Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agtr1b |
G |
T |
3: 20,369,943 (GRCm39) |
A221D |
probably benign |
Het |
Aldh18a1 |
A |
T |
19: 40,559,005 (GRCm39) |
D280E |
probably benign |
Het |
Apob |
G |
A |
12: 8,039,194 (GRCm39) |
D475N |
probably benign |
Het |
Bmi1 |
C |
T |
2: 18,689,186 (GRCm39) |
T290I |
probably benign |
Het |
Brd8 |
A |
T |
18: 34,746,292 (GRCm39) |
D139E |
possibly damaging |
Het |
Cacna1e |
C |
A |
1: 154,317,270 (GRCm39) |
V1467F |
possibly damaging |
Het |
Cdh15 |
A |
G |
8: 123,591,086 (GRCm39) |
D445G |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,481,123 (GRCm39) |
L290H |
probably damaging |
Het |
Chi3l1 |
T |
A |
1: 134,109,996 (GRCm39) |
M1K |
probably null |
Het |
Crybg2 |
T |
C |
4: 133,808,737 (GRCm39) |
S1404P |
probably damaging |
Het |
Cubn |
C |
A |
2: 13,285,006 (GRCm39) |
C3470F |
probably damaging |
Het |
Cyp20a1 |
T |
C |
1: 60,391,331 (GRCm39) |
|
probably null |
Het |
Cyp24a1 |
G |
T |
2: 170,328,704 (GRCm39) |
T408K |
probably benign |
Het |
Cyp2a12 |
A |
T |
7: 26,730,577 (GRCm39) |
I181F |
possibly damaging |
Het |
Dnm1l |
A |
T |
16: 16,149,952 (GRCm39) |
I268N |
probably damaging |
Het |
Eif2a |
A |
G |
3: 58,464,517 (GRCm39) |
|
probably null |
Het |
Epg5 |
T |
C |
18: 78,005,613 (GRCm39) |
F701S |
probably damaging |
Het |
Fbxo46 |
T |
C |
7: 18,870,466 (GRCm39) |
S362P |
possibly damaging |
Het |
Fgf22 |
A |
G |
10: 79,592,830 (GRCm39) |
|
probably benign |
Het |
Fhod1 |
A |
C |
8: 106,063,982 (GRCm39) |
|
probably benign |
Het |
Flnc |
T |
A |
6: 29,459,062 (GRCm39) |
V2448D |
probably damaging |
Het |
Gm2696 |
G |
T |
10: 77,671,972 (GRCm39) |
|
probably benign |
Het |
Gmpr |
T |
C |
13: 45,685,874 (GRCm39) |
S214P |
possibly damaging |
Het |
Krt6a |
A |
G |
15: 101,600,744 (GRCm39) |
V308A |
probably damaging |
Het |
Lig3 |
T |
A |
11: 82,684,833 (GRCm39) |
|
probably null |
Het |
Lrrc37a |
T |
A |
11: 103,394,877 (GRCm39) |
N183Y |
probably benign |
Het |
Mapk8ip3 |
C |
A |
17: 25,125,879 (GRCm39) |
G422V |
probably damaging |
Het |
Mks1 |
T |
C |
11: 87,746,325 (GRCm39) |
S97P |
probably benign |
Het |
Mphosph9 |
A |
T |
5: 124,463,024 (GRCm39) |
V7E |
probably damaging |
Het |
Msh5 |
A |
G |
17: 35,248,900 (GRCm39) |
L711P |
probably damaging |
Het |
Naga |
T |
A |
15: 82,216,404 (GRCm39) |
|
probably null |
Het |
Nherf4 |
A |
G |
9: 44,159,980 (GRCm39) |
V380A |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,524,953 (GRCm39) |
T176S |
possibly damaging |
Het |
Nqo1 |
T |
C |
8: 108,115,582 (GRCm39) |
N232D |
probably benign |
Het |
Or1j21 |
C |
G |
2: 36,683,585 (GRCm39) |
N112K |
possibly damaging |
Het |
Or2b6 |
T |
A |
13: 21,823,418 (GRCm39) |
I92L |
probably damaging |
Het |
P2ry6 |
A |
G |
7: 100,587,603 (GRCm39) |
F252S |
probably damaging |
Het |
P3h3 |
G |
A |
6: 124,831,835 (GRCm39) |
R317W |
probably benign |
Het |
Pakap |
T |
A |
4: 57,710,173 (GRCm39) |
C373S |
probably damaging |
Het |
Phkb |
T |
A |
8: 86,602,327 (GRCm39) |
D39E |
probably benign |
Het |
Psg16 |
G |
A |
7: 16,822,112 (GRCm39) |
G23D |
probably damaging |
Het |
Ptgr2 |
T |
A |
12: 84,349,111 (GRCm39) |
I150K |
probably benign |
Het |
Ptprf |
A |
G |
4: 118,070,011 (GRCm39) |
V1457A |
probably benign |
Het |
Sart3 |
A |
T |
5: 113,889,301 (GRCm39) |
Y508N |
probably benign |
Het |
Sh3bp1 |
C |
T |
15: 78,795,715 (GRCm39) |
P615S |
probably damaging |
Het |
Ska3 |
A |
T |
14: 58,054,148 (GRCm39) |
N267K |
probably benign |
Het |
Slc26a7 |
A |
G |
4: 14,524,498 (GRCm39) |
I462T |
probably benign |
Het |
Slu7 |
C |
T |
11: 43,332,316 (GRCm39) |
A244V |
probably benign |
Het |
Smarca4 |
C |
T |
9: 21,548,671 (GRCm39) |
P319L |
probably damaging |
Het |
Smg9 |
A |
G |
7: 24,120,286 (GRCm39) |
D420G |
probably benign |
Het |
Strc |
T |
A |
2: 121,205,439 (GRCm39) |
D25V |
probably benign |
Het |
Syne2 |
T |
G |
12: 76,108,424 (GRCm39) |
V936G |
probably damaging |
Het |
Tbc1d7 |
C |
T |
13: 43,306,409 (GRCm39) |
|
probably benign |
Het |
Terb1 |
C |
A |
8: 105,173,831 (GRCm39) |
D751Y |
probably damaging |
Het |
Trpc1 |
A |
G |
9: 95,603,303 (GRCm39) |
Y410H |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,089,043 (GRCm39) |
N333D |
probably benign |
Het |
Usp34 |
T |
C |
11: 23,402,520 (GRCm39) |
S2438P |
probably damaging |
Het |
Vps35l |
T |
C |
7: 118,353,072 (GRCm39) |
V189A |
probably benign |
Het |
Zbtb17 |
G |
A |
4: 141,190,694 (GRCm39) |
G171S |
probably benign |
Het |
Zfp7 |
G |
A |
15: 76,774,810 (GRCm39) |
G284D |
possibly damaging |
Het |
Zfyve26 |
A |
G |
12: 79,286,776 (GRCm39) |
S2271P |
probably damaging |
Het |
Zscan18 |
G |
A |
7: 12,509,147 (GRCm39) |
|
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 |
|
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 |
|