Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afmid |
G |
A |
11: 117,725,648 (GRCm39) |
V120M |
possibly damaging |
Het |
Aldh1l1 |
T |
C |
6: 90,567,776 (GRCm39) |
L680P |
probably damaging |
Het |
Alox12 |
A |
T |
11: 70,138,104 (GRCm39) |
D410E |
probably benign |
Het |
Amt |
T |
A |
9: 108,178,579 (GRCm39) |
V365E |
probably damaging |
Het |
Ano9 |
A |
G |
7: 140,687,353 (GRCm39) |
S321P |
probably damaging |
Het |
Atp2c2 |
A |
T |
8: 120,479,771 (GRCm39) |
I767F |
probably damaging |
Het |
Bag1 |
A |
T |
4: 40,936,643 (GRCm39) |
Y338N |
probably benign |
Het |
Bcr |
T |
A |
10: 74,990,796 (GRCm39) |
D767E |
probably benign |
Het |
Chfr |
A |
T |
5: 110,302,705 (GRCm39) |
Q350L |
probably damaging |
Het |
Cops3 |
A |
T |
11: 59,721,043 (GRCm39) |
L124H |
probably damaging |
Het |
Ddx60 |
T |
C |
8: 62,437,149 (GRCm39) |
Y988H |
probably benign |
Het |
Dnajc2 |
A |
T |
5: 21,975,479 (GRCm39) |
|
probably benign |
Het |
Dym |
C |
T |
18: 75,215,527 (GRCm39) |
Q238* |
probably null |
Het |
Fbn1 |
A |
T |
2: 125,193,945 (GRCm39) |
C1341S |
possibly damaging |
Het |
Fryl |
G |
T |
5: 73,212,203 (GRCm39) |
N2308K |
probably benign |
Het |
Gbp2b |
G |
T |
3: 142,309,873 (GRCm39) |
R221L |
probably damaging |
Het |
Gpat2 |
A |
G |
2: 127,269,251 (GRCm39) |
N8S |
probably benign |
Het |
Gvin2 |
T |
C |
7: 105,545,972 (GRCm39) |
K2360R |
probably damaging |
Het |
Hycc2 |
A |
T |
1: 58,574,561 (GRCm39) |
W327R |
probably damaging |
Het |
Inhbe |
C |
A |
10: 127,186,645 (GRCm39) |
L178F |
probably damaging |
Het |
Ipo5 |
T |
C |
14: 121,181,212 (GRCm39) |
Y913H |
possibly damaging |
Het |
Kif21b |
T |
A |
1: 136,099,968 (GRCm39) |
D1507E |
possibly damaging |
Het |
Lnx2 |
A |
G |
5: 146,964,984 (GRCm39) |
V413A |
probably damaging |
Het |
Lrrc40 |
C |
A |
3: 157,742,410 (GRCm39) |
F16L |
probably damaging |
Het |
Magi2 |
A |
G |
5: 19,432,581 (GRCm39) |
K99E |
probably damaging |
Het |
Me3 |
A |
G |
7: 89,495,461 (GRCm39) |
I357M |
probably benign |
Het |
Med30 |
A |
G |
15: 52,582,761 (GRCm39) |
Y66C |
probably benign |
Het |
Mief2 |
A |
T |
11: 60,621,783 (GRCm39) |
S118C |
probably damaging |
Het |
Mylip |
A |
G |
13: 45,544,722 (GRCm39) |
S49G |
probably benign |
Het |
Ncoa7 |
T |
A |
10: 30,528,972 (GRCm39) |
D107V |
probably damaging |
Het |
Nvl |
C |
A |
1: 180,934,541 (GRCm39) |
V655F |
probably damaging |
Het |
Olfml2b |
C |
T |
1: 170,508,645 (GRCm39) |
T501I |
probably benign |
Het |
Ormdl2 |
T |
C |
10: 128,656,186 (GRCm39) |
I40V |
probably benign |
Het |
Pde6b |
G |
T |
5: 108,568,142 (GRCm39) |
|
probably benign |
Het |
Ralgapa1 |
A |
C |
12: 55,720,292 (GRCm39) |
L1785W |
probably damaging |
Het |
Rnf112 |
A |
T |
11: 61,341,078 (GRCm39) |
|
probably null |
Het |
Sema3c |
A |
T |
5: 17,781,866 (GRCm39) |
M1L |
possibly damaging |
Het |
Sema3c |
T |
A |
5: 17,867,972 (GRCm39) |
Y128N |
probably damaging |
Het |
Sema4b |
G |
A |
7: 79,866,789 (GRCm39) |
G255D |
probably damaging |
Het |
Setd1a |
C |
T |
7: 127,394,997 (GRCm39) |
|
probably benign |
Het |
Sirpb1a |
A |
C |
3: 15,482,111 (GRCm39) |
S72R |
possibly damaging |
Het |
Slu7 |
T |
A |
11: 43,332,849 (GRCm39) |
|
probably null |
Het |
Spata19 |
T |
C |
9: 27,309,276 (GRCm39) |
V59A |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Suclg1 |
T |
A |
6: 73,237,504 (GRCm39) |
V83E |
probably damaging |
Het |
Syncrip |
G |
T |
9: 88,338,457 (GRCm39) |
R536S |
probably benign |
Het |
Tap2 |
T |
C |
17: 34,424,432 (GRCm39) |
V55A |
probably damaging |
Het |
Tekt4 |
T |
C |
17: 25,692,732 (GRCm39) |
I186T |
possibly damaging |
Het |
Trpc6 |
C |
A |
9: 8,643,602 (GRCm39) |
D462E |
possibly damaging |
Het |
Ubqln3 |
T |
G |
7: 103,791,170 (GRCm39) |
T307P |
probably damaging |
Het |
Vmn1r64 |
A |
T |
7: 5,886,727 (GRCm39) |
I272K |
probably benign |
Het |
Xpr1 |
T |
C |
1: 155,166,026 (GRCm39) |
T574A |
probably benign |
Het |
Zfc3h1 |
A |
G |
10: 115,247,859 (GRCm39) |
T1021A |
possibly damaging |
Het |
Zfp512 |
A |
T |
5: 31,628,501 (GRCm39) |
H159L |
probably damaging |
Het |
|
Other mutations in Ift52 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02006:Ift52
|
APN |
2 |
162,865,289 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02164:Ift52
|
APN |
2 |
162,867,384 (GRCm39) |
splice site |
probably null |
|
IGL02876:Ift52
|
APN |
2 |
162,878,627 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03136:Ift52
|
APN |
2 |
162,867,254 (GRCm39) |
nonsense |
probably null |
|
IGL03292:Ift52
|
APN |
2 |
162,865,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R1115:Ift52
|
UTSW |
2 |
162,871,702 (GRCm39) |
missense |
probably benign |
0.34 |
R1502:Ift52
|
UTSW |
2 |
162,871,782 (GRCm39) |
critical splice donor site |
probably null |
|
R1775:Ift52
|
UTSW |
2 |
162,867,275 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2204:Ift52
|
UTSW |
2 |
162,873,150 (GRCm39) |
missense |
probably benign |
0.07 |
R2259:Ift52
|
UTSW |
2 |
162,870,013 (GRCm39) |
missense |
probably benign |
0.04 |
R2348:Ift52
|
UTSW |
2 |
162,887,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R4820:Ift52
|
UTSW |
2 |
162,873,108 (GRCm39) |
missense |
probably benign |
0.06 |
R5464:Ift52
|
UTSW |
2 |
162,871,735 (GRCm39) |
missense |
probably benign |
0.20 |
R7054:Ift52
|
UTSW |
2 |
162,871,716 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1088:Ift52
|
UTSW |
2 |
162,865,278 (GRCm39) |
missense |
possibly damaging |
0.86 |
|