Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg1 |
G |
A |
9: 54,517,083 (GRCm39) |
P577S |
probably damaging |
Het |
Adal |
T |
C |
2: 120,985,236 (GRCm39) |
V269A |
possibly damaging |
Het |
Adam33 |
T |
C |
2: 130,898,250 (GRCm39) |
T155A |
probably benign |
Het |
Adgre1 |
A |
T |
17: 57,752,061 (GRCm39) |
E603V |
possibly damaging |
Het |
Adgrf4 |
T |
C |
17: 42,978,441 (GRCm39) |
T301A |
probably damaging |
Het |
Agtpbp1 |
G |
T |
13: 59,630,385 (GRCm39) |
A782E |
possibly damaging |
Het |
Ank3 |
A |
T |
10: 69,811,925 (GRCm39) |
K1197N |
possibly damaging |
Het |
Anxa9 |
A |
T |
3: 95,213,207 (GRCm39) |
D46E |
probably damaging |
Het |
Atg9a |
T |
C |
1: 75,161,927 (GRCm39) |
T540A |
probably damaging |
Het |
Atg9a |
A |
G |
1: 75,163,009 (GRCm39) |
Y364H |
probably damaging |
Het |
Bltp1 |
A |
C |
3: 37,067,030 (GRCm39) |
E73A |
|
Het |
Cd300c2 |
C |
T |
11: 114,891,634 (GRCm39) |
G80D |
possibly damaging |
Het |
Cebpz |
T |
C |
17: 79,230,685 (GRCm39) |
E844G |
probably benign |
Het |
Cftr |
A |
G |
6: 18,220,696 (GRCm39) |
N189S |
probably damaging |
Het |
Dhrs13 |
G |
T |
11: 77,924,302 (GRCm39) |
R116I |
unknown |
Het |
Dnah10 |
A |
G |
5: 124,827,858 (GRCm39) |
M735V |
probably benign |
Het |
Dnajb8 |
C |
T |
6: 88,199,940 (GRCm39) |
R159C |
possibly damaging |
Het |
E130208F15Rik |
C |
A |
7: 30,021,619 (GRCm39) |
S93* |
probably null |
Het |
E330034G19Rik |
T |
C |
14: 24,346,104 (GRCm39) |
I92T |
|
Het |
Eef1d |
A |
T |
15: 75,768,309 (GRCm39) |
V511D |
probably damaging |
Het |
Efna1 |
T |
G |
3: 89,183,520 (GRCm39) |
E102A |
probably damaging |
Het |
H2-M11 |
C |
A |
17: 36,858,860 (GRCm39) |
F133L |
probably damaging |
Het |
Htr3b |
G |
T |
9: 48,847,343 (GRCm39) |
|
probably null |
Het |
Kcns3 |
A |
G |
12: 11,142,253 (GRCm39) |
S149P |
probably damaging |
Het |
Lhx4 |
T |
A |
1: 155,586,214 (GRCm39) |
|
probably null |
Het |
Lrp1 |
C |
T |
10: 127,412,354 (GRCm39) |
V1317M |
probably damaging |
Het |
Mphosph9 |
A |
G |
5: 124,405,174 (GRCm39) |
I799T |
probably damaging |
Het |
Muc1 |
C |
T |
3: 89,138,906 (GRCm39) |
A505V |
probably damaging |
Het |
Muc6 |
C |
A |
7: 141,235,673 (GRCm39) |
|
probably null |
Het |
Mylk |
A |
G |
16: 34,820,721 (GRCm39) |
D1891G |
probably damaging |
Het |
Nfe2l3 |
A |
T |
6: 51,428,065 (GRCm39) |
H209L |
probably benign |
Het |
Nprl2 |
A |
C |
9: 107,421,947 (GRCm39) |
Y241S |
probably damaging |
Het |
Oprm1 |
A |
T |
10: 6,780,442 (GRCm39) |
Q368L |
probably benign |
Het |
Or4g7 |
T |
A |
2: 111,309,753 (GRCm39) |
M208K |
possibly damaging |
Het |
Pcm1 |
C |
T |
8: 41,766,974 (GRCm39) |
R1593C |
probably damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,162,878 (GRCm39) |
|
probably null |
Het |
Pnoc |
A |
G |
14: 65,642,521 (GRCm39) |
S81P |
probably benign |
Het |
Prkg2 |
T |
A |
5: 99,114,393 (GRCm39) |
D585V |
probably damaging |
Het |
Prpf38b |
A |
T |
3: 108,815,148 (GRCm39) |
|
probably benign |
Het |
Ranbp3l |
G |
T |
15: 9,065,059 (GRCm39) |
S482I |
probably benign |
Het |
Rapgef4 |
T |
C |
2: 72,056,364 (GRCm39) |
F651L |
probably benign |
Het |
Rasgrf1 |
A |
G |
9: 89,793,675 (GRCm39) |
T151A |
unknown |
Het |
Rnf215 |
T |
C |
11: 4,085,544 (GRCm39) |
L91P |
possibly damaging |
Het |
Rph3a |
T |
C |
5: 121,099,312 (GRCm39) |
H193R |
probably benign |
Het |
Rps17 |
C |
T |
7: 80,994,750 (GRCm39) |
V4I |
probably benign |
Het |
Sec61a2 |
A |
T |
2: 5,881,728 (GRCm39) |
F234Y |
possibly damaging |
Het |
Serpinb8 |
T |
C |
1: 107,526,736 (GRCm39) |
L92P |
probably damaging |
Het |
Slc1a6 |
A |
T |
10: 78,632,091 (GRCm39) |
I306F |
possibly damaging |
Het |
Slc26a11 |
T |
C |
11: 119,270,692 (GRCm39) |
V538A |
possibly damaging |
Het |
Slc27a1 |
G |
A |
8: 72,032,566 (GRCm39) |
S193N |
probably benign |
Het |
Slc9b1 |
T |
C |
3: 135,097,948 (GRCm39) |
S393P |
probably damaging |
Het |
Slfn3 |
T |
A |
11: 83,105,332 (GRCm39) |
I320K |
possibly damaging |
Het |
Spata31f1a |
T |
A |
4: 42,848,542 (GRCm39) |
M1205L |
probably benign |
Het |
Tgfbr1 |
A |
T |
4: 47,406,924 (GRCm39) |
I420F |
probably benign |
Het |
Tnik |
A |
T |
3: 28,658,482 (GRCm39) |
D589V |
possibly damaging |
Het |
Trappc8 |
A |
C |
18: 21,006,938 (GRCm39) |
|
probably null |
Het |
Ttbk1 |
A |
G |
17: 46,791,087 (GRCm39) |
S66P |
possibly damaging |
Het |
Unc13c |
A |
G |
9: 73,392,220 (GRCm39) |
V2044A |
probably benign |
Het |
Usp53 |
T |
C |
3: 122,741,045 (GRCm39) |
E735G |
probably benign |
Het |
Vmn2r-ps158 |
T |
A |
7: 42,673,462 (GRCm39) |
N180K |
probably benign |
Het |
Zfyve26 |
A |
T |
12: 79,302,037 (GRCm39) |
V1853D |
probably damaging |
Het |
Zkscan17 |
A |
G |
11: 59,394,574 (GRCm39) |
V9A |
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 |
|
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 |
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 |
|