Mutagenetix > Incidental Mutation

Incidental Mutation 'R6861:Lrp2'

535491

Institutional Source

Beutler Lab

Gene Symbol

Lrp2

Ensembl Gene

ENSMUSG00000027070

Gene Name

low density lipoprotein receptor-related protein 2

Synonyms

Gp330, D230004K18Rik, b2b1625.2Clo, Megalin

MMRRC Submission

044962-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6861 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

69424340-69586065 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 69513377 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 879 (S879R)

Ref Sequence

ENSEMBL: ENSMUSP00000097628 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080953] [ENSMUST00000100051]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000080953
AA Change: S879R

PolyPhen 2 Score 0.584 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000079752
Gene: ENSMUSG00000027070
AA Change: S879R

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

Predicted Effect

possibly damaging
Transcript: ENSMUST00000100051
AA Change: S879R

PolyPhen 2 Score 0.767 (Sensitivity: 0.85; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000097628
Gene: ENSMUSG00000027070
AA Change: S879R

Domain	Start	End	E-Value	Type
signal peptide	1	25	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	6.18e-10	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

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: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9030624J02Rik	A	G	7: 118,743,675 (GRCm38)	H32R	probably damaging	Het
Adamtsl4	G	A	3: 95,680,884 (GRCm38)	R598C	probably damaging	Het
Adra2a	T	C	19: 54,046,387 (GRCm38)	L58P	probably damaging	Het
Alox5ap	A	G	5: 149,265,117 (GRCm38)	D2G	probably damaging	Het
Arid1b	G	A	17: 5,327,686 (GRCm38)	V1238M	possibly damaging	Het
Bank1	A	G	3: 136,255,003 (GRCm38)	V31A	probably benign	Het
Bptf	G	A	11: 107,062,565 (GRCm38)	T2117M	probably damaging	Het
Cadps	G	A	14: 12,522,401 (GRCm38)	R588*	probably null	Het
Cavin4	A	G	4: 48,672,214 (GRCm38)	I220V	probably benign	Het
Cep192	G	A	18: 67,841,628 (GRCm38)	M1267I	probably benign	Het
Cers5	G	A	15: 99,772,363 (GRCm38)		probably benign	Het
Cfap65	A	T	1: 74,925,115 (GRCm38)	I558N	probably damaging	Het
Cfh	A	T	1: 140,100,883 (GRCm38)	S1025T	probably benign	Het
Cftr	A	G	6: 18,268,108 (GRCm38)	I689V	probably benign	Het
Cgrrf1	T	C	14: 46,832,328 (GRCm38)	I18T	probably damaging	Het
CK137956	A	G	4: 127,970,726 (GRCm38)	S37P	probably damaging	Het
Clca4a	T	C	3: 144,970,655 (GRCm38)	D88G	probably benign	Het
Col11a1	G	A	3: 114,167,492 (GRCm38)	G1166D	probably damaging	Het
Col24a1	G	A	3: 145,460,834 (GRCm38)	G1075S	probably damaging	Het
Crispld2	C	T	8: 120,026,113 (GRCm38)	T299M	probably damaging	Het
Cyb561a3	T	A	19: 10,585,337 (GRCm38)	Y114N	probably damaging	Het
Cyp3a57	T	A	5: 145,370,963 (GRCm38)	W147R	possibly damaging	Het
Dnah2	C	A	11: 69,455,963 (GRCm38)	R2599L	possibly damaging	Het
Dock1	T	A	7: 134,771,478 (GRCm38)	S525T	probably benign	Het
Drc7	T	G	8: 95,062,397 (GRCm38)		probably null	Het
Efhd2	G	T	4: 141,859,881 (GRCm38)		probably null	Het
Epb41l1	A	T	2: 156,525,222 (GRCm38)	E658D	probably benign	Het
Evi5	C	T	5: 107,748,318 (GRCm38)	S753N	probably benign	Het
Exoc3	A	T	13: 74,189,200 (GRCm38)	D427E	probably benign	Het
Fbxw9	A	G	8: 85,066,111 (GRCm38)	D363G	probably damaging	Het
Fcer2a	T	C	8: 3,682,910 (GRCm38)	Y277C	probably damaging	Het
Fstl5	A	T	3: 76,322,216 (GRCm38)	Y108F	probably damaging	Het
Gcn1l1	A	G	5: 115,611,049 (GRCm38)	D1880G	probably benign	Het
Gm4924	T	A	10: 82,379,114 (GRCm38)	Y915*	probably null	Het
Gm996	C	CTCTA	2: 25,579,721 (GRCm38)		probably null	Het
Gpr139	T	A	7: 119,144,652 (GRCm38)	I237F	probably benign	Het
Hao2	A	G	3: 98,877,182 (GRCm38)	L289S	probably damaging	Het
Hexim1	A	G	11: 103,116,967 (GRCm38)	S16G	probably benign	Het
Hmgcs1	T	A	13: 119,699,999 (GRCm38)	M109K	probably damaging	Het
Hs3st4	T	A	7: 124,396,829 (GRCm38)	N239K	possibly damaging	Het
Hsd3b5	T	A	3: 98,622,012 (GRCm38)	N101Y	probably damaging	Het
Idh2	G	A	7: 80,098,218 (GRCm38)	P245S	probably damaging	Het
Irx3	A	G	8: 91,798,902 (GRCm38)		probably benign	Het
Lilra5	A	T	7: 4,241,932 (GRCm38)	D234V	probably benign	Het
Lrfn5	G	A	12: 61,839,690 (GRCm38)	S88N	probably damaging	Het
Lsm11	A	G	11: 45,933,954 (GRCm38)	S249P	probably benign	Het
Ltbp1	C	T	17: 75,227,192 (GRCm38)	A543V	possibly damaging	Het
Mbd1	GTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	GTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC	18: 74,273,574 (GRCm38)			Het
Mier2	C	T	10: 79,541,156 (GRCm38)		probably benign	Het
Mup6	G	C	4: 60,004,093 (GRCm38)	G70A	probably benign	Het
Neb	A	G	2: 52,195,720 (GRCm38)	L5258P	probably damaging	Het
Nlrc5	G	A	8: 94,521,229 (GRCm38)		probably benign	Het
Nr6a1	A	T	2: 38,740,585 (GRCm38)	F207I	possibly damaging	Het
Olfr1385	A	T	11: 49,494,805 (GRCm38)	T91S	probably benign	Het
Olfr181	A	T	16: 58,926,504 (GRCm38)	D22E	probably benign	Het
Olfr902	T	C	9: 38,449,435 (GRCm38)	C188R	probably damaging	Het
Osbp2	A	G	11: 3,715,191 (GRCm38)	V51A	possibly damaging	Het
Papln	G	T	12: 83,774,949 (GRCm38)	C317F	probably damaging	Het
Pdcd7	T	C	9: 65,358,622 (GRCm38)	S454P	probably damaging	Het
Pde4a	C	T	9: 21,205,301 (GRCm38)	T473I	probably damaging	Het
Peg10	C	CCCATCAGGA	6: 4,756,351 (GRCm38)		probably benign	Het
Peg10	CC	CCCCATCAGGC	6: 4,756,350 (GRCm38)		probably benign	Het
Peg3	G	T	7: 6,711,386 (GRCm38)	S279*	probably null	Het
Rbl1	A	G	2: 157,152,967 (GRCm38)	Y929H	probably damaging	Het
Rsf1	G	GACGGCGGCA	7: 97,579,909 (GRCm38)		probably benign	Het
Sall3	C	A	18: 80,974,375 (GRCm38)	E113*	probably null	Het
Scn5a	A	C	9: 119,530,023 (GRCm38)	F653V	probably damaging	Het
Selenok	T	A	14: 29,970,048 (GRCm38)	N14K	possibly damaging	Het
Slc22a20	T	C	19: 5,971,810 (GRCm38)	T426A	probably benign	Het
Slc4a2	T	A	5: 24,435,009 (GRCm38)	S563T	probably damaging	Het
Sspo	T	A	6: 48,487,955 (GRCm38)	S3798T	probably benign	Het
Stag3	G	T	5: 138,304,707 (GRCm38)	R63L	possibly damaging	Het
Stard9	A	T	2: 120,705,186 (GRCm38)	M3975L	probably benign	Het
Syne2	C	A	12: 75,909,266 (GRCm38)	T582K	probably damaging	Het
Synj1	G	A	16: 90,963,880 (GRCm38)	Q748*	probably null	Het
Tas2r109	T	C	6: 132,980,085 (GRCm38)	D294G	probably benign	Het
Tbl1xr1	C	T	3: 22,191,439 (GRCm38)	T203M	possibly damaging	Het
Tbl1xr1	T	A	3: 22,191,539 (GRCm38)		probably null	Het
Tcf7l2	A	G	19: 55,742,523 (GRCm38)	D19G	probably damaging	Het
Tecta	A	G	9: 42,337,337 (GRCm38)	V1923A	possibly damaging	Het
Tg	T	A	15: 66,688,891 (GRCm38)	M1034K	probably benign	Het
Ttf2	T	C	3: 100,969,625 (GRCm38)	E8G	possibly damaging	Het
Vps13b	T	A	15: 35,576,395 (GRCm38)	V983E	probably damaging	Het
Vwa2	T	C	19: 56,901,593 (GRCm38)	V210A	probably benign	Het
Xkr6	T	A	14: 63,819,644 (GRCm38)	Y335N	probably benign	Het
Zfp97	A	G	17: 17,145,175 (GRCm38)	H312R	probably damaging	Het

Other mutations in Lrp2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00094:Lrp2	APN	2	69,507,779 (GRCm38)	missense	probably damaging	1.00
IGL00594:Lrp2	APN	2	69,486,280 (GRCm38)	missense	probably benign	0.00
IGL00782:Lrp2	APN	2	69,501,645 (GRCm38)	missense	probably benign	0.14
IGL00821:Lrp2	APN	2	69,459,516 (GRCm38)	missense	probably damaging	1.00
IGL00897:Lrp2	APN	2	69,521,881 (GRCm38)	missense	possibly damaging	0.86
IGL01065:Lrp2	APN	2	69,469,436 (GRCm38)	missense	possibly damaging	0.94
IGL01087:Lrp2	APN	2	69,524,073 (GRCm38)	missense	probably damaging	1.00
IGL01095:Lrp2	APN	2	69,492,432 (GRCm38)	nonsense	probably null
IGL01131:Lrp2	APN	2	69,499,239 (GRCm38)	missense	probably damaging	1.00
IGL01350:Lrp2	APN	2	69,510,984 (GRCm38)	missense	probably damaging	0.96
IGL01352:Lrp2	APN	2	69,503,526 (GRCm38)	missense	possibly damaging	0.77
IGL01358:Lrp2	APN	2	69,552,470 (GRCm38)	splice site	probably benign
IGL01375:Lrp2	APN	2	69,478,566 (GRCm38)	splice site	probably benign
IGL01384:Lrp2	APN	2	69,483,502 (GRCm38)	missense	probably damaging	1.00
IGL01384:Lrp2	APN	2	69,453,812 (GRCm38)	missense	probably null	1.00
IGL01411:Lrp2	APN	2	69,482,267 (GRCm38)	missense	probably damaging	1.00
IGL01418:Lrp2	APN	2	69,525,286 (GRCm38)	missense	probably benign
IGL01444:Lrp2	APN	2	69,443,716 (GRCm38)	missense	possibly damaging	0.94
IGL01464:Lrp2	APN	2	69,472,439 (GRCm38)	missense	probably damaging	0.98
IGL01528:Lrp2	APN	2	69,492,460 (GRCm38)	missense	probably damaging	1.00
IGL01663:Lrp2	APN	2	69,428,706 (GRCm38)	missense	probably benign
IGL01761:Lrp2	APN	2	69,481,235 (GRCm38)	missense	possibly damaging	0.85
IGL01780:Lrp2	APN	2	69,486,184 (GRCm38)	missense	possibly damaging	0.66
IGL01994:Lrp2	APN	2	69,483,601 (GRCm38)	missense	probably benign	0.08
IGL02015:Lrp2	APN	2	69,527,578 (GRCm38)	missense	probably benign	0.00
IGL02104:Lrp2	APN	2	69,510,418 (GRCm38)	missense	probably damaging	1.00
IGL02132:Lrp2	APN	2	69,537,616 (GRCm38)	missense	probably benign	0.01
IGL02134:Lrp2	APN	2	69,513,379 (GRCm38)	critical splice acceptor site	probably null
IGL02197:Lrp2	APN	2	69,466,880 (GRCm38)	missense	probably benign	0.01
IGL02212:Lrp2	APN	2	69,451,264 (GRCm38)	missense	probably benign	0.00
IGL02240:Lrp2	APN	2	69,535,046 (GRCm38)	missense	probably benign
IGL02248:Lrp2	APN	2	69,482,808 (GRCm38)	missense	probably damaging	1.00
IGL02369:Lrp2	APN	2	69,464,636 (GRCm38)	missense	probably damaging	1.00
IGL02416:Lrp2	APN	2	69,469,633 (GRCm38)	missense	probably damaging	1.00
IGL02417:Lrp2	APN	2	69,461,305 (GRCm38)	missense	probably damaging	1.00
IGL02458:Lrp2	APN	2	69,521,773 (GRCm38)	missense	probably damaging	0.97
IGL02479:Lrp2	APN	2	69,464,801 (GRCm38)	splice site	probably benign
IGL02508:Lrp2	APN	2	69,503,430 (GRCm38)	missense	probably benign	0.04
IGL02751:Lrp2	APN	2	69,533,462 (GRCm38)	missense	possibly damaging	0.56
IGL02814:Lrp2	APN	2	69,506,736 (GRCm38)	missense	probably damaging	1.00
IGL02867:Lrp2	APN	2	69,552,450 (GRCm38)	missense	possibly damaging	0.67
IGL02889:Lrp2	APN	2	69,552,450 (GRCm38)	missense	possibly damaging	0.67
IGL02943:Lrp2	APN	2	69,455,510 (GRCm38)	missense	possibly damaging	0.86
IGL02948:Lrp2	APN	2	69,487,837 (GRCm38)	missense	probably damaging	1.00
IGL02960:Lrp2	APN	2	69,455,453 (GRCm38)	splice site	probably benign
IGL02990:Lrp2	APN	2	69,441,396 (GRCm38)	missense	possibly damaging	0.56
IGL03027:Lrp2	APN	2	69,537,553 (GRCm38)	missense	probably benign	0.43
IGL03038:Lrp2	APN	2	69,475,464 (GRCm38)	missense	probably damaging	0.99
IGL03064:Lrp2	APN	2	69,483,133 (GRCm38)	missense	probably damaging	0.98
IGL03107:Lrp2	APN	2	69,454,833 (GRCm38)	missense	probably damaging	1.00
IGL03141:Lrp2	APN	2	69,477,026 (GRCm38)	missense	probably damaging	0.99
IGL03154:Lrp2	APN	2	69,549,042 (GRCm38)	missense	probably damaging	1.00
IGL03155:Lrp2	APN	2	69,455,452 (GRCm38)	splice site	probably benign
IGL03163:Lrp2	APN	2	69,501,526 (GRCm38)	nonsense	probably null
IGL03164:Lrp2	APN	2	69,464,699 (GRCm38)	missense	probably damaging	1.00
IGL03169:Lrp2	APN	2	69,523,194 (GRCm38)	missense	probably damaging	1.00
IGL03174:Lrp2	APN	2	69,466,265 (GRCm38)	missense	probably damaging	1.00
IGL03189:Lrp2	APN	2	69,438,478 (GRCm38)	splice site	probably benign
IGL03288:Lrp2	APN	2	69,426,039 (GRCm38)	missense	probably benign	0.02
IGL03350:Lrp2	APN	2	69,438,453 (GRCm38)	missense	probably damaging	1.00
IGL03378:Lrp2	APN	2	69,431,152 (GRCm38)	missense	probably damaging	1.00
casual	UTSW	2	69,499,263 (GRCm38)	missense	probably benign
nonchalant	UTSW	2	69,489,329 (GRCm38)	missense	probably damaging	1.00
Presto	UTSW	2	69,459,531 (GRCm38)	nonsense	probably null
relaxed	UTSW	2	69,535,005 (GRCm38)	missense	probably damaging	1.00
unguarded	UTSW	2	69,465,758 (GRCm38)	missense	probably benign	0.00
Unintended	UTSW	2	69,518,443 (GRCm38)	missense	probably damaging	1.00
BB009:Lrp2	UTSW	2	69,426,027 (GRCm38)	missense	probably benign	0.00
BB019:Lrp2	UTSW	2	69,426,027 (GRCm38)	missense	probably benign	0.00
IGL02835:Lrp2	UTSW	2	69,505,304 (GRCm38)	missense	probably damaging	1.00
IGL03055:Lrp2	UTSW	2	69,458,448 (GRCm38)	missense	probably damaging	1.00
PIT4362001:Lrp2	UTSW	2	69,537,538 (GRCm38)	missense	probably damaging	1.00
PIT4504001:Lrp2	UTSW	2	69,475,403 (GRCm38)	missense	probably damaging	1.00
R0008:Lrp2	UTSW	2	69,516,551 (GRCm38)	missense	probably benign	0.42
R0008:Lrp2	UTSW	2	69,516,551 (GRCm38)	missense	probably benign	0.42
R0044:Lrp2	UTSW	2	69,527,555 (GRCm38)	missense	probably benign	0.01
R0044:Lrp2	UTSW	2	69,527,555 (GRCm38)	missense	probably damaging	0.96
R0048:Lrp2	UTSW	2	69,465,627 (GRCm38)	missense	probably damaging	1.00
R0098:Lrp2	UTSW	2	69,475,412 (GRCm38)	missense	probably damaging	1.00
R0098:Lrp2	UTSW	2	69,475,412 (GRCm38)	missense	probably damaging	1.00
R0103:Lrp2	UTSW	2	69,477,040 (GRCm38)	missense	probably benign
R0167:Lrp2	UTSW	2	69,425,658 (GRCm38)	missense	possibly damaging	0.95
R0226:Lrp2	UTSW	2	69,537,563 (GRCm38)	missense	probably null	1.00
R0243:Lrp2	UTSW	2	69,428,630 (GRCm38)	missense	probably benign	0.00
R0308:Lrp2	UTSW	2	69,482,982 (GRCm38)	splice site	probably benign
R0323:Lrp2	UTSW	2	69,469,639 (GRCm38)	missense	probably damaging	1.00
R0372:Lrp2	UTSW	2	69,535,043 (GRCm38)	missense	probably benign	0.10
R0374:Lrp2	UTSW	2	69,430,307 (GRCm38)	missense	probably damaging	1.00
R0391:Lrp2	UTSW	2	69,460,337 (GRCm38)	splice site	probably benign
R0391:Lrp2	UTSW	2	69,456,858 (GRCm38)	missense	probably damaging	0.99
R0395:Lrp2	UTSW	2	69,433,077 (GRCm38)	missense	possibly damaging	0.89
R0401:Lrp2	UTSW	2	69,479,148 (GRCm38)	missense	probably damaging	0.98
R0471:Lrp2	UTSW	2	69,525,234 (GRCm38)	missense	probably damaging	0.97
R0483:Lrp2	UTSW	2	69,507,801 (GRCm38)	missense	probably damaging	0.99
R0502:Lrp2	UTSW	2	69,511,017 (GRCm38)	missense	probably damaging	1.00
R0542:Lrp2	UTSW	2	69,428,654 (GRCm38)	missense	probably benign	0.00
R0544:Lrp2	UTSW	2	69,491,931 (GRCm38)	missense	probably benign	0.18
R0548:Lrp2	UTSW	2	69,537,638 (GRCm38)	splice site	probably benign
R0593:Lrp2	UTSW	2	69,467,006 (GRCm38)	missense	probably benign
R0608:Lrp2	UTSW	2	69,486,243 (GRCm38)	missense	probably benign	0.02
R0633:Lrp2	UTSW	2	69,448,120 (GRCm38)	missense	probably damaging	1.00
R0691:Lrp2	UTSW	2	69,451,380 (GRCm38)	missense	probably benign	0.19
R0718:Lrp2	UTSW	2	69,510,948 (GRCm38)	missense	probably damaging	1.00
R0737:Lrp2	UTSW	2	69,448,169 (GRCm38)	missense	probably damaging	0.96
R0771:Lrp2	UTSW	2	69,507,990 (GRCm38)	missense	probably damaging	1.00
R0784:Lrp2	UTSW	2	69,518,365 (GRCm38)	missense	probably benign	0.32
R0885:Lrp2	UTSW	2	69,482,353 (GRCm38)	missense	possibly damaging	0.75
R0947:Lrp2	UTSW	2	69,487,838 (GRCm38)	missense	probably damaging	1.00
R1235:Lrp2	UTSW	2	69,524,036 (GRCm38)	missense	probably damaging	1.00
R1293:Lrp2	UTSW	2	69,523,302 (GRCm38)	splice site	probably null
R1301:Lrp2	UTSW	2	69,428,604 (GRCm38)	missense	probably damaging	0.98
R1387:Lrp2	UTSW	2	69,456,918 (GRCm38)	missense	probably damaging	1.00
R1459:Lrp2	UTSW	2	69,483,394 (GRCm38)	missense	probably damaging	0.99
R1459:Lrp2	UTSW	2	69,460,477 (GRCm38)	missense	probably damaging	1.00
R1529:Lrp2	UTSW	2	69,523,182 (GRCm38)	missense	probably damaging	1.00
R1543:Lrp2	UTSW	2	69,500,730 (GRCm38)	missense	probably damaging	1.00
R1546:Lrp2	UTSW	2	69,502,610 (GRCm38)	missense	probably damaging	1.00
R1550:Lrp2	UTSW	2	69,502,661 (GRCm38)	missense	possibly damaging	0.74
R1590:Lrp2	UTSW	2	69,466,763 (GRCm38)	critical splice donor site	probably null
R1689:Lrp2	UTSW	2	69,503,529 (GRCm38)	missense	probably benign	0.09
R1693:Lrp2	UTSW	2	69,510,418 (GRCm38)	missense	probably damaging	1.00
R1753:Lrp2	UTSW	2	69,496,489 (GRCm38)	missense	possibly damaging	0.87
R1799:Lrp2	UTSW	2	69,503,530 (GRCm38)	missense	probably benign	0.04
R1834:Lrp2	UTSW	2	69,466,880 (GRCm38)	missense	probably benign	0.01
R1921:Lrp2	UTSW	2	69,523,287 (GRCm38)	missense	probably damaging	1.00
R2000:Lrp2	UTSW	2	69,467,090 (GRCm38)	missense	probably damaging	1.00
R2077:Lrp2	UTSW	2	69,507,843 (GRCm38)	missense	probably damaging	1.00
R2092:Lrp2	UTSW	2	69,536,021 (GRCm38)	missense	probably benign	0.25
R2093:Lrp2	UTSW	2	69,536,021 (GRCm38)	missense	probably benign	0.25
R2108:Lrp2	UTSW	2	69,506,624 (GRCm38)	missense	possibly damaging	0.75
R2117:Lrp2	UTSW	2	69,483,385 (GRCm38)	missense	probably benign	0.05
R2122:Lrp2	UTSW	2	69,483,707 (GRCm38)	missense	probably damaging	1.00
R2134:Lrp2	UTSW	2	69,511,067 (GRCm38)	missense	probably damaging	1.00
R2207:Lrp2	UTSW	2	69,467,028 (GRCm38)	missense	possibly damaging	0.94
R2248:Lrp2	UTSW	2	69,511,010 (GRCm38)	missense	probably damaging	1.00
R2264:Lrp2	UTSW	2	69,482,366 (GRCm38)	missense	possibly damaging	0.88
R2316:Lrp2	UTSW	2	69,491,847 (GRCm38)	missense	possibly damaging	0.75
R2513:Lrp2	UTSW	2	69,506,374 (GRCm38)	splice site	probably null
R2984:Lrp2	UTSW	2	69,425,814 (GRCm38)	splice site	probably null
R3085:Lrp2	UTSW	2	69,467,135 (GRCm38)	missense	probably benign	0.05
R3103:Lrp2	UTSW	2	69,431,984 (GRCm38)	missense	probably benign	0.00
R3727:Lrp2	UTSW	2	69,510,429 (GRCm38)	missense	probably damaging	1.00
R3730:Lrp2	UTSW	2	69,464,579 (GRCm38)	missense	probably damaging	0.99
R3730:Lrp2	UTSW	2	69,534,907 (GRCm38)	critical splice donor site	probably null
R3731:Lrp2	UTSW	2	69,464,579 (GRCm38)	missense	probably damaging	0.99
R3731:Lrp2	UTSW	2	69,534,907 (GRCm38)	critical splice donor site	probably null
R3764:Lrp2	UTSW	2	69,496,336 (GRCm38)	missense	probably damaging	1.00
R3768:Lrp2	UTSW	2	69,505,105 (GRCm38)	missense	probably benign	0.34
R3778:Lrp2	UTSW	2	69,509,204 (GRCm38)	missense	probably benign	0.00
R3808:Lrp2	UTSW	2	69,501,548 (GRCm38)	missense	probably damaging	1.00
R3809:Lrp2	UTSW	2	69,501,548 (GRCm38)	missense	probably damaging	1.00
R3813:Lrp2	UTSW	2	69,464,579 (GRCm38)	missense	probably damaging	0.99
R3828:Lrp2	UTSW	2	69,426,012 (GRCm38)	missense	probably benign	0.03
R3852:Lrp2	UTSW	2	69,537,565 (GRCm38)	missense	probably damaging	0.96
R3877:Lrp2	UTSW	2	69,459,472 (GRCm38)	critical splice donor site	probably null
R3877:Lrp2	UTSW	2	69,549,047 (GRCm38)	missense	probably damaging	1.00
R3922:Lrp2	UTSW	2	69,506,376 (GRCm38)	missense	probably benign
R4081:Lrp2	UTSW	2	69,513,273 (GRCm38)	missense	probably damaging	0.98
R4082:Lrp2	UTSW	2	69,513,273 (GRCm38)	missense	probably damaging	0.98
R4118:Lrp2	UTSW	2	69,430,262 (GRCm38)	critical splice donor site	probably null
R4193:Lrp2	UTSW	2	69,467,143 (GRCm38)	missense	probably damaging	1.00
R4284:Lrp2	UTSW	2	69,480,094 (GRCm38)	missense	possibly damaging	0.95
R4322:Lrp2	UTSW	2	69,425,991 (GRCm38)	nonsense	probably null
R4352:Lrp2	UTSW	2	69,432,182 (GRCm38)	critical splice donor site	probably null
R4407:Lrp2	UTSW	2	69,502,517 (GRCm38)	missense	probably damaging	1.00
R4408:Lrp2	UTSW	2	69,467,169 (GRCm38)	missense	probably benign	0.09
R4416:Lrp2	UTSW	2	69,527,231 (GRCm38)	missense	probably benign	0.18
R4426:Lrp2	UTSW	2	69,506,348 (GRCm38)	missense	probably benign	0.00
R4510:Lrp2	UTSW	2	69,480,062 (GRCm38)	missense	possibly damaging	0.58
R4511:Lrp2	UTSW	2	69,480,062 (GRCm38)	missense	possibly damaging	0.58
R4553:Lrp2	UTSW	2	69,513,285 (GRCm38)	missense	probably benign	0.13
R4591:Lrp2	UTSW	2	69,536,075 (GRCm38)	missense	probably damaging	1.00
R4612:Lrp2	UTSW	2	69,458,427 (GRCm38)	nonsense	probably null
R4622:Lrp2	UTSW	2	69,460,349 (GRCm38)	missense	possibly damaging	0.87
R4632:Lrp2	UTSW	2	69,489,129 (GRCm38)	splice site	probably null
R4633:Lrp2	UTSW	2	69,461,417 (GRCm38)	missense	probably benign	0.16
R4636:Lrp2	UTSW	2	69,436,639 (GRCm38)	missense	possibly damaging	0.93
R4657:Lrp2	UTSW	2	69,466,993 (GRCm38)	missense	probably damaging	1.00
R4667:Lrp2	UTSW	2	69,489,298 (GRCm38)	missense	probably benign	0.02
R4712:Lrp2	UTSW	2	69,506,551 (GRCm38)	missense	probably damaging	1.00
R4713:Lrp2	UTSW	2	69,487,966 (GRCm38)	missense	probably damaging	1.00
R4720:Lrp2	UTSW	2	69,481,173 (GRCm38)	missense	probably damaging	0.99
R4732:Lrp2	UTSW	2	69,533,555 (GRCm38)	missense	probably benign
R4733:Lrp2	UTSW	2	69,533,555 (GRCm38)	missense	probably benign
R4777:Lrp2	UTSW	2	69,482,264 (GRCm38)	missense	probably damaging	1.00
R4779:Lrp2	UTSW	2	69,459,715 (GRCm38)	missense	possibly damaging	0.75
R4786:Lrp2	UTSW	2	69,537,956 (GRCm38)	missense	probably damaging	1.00
R4842:Lrp2	UTSW	2	69,469,411 (GRCm38)	missense	probably benign	0.06
R4845:Lrp2	UTSW	2	69,509,241 (GRCm38)	missense	possibly damaging	0.71
R4846:Lrp2	UTSW	2	69,479,113 (GRCm38)	missense	probably damaging	1.00
R4938:Lrp2	UTSW	2	69,472,368 (GRCm38)	missense	probably damaging	0.98
R4951:Lrp2	UTSW	2	69,535,988 (GRCm38)	missense	probably damaging	1.00
R4990:Lrp2	UTSW	2	69,481,388 (GRCm38)	missense	probably benign	0.01
R5075:Lrp2	UTSW	2	69,465,758 (GRCm38)	missense	probably benign	0.00
R5078:Lrp2	UTSW	2	69,501,530 (GRCm38)	missense	possibly damaging	0.93
R5102:Lrp2	UTSW	2	69,489,158 (GRCm38)	missense	probably damaging	0.98
R5124:Lrp2	UTSW	2	69,501,490 (GRCm38)	missense	probably damaging	0.97
R5131:Lrp2	UTSW	2	69,430,342 (GRCm38)	missense	possibly damaging	0.74
R5141:Lrp2	UTSW	2	69,552,349 (GRCm38)	splice site	probably null
R5223:Lrp2	UTSW	2	69,524,053 (GRCm38)	missense	probably damaging	0.99
R5236:Lrp2	UTSW	2	69,456,819 (GRCm38)	splice site	probably null
R5267:Lrp2	UTSW	2	69,548,978 (GRCm38)	missense	possibly damaging	0.83
R5290:Lrp2	UTSW	2	69,513,354 (GRCm38)	missense	probably damaging	1.00
R5333:Lrp2	UTSW	2	69,525,228 (GRCm38)	missense	probably benign	0.01
R5355:Lrp2	UTSW	2	69,454,838 (GRCm38)	nonsense	probably null
R5356:Lrp2	UTSW	2	69,464,708 (GRCm38)	missense	possibly damaging	0.74
R5369:Lrp2	UTSW	2	69,459,560 (GRCm38)	missense	probably benign	0.04
R5486:Lrp2	UTSW	2	69,437,465 (GRCm38)	missense	probably benign	0.04
R5554:Lrp2	UTSW	2	69,552,424 (GRCm38)	missense	possibly damaging	0.92
R5584:Lrp2	UTSW	2	69,451,288 (GRCm38)	missense	probably damaging	1.00
R5585:Lrp2	UTSW	2	69,464,624 (GRCm38)	missense	possibly damaging	0.77
R5587:Lrp2	UTSW	2	69,499,263 (GRCm38)	missense	probably benign
R5605:Lrp2	UTSW	2	69,523,299 (GRCm38)	missense	probably damaging	1.00
R5637:Lrp2	UTSW	2	69,472,418 (GRCm38)	missense	probably damaging	1.00
R5647:Lrp2	UTSW	2	69,519,914 (GRCm38)	missense	probably null	0.80
R5686:Lrp2	UTSW	2	69,511,061 (GRCm38)	missense	possibly damaging	0.88
R5691:Lrp2	UTSW	2	69,502,553 (GRCm38)	missense	probably damaging	1.00
R5724:Lrp2	UTSW	2	69,451,382 (GRCm38)	missense	probably damaging	0.99
R5726:Lrp2	UTSW	2	69,509,147 (GRCm38)	missense	probably damaging	1.00
R5743:Lrp2	UTSW	2	69,466,877 (GRCm38)	missense	probably damaging	1.00
R5777:Lrp2	UTSW	2	69,455,525 (GRCm38)	missense	probably damaging	1.00
R5841:Lrp2	UTSW	2	69,480,153 (GRCm38)	missense	probably benign	0.00
R5892:Lrp2	UTSW	2	69,442,776 (GRCm38)	missense	probably benign
R5951:Lrp2	UTSW	2	69,496,323 (GRCm38)	splice site	probably null
R5974:Lrp2	UTSW	2	69,459,548 (GRCm38)	missense	probably damaging	1.00
R5980:Lrp2	UTSW	2	69,535,005 (GRCm38)	missense	probably damaging	1.00
R6046:Lrp2	UTSW	2	69,506,754 (GRCm38)	missense	probably damaging	1.00
R6113:Lrp2	UTSW	2	69,483,557 (GRCm38)	missense	possibly damaging	0.76
R6146:Lrp2	UTSW	2	69,511,001 (GRCm38)	missense	probably benign	0.00
R6177:Lrp2	UTSW	2	69,510,419 (GRCm38)	frame shift	probably null
R6180:Lrp2	UTSW	2	69,503,524 (GRCm38)	missense	possibly damaging	0.85
R6219:Lrp2	UTSW	2	69,469,478 (GRCm38)	missense	probably damaging	1.00
R6228:Lrp2	UTSW	2	69,482,366 (GRCm38)	missense	possibly damaging	0.88
R6265:Lrp2	UTSW	2	69,466,340 (GRCm38)	missense	probably damaging	1.00
R6312:Lrp2	UTSW	2	69,436,681 (GRCm38)	missense	probably damaging	1.00
R6337:Lrp2	UTSW	2	69,438,467 (GRCm38)	missense	probably damaging	1.00
R6376:Lrp2	UTSW	2	69,483,443 (GRCm38)	missense	probably benign	0.02
R6385:Lrp2	UTSW	2	69,495,784 (GRCm38)	missense	probably benign	0.22
R6429:Lrp2	UTSW	2	69,461,287 (GRCm38)	missense	probably damaging	1.00
R6458:Lrp2	UTSW	2	69,505,156 (GRCm38)	missense	probably benign	0.00
R6524:Lrp2	UTSW	2	69,436,639 (GRCm38)	missense	possibly damaging	0.93
R6555:Lrp2	UTSW	2	69,509,303 (GRCm38)	missense	probably benign	0.00
R6594:Lrp2	UTSW	2	69,439,923 (GRCm38)	missense	possibly damaging	0.58
R6599:Lrp2	UTSW	2	69,469,405 (GRCm38)	missense	probably damaging	1.00
R6655:Lrp2	UTSW	2	69,453,858 (GRCm38)	missense	probably benign	0.01
R6718:Lrp2	UTSW	2	69,483,780 (GRCm38)	missense	probably benign	0.09
R6736:Lrp2	UTSW	2	69,448,211 (GRCm38)	missense	probably benign	0.02
R6738:Lrp2	UTSW	2	69,458,488 (GRCm38)	missense	probably damaging	0.97
R6799:Lrp2	UTSW	2	69,483,904 (GRCm38)	missense	probably damaging	1.00
R6846:Lrp2	UTSW	2	69,518,443 (GRCm38)	missense	probably damaging	1.00
R6856:Lrp2	UTSW	2	69,513,268 (GRCm38)	missense	probably damaging	1.00
R6888:Lrp2	UTSW	2	69,524,141 (GRCm38)	missense	probably damaging	0.98
R6897:Lrp2	UTSW	2	69,510,502 (GRCm38)	missense	probably benign
R6902:Lrp2	UTSW	2	69,459,503 (GRCm38)	missense	probably damaging	1.00
R6908:Lrp2	UTSW	2	69,472,365 (GRCm38)	missense	probably damaging	1.00
R6918:Lrp2	UTSW	2	69,489,305 (GRCm38)	missense	probably damaging	1.00
R6989:Lrp2	UTSW	2	69,472,455 (GRCm38)	missense	probably damaging	1.00
R7022:Lrp2	UTSW	2	69,483,208 (GRCm38)	missense	probably damaging	1.00
R7025:Lrp2	UTSW	2	69,483,028 (GRCm38)	missense	possibly damaging	0.90
R7026:Lrp2	UTSW	2	69,521,787 (GRCm38)	missense	probably damaging	0.97
R7138:Lrp2	UTSW	2	69,465,745 (GRCm38)	missense	possibly damaging	0.94
R7145:Lrp2	UTSW	2	69,454,808 (GRCm38)	critical splice donor site	probably null
R7150:Lrp2	UTSW	2	69,488,051 (GRCm38)	missense	probably damaging	0.99
R7165:Lrp2	UTSW	2	69,506,573 (GRCm38)	missense	probably damaging	0.99
R7174:Lrp2	UTSW	2	69,433,072 (GRCm38)	missense	probably benign	0.11
R7204:Lrp2	UTSW	2	69,472,533 (GRCm38)	missense	probably benign	0.25
R7275:Lrp2	UTSW	2	69,459,531 (GRCm38)	nonsense	probably null
R7278:Lrp2	UTSW	2	69,486,352 (GRCm38)	missense	probably damaging	1.00
R7296:Lrp2	UTSW	2	69,482,381 (GRCm38)	missense	probably benign	0.04
R7315:Lrp2	UTSW	2	69,491,822 (GRCm38)	missense	probably damaging	0.98
R7342:Lrp2	UTSW	2	69,479,290 (GRCm38)	missense	possibly damaging	0.95
R7351:Lrp2	UTSW	2	69,448,142 (GRCm38)	missense	probably damaging	1.00
R7352:Lrp2	UTSW	2	69,472,397 (GRCm38)	missense	probably benign	0.04
R7366:Lrp2	UTSW	2	69,483,806 (GRCm38)	missense	probably damaging	1.00
R7373:Lrp2	UTSW	2	69,500,692 (GRCm38)	missense	probably damaging	1.00
R7446:Lrp2	UTSW	2	69,459,674 (GRCm38)	missense	probably damaging	0.99
R7446:Lrp2	UTSW	2	69,432,213 (GRCm38)	missense	probably damaging	1.00
R7451:Lrp2	UTSW	2	69,513,333 (GRCm38)	missense	probably damaging	1.00
R7492:Lrp2	UTSW	2	69,537,581 (GRCm38)	missense	probably damaging	0.99
R7571:Lrp2	UTSW	2	69,516,403 (GRCm38)	missense	probably damaging	1.00
R7638:Lrp2	UTSW	2	69,477,008 (GRCm38)	critical splice donor site	probably null
R7664:Lrp2	UTSW	2	69,506,732 (GRCm38)	missense	probably damaging	1.00
R7686:Lrp2	UTSW	2	69,489,237 (GRCm38)	missense	probably damaging	1.00
R7711:Lrp2	UTSW	2	69,479,343 (GRCm38)	critical splice acceptor site	probably null
R7737:Lrp2	UTSW	2	69,496,438 (GRCm38)	missense	possibly damaging	0.77
R7763:Lrp2	UTSW	2	69,503,388 (GRCm38)	missense	probably damaging	0.99
R7775:Lrp2	UTSW	2	69,501,539 (GRCm38)	missense	possibly damaging	0.74
R7824:Lrp2	UTSW	2	69,501,539 (GRCm38)	missense	possibly damaging	0.74
R7840:Lrp2	UTSW	2	69,464,784 (GRCm38)	missense	probably damaging	0.98
R7878:Lrp2	UTSW	2	69,507,809 (GRCm38)	missense	probably damaging	1.00
R7878:Lrp2	UTSW	2	69,507,810 (GRCm38)	missense	probably damaging	1.00
R7895:Lrp2	UTSW	2	69,458,479 (GRCm38)	missense	probably damaging	0.97
R7898:Lrp2	UTSW	2	69,441,366 (GRCm38)	missense	probably benign	0.00
R7912:Lrp2	UTSW	2	69,428,672 (GRCm38)	missense	probably benign	0.03
R7923:Lrp2	UTSW	2	69,438,388 (GRCm38)	missense	possibly damaging	0.75
R7932:Lrp2	UTSW	2	69,426,027 (GRCm38)	missense	probably benign	0.00
R7940:Lrp2	UTSW	2	69,432,197 (GRCm38)	missense	possibly damaging	0.91
R7954:Lrp2	UTSW	2	69,503,523 (GRCm38)	missense	possibly damaging	0.61
R8007:Lrp2	UTSW	2	69,506,505 (GRCm38)	missense	probably benign	0.02
R8084:Lrp2	UTSW	2	69,509,369 (GRCm38)	missense	probably damaging	0.97
R8087:Lrp2	UTSW	2	69,448,129 (GRCm38)	missense	probably damaging	1.00
R8090:Lrp2	UTSW	2	69,464,745 (GRCm38)	missense	possibly damaging	0.94
R8110:Lrp2	UTSW	2	69,506,453 (GRCm38)	missense	probably benign
R8129:Lrp2	UTSW	2	69,430,280 (GRCm38)	missense	possibly damaging	0.75
R8155:Lrp2	UTSW	2	69,482,998 (GRCm38)	missense	possibly damaging	0.74
R8182:Lrp2	UTSW	2	69,489,329 (GRCm38)	missense	probably damaging	1.00
R8239:Lrp2	UTSW	2	69,481,267 (GRCm38)	nonsense	probably null
R8247:Lrp2	UTSW	2	69,431,087 (GRCm38)	missense	possibly damaging	0.76
R8327:Lrp2	UTSW	2	69,491,924 (GRCm38)	missense	probably damaging	1.00
R8355:Lrp2	UTSW	2	69,516,484 (GRCm38)	missense	probably damaging	0.99
R8404:Lrp2	UTSW	2	69,514,241 (GRCm38)	nonsense	probably null
R8427:Lrp2	UTSW	2	69,451,297 (GRCm38)	missense	probably damaging	0.97
R8463:Lrp2	UTSW	2	69,491,906 (GRCm38)	missense	probably damaging	1.00
R8502:Lrp2	UTSW	2	69,514,241 (GRCm38)	nonsense	probably null
R8529:Lrp2	UTSW	2	69,500,642 (GRCm38)	missense	probably damaging	0.96
R8673:Lrp2	UTSW	2	69,472,460 (GRCm38)	missense	probably damaging	1.00
R8698:Lrp2	UTSW	2	69,458,423 (GRCm38)	missense	probably benign	0.37
R8698:Lrp2	UTSW	2	69,448,239 (GRCm38)	missense	probably benign	0.39
R8708:Lrp2	UTSW	2	69,459,613 (GRCm38)	missense	probably damaging	1.00
R8716:Lrp2	UTSW	2	69,443,794 (GRCm38)	missense	probably benign	0.04
R8723:Lrp2	UTSW	2	69,486,304 (GRCm38)	missense	probably damaging	1.00
R8787:Lrp2	UTSW	2	69,552,401 (GRCm38)	missense	probably damaging	1.00
R8903:Lrp2	UTSW	2	69,549,038 (GRCm38)	missense	possibly damaging	0.68
R8944:Lrp2	UTSW	2	69,511,004 (GRCm38)	missense	probably damaging	1.00
R9069:Lrp2	UTSW	2	69,501,652 (GRCm38)	missense	probably damaging	1.00
R9076:Lrp2	UTSW	2	69,519,916 (GRCm38)	missense	probably benign	0.01
R9155:Lrp2	UTSW	2	69,461,369 (GRCm38)	nonsense	probably null
R9173:Lrp2	UTSW	2	69,469,387 (GRCm38)	missense	probably damaging	1.00
R9254:Lrp2	UTSW	2	69,503,547 (GRCm38)	missense	probably benign	0.09
R9256:Lrp2	UTSW	2	69,510,959 (GRCm38)	missense	probably benign	0.03
R9291:Lrp2	UTSW	2	69,480,035 (GRCm38)	missense	probably damaging	1.00
R9335:Lrp2	UTSW	2	69,428,639 (GRCm38)	missense	probably benign	0.01
R9357:Lrp2	UTSW	2	69,506,573 (GRCm38)	missense	probably damaging	0.99
R9368:Lrp2	UTSW	2	69,527,635 (GRCm38)	missense	probably damaging	0.99
R9453:Lrp2	UTSW	2	69,458,488 (GRCm38)	missense	probably damaging	1.00
R9546:Lrp2	UTSW	2	69,456,821 (GRCm38)	critical splice donor site	probably null
R9554:Lrp2	UTSW	2	69,431,153 (GRCm38)	missense	probably damaging	1.00
R9597:Lrp2	UTSW	2	69,430,359 (GRCm38)	missense	probably benign	0.02
R9601:Lrp2	UTSW	2	69,459,584 (GRCm38)	missense	probably damaging	1.00
R9623:Lrp2	UTSW	2	69,477,079 (GRCm38)	missense	probably benign	0.09
RF016:Lrp2	UTSW	2	69,509,205 (GRCm38)	missense	probably benign
X0011:Lrp2	UTSW	2	69,519,998 (GRCm38)	missense	probably damaging	1.00
X0023:Lrp2	UTSW	2	69,436,600 (GRCm38)	missense	probably damaging	0.99
Z1176:Lrp2	UTSW	2	69,507,881 (GRCm38)	missense	possibly damaging	0.88
Z1176:Lrp2	UTSW	2	69,480,042 (GRCm38)	missense	possibly damaging	0.66
Z1177:Lrp2	UTSW	2	69,496,468 (GRCm38)	missense	probably damaging	1.00
Z1177:Lrp2	UTSW	2	69,472,453 (GRCm38)	missense	probably benign	0.03
Z1177:Lrp2	UTSW	2	69,451,280 (GRCm38)	missense	probably damaging	1.00
Z1177:Lrp2	UTSW	2	69,509,289 (GRCm38)	missense	probably benign	0.00
Z1177:Lrp2	UTSW	2	69,501,641 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGGTTCTGTGGCAAACATATACC -3'
(R):5'- AGGGCAGAAGCATGTTTAGTC -3'

Sequencing Primer
(F):5'- GTGGCAAACATATACCTTTTGTTGCC -3'
(R):5'- GTCTATTTCTCAAGGAGGAAACAC -3'

Posted On

2018-09-12