:Lrp2	UTSW	2	69,335,449 (GRCm39)	missense	probably benign	0.34
R3778:Lrp2	UTSW	2	69,339,548 (GRCm39)	missense	probably benign	0.00
R3808:Lrp2	UTSW	2	69,331,892 (GRCm39)	missense	probably damaging	1.00
R3809:Lrp2	UTSW	2	69,331,892 (GRCm39)	missense	probably damaging	1.00
R3813:Lrp2	UTSW	2	69,294,923 (GRCm39)	missense	probably damaging	0.99
R3828:Lrp2	UTSW	2	69,256,356 (GRCm39)	missense	probably benign	0.03
R3852:Lrp2	UTSW	2	69,367,909 (GRCm39)	missense	probably damaging	0.96
R3877:Lrp2	UTSW	2	69,289,816 (GRCm39)	critical splice donor site	probably null
R3877:Lrp2	UTSW	2	69,379,391 (GRCm39)	missense	probably damaging	1.00
R3922:Lrp2	UTSW	2	69,336,720 (GRCm39)	missense	probably benign
R4081:Lrp2	UTSW	2	69,343,617 (GRCm39)	missense	probably damaging	0.98
R4082:Lrp2	UTSW	2	69,343,617 (GRCm39)	missense	probably damaging	0.98
R4118:Lrp2	UTSW	2	69,260,606 (GRCm39)	critical splice donor site	probably null
R4193:Lrp2	UTSW	2	69,297,487 (GRCm39)	missense	probably damaging	1.00
R4284:Lrp2	UTSW	2	69,310,438 (GRCm39)	missense	possibly damaging	0.95
R4322:Lrp2	UTSW	2	69,256,335 (GRCm39)	nonsense	probably null
R4352:Lrp2	UTSW	2	69,262,526 (GRCm39)	critical splice donor site	probably null
R4407:Lrp2	UTSW	2	69,332,861 (GRCm39)	missense	probably damaging	1.00
R4408:Lrp2	UTSW	2	69,297,513 (GRCm39)	missense	probably benign	0.09
R4416:Lrp2	UTSW	2	69,357,575 (GRCm39)	missense	probably benign	0.18
R4426:Lrp2	UTSW	2	69,336,692 (GRCm39)	missense	probably benign	0.00
R4510:Lrp2	UTSW	2	69,310,406 (GRCm39)	missense	possibly damaging	0.58
R4511:Lrp2	UTSW	2	69,310,406 (GRCm39)	missense	possibly damaging	0.58
R4553:Lrp2	UTSW	2	69,343,629 (GRCm39)	missense	probably benign	0.13
R4591:Lrp2	UTSW	2	69,366,419 (GRCm39)	missense	probably damaging	1.00
R4612:Lrp2	UTSW	2	69,288,771 (GRCm39)	nonsense	probably null
R4622:Lrp2	UTSW	2	69,290,693 (GRCm39)	missense	possibly damaging	0.87
R4632:Lrp2	UTSW	2	69,319,473 (GRCm39)	splice site	probably null
R4633:Lrp2	UTSW	2	69,291,761 (GRCm39)	missense	probably benign	0.16
R4636:Lrp2	UTSW	2	69,266,983 (GRCm39)	missense	possibly damaging	0.93
R4657:Lrp2	UTSW	2	69,297,337 (GRCm39)	missense	probably damaging	1.00
R4667:Lrp2	UTSW	2	69,319,642 (GRCm39)	missense	probably benign	0.02
R4712:Lrp2	UTSW	2	69,336,895 (GRCm39)	missense	probably damaging	1.00
R4713:Lrp2	UTSW	2	69,318,310 (GRCm39)	missense	probably damaging	1.00
R4720:Lrp2	UTSW	2	69,311,517 (GRCm39)	missense	probably damaging	0.99
R4732:Lrp2	UTSW	2	69,363,899 (GRCm39)	missense	probably benign
R4733:Lrp2	UTSW	2	69,363,899 (GRCm39)	missense	probably benign
R4777:Lrp2	UTSW	2	69,312,608 (GRCm39)	missense	probably damaging	1.00
R4779:Lrp2	UTSW	2	69,290,059 (GRCm39)	missense	possibly damaging	0.75
R4786:Lrp2	UTSW	2	69,368,300 (GRCm39)	missense	probably damaging	1.00
R4842:Lrp2	UTSW	2	69,299,755 (GRCm39)	missense	probably benign	0.06
R4845:Lrp2	UTSW	2	69,339,585 (GRCm39)	missense	possibly damaging	0.71
R4846:Lrp2	UTSW	2	69,309,457 (GRCm39)	missense	probably damaging	1.00
R4938:Lrp2	UTSW	2	69,302,712 (GRCm39)	missense	probably damaging	0.98
R4951:Lrp2	UTSW	2	69,366,332 (GRCm39)	missense	probably damaging	1.00
R4990:Lrp2	UTSW	2	69,311,732 (GRCm39)	missense	probably benign	0.01
R5075:Lrp2	UTSW	2	69,296,102 (GRCm39)	missense	probably benign	0.00
R5078:Lrp2	UTSW	2	69,331,874 (GRCm39)	missense	possibly damaging	0.93
R5102:Lrp2	UTSW	2	69,319,502 (GRCm39)	missense	probably damaging	0.98
R5124:Lrp2	UTSW	2	69,331,834 (GRCm39)	missense	probably damaging	0.97
R5131:Lrp2	UTSW	2	69,260,686 (GRCm39)	missense	possibly damaging	0.74
R5141:Lrp2	UTSW	2	69,382,693 (GRCm39)	splice site	probably null
R5223:Lrp2	UTSW	2	69,354,397 (GRCm39)	missense	probably damaging	0.99
R5236:Lrp2	UTSW	2	69,287,163 (GRCm39)	splice site	probably null
R5267:Lrp2	UTSW	2	69,379,322 (GRCm39)	missense	possibly damaging	0.83
R5290:Lrp2	UTSW	2	69,343,698 (GRCm39)	missense	probably damaging	1.00
R5333:Lrp2	UTSW	2	69,355,572 (GRCm39)	missense	probably benign	0.01
R5355:Lrp2	UTSW	2	69,285,182 (GRCm39)	nonsense	probably null
R5356:Lrp2	UTSW	2	69,295,052 (GRCm39)	missense	possibly damaging	0.74
R5369:Lrp2	UTSW	2	69,289,904 (GRCm39)	missense	probably benign	0.04
R5486:Lrp2	UTSW	2	69,267,809 (GRCm39)	missense	probably benign	0.04
R5554:Lrp2	UTSW	2	69,382,768 (GRCm39)	missense	possibly damaging	0.92
R5584:Lrp2	UTSW	2	69,281,632 (GRCm39)	missense	probably damaging	1.00
R5585:Lrp2	UTSW	2	69,294,968 (GRCm39)	missense	possibly damaging	0.77
R5587:Lrp2	UTSW	2	69,329,607 (GRCm39)	missense	probably benign
R5605:Lrp2	UTSW	2	69,353,643 (GRCm39)	missense	probably damaging	1.00
R5637:Lrp2	UTSW	2	69,302,762 (GRCm39)	missense	probably damaging	1.00
R5647:Lrp2	UTSW	2	69,350,258 (GRCm39)	missense	probably null	0.80
R5686:Lrp2	UTSW	2	69,341,405 (GRCm39)	missense	possibly damaging	0.88
R5691:Lrp2	UTSW	2	69,332,897 (GRCm39)	missense	probably damaging	1.00
R5724:Lrp2	UTSW	2	69,281,726 (GRCm39)	missense	probably damaging	0.99
R5726:Lrp2	UTSW	2	69,339,491 (GRCm39)	missense	probably damaging	1.00
R5743:Lrp2	UTSW	2	69,297,221 (GRCm39)	missense	probably damaging	1.00
R5777:Lrp2	UTSW	2	69,285,869 (GRCm39)	missense	probably damaging	1.00
R5841:Lrp2	UTSW	2	69,310,497 (GRCm39)	missense	probably benign	0.00
R5892:Lrp2	UTSW	2	69,273,120 (GRCm39)	missense	probably benign
R5951:Lrp2	UTSW	2	69,326,667 (GRCm39)	splice site	probably null
R5974:Lrp2	UTSW	2	69,289,892 (GRCm39)	missense	probably damaging	1.00
R5980:Lrp2	UTSW	2	69,365,349 (GRCm39)	missense	probably damaging	1.00
R6046:Lrp2	UTSW	2	69,337,098 (GRCm39)	missense	probably damaging	1.00
R6113:Lrp2	UTSW	2	69,313,901 (GRCm39)	missense	possibly damaging	0.76
R6146:Lrp2	UTSW	2	69,341,345 (GRCm39)	missense	probably benign	0.00
R6177:Lrp2	UTSW	2	69,340,763 (GRCm39)	frame shift	probably null
R6180:Lrp2	UTSW	2	69,333,868 (GRCm39)	missense	possibly damaging	0.85
R6219:Lrp2	UTSW	2	69,299,822 (GRCm39)	missense	probably damaging	1.00
R6228:Lrp2	UTSW	2	69,312,710 (GRCm39)	missense	possibly damaging	0.88
R6265:Lrp2	UTSW	2	69,296,684 (GRCm39)	missense	probably damaging	1.00
R6312:Lrp2	UTSW	2	69,267,025 (GRCm39)	missense	probably damaging	1.00
R6337:Lrp2	UTSW	2	69,268,811 (GRCm39)	missense	probably damaging	1.00
R6376:Lrp2	UTSW	2	69,313,787 (GRCm39)	missense	probably benign	0.02
R6385:Lrp2	UTSW	2	69,326,128 (GRCm39)	missense	probably benign	0.22
R6429:Lrp2	UTSW	2	69,291,631 (GRCm39)	missense	probably damaging	1.00
R6458:Lrp2	UTSW	2	69,335,500 (GRCm39)	missense	probably benign	0.00
R6524:Lrp2	UTSW	2	69,266,983 (GRCm39)	missense	possibly damaging	0.93
R6555:Lrp2	UTSW	2	69,339,647 (GRCm39)	missense	probably benign	0.00
R6594:Lrp2	UTSW	2	69,270,267 (GRCm39)	missense	possibly damaging	0.58
R6599:Lrp2	UTSW	2	69,299,749 (GRCm39)	missense	probably damaging	1.00
R6655:Lrp2	UTSW	2	69,284,202 (GRCm39)	missense	probably benign	0.01
R6718:Lrp2	UTSW	2	69,314,124 (GRCm39)	missense	probably benign	0.09
R6736:Lrp2	UTSW	2	69,278,555 (GRCm39)	missense	probably benign	0.02
R6738:Lrp2	UTSW	2	69,288,832 (GRCm39)	missense	probably damaging	0.97
R6799:Lrp2	UTSW	2	69,314,248 (GRCm39)	missense	probably damaging	1.00
R6846:Lrp2	UTSW	2	69,348,787 (GRCm39)	missense	probably damaging	1.00
R6856:Lrp2	UTSW	2	69,343,612 (GRCm39)	missense	probably damaging	1.00
R6861:Lrp2	UTSW	2	69,343,721 (GRCm39)	missense	possibly damaging	0.77
R6888:Lrp2	UTSW	2	69,354,485 (GRCm39)	missense	probably damaging	0.98
R6897:Lrp2	UTSW	2	69,340,846 (GRCm39)	missense	probably benign
R6902:Lrp2	UTSW	2	69,289,847 (GRCm39)	missense	probably damaging	1.00
R6908:Lrp2	UTSW	2	69,302,709 (GRCm39)	missense	probably damaging	1.00
R6918:Lrp2	UTSW	2	69,319,649 (GRCm39)	missense	probably damaging	1.00
R6989:Lrp2	UTSW	2	69,302,799 (GRCm39)	missense	probably damaging	1.00
R7022:Lrp2	UTSW	2	69,313,552 (GRCm39)	missense	probably damaging	1.00
R7025:Lrp2	UTSW	2	69,313,372 (GRCm39)	missense	possibly damaging	0.90
R7026:Lrp2	UTSW	2	69,352,131 (GRCm39)	missense	probably damaging	0.97
R7138:Lrp2	UTSW	2	69,296,089 (GRCm39)	missense	possibly damaging	0.94
R7145:Lrp2	UTSW	2	69,285,152 (GRCm39)	critical splice donor site	probably null
R7150:Lrp2	UTSW	2	69,318,395 (GRCm39)	missense	probably damaging	0.99
R7165:Lrp2	UTSW	2	69,336,917 (GRCm39)	missense	probably damaging	0.99
R7174:Lrp2	UTSW	2	69,263,416 (GRCm39)	missense	probably benign	0.11
R7204:Lrp2	UTSW	2	69,302,877 (GRCm39)	missense	probably benign	0.25
R7275:Lrp2	UTSW	2	69,289,875 (GRCm39)	nonsense	probably null
R7278:Lrp2	UTSW	2	69,316,696 (GRCm39)	missense	probably damaging	1.00
R7296:Lrp2	UTSW	2	69,312,725 (GRCm39)	missense	probably benign	0.04
R7315:Lrp2	UTSW	2	69,322,166 (GRCm39)	missense	probably damaging	0.98
R7342:Lrp2	UTSW	2	69,309,634 (GRCm39)	missense	possibly damaging	0.95
R7351:Lrp2	UTSW	2	69,278,486 (GRCm39)	missense	probably damaging	1.00
R7352:Lrp2	UTSW	2	69,302,741 (GRCm39)	missense	probably benign	0.04
R7366:Lrp2	UTSW	2	69,314,150 (GRCm39)	missense	probably damaging	1.00
R7373:Lrp2	UTSW	2	69,331,036 (GRCm39)	missense	probably damaging	1.00
R7446:Lrp2	UTSW	2	69,290,018 (GRCm39)	missense	probably damaging	0.99
R7446:Lrp2	UTSW	2	69,262,557 (GRCm39)	missense	probably damaging	1.00
R7451:Lrp2	UTSW	2	69,343,677 (GRCm39)	missense	probably damaging	1.00
R7492:Lrp2	UTSW	2	69,367,925 (GRCm39)	missense	probably damaging	0.99
R7571:Lrp2	UTSW	2	69,346,747 (GRCm39)	missense	probably damaging	1.00
R7638:Lrp2	UTSW	2	69,307,352 (GRCm39)	critical splice donor site	probably null
R7664:Lrp2	UTSW	2	69,337,076 (GRCm39)	missense	probably damaging	1.00
R7686:Lrp2	UTSW	2	69,319,581 (GRCm39)	missense	probably damaging	1.00
R7711:Lrp2	UTSW	2	69,309,687 (GRCm39)	critical splice acceptor site	probably null
R7737:Lrp2	UTSW	2	69,326,782 (GRCm39)	missense	possibly damaging	0.77
R7763:Lrp2	UTSW	2	69,333,732 (GRCm39)	missense	probably damaging	0.99
R7775:Lrp2	UTSW	2	69,331,883 (GRCm39)	missense	possibly damaging	0.74
R7824:Lrp2	UTSW	2	69,331,883 (GRCm39)	missense	possibly damaging	0.74
R7840:Lrp2	UTSW	2	69,295,128 (GRCm39)	missense	probably damaging	0.98
R7878:Lrp2	UTSW	2	69,338,153 (GRCm39)	missense	probably damaging	1.00
R7878:Lrp2	UTSW	2	69,338,154 (GRCm39)	missense	probably damaging	1.00
R7895:Lrp2	UTSW	2	69,288,823 (GRCm39)	missense	probably damaging	0.97
R7898:Lrp2	UTSW	2	69,271,710 (GRCm39)	missense	probably benign	0.00
R7912:Lrp2	UTSW	2	69,259,016 (GRCm39)	missense	probably benign	0.03
R7923:Lrp2	UTSW	2	69,268,732 (GRCm39)	missense	possibly damaging	0.75
R7932:Lrp2	UTSW	2	69,256,371 (GRCm39)	missense	probably benign	0.00
R7940:Lrp2	UTSW	2	69,262,541 (GRCm39)	missense	possibly damaging	0.91
R7954:Lrp2	UTSW	2	69,333,867 (GRCm39)	missense	possibly damaging	0.61
R8007:Lrp2	UTSW	2	69,336,849 (GRCm39)	missense	probably benign	0.02
R8084:Lrp2	UTSW	2	69,339,713 (GRCm39)	missense	probably damaging	0.97
R8087:Lrp2	UTSW	2	69,278,473 (GRCm39)	missense	probably damaging	1.00
R8090:Lrp2	UTSW	2	69,295,089 (GRCm39)	missense	possibly damaging	0.94
R8110:Lrp2	UTSW	2	69,336,797 (GRCm39)	missense	probably benign
R8129:Lrp2	UTSW	2	69,260,624 (GRCm39)	missense	possibly damaging	0.75
R8155:Lrp2	UTSW	2	69,313,342 (GRCm39)	missense	possibly damaging	0.74
R8182:Lrp2	UTSW	2	69,319,673 (GRCm39)	missense	probably damaging	1.00
R8239:Lrp2	UTSW	2	69,311,611 (GRCm39)	nonsense	probably null
R8247:Lrp2	UTSW	2	69,261,431 (GRCm39)	missense	possibly damaging	0.76
R8327:Lrp2	UTSW	2	69,322,268 (GRCm39)	missense	probably damaging	1.00
R8355:Lrp2	UTSW	2	69,346,828 (GRCm39)	missense	probably damaging	0.99
R8404:Lrp2	UTSW	2	69,344,585 (GRCm39)	nonsense	probably null
R8427:Lrp2	UTSW	2	69,281,641 (GRCm39)	missense	probably damaging	0.97
R8463:Lrp2	UTSW	2	69,322,250 (GRCm39)	missense	probably damaging	1.00
R8502:Lrp2	UTSW	2	69,344,585 (GRCm39)	nonsense	probably null
R8529:Lrp2	UTSW	2	69,330,986 (GRCm39)	missense	probably damaging	0.96
R8673:Lrp2	UTSW	2	69,302,804 (GRCm39)	missense	probably damaging	1.00
R8698:Lrp2	UTSW	2	69,288,767 (GRCm39)	missense	probably benign	0.37
R8698:Lrp2	UTSW	2	69,278,583 (GRCm39)	missense	probably benign	0.39
R8708:Lrp2	UTSW	2	69,289,957 (GRCm39)	missense	probably damaging	1.00
R8716:Lrp2	UTSW	2	69,274,138 (GRCm39)	missense	probably benign	0.04
R8723:Lrp2	UTSW	2	69,316,648 (GRCm39)	missense	probably damaging	1.00
R8787:Lrp2	UTSW	2	69,382,745 (GRCm39)	missense	probably damaging	1.00
R8903:Lrp2	UTSW	2	69,379,382 (GRCm39)	missense	possibly damaging	0.68
R8944:Lrp2	UTSW	2	69,341,348 (GRCm39)	missense	probably damaging	1.00
R9069:Lrp2	UTSW	2	69,331,996 (GRCm39)	missense	probably damaging	1.00
R9076:Lrp2	UTSW	2	69,350,260 (GRCm39)	missense	probably benign	0.01
R9155:Lrp2	UTSW	2	69,291,713 (GRCm39)	nonsense	probably null
R9173:Lrp2	UTSW	2	69,299,731 (GRCm39)	missense	probably damaging	1.00
R9254:Lrp2	UTSW	2	69,333,891 (GRCm39)	missense	probably benign	0.09
R9256:Lrp2	UTSW	2	69,341,303 (GRCm39)	missense	probably benign	0.03
R9291:Lrp2	UTSW	2	69,310,379 (GRCm39)	missense	probably damaging	1.00
R9335:Lrp2	UTSW	2	69,258,983 (GRCm39)	missense	probably benign	0.01
R9357:Lrp2	UTSW	2	69,336,917 (GRCm39)	missense	probably damaging	0.99
R9368:Lrp2	UTSW	2	69,357,979 (GRCm39)	missense	probably damaging	0.99
R9453:Lrp2	UTSW	2	69,288,832 (GRCm39)	missense	probably damaging	1.00
R9546:Lrp2	UTSW	2	69,287,165 (GRCm39)	critical splice donor site	probably null
R9554:Lrp2	UTSW	2	69,261,497 (GRCm39)	missense	probably damaging	1.00
R9597:Lrp2	UTSW	2	69,260,703 (GRCm39)	missense	probably benign	0.02
R9601:Lrp2	UTSW	2	69,289,928 (GRCm39)	missense	probably damaging	1.00
R9623:Lrp2	UTSW	2	69,307,423 (GRCm39)	missense	probably benign	0.09
RF016:Lrp2	UTSW	2	69,339,549 (GRCm39)	missense	probably benign
X0011:Lrp2	UTSW	2	69,350,342 (GRCm39)	missense	probably damaging	1.00
X0023:Lrp2	UTSW	2	69,266,944 (GRCm39)	missense	probably damaging	0.99
Z1176:Lrp2	UTSW	2	69,338,225 (GRCm39)	missense	possibly damaging	0.88
Z1176:Lrp2	UTSW	2	69,310,386 (GRCm39)	missense	possibly damaging	0.66
Z1177:Lrp2	UTSW	2	69,326,812 (GRCm39)	missense	probably damaging	1.00
Z1177:Lrp2	UTSW	2	69,302,797 (GRCm39)	missense	probably benign	0.03
Z1177:Lrp2	UTSW	2	69,281,624 (GRCm39)	missense	probably damaging	1.00
Z1177:Lrp2	UTSW	2	69,339,633 (GRCm39)	missense	probably benign	0.00
Z1177:Lrp2	UTSW	2	69,331,985 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCTTGGAAAGGCAGGTTATG -3'
(R):5'- ATGGCAGTCGTTACCCAACTC -3'

Sequencing Primer
(F):5'- GAGGGTCAAAGTGTAAACTTCTC -3'
(R):5'- AACTCCTTATGGCATCACCG -3'

Posted On

2014-09-18