Incidental Mutation 'R0646:Lrrc37'
ID |
57184 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Lrrc37
|
Ensembl Gene |
ENSMUSG00000034239 |
Gene Name |
leucine rich repeat containing 37 |
Synonyms |
LOC380730, Gm884 |
MMRRC Submission |
038831-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.266)
|
Stock # |
R0646 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
103425403-103511966 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 103503986 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Stop codon
at position 485
(K485*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129662
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059279]
[ENSMUST00000167262]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000059279
AA Change: K2661*
|
SMART Domains |
Protein: ENSMUSP00000058511 Gene: ENSMUSG00000034239 AA Change: K2661*
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 |
probably null
Transcript: ENSMUST00000167262
AA Change: K485*
|
SMART Domains |
Protein: ENSMUSP00000129662 Gene: ENSMUSG00000034239 AA Change: K485*
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 |
0.9755 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.7%
|
Validation Efficiency |
95% (123/130) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 125 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
C |
T |
7: 29,260,710 (GRCm39) |
|
noncoding transcript |
Het |
Abcb11 |
A |
G |
2: 69,115,627 (GRCm39) |
I579T |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,830 (GRCm39) |
N400S |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,781,855 (GRCm39) |
L577P |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,852 (GRCm39) |
N422K |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,990,766 (GRCm39) |
K4017* |
probably null |
Het |
Akap13 |
C |
A |
7: 75,397,494 (GRCm39) |
Q2575K |
probably damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,144,541 (GRCm39) |
I339K |
probably damaging |
Het |
Alox15 |
G |
T |
11: 70,236,450 (GRCm39) |
Y483* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,006,913 (GRCm39) |
I713F |
probably damaging |
Het |
Amph |
A |
T |
13: 19,297,286 (GRCm39) |
E344V |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,436,959 (GRCm39) |
Y250H |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,932,807 (GRCm39) |
S1032P |
probably damaging |
Het |
Armc8 |
C |
A |
9: 99,387,741 (GRCm39) |
L393F |
probably damaging |
Het |
Bpnt1 |
A |
G |
1: 185,077,623 (GRCm39) |
|
probably null |
Het |
Cachd1 |
G |
A |
4: 100,845,418 (GRCm39) |
R970H |
probably damaging |
Het |
Cd207 |
T |
C |
6: 83,652,738 (GRCm39) |
T131A |
probably benign |
Het |
Cd83 |
G |
A |
13: 43,951,009 (GRCm39) |
V54I |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,752,115 (GRCm39) |
K1086E |
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,941,328 (GRCm39) |
V1837E |
probably benign |
Het |
Clcnka |
T |
A |
4: 141,123,917 (GRCm39) |
H89L |
probably benign |
Het |
Cnga4 |
T |
C |
7: 105,054,182 (GRCm39) |
I50T |
possibly damaging |
Het |
Cog5 |
A |
G |
12: 31,887,358 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,278,322 (GRCm39) |
|
probably null |
Het |
Col28a1 |
T |
G |
6: 8,175,291 (GRCm39) |
I186L |
possibly damaging |
Het |
Col4a2 |
T |
A |
8: 11,481,252 (GRCm39) |
M808K |
probably benign |
Het |
Copb2 |
A |
G |
9: 98,445,528 (GRCm39) |
|
probably benign |
Het |
Dbnl |
G |
A |
11: 5,745,441 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,552,493 (GRCm39) |
T51A |
possibly damaging |
Het |
Dcp1a |
A |
T |
14: 30,224,842 (GRCm39) |
M123L |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,123,659 (GRCm39) |
F217I |
probably benign |
Het |
Dlc1 |
T |
C |
8: 37,325,205 (GRCm39) |
T367A |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,888,863 (GRCm39) |
T834S |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,903,147 (GRCm39) |
S929P |
probably damaging |
Het |
Dnase1l2 |
C |
A |
17: 24,660,056 (GRCm39) |
V271L |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,229,114 (GRCm39) |
Y392C |
probably damaging |
Het |
Edn1 |
T |
C |
13: 42,458,718 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,611,327 (GRCm39) |
D390N |
probably benign |
Het |
Eps8l3 |
T |
C |
3: 107,792,126 (GRCm39) |
L351P |
probably damaging |
Het |
F12 |
G |
A |
13: 55,570,296 (GRCm39) |
|
probably benign |
Het |
Fam47e |
T |
C |
5: 92,726,317 (GRCm39) |
|
probably benign |
Het |
Fcrl5 |
C |
A |
3: 87,349,320 (GRCm39) |
Q32K |
probably benign |
Het |
Fndc1 |
C |
T |
17: 7,960,505 (GRCm39) |
V1637I |
possibly damaging |
Het |
Foxg1 |
G |
T |
12: 49,431,350 (GRCm39) |
|
probably benign |
Het |
Frrs1 |
A |
T |
3: 116,696,070 (GRCm39) |
I530F |
possibly damaging |
Het |
Galnt5 |
A |
T |
2: 57,889,097 (GRCm39) |
K232N |
probably benign |
Het |
Ggt5 |
G |
A |
10: 75,438,482 (GRCm39) |
V68M |
probably damaging |
Het |
Gm16519 |
T |
C |
17: 71,236,101 (GRCm39) |
C17R |
probably benign |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Gm9631 |
T |
G |
11: 121,836,455 (GRCm39) |
D28A |
probably damaging |
Het |
Gpx2 |
T |
C |
12: 76,842,087 (GRCm39) |
I21M |
probably benign |
Het |
H2-Q2 |
T |
G |
17: 35,564,661 (GRCm39) |
D354E |
probably damaging |
Het |
Icam2 |
A |
T |
11: 106,271,717 (GRCm39) |
I71K |
probably damaging |
Het |
Il12a |
T |
C |
3: 68,605,223 (GRCm39) |
|
probably benign |
Het |
Insm2 |
C |
G |
12: 55,647,225 (GRCm39) |
A323G |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,104,835 (GRCm39) |
T1064A |
probably benign |
Het |
Itgad |
T |
A |
7: 127,773,176 (GRCm39) |
V11E |
possibly damaging |
Het |
Kctd15 |
C |
T |
7: 34,344,306 (GRCm39) |
S115N |
probably damaging |
Het |
Klra5 |
A |
G |
6: 129,880,527 (GRCm39) |
W124R |
probably damaging |
Het |
Kng2 |
T |
A |
16: 22,806,486 (GRCm39) |
D571V |
probably benign |
Het |
Kpna6 |
A |
T |
4: 129,544,583 (GRCm39) |
F380I |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,762,169 (GRCm39) |
Y109* |
probably null |
Het |
Man2a2 |
T |
C |
7: 80,012,945 (GRCm39) |
H540R |
possibly damaging |
Het |
Map2k4 |
T |
C |
11: 65,603,101 (GRCm39) |
E188G |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,895,252 (GRCm39) |
|
probably benign |
Het |
Mbtd1 |
A |
G |
11: 93,796,038 (GRCm39) |
D25G |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,221,915 (GRCm39) |
Q238L |
possibly damaging |
Het |
Mmachc |
A |
G |
4: 116,560,851 (GRCm39) |
Y215H |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,568,811 (GRCm39) |
Y1110* |
probably null |
Het |
Nek2 |
A |
G |
1: 191,554,331 (GRCm39) |
N57D |
probably damaging |
Het |
Nek7 |
ACCCC |
ACCC |
1: 138,443,431 (GRCm39) |
|
probably null |
Het |
Neo1 |
G |
T |
9: 58,838,317 (GRCm39) |
T489K |
probably damaging |
Het |
Neu1 |
T |
A |
17: 35,153,736 (GRCm39) |
Y387N |
probably damaging |
Het |
Nfasc |
A |
T |
1: 132,536,176 (GRCm39) |
C586* |
probably null |
Het |
Nle1 |
G |
A |
11: 82,795,671 (GRCm39) |
L259F |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,110,105 (GRCm39) |
Q309* |
probably null |
Het |
Nufip2 |
C |
T |
11: 77,577,279 (GRCm39) |
H76Y |
probably benign |
Het |
Or10ak16 |
A |
C |
4: 118,750,687 (GRCm39) |
T136P |
probably damaging |
Het |
Or2y13 |
A |
T |
11: 49,415,405 (GRCm39) |
N285I |
probably damaging |
Het |
Or4k6 |
A |
T |
14: 50,476,096 (GRCm39) |
I82N |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,018 (GRCm39) |
I307N |
probably benign |
Het |
Or52r1c |
T |
C |
7: 102,735,358 (GRCm39) |
F206S |
probably damaging |
Het |
Or9s18 |
A |
T |
13: 65,300,877 (GRCm39) |
I280F |
probably damaging |
Het |
Pcdhb5 |
A |
G |
18: 37,454,675 (GRCm39) |
T352A |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,476,442 (GRCm39) |
D526V |
probably damaging |
Het |
Phkg1 |
A |
T |
5: 129,893,394 (GRCm39) |
|
probably null |
Het |
Plg |
C |
T |
17: 12,637,623 (GRCm39) |
T744M |
probably damaging |
Het |
Plxnd1 |
A |
C |
6: 115,935,660 (GRCm39) |
|
probably benign |
Het |
Poglut1 |
A |
T |
16: 38,349,837 (GRCm39) |
I312N |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
A |
G |
4: 122,737,892 (GRCm39) |
M77V |
probably benign |
Het |
Pramel26 |
A |
C |
4: 143,539,155 (GRCm39) |
S113A |
possibly damaging |
Het |
Pramel5 |
G |
T |
4: 143,998,190 (GRCm39) |
T351N |
probably damaging |
Het |
Psmb4 |
G |
A |
3: 94,792,275 (GRCm39) |
R216C |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,002,640 (GRCm39) |
T699A |
probably damaging |
Het |
Retreg3 |
A |
T |
11: 100,989,455 (GRCm39) |
|
probably benign |
Het |
Sanbr |
C |
T |
11: 23,525,491 (GRCm39) |
R716H |
probably damaging |
Het |
Scaper |
G |
A |
9: 55,665,340 (GRCm39) |
A389V |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,825,245 (GRCm39) |
D225N |
possibly damaging |
Het |
Slco1a1 |
T |
G |
6: 141,871,480 (GRCm39) |
|
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Sod3 |
A |
T |
5: 52,525,421 (GRCm39) |
D40V |
probably benign |
Het |
Sorcs3 |
C |
A |
19: 48,194,734 (GRCm39) |
A39E |
probably benign |
Het |
Spon1 |
A |
T |
7: 113,639,056 (GRCm39) |
T761S |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,720,004 (GRCm39) |
|
probably null |
Het |
Synm |
T |
A |
7: 67,408,916 (GRCm39) |
D154V |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,098 (GRCm39) |
E406G |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,975,382 (GRCm39) |
L8* |
probably null |
Het |
Tec |
G |
A |
5: 72,980,840 (GRCm39) |
L33F |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,072,354 (GRCm39) |
S2634T |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,601,475 (GRCm39) |
Y162N |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,690,123 (GRCm39) |
V853I |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,068,240 (GRCm39) |
K1748E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,822 (GRCm39) |
|
probably benign |
Het |
Usp36 |
C |
T |
11: 118,163,847 (GRCm39) |
D234N |
probably damaging |
Het |
Usp40 |
G |
A |
1: 87,906,244 (GRCm39) |
P664S |
probably benign |
Het |
Vmn1r54 |
T |
A |
6: 90,246,635 (GRCm39) |
L183H |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,676 (GRCm39) |
I185L |
probably benign |
Het |
Wnt8a |
A |
T |
18: 34,680,618 (GRCm39) |
R328W |
probably benign |
Het |
Yars1 |
A |
G |
4: 129,107,732 (GRCm39) |
|
probably benign |
Het |
Zbtb49 |
A |
C |
5: 38,358,018 (GRCm39) |
M745R |
probably damaging |
Het |
Zeb1 |
T |
G |
18: 5,759,027 (GRCm39) |
F162V |
probably damaging |
Het |
Zfp369 |
A |
T |
13: 65,445,362 (GRCm39) |
H835L |
probably damaging |
Het |
Zic5 |
A |
G |
14: 122,701,351 (GRCm39) |
V460A |
unknown |
Het |
Zp3 |
A |
G |
5: 136,013,210 (GRCm39) |
N181D |
possibly damaging |
Het |
|
Other mutations in Lrrc37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00572:Lrrc37
|
APN |
11 |
103,506,236 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00576:Lrrc37
|
APN |
11 |
103,508,212 (GRCm39) |
unclassified |
probably benign |
|
IGL00813:Lrrc37
|
APN |
11 |
103,505,324 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01311:Lrrc37
|
APN |
11 |
103,425,502 (GRCm39) |
missense |
unknown |
|
IGL01946:Lrrc37
|
APN |
11 |
103,503,759 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02217:Lrrc37
|
APN |
11 |
103,503,697 (GRCm39) |
splice site |
probably benign |
|
IGL02556:Lrrc37
|
APN |
11 |
103,504,109 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02825:Lrrc37
|
APN |
11 |
103,507,894 (GRCm39) |
unclassified |
probably benign |
|
IGL02868:Lrrc37
|
APN |
11 |
103,505,965 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02904:Lrrc37
|
APN |
11 |
103,507,187 (GRCm39) |
unclassified |
probably benign |
|
IGL03008:Lrrc37
|
APN |
11 |
103,511,293 (GRCm39) |
missense |
unknown |
|
IGL03120:Lrrc37
|
APN |
11 |
103,507,801 (GRCm39) |
unclassified |
probably benign |
|
IGL03159:Lrrc37
|
APN |
11 |
103,495,328 (GRCm39) |
splice site |
probably benign |
|
IGL03181:Lrrc37
|
APN |
11 |
103,507,242 (GRCm39) |
unclassified |
probably benign |
|
IGL03202:Lrrc37
|
APN |
11 |
103,506,199 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03263:Lrrc37
|
APN |
11 |
103,504,525 (GRCm39) |
missense |
possibly damaging |
0.86 |
esteemed
|
UTSW |
11 |
103,509,656 (GRCm39) |
missense |
unknown |
|
lauded
|
UTSW |
11 |
103,503,929 (GRCm39) |
missense |
possibly damaging |
0.62 |
PIT4486001:Lrrc37
|
UTSW |
11 |
103,509,027 (GRCm39) |
missense |
unknown |
|
R0040:Lrrc37
|
UTSW |
11 |
103,433,816 (GRCm39) |
missense |
probably damaging |
0.99 |
R0135:Lrrc37
|
UTSW |
11 |
103,508,873 (GRCm39) |
unclassified |
probably benign |
|
R0141:Lrrc37
|
UTSW |
11 |
103,504,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Lrrc37
|
UTSW |
11 |
103,494,067 (GRCm39) |
missense |
probably benign |
0.08 |
R0547:Lrrc37
|
UTSW |
11 |
103,510,990 (GRCm39) |
missense |
unknown |
|
R0685:Lrrc37
|
UTSW |
11 |
103,507,714 (GRCm39) |
unclassified |
probably benign |
|
R0732:Lrrc37
|
UTSW |
11 |
103,510,664 (GRCm39) |
missense |
unknown |
|
R1015:Lrrc37
|
UTSW |
11 |
103,436,622 (GRCm39) |
missense |
probably benign |
0.01 |
R1166:Lrrc37
|
UTSW |
11 |
103,506,209 (GRCm39) |
missense |
probably benign |
0.21 |
R1168:Lrrc37
|
UTSW |
11 |
103,509,776 (GRCm39) |
unclassified |
probably benign |
|
R1257:Lrrc37
|
UTSW |
11 |
103,425,467 (GRCm39) |
missense |
unknown |
|
R1545:Lrrc37
|
UTSW |
11 |
103,499,745 (GRCm39) |
missense |
probably benign |
0.16 |
R1570:Lrrc37
|
UTSW |
11 |
103,500,764 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1677:Lrrc37
|
UTSW |
11 |
103,505,768 (GRCm39) |
missense |
probably benign |
0.19 |
R1703:Lrrc37
|
UTSW |
11 |
103,431,700 (GRCm39) |
missense |
probably benign |
0.39 |
R1719:Lrrc37
|
UTSW |
11 |
103,507,897 (GRCm39) |
unclassified |
probably benign |
|
R1752:Lrrc37
|
UTSW |
11 |
103,505,381 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1870:Lrrc37
|
UTSW |
11 |
103,511,431 (GRCm39) |
missense |
unknown |
|
R2155:Lrrc37
|
UTSW |
11 |
103,511,285 (GRCm39) |
missense |
unknown |
|
R2191:Lrrc37
|
UTSW |
11 |
103,509,793 (GRCm39) |
unclassified |
probably benign |
|
R2271:Lrrc37
|
UTSW |
11 |
103,505,033 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2378:Lrrc37
|
UTSW |
11 |
103,510,537 (GRCm39) |
unclassified |
probably benign |
|
R2405:Lrrc37
|
UTSW |
11 |
103,511,810 (GRCm39) |
missense |
unknown |
|
R2864:Lrrc37
|
UTSW |
11 |
103,431,744 (GRCm39) |
missense |
probably benign |
0.34 |
R3011:Lrrc37
|
UTSW |
11 |
103,503,929 (GRCm39) |
missense |
possibly damaging |
0.62 |
R3415:Lrrc37
|
UTSW |
11 |
103,505,435 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3417:Lrrc37
|
UTSW |
11 |
103,505,435 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3835:Lrrc37
|
UTSW |
11 |
103,510,836 (GRCm39) |
missense |
unknown |
|
R3974:Lrrc37
|
UTSW |
11 |
103,509,927 (GRCm39) |
unclassified |
probably benign |
|
R4019:Lrrc37
|
UTSW |
11 |
103,506,119 (GRCm39) |
missense |
probably benign |
0.19 |
R4020:Lrrc37
|
UTSW |
11 |
103,506,119 (GRCm39) |
missense |
probably benign |
0.19 |
R4176:Lrrc37
|
UTSW |
11 |
103,427,426 (GRCm39) |
missense |
unknown |
|
R4361:Lrrc37
|
UTSW |
11 |
103,508,327 (GRCm39) |
frame shift |
probably null |
|
R4418:Lrrc37
|
UTSW |
11 |
103,509,140 (GRCm39) |
unclassified |
probably benign |
|
R4633:Lrrc37
|
UTSW |
11 |
103,509,957 (GRCm39) |
unclassified |
probably benign |
|
R4693:Lrrc37
|
UTSW |
11 |
103,510,686 (GRCm39) |
missense |
unknown |
|
R4758:Lrrc37
|
UTSW |
11 |
103,505,290 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4878:Lrrc37
|
UTSW |
11 |
103,508,717 (GRCm39) |
unclassified |
probably benign |
|
R4887:Lrrc37
|
UTSW |
11 |
103,505,698 (GRCm39) |
missense |
probably benign |
0.03 |
R4944:Lrrc37
|
UTSW |
11 |
103,504,286 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4952:Lrrc37
|
UTSW |
11 |
103,505,033 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5030:Lrrc37
|
UTSW |
11 |
103,425,675 (GRCm39) |
missense |
unknown |
|
R5183:Lrrc37
|
UTSW |
11 |
103,433,947 (GRCm39) |
missense |
probably damaging |
0.99 |
R5294:Lrrc37
|
UTSW |
11 |
103,507,057 (GRCm39) |
unclassified |
probably benign |
|
R5317:Lrrc37
|
UTSW |
11 |
103,504,971 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5334:Lrrc37
|
UTSW |
11 |
103,504,699 (GRCm39) |
missense |
probably benign |
0.18 |
R5426:Lrrc37
|
UTSW |
11 |
103,511,586 (GRCm39) |
missense |
unknown |
|
R5467:Lrrc37
|
UTSW |
11 |
103,494,091 (GRCm39) |
nonsense |
probably null |
|
R5518:Lrrc37
|
UTSW |
11 |
103,506,079 (GRCm39) |
missense |
probably benign |
0.03 |
R5634:Lrrc37
|
UTSW |
11 |
103,432,840 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5647:Lrrc37
|
UTSW |
11 |
103,508,300 (GRCm39) |
unclassified |
probably benign |
|
R5663:Lrrc37
|
UTSW |
11 |
103,503,949 (GRCm39) |
missense |
probably benign |
0.01 |
R5668:Lrrc37
|
UTSW |
11 |
103,507,880 (GRCm39) |
unclassified |
probably benign |
|
R5763:Lrrc37
|
UTSW |
11 |
103,504,469 (GRCm39) |
missense |
probably damaging |
0.97 |
R5829:Lrrc37
|
UTSW |
11 |
103,432,712 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5871:Lrrc37
|
UTSW |
11 |
103,507,280 (GRCm39) |
unclassified |
probably benign |
|
R5905:Lrrc37
|
UTSW |
11 |
103,505,081 (GRCm39) |
missense |
probably damaging |
0.98 |
R5940:Lrrc37
|
UTSW |
11 |
103,504,712 (GRCm39) |
missense |
probably benign |
0.18 |
R5964:Lrrc37
|
UTSW |
11 |
103,432,946 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5988:Lrrc37
|
UTSW |
11 |
103,506,722 (GRCm39) |
unclassified |
probably benign |
|
R5992:Lrrc37
|
UTSW |
11 |
103,504,618 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6114:Lrrc37
|
UTSW |
11 |
103,508,617 (GRCm39) |
unclassified |
probably benign |
|
R6154:Lrrc37
|
UTSW |
11 |
103,504,969 (GRCm39) |
missense |
probably benign |
0.33 |
R6233:Lrrc37
|
UTSW |
11 |
103,504,214 (GRCm39) |
missense |
probably damaging |
0.98 |
R6301:Lrrc37
|
UTSW |
11 |
103,509,756 (GRCm39) |
unclassified |
probably benign |
|
R6362:Lrrc37
|
UTSW |
11 |
103,511,478 (GRCm39) |
missense |
unknown |
|
R6471:Lrrc37
|
UTSW |
11 |
103,510,448 (GRCm39) |
unclassified |
probably benign |
|
R6806:Lrrc37
|
UTSW |
11 |
103,511,950 (GRCm39) |
missense |
unknown |
|
R6962:Lrrc37
|
UTSW |
11 |
103,505,126 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6996:Lrrc37
|
UTSW |
11 |
103,509,583 (GRCm39) |
nonsense |
probably null |
|
R7028:Lrrc37
|
UTSW |
11 |
103,505,363 (GRCm39) |
missense |
probably benign |
0.28 |
R7034:Lrrc37
|
UTSW |
11 |
103,506,638 (GRCm39) |
unclassified |
probably benign |
|
R7036:Lrrc37
|
UTSW |
11 |
103,506,638 (GRCm39) |
unclassified |
probably benign |
|
R7113:Lrrc37
|
UTSW |
11 |
103,509,625 (GRCm39) |
missense |
unknown |
|
R7405:Lrrc37
|
UTSW |
11 |
103,505,987 (GRCm39) |
missense |
probably benign |
0.02 |
R7420:Lrrc37
|
UTSW |
11 |
103,504,451 (GRCm39) |
missense |
probably benign |
0.11 |
R7461:Lrrc37
|
UTSW |
11 |
103,507,116 (GRCm39) |
missense |
unknown |
|
R7544:Lrrc37
|
UTSW |
11 |
103,506,274 (GRCm39) |
missense |
probably benign |
0.01 |
R7613:Lrrc37
|
UTSW |
11 |
103,507,116 (GRCm39) |
missense |
unknown |
|
R7711:Lrrc37
|
UTSW |
11 |
103,505,738 (GRCm39) |
missense |
probably benign |
0.02 |
R7714:Lrrc37
|
UTSW |
11 |
103,507,719 (GRCm39) |
missense |
unknown |
|
R7747:Lrrc37
|
UTSW |
11 |
103,505,081 (GRCm39) |
missense |
probably damaging |
0.98 |
R7814:Lrrc37
|
UTSW |
11 |
103,504,999 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8053:Lrrc37
|
UTSW |
11 |
103,495,392 (GRCm39) |
missense |
unknown |
|
R8063:Lrrc37
|
UTSW |
11 |
103,433,087 (GRCm39) |
missense |
unknown |
|
R8116:Lrrc37
|
UTSW |
11 |
103,434,115 (GRCm39) |
missense |
unknown |
|
R8124:Lrrc37
|
UTSW |
11 |
103,511,257 (GRCm39) |
missense |
unknown |
|
R8141:Lrrc37
|
UTSW |
11 |
103,511,855 (GRCm39) |
missense |
unknown |
|
R8163:Lrrc37
|
UTSW |
11 |
103,506,688 (GRCm39) |
missense |
unknown |
|
R8270:Lrrc37
|
UTSW |
11 |
103,434,141 (GRCm39) |
missense |
unknown |
|
R8348:Lrrc37
|
UTSW |
11 |
103,511,726 (GRCm39) |
missense |
unknown |
|
R8362:Lrrc37
|
UTSW |
11 |
103,506,163 (GRCm39) |
missense |
probably benign |
0.34 |
R8448:Lrrc37
|
UTSW |
11 |
103,511,726 (GRCm39) |
missense |
unknown |
|
R8465:Lrrc37
|
UTSW |
11 |
103,506,947 (GRCm39) |
unclassified |
probably benign |
|
R8473:Lrrc37
|
UTSW |
11 |
103,434,266 (GRCm39) |
missense |
unknown |
|
R8781:Lrrc37
|
UTSW |
11 |
103,508,958 (GRCm39) |
missense |
unknown |
|
R8821:Lrrc37
|
UTSW |
11 |
103,510,470 (GRCm39) |
missense |
unknown |
|
R8859:Lrrc37
|
UTSW |
11 |
103,506,370 (GRCm39) |
missense |
unknown |
|
R8888:Lrrc37
|
UTSW |
11 |
103,509,656 (GRCm39) |
missense |
unknown |
|
R8895:Lrrc37
|
UTSW |
11 |
103,509,656 (GRCm39) |
missense |
unknown |
|
R9083:Lrrc37
|
UTSW |
11 |
103,509,830 (GRCm39) |
missense |
unknown |
|
R9085:Lrrc37
|
UTSW |
11 |
103,507,565 (GRCm39) |
missense |
unknown |
|
R9088:Lrrc37
|
UTSW |
11 |
103,511,762 (GRCm39) |
missense |
unknown |
|
R9124:Lrrc37
|
UTSW |
11 |
103,509,721 (GRCm39) |
missense |
unknown |
|
R9177:Lrrc37
|
UTSW |
11 |
103,508,263 (GRCm39) |
missense |
unknown |
|
R9238:Lrrc37
|
UTSW |
11 |
103,509,859 (GRCm39) |
missense |
unknown |
|
R9267:Lrrc37
|
UTSW |
11 |
103,495,406 (GRCm39) |
missense |
unknown |
|
R9444:Lrrc37
|
UTSW |
11 |
103,508,846 (GRCm39) |
nonsense |
probably null |
|
R9517:Lrrc37
|
UTSW |
11 |
103,433,416 (GRCm39) |
missense |
unknown |
|
R9564:Lrrc37
|
UTSW |
11 |
103,503,822 (GRCm39) |
missense |
unknown |
|
R9632:Lrrc37
|
UTSW |
11 |
103,433,252 (GRCm39) |
missense |
unknown |
|
R9741:Lrrc37
|
UTSW |
11 |
103,504,255 (GRCm39) |
missense |
possibly damaging |
0.68 |
Z1176:Lrrc37
|
UTSW |
11 |
103,504,507 (GRCm39) |
missense |
probably benign |
0.45 |
|
Predicted Primers |
PCR Primer
(F):5'- CAGTGTCTCATTTTCACACACGCAG -3'
(R):5'- CAATGCATCTTCAAGTCCCAATGCC -3'
Sequencing Primer
(F):5'- CACGCAGAAGTCACATATTTTGG -3'
(R):5'- TCCTTCAGAGATACCTGTGGAGAC -3'
|
Posted On |
2013-07-11 |