Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
G |
1: 130,668,740 (GRCm39) |
S36G |
probably damaging |
Het |
Aarsd1 |
T |
C |
11: 101,301,203 (GRCm39) |
N280D |
probably benign |
Het |
Abca2 |
T |
A |
2: 25,335,686 (GRCm39) |
M2099K |
probably damaging |
Het |
Abcb5 |
T |
A |
12: 118,875,278 (GRCm39) |
E631D |
probably benign |
Het |
Acss2 |
T |
A |
2: 155,415,149 (GRCm39) |
L682Q |
probably null |
Het |
Adamts14 |
G |
A |
10: 61,034,267 (GRCm39) |
P1207L |
probably benign |
Het |
Adora1 |
G |
A |
1: 134,130,748 (GRCm39) |
R308* |
probably null |
Het |
Arcn1 |
A |
T |
9: 44,668,444 (GRCm39) |
V264E |
probably benign |
Het |
B3galt1 |
G |
A |
2: 67,949,112 (GRCm39) |
G276S |
probably damaging |
Het |
Bms1 |
A |
T |
6: 118,382,179 (GRCm39) |
M453K |
possibly damaging |
Het |
Bnip3l |
T |
C |
14: 67,225,180 (GRCm39) |
Y218C |
probably damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,390,805 (GRCm39) |
E379G |
probably null |
Het |
Cacng6 |
G |
A |
7: 3,483,376 (GRCm39) |
G235R |
probably damaging |
Het |
Capn8 |
A |
T |
1: 182,456,169 (GRCm39) |
T640S |
probably benign |
Het |
Ccdc106 |
T |
C |
7: 5,063,159 (GRCm39) |
|
probably benign |
Het |
Ccdc33 |
A |
T |
9: 57,993,860 (GRCm39) |
N95K |
probably benign |
Het |
Cemip |
A |
T |
7: 83,604,509 (GRCm39) |
N844K |
probably damaging |
Het |
Chrdl2 |
A |
T |
7: 99,677,948 (GRCm39) |
T284S |
probably damaging |
Het |
Ckm |
A |
G |
7: 19,154,090 (GRCm39) |
Y279C |
probably damaging |
Het |
Clvs1 |
A |
T |
4: 9,424,261 (GRCm39) |
I236F |
probably damaging |
Het |
Col9a1 |
T |
C |
1: 24,234,620 (GRCm39) |
|
probably null |
Het |
Csmd1 |
T |
C |
8: 17,266,728 (GRCm39) |
E66G |
possibly damaging |
Het |
Ctdsp2 |
A |
G |
10: 126,831,923 (GRCm39) |
D26G |
probably damaging |
Het |
Ctsll3 |
C |
A |
13: 60,946,721 (GRCm39) |
|
probably null |
Het |
Cyp2d12 |
A |
T |
15: 82,439,423 (GRCm39) |
M26L |
probably benign |
Het |
Cyp8b1 |
C |
T |
9: 121,743,950 (GRCm39) |
D461N |
probably damaging |
Het |
Dbt |
A |
T |
3: 116,322,220 (GRCm39) |
|
probably benign |
Het |
Dnah7c |
A |
G |
1: 46,704,728 (GRCm39) |
D2247G |
probably benign |
Het |
Dsg1c |
A |
G |
18: 20,400,994 (GRCm39) |
I166V |
possibly damaging |
Het |
Duoxa1 |
T |
A |
2: 122,134,361 (GRCm39) |
E252D |
probably damaging |
Het |
Ezr |
T |
A |
17: 7,020,448 (GRCm39) |
K211M |
probably damaging |
Het |
Faap100 |
T |
A |
11: 120,268,458 (GRCm39) |
E105V |
possibly damaging |
Het |
Fahd2a |
T |
C |
2: 127,283,878 (GRCm39) |
D54G |
possibly damaging |
Het |
Fbxo9 |
A |
T |
9: 78,003,146 (GRCm39) |
|
probably null |
Het |
Fndc1 |
A |
G |
17: 7,991,540 (GRCm39) |
S719P |
unknown |
Het |
Gas7 |
G |
T |
11: 67,552,916 (GRCm39) |
G159C |
probably damaging |
Het |
Gba2 |
T |
C |
4: 43,574,063 (GRCm39) |
D130G |
probably damaging |
Het |
Gli3 |
T |
G |
13: 15,723,092 (GRCm39) |
S78A |
probably damaging |
Het |
Gtpbp6 |
A |
G |
5: 110,254,770 (GRCm39) |
F101S |
probably damaging |
Het |
Gzme |
G |
A |
14: 56,355,224 (GRCm39) |
H236Y |
probably benign |
Het |
Hira |
T |
C |
16: 18,773,508 (GRCm39) |
Y943H |
probably damaging |
Het |
Hmbox1 |
G |
A |
14: 65,134,144 (GRCm39) |
S152L |
possibly damaging |
Het |
Ibtk |
A |
G |
9: 85,619,519 (GRCm39) |
|
probably null |
Het |
Jade1 |
T |
C |
3: 41,568,413 (GRCm39) |
I827T |
possibly damaging |
Het |
Jakmip3 |
A |
T |
7: 138,627,164 (GRCm39) |
E389D |
possibly damaging |
Het |
Klhdc8b |
A |
T |
9: 108,326,241 (GRCm39) |
|
probably benign |
Het |
Lama2 |
T |
C |
10: 27,014,942 (GRCm39) |
T1589A |
probably benign |
Het |
Lbx2 |
A |
C |
6: 83,064,784 (GRCm39) |
K107T |
probably damaging |
Het |
Ldha |
A |
G |
7: 46,503,522 (GRCm39) |
M259V |
probably benign |
Het |
Lrrtm4 |
A |
G |
6: 79,999,620 (GRCm39) |
K344R |
probably damaging |
Het |
Ltb |
A |
T |
17: 35,414,935 (GRCm39) |
E245V |
probably damaging |
Het |
Macf1 |
GCCCCC |
GCCCCCC |
4: 123,244,784 (GRCm39) |
|
probably null |
Het |
Map3k13 |
T |
A |
16: 21,740,397 (GRCm39) |
S575T |
possibly damaging |
Het |
Mcpt2 |
A |
T |
14: 56,280,833 (GRCm39) |
I74F |
probably damaging |
Het |
Mpeg1 |
T |
A |
19: 12,439,013 (GRCm39) |
V157D |
probably damaging |
Het |
Mrpl21 |
A |
T |
19: 3,337,009 (GRCm39) |
|
probably null |
Het |
Nagpa |
T |
C |
16: 5,017,877 (GRCm39) |
T99A |
possibly damaging |
Het |
Nphs1 |
A |
T |
7: 30,163,250 (GRCm39) |
I469F |
probably benign |
Het |
Nyap2 |
A |
G |
1: 81,169,756 (GRCm39) |
E171G |
possibly damaging |
Het |
Oas1e |
A |
G |
5: 120,930,006 (GRCm39) |
Y171H |
probably damaging |
Het |
Or10ag59 |
T |
A |
2: 87,406,043 (GRCm39) |
V205D |
probably damaging |
Het |
Or2y1f |
T |
C |
11: 49,184,493 (GRCm39) |
L115P |
probably damaging |
Het |
Or5ac23 |
T |
C |
16: 59,149,461 (GRCm39) |
K137R |
probably benign |
Het |
Or5h26 |
T |
C |
16: 58,987,983 (GRCm39) |
I174M |
possibly damaging |
Het |
Otud7b |
C |
A |
3: 96,063,055 (GRCm39) |
Q765K |
probably benign |
Het |
Pdzd7 |
A |
G |
19: 45,017,216 (GRCm39) |
V851A |
probably benign |
Het |
Pi4ka |
T |
G |
16: 17,143,277 (GRCm39) |
K794T |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,410,258 (GRCm39) |
N2588K |
probably damaging |
Het |
Pla2g6 |
A |
T |
15: 79,186,837 (GRCm39) |
M471K |
probably benign |
Het |
Plagl2 |
T |
C |
2: 153,077,759 (GRCm39) |
H74R |
possibly damaging |
Het |
Prf1 |
T |
A |
10: 61,136,037 (GRCm39) |
N104K |
probably benign |
Het |
Ptprf |
A |
T |
4: 118,093,586 (GRCm39) |
I358N |
probably damaging |
Het |
Rcsd1 |
A |
G |
1: 165,482,872 (GRCm39) |
|
probably null |
Het |
Rev1 |
G |
A |
1: 38,147,532 (GRCm39) |
R3* |
probably null |
Het |
Rp1 |
T |
C |
1: 4,419,583 (GRCm39) |
|
probably null |
Het |
Rrp12 |
G |
A |
19: 41,881,035 (GRCm39) |
T132I |
probably damaging |
Het |
Sema3a |
T |
C |
5: 13,649,357 (GRCm39) |
V702A |
probably benign |
Het |
Serpinb12 |
A |
G |
1: 106,884,174 (GRCm39) |
N307D |
probably damaging |
Het |
Slc35d1 |
A |
G |
4: 103,070,383 (GRCm39) |
L103P |
probably damaging |
Het |
Smyd4 |
T |
C |
11: 75,281,765 (GRCm39) |
C413R |
probably damaging |
Het |
Stab1 |
G |
A |
14: 30,883,793 (GRCm39) |
Q255* |
probably null |
Het |
Synpo |
T |
A |
18: 60,736,918 (GRCm39) |
I343F |
possibly damaging |
Het |
Tcirg1 |
A |
G |
19: 3,952,342 (GRCm39) |
|
probably null |
Het |
Tmem132c |
A |
G |
5: 127,640,816 (GRCm39) |
T996A |
possibly damaging |
Het |
Trim10 |
A |
G |
17: 37,181,081 (GRCm39) |
E104G |
probably damaging |
Het |
Trpc1 |
T |
C |
9: 95,603,524 (GRCm39) |
|
probably null |
Het |
Tspo2 |
A |
T |
17: 48,756,887 (GRCm39) |
|
probably benign |
Het |
Ugt2a3 |
A |
T |
5: 87,479,174 (GRCm39) |
I258N |
probably damaging |
Het |
Usp34 |
T |
C |
11: 23,418,846 (GRCm39) |
L2998P |
probably damaging |
Het |
Vmn1r45 |
A |
C |
6: 89,910,123 (GRCm39) |
D162E |
possibly damaging |
Het |
Vmn2r117 |
A |
T |
17: 23,696,848 (GRCm39) |
Y186* |
probably null |
Het |
Vmn2r67 |
A |
G |
7: 84,785,698 (GRCm39) |
F769S |
probably damaging |
Het |
Zbtb17 |
A |
G |
4: 141,192,942 (GRCm39) |
I514V |
probably benign |
Het |
Zfp329 |
A |
C |
7: 12,545,421 (GRCm39) |
D34E |
probably benign |
Het |
|
Other mutations in Celsr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Celsr3
|
APN |
9 |
108,726,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00536:Celsr3
|
APN |
9 |
108,706,391 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00552:Celsr3
|
APN |
9 |
108,718,462 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00801:Celsr3
|
APN |
9 |
108,719,775 (GRCm39) |
missense |
probably benign |
|
IGL01420:Celsr3
|
APN |
9 |
108,718,389 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01541:Celsr3
|
APN |
9 |
108,708,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,711,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,714,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01631:Celsr3
|
APN |
9 |
108,714,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01777:Celsr3
|
APN |
9 |
108,713,141 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01938:Celsr3
|
APN |
9 |
108,705,614 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02135:Celsr3
|
APN |
9 |
108,704,755 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02231:Celsr3
|
APN |
9 |
108,719,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:Celsr3
|
APN |
9 |
108,707,159 (GRCm39) |
missense |
probably benign |
|
IGL02392:Celsr3
|
APN |
9 |
108,711,920 (GRCm39) |
splice site |
probably benign |
|
IGL02416:Celsr3
|
APN |
9 |
108,709,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02421:Celsr3
|
APN |
9 |
108,717,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Celsr3
|
APN |
9 |
108,720,092 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02798:Celsr3
|
APN |
9 |
108,720,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Celsr3
|
APN |
9 |
108,726,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Celsr3
|
APN |
9 |
108,723,134 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02986:Celsr3
|
APN |
9 |
108,718,454 (GRCm39) |
splice site |
probably null |
|
IGL03089:Celsr3
|
APN |
9 |
108,703,806 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03162:Celsr3
|
APN |
9 |
108,719,757 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Celsr3
|
APN |
9 |
108,713,724 (GRCm39) |
splice site |
probably benign |
|
Diminishment
|
UTSW |
9 |
108,719,907 (GRCm39) |
intron |
probably benign |
|
little_d
|
UTSW |
9 |
108,704,891 (GRCm39) |
missense |
probably damaging |
0.98 |
nogal
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
F6893:Celsr3
|
UTSW |
9 |
108,712,266 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4243001:Celsr3
|
UTSW |
9 |
108,709,507 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4810001:Celsr3
|
UTSW |
9 |
108,722,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Celsr3
|
UTSW |
9 |
108,704,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0243:Celsr3
|
UTSW |
9 |
108,720,923 (GRCm39) |
splice site |
probably benign |
|
R0382:Celsr3
|
UTSW |
9 |
108,706,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Celsr3
|
UTSW |
9 |
108,706,272 (GRCm39) |
nonsense |
probably null |
|
R0510:Celsr3
|
UTSW |
9 |
108,704,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0630:Celsr3
|
UTSW |
9 |
108,704,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R0656:Celsr3
|
UTSW |
9 |
108,711,854 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0764:Celsr3
|
UTSW |
9 |
108,705,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Celsr3
|
UTSW |
9 |
108,719,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Celsr3
|
UTSW |
9 |
108,723,224 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1015:Celsr3
|
UTSW |
9 |
108,710,375 (GRCm39) |
missense |
probably benign |
0.17 |
R1321:Celsr3
|
UTSW |
9 |
108,713,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R1423:Celsr3
|
UTSW |
9 |
108,704,104 (GRCm39) |
missense |
probably benign |
0.00 |
R1497:Celsr3
|
UTSW |
9 |
108,726,064 (GRCm39) |
missense |
probably benign |
0.14 |
R1520:Celsr3
|
UTSW |
9 |
108,725,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Celsr3
|
UTSW |
9 |
108,726,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R1569:Celsr3
|
UTSW |
9 |
108,706,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Celsr3
|
UTSW |
9 |
108,720,151 (GRCm39) |
nonsense |
probably null |
|
R1753:Celsr3
|
UTSW |
9 |
108,709,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R1764:Celsr3
|
UTSW |
9 |
108,706,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Celsr3
|
UTSW |
9 |
108,711,825 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1838:Celsr3
|
UTSW |
9 |
108,707,105 (GRCm39) |
missense |
probably benign |
|
R1839:Celsr3
|
UTSW |
9 |
108,707,105 (GRCm39) |
missense |
probably benign |
|
R1874:Celsr3
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
R1875:Celsr3
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
R1953:Celsr3
|
UTSW |
9 |
108,720,381 (GRCm39) |
missense |
probably benign |
0.19 |
R1960:Celsr3
|
UTSW |
9 |
108,723,016 (GRCm39) |
missense |
probably benign |
|
R2113:Celsr3
|
UTSW |
9 |
108,715,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Celsr3
|
UTSW |
9 |
108,720,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2369:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2373:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2374:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2375:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2844:Celsr3
|
UTSW |
9 |
108,706,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2968:Celsr3
|
UTSW |
9 |
108,709,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Celsr3
|
UTSW |
9 |
108,714,338 (GRCm39) |
missense |
probably benign |
0.31 |
R3159:Celsr3
|
UTSW |
9 |
108,704,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3791:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R4194:Celsr3
|
UTSW |
9 |
108,720,501 (GRCm39) |
critical splice donor site |
probably null |
|
R4329:Celsr3
|
UTSW |
9 |
108,723,248 (GRCm39) |
missense |
probably benign |
0.00 |
R4365:Celsr3
|
UTSW |
9 |
108,707,046 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4419:Celsr3
|
UTSW |
9 |
108,720,443 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4484:Celsr3
|
UTSW |
9 |
108,723,262 (GRCm39) |
critical splice donor site |
probably null |
|
R4582:Celsr3
|
UTSW |
9 |
108,722,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R4681:Celsr3
|
UTSW |
9 |
108,704,953 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4729:Celsr3
|
UTSW |
9 |
108,724,851 (GRCm39) |
missense |
probably benign |
0.05 |
R4881:Celsr3
|
UTSW |
9 |
108,721,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Celsr3
|
UTSW |
9 |
108,726,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Celsr3
|
UTSW |
9 |
108,714,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R5207:Celsr3
|
UTSW |
9 |
108,709,958 (GRCm39) |
missense |
probably benign |
0.01 |
R5290:Celsr3
|
UTSW |
9 |
108,720,357 (GRCm39) |
missense |
probably benign |
0.01 |
R5345:Celsr3
|
UTSW |
9 |
108,709,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Celsr3
|
UTSW |
9 |
108,709,224 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5396:Celsr3
|
UTSW |
9 |
108,705,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5414:Celsr3
|
UTSW |
9 |
108,717,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5452:Celsr3
|
UTSW |
9 |
108,721,233 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5467:Celsr3
|
UTSW |
9 |
108,705,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Celsr3
|
UTSW |
9 |
108,721,743 (GRCm39) |
critical splice donor site |
probably null |
|
R5629:Celsr3
|
UTSW |
9 |
108,726,266 (GRCm39) |
missense |
probably benign |
0.41 |
R5637:Celsr3
|
UTSW |
9 |
108,714,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Celsr3
|
UTSW |
9 |
108,715,671 (GRCm39) |
missense |
probably benign |
0.03 |
R5739:Celsr3
|
UTSW |
9 |
108,704,357 (GRCm39) |
missense |
probably benign |
|
R5785:Celsr3
|
UTSW |
9 |
108,704,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Celsr3
|
UTSW |
9 |
108,722,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R5961:Celsr3
|
UTSW |
9 |
108,708,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Celsr3
|
UTSW |
9 |
108,714,350 (GRCm39) |
missense |
probably benign |
0.01 |
R6176:Celsr3
|
UTSW |
9 |
108,705,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Celsr3
|
UTSW |
9 |
108,706,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R6468:Celsr3
|
UTSW |
9 |
108,712,989 (GRCm39) |
missense |
probably benign |
0.08 |
R6481:Celsr3
|
UTSW |
9 |
108,714,283 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6547:Celsr3
|
UTSW |
9 |
108,706,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Celsr3
|
UTSW |
9 |
108,704,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6870:Celsr3
|
UTSW |
9 |
108,706,390 (GRCm39) |
missense |
probably benign |
0.02 |
R6977:Celsr3
|
UTSW |
9 |
108,704,914 (GRCm39) |
missense |
probably benign |
|
R7061:Celsr3
|
UTSW |
9 |
108,724,793 (GRCm39) |
nonsense |
probably null |
|
R7122:Celsr3
|
UTSW |
9 |
108,705,766 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7156:Celsr3
|
UTSW |
9 |
108,715,203 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7166:Celsr3
|
UTSW |
9 |
108,720,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Celsr3
|
UTSW |
9 |
108,722,961 (GRCm39) |
missense |
probably benign |
|
R7213:Celsr3
|
UTSW |
9 |
108,726,239 (GRCm39) |
missense |
probably damaging |
0.98 |
R7314:Celsr3
|
UTSW |
9 |
108,706,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7478:Celsr3
|
UTSW |
9 |
108,720,777 (GRCm39) |
missense |
probably benign |
0.37 |
R7508:Celsr3
|
UTSW |
9 |
108,713,821 (GRCm39) |
missense |
probably benign |
|
R7554:Celsr3
|
UTSW |
9 |
108,718,408 (GRCm39) |
missense |
probably benign |
|
R7615:Celsr3
|
UTSW |
9 |
108,714,851 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7653:Celsr3
|
UTSW |
9 |
108,712,269 (GRCm39) |
nonsense |
probably null |
|
R7747:Celsr3
|
UTSW |
9 |
108,707,177 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7881:Celsr3
|
UTSW |
9 |
108,705,271 (GRCm39) |
missense |
probably benign |
0.28 |
R7935:Celsr3
|
UTSW |
9 |
108,706,840 (GRCm39) |
missense |
probably benign |
0.01 |
R7995:Celsr3
|
UTSW |
9 |
108,722,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R8006:Celsr3
|
UTSW |
9 |
108,706,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R8077:Celsr3
|
UTSW |
9 |
108,705,530 (GRCm39) |
missense |
probably benign |
0.15 |
R8284:Celsr3
|
UTSW |
9 |
108,723,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R8291:Celsr3
|
UTSW |
9 |
108,715,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8322:Celsr3
|
UTSW |
9 |
108,725,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Celsr3
|
UTSW |
9 |
108,718,471 (GRCm39) |
frame shift |
probably null |
|
R8337:Celsr3
|
UTSW |
9 |
108,718,471 (GRCm39) |
frame shift |
probably null |
|
R8338:Celsr3
|
UTSW |
9 |
108,704,539 (GRCm39) |
nonsense |
probably null |
|
R8353:Celsr3
|
UTSW |
9 |
108,703,734 (GRCm39) |
missense |
probably benign |
0.00 |
R8407:Celsr3
|
UTSW |
9 |
108,706,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8408:Celsr3
|
UTSW |
9 |
108,708,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R8459:Celsr3
|
UTSW |
9 |
108,706,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Celsr3
|
UTSW |
9 |
108,715,319 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8713:Celsr3
|
UTSW |
9 |
108,707,062 (GRCm39) |
missense |
probably benign |
|
R8728:Celsr3
|
UTSW |
9 |
108,723,940 (GRCm39) |
missense |
probably benign |
0.24 |
R8829:Celsr3
|
UTSW |
9 |
108,717,582 (GRCm39) |
missense |
probably benign |
|
R8877:Celsr3
|
UTSW |
9 |
108,706,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Celsr3
|
UTSW |
9 |
108,718,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Celsr3
|
UTSW |
9 |
108,706,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9072:Celsr3
|
UTSW |
9 |
108,704,293 (GRCm39) |
missense |
probably benign |
|
R9157:Celsr3
|
UTSW |
9 |
108,707,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R9183:Celsr3
|
UTSW |
9 |
108,706,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Celsr3
|
UTSW |
9 |
108,715,689 (GRCm39) |
missense |
probably benign |
0.27 |
R9361:Celsr3
|
UTSW |
9 |
108,726,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Celsr3
|
UTSW |
9 |
108,706,961 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9407:Celsr3
|
UTSW |
9 |
108,723,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Celsr3
|
UTSW |
9 |
108,726,032 (GRCm39) |
missense |
probably benign |
0.00 |
R9607:Celsr3
|
UTSW |
9 |
108,717,701 (GRCm39) |
critical splice donor site |
probably null |
|
R9626:Celsr3
|
UTSW |
9 |
108,726,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Celsr3
|
UTSW |
9 |
108,703,559 (GRCm39) |
nonsense |
probably null |
|
R9630:Celsr3
|
UTSW |
9 |
108,704,296 (GRCm39) |
missense |
probably benign |
|
R9645:Celsr3
|
UTSW |
9 |
108,704,691 (GRCm39) |
nonsense |
probably null |
|
R9683:Celsr3
|
UTSW |
9 |
108,704,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Celsr3
|
UTSW |
9 |
108,728,502 (GRCm39) |
missense |
probably benign |
0.00 |
R9798:Celsr3
|
UTSW |
9 |
108,705,794 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Celsr3
|
UTSW |
9 |
108,726,256 (GRCm39) |
missense |
probably benign |
|
X0018:Celsr3
|
UTSW |
9 |
108,717,611 (GRCm39) |
missense |
probably benign |
0.01 |
X0018:Celsr3
|
UTSW |
9 |
108,704,977 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0026:Celsr3
|
UTSW |
9 |
108,706,129 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Celsr3
|
UTSW |
9 |
108,703,676 (GRCm39) |
missense |
probably benign |
0.34 |
|