Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
C |
7: 120,139,969 (GRCm39) |
|
probably null |
Het |
Acap2 |
C |
A |
16: 30,928,543 (GRCm39) |
C475F |
probably damaging |
Het |
Ace |
C |
A |
11: 105,879,284 (GRCm39) |
P603Q |
possibly damaging |
Het |
Adamts20 |
C |
G |
15: 94,243,659 (GRCm39) |
V657L |
possibly damaging |
Het |
Antxr2 |
A |
G |
5: 98,125,458 (GRCm39) |
|
probably null |
Het |
Atp6v1b2 |
G |
A |
8: 69,554,089 (GRCm39) |
V89I |
probably benign |
Het |
Cacna1e |
G |
A |
1: 154,353,542 (GRCm39) |
P676L |
probably damaging |
Het |
Camsap3 |
A |
T |
8: 3,654,276 (GRCm39) |
I649F |
probably damaging |
Het |
Camta1 |
G |
T |
4: 151,159,695 (GRCm39) |
S490R |
probably damaging |
Het |
Celsr1 |
A |
G |
15: 85,809,719 (GRCm39) |
I2221T |
probably damaging |
Het |
Cfd |
A |
T |
10: 79,727,959 (GRCm39) |
D164V |
probably damaging |
Het |
Cfdp1 |
T |
C |
8: 112,495,384 (GRCm39) |
D278G |
probably damaging |
Het |
Cntn6 |
A |
T |
6: 104,809,523 (GRCm39) |
L519F |
probably damaging |
Het |
Col4a4 |
C |
T |
1: 82,471,312 (GRCm39) |
G681E |
unknown |
Het |
Cybrd1 |
T |
C |
2: 70,967,989 (GRCm39) |
|
probably null |
Het |
Cyp2e1 |
T |
C |
7: 140,343,906 (GRCm39) |
L48P |
probably damaging |
Het |
Eddm13 |
T |
C |
7: 6,269,346 (GRCm39) |
|
probably null |
Het |
Ep400 |
G |
A |
5: 110,849,594 (GRCm39) |
T1409I |
unknown |
Het |
Exosc7 |
A |
T |
9: 122,947,972 (GRCm39) |
D47V |
probably damaging |
Het |
Fgr |
T |
C |
4: 132,722,342 (GRCm39) |
F204L |
probably damaging |
Het |
Gm10100 |
G |
A |
10: 77,562,560 (GRCm39) |
V81M |
probably benign |
Het |
Gm12367 |
T |
C |
4: 35,235,690 (GRCm39) |
|
noncoding transcript |
Het |
Grxcr1 |
C |
A |
5: 68,323,538 (GRCm39) |
T272K |
probably damaging |
Het |
Kcna5 |
C |
T |
6: 126,511,859 (GRCm39) |
D90N |
probably benign |
Het |
Kdm5b |
T |
A |
1: 134,536,635 (GRCm39) |
Y618* |
probably null |
Het |
Lama5 |
T |
A |
2: 179,832,539 (GRCm39) |
H1670L |
possibly damaging |
Het |
Mtus2 |
C |
T |
5: 148,243,518 (GRCm39) |
Q113* |
probably null |
Het |
Ncam1 |
A |
C |
9: 49,456,054 (GRCm39) |
D521E |
probably benign |
Het |
Nkapl |
T |
C |
13: 21,651,740 (GRCm39) |
H291R |
possibly damaging |
Het |
Nlrp1b |
T |
G |
11: 71,062,967 (GRCm39) |
N695H |
probably damaging |
Het |
Npc1l1 |
T |
A |
11: 6,164,733 (GRCm39) |
Q1105H |
probably damaging |
Het |
Paxip1 |
C |
G |
5: 27,986,453 (GRCm39) |
|
probably benign |
Het |
Pign |
A |
T |
1: 105,583,695 (GRCm39) |
W136R |
probably damaging |
Het |
Pira1 |
T |
C |
7: 3,741,856 (GRCm39) |
T175A |
possibly damaging |
Het |
Pkn3 |
T |
A |
2: 29,971,086 (GRCm39) |
S222T |
probably damaging |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Ppfibp1 |
T |
A |
6: 146,898,338 (GRCm39) |
I98N |
probably damaging |
Het |
Ppfibp1 |
T |
G |
6: 146,917,828 (GRCm39) |
S484A |
probably damaging |
Het |
Ppp1r7 |
T |
C |
1: 93,280,312 (GRCm39) |
F127L |
probably damaging |
Het |
Pramel1 |
T |
C |
4: 143,123,954 (GRCm39) |
Y210H |
probably benign |
Het |
Ripply1 |
TTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCT |
TTCCTCCTCCTCCTCCTCCTCCTCCTCCT |
X: 138,680,599 (GRCm39) |
|
probably benign |
Het |
Rnf225 |
A |
G |
7: 12,661,932 (GRCm39) |
D37G |
probably damaging |
Het |
Smpd2 |
A |
G |
10: 41,363,967 (GRCm39) |
|
probably null |
Het |
Spata31h1 |
T |
C |
10: 82,119,561 (GRCm39) |
Q4483R |
probably damaging |
Het |
Tmem38b |
C |
T |
4: 53,859,945 (GRCm39) |
R242W |
probably benign |
Het |
Topaz1 |
A |
T |
9: 122,603,158 (GRCm39) |
K1035I |
possibly damaging |
Het |
Trhr |
T |
C |
15: 44,060,873 (GRCm39) |
I131T |
possibly damaging |
Het |
Usp1 |
A |
G |
4: 98,819,294 (GRCm39) |
D252G |
probably benign |
Het |
Usp14 |
C |
T |
18: 10,018,023 (GRCm39) |
E90K |
probably damaging |
Het |
Yme1l1 |
T |
G |
2: 23,052,569 (GRCm39) |
D74E |
probably benign |
Het |
Ythdc2 |
T |
A |
18: 44,990,092 (GRCm39) |
L732Q |
possibly damaging |
Het |
Zbbx |
G |
T |
3: 74,990,977 (GRCm39) |
A289D |
probably damaging |
Het |
Zfhx3 |
G |
A |
8: 109,673,446 (GRCm39) |
V1499I |
possibly damaging |
Het |
Zfp622 |
T |
C |
15: 25,996,285 (GRCm39) |
V184A |
possibly damaging |
Het |
|
Other mutations in Rad21l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00435:Rad21l
|
APN |
2 |
151,495,436 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00815:Rad21l
|
APN |
2 |
151,509,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00847:Rad21l
|
APN |
2 |
151,502,635 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01545:Rad21l
|
APN |
2 |
151,497,084 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02983:Rad21l
|
APN |
2 |
151,497,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Rad21l
|
APN |
2 |
151,510,389 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Rad21l
|
UTSW |
2 |
151,496,567 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0219:Rad21l
|
UTSW |
2 |
151,496,508 (GRCm39) |
splice site |
probably benign |
|
R0382:Rad21l
|
UTSW |
2 |
151,487,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Rad21l
|
UTSW |
2 |
151,493,851 (GRCm39) |
missense |
probably benign |
|
R0511:Rad21l
|
UTSW |
2 |
151,490,989 (GRCm39) |
splice site |
probably benign |
|
R1555:Rad21l
|
UTSW |
2 |
151,500,348 (GRCm39) |
missense |
probably benign |
0.03 |
R1606:Rad21l
|
UTSW |
2 |
151,496,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Rad21l
|
UTSW |
2 |
151,510,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Rad21l
|
UTSW |
2 |
151,497,179 (GRCm39) |
missense |
probably benign |
0.04 |
R1999:Rad21l
|
UTSW |
2 |
151,496,621 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2060:Rad21l
|
UTSW |
2 |
151,487,349 (GRCm39) |
missense |
probably benign |
0.21 |
R2068:Rad21l
|
UTSW |
2 |
151,509,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R3037:Rad21l
|
UTSW |
2 |
151,502,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R4805:Rad21l
|
UTSW |
2 |
151,509,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R5185:Rad21l
|
UTSW |
2 |
151,499,382 (GRCm39) |
missense |
probably benign |
0.01 |
R5504:Rad21l
|
UTSW |
2 |
151,510,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R5530:Rad21l
|
UTSW |
2 |
151,499,430 (GRCm39) |
missense |
probably benign |
0.00 |
R6113:Rad21l
|
UTSW |
2 |
151,499,398 (GRCm39) |
missense |
probably damaging |
0.98 |
R6233:Rad21l
|
UTSW |
2 |
151,495,462 (GRCm39) |
missense |
probably benign |
|
R7096:Rad21l
|
UTSW |
2 |
151,509,840 (GRCm39) |
missense |
probably benign |
0.31 |
R7337:Rad21l
|
UTSW |
2 |
151,500,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7822:Rad21l
|
UTSW |
2 |
151,497,045 (GRCm39) |
missense |
probably benign |
|
R8315:Rad21l
|
UTSW |
2 |
151,497,160 (GRCm39) |
missense |
probably benign |
0.00 |
R8368:Rad21l
|
UTSW |
2 |
151,495,390 (GRCm39) |
missense |
probably benign |
|
R8673:Rad21l
|
UTSW |
2 |
151,502,718 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8698:Rad21l
|
UTSW |
2 |
151,487,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R8769:Rad21l
|
UTSW |
2 |
151,509,838 (GRCm39) |
missense |
probably benign |
0.05 |
R9308:Rad21l
|
UTSW |
2 |
151,491,049 (GRCm39) |
missense |
probably benign |
0.07 |
Z1088:Rad21l
|
UTSW |
2 |
151,509,939 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rad21l
|
UTSW |
2 |
151,497,152 (GRCm39) |
missense |
probably damaging |
0.99 |
|