Mutagenetix > Incidental Mutation

Incidental Mutation 'R6190:Lrrc37a'

502496

Institutional Source

Beutler Lab

Gene Symbol

Lrrc37a

Ensembl Gene

ENSMUSG00000078632

Gene Name

leucine rich repeat containing 37A

Synonyms

LOC237954

MMRRC Submission

044330-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.099) question?

Stock #

R6190 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

103341535-103395423 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 103392042 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Lysine at position 1128 (Q1128K)

Ref Sequence

ENSEMBL: ENSMUSP00000121903 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000153273]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000153273
AA Change: Q1128K

PolyPhen 2 Score 0.669 (Sensitivity: 0.86; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000121903
Gene: ENSMUSG00000078632
AA Change: Q1128K

Domain	Start	End	E-Value	Type
Pfam:LRRC37	199	269	2.6e-15	PFAM
low complexity region	313	329	N/A	INTRINSIC
Pfam:LRRC37	363	432	4e-18	PFAM
low complexity region	457	467	N/A	INTRINSIC
low complexity region	480	492	N/A	INTRINSIC
Pfam:LRRC37	550	619	2.1e-21	PFAM
Pfam:LRRC37	637	704	2.9e-12	PFAM
Pfam:LRRC37	780	851	2.5e-12	PFAM
Pfam:LRRC37	1078	1148	2.7e-18	PFAM
Pfam:LRRC37	1149	1190	2.1e-7	PFAM
Pfam:LRRC37	1187	1258	2.5e-25	PFAM
Pfam:LRRC37	1255	1300	2.6e-7	PFAM
Pfam:LRRC37	1299	1370	2.4e-27	PFAM
Pfam:LRRC37	1369	1420	2.9e-8	PFAM
Pfam:LRRC37	1419	1488	1.3e-24	PFAM
Pfam:LRRC37	1509	1578	9.2e-21	PFAM
Pfam:LRRC37	1575	1620	1.7e-6	PFAM
Pfam:LRRC37	1619	1686	1.7e-20	PFAM
Pfam:LRRC37	1690	1736	7e-10	PFAM
Pfam:LRRC37	1733	1799	7.5e-17	PFAM
Pfam:LRRC37	1789	1854	5.1e-12	PFAM
Pfam:LRRC37	1850	1921	4.2e-21	PFAM
Pfam:LRRC37	1915	1969	1.1e-9	PFAM
low complexity region	2143	2167	N/A	INTRINSIC
low complexity region	2185	2209	N/A	INTRINSIC
low complexity region	2228	2249	N/A	INTRINSIC
low complexity region	2262	2274	N/A	INTRINSIC
low complexity region	2284	2297	N/A	INTRINSIC
LRR	2419	2438	3.09e1	SMART
LRR	2439	2462	9.96e-1	SMART
LRR	2463	2486	8.24e0	SMART
LRR	2490	2514	3.18e1	SMART
low complexity region	2535	2547	N/A	INTRINSIC
coiled coil region	2712	2735	N/A	INTRINSIC
low complexity region	2861	2871	N/A	INTRINSIC
low complexity region	2937	2950	N/A	INTRINSIC
Pfam:LRRC37AB_C	3063	3209	1.1e-77	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abat	T	A	16: 8,423,472 (GRCm39)	L224Q	probably damaging	Het
Abcc5	A	G	16: 20,211,529 (GRCm39)	M478T	probably benign	Het
Acot10	T	C	15: 20,665,871 (GRCm39)	D290G	possibly damaging	Het
Actr3b	A	G	5: 26,036,688 (GRCm39)	Q167R	probably benign	Het
Actr8	C	T	14: 29,713,674 (GRCm39)	R565*	probably null	Het
Adcy7	C	T	8: 89,052,358 (GRCm39)		probably null	Het
Adgrb3	C	T	1: 25,459,728 (GRCm39)	V576I	probably benign	Het
Adgrv1	T	A	13: 81,607,882 (GRCm39)		probably null	Het
Adgrv1	A	T	13: 81,672,898 (GRCm39)		probably null	Het
Ak2	A	G	4: 128,892,976 (GRCm39)	D45G	probably damaging	Het
Ak9	C	G	10: 41,298,403 (GRCm39)	Q1489E	unknown	Het
Ak9	A	T	10: 41,298,404 (GRCm39)	Q1489L	unknown	Het
Akap12	C	A	10: 4,306,268 (GRCm39)	S1026Y	possibly damaging	Het
Ankhd1	T	G	18: 36,744,862 (GRCm39)	S601A	possibly damaging	Het
Apba2	A	T	7: 64,389,628 (GRCm39)	E508V	probably damaging	Het
Arhgap18	A	G	10: 26,722,031 (GRCm39)	M1V	probably null	Het
Arhgef10l	G	A	4: 140,270,073 (GRCm39)	T865M	possibly damaging	Het
Bdh1	T	A	16: 31,268,715 (GRCm39)	V150D	probably damaging	Het
Becn1	A	G	11: 101,186,200 (GRCm39)	C135R	probably damaging	Het
C2cd4d	A	G	3: 94,271,226 (GRCm39)	D164G	probably benign	Het
Cacna1e	C	A	1: 154,362,316 (GRCm39)	V424F	possibly damaging	Het
Capn7	C	A	14: 31,085,560 (GRCm39)	T511K	probably benign	Het
Cdc5l	G	A	17: 45,718,943 (GRCm39)	P558S	probably benign	Het
Cep170	T	A	1: 176,609,975 (GRCm39)	H112L	probably damaging	Het
Cfap61	C	T	2: 145,789,053 (GRCm39)	T19M	probably benign	Het
Clca3a1	A	G	3: 144,463,821 (GRCm39)	V152A	probably benign	Het
Cnot10	G	T	9: 114,461,791 (GRCm39)	T24K	probably damaging	Het
Cntnap5b	T	A	1: 100,306,800 (GRCm39)	I839N	possibly damaging	Het
Cyp4f13	A	T	17: 33,148,847 (GRCm39)	D299E	probably damaging	Het
Dclk1	A	G	3: 55,395,232 (GRCm39)	E128G	probably damaging	Het
Dennd1b	T	C	1: 139,061,413 (GRCm39)	I365T	probably damaging	Het
Dgcr8	T	C	16: 18,102,274 (GRCm39)	T3A	probably damaging	Het
Dld	A	C	12: 31,394,847 (GRCm39)	I58S	probably damaging	Het
Dlg5	T	A	14: 24,240,506 (GRCm39)	R248S	probably damaging	Het
Eml2	G	A	7: 18,935,088 (GRCm39)	V432I	probably damaging	Het
Faf1	C	T	4: 109,719,012 (GRCm39)	L373F	probably damaging	Het
Fam171b	C	T	2: 83,707,042 (GRCm39)	T304I	probably benign	Het
Fcgrt	A	T	7: 44,751,622 (GRCm39)		probably null	Het
Gimap9	T	C	6: 48,655,285 (GRCm39)	W291R	probably damaging	Het
Gm4847	G	A	1: 166,457,892 (GRCm39)	A487V	probably damaging	Het
Gria4	T	A	9: 4,420,199 (GRCm39)	I888F	probably benign	Het
Hapln2	T	A	3: 87,930,600 (GRCm39)	I224F	probably damaging	Het
Herc1	T	G	9: 66,283,663 (GRCm39)	L332R	possibly damaging	Het
Hmgxb4	T	C	8: 75,749,927 (GRCm39)	V481A	probably benign	Het
Htr1d	T	C	4: 136,170,109 (GRCm39)	S113P	probably damaging	Het
Ift81	T	C	5: 122,689,163 (GRCm39)	Q651R	probably benign	Het
Il17ra	T	C	6: 120,452,234 (GRCm39)	S199P	probably damaging	Het
Itih2	T	C	2: 10,103,318 (GRCm39)	N723S	probably benign	Het
Jak1	A	T	4: 101,032,325 (GRCm39)	V427E	probably damaging	Het
Krt23	C	T	11: 99,376,584 (GRCm39)	D191N	probably damaging	Het
Lingo1	T	A	9: 56,526,934 (GRCm39)	I552F	possibly damaging	Het
Llgl2	G	A	11: 115,737,812 (GRCm39)	R199Q	probably benign	Het
Lrrc74a	T	C	12: 86,783,263 (GRCm39)	V36A	probably benign	Het
M1ap	T	A	6: 82,980,877 (GRCm39)	D254E	possibly damaging	Het
Mal2	C	T	15: 54,434,794 (GRCm39)		probably benign	Het
Mbnl2	A	G	14: 120,622,833 (GRCm39)	T124A	probably benign	Het
Nfatc1	A	G	18: 80,755,885 (GRCm39)	S33P	probably benign	Het
Nfkbid	A	G	7: 30,125,162 (GRCm39)	N253S	probably damaging	Het
Ngfr	T	A	11: 95,465,267 (GRCm39)	I194F	probably benign	Het
Nhsl1	A	G	10: 18,345,789 (GRCm39)		probably benign	Het
Nol9	T	A	4: 152,125,691 (GRCm39)	I214N	possibly damaging	Het
Or1o3	A	G	17: 37,573,635 (GRCm39)	S307P	probably benign	Het
Or5p56	T	C	7: 107,590,307 (GRCm39)	L245P	probably damaging	Het
Or8k3	T	A	2: 86,058,578 (GRCm39)	T246S	possibly damaging	Het
Pax3	C	T	1: 78,169,186 (GRCm39)	S160N	possibly damaging	Het
Pde3b	A	G	7: 114,122,267 (GRCm39)		probably null	Het
Pde5a	A	C	3: 122,522,956 (GRCm39)	E21A	probably benign	Het
Plcxd1	A	G	5: 110,250,469 (GRCm39)	E270G	probably damaging	Het
Plxna1	T	A	6: 89,333,586 (GRCm39)	K348*	probably null	Het
Pramel34	A	T	5: 93,785,937 (GRCm39)	N114K	probably benign	Het
Prb1b	T	A	6: 132,289,692 (GRCm39)	H44L	unknown	Het
Psg21	G	T	7: 18,388,926 (GRCm39)	D55E	possibly damaging	Het
Rasa1	C	A	13: 85,381,814 (GRCm39)	A493S	probably benign	Het
Raver2	A	G	4: 100,990,814 (GRCm39)	I396V	probably benign	Het
Rpa2	A	G	4: 132,502,331 (GRCm39)	K138E	probably benign	Het
Rsad1	T	C	11: 94,439,062 (GRCm39)	N133D	probably damaging	Het
Rusc1	T	C	3: 88,999,188 (GRCm39)	D198G	probably benign	Het
Samsn1	A	T	16: 75,667,803 (GRCm39)	Y258N	probably damaging	Het
Scap	A	G	9: 110,203,135 (GRCm39)	N270D	probably benign	Het
Shisal2a	A	T	4: 108,225,052 (GRCm39)	I170N	probably damaging	Het
Smpd4	T	C	16: 17,449,877 (GRCm39)	Y200H	probably damaging	Het
Steap2	A	G	5: 5,725,881 (GRCm39)	V381A	probably damaging	Het
Syk	C	T	13: 52,765,089 (GRCm39)	T72I	probably damaging	Het
Tbc1d14	T	C	5: 36,729,228 (GRCm39)	D66G	possibly damaging	Het
Tcp11	A	G	17: 28,290,691 (GRCm39)	Y223H	probably benign	Het
Timm9	A	G	12: 71,173,124 (GRCm39)	S8P	probably benign	Het
Tmpo	T	C	10: 91,000,069 (GRCm39)		probably null	Het
Vezf1	T	C	11: 87,967,012 (GRCm39)	M81T	probably benign	Het
Vipr1	T	A	9: 121,493,719 (GRCm39)	W257R	probably damaging	Het
Vmn1r237	G	A	17: 21,534,556 (GRCm39)	G93D	probably damaging	Het
Vmn2r6	A	G	3: 64,445,424 (GRCm39)	V678A	probably benign	Het
Vmn2r85	T	C	10: 130,261,330 (GRCm39)	T336A	possibly damaging	Het
Xpnpep3	C	A	15: 81,322,300 (GRCm39)	D296E	probably benign	Het
Zfp35	C	A	18: 24,137,118 (GRCm39)	H487Q	probably benign	Het
Zfp606	A	T	7: 12,227,928 (GRCm39)	Y625F	probably damaging	Het
Zfp677	A	G	17: 21,617,530 (GRCm39)	T196A	possibly damaging	Het
Zmym1	T	C	4: 126,941,677 (GRCm39)	I904V	probably damaging	Het

Other mutations in Lrrc37a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00518:Lrrc37a	APN	11	103,391,177 (GRCm39)	missense	probably benign	0.09
IGL01339:Lrrc37a	APN	11	103,388,763 (GRCm39)	missense	unknown
IGL01352:Lrrc37a	APN	11	103,390,181 (GRCm39)	missense	probably benign	0.39
IGL01382:Lrrc37a	APN	11	103,389,581 (GRCm39)	missense	probably damaging	0.99
IGL01395:Lrrc37a	APN	11	103,394,687 (GRCm39)	missense	probably benign	0.24
IGL01645:Lrrc37a	APN	11	103,395,090 (GRCm39)	missense	probably benign	0.01
IGL01925:Lrrc37a	APN	11	103,389,245 (GRCm39)	missense	probably benign	0.01
IGL02006:Lrrc37a	APN	11	103,347,317 (GRCm39)	missense	probably damaging	1.00
IGL02127:Lrrc37a	APN	11	103,395,365 (GRCm39)	missense	probably benign	0.01
IGL02184:Lrrc37a	APN	11	103,388,435 (GRCm39)	missense	unknown
IGL02218:Lrrc37a	APN	11	103,391,207 (GRCm39)	missense	probably benign	0.03
IGL02436:Lrrc37a	APN	11	103,389,003 (GRCm39)	missense	unknown
IGL02487:Lrrc37a	APN	11	103,386,863 (GRCm39)	missense	unknown
IGL02597:Lrrc37a	APN	11	103,395,113 (GRCm39)	missense	probably benign	0.01
IGL02634:Lrrc37a	APN	11	103,389,938 (GRCm39)	missense	probably benign	0.09
IGL02818:Lrrc37a	APN	11	103,392,132 (GRCm39)	missense	possibly damaging	0.47
IGL02829:Lrrc37a	APN	11	103,382,000 (GRCm39)	missense	unknown
IGL02987:Lrrc37a	APN	11	103,391,239 (GRCm39)	missense	probably benign	0.03
IGL03081:Lrrc37a	APN	11	103,347,421 (GRCm39)	missense	unknown
IGL03210:Lrrc37a	APN	11	103,390,331 (GRCm39)	missense	probably benign	0.29
IGL03239:Lrrc37a	APN	11	103,390,233 (GRCm39)	missense	probably benign	0.03
IGL03285:Lrrc37a	APN	11	103,388,499 (GRCm39)	missense	unknown
IGL03296:Lrrc37a	APN	11	103,388,499 (GRCm39)	missense	unknown
IGL03299:Lrrc37a	APN	11	103,388,499 (GRCm39)	missense	unknown
IGL03370:Lrrc37a	APN	11	103,388,499 (GRCm39)	missense	unknown
IGL03390:Lrrc37a	APN	11	103,386,857 (GRCm39)	missense	unknown
Lark	UTSW	11	103,355,180 (GRCm39)	critical splice donor site	probably null
Longspur	UTSW	11	103,393,140 (GRCm39)	missense	probably benign	0.42
F5770:Lrrc37a	UTSW	11	103,346,338 (GRCm39)	missense	possibly damaging	0.95
P0035:Lrrc37a	UTSW	11	103,393,958 (GRCm39)	missense	possibly damaging	0.84
PIT4458001:Lrrc37a	UTSW	11	103,395,338 (GRCm39)	missense	probably benign	0.04
R0112:Lrrc37a	UTSW	11	103,391,739 (GRCm39)	missense	probably benign	0.19
R0194:Lrrc37a	UTSW	11	103,390,616 (GRCm39)	missense	possibly damaging	0.82
R0360:Lrrc37a	UTSW	11	103,391,466 (GRCm39)	missense	possibly damaging	0.89
R0364:Lrrc37a	UTSW	11	103,391,466 (GRCm39)	missense	possibly damaging	0.89
R0395:Lrrc37a	UTSW	11	103,355,221 (GRCm39)	missense	unknown
R0418:Lrrc37a	UTSW	11	103,394,264 (GRCm39)	missense	probably benign	0.03
R0505:Lrrc37a	UTSW	11	103,393,851 (GRCm39)	missense	probably benign	0.10
R0583:Lrrc37a	UTSW	11	103,389,263 (GRCm39)	missense	probably benign	0.01
R1078:Lrrc37a	UTSW	11	103,388,457 (GRCm39)	missense	unknown
R1581:Lrrc37a	UTSW	11	103,347,843 (GRCm39)	nonsense	probably null
R1888:Lrrc37a	UTSW	11	103,389,587 (GRCm39)	missense	probably benign	0.18
R1888:Lrrc37a	UTSW	11	103,389,587 (GRCm39)	missense	probably benign	0.18
R1907:Lrrc37a	UTSW	11	103,347,982 (GRCm39)	missense	unknown
R1982:Lrrc37a	UTSW	11	103,389,792 (GRCm39)	missense	probably benign	0.20
R1991:Lrrc37a	UTSW	11	103,391,087 (GRCm39)	missense	probably benign	0.29
R2017:Lrrc37a	UTSW	11	103,391,951 (GRCm39)	missense	probably benign	0.03
R2103:Lrrc37a	UTSW	11	103,391,087 (GRCm39)	missense	probably benign	0.29
R2110:Lrrc37a	UTSW	11	103,388,648 (GRCm39)	missense	unknown
R2190:Lrrc37a	UTSW	11	103,390,869 (GRCm39)	missense	possibly damaging	0.82
R2252:Lrrc37a	UTSW	11	103,392,293 (GRCm39)	missense	probably benign	0.01
R2253:Lrrc37a	UTSW	11	103,392,293 (GRCm39)	missense	probably benign	0.01
R2894:Lrrc37a	UTSW	11	103,388,690 (GRCm39)	missense	unknown
R2899:Lrrc37a	UTSW	11	103,388,690 (GRCm39)	missense	unknown
R3439:Lrrc37a	UTSW	11	103,388,690 (GRCm39)	missense	unknown
R3899:Lrrc37a	UTSW	11	103,388,372 (GRCm39)	missense	unknown
R3916:Lrrc37a	UTSW	11	103,346,344 (GRCm39)	missense	possibly damaging	0.83
R3921:Lrrc37a	UTSW	11	103,392,296 (GRCm39)	missense	probably benign	0.10
R3977:Lrrc37a	UTSW	11	103,348,430 (GRCm39)	missense	unknown
R4043:Lrrc37a	UTSW	11	103,389,479 (GRCm39)	missense	possibly damaging	0.95
R4077:Lrrc37a	UTSW	11	103,388,808 (GRCm39)	missense	unknown
R4237:Lrrc37a	UTSW	11	103,393,115 (GRCm39)	missense	probably damaging	0.97
R4461:Lrrc37a	UTSW	11	103,355,180 (GRCm39)	critical splice donor site	probably null
R4498:Lrrc37a	UTSW	11	103,392,624 (GRCm39)	missense	probably benign	0.20
R4593:Lrrc37a	UTSW	11	103,389,795 (GRCm39)	missense	possibly damaging	0.64
R4670:Lrrc37a	UTSW	11	103,395,363 (GRCm39)	missense	probably benign	0.10
R4698:Lrrc37a	UTSW	11	103,394,930 (GRCm39)	missense	possibly damaging	0.83
R4750:Lrrc37a	UTSW	11	103,346,306 (GRCm39)	missense	probably benign	0.24
R4805:Lrrc37a	UTSW	11	103,395,135 (GRCm39)	missense	probably benign	0.01
R4940:Lrrc37a	UTSW	11	103,388,438 (GRCm39)	missense	unknown
R4983:Lrrc37a	UTSW	11	103,388,444 (GRCm39)	missense	unknown
R4989:Lrrc37a	UTSW	11	103,347,565 (GRCm39)	missense	unknown
R5046:Lrrc37a	UTSW	11	103,389,066 (GRCm39)	missense	unknown
R5217:Lrrc37a	UTSW	11	103,347,780 (GRCm39)	missense	unknown
R5300:Lrrc37a	UTSW	11	103,347,784 (GRCm39)	missense	unknown
R5509:Lrrc37a	UTSW	11	103,391,361 (GRCm39)	missense	probably benign	0.23
R5550:Lrrc37a	UTSW	11	103,389,003 (GRCm39)	missense	unknown
R5655:Lrrc37a	UTSW	11	103,389,381 (GRCm39)	missense	probably benign	0.28
R5668:Lrrc37a	UTSW	11	103,391,001 (GRCm39)	missense	probably benign	0.03
R5750:Lrrc37a	UTSW	11	103,348,923 (GRCm39)	missense	unknown
R5815:Lrrc37a	UTSW	11	103,394,612 (GRCm39)	missense	probably benign	0.01
R5976:Lrrc37a	UTSW	11	103,389,897 (GRCm39)	missense	possibly damaging	0.73
R5990:Lrrc37a	UTSW	11	103,391,784 (GRCm39)	missense	probably benign	0.19
R6004:Lrrc37a	UTSW	11	103,393,362 (GRCm39)	missense	possibly damaging	0.56
R6019:Lrrc37a	UTSW	11	103,347,422 (GRCm39)	missense	unknown
R6056:Lrrc37a	UTSW	11	103,388,484 (GRCm39)	missense	unknown
R6125:Lrrc37a	UTSW	11	103,392,386 (GRCm39)	missense	probably benign	0.19
R6295:Lrrc37a	UTSW	11	103,388,459 (GRCm39)	missense	unknown
R6320:Lrrc37a	UTSW	11	103,394,877 (GRCm39)	missense	probably benign	0.10
R6354:Lrrc37a	UTSW	11	103,355,213 (GRCm39)	missense	unknown
R6375:Lrrc37a	UTSW	11	103,391,915 (GRCm39)	missense	probably benign	0.19
R6406:Lrrc37a	UTSW	11	103,388,361 (GRCm39)	missense	unknown
R6468:Lrrc37a	UTSW	11	103,351,666 (GRCm39)	missense	unknown
R6490:Lrrc37a	UTSW	11	103,347,486 (GRCm39)	missense	unknown
R6502:Lrrc37a	UTSW	11	103,383,005 (GRCm39)	missense	unknown
R6509:Lrrc37a	UTSW	11	103,395,240 (GRCm39)	missense	probably benign	0.04
R6749:Lrrc37a	UTSW	11	103,392,923 (GRCm39)	missense	probably benign	0.29
R6768:Lrrc37a	UTSW	11	103,390,949 (GRCm39)	missense	probably benign	0.36
R6912:Lrrc37a	UTSW	11	103,348,369 (GRCm39)	missense	unknown
R7081:Lrrc37a	UTSW	11	103,348,781 (GRCm39)	missense	unknown
R7083:Lrrc37a	UTSW	11	103,394,166 (GRCm39)	missense	probably benign	0.03
R7154:Lrrc37a	UTSW	11	103,393,682 (GRCm39)	missense	probably benign	0.03
R7195:Lrrc37a	UTSW	11	103,348,601 (GRCm39)	missense	unknown
R7265:Lrrc37a	UTSW	11	103,389,767 (GRCm39)	missense	probably benign	0.09
R7276:Lrrc37a	UTSW	11	103,347,572 (GRCm39)	missense	unknown
R7362:Lrrc37a	UTSW	11	103,348,335 (GRCm39)	missense	unknown
R7450:Lrrc37a	UTSW	11	103,389,152 (GRCm39)	missense	probably benign	0.01
R7458:Lrrc37a	UTSW	11	103,388,258 (GRCm39)	missense	unknown
R7487:Lrrc37a	UTSW	11	103,389,045 (GRCm39)	missense	unknown
R7535:Lrrc37a	UTSW	11	103,392,683 (GRCm39)	missense	possibly damaging	0.68
R7593:Lrrc37a	UTSW	11	103,391,778 (GRCm39)	missense	probably benign	0.03
R7677:Lrrc37a	UTSW	11	103,390,464 (GRCm39)	missense	probably benign	0.26
R7686:Lrrc37a	UTSW	11	103,389,062 (GRCm39)	missense	unknown
R7694:Lrrc37a	UTSW	11	103,395,204 (GRCm39)	missense	probably benign	0.12
R7696:Lrrc37a	UTSW	11	103,389,263 (GRCm39)	missense	probably benign	0.01
R7717:Lrrc37a	UTSW	11	103,395,126 (GRCm39)	missense	probably benign	0.01
R7736:Lrrc37a	UTSW	11	103,388,285 (GRCm39)	missense	unknown
R7841:Lrrc37a	UTSW	11	103,391,931 (GRCm39)	missense	probably benign	0.03
R7885:Lrrc37a	UTSW	11	103,393,868 (GRCm39)	missense	probably benign	0.01
R7888:Lrrc37a	UTSW	11	103,392,307 (GRCm39)	missense	probably benign	0.19
R7993:Lrrc37a	UTSW	11	103,348,787 (GRCm39)	missense	unknown
R8051:Lrrc37a	UTSW	11	103,393,952 (GRCm39)	missense	possibly damaging	0.48
R8082:Lrrc37a	UTSW	11	103,348,248 (GRCm39)	missense	unknown
R8097:Lrrc37a	UTSW	11	103,394,925 (GRCm39)	missense	probably benign	0.04
R8108:Lrrc37a	UTSW	11	103,393,883 (GRCm39)	missense	probably benign	0.24
R8269:Lrrc37a	UTSW	11	103,388,724 (GRCm39)	missense	unknown
R8311:Lrrc37a	UTSW	11	103,394,247 (GRCm39)	missense	probably benign	0.05
R8403:Lrrc37a	UTSW	11	103,392,411 (GRCm39)	missense	probably benign	0.10
R8408:Lrrc37a	UTSW	11	103,351,635 (GRCm39)	missense	unknown
R8529:Lrrc37a	UTSW	11	103,348,373 (GRCm39)	missense	unknown
R8711:Lrrc37a	UTSW	11	103,388,350 (GRCm39)	nonsense	probably null
R8757:Lrrc37a	UTSW	11	103,348,766 (GRCm39)	missense	unknown
R8759:Lrrc37a	UTSW	11	103,348,766 (GRCm39)	missense	unknown
R8769:Lrrc37a	UTSW	11	103,389,536 (GRCm39)	missense	probably benign	0.10
R8785:Lrrc37a	UTSW	11	103,347,242 (GRCm39)	missense	probably damaging	1.00
R8837:Lrrc37a	UTSW	11	103,394,795 (GRCm39)	missense	probably benign	0.43
R8850:Lrrc37a	UTSW	11	103,393,481 (GRCm39)	missense
R8871:Lrrc37a	UTSW	11	103,347,375 (GRCm39)	missense	unknown
R8894:Lrrc37a	UTSW	11	103,347,449 (GRCm39)	missense	unknown
R8971:Lrrc37a	UTSW	11	103,391,490 (GRCm39)	missense	probably benign	0.19
R8979:Lrrc37a	UTSW	11	103,393,833 (GRCm39)	missense	possibly damaging	0.48
R9012:Lrrc37a	UTSW	11	103,389,978 (GRCm39)	missense	probably benign	0.05
R9047:Lrrc37a	UTSW	11	103,391,375 (GRCm39)	missense	probably damaging	0.97
R9167:Lrrc37a	UTSW	11	103,347,658 (GRCm39)	missense	unknown
R9171:Lrrc37a	UTSW	11	103,393,140 (GRCm39)	missense	probably benign	0.42
R9194:Lrrc37a	UTSW	11	103,391,676 (GRCm39)	missense	probably benign	0.03
R9258:Lrrc37a	UTSW	11	103,393,022 (GRCm39)	missense	probably benign	0.20
R9282:Lrrc37a	UTSW	11	103,391,633 (GRCm39)	missense	probably benign	0.03
R9294:Lrrc37a	UTSW	11	103,395,359 (GRCm39)	missense	probably benign	0.10
R9349:Lrrc37a	UTSW	11	103,388,454 (GRCm39)	missense	unknown
R9560:Lrrc37a	UTSW	11	103,347,420 (GRCm39)	missense	unknown
R9595:Lrrc37a	UTSW	11	103,392,552 (GRCm39)	missense	probably benign	0.01
R9628:Lrrc37a	UTSW	11	103,394,330 (GRCm39)	missense	probably benign	0.03
V7580:Lrrc37a	UTSW	11	103,346,338 (GRCm39)	missense	possibly damaging	0.95
X0018:Lrrc37a	UTSW	11	103,390,370 (GRCm39)	missense	possibly damaging	0.78
Z1176:Lrrc37a	UTSW	11	103,391,920 (GRCm39)	missense	probably benign	0.09
Z1176:Lrrc37a	UTSW	11	103,389,860 (GRCm39)	missense	possibly damaging	0.68
Z1176:Lrrc37a	UTSW	11	103,347,312 (GRCm39)	missense	probably damaging	1.00
Z1177:Lrrc37a	UTSW	11	103,391,346 (GRCm39)	missense	probably benign	0.43
Z1177:Lrrc37a	UTSW	11	103,390,793 (GRCm39)	missense	possibly damaging	0.46
Z1177:Lrrc37a	UTSW	11	103,393,853 (GRCm39)	missense	probably benign	0.20
Z1177:Lrrc37a	UTSW	11	103,391,424 (GRCm39)	missense	probably benign	0.20

Predicted Primers

PCR Primer
(F):5'- GAAGTTCCTCAGGAGTTGGC -3'
(R):5'- AATGTAGGACCATCTCTAGTGC -3'

Sequencing Primer
(F):5'- CCTCAGGAGTTGGCTGTGGAC -3'
(R):5'- TAGGACCATCTCTAGTGCTACAG -3'

Posted On

2018-02-27