Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029F12Rik |
A |
T |
13: 97,159,038 (GRCm39) |
V122D |
unknown |
Het |
4930579F01Rik |
T |
G |
3: 137,870,134 (GRCm39) |
Y199S |
possibly damaging |
Het |
Abca6 |
T |
A |
11: 110,073,750 (GRCm39) |
I1434F |
probably benign |
Het |
Acsm1 |
T |
C |
7: 119,257,635 (GRCm39) |
V467A |
possibly damaging |
Het |
Alg3 |
T |
C |
16: 20,425,285 (GRCm39) |
T260A |
possibly damaging |
Het |
Aoc1 |
A |
G |
6: 48,883,254 (GRCm39) |
|
probably null |
Het |
Ap5b1 |
C |
T |
19: 5,620,815 (GRCm39) |
T745I |
possibly damaging |
Het |
Atp6v1c2 |
T |
G |
12: 17,341,441 (GRCm39) |
K272Q |
possibly damaging |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Cert1 |
T |
G |
13: 96,735,982 (GRCm39) |
Y181D |
probably benign |
Het |
Clcn7 |
C |
T |
17: 25,372,058 (GRCm39) |
A426V |
possibly damaging |
Het |
Dst |
T |
A |
1: 34,267,738 (GRCm39) |
V2720E |
probably damaging |
Het |
Efr3a |
C |
T |
15: 65,742,999 (GRCm39) |
|
probably benign |
Het |
Fam83g |
T |
C |
11: 61,575,609 (GRCm39) |
S84P |
probably benign |
Het |
Gm7251 |
T |
C |
13: 49,959,382 (GRCm39) |
|
noncoding transcript |
Het |
Gnptab |
T |
G |
10: 88,265,323 (GRCm39) |
S312A |
possibly damaging |
Het |
Grap2 |
C |
A |
15: 80,532,076 (GRCm39) |
S230R |
possibly damaging |
Het |
Grm6 |
T |
A |
11: 50,750,483 (GRCm39) |
C549S |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,245,903 (GRCm39) |
L1504* |
probably null |
Het |
Iars1 |
A |
G |
13: 49,878,172 (GRCm39) |
M899V |
probably benign |
Het |
Il1rl1 |
T |
A |
1: 40,481,463 (GRCm39) |
|
probably benign |
Het |
Kcna4 |
T |
C |
2: 107,126,963 (GRCm39) |
Y566H |
possibly damaging |
Het |
Kcnn2 |
T |
C |
18: 45,694,340 (GRCm39) |
I175T |
probably damaging |
Het |
Kcnt1 |
C |
T |
2: 25,791,877 (GRCm39) |
T609I |
probably damaging |
Het |
Kif3b |
A |
G |
2: 153,159,194 (GRCm39) |
R332G |
probably damaging |
Het |
Mansc1 |
T |
C |
6: 134,598,800 (GRCm39) |
D39G |
probably damaging |
Het |
Med12 |
T |
C |
X: 100,331,948 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
G |
T |
9: 7,384,935 (GRCm39) |
T238K |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,594,897 (GRCm39) |
S1435P |
probably damaging |
Het |
Npc1l1 |
A |
G |
11: 6,178,157 (GRCm39) |
S418P |
probably benign |
Het |
Or14j1 |
T |
C |
17: 38,146,832 (GRCm39) |
V314A |
probably benign |
Het |
Or2ab1 |
T |
C |
11: 58,488,408 (GRCm39) |
V62A |
possibly damaging |
Het |
Or3a1b |
A |
G |
11: 74,012,113 (GRCm39) |
|
probably benign |
Het |
Or52a24 |
A |
G |
7: 103,381,676 (GRCm39) |
Y181C |
probably damaging |
Het |
Or52h1 |
A |
C |
7: 103,829,432 (GRCm39) |
M61R |
probably damaging |
Het |
Or6ae1 |
G |
T |
7: 139,742,607 (GRCm39) |
D85E |
probably benign |
Het |
Or8b3b |
T |
C |
9: 38,584,711 (GRCm39) |
T23A |
probably damaging |
Het |
Otoa |
A |
G |
7: 120,721,247 (GRCm39) |
T421A |
probably benign |
Het |
Otulin |
G |
A |
15: 27,608,823 (GRCm39) |
A42V |
probably damaging |
Het |
Pcdhb1 |
T |
A |
18: 37,398,838 (GRCm39) |
V263E |
probably benign |
Het |
Pfkfb4 |
C |
T |
9: 108,854,178 (GRCm39) |
R351W |
probably damaging |
Het |
Phip |
A |
T |
9: 82,775,423 (GRCm39) |
V1053D |
probably damaging |
Het |
Pkd1 |
G |
A |
17: 24,794,901 (GRCm39) |
R2196H |
probably benign |
Het |
Plin4 |
T |
A |
17: 56,409,131 (GRCm39) |
Q1363L |
probably damaging |
Het |
Pp2d1 |
C |
A |
17: 53,814,949 (GRCm39) |
V592L |
probably damaging |
Het |
Pramel51 |
T |
C |
12: 88,145,242 (GRCm39) |
D28G |
possibly damaging |
Het |
Prkdc |
T |
G |
16: 15,535,048 (GRCm39) |
M1649R |
probably benign |
Het |
Ptk2b |
T |
C |
14: 66,450,931 (GRCm39) |
K12E |
probably benign |
Het |
Rars2 |
G |
A |
4: 34,657,219 (GRCm39) |
V522I |
probably damaging |
Het |
Rpgrip1 |
T |
A |
14: 52,384,831 (GRCm39) |
N646K |
possibly damaging |
Het |
Sars2 |
A |
G |
7: 28,451,950 (GRCm39) |
|
probably benign |
Het |
Sgo2b |
T |
C |
8: 64,384,316 (GRCm39) |
T227A |
possibly damaging |
Het |
Smc1b |
T |
C |
15: 84,982,186 (GRCm39) |
T703A |
probably benign |
Het |
Stk32a |
G |
T |
18: 43,446,572 (GRCm39) |
D341Y |
probably benign |
Het |
Thap11 |
T |
C |
8: 106,582,546 (GRCm39) |
V185A |
possibly damaging |
Het |
Ttll10 |
C |
A |
4: 156,132,890 (GRCm39) |
V65F |
probably benign |
Het |
Ube2q1 |
T |
A |
3: 89,687,769 (GRCm39) |
N111K |
possibly damaging |
Het |
Upf2 |
C |
A |
2: 6,031,134 (GRCm39) |
|
probably benign |
Het |
Utp25 |
A |
T |
1: 192,800,586 (GRCm39) |
D411E |
probably benign |
Het |
Vasp |
T |
A |
7: 18,991,637 (GRCm39) |
|
probably benign |
Het |
Vmn2r104 |
C |
T |
17: 20,262,056 (GRCm39) |
W358* |
probably null |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Wdfy3 |
C |
T |
5: 102,046,376 (GRCm39) |
G1826R |
possibly damaging |
Het |
Wdr7 |
T |
A |
18: 63,910,616 (GRCm39) |
Y669* |
probably null |
Het |
Wdr72 |
T |
A |
9: 74,189,011 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Clec14a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01933:Clec14a
|
APN |
12 |
58,315,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02109:Clec14a
|
APN |
12 |
58,314,934 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02136:Clec14a
|
APN |
12 |
58,315,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02818:Clec14a
|
APN |
12 |
58,314,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Clec14a
|
UTSW |
12 |
58,315,580 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0382:Clec14a
|
UTSW |
12 |
58,315,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R0419:Clec14a
|
UTSW |
12 |
58,314,451 (GRCm39) |
missense |
probably damaging |
0.97 |
R2972:Clec14a
|
UTSW |
12 |
58,314,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R3796:Clec14a
|
UTSW |
12 |
58,314,695 (GRCm39) |
missense |
probably benign |
0.34 |
R3797:Clec14a
|
UTSW |
12 |
58,314,695 (GRCm39) |
missense |
probably benign |
0.34 |
R3876:Clec14a
|
UTSW |
12 |
58,315,430 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4602:Clec14a
|
UTSW |
12 |
58,314,767 (GRCm39) |
missense |
probably benign |
0.03 |
R4708:Clec14a
|
UTSW |
12 |
58,314,489 (GRCm39) |
missense |
probably benign |
0.00 |
R4994:Clec14a
|
UTSW |
12 |
58,315,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R5193:Clec14a
|
UTSW |
12 |
58,315,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Clec14a
|
UTSW |
12 |
58,315,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Clec14a
|
UTSW |
12 |
58,314,612 (GRCm39) |
missense |
probably benign |
0.05 |
R6318:Clec14a
|
UTSW |
12 |
58,315,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R6388:Clec14a
|
UTSW |
12 |
58,314,243 (GRCm39) |
makesense |
probably null |
|
R6828:Clec14a
|
UTSW |
12 |
58,315,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Clec14a
|
UTSW |
12 |
58,315,580 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7418:Clec14a
|
UTSW |
12 |
58,315,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R7635:Clec14a
|
UTSW |
12 |
58,315,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Clec14a
|
UTSW |
12 |
58,314,543 (GRCm39) |
missense |
probably benign |
0.05 |
R7908:Clec14a
|
UTSW |
12 |
58,314,465 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8844:Clec14a
|
UTSW |
12 |
58,315,599 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9294:Clec14a
|
UTSW |
12 |
58,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R9477:Clec14a
|
UTSW |
12 |
58,314,620 (GRCm39) |
missense |
probably benign |
0.01 |
R9711:Clec14a
|
UTSW |
12 |
58,314,432 (GRCm39) |
missense |
probably damaging |
0.97 |
X0024:Clec14a
|
UTSW |
12 |
58,315,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|