Mutagenetix > Incidental Mutation

Incidental Mutation 'V7580:Lrrc37a'

69421

Institutional Source

Beutler Lab

Gene Symbol

Lrrc37a

Ensembl Gene

ENSMUSG00000078632

Gene Name

leucine rich repeat containing 37A

Synonyms

LOC237954

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.124) question?

Stock #

V7580 () of strain stinger

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

103451955-103504597 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 103455512 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Threonine at position 3176 (N3176T)

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: N3176T

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000121903
Gene: ENSMUSG00000078632
AA Change: N3176T

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

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.5%
3x: 99.0%
10x: 97.8%
20x: 96.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb5	T	A	12: 118,886,179 (GRCm38)	M950L	probably benign	Het
Atp6v1h	A	G	1: 5,124,443 (GRCm38)	T282A	possibly damaging	Het
Casp8ap2	C	T	4: 32,639,944 (GRCm38)	H333Y	probably benign	Het
Cd36	ACTGTCTGT	ACTGT	5: 17,820,528 (GRCm38)		probably null	Het
Cfi	T	A	3: 129,854,992 (GRCm38)	I175K	possibly damaging	Het
D630003M21Rik	T	C	2: 158,201,011 (GRCm38)	T870A	probably benign	Het
Dnah12	T	A	14: 26,773,093 (GRCm38)	N1369K	possibly damaging	Het
Dnajc22	T	A	15: 99,101,482 (GRCm38)	Y183N	probably damaging	Het
Erv3	T	C	2: 131,855,926 (GRCm38)	H171R	possibly damaging	Het
Fam221b	T	C	4: 43,665,865 (GRCm38)	T249A	probably benign	Het
Gm10770	T	A	2: 150,179,484 (GRCm38)	K38*	probably null	Het
Gm4787	G	A	12: 81,377,567 (GRCm38)	Q606*	probably null	Het
Izumo4	A	T	10: 80,703,891 (GRCm38)	T155S	probably benign	Het
Kcnb2	A	G	1: 15,710,091 (GRCm38)	I396V	probably benign	Het
Klc1	A	T	12: 111,774,572 (GRCm38)	I161F	probably benign	Het
Lpar5	C	A	6: 125,081,727 (GRCm38)	A137E	possibly damaging	Het
Lrp4	C	T	2: 91,488,518 (GRCm38)	S900L	possibly damaging	Het
Med20	G	A	17: 47,618,832 (GRCm38)	V65M	probably damaging	Het
Mylk	G	T	16: 34,995,204 (GRCm38)		probably null	Het
Numbl	T	C	7: 27,279,602 (GRCm38)	S379P	probably benign	Het
Olfr1406	G	T	1: 173,183,964 (GRCm38)	L157I	probably benign	Het
Olfr1440	G	A	19: 12,394,550 (GRCm38)	V96I	probably benign	Het
Otop3	T	A	11: 115,344,838 (GRCm38)	L432Q	probably damaging	Het
Papln	C	T	12: 83,778,834 (GRCm38)	R608C	possibly damaging	Het
Pelp1	T	A	11: 70,398,150 (GRCm38)	T257S	probably damaging	Het
Pigx	T	C	16: 32,087,422 (GRCm38)	D129G	probably damaging	Het
Pik3cd	A	C	4: 149,657,319 (GRCm38)	L390R	probably damaging	Het
Plekhb1	T	C	7: 100,654,618 (GRCm38)	T112A	probably benign	Het
Ppwd1	A	G	13: 104,220,237 (GRCm38)	Y257H	probably damaging	Het
Recql4	T	C	15: 76,706,169 (GRCm38)	D705G	possibly damaging	Het
Ror1	A	G	4: 100,440,933 (GRCm38)	Q501R	probably damaging	Het
Slc30a4	T	A	2: 122,689,538 (GRCm38)	M136L	probably benign	Het
Spaca1	T	C	4: 34,039,311 (GRCm38)	E192G	probably damaging	Het
Spata31	C	A	13: 64,921,648 (GRCm38)	P537T	probably benign	Het
Sptbn2	C	T	19: 4,750,632 (GRCm38)	R2292C	probably damaging	Het
Tnrc6c	G	A	11: 117,723,326 (GRCm38)	R770H	probably damaging	Het
Trps1	T	C	15: 50,831,577 (GRCm38)	K150E	probably damaging	Het
Tspyl3	A	G	2: 153,225,060 (GRCm38)	V86A	probably benign	Het
Zfp292	C	T	4: 34,806,783 (GRCm38)	C2087Y	possibly damaging	Het
Zmynd8	G	A	2: 165,812,394 (GRCm38)	R724*	probably null	Het

Other mutations in Lrrc37a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00518:Lrrc37a	APN	11	103,500,351 (GRCm38)	missense	probably benign	0.09
IGL01339:Lrrc37a	APN	11	103,497,937 (GRCm38)	missense	unknown
IGL01352:Lrrc37a	APN	11	103,499,355 (GRCm38)	missense	probably benign	0.39
IGL01382:Lrrc37a	APN	11	103,498,755 (GRCm38)	missense	probably damaging	0.99
IGL01395:Lrrc37a	APN	11	103,503,861 (GRCm38)	missense	probably benign	0.24
IGL01645:Lrrc37a	APN	11	103,504,264 (GRCm38)	missense	probably benign	0.01
IGL01925:Lrrc37a	APN	11	103,498,419 (GRCm38)	missense	probably benign	0.01
IGL02006:Lrrc37a	APN	11	103,456,491 (GRCm38)	missense	probably damaging	1.00
IGL02127:Lrrc37a	APN	11	103,504,539 (GRCm38)	missense	probably benign	0.01
IGL02184:Lrrc37a	APN	11	103,497,609 (GRCm38)	missense	unknown
IGL02218:Lrrc37a	APN	11	103,500,381 (GRCm38)	missense	probably benign	0.03
IGL02436:Lrrc37a	APN	11	103,498,177 (GRCm38)	missense	unknown
IGL02487:Lrrc37a	APN	11	103,496,037 (GRCm38)	missense	unknown
IGL02597:Lrrc37a	APN	11	103,504,287 (GRCm38)	missense	probably benign	0.01
IGL02634:Lrrc37a	APN	11	103,499,112 (GRCm38)	missense	probably benign	0.09
IGL02818:Lrrc37a	APN	11	103,501,306 (GRCm38)	missense	possibly damaging	0.47
IGL02829:Lrrc37a	APN	11	103,491,174 (GRCm38)	missense	unknown
IGL02987:Lrrc37a	APN	11	103,500,413 (GRCm38)	missense	probably benign	0.03
IGL03081:Lrrc37a	APN	11	103,456,595 (GRCm38)	missense	unknown
IGL03210:Lrrc37a	APN	11	103,499,505 (GRCm38)	missense	probably benign	0.29
IGL03239:Lrrc37a	APN	11	103,499,407 (GRCm38)	missense	probably benign	0.03
IGL03285:Lrrc37a	APN	11	103,497,673 (GRCm38)	missense	unknown
IGL03296:Lrrc37a	APN	11	103,497,673 (GRCm38)	missense	unknown
IGL03299:Lrrc37a	APN	11	103,497,673 (GRCm38)	missense	unknown
IGL03370:Lrrc37a	APN	11	103,497,673 (GRCm38)	missense	unknown
IGL03390:Lrrc37a	APN	11	103,496,031 (GRCm38)	missense	unknown
Lark	UTSW	11	103,464,354 (GRCm38)	critical splice donor site	probably null
Longspur	UTSW	11	103,502,314 (GRCm38)	missense	probably benign	0.42
F5770:Lrrc37a	UTSW	11	103,455,512 (GRCm38)	missense	possibly damaging	0.95
P0035:Lrrc37a	UTSW	11	103,503,132 (GRCm38)	missense	possibly damaging	0.84
PIT4458001:Lrrc37a	UTSW	11	103,504,512 (GRCm38)	missense	probably benign	0.04
R0112:Lrrc37a	UTSW	11	103,500,913 (GRCm38)	missense	probably benign	0.19
R0194:Lrrc37a	UTSW	11	103,499,790 (GRCm38)	missense	possibly damaging	0.82
R0360:Lrrc37a	UTSW	11	103,500,640 (GRCm38)	missense	possibly damaging	0.89
R0364:Lrrc37a	UTSW	11	103,500,640 (GRCm38)	missense	possibly damaging	0.89
R0395:Lrrc37a	UTSW	11	103,464,395 (GRCm38)	missense	unknown
R0418:Lrrc37a	UTSW	11	103,503,438 (GRCm38)	missense	probably benign	0.03
R0505:Lrrc37a	UTSW	11	103,503,025 (GRCm38)	missense	probably benign	0.10
R0583:Lrrc37a	UTSW	11	103,498,437 (GRCm38)	missense	probably benign	0.01
R1078:Lrrc37a	UTSW	11	103,497,631 (GRCm38)	missense	unknown
R1581:Lrrc37a	UTSW	11	103,457,017 (GRCm38)	nonsense	probably null
R1888:Lrrc37a	UTSW	11	103,498,761 (GRCm38)	missense	probably benign	0.18
R1888:Lrrc37a	UTSW	11	103,498,761 (GRCm38)	missense	probably benign	0.18
R1907:Lrrc37a	UTSW	11	103,457,156 (GRCm38)	missense	unknown
R1982:Lrrc37a	UTSW	11	103,498,966 (GRCm38)	missense	probably benign	0.20
R1991:Lrrc37a	UTSW	11	103,500,261 (GRCm38)	missense	probably benign	0.29
R2017:Lrrc37a	UTSW	11	103,501,125 (GRCm38)	missense	probably benign	0.03
R2103:Lrrc37a	UTSW	11	103,500,261 (GRCm38)	missense	probably benign	0.29
R2110:Lrrc37a	UTSW	11	103,497,822 (GRCm38)	missense	unknown
R2190:Lrrc37a	UTSW	11	103,500,043 (GRCm38)	missense	possibly damaging	0.82
R2252:Lrrc37a	UTSW	11	103,501,467 (GRCm38)	missense	probably benign	0.01
R2253:Lrrc37a	UTSW	11	103,501,467 (GRCm38)	missense	probably benign	0.01
R2894:Lrrc37a	UTSW	11	103,497,864 (GRCm38)	missense	unknown
R2899:Lrrc37a	UTSW	11	103,497,864 (GRCm38)	missense	unknown
R3439:Lrrc37a	UTSW	11	103,497,864 (GRCm38)	missense	unknown
R3899:Lrrc37a	UTSW	11	103,497,546 (GRCm38)	missense	unknown
R3916:Lrrc37a	UTSW	11	103,455,518 (GRCm38)	missense	possibly damaging	0.83
R3921:Lrrc37a	UTSW	11	103,501,470 (GRCm38)	missense	probably benign	0.10
R3977:Lrrc37a	UTSW	11	103,457,604 (GRCm38)	missense	unknown
R4043:Lrrc37a	UTSW	11	103,498,653 (GRCm38)	missense	possibly damaging	0.95
R4077:Lrrc37a	UTSW	11	103,497,982 (GRCm38)	missense	unknown
R4237:Lrrc37a	UTSW	11	103,502,289 (GRCm38)	missense	probably damaging	0.97
R4461:Lrrc37a	UTSW	11	103,464,354 (GRCm38)	critical splice donor site	probably null
R4498:Lrrc37a	UTSW	11	103,501,798 (GRCm38)	missense	probably benign	0.20
R4593:Lrrc37a	UTSW	11	103,498,969 (GRCm38)	missense	possibly damaging	0.64
R4670:Lrrc37a	UTSW	11	103,504,537 (GRCm38)	missense	probably benign	0.10
R4698:Lrrc37a	UTSW	11	103,504,104 (GRCm38)	missense	possibly damaging	0.83
R4750:Lrrc37a	UTSW	11	103,455,480 (GRCm38)	missense	probably benign	0.24
R4805:Lrrc37a	UTSW	11	103,504,309 (GRCm38)	missense	probably benign	0.01
R4940:Lrrc37a	UTSW	11	103,497,612 (GRCm38)	missense	unknown
R4983:Lrrc37a	UTSW	11	103,497,618 (GRCm38)	missense	unknown
R4989:Lrrc37a	UTSW	11	103,456,739 (GRCm38)	missense	unknown
R5046:Lrrc37a	UTSW	11	103,498,240 (GRCm38)	missense	unknown
R5217:Lrrc37a	UTSW	11	103,456,954 (GRCm38)	missense	unknown
R5300:Lrrc37a	UTSW	11	103,456,958 (GRCm38)	missense	unknown
R5509:Lrrc37a	UTSW	11	103,500,535 (GRCm38)	missense	probably benign	0.23
R5550:Lrrc37a	UTSW	11	103,498,177 (GRCm38)	missense	unknown
R5655:Lrrc37a	UTSW	11	103,498,555 (GRCm38)	missense	probably benign	0.28
R5668:Lrrc37a	UTSW	11	103,500,175 (GRCm38)	missense	probably benign	0.03
R5750:Lrrc37a	UTSW	11	103,458,097 (GRCm38)	missense	unknown
R5815:Lrrc37a	UTSW	11	103,503,786 (GRCm38)	missense	probably benign	0.01
R5976:Lrrc37a	UTSW	11	103,499,071 (GRCm38)	missense	possibly damaging	0.73
R5990:Lrrc37a	UTSW	11	103,500,958 (GRCm38)	missense	probably benign	0.19
R6004:Lrrc37a	UTSW	11	103,502,536 (GRCm38)	missense	possibly damaging	0.56
R6019:Lrrc37a	UTSW	11	103,456,596 (GRCm38)	missense	unknown
R6056:Lrrc37a	UTSW	11	103,497,658 (GRCm38)	missense	unknown
R6125:Lrrc37a	UTSW	11	103,501,560 (GRCm38)	missense	probably benign	0.19
R6190:Lrrc37a	UTSW	11	103,501,216 (GRCm38)	missense	possibly damaging	0.67
R6295:Lrrc37a	UTSW	11	103,497,633 (GRCm38)	missense	unknown
R6320:Lrrc37a	UTSW	11	103,504,051 (GRCm38)	missense	probably benign	0.10
R6354:Lrrc37a	UTSW	11	103,464,387 (GRCm38)	missense	unknown
R6375:Lrrc37a	UTSW	11	103,501,089 (GRCm38)	missense	probably benign	0.19
R6406:Lrrc37a	UTSW	11	103,497,535 (GRCm38)	missense	unknown
R6468:Lrrc37a	UTSW	11	103,460,840 (GRCm38)	missense	unknown
R6490:Lrrc37a	UTSW	11	103,456,660 (GRCm38)	missense	unknown
R6502:Lrrc37a	UTSW	11	103,492,179 (GRCm38)	missense	unknown
R6509:Lrrc37a	UTSW	11	103,504,414 (GRCm38)	missense	probably benign	0.04
R6749:Lrrc37a	UTSW	11	103,502,097 (GRCm38)	missense	probably benign	0.29
R6768:Lrrc37a	UTSW	11	103,500,123 (GRCm38)	missense	probably benign	0.36
R6912:Lrrc37a	UTSW	11	103,457,543 (GRCm38)	missense	unknown
R7081:Lrrc37a	UTSW	11	103,457,955 (GRCm38)	missense	unknown
R7083:Lrrc37a	UTSW	11	103,503,340 (GRCm38)	missense	probably benign	0.03
R7154:Lrrc37a	UTSW	11	103,502,856 (GRCm38)	missense	probably benign	0.03
R7195:Lrrc37a	UTSW	11	103,457,775 (GRCm38)	missense	unknown
R7265:Lrrc37a	UTSW	11	103,498,941 (GRCm38)	missense	probably benign	0.09
R7276:Lrrc37a	UTSW	11	103,456,746 (GRCm38)	missense	unknown
R7362:Lrrc37a	UTSW	11	103,457,509 (GRCm38)	missense	unknown
R7450:Lrrc37a	UTSW	11	103,498,326 (GRCm38)	missense	probably benign	0.01
R7458:Lrrc37a	UTSW	11	103,497,432 (GRCm38)	missense	unknown
R7487:Lrrc37a	UTSW	11	103,498,219 (GRCm38)	missense	unknown
R7535:Lrrc37a	UTSW	11	103,501,857 (GRCm38)	missense	possibly damaging	0.68
R7593:Lrrc37a	UTSW	11	103,500,952 (GRCm38)	missense	probably benign	0.03
R7677:Lrrc37a	UTSW	11	103,499,638 (GRCm38)	missense	probably benign	0.26
R7686:Lrrc37a	UTSW	11	103,498,236 (GRCm38)	missense	unknown
R7694:Lrrc37a	UTSW	11	103,504,378 (GRCm38)	missense	probably benign	0.12
R7696:Lrrc37a	UTSW	11	103,498,437 (GRCm38)	missense	probably benign	0.01
R7717:Lrrc37a	UTSW	11	103,504,300 (GRCm38)	missense	probably benign	0.01
R7736:Lrrc37a	UTSW	11	103,497,459 (GRCm38)	missense	unknown
R7841:Lrrc37a	UTSW	11	103,501,105 (GRCm38)	missense	probably benign	0.03
R7885:Lrrc37a	UTSW	11	103,503,042 (GRCm38)	missense	probably benign	0.01
R7888:Lrrc37a	UTSW	11	103,501,481 (GRCm38)	missense	probably benign	0.19
R7993:Lrrc37a	UTSW	11	103,457,961 (GRCm38)	missense	unknown
R8051:Lrrc37a	UTSW	11	103,503,126 (GRCm38)	missense	possibly damaging	0.48
R8082:Lrrc37a	UTSW	11	103,457,422 (GRCm38)	missense	unknown
R8097:Lrrc37a	UTSW	11	103,504,099 (GRCm38)	missense	probably benign	0.04
R8108:Lrrc37a	UTSW	11	103,503,057 (GRCm38)	missense	probably benign	0.24
R8269:Lrrc37a	UTSW	11	103,497,898 (GRCm38)	missense	unknown
R8311:Lrrc37a	UTSW	11	103,503,421 (GRCm38)	missense	probably benign	0.05
R8403:Lrrc37a	UTSW	11	103,501,585 (GRCm38)	missense	probably benign	0.10
R8408:Lrrc37a	UTSW	11	103,460,809 (GRCm38)	missense	unknown
R8529:Lrrc37a	UTSW	11	103,457,547 (GRCm38)	missense	unknown
R8711:Lrrc37a	UTSW	11	103,497,524 (GRCm38)	nonsense	probably null
R8757:Lrrc37a	UTSW	11	103,457,940 (GRCm38)	missense	unknown
R8759:Lrrc37a	UTSW	11	103,457,940 (GRCm38)	missense	unknown
R8769:Lrrc37a	UTSW	11	103,498,710 (GRCm38)	missense	probably benign	0.10
R8785:Lrrc37a	UTSW	11	103,456,416 (GRCm38)	missense	probably damaging	1.00
R8837:Lrrc37a	UTSW	11	103,503,969 (GRCm38)	missense	probably benign	0.43
R8850:Lrrc37a	UTSW	11	103,502,655 (GRCm38)	missense
R8871:Lrrc37a	UTSW	11	103,456,549 (GRCm38)	missense	unknown
R8894:Lrrc37a	UTSW	11	103,456,623 (GRCm38)	missense	unknown
R8971:Lrrc37a	UTSW	11	103,500,664 (GRCm38)	missense	probably benign	0.19
R8979:Lrrc37a	UTSW	11	103,503,007 (GRCm38)	missense	possibly damaging	0.48
R9012:Lrrc37a	UTSW	11	103,499,152 (GRCm38)	missense	probably benign	0.05
R9047:Lrrc37a	UTSW	11	103,500,549 (GRCm38)	missense	probably damaging	0.97
R9167:Lrrc37a	UTSW	11	103,456,832 (GRCm38)	missense	unknown
R9171:Lrrc37a	UTSW	11	103,502,314 (GRCm38)	missense	probably benign	0.42
R9194:Lrrc37a	UTSW	11	103,500,850 (GRCm38)	missense	probably benign	0.03
R9258:Lrrc37a	UTSW	11	103,502,196 (GRCm38)	missense	probably benign	0.20
R9282:Lrrc37a	UTSW	11	103,500,807 (GRCm38)	missense	probably benign	0.03
R9294:Lrrc37a	UTSW	11	103,504,533 (GRCm38)	missense	probably benign	0.10
R9349:Lrrc37a	UTSW	11	103,497,628 (GRCm38)	missense	unknown
R9560:Lrrc37a	UTSW	11	103,456,594 (GRCm38)	missense	unknown
R9595:Lrrc37a	UTSW	11	103,501,726 (GRCm38)	missense	probably benign	0.01
R9628:Lrrc37a	UTSW	11	103,503,504 (GRCm38)	missense	probably benign	0.03
X0018:Lrrc37a	UTSW	11	103,499,544 (GRCm38)	missense	possibly damaging	0.78
Z1176:Lrrc37a	UTSW	11	103,501,094 (GRCm38)	missense	probably benign	0.09
Z1176:Lrrc37a	UTSW	11	103,499,034 (GRCm38)	missense	possibly damaging	0.68
Z1176:Lrrc37a	UTSW	11	103,456,486 (GRCm38)	missense	probably damaging	1.00
Z1177:Lrrc37a	UTSW	11	103,500,520 (GRCm38)	missense	probably benign	0.43
Z1177:Lrrc37a	UTSW	11	103,499,967 (GRCm38)	missense	possibly damaging	0.46
Z1177:Lrrc37a	UTSW	11	103,503,027 (GRCm38)	missense	probably benign	0.20
Z1177:Lrrc37a	UTSW	11	103,500,598 (GRCm38)	missense	probably benign	0.20

Predicted Primers

PCR Primer
(F):5'- ATCGAGGAGACATGCTTCCCAGAC -3'
(R):5'- CAAATTCATGGCGGCCTTCTTCAC -3'

Sequencing Primer
(F):5'- ACACGGGGACATCACTTG -3'
(R):5'- GGCCTTCTTCACTTCCCATAG -3'

Posted On

2013-09-04