Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
A |
T |
7: 119,140,075 (GRCm39) |
E492V |
probably damaging |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
Atr |
T |
C |
9: 95,789,376 (GRCm39) |
F1511L |
probably damaging |
Het |
Bdkrb2 |
G |
T |
12: 105,558,416 (GRCm39) |
R219L |
probably benign |
Het |
Bhmt2 |
A |
T |
13: 93,798,837 (GRCm39) |
M328K |
probably benign |
Het |
Btbd3 |
A |
G |
2: 138,125,881 (GRCm39) |
D286G |
probably benign |
Het |
Bub1b |
T |
G |
2: 118,437,167 (GRCm39) |
L122V |
probably benign |
Het |
Caml |
T |
C |
13: 55,772,820 (GRCm39) |
S155P |
probably damaging |
Het |
Cfap43 |
T |
C |
19: 47,824,150 (GRCm39) |
K74E |
probably benign |
Het |
Chst4 |
A |
G |
8: 110,757,255 (GRCm39) |
S120P |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 113,860,213 (GRCm39) |
D213G |
unknown |
Het |
Cripto |
C |
A |
9: 110,772,235 (GRCm39) |
V54L |
probably benign |
Het |
Cxcl10 |
TACTCAC |
TACTCACTCAC |
5: 92,495,941 (GRCm39) |
|
probably null |
Het |
Cxcl10 |
CAC |
CACTAAC |
5: 92,495,945 (GRCm39) |
|
probably null |
Het |
Cyp26b1 |
A |
T |
6: 84,553,653 (GRCm39) |
I167N |
possibly damaging |
Het |
Dchs1 |
A |
G |
7: 105,406,921 (GRCm39) |
S2195P |
probably benign |
Het |
Ddx25 |
T |
A |
9: 35,458,142 (GRCm39) |
K326* |
probably null |
Het |
Dip2c |
A |
T |
13: 9,543,162 (GRCm39) |
Y36F |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,586,068 (GRCm39) |
D538G |
probably damaging |
Het |
E4f1 |
C |
T |
17: 24,670,523 (GRCm39) |
D55N |
probably damaging |
Het |
Emp1 |
G |
T |
6: 135,358,077 (GRCm39) |
W141L |
probably damaging |
Het |
Faim2 |
T |
A |
15: 99,398,135 (GRCm39) |
H271L |
probably benign |
Het |
Fbxw9 |
T |
C |
8: 85,792,707 (GRCm39) |
M352T |
possibly damaging |
Het |
Fcrl2 |
A |
T |
3: 87,164,167 (GRCm39) |
F321I |
probably benign |
Het |
Frzb |
C |
T |
2: 80,268,834 (GRCm39) |
|
probably null |
Het |
Gal3st1 |
G |
T |
11: 3,948,931 (GRCm39) |
K379N |
probably damaging |
Het |
Gm5519 |
G |
A |
19: 33,800,372 (GRCm39) |
C22Y |
possibly damaging |
Het |
Gpn3 |
T |
C |
5: 122,516,583 (GRCm39) |
F71L |
probably benign |
Het |
H2-M9 |
A |
G |
17: 36,952,545 (GRCm39) |
V167A |
probably benign |
Het |
Hars1 |
A |
G |
18: 36,904,467 (GRCm39) |
F182L |
possibly damaging |
Het |
Hid1 |
T |
C |
11: 115,243,543 (GRCm39) |
T502A |
probably benign |
Het |
Hipk3 |
G |
T |
2: 104,302,021 (GRCm39) |
T57K |
probably benign |
Het |
Iqsec2 |
A |
G |
X: 150,927,727 (GRCm39) |
S87G |
probably benign |
Het |
Itpk1 |
G |
A |
12: 102,572,378 (GRCm39) |
L112F |
probably damaging |
Het |
Klk1b9 |
T |
A |
7: 43,443,817 (GRCm39) |
D110E |
possibly damaging |
Het |
Lemd3 |
A |
T |
10: 120,785,246 (GRCm39) |
M535K |
possibly damaging |
Het |
Lipg |
A |
T |
18: 75,078,894 (GRCm39) |
S453T |
possibly damaging |
Het |
Lrrc75a |
A |
T |
11: 62,500,069 (GRCm39) |
W150R |
probably damaging |
Het |
Lyg1 |
T |
C |
1: 37,986,305 (GRCm39) |
E143G |
probably damaging |
Het |
Map3k1 |
A |
G |
13: 111,892,177 (GRCm39) |
V1026A |
probably benign |
Het |
Mgat3 |
T |
A |
15: 80,095,838 (GRCm39) |
F222I |
probably benign |
Het |
Mindy4 |
A |
T |
6: 55,232,601 (GRCm39) |
N348I |
possibly damaging |
Het |
Ms4a20 |
T |
C |
19: 11,089,741 (GRCm39) |
Y48C |
probably damaging |
Het |
Myo1b |
A |
C |
1: 51,817,684 (GRCm39) |
F532C |
probably damaging |
Het |
Naif1 |
T |
A |
2: 32,342,558 (GRCm39) |
N36K |
probably damaging |
Het |
Nkpd1 |
C |
A |
7: 19,258,012 (GRCm39) |
A597E |
possibly damaging |
Het |
Npr2 |
A |
G |
4: 43,647,260 (GRCm39) |
D772G |
possibly damaging |
Het |
Or52n4 |
T |
G |
7: 104,294,204 (GRCm39) |
D123A |
probably damaging |
Het |
Or6a2 |
T |
C |
7: 106,600,791 (GRCm39) |
N92S |
probably benign |
Het |
Pcolce2 |
A |
T |
9: 95,576,793 (GRCm39) |
M355L |
probably benign |
Het |
Pdgfra |
A |
T |
5: 75,334,108 (GRCm39) |
I394F |
probably damaging |
Het |
Pdzrn3 |
G |
A |
6: 101,127,838 (GRCm39) |
R943C |
probably damaging |
Het |
Pml |
A |
G |
9: 58,141,821 (GRCm39) |
V337A |
probably damaging |
Het |
Pnpla2 |
T |
A |
7: 141,038,794 (GRCm39) |
M321K |
probably benign |
Het |
Poln |
A |
T |
5: 34,261,284 (GRCm39) |
N546K |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Prss28 |
T |
A |
17: 25,529,029 (GRCm39) |
F123L |
possibly damaging |
Het |
Psg18 |
A |
G |
7: 18,080,004 (GRCm39) |
V399A |
probably benign |
Het |
Rab5a |
T |
C |
17: 53,813,443 (GRCm39) |
C212R |
probably damaging |
Het |
Ranbp6 |
A |
T |
19: 29,789,679 (GRCm39) |
D224E |
probably benign |
Het |
Recql4 |
T |
C |
15: 76,588,239 (GRCm39) |
I1104M |
possibly damaging |
Het |
Rhbdl3 |
T |
A |
11: 80,244,418 (GRCm39) |
V375E |
possibly damaging |
Het |
Senp6 |
T |
A |
9: 80,024,007 (GRCm39) |
N423K |
possibly damaging |
Het |
Sertad2 |
C |
G |
11: 20,598,091 (GRCm39) |
L96V |
probably benign |
Het |
Slc33a1 |
T |
A |
3: 63,861,315 (GRCm39) |
T296S |
probably benign |
Het |
Smurf2 |
G |
A |
11: 106,743,444 (GRCm39) |
P188S |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,039,180 (GRCm39) |
Y1174* |
probably null |
Het |
Stra6l |
A |
T |
4: 45,864,982 (GRCm39) |
T103S |
probably benign |
Het |
Swt1 |
C |
T |
1: 151,281,272 (GRCm39) |
A352T |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,668,769 (GRCm39) |
V1097A |
possibly damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,361 (GRCm39) |
N409K |
possibly damaging |
Het |
Tlr6 |
G |
T |
5: 65,112,593 (GRCm39) |
H105N |
probably benign |
Het |
Tmprss9 |
A |
C |
10: 80,715,692 (GRCm39) |
T15P |
possibly damaging |
Het |
Tnik |
C |
T |
3: 28,587,089 (GRCm39) |
T120M |
probably damaging |
Het |
Tnr |
T |
A |
1: 159,685,780 (GRCm39) |
I337N |
probably damaging |
Het |
Top3a |
A |
G |
11: 60,641,419 (GRCm39) |
Y422H |
probably benign |
Het |
Trim67 |
A |
G |
8: 125,555,820 (GRCm39) |
N768S |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,536,310 (GRCm39) |
V35016A |
probably benign |
Het |
Utrn |
A |
C |
10: 12,357,052 (GRCm39) |
S312R |
probably damaging |
Het |
Vdac2 |
A |
G |
14: 21,887,879 (GRCm39) |
Y62C |
probably damaging |
Het |
Vwa5b2 |
A |
G |
16: 20,423,734 (GRCm39) |
T1216A |
probably benign |
Het |
Wfdc16 |
T |
C |
2: 164,480,403 (GRCm39) |
K31E |
possibly damaging |
Het |
Wtip |
C |
T |
7: 33,824,921 (GRCm39) |
C221Y |
probably damaging |
Het |
Xrn1 |
A |
G |
9: 95,873,064 (GRCm39) |
D640G |
possibly damaging |
Het |
Zdhhc5 |
T |
C |
2: 84,522,685 (GRCm39) |
R293G |
probably benign |
Het |
Zfp536 |
T |
C |
7: 37,269,059 (GRCm39) |
D119G |
probably damaging |
Het |
Zfp81 |
T |
C |
17: 33,554,254 (GRCm39) |
T187A |
probably benign |
Het |
Zfp810 |
C |
T |
9: 22,190,122 (GRCm39) |
G262D |
possibly damaging |
Het |
Zfp963 |
A |
C |
8: 70,195,669 (GRCm39) |
I203M |
possibly damaging |
Het |
Zfpm2 |
T |
C |
15: 40,965,075 (GRCm39) |
M520T |
probably damaging |
Het |
Zswim8 |
G |
A |
14: 20,763,181 (GRCm39) |
R360Q |
possibly damaging |
Het |
Zwilch |
T |
A |
9: 64,065,999 (GRCm39) |
H254L |
possibly damaging |
Het |
|
Other mutations in Rev1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Rev1
|
APN |
1 |
38,138,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01065:Rev1
|
APN |
1 |
38,138,090 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01393:Rev1
|
APN |
1 |
38,131,144 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03003:Rev1
|
APN |
1 |
38,127,154 (GRCm39) |
missense |
possibly damaging |
0.77 |
H8562:Rev1
|
UTSW |
1 |
38,095,848 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT1430001:Rev1
|
UTSW |
1 |
38,095,337 (GRCm39) |
unclassified |
probably benign |
|
R0409:Rev1
|
UTSW |
1 |
38,113,449 (GRCm39) |
nonsense |
probably null |
|
R0606:Rev1
|
UTSW |
1 |
38,098,204 (GRCm39) |
missense |
probably null |
1.00 |
R1134:Rev1
|
UTSW |
1 |
38,096,768 (GRCm39) |
missense |
probably benign |
0.04 |
R1208:Rev1
|
UTSW |
1 |
38,098,199 (GRCm39) |
unclassified |
probably benign |
|
R1440:Rev1
|
UTSW |
1 |
38,127,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Rev1
|
UTSW |
1 |
38,127,653 (GRCm39) |
missense |
probably benign |
0.00 |
R1627:Rev1
|
UTSW |
1 |
38,094,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R3845:Rev1
|
UTSW |
1 |
38,138,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R3948:Rev1
|
UTSW |
1 |
38,113,414 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4074:Rev1
|
UTSW |
1 |
38,093,319 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4075:Rev1
|
UTSW |
1 |
38,093,319 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4076:Rev1
|
UTSW |
1 |
38,093,319 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4248:Rev1
|
UTSW |
1 |
38,146,729 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4293:Rev1
|
UTSW |
1 |
38,147,500 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4548:Rev1
|
UTSW |
1 |
38,098,275 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4610:Rev1
|
UTSW |
1 |
38,092,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Rev1
|
UTSW |
1 |
38,118,337 (GRCm39) |
intron |
probably benign |
|
R5032:Rev1
|
UTSW |
1 |
38,113,570 (GRCm39) |
intron |
probably benign |
|
R5286:Rev1
|
UTSW |
1 |
38,094,407 (GRCm39) |
nonsense |
probably null |
|
R5311:Rev1
|
UTSW |
1 |
38,118,474 (GRCm39) |
missense |
probably benign |
0.00 |
R5327:Rev1
|
UTSW |
1 |
38,147,532 (GRCm39) |
nonsense |
probably null |
|
R6363:Rev1
|
UTSW |
1 |
38,110,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Rev1
|
UTSW |
1 |
38,093,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7072:Rev1
|
UTSW |
1 |
38,106,626 (GRCm39) |
nonsense |
probably null |
|
R7132:Rev1
|
UTSW |
1 |
38,110,530 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7264:Rev1
|
UTSW |
1 |
38,124,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R7298:Rev1
|
UTSW |
1 |
38,092,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:Rev1
|
UTSW |
1 |
38,113,488 (GRCm39) |
nonsense |
probably null |
|
R7395:Rev1
|
UTSW |
1 |
38,127,146 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7829:Rev1
|
UTSW |
1 |
38,095,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R8053:Rev1
|
UTSW |
1 |
38,102,222 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8093:Rev1
|
UTSW |
1 |
38,114,097 (GRCm39) |
intron |
probably benign |
|
R8356:Rev1
|
UTSW |
1 |
38,098,324 (GRCm39) |
nonsense |
probably null |
|
R8456:Rev1
|
UTSW |
1 |
38,098,324 (GRCm39) |
nonsense |
probably null |
|
R8461:Rev1
|
UTSW |
1 |
38,122,868 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8724:Rev1
|
UTSW |
1 |
38,127,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R8757:Rev1
|
UTSW |
1 |
38,098,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Rev1
|
UTSW |
1 |
38,098,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R8945:Rev1
|
UTSW |
1 |
38,122,824 (GRCm39) |
missense |
probably damaging |
0.98 |
R9309:Rev1
|
UTSW |
1 |
38,093,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R9433:Rev1
|
UTSW |
1 |
38,092,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R9500:Rev1
|
UTSW |
1 |
38,102,214 (GRCm39) |
nonsense |
probably null |
|
X0017:Rev1
|
UTSW |
1 |
38,092,742 (GRCm39) |
missense |
probably damaging |
1.00 |
|