Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd2 |
T |
C |
15: 91,063,347 (GRCm39) |
E447G |
probably benign |
Het |
Actn4 |
T |
C |
7: 28,598,071 (GRCm39) |
T510A |
probably benign |
Het |
Adgrb3 |
A |
G |
1: 25,133,153 (GRCm39) |
M1311T |
possibly damaging |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Bicdl1 |
G |
T |
5: 115,789,326 (GRCm39) |
|
probably benign |
Het |
Bmyc |
T |
C |
2: 25,597,346 (GRCm39) |
S137P |
probably damaging |
Het |
Camsap3 |
C |
T |
8: 3,654,708 (GRCm39) |
R782C |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,644 (GRCm39) |
T292I |
possibly damaging |
Het |
Chmp7 |
C |
T |
14: 69,956,899 (GRCm39) |
M336I |
probably benign |
Het |
Cnnm2 |
A |
G |
19: 46,751,562 (GRCm39) |
T451A |
probably damaging |
Het |
Eed |
T |
C |
7: 89,629,676 (GRCm39) |
K20E |
possibly damaging |
Het |
Eps15 |
T |
A |
4: 109,220,383 (GRCm39) |
M180K |
probably benign |
Het |
Esr1 |
T |
C |
10: 4,947,905 (GRCm39) |
I486T |
probably damaging |
Het |
Etnppl |
A |
G |
3: 130,422,393 (GRCm39) |
I207V |
possibly damaging |
Het |
Fancg |
G |
A |
4: 43,007,039 (GRCm39) |
P246L |
probably damaging |
Het |
Fcrl1 |
G |
A |
3: 87,293,030 (GRCm39) |
C249Y |
possibly damaging |
Het |
Foxred2 |
A |
G |
15: 77,839,961 (GRCm39) |
F110L |
possibly damaging |
Het |
Fsip2 |
A |
T |
2: 82,816,626 (GRCm39) |
N4120Y |
probably damaging |
Het |
Gm4884 |
C |
T |
7: 40,693,255 (GRCm39) |
S408L |
probably benign |
Het |
Gm9476 |
T |
C |
10: 100,142,474 (GRCm39) |
|
noncoding transcript |
Het |
Gria1 |
T |
C |
11: 57,127,836 (GRCm39) |
|
probably null |
Het |
H6pd |
T |
A |
4: 150,066,971 (GRCm39) |
I472F |
possibly damaging |
Het |
Hydin |
A |
T |
8: 111,137,092 (GRCm39) |
M632L |
probably benign |
Het |
Hyou1 |
C |
T |
9: 44,300,167 (GRCm39) |
P819S |
probably damaging |
Het |
Il6st |
A |
G |
13: 112,618,075 (GRCm39) |
E163G |
probably damaging |
Het |
Kcnk1 |
T |
C |
8: 126,722,278 (GRCm39) |
V27A |
possibly damaging |
Het |
Kdelr3 |
T |
C |
15: 79,407,114 (GRCm39) |
|
probably null |
Het |
Klk1b22 |
A |
G |
7: 43,765,399 (GRCm39) |
N117S |
possibly damaging |
Het |
Klrh1 |
T |
C |
6: 129,752,796 (GRCm39) |
D3G |
probably benign |
Het |
Lpp |
C |
A |
16: 24,500,591 (GRCm39) |
C134* |
probably null |
Het |
Lrrc37a |
G |
A |
11: 103,347,843 (GRCm39) |
R2951* |
probably null |
Het |
Luzp2 |
T |
A |
7: 54,899,238 (GRCm39) |
D285E |
possibly damaging |
Het |
Ly75 |
C |
T |
2: 60,158,237 (GRCm39) |
R1016H |
probably damaging |
Het |
Mesp2 |
T |
A |
7: 79,462,289 (GRCm39) |
S282T |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,659,289 (GRCm39) |
D776G |
probably damaging |
Het |
Nr2e1 |
T |
C |
10: 42,443,964 (GRCm39) |
T253A |
probably benign |
Het |
Nup214 |
C |
T |
2: 31,924,478 (GRCm39) |
S1669F |
probably damaging |
Het |
Or1r1 |
A |
T |
11: 73,875,347 (GRCm39) |
L29H |
probably damaging |
Het |
Padi6 |
T |
C |
4: 140,463,147 (GRCm39) |
Y146C |
probably damaging |
Het |
Pank4 |
C |
T |
4: 155,059,108 (GRCm39) |
R414W |
probably damaging |
Het |
Pclo |
T |
G |
5: 14,571,296 (GRCm39) |
I227S |
probably benign |
Het |
Plppr4 |
A |
G |
3: 117,121,915 (GRCm39) |
V221A |
possibly damaging |
Het |
Pradc1 |
G |
A |
6: 85,425,568 (GRCm39) |
R25C |
probably damaging |
Het |
Rfwd3 |
C |
T |
8: 112,014,874 (GRCm39) |
R326Q |
probably damaging |
Het |
Rnd2 |
A |
G |
11: 101,362,022 (GRCm39) |
T192A |
probably benign |
Het |
Rtbdn |
A |
G |
8: 85,681,695 (GRCm39) |
E131G |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,809,449 (GRCm39) |
V792A |
probably benign |
Het |
Sacs |
G |
T |
14: 61,451,128 (GRCm39) |
Q4391H |
probably damaging |
Het |
Scd2 |
A |
G |
19: 44,286,538 (GRCm39) |
S123G |
probably benign |
Het |
Septin9 |
A |
G |
11: 117,181,421 (GRCm39) |
R74G |
probably damaging |
Het |
Sipa1l2 |
T |
A |
8: 126,218,356 (GRCm39) |
Q327L |
probably damaging |
Het |
Skor1 |
T |
C |
9: 63,053,505 (GRCm39) |
T127A |
probably damaging |
Het |
Sphk2 |
A |
G |
7: 45,362,920 (GRCm39) |
V57A |
probably damaging |
Het |
Tfec |
A |
T |
6: 16,844,243 (GRCm39) |
D101E |
probably damaging |
Het |
Tmem43 |
T |
A |
6: 91,455,717 (GRCm39) |
H109Q |
probably benign |
Het |
Tmem67 |
C |
A |
4: 12,047,814 (GRCm39) |
S839I |
probably damaging |
Het |
Trpv5 |
T |
C |
6: 41,630,074 (GRCm39) |
Y672C |
probably damaging |
Het |
Ttc39d |
A |
C |
17: 80,523,913 (GRCm39) |
S191R |
probably benign |
Het |
Ttll1 |
C |
T |
15: 83,380,478 (GRCm39) |
V296M |
probably damaging |
Het |
Upp2 |
A |
C |
2: 58,664,177 (GRCm39) |
K130T |
possibly damaging |
Het |
Vmn2r5 |
A |
G |
3: 64,398,640 (GRCm39) |
C780R |
probably damaging |
Het |
Wars1 |
C |
A |
12: 108,841,635 (GRCm39) |
E171* |
probably null |
Het |
Zeb2 |
A |
T |
2: 44,887,012 (GRCm39) |
S637T |
probably damaging |
Het |
Zfp27 |
T |
A |
7: 29,595,549 (GRCm39) |
T139S |
possibly damaging |
Het |
Zfp941 |
A |
T |
7: 140,392,033 (GRCm39) |
L442Q |
probably benign |
Het |
|
Other mutations in Cibar1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02514:Cibar1
|
APN |
4 |
12,164,080 (GRCm39) |
splice site |
probably benign |
|
R0558:Cibar1
|
UTSW |
4 |
12,164,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R0616:Cibar1
|
UTSW |
4 |
12,168,234 (GRCm39) |
nonsense |
probably null |
|
R1862:Cibar1
|
UTSW |
4 |
12,155,717 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2027:Cibar1
|
UTSW |
4 |
12,171,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Cibar1
|
UTSW |
4 |
12,169,041 (GRCm39) |
splice site |
probably benign |
|
R2212:Cibar1
|
UTSW |
4 |
12,171,696 (GRCm39) |
critical splice donor site |
probably null |
|
R3053:Cibar1
|
UTSW |
4 |
12,157,767 (GRCm39) |
splice site |
probably null |
|
R4441:Cibar1
|
UTSW |
4 |
12,157,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Cibar1
|
UTSW |
4 |
12,155,689 (GRCm39) |
missense |
probably benign |
0.03 |
R5290:Cibar1
|
UTSW |
4 |
12,171,195 (GRCm39) |
missense |
probably benign |
0.08 |
R5928:Cibar1
|
UTSW |
4 |
12,171,919 (GRCm39) |
unclassified |
probably benign |
|
R6529:Cibar1
|
UTSW |
4 |
12,168,978 (GRCm39) |
missense |
probably damaging |
0.98 |
R6909:Cibar1
|
UTSW |
4 |
12,168,309 (GRCm39) |
missense |
probably benign |
0.05 |
R8182:Cibar1
|
UTSW |
4 |
12,171,842 (GRCm39) |
missense |
probably benign |
0.00 |
R8292:Cibar1
|
UTSW |
4 |
12,153,963 (GRCm39) |
missense |
possibly damaging |
0.85 |
|