Mutagenetix > Incidental Mutation

Incidental Mutation 'R0226:Lrrc37'

33950

Institutional Source

Beutler Lab

Gene Symbol

Lrrc37

Ensembl Gene

ENSMUSG00000034239

Gene Name

leucine rich repeat containing 37

Synonyms

LOC380730, Gm884

MMRRC Submission

038471-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.154) question?

Stock #

R0226 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

103534577-103621140 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 103603241 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 663 (F663L)

Ref Sequence

ENSEMBL: ENSMUSP00000129662 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000059279] [ENSMUST00000167262]

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000059279
AA Change: F2839L

SMART Domains

Protein: ENSMUSP00000058511
Gene: ENSMUSG00000034239
AA Change: F2839L

Domain	Start	End	E-Value	Type
Pfam:LRRC37	149	223	5.4e-10	PFAM
low complexity region	244	264	N/A	INTRINSIC
low complexity region	298	308	N/A	INTRINSIC
Pfam:LRRC37	335	403	1.9e-14	PFAM
Pfam:LRRC37	419	514	1.2e-8	PFAM
Pfam:LRRC37	565	620	2e-10	PFAM
Pfam:LRRC37	669	739	7.6e-18	PFAM
Pfam:LRRC37	741	792	1.6e-9	PFAM
Pfam:LRRC37	789	860	1.4e-23	PFAM
Pfam:LRRC37	861	914	2.8e-9	PFAM
Pfam:LRRC37	911	983	1.9e-23	PFAM
Pfam:LRRC37	979	1038	1e-8	PFAM
Pfam:LRRC37	1034	1105	2.7e-24	PFAM
Pfam:LRRC37	1105	1158	2.3e-9	PFAM
Pfam:LRRC37	1155	1219	2.4e-17	PFAM
Pfam:LRRC37	1222	1265	9.2e-7	PFAM
Pfam:LRRC37	1263	1330	4.9e-24	PFAM
Pfam:LRRC37	1331	1384	1.4e-10	PFAM
Pfam:LRRC37	1380	1451	4.3e-15	PFAM
Pfam:LRRC37	1487	1558	1.9e-15	PFAM
Pfam:LRRC37	1594	1665	2.9e-18	PFAM
Pfam:LRRC37	1701	1772	5.6e-23	PFAM
Pfam:LRRC37	1808	1910	2.8e-18	PFAM
Pfam:LRRC37	1915	1986	7.2e-17	PFAM
Pfam:LRRC37	2022	2093	4.9e-22	PFAM
Pfam:LRRC37	2129	2200	4.4e-22	PFAM
Pfam:LRRC37	2236	2307	2.1e-21	PFAM
Pfam:LRRC37	2343	2414	3.8e-17	PFAM
Pfam:LRRC37	2449	2519	1.6e-19	PFAM
LRR	2777	2796	3.09e1	SMART
LRR_TYP	2797	2820	2.09e-3	SMART
LRR	2821	2844	4.44e0	SMART
LRR	2848	2872	8.26e1	SMART
low complexity region	2991	3002	N/A	INTRINSIC
low complexity region	3220	3230	N/A	INTRINSIC
low complexity region	3382	3393	N/A	INTRINSIC
Pfam:LRRC37AB_C	3424	3570	7.7e-76	PFAM
low complexity region	3571	3589	N/A	INTRINSIC
low complexity region	3622	3640	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000119578

Predicted Effect

probably benign
Transcript: ENSMUST00000167262
AA Change: F663L

PolyPhen 2 Score 0.082 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000129662
Gene: ENSMUSG00000034239
AA Change: F663L

Domain	Start	End	E-Value	Type
internal_repeat_1	1	70	1.46e-11	PROSPERO
internal_repeat_1	108	290	1.46e-11	PROSPERO
LRR	601	620	3.09e1	SMART
LRR_TYP	621	644	2.09e-3	SMART
LRR	645	668	4.44e0	SMART
LRR	672	696	8.26e1	SMART
low complexity region	815	826	N/A	INTRINSIC
low complexity region	1044	1054	N/A	INTRINSIC
low complexity region	1206	1217	N/A	INTRINSIC
Pfam:LRRC37AB_C	1243	1396	1.2e-92	PFAM
low complexity region	1446	1464	N/A	INTRINSIC

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.4%

Validation Efficiency

100% (98/98)

Allele List at MGI

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700129C05Rik	G	T	14: 59,142,120 (GRCm38)	T54K	possibly damaging	Het
2210408I21Rik	A	T	13: 77,303,425 (GRCm38)	E876V	possibly damaging	Het
Aasdh	A	T	5: 76,902,002 (GRCm38)	L49Q	probably damaging	Het
Abca8b	T	C	11: 109,957,018 (GRCm38)		probably null	Het
Ablim1	A	T	19: 57,043,870 (GRCm38)	L556Q	probably damaging	Het
Afdn	A	G	17: 13,899,146 (GRCm38)	T1700A	probably benign	Het
Agl	G	A	3: 116,752,071 (GRCm38)	R1359C	probably damaging	Het
Agpat3	T	A	10: 78,278,029 (GRCm38)	H275L	possibly damaging	Het
Ahcyl1	A	T	3: 107,670,270 (GRCm38)	C180*	probably null	Het
Aim2	A	G	1: 173,462,333 (GRCm38)		probably benign	Het
Angpt1	T	C	15: 42,468,235 (GRCm38)	N320S	probably benign	Het
Ankrd52	T	A	10: 128,389,858 (GRCm38)		probably null	Het
Ap1g1	C	T	8: 109,855,062 (GRCm38)	S654L	probably benign	Het
Bpifa1	T	A	2: 154,146,057 (GRCm38)	S173R	probably benign	Het
Brd8	T	C	18: 34,603,894 (GRCm38)		probably benign	Het
Btbd9	C	T	17: 30,274,942 (GRCm38)	D492N	possibly damaging	Het
C1qtnf2	A	G	11: 43,490,843 (GRCm38)	T161A	probably benign	Het
Car6	T	C	4: 150,187,508 (GRCm38)	Y228C	probably damaging	Het
Ccdc149	A	G	5: 52,400,217 (GRCm38)	L273P	probably damaging	Het
Cit	G	A	5: 115,984,840 (GRCm38)	R1405Q	probably damaging	Het
Cox17	T	C	16: 38,349,276 (GRCm38)	L48P	probably damaging	Het
Cttn	A	G	7: 144,441,852 (GRCm38)		probably benign	Het
Cyp4f18	T	C	8: 71,989,775 (GRCm38)		probably benign	Het
Dtnbp1	A	G	13: 44,923,193 (GRCm38)	L175P	probably damaging	Het
Efl1	T	C	7: 82,693,011 (GRCm38)		probably benign	Het
Fbn1	C	T	2: 125,320,910 (GRCm38)	R2152Q	possibly damaging	Het
Fignl1	A	T	11: 11,801,061 (GRCm38)	S665T	probably benign	Het
Gm9843	A	T	16: 76,403,561 (GRCm38)		noncoding transcript	Het
Gpr155	C	T	2: 73,367,592 (GRCm38)	V395I	probably benign	Het
Greb1l	T	C	18: 10,522,076 (GRCm38)		probably benign	Het
Hdgfl1	A	T	13: 26,769,996 (GRCm38)	H31Q	probably benign	Het
Heatr1	T	C	13: 12,410,562 (GRCm38)	S628P	probably damaging	Het
Hivep2	A	G	10: 14,129,712 (GRCm38)	T685A	probably benign	Het
Hmgcl	T	G	4: 135,958,728 (GRCm38)	V168G	probably damaging	Het
Itch	T	C	2: 155,199,394 (GRCm38)	I454T	probably benign	Het
Itih2	T	C	2: 10,115,299 (GRCm38)	D309G	possibly damaging	Het
Kcmf1	T	C	6: 72,842,952 (GRCm38)	I304V	probably benign	Het
Kcnh1	G	A	1: 192,276,804 (GRCm38)	W222*	probably null	Het
Kcnh1	G	T	1: 192,276,805 (GRCm38)	W222C	probably damaging	Het
Kif24	T	A	4: 41,414,939 (GRCm38)	K287*	probably null	Het
Lrig3	A	G	10: 125,972,117 (GRCm38)		probably benign	Het
Lrp2	A	T	2: 69,537,563 (GRCm38)	C202S	probably null	Het
Lrrn2	A	G	1: 132,937,820 (GRCm38)	N208D	probably damaging	Het
Mcm5	C	T	8: 75,126,252 (GRCm38)	T664I	possibly damaging	Het
Mfsd10	A	G	5: 34,634,446 (GRCm38)	L365S	probably benign	Het
Mfsd6	A	G	1: 52,658,690 (GRCm38)		probably benign	Het
Mgat4e	A	G	1: 134,541,103 (GRCm38)	V401A	probably benign	Het
Mllt3	C	A	4: 87,840,732 (GRCm38)	V360L	probably benign	Het
Mrm1	G	A	11: 84,819,170 (GRCm38)	A68V	possibly damaging	Het
Myo19	A	G	11: 84,897,732 (GRCm38)		probably benign	Het
Myo3b	A	G	2: 70,217,166 (GRCm38)	T311A	probably benign	Het
Myo5b	T	C	18: 74,742,180 (GRCm38)	F1552L	probably benign	Het
Myo7b	C	T	18: 31,972,896 (GRCm38)	V1353I	probably benign	Het
Myo9b	T	C	8: 71,353,832 (GRCm38)	S1512P	probably damaging	Het
Nanos3	C	T	8: 84,176,134 (GRCm38)	R133Q	probably damaging	Het
Osbpl3	A	G	6: 50,353,008 (GRCm38)	W63R	probably damaging	Het
Pcdh17	T	C	14: 84,448,201 (GRCm38)	S703P	probably damaging	Het
Pclo	T	C	5: 14,765,223 (GRCm38)	I1231T	probably damaging	Het
Pex16	A	C	2: 92,375,687 (GRCm38)		probably benign	Het
Pfkl	T	C	10: 77,992,534 (GRCm38)	N399S	probably benign	Het
Pkhd1l1	G	A	15: 44,526,784 (GRCm38)	R1432K	possibly damaging	Het
Prdm1	T	A	10: 44,456,696 (GRCm38)	T106S	probably benign	Het
Prrc1	A	G	18: 57,363,291 (GRCm38)	M105V	probably benign	Het
Psg26	A	G	7: 18,483,958 (GRCm38)	C12R	possibly damaging	Het
Rnf43	A	T	11: 87,731,437 (GRCm38)	S455C	probably damaging	Het
Ryr2	T	C	13: 11,772,556 (GRCm38)	K977R	probably damaging	Het
Sart1	C	T	19: 5,381,122 (GRCm38)		probably benign	Het
Sec14l5	A	G	16: 5,180,303 (GRCm38)	S509G	probably benign	Het
Sin3b	A	T	8: 72,744,508 (GRCm38)	E361V	probably benign	Het
Slc35e3	C	T	10: 117,740,890 (GRCm38)	E179K	possibly damaging	Het
Sntb2	T	C	8: 107,001,583 (GRCm38)	S388P	probably damaging	Het
Srms	A	G	2: 181,212,382 (GRCm38)	S131P	probably benign	Het
Sting1	A	T	18: 35,739,088 (GRCm38)	F120L	probably benign	Het
Stxbp5	T	C	10: 9,866,698 (GRCm38)		probably benign	Het
Taar2	G	A	10: 23,941,495 (GRCm38)	R311H	probably benign	Het
Taar2	T	C	10: 23,941,063 (GRCm38)	V167A	probably damaging	Het
Thsd7a	A	G	6: 12,321,900 (GRCm38)	Y1516H	possibly damaging	Het
Tlk1	T	A	2: 70,714,169 (GRCm38)		probably benign	Het
Tnfaip3	T	C	10: 19,002,747 (GRCm38)	K771R	probably damaging	Het
Treml1	C	T	17: 48,360,458 (GRCm38)	L124F	probably damaging	Het
Ttn	G	T	2: 76,780,797 (GRCm38)	Q9137K	possibly damaging	Het
Unkl	T	A	17: 25,230,711 (GRCm38)	I469N	probably damaging	Het
Vmn1r173	G	T	7: 23,703,083 (GRCm38)	V248L	possibly damaging	Het
Vps35	T	C	8: 85,273,575 (GRCm38)	Q474R	probably damaging	Het
Wdr17	T	A	8: 54,663,008 (GRCm38)	T580S	probably benign	Het
Xpnpep1	T	C	19: 53,010,152 (GRCm38)	K222E	probably benign	Het
Ylpm1	A	G	12: 85,049,737 (GRCm38)	T1446A	probably benign	Het
Zfp277	A	G	12: 40,364,162 (GRCm38)	L228S	possibly damaging	Het
Zfp941	T	A	7: 140,813,275 (GRCm38)	K57M	probably damaging	Het
Zmpste24	A	T	4: 121,081,209 (GRCm38)	S244R	probably benign	Het

Other mutations in Lrrc37

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00572:Lrrc37	APN	11	103,615,410 (GRCm38)	missense	probably benign	0.01
IGL00576:Lrrc37	APN	11	103,617,386 (GRCm38)	unclassified	probably benign
IGL00813:Lrrc37	APN	11	103,614,498 (GRCm38)	missense	probably benign	0.05
IGL01311:Lrrc37	APN	11	103,534,676 (GRCm38)	missense	unknown
IGL01946:Lrrc37	APN	11	103,612,933 (GRCm38)	missense	probably benign	0.28
IGL02217:Lrrc37	APN	11	103,612,871 (GRCm38)	splice site	probably benign
IGL02556:Lrrc37	APN	11	103,613,283 (GRCm38)	missense	probably benign	0.01
IGL02825:Lrrc37	APN	11	103,617,068 (GRCm38)	unclassified	probably benign
IGL02868:Lrrc37	APN	11	103,615,139 (GRCm38)	missense	probably benign	0.10
IGL02904:Lrrc37	APN	11	103,616,361 (GRCm38)	unclassified	probably benign
IGL03008:Lrrc37	APN	11	103,620,467 (GRCm38)	missense	unknown
IGL03120:Lrrc37	APN	11	103,616,975 (GRCm38)	unclassified	probably benign
IGL03159:Lrrc37	APN	11	103,604,502 (GRCm38)	splice site	probably benign
IGL03181:Lrrc37	APN	11	103,616,416 (GRCm38)	unclassified	probably benign
IGL03202:Lrrc37	APN	11	103,615,373 (GRCm38)	missense	probably benign	0.03
IGL03263:Lrrc37	APN	11	103,613,699 (GRCm38)	missense	possibly damaging	0.86
esteemed	UTSW	11	103,618,830 (GRCm38)	missense	unknown
lauded	UTSW	11	103,613,103 (GRCm38)	missense	possibly damaging	0.62
PIT4486001:Lrrc37	UTSW	11	103,618,201 (GRCm38)	missense	unknown
R0040:Lrrc37	UTSW	11	103,542,990 (GRCm38)	missense	probably damaging	0.99
R0135:Lrrc37	UTSW	11	103,618,047 (GRCm38)	unclassified	probably benign
R0141:Lrrc37	UTSW	11	103,613,686 (GRCm38)	missense	probably damaging	1.00
R0547:Lrrc37	UTSW	11	103,620,164 (GRCm38)	missense	unknown
R0646:Lrrc37	UTSW	11	103,613,160 (GRCm38)	nonsense	probably null
R0685:Lrrc37	UTSW	11	103,616,888 (GRCm38)	unclassified	probably benign
R0732:Lrrc37	UTSW	11	103,619,838 (GRCm38)	missense	unknown
R1015:Lrrc37	UTSW	11	103,545,796 (GRCm38)	missense	probably benign	0.01
R1166:Lrrc37	UTSW	11	103,615,383 (GRCm38)	missense	probably benign	0.21
R1168:Lrrc37	UTSW	11	103,618,950 (GRCm38)	unclassified	probably benign
R1257:Lrrc37	UTSW	11	103,534,641 (GRCm38)	missense	unknown
R1545:Lrrc37	UTSW	11	103,608,919 (GRCm38)	missense	probably benign	0.16
R1570:Lrrc37	UTSW	11	103,609,938 (GRCm38)	missense	possibly damaging	0.76
R1677:Lrrc37	UTSW	11	103,614,942 (GRCm38)	missense	probably benign	0.19
R1703:Lrrc37	UTSW	11	103,540,874 (GRCm38)	missense	probably benign	0.39
R1719:Lrrc37	UTSW	11	103,617,071 (GRCm38)	unclassified	probably benign
R1752:Lrrc37	UTSW	11	103,614,555 (GRCm38)	missense	possibly damaging	0.67
R1870:Lrrc37	UTSW	11	103,620,605 (GRCm38)	missense	unknown
R2155:Lrrc37	UTSW	11	103,620,459 (GRCm38)	missense	unknown
R2191:Lrrc37	UTSW	11	103,618,967 (GRCm38)	unclassified	probably benign
R2271:Lrrc37	UTSW	11	103,614,207 (GRCm38)	missense	possibly damaging	0.53
R2378:Lrrc37	UTSW	11	103,619,711 (GRCm38)	unclassified	probably benign
R2405:Lrrc37	UTSW	11	103,620,984 (GRCm38)	missense	unknown
R2864:Lrrc37	UTSW	11	103,540,918 (GRCm38)	missense	probably benign	0.34
R3011:Lrrc37	UTSW	11	103,613,103 (GRCm38)	missense	possibly damaging	0.62
R3415:Lrrc37	UTSW	11	103,614,609 (GRCm38)	missense	possibly damaging	0.82
R3417:Lrrc37	UTSW	11	103,614,609 (GRCm38)	missense	possibly damaging	0.82
R3835:Lrrc37	UTSW	11	103,620,010 (GRCm38)	missense	unknown
R3974:Lrrc37	UTSW	11	103,619,101 (GRCm38)	unclassified	probably benign
R4019:Lrrc37	UTSW	11	103,615,293 (GRCm38)	missense	probably benign	0.19
R4020:Lrrc37	UTSW	11	103,615,293 (GRCm38)	missense	probably benign	0.19
R4176:Lrrc37	UTSW	11	103,536,600 (GRCm38)	missense	unknown
R4361:Lrrc37	UTSW	11	103,617,501 (GRCm38)	frame shift	probably null
R4418:Lrrc37	UTSW	11	103,618,314 (GRCm38)	unclassified	probably benign
R4633:Lrrc37	UTSW	11	103,619,131 (GRCm38)	unclassified	probably benign
R4693:Lrrc37	UTSW	11	103,619,860 (GRCm38)	missense	unknown
R4758:Lrrc37	UTSW	11	103,614,464 (GRCm38)	missense	possibly damaging	0.48
R4878:Lrrc37	UTSW	11	103,617,891 (GRCm38)	unclassified	probably benign
R4887:Lrrc37	UTSW	11	103,614,872 (GRCm38)	missense	probably benign	0.03
R4944:Lrrc37	UTSW	11	103,613,460 (GRCm38)	missense	possibly damaging	0.68
R4952:Lrrc37	UTSW	11	103,614,207 (GRCm38)	missense	possibly damaging	0.53
R5030:Lrrc37	UTSW	11	103,534,849 (GRCm38)	missense	unknown
R5183:Lrrc37	UTSW	11	103,543,121 (GRCm38)	missense	probably damaging	0.99
R5294:Lrrc37	UTSW	11	103,616,231 (GRCm38)	unclassified	probably benign
R5317:Lrrc37	UTSW	11	103,614,145 (GRCm38)	missense	possibly damaging	0.73
R5334:Lrrc37	UTSW	11	103,613,873 (GRCm38)	missense	probably benign	0.18
R5426:Lrrc37	UTSW	11	103,620,760 (GRCm38)	missense	unknown
R5467:Lrrc37	UTSW	11	103,603,265 (GRCm38)	nonsense	probably null
R5518:Lrrc37	UTSW	11	103,615,253 (GRCm38)	missense	probably benign	0.03
R5634:Lrrc37	UTSW	11	103,542,014 (GRCm38)	missense	possibly damaging	0.95
R5647:Lrrc37	UTSW	11	103,617,474 (GRCm38)	unclassified	probably benign
R5663:Lrrc37	UTSW	11	103,613,123 (GRCm38)	missense	probably benign	0.01
R5668:Lrrc37	UTSW	11	103,617,054 (GRCm38)	unclassified	probably benign
R5763:Lrrc37	UTSW	11	103,613,643 (GRCm38)	missense	probably damaging	0.97
R5829:Lrrc37	UTSW	11	103,541,886 (GRCm38)	missense	possibly damaging	0.95
R5871:Lrrc37	UTSW	11	103,616,454 (GRCm38)	unclassified	probably benign
R5905:Lrrc37	UTSW	11	103,614,255 (GRCm38)	missense	probably damaging	0.98
R5940:Lrrc37	UTSW	11	103,613,886 (GRCm38)	missense	probably benign	0.18
R5964:Lrrc37	UTSW	11	103,542,120 (GRCm38)	missense	possibly damaging	0.92
R5988:Lrrc37	UTSW	11	103,615,896 (GRCm38)	unclassified	probably benign
R5992:Lrrc37	UTSW	11	103,613,792 (GRCm38)	missense	possibly damaging	0.81
R6114:Lrrc37	UTSW	11	103,617,791 (GRCm38)	unclassified	probably benign
R6154:Lrrc37	UTSW	11	103,614,143 (GRCm38)	missense	probably benign	0.33
R6233:Lrrc37	UTSW	11	103,613,388 (GRCm38)	missense	probably damaging	0.98
R6301:Lrrc37	UTSW	11	103,618,930 (GRCm38)	unclassified	probably benign
R6362:Lrrc37	UTSW	11	103,620,652 (GRCm38)	missense	unknown
R6471:Lrrc37	UTSW	11	103,619,622 (GRCm38)	unclassified	probably benign
R6806:Lrrc37	UTSW	11	103,621,124 (GRCm38)	missense	unknown
R6962:Lrrc37	UTSW	11	103,614,300 (GRCm38)	missense	possibly damaging	0.67
R6996:Lrrc37	UTSW	11	103,618,757 (GRCm38)	nonsense	probably null
R7028:Lrrc37	UTSW	11	103,614,537 (GRCm38)	missense	probably benign	0.28
R7034:Lrrc37	UTSW	11	103,615,812 (GRCm38)	unclassified	probably benign
R7036:Lrrc37	UTSW	11	103,615,812 (GRCm38)	unclassified	probably benign
R7113:Lrrc37	UTSW	11	103,618,799 (GRCm38)	missense	unknown
R7405:Lrrc37	UTSW	11	103,615,161 (GRCm38)	missense	probably benign	0.02
R7420:Lrrc37	UTSW	11	103,613,625 (GRCm38)	missense	probably benign	0.11
R7461:Lrrc37	UTSW	11	103,616,290 (GRCm38)	missense	unknown
R7544:Lrrc37	UTSW	11	103,615,448 (GRCm38)	missense	probably benign	0.01
R7613:Lrrc37	UTSW	11	103,616,290 (GRCm38)	missense	unknown
R7711:Lrrc37	UTSW	11	103,614,912 (GRCm38)	missense	probably benign	0.02
R7714:Lrrc37	UTSW	11	103,616,893 (GRCm38)	missense	unknown
R7747:Lrrc37	UTSW	11	103,614,255 (GRCm38)	missense	probably damaging	0.98
R7814:Lrrc37	UTSW	11	103,614,173 (GRCm38)	missense	possibly damaging	0.53
R8053:Lrrc37	UTSW	11	103,604,566 (GRCm38)	missense	unknown
R8063:Lrrc37	UTSW	11	103,542,261 (GRCm38)	missense	unknown
R8116:Lrrc37	UTSW	11	103,543,289 (GRCm38)	missense	unknown
R8124:Lrrc37	UTSW	11	103,620,431 (GRCm38)	missense	unknown
R8141:Lrrc37	UTSW	11	103,621,029 (GRCm38)	missense	unknown
R8163:Lrrc37	UTSW	11	103,615,862 (GRCm38)	missense	unknown
R8270:Lrrc37	UTSW	11	103,543,315 (GRCm38)	missense	unknown
R8348:Lrrc37	UTSW	11	103,620,900 (GRCm38)	missense	unknown
R8362:Lrrc37	UTSW	11	103,615,337 (GRCm38)	missense	probably benign	0.34
R8448:Lrrc37	UTSW	11	103,620,900 (GRCm38)	missense	unknown
R8465:Lrrc37	UTSW	11	103,616,121 (GRCm38)	unclassified	probably benign
R8473:Lrrc37	UTSW	11	103,543,440 (GRCm38)	missense	unknown
R8781:Lrrc37	UTSW	11	103,618,132 (GRCm38)	missense	unknown
R8821:Lrrc37	UTSW	11	103,619,644 (GRCm38)	missense	unknown
R8859:Lrrc37	UTSW	11	103,615,544 (GRCm38)	missense	unknown
R8888:Lrrc37	UTSW	11	103,618,830 (GRCm38)	missense	unknown
R8895:Lrrc37	UTSW	11	103,618,830 (GRCm38)	missense	unknown
R9083:Lrrc37	UTSW	11	103,619,004 (GRCm38)	missense	unknown
R9085:Lrrc37	UTSW	11	103,616,739 (GRCm38)	missense	unknown
R9088:Lrrc37	UTSW	11	103,620,936 (GRCm38)	missense	unknown
R9124:Lrrc37	UTSW	11	103,618,895 (GRCm38)	missense	unknown
R9177:Lrrc37	UTSW	11	103,617,437 (GRCm38)	missense	unknown
R9238:Lrrc37	UTSW	11	103,619,033 (GRCm38)	missense	unknown
R9267:Lrrc37	UTSW	11	103,604,580 (GRCm38)	missense	unknown
R9444:Lrrc37	UTSW	11	103,618,020 (GRCm38)	nonsense	probably null
R9517:Lrrc37	UTSW	11	103,542,590 (GRCm38)	missense	unknown
R9564:Lrrc37	UTSW	11	103,612,996 (GRCm38)	missense	unknown
R9632:Lrrc37	UTSW	11	103,542,426 (GRCm38)	missense	unknown
R9741:Lrrc37	UTSW	11	103,613,429 (GRCm38)	missense	possibly damaging	0.68
Z1176:Lrrc37	UTSW	11	103,613,681 (GRCm38)	missense	probably benign	0.45

Predicted Primers

PCR Primer
(F):5'- GGGTATCAGAAGTCCAGCCACCA -3'
(R):5'- ggttgtgaaaccctgTCCTAGAGAAGT -3'

Sequencing Primer
(F):5'- aacacagccacagcaaaag -3'
(R):5'- cctgTCCTAGAGAAGTAAGATCATTG -3'

Posted On

2013-05-09