Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A130051J06Rik |
C |
T |
15: 95,688,641 (GRCm39) |
|
probably benign |
Het |
A630001G21Rik |
T |
A |
1: 85,651,106 (GRCm39) |
R110W |
probably benign |
Het |
Abca4 |
T |
C |
3: 121,928,915 (GRCm39) |
|
probably null |
Het |
Abcc3 |
T |
C |
11: 94,241,894 (GRCm39) |
N1379S |
probably damaging |
Het |
Actrt3 |
A |
C |
3: 30,652,276 (GRCm39) |
F273V |
probably benign |
Het |
Adam22 |
T |
C |
5: 8,417,217 (GRCm39) |
D75G |
probably benign |
Het |
Ash1l |
C |
A |
3: 88,961,805 (GRCm39) |
D2392E |
possibly damaging |
Het |
Ash1l |
T |
C |
3: 88,965,933 (GRCm39) |
I2445T |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,164,071 (GRCm39) |
H1137Q |
probably damaging |
Het |
Cacna2d2 |
A |
G |
9: 107,401,851 (GRCm39) |
I762V |
probably benign |
Het |
Ccdc127 |
T |
A |
13: 74,505,187 (GRCm39) |
|
probably benign |
Het |
Ccdc91 |
C |
G |
6: 147,477,001 (GRCm39) |
L230V |
unknown |
Het |
Cdk13 |
A |
G |
13: 17,894,240 (GRCm39) |
I1129T |
probably damaging |
Het |
Cnot1 |
C |
T |
8: 96,470,924 (GRCm39) |
R1308H |
possibly damaging |
Het |
Crhr2 |
T |
C |
6: 55,080,207 (GRCm39) |
H144R |
probably damaging |
Het |
Dnmt1 |
T |
C |
9: 20,823,891 (GRCm39) |
N993S |
possibly damaging |
Het |
Eif4g1 |
T |
A |
16: 20,507,761 (GRCm39) |
V1182D |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fam234a |
T |
A |
17: 26,433,627 (GRCm39) |
Q399L |
possibly damaging |
Het |
Fyb1 |
A |
T |
15: 6,610,350 (GRCm39) |
K308* |
probably null |
Het |
Gfral |
C |
T |
9: 76,104,328 (GRCm39) |
R228Q |
probably benign |
Het |
Gm10309 |
A |
T |
17: 86,806,421 (GRCm39) |
|
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Gm5501 |
G |
A |
18: 9,917,417 (GRCm39) |
|
noncoding transcript |
Het |
Gm6309 |
A |
T |
5: 146,104,992 (GRCm39) |
V307D |
probably benign |
Het |
Gm9871 |
T |
A |
6: 101,773,148 (GRCm39) |
|
noncoding transcript |
Het |
Greb1l |
G |
A |
18: 10,542,427 (GRCm39) |
E1341K |
probably damaging |
Het |
Herc3 |
T |
A |
6: 58,871,528 (GRCm39) |
V70E |
possibly damaging |
Het |
Hes7 |
A |
G |
11: 69,012,415 (GRCm39) |
E41G |
probably damaging |
Het |
Ifi27l2b |
T |
C |
12: 103,422,046 (GRCm39) |
D106G |
unknown |
Het |
Igfbp6 |
A |
T |
15: 102,056,616 (GRCm39) |
Y184F |
probably damaging |
Het |
Isyna1 |
A |
G |
8: 71,047,352 (GRCm39) |
Y25C |
probably damaging |
Het |
Kcng3 |
G |
T |
17: 83,938,563 (GRCm39) |
T162K |
possibly damaging |
Het |
Krt36 |
T |
C |
11: 99,994,987 (GRCm39) |
D195G |
possibly damaging |
Het |
Lrwd1 |
A |
T |
5: 136,161,093 (GRCm39) |
|
probably null |
Het |
Lsg1 |
C |
T |
16: 30,380,593 (GRCm39) |
A615T |
probably benign |
Het |
Myo5a |
A |
T |
9: 75,059,213 (GRCm39) |
E480D |
probably damaging |
Het |
Myrf |
T |
A |
19: 10,194,087 (GRCm39) |
D690V |
probably damaging |
Het |
N4bp1 |
T |
C |
8: 87,578,312 (GRCm39) |
I684M |
probably damaging |
Het |
Nlrc3 |
C |
T |
16: 3,781,589 (GRCm39) |
A607T |
probably damaging |
Het |
Nuak1 |
A |
T |
10: 84,245,584 (GRCm39) |
I87N |
probably damaging |
Het |
Odad2 |
G |
T |
18: 7,211,496 (GRCm39) |
Q793K |
probably benign |
Het |
Or5p66 |
T |
G |
7: 107,885,599 (GRCm39) |
T245P |
probably damaging |
Het |
Or5w11 |
T |
C |
2: 87,459,475 (GRCm39) |
|
probably null |
Het |
Or8b4 |
A |
T |
9: 37,830,647 (GRCm39) |
E236D |
probably damaging |
Het |
Osbpl9 |
T |
A |
4: 108,919,763 (GRCm39) |
R689* |
probably null |
Het |
Ppargc1b |
T |
A |
18: 61,440,639 (GRCm39) |
M744L |
probably benign |
Het |
Prss40 |
A |
T |
1: 34,591,598 (GRCm39) |
|
probably benign |
Het |
Ptprd |
T |
A |
4: 75,972,839 (GRCm39) |
|
probably null |
Het |
Rft1 |
T |
C |
14: 30,385,183 (GRCm39) |
|
probably benign |
Het |
Rnaset2a |
T |
C |
17: 8,350,879 (GRCm39) |
Y167C |
probably damaging |
Het |
Schip1 |
T |
C |
3: 68,315,560 (GRCm39) |
|
probably benign |
Het |
Scn5a |
A |
C |
9: 119,359,118 (GRCm39) |
L643R |
possibly damaging |
Het |
Shroom3 |
T |
A |
5: 93,090,877 (GRCm39) |
M1128K |
probably benign |
Het |
Skint8 |
C |
A |
4: 111,807,390 (GRCm39) |
L359M |
probably damaging |
Het |
Slc14a2 |
A |
G |
18: 78,252,257 (GRCm39) |
L18P |
probably benign |
Het |
Slc22a3 |
C |
T |
17: 12,642,691 (GRCm39) |
V509M |
probably damaging |
Het |
Slc7a5 |
A |
C |
8: 122,610,381 (GRCm39) |
F478V |
probably benign |
Het |
Smc1b |
T |
A |
15: 84,980,859 (GRCm39) |
N803I |
probably benign |
Het |
Snf8 |
T |
A |
11: 95,932,551 (GRCm39) |
N115K |
probably damaging |
Het |
Stox2 |
T |
A |
8: 47,866,172 (GRCm39) |
K57* |
probably null |
Het |
Tmem248 |
T |
A |
5: 130,258,429 (GRCm39) |
F41I |
probably damaging |
Het |
Tmprss7 |
T |
C |
16: 45,506,793 (GRCm39) |
S90G |
probably damaging |
Het |
Top3b |
T |
C |
16: 16,703,700 (GRCm39) |
V285A |
probably damaging |
Het |
Tsen15 |
T |
C |
1: 152,247,534 (GRCm39) |
T153A |
probably damaging |
Het |
Usp34 |
T |
G |
11: 23,304,846 (GRCm39) |
S360A |
probably benign |
Het |
Wdr24 |
T |
C |
17: 26,047,314 (GRCm39) |
|
probably null |
Het |
Zbtb2 |
G |
A |
10: 4,319,456 (GRCm39) |
T190I |
probably benign |
Het |
Zranb3 |
T |
C |
1: 127,891,613 (GRCm39) |
S788G |
probably benign |
Het |
|
Other mutations in Rftn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00565:Rftn2
|
APN |
1 |
55,243,444 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01691:Rftn2
|
APN |
1 |
55,253,445 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02412:Rftn2
|
APN |
1 |
55,245,497 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02458:Rftn2
|
APN |
1 |
55,250,351 (GRCm39) |
nonsense |
probably null |
|
1mM(1):Rftn2
|
UTSW |
1 |
55,245,754 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0446:Rftn2
|
UTSW |
1 |
55,253,354 (GRCm39) |
missense |
probably damaging |
0.99 |
R1167:Rftn2
|
UTSW |
1 |
55,243,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Rftn2
|
UTSW |
1 |
55,250,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R4171:Rftn2
|
UTSW |
1 |
55,253,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Rftn2
|
UTSW |
1 |
55,233,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R4487:Rftn2
|
UTSW |
1 |
55,241,311 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4833:Rftn2
|
UTSW |
1 |
55,253,399 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4863:Rftn2
|
UTSW |
1 |
55,211,198 (GRCm39) |
missense |
probably benign |
0.01 |
R6801:Rftn2
|
UTSW |
1 |
55,233,418 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6937:Rftn2
|
UTSW |
1 |
55,233,508 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6939:Rftn2
|
UTSW |
1 |
55,233,508 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7344:Rftn2
|
UTSW |
1 |
55,265,311 (GRCm39) |
nonsense |
probably null |
|
R7401:Rftn2
|
UTSW |
1 |
55,233,401 (GRCm39) |
critical splice donor site |
probably null |
|
R7517:Rftn2
|
UTSW |
1 |
55,234,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R8512:Rftn2
|
UTSW |
1 |
55,253,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R9207:Rftn2
|
UTSW |
1 |
55,224,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9501:Rftn2
|
UTSW |
1 |
55,241,355 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0022:Rftn2
|
UTSW |
1 |
55,253,295 (GRCm39) |
missense |
probably benign |
0.05 |
|