Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
G |
A |
15: 101,108,720 (GRCm39) |
V499M |
possibly damaging |
Het |
Adam5 |
G |
A |
8: 25,294,475 (GRCm39) |
Q375* |
probably null |
Het |
Adgrf1 |
G |
A |
17: 43,606,055 (GRCm39) |
E60K |
probably benign |
Het |
Alb |
T |
C |
5: 90,610,630 (GRCm39) |
V70A |
probably damaging |
Het |
Aph1b |
T |
A |
9: 66,695,709 (GRCm39) |
|
probably benign |
Het |
Aste1 |
G |
A |
9: 105,274,189 (GRCm39) |
R143Q |
possibly damaging |
Het |
Aste1 |
A |
T |
9: 105,274,995 (GRCm39) |
T351S |
probably damaging |
Het |
Bace2 |
T |
A |
16: 97,214,670 (GRCm39) |
L286Q |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,516,163 (GRCm39) |
G235R |
probably damaging |
Het |
Bpnt2 |
C |
T |
4: 4,769,376 (GRCm39) |
M246I |
probably benign |
Het |
Brwd1 |
A |
T |
16: 95,848,630 (GRCm39) |
H516Q |
probably damaging |
Het |
Cc2d2a |
C |
A |
5: 43,842,486 (GRCm39) |
|
probably null |
Het |
Cdh22 |
T |
A |
2: 164,988,646 (GRCm39) |
E236D |
probably benign |
Het |
Celsr2 |
T |
A |
3: 108,306,218 (GRCm39) |
T2029S |
probably benign |
Het |
Col11a1 |
A |
G |
3: 113,975,043 (GRCm39) |
D1234G |
probably benign |
Het |
Cplane1 |
C |
A |
15: 8,216,942 (GRCm39) |
P720Q |
possibly damaging |
Het |
Cpt2 |
A |
G |
4: 107,764,957 (GRCm39) |
I269T |
probably damaging |
Het |
Dcaf7 |
T |
A |
11: 105,945,619 (GRCm39) |
S323T |
probably benign |
Het |
Ddias |
G |
T |
7: 92,508,608 (GRCm39) |
Q436K |
probably benign |
Het |
Dlec1 |
G |
A |
9: 118,972,335 (GRCm39) |
|
probably null |
Het |
Dock5 |
T |
A |
14: 68,073,859 (GRCm39) |
I294F |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,173,794 (GRCm39) |
D2306E |
possibly damaging |
Het |
Gm4787 |
T |
A |
12: 81,424,280 (GRCm39) |
D626V |
probably damaging |
Het |
Gm6563 |
A |
G |
19: 23,653,290 (GRCm39) |
T27A |
probably benign |
Het |
Hadhb |
T |
C |
5: 30,373,568 (GRCm39) |
|
probably null |
Het |
Hsph1 |
A |
T |
5: 149,551,029 (GRCm39) |
W406R |
probably null |
Het |
Ighv1-66 |
C |
T |
12: 115,557,002 (GRCm39) |
G27R |
possibly damaging |
Het |
Krt26 |
T |
C |
11: 99,228,426 (GRCm39) |
E102G |
probably damaging |
Het |
Krt34 |
T |
A |
11: 99,930,971 (GRCm39) |
|
probably null |
Het |
Krt36 |
T |
C |
11: 99,993,635 (GRCm39) |
D401G |
possibly damaging |
Het |
Loxhd1 |
G |
A |
18: 77,518,827 (GRCm39) |
G326S |
probably damaging |
Het |
Lrrc8b |
A |
G |
5: 105,633,802 (GRCm39) |
N758S |
probably damaging |
Het |
Mrtfb |
A |
T |
16: 13,202,056 (GRCm39) |
|
probably null |
Het |
Muc4 |
C |
T |
16: 32,574,421 (GRCm39) |
T957I |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,358,743 (GRCm39) |
Y831C |
probably damaging |
Het |
Nfatc1 |
A |
T |
18: 80,678,859 (GRCm39) |
V829E |
probably benign |
Het |
Nmnat1 |
G |
A |
4: 149,557,827 (GRCm39) |
L72F |
possibly damaging |
Het |
Or4f14d |
A |
T |
2: 111,960,330 (GRCm39) |
D275E |
possibly damaging |
Het |
Pcdh7 |
T |
A |
5: 58,286,407 (GRCm39) |
V1161E |
probably damaging |
Het |
Raver1 |
A |
G |
9: 21,001,576 (GRCm39) |
Y86H |
probably benign |
Het |
Recql4 |
G |
T |
15: 76,588,705 (GRCm39) |
H1035Q |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,411,284 (GRCm39) |
M814K |
probably benign |
Het |
Sh3d19 |
T |
G |
3: 85,992,184 (GRCm39) |
W71G |
probably benign |
Het |
Sidt1 |
T |
C |
16: 44,065,529 (GRCm39) |
Y759C |
probably damaging |
Het |
Spg11 |
G |
T |
2: 121,943,560 (GRCm39) |
D197E |
probably damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Ssc5d |
A |
T |
7: 4,939,328 (GRCm39) |
D588V |
probably damaging |
Het |
Supt20 |
C |
A |
3: 54,614,537 (GRCm39) |
T181K |
probably damaging |
Het |
Szt2 |
A |
T |
4: 118,244,015 (GRCm39) |
S1363R |
probably benign |
Het |
Tbcel |
G |
A |
9: 42,375,169 (GRCm39) |
|
probably null |
Het |
Ube2e3 |
T |
C |
2: 78,749,158 (GRCm39) |
L169P |
probably damaging |
Het |
Wrn |
A |
G |
8: 33,778,796 (GRCm39) |
F595S |
probably benign |
Het |
Zfp473 |
G |
T |
7: 44,382,323 (GRCm39) |
P670Q |
probably damaging |
Het |
Zw10 |
C |
T |
9: 48,986,299 (GRCm39) |
A660V |
probably benign |
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 |
|
R1522:Celsr1
|
UTSW |
15 |
85,815,477 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
|
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 |
|