Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,902,963 (GRCm39) |
T421A |
probably damaging |
Het |
Adamts12 |
T |
C |
15: 11,317,443 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
T |
13: 81,567,588 (GRCm39) |
V5195E |
probably benign |
Het |
Adora2b |
C |
T |
11: 62,139,983 (GRCm39) |
A19V |
possibly damaging |
Het |
Ankrd28 |
A |
G |
14: 31,477,698 (GRCm39) |
C115R |
probably benign |
Het |
Ankrd35 |
T |
A |
3: 96,587,003 (GRCm39) |
L106* |
probably null |
Het |
Ankrd44 |
G |
A |
1: 54,801,538 (GRCm39) |
A263V |
probably damaging |
Het |
Apol7b |
T |
C |
15: 77,308,120 (GRCm39) |
K125R |
possibly damaging |
Het |
Cacna1c |
A |
T |
6: 118,719,232 (GRCm39) |
L245* |
probably null |
Het |
Cbll1 |
A |
T |
12: 31,538,199 (GRCm39) |
H185Q |
probably damaging |
Het |
Ccdc150 |
A |
C |
1: 54,311,641 (GRCm39) |
N209T |
probably benign |
Het |
Ccdc88a |
T |
A |
11: 29,448,416 (GRCm39) |
N1465K |
possibly damaging |
Het |
Cfap54 |
C |
A |
10: 92,864,562 (GRCm39) |
G124* |
probably null |
Het |
Chml |
A |
T |
1: 175,514,601 (GRCm39) |
L440H |
probably damaging |
Het |
Chrnd |
A |
T |
1: 87,122,603 (GRCm39) |
Q128L |
probably damaging |
Het |
Clvs2 |
A |
T |
10: 33,498,677 (GRCm39) |
D84E |
probably benign |
Het |
Ctif |
CGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACAC |
CGGGGCACACTTTGCTCTTACCTCCCGGAGGCACGTGTAGATGGGGCACAC |
18: 75,604,874 (GRCm39) |
|
probably benign |
Het |
Cyp2c40 |
T |
A |
19: 39,755,926 (GRCm39) |
I463F |
possibly damaging |
Het |
Cyp51 |
C |
A |
5: 4,136,519 (GRCm39) |
R425L |
probably damaging |
Het |
Daam1 |
A |
G |
12: 71,992,018 (GRCm39) |
T279A |
unknown |
Het |
Ebf2 |
G |
T |
14: 67,665,554 (GRCm39) |
V571F |
probably benign |
Het |
Elapor2 |
T |
A |
5: 9,487,792 (GRCm39) |
N559K |
probably damaging |
Het |
Elavl4 |
A |
T |
4: 110,063,776 (GRCm39) |
I275N |
probably damaging |
Het |
F11r |
A |
G |
1: 171,288,505 (GRCm39) |
Q116R |
probably benign |
Het |
Gatad1 |
A |
C |
5: 3,691,544 (GRCm39) |
L4R |
probably damaging |
Het |
Gcn1 |
T |
A |
5: 115,727,153 (GRCm39) |
M670K |
probably benign |
Het |
Greb1 |
A |
T |
12: 16,774,885 (GRCm39) |
F171I |
probably damaging |
Het |
Grin2b |
A |
G |
6: 136,021,007 (GRCm39) |
V98A |
probably damaging |
Het |
Helz2 |
A |
T |
2: 180,871,407 (GRCm39) |
V2735E |
probably damaging |
Het |
Hrct1 |
A |
T |
4: 43,727,564 (GRCm39) |
|
probably benign |
Het |
Ighv1-11 |
C |
T |
12: 114,575,864 (GRCm39) |
R117K |
probably damaging |
Het |
Igkv12-46 |
A |
T |
6: 69,741,754 (GRCm39) |
S34T |
probably damaging |
Het |
Il27ra |
T |
A |
8: 84,767,711 (GRCm39) |
N71Y |
probably damaging |
Het |
Iqca1 |
G |
T |
1: 90,067,649 (GRCm39) |
H201N |
probably benign |
Het |
Itgb1bp1 |
C |
T |
12: 21,324,864 (GRCm39) |
R64Q |
probably damaging |
Het |
Katnb1 |
T |
C |
8: 95,809,519 (GRCm39) |
L13S |
probably damaging |
Het |
Kif26b |
G |
A |
1: 178,743,714 (GRCm39) |
R1270Q |
probably benign |
Het |
Klhdc2 |
A |
T |
12: 69,347,065 (GRCm39) |
R77* |
probably null |
Het |
Klra10 |
A |
T |
6: 130,249,617 (GRCm39) |
|
probably null |
Het |
Large1 |
A |
T |
8: 73,542,612 (GRCm39) |
I704N |
probably damaging |
Het |
Lrp1b |
G |
A |
2: 40,888,196 (GRCm39) |
H2241Y |
probably benign |
Het |
Lrpap1 |
T |
A |
5: 35,255,001 (GRCm39) |
M212L |
probably benign |
Het |
Mab21l1 |
A |
G |
3: 55,690,348 (GRCm39) |
|
probably benign |
Het |
Map4k4 |
A |
T |
1: 40,039,740 (GRCm39) |
Q44L |
probably damaging |
Het |
Map7d1 |
A |
G |
4: 126,130,475 (GRCm39) |
S412P |
probably damaging |
Het |
Me1 |
A |
T |
9: 86,480,844 (GRCm39) |
F354I |
probably damaging |
Het |
Nlrp1b |
A |
G |
11: 71,108,658 (GRCm39) |
V281A |
probably damaging |
Het |
Nrip2 |
A |
G |
6: 128,385,288 (GRCm39) |
T240A |
possibly damaging |
Het |
Nsmaf |
A |
G |
4: 6,428,471 (GRCm39) |
V203A |
probably damaging |
Het |
Or12e8 |
T |
A |
2: 87,187,950 (GRCm39) |
I54K |
possibly damaging |
Het |
Or4g17 |
A |
T |
2: 111,209,645 (GRCm39) |
Q100L |
probably damaging |
Het |
Or4n5 |
A |
T |
14: 50,132,509 (GRCm39) |
M250K |
probably benign |
Het |
Or8g2 |
A |
G |
9: 39,821,495 (GRCm39) |
Y132C |
probably damaging |
Het |
P4ha2 |
T |
C |
11: 54,004,995 (GRCm39) |
F124L |
probably benign |
Het |
Pcdha9 |
A |
T |
18: 37,131,750 (GRCm39) |
D273V |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Plxnd1 |
G |
T |
6: 115,949,506 (GRCm39) |
S760* |
probably null |
Het |
Polr1b |
A |
G |
2: 128,957,576 (GRCm39) |
T544A |
probably benign |
Het |
Polr2g |
T |
C |
19: 8,771,513 (GRCm39) |
D153G |
probably damaging |
Het |
Pramel12 |
T |
C |
4: 143,144,229 (GRCm39) |
Y192H |
probably benign |
Het |
Rad51ap2 |
A |
C |
12: 11,506,255 (GRCm39) |
E59A |
possibly damaging |
Het |
Rrm1 |
A |
T |
7: 102,105,739 (GRCm39) |
Y285F |
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,667,015 (GRCm39) |
|
probably null |
Het |
Scaf4 |
GGCTGCTGCTGCTGCTGCTGCTGCTG |
GGCTGCTGCTGCTGCTGCTGCTG |
16: 90,026,745 (GRCm39) |
|
probably benign |
Het |
Sftpd |
A |
G |
14: 40,905,001 (GRCm39) |
V30A |
probably benign |
Het |
Sirt6 |
A |
G |
10: 81,462,378 (GRCm39) |
V7A |
probably benign |
Het |
Ska1 |
C |
T |
18: 74,330,639 (GRCm39) |
V188M |
probably damaging |
Het |
Skint8 |
G |
A |
4: 111,794,241 (GRCm39) |
M210I |
probably benign |
Het |
Slc6a11 |
A |
G |
6: 114,202,782 (GRCm39) |
|
probably null |
Het |
Slc6a2 |
A |
T |
8: 93,715,702 (GRCm39) |
H280L |
probably benign |
Het |
Sptan1 |
T |
C |
2: 29,873,744 (GRCm39) |
V208A |
possibly damaging |
Het |
Taf6l |
T |
A |
19: 8,752,135 (GRCm39) |
T518S |
probably benign |
Het |
Thoc2l |
T |
C |
5: 104,665,652 (GRCm39) |
V58A |
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,656,266 (GRCm39) |
M59T |
probably benign |
Het |
Unc5cl |
A |
G |
17: 48,769,361 (GRCm39) |
T282A |
probably benign |
Het |
Vav3 |
A |
G |
3: 109,590,229 (GRCm39) |
K260E |
probably damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,315,926 (GRCm39) |
V631A |
probably damaging |
Het |
Zfp938 |
A |
T |
10: 82,061,287 (GRCm39) |
F444L |
possibly damaging |
Het |
|
Other mutations in Foxred2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01394:Foxred2
|
APN |
15 |
77,839,820 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01479:Foxred2
|
APN |
15 |
77,836,489 (GRCm39) |
splice site |
probably null |
|
IGL01748:Foxred2
|
APN |
15 |
77,836,546 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02160:Foxred2
|
APN |
15 |
77,839,850 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02328:Foxred2
|
APN |
15 |
77,840,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02630:Foxred2
|
APN |
15 |
77,831,362 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02672:Foxred2
|
APN |
15 |
77,829,777 (GRCm39) |
critical splice donor site |
probably null |
|
soma
|
UTSW |
15 |
77,837,558 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0271:Foxred2
|
UTSW |
15 |
77,827,590 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1386:Foxred2
|
UTSW |
15 |
77,832,721 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1581:Foxred2
|
UTSW |
15 |
77,839,961 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4399:Foxred2
|
UTSW |
15 |
77,839,880 (GRCm39) |
missense |
probably benign |
0.06 |
R4399:Foxred2
|
UTSW |
15 |
77,837,558 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4528:Foxred2
|
UTSW |
15 |
77,827,449 (GRCm39) |
missense |
probably benign |
0.01 |
R4937:Foxred2
|
UTSW |
15 |
77,840,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5165:Foxred2
|
UTSW |
15 |
77,840,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Foxred2
|
UTSW |
15 |
77,836,598 (GRCm39) |
missense |
probably benign |
0.00 |
R5893:Foxred2
|
UTSW |
15 |
77,831,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R6336:Foxred2
|
UTSW |
15 |
77,839,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R6370:Foxred2
|
UTSW |
15 |
77,827,506 (GRCm39) |
missense |
probably benign |
0.01 |
R6426:Foxred2
|
UTSW |
15 |
77,837,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Foxred2
|
UTSW |
15 |
77,831,285 (GRCm39) |
missense |
probably benign |
0.01 |
R6891:Foxred2
|
UTSW |
15 |
77,839,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R6934:Foxred2
|
UTSW |
15 |
77,836,530 (GRCm39) |
nonsense |
probably null |
|
R7193:Foxred2
|
UTSW |
15 |
77,836,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7821:Foxred2
|
UTSW |
15 |
77,827,550 (GRCm39) |
missense |
probably benign |
0.01 |
R8401:Foxred2
|
UTSW |
15 |
77,836,191 (GRCm39) |
missense |
probably damaging |
0.98 |
R8540:Foxred2
|
UTSW |
15 |
77,836,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8844:Foxred2
|
UTSW |
15 |
77,832,677 (GRCm39) |
missense |
probably benign |
0.00 |
R8916:Foxred2
|
UTSW |
15 |
77,837,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R9104:Foxred2
|
UTSW |
15 |
77,836,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R9153:Foxred2
|
UTSW |
15 |
77,839,787 (GRCm39) |
critical splice donor site |
probably null |
|
R9205:Foxred2
|
UTSW |
15 |
77,836,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Foxred2
|
UTSW |
15 |
77,836,206 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Foxred2
|
UTSW |
15 |
77,836,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|