Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
T |
C |
6: 83,139,568 (GRCm39) |
S498P |
probably damaging |
Het |
3100002H09Rik |
A |
G |
4: 124,504,487 (GRCm39) |
W22R |
probably damaging |
Het |
AA986860 |
A |
G |
1: 130,670,831 (GRCm39) |
E351G |
probably damaging |
Het |
Acsl5 |
T |
C |
19: 55,268,924 (GRCm39) |
V195A |
probably benign |
Het |
Actmap |
A |
G |
7: 26,902,105 (GRCm39) |
H244R |
probably damaging |
Het |
Adamts10 |
A |
G |
17: 33,756,293 (GRCm39) |
D312G |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,452,466 (GRCm39) |
M211V |
probably damaging |
Het |
Ankfy1 |
C |
T |
11: 72,646,693 (GRCm39) |
R859* |
probably null |
Het |
Atp8b1 |
T |
A |
18: 64,683,503 (GRCm39) |
I742L |
probably benign |
Het |
B3galnt2 |
T |
A |
13: 14,145,354 (GRCm39) |
V89E |
probably damaging |
Het |
Brinp3 |
A |
C |
1: 146,777,628 (GRCm39) |
T692P |
probably damaging |
Het |
C9 |
T |
A |
15: 6,516,243 (GRCm39) |
F349I |
probably damaging |
Het |
Cacna1a |
T |
A |
8: 85,360,062 (GRCm39) |
M1976K |
probably benign |
Het |
Castor2 |
T |
G |
5: 134,154,726 (GRCm39) |
S43R |
probably damaging |
Het |
Ccdc180 |
T |
C |
4: 45,927,975 (GRCm39) |
V1170A |
possibly damaging |
Het |
Ces1f |
A |
T |
8: 93,998,517 (GRCm39) |
Y160N |
possibly damaging |
Het |
Cfap45 |
A |
G |
1: 172,368,139 (GRCm39) |
E377G |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,460,932 (GRCm39) |
M240L |
probably benign |
Het |
Clnk |
G |
A |
5: 38,952,309 (GRCm39) |
T10M |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,045,291 (GRCm39) |
I781K |
possibly damaging |
Het |
Col11a2 |
G |
A |
17: 34,274,228 (GRCm39) |
G375S |
probably damaging |
Het |
Col6a5 |
T |
A |
9: 105,817,193 (GRCm39) |
I373F |
unknown |
Het |
Dmxl1 |
C |
T |
18: 49,985,434 (GRCm39) |
A227V |
probably benign |
Het |
Dok5 |
A |
G |
2: 170,574,052 (GRCm39) |
N4D |
probably benign |
Het |
Dpysl3 |
A |
T |
18: 43,496,622 (GRCm39) |
V138D |
probably damaging |
Het |
Efs |
A |
T |
14: 55,157,172 (GRCm39) |
Y380N |
probably damaging |
Het |
Eme2 |
G |
A |
17: 25,111,892 (GRCm39) |
S263F |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,546,275 (GRCm39) |
Q855R |
possibly damaging |
Het |
Fcrl2 |
A |
C |
3: 87,164,014 (GRCm39) |
S372A |
possibly damaging |
Het |
Gadl1 |
C |
T |
9: 115,773,297 (GRCm39) |
A113V |
probably damaging |
Het |
Gda |
T |
A |
19: 21,389,903 (GRCm39) |
E219D |
probably benign |
Het |
Gli1 |
A |
T |
10: 127,168,446 (GRCm39) |
M469K |
probably damaging |
Het |
Gm4847 |
A |
T |
1: 166,469,219 (GRCm39) |
S148R |
probably damaging |
Het |
Golga2 |
T |
C |
2: 32,192,216 (GRCm39) |
V325A |
probably benign |
Het |
Hpf1 |
A |
G |
8: 61,349,783 (GRCm39) |
D137G |
probably damaging |
Het |
Htr2a |
C |
G |
14: 74,943,293 (GRCm39) |
S291* |
probably null |
Het |
Itga5 |
G |
A |
15: 103,265,209 (GRCm39) |
Q233* |
probably null |
Het |
Jazf1 |
C |
A |
6: 52,789,168 (GRCm39) |
R102L |
probably damaging |
Het |
Kif6 |
T |
G |
17: 50,021,141 (GRCm39) |
L322R |
probably damaging |
Het |
Ktn1 |
A |
C |
14: 47,904,873 (GRCm39) |
K217T |
probably damaging |
Het |
Lig4 |
A |
T |
8: 10,023,012 (GRCm39) |
V256E |
possibly damaging |
Het |
Lrp1 |
G |
T |
10: 127,403,233 (GRCm39) |
D2113E |
probably damaging |
Het |
Lrp1 |
A |
T |
10: 127,411,155 (GRCm39) |
D1399E |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,979,443 (GRCm39) |
E717G |
probably damaging |
Het |
Mndal |
G |
T |
1: 173,699,032 (GRCm39) |
P155H |
possibly damaging |
Het |
Mycbpap |
A |
G |
11: 94,402,449 (GRCm39) |
|
probably null |
Het |
Nedd1 |
T |
C |
10: 92,555,476 (GRCm39) |
E3G |
probably damaging |
Het |
Nlgn1 |
A |
T |
3: 25,490,073 (GRCm39) |
N551K |
probably damaging |
Het |
Nup210 |
G |
A |
6: 91,046,148 (GRCm39) |
P595L |
possibly damaging |
Het |
Or2ag15 |
A |
G |
7: 106,340,212 (GRCm39) |
C310R |
probably benign |
Het |
Or2g25 |
A |
T |
17: 37,970,661 (GRCm39) |
C188S |
probably damaging |
Het |
Or4k52 |
A |
T |
2: 111,610,693 (GRCm39) |
|
probably null |
Het |
Or5ac17 |
T |
G |
16: 59,036,347 (GRCm39) |
T210P |
probably damaging |
Het |
Or5p56 |
A |
G |
7: 107,589,740 (GRCm39) |
H56R |
probably benign |
Het |
Pank3 |
G |
A |
11: 35,672,508 (GRCm39) |
V304M |
probably benign |
Het |
Phf3 |
G |
A |
1: 30,844,729 (GRCm39) |
T1410I |
probably benign |
Het |
Ppm1k |
A |
G |
6: 57,502,142 (GRCm39) |
I7T |
possibly damaging |
Het |
Ppp1r12c |
T |
C |
7: 4,500,424 (GRCm39) |
D73G |
probably damaging |
Het |
Prelid2 |
T |
G |
18: 42,014,332 (GRCm39) |
M165L |
probably benign |
Het |
Prkd3 |
A |
C |
17: 79,260,125 (GRCm39) |
L826R |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,814,433 (GRCm39) |
N778I |
probably damaging |
Het |
Ptprm |
T |
C |
17: 67,000,866 (GRCm39) |
D1063G |
possibly damaging |
Het |
Rab27a |
C |
A |
9: 72,982,764 (GRCm39) |
T23N |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,044,205 (GRCm39) |
F949L |
probably benign |
Het |
Rbm33 |
A |
G |
5: 28,542,002 (GRCm39) |
N68D |
probably damaging |
Het |
Rgl1 |
A |
T |
1: 152,462,284 (GRCm39) |
L109Q |
probably damaging |
Het |
Rnf20 |
A |
G |
4: 49,638,197 (GRCm39) |
N103S |
possibly damaging |
Het |
Sbno1 |
G |
A |
5: 124,530,675 (GRCm39) |
L875F |
probably damaging |
Het |
Scube1 |
T |
A |
15: 83,512,277 (GRCm39) |
|
probably null |
Het |
Selenbp1 |
G |
A |
3: 94,844,669 (GRCm39) |
V109M |
probably damaging |
Het |
Serpina3c |
T |
A |
12: 104,117,805 (GRCm39) |
I178F |
probably damaging |
Het |
Shisa8 |
C |
T |
15: 82,092,702 (GRCm39) |
G63D |
probably damaging |
Het |
Snx14 |
T |
C |
9: 88,284,277 (GRCm39) |
R464G |
possibly damaging |
Het |
Snx25 |
A |
T |
8: 46,577,119 (GRCm39) |
M1K |
probably null |
Het |
Sorcs3 |
C |
A |
19: 48,694,448 (GRCm39) |
T574K |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,150,557 (GRCm39) |
E6528G |
probably damaging |
Het |
Syt5 |
T |
C |
7: 4,543,245 (GRCm39) |
E338G |
probably damaging |
Het |
Tbk1 |
T |
C |
10: 121,387,223 (GRCm39) |
K691E |
probably benign |
Het |
Tenm3 |
G |
A |
8: 48,848,611 (GRCm39) |
T11I |
probably damaging |
Het |
Thrb |
A |
G |
14: 18,002,597 (GRCm38) |
H87R |
probably damaging |
Het |
Tlr4 |
T |
A |
4: 66,757,933 (GRCm39) |
M242K |
possibly damaging |
Het |
Tm4sf19 |
T |
C |
16: 32,224,820 (GRCm39) |
M56T |
possibly damaging |
Het |
Tmem212 |
T |
A |
3: 27,940,620 (GRCm39) |
R66* |
probably null |
Het |
Tmem39b |
G |
T |
4: 129,578,275 (GRCm39) |
D315E |
probably benign |
Het |
Tnxb |
T |
C |
17: 34,937,612 (GRCm39) |
F3834L |
probably damaging |
Het |
Trim36 |
A |
T |
18: 46,319,250 (GRCm39) |
L225* |
probably null |
Het |
Trim42 |
A |
T |
9: 97,247,732 (GRCm39) |
H321Q |
probably damaging |
Het |
Trio |
G |
T |
15: 27,732,726 (GRCm39) |
Q3052K |
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,955,698 (GRCm39) |
I1091T |
probably benign |
Het |
Tst |
T |
C |
15: 78,284,143 (GRCm39) |
E228G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,702,060 (GRCm39) |
|
probably benign |
Het |
Uap1 |
A |
C |
1: 169,978,510 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 188,530,011 (GRCm39) |
S3267P |
possibly damaging |
Het |
Usp5 |
T |
C |
6: 124,802,129 (GRCm39) |
T38A |
probably benign |
Het |
Uvssa |
A |
T |
5: 33,545,152 (GRCm39) |
Q84L |
probably damaging |
Het |
Vmn1r159 |
T |
G |
7: 22,542,693 (GRCm39) |
H113P |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,824,742 (GRCm39) |
|
probably null |
Het |
Zfp182 |
T |
A |
X: 20,897,799 (GRCm39) |
I166L |
probably benign |
Het |
Zfp811 |
A |
T |
17: 33,016,622 (GRCm39) |
Y472N |
probably damaging |
Het |
|
Other mutations in Celsr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Celsr1
|
APN |
15 |
85,815,546 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00519:Celsr1
|
APN |
15 |
85,915,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00909:Celsr1
|
APN |
15 |
85,806,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Celsr1
|
APN |
15 |
85,914,692 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01726:Celsr1
|
APN |
15 |
85,810,391 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01910:Celsr1
|
APN |
15 |
85,814,096 (GRCm39) |
missense |
probably benign |
|
IGL01931:Celsr1
|
APN |
15 |
85,791,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01952:Celsr1
|
APN |
15 |
85,847,424 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02090:Celsr1
|
APN |
15 |
85,791,922 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02191:Celsr1
|
APN |
15 |
85,863,205 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02372:Celsr1
|
APN |
15 |
85,814,108 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02413:Celsr1
|
APN |
15 |
85,915,427 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02478:Celsr1
|
APN |
15 |
85,825,337 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02507:Celsr1
|
APN |
15 |
85,784,889 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02508:Celsr1
|
APN |
15 |
85,914,818 (GRCm39) |
nonsense |
probably null |
|
IGL02899:Celsr1
|
APN |
15 |
85,915,927 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02939:Celsr1
|
APN |
15 |
85,785,673 (GRCm39) |
missense |
probably benign |
|
IGL03212:Celsr1
|
APN |
15 |
85,814,878 (GRCm39) |
missense |
probably benign |
0.04 |
P0028:Celsr1
|
UTSW |
15 |
85,806,436 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4305001:Celsr1
|
UTSW |
15 |
85,785,138 (GRCm39) |
missense |
possibly damaging |
0.87 |
PIT4480001:Celsr1
|
UTSW |
15 |
85,916,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R0018:Celsr1
|
UTSW |
15 |
85,915,243 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0018:Celsr1
|
UTSW |
15 |
85,915,243 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0038:Celsr1
|
UTSW |
15 |
85,813,620 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0057:Celsr1
|
UTSW |
15 |
85,914,963 (GRCm39) |
missense |
probably benign |
0.02 |
R0060:Celsr1
|
UTSW |
15 |
85,806,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R0060:Celsr1
|
UTSW |
15 |
85,806,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R0279:Celsr1
|
UTSW |
15 |
85,787,065 (GRCm39) |
missense |
probably benign |
0.00 |
R0570:Celsr1
|
UTSW |
15 |
85,787,566 (GRCm39) |
missense |
probably benign |
0.18 |
R0611:Celsr1
|
UTSW |
15 |
85,816,524 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0731:Celsr1
|
UTSW |
15 |
85,785,798 (GRCm39) |
missense |
probably benign |
|
R0792:Celsr1
|
UTSW |
15 |
85,815,477 (GRCm39) |
missense |
probably benign |
0.02 |
R0943:Celsr1
|
UTSW |
15 |
85,787,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0989:Celsr1
|
UTSW |
15 |
85,915,480 (GRCm39) |
missense |
probably benign |
0.39 |
R1118:Celsr1
|
UTSW |
15 |
85,916,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Celsr1
|
UTSW |
15 |
85,788,175 (GRCm39) |
missense |
probably benign |
0.01 |
R1239:Celsr1
|
UTSW |
15 |
85,863,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R1405:Celsr1
|
UTSW |
15 |
85,789,635 (GRCm39) |
splice site |
probably null |
|
R1405:Celsr1
|
UTSW |
15 |
85,789,635 (GRCm39) |
splice site |
probably null |
|
R1662:Celsr1
|
UTSW |
15 |
85,915,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Celsr1
|
UTSW |
15 |
85,816,658 (GRCm39) |
missense |
probably benign |
0.00 |
R1795:Celsr1
|
UTSW |
15 |
85,914,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R1799:Celsr1
|
UTSW |
15 |
85,916,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Celsr1
|
UTSW |
15 |
85,916,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R2040:Celsr1
|
UTSW |
15 |
85,917,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Celsr1
|
UTSW |
15 |
85,914,748 (GRCm39) |
missense |
probably benign |
0.02 |
R2131:Celsr1
|
UTSW |
15 |
85,847,424 (GRCm39) |
missense |
probably benign |
0.35 |
R2132:Celsr1
|
UTSW |
15 |
85,916,168 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2189:Celsr1
|
UTSW |
15 |
85,863,431 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2192:Celsr1
|
UTSW |
15 |
85,800,924 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4213:Celsr1
|
UTSW |
15 |
85,916,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Celsr1
|
UTSW |
15 |
85,863,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R4414:Celsr1
|
UTSW |
15 |
85,812,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4414:Celsr1
|
UTSW |
15 |
85,847,334 (GRCm39) |
missense |
probably benign |
0.00 |
R4416:Celsr1
|
UTSW |
15 |
85,812,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4645:Celsr1
|
UTSW |
15 |
85,800,957 (GRCm39) |
missense |
probably benign |
0.35 |
R4666:Celsr1
|
UTSW |
15 |
85,914,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Celsr1
|
UTSW |
15 |
85,816,661 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4735:Celsr1
|
UTSW |
15 |
85,790,230 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4804:Celsr1
|
UTSW |
15 |
85,822,154 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4995:Celsr1
|
UTSW |
15 |
85,822,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Celsr1
|
UTSW |
15 |
85,823,335 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5218:Celsr1
|
UTSW |
15 |
85,816,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R5280:Celsr1
|
UTSW |
15 |
85,814,747 (GRCm39) |
missense |
probably benign |
|
R5310:Celsr1
|
UTSW |
15 |
85,810,423 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5388:Celsr1
|
UTSW |
15 |
85,809,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R5484:Celsr1
|
UTSW |
15 |
85,815,483 (GRCm39) |
missense |
probably benign |
0.00 |
R5639:Celsr1
|
UTSW |
15 |
85,914,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5758:Celsr1
|
UTSW |
15 |
85,825,465 (GRCm39) |
missense |
probably benign |
0.27 |
R5778:Celsr1
|
UTSW |
15 |
85,917,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Celsr1
|
UTSW |
15 |
85,788,215 (GRCm39) |
missense |
probably benign |
0.02 |
R5915:Celsr1
|
UTSW |
15 |
85,914,550 (GRCm39) |
missense |
probably damaging |
0.96 |
R5915:Celsr1
|
UTSW |
15 |
85,822,176 (GRCm39) |
missense |
probably benign |
|
R5932:Celsr1
|
UTSW |
15 |
85,916,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Celsr1
|
UTSW |
15 |
85,916,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R5975:Celsr1
|
UTSW |
15 |
85,803,239 (GRCm39) |
splice site |
probably null |
|
R6050:Celsr1
|
UTSW |
15 |
85,814,812 (GRCm39) |
missense |
probably benign |
0.00 |
R6117:Celsr1
|
UTSW |
15 |
85,816,612 (GRCm39) |
missense |
probably benign |
0.04 |
R6178:Celsr1
|
UTSW |
15 |
85,785,222 (GRCm39) |
missense |
probably benign |
0.08 |
R6186:Celsr1
|
UTSW |
15 |
85,805,394 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6212:Celsr1
|
UTSW |
15 |
85,800,888 (GRCm39) |
missense |
probably benign |
0.25 |
R6307:Celsr1
|
UTSW |
15 |
85,812,531 (GRCm39) |
missense |
probably benign |
|
R6320:Celsr1
|
UTSW |
15 |
85,785,160 (GRCm39) |
missense |
probably benign |
0.13 |
R6349:Celsr1
|
UTSW |
15 |
85,915,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Celsr1
|
UTSW |
15 |
85,809,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R6504:Celsr1
|
UTSW |
15 |
85,863,121 (GRCm39) |
missense |
probably benign |
0.07 |
R6607:Celsr1
|
UTSW |
15 |
85,847,486 (GRCm39) |
missense |
probably benign |
|
R6615:Celsr1
|
UTSW |
15 |
85,786,315 (GRCm39) |
critical splice donor site |
probably null |
|
R6661:Celsr1
|
UTSW |
15 |
85,803,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R6722:Celsr1
|
UTSW |
15 |
85,790,115 (GRCm39) |
critical splice donor site |
probably null |
|
R6743:Celsr1
|
UTSW |
15 |
85,791,799 (GRCm39) |
missense |
probably damaging |
0.96 |
R6746:Celsr1
|
UTSW |
15 |
85,915,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R6772:Celsr1
|
UTSW |
15 |
85,914,983 (GRCm39) |
missense |
probably benign |
|
R6838:Celsr1
|
UTSW |
15 |
85,823,395 (GRCm39) |
missense |
probably benign |
|
R6886:Celsr1
|
UTSW |
15 |
85,915,855 (GRCm39) |
missense |
probably benign |
0.00 |
R7030:Celsr1
|
UTSW |
15 |
85,789,679 (GRCm39) |
missense |
probably damaging |
0.99 |
R7060:Celsr1
|
UTSW |
15 |
85,916,856 (GRCm39) |
missense |
probably benign |
0.07 |
R7080:Celsr1
|
UTSW |
15 |
85,816,652 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7325:Celsr1
|
UTSW |
15 |
85,917,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R7357:Celsr1
|
UTSW |
15 |
85,914,715 (GRCm39) |
missense |
probably benign |
0.00 |
R7371:Celsr1
|
UTSW |
15 |
85,914,875 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7446:Celsr1
|
UTSW |
15 |
85,791,874 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7465:Celsr1
|
UTSW |
15 |
85,917,593 (GRCm39) |
missense |
probably benign |
|
R7491:Celsr1
|
UTSW |
15 |
85,916,719 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7639:Celsr1
|
UTSW |
15 |
85,814,073 (GRCm39) |
missense |
probably benign |
0.00 |
R7685:Celsr1
|
UTSW |
15 |
85,862,933 (GRCm39) |
nonsense |
probably null |
|
R7741:Celsr1
|
UTSW |
15 |
85,863,303 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7768:Celsr1
|
UTSW |
15 |
85,816,610 (GRCm39) |
missense |
probably benign |
|
R7974:Celsr1
|
UTSW |
15 |
85,915,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7977:Celsr1
|
UTSW |
15 |
85,917,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Celsr1
|
UTSW |
15 |
85,917,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8073:Celsr1
|
UTSW |
15 |
85,823,356 (GRCm39) |
missense |
probably benign |
0.00 |
R8099:Celsr1
|
UTSW |
15 |
85,915,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R8190:Celsr1
|
UTSW |
15 |
85,787,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R8210:Celsr1
|
UTSW |
15 |
85,863,436 (GRCm39) |
missense |
probably benign |
0.00 |
R8289:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8290:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8292:Celsr1
|
UTSW |
15 |
85,791,819 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8328:Celsr1
|
UTSW |
15 |
85,806,445 (GRCm39) |
missense |
probably benign |
0.00 |
R8330:Celsr1
|
UTSW |
15 |
85,816,501 (GRCm39) |
missense |
probably damaging |
0.99 |
R8333:Celsr1
|
UTSW |
15 |
85,915,615 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8352:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8384:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8452:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8463:Celsr1
|
UTSW |
15 |
85,914,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R8479:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8480:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8493:Celsr1
|
UTSW |
15 |
85,822,207 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8498:Celsr1
|
UTSW |
15 |
85,823,306 (GRCm39) |
missense |
probably benign |
0.01 |
R8506:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8771:Celsr1
|
UTSW |
15 |
85,788,175 (GRCm39) |
missense |
probably benign |
0.01 |
R8891:Celsr1
|
UTSW |
15 |
85,822,194 (GRCm39) |
missense |
probably benign |
0.01 |
R8905:Celsr1
|
UTSW |
15 |
85,788,269 (GRCm39) |
intron |
probably benign |
|
R8924:Celsr1
|
UTSW |
15 |
85,916,671 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8979:Celsr1
|
UTSW |
15 |
85,847,340 (GRCm39) |
missense |
probably damaging |
0.96 |
R9069:Celsr1
|
UTSW |
15 |
85,914,772 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9115:Celsr1
|
UTSW |
15 |
85,803,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R9194:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9196:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9198:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9200:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9201:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9202:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9203:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9222:Celsr1
|
UTSW |
15 |
85,815,471 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9236:Celsr1
|
UTSW |
15 |
85,915,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9386:Celsr1
|
UTSW |
15 |
85,863,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9401:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9415:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9428:Celsr1
|
UTSW |
15 |
85,815,549 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9435:Celsr1
|
UTSW |
15 |
85,806,535 (GRCm39) |
splice site |
probably benign |
|
R9493:Celsr1
|
UTSW |
15 |
85,785,346 (GRCm39) |
missense |
probably damaging |
0.98 |
R9495:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9499:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9607:Celsr1
|
UTSW |
15 |
85,915,229 (GRCm39) |
missense |
|
|
R9673:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
Z1176:Celsr1
|
UTSW |
15 |
85,847,301 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Celsr1
|
UTSW |
15 |
85,863,052 (GRCm39) |
missense |
probably damaging |
1.00 |
|