Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
A |
17: 9,226,939 (GRCm39) |
V498D |
unknown |
Het |
Actn1 |
C |
T |
12: 80,245,754 (GRCm39) |
|
probably benign |
Het |
Actrt2 |
T |
C |
4: 154,751,176 (GRCm39) |
E320G |
probably damaging |
Het |
Adamts7 |
C |
T |
9: 90,076,239 (GRCm39) |
Q1265* |
probably null |
Het |
Adra1a |
A |
G |
14: 66,875,064 (GRCm39) |
N13S |
probably benign |
Het |
Alpk3 |
G |
T |
7: 80,707,403 (GRCm39) |
R9L |
unknown |
Het |
Ankrd42 |
A |
G |
7: 92,263,674 (GRCm39) |
F225L |
probably benign |
Het |
C3 |
T |
C |
17: 57,528,011 (GRCm39) |
E736G |
probably benign |
Het |
Ccng1 |
A |
G |
11: 40,644,826 (GRCm39) |
S24P |
probably benign |
Het |
Cdc42bpa |
A |
T |
1: 179,894,816 (GRCm39) |
N332I |
probably damaging |
Het |
Cep131 |
G |
A |
11: 119,972,074 (GRCm39) |
P90S |
probably benign |
Het |
Chd8 |
A |
G |
14: 52,441,904 (GRCm39) |
S2154P |
probably damaging |
Het |
Cilp |
A |
G |
9: 65,186,535 (GRCm39) |
S877G |
probably benign |
Het |
Clic6 |
T |
A |
16: 92,324,987 (GRCm39) |
S382T |
possibly damaging |
Het |
Coq8a |
G |
T |
1: 180,006,773 (GRCm39) |
P85Q |
probably benign |
Het |
Creb3l4 |
A |
G |
3: 90,145,225 (GRCm39) |
I309T |
probably benign |
Het |
Cux2 |
T |
C |
5: 122,007,306 (GRCm39) |
E785G |
probably benign |
Het |
Cyfip2 |
A |
G |
11: 46,144,800 (GRCm39) |
F685L |
possibly damaging |
Het |
Epha6 |
T |
C |
16: 60,026,035 (GRCm39) |
D469G |
probably benign |
Het |
Erc1 |
A |
T |
6: 119,607,616 (GRCm39) |
V962E |
probably damaging |
Het |
Esrrb |
A |
T |
12: 86,517,038 (GRCm39) |
S57C |
probably damaging |
Het |
Farsb |
C |
T |
1: 78,401,678 (GRCm39) |
|
probably benign |
Het |
Frem3 |
T |
C |
8: 81,338,907 (GRCm39) |
V400A |
probably damaging |
Het |
Frem3 |
A |
T |
8: 81,342,851 (GRCm39) |
M1715L |
probably benign |
Het |
Frmpd1 |
A |
G |
4: 45,279,632 (GRCm39) |
T786A |
probably benign |
Het |
Gapvd1 |
A |
T |
2: 34,594,330 (GRCm39) |
S886T |
possibly damaging |
Het |
Gba2 |
A |
G |
4: 43,568,077 (GRCm39) |
S737P |
probably damaging |
Het |
Gm525 |
A |
G |
11: 88,979,479 (GRCm39) |
N85S |
probably damaging |
Het |
Gnpda1 |
T |
A |
18: 38,465,091 (GRCm39) |
D175V |
probably benign |
Het |
Heatr5b |
T |
C |
17: 79,123,015 (GRCm39) |
I655V |
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,591,469 (GRCm39) |
T1910I |
probably benign |
Het |
Idh1 |
CA |
CAA |
1: 65,204,347 (GRCm39) |
|
probably null |
Het |
Ier2 |
A |
T |
8: 85,389,096 (GRCm39) |
D95E |
probably damaging |
Het |
Ifi208 |
A |
G |
1: 173,523,370 (GRCm39) |
R547G |
possibly damaging |
Het |
Itih3 |
T |
A |
14: 30,634,854 (GRCm39) |
S639C |
possibly damaging |
Het |
Kif19b |
A |
G |
5: 140,461,785 (GRCm39) |
E529G |
probably damaging |
Het |
Marchf7 |
G |
A |
2: 60,074,015 (GRCm39) |
|
probably null |
Het |
Mep1b |
A |
C |
18: 21,224,325 (GRCm39) |
T373P |
probably damaging |
Het |
Mlh3 |
G |
A |
12: 85,282,497 (GRCm39) |
P1379S |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,605,032 (GRCm39) |
K1014* |
probably null |
Het |
Nme1 |
A |
T |
11: 93,851,658 (GRCm39) |
F78I |
probably benign |
Het |
Nos3 |
T |
A |
5: 24,576,745 (GRCm39) |
V458D |
probably damaging |
Het |
Noxa1 |
A |
G |
2: 24,984,852 (GRCm39) |
F29L |
probably benign |
Het |
Nrcam |
G |
A |
12: 44,624,958 (GRCm39) |
G1055D |
probably benign |
Het |
Nutf2 |
A |
T |
8: 106,602,171 (GRCm39) |
|
probably benign |
Het |
Oog3 |
A |
G |
4: 143,884,556 (GRCm39) |
I460T |
probably benign |
Het |
Or4b1b |
A |
T |
2: 90,112,150 (GRCm39) |
Y256* |
probably null |
Het |
Or4c113 |
T |
C |
2: 88,885,477 (GRCm39) |
M98V |
probably benign |
Het |
Or5p78 |
A |
T |
7: 108,211,580 (GRCm39) |
D22V |
probably benign |
Het |
Or7e175 |
A |
T |
9: 20,048,630 (GRCm39) |
M73L |
possibly damaging |
Het |
Pde2a |
A |
T |
7: 101,155,136 (GRCm39) |
Y559F |
possibly damaging |
Het |
Pde6d |
G |
A |
1: 86,475,209 (GRCm39) |
Q61* |
probably null |
Het |
Pdpr |
A |
G |
8: 111,852,240 (GRCm39) |
T536A |
possibly damaging |
Het |
Pias4 |
T |
A |
10: 80,999,846 (GRCm39) |
K69M |
probably damaging |
Het |
Pigo |
A |
T |
4: 43,023,787 (GRCm39) |
D188E |
possibly damaging |
Het |
Pik3r2 |
A |
G |
8: 71,224,007 (GRCm39) |
V270A |
probably benign |
Het |
Plod2 |
T |
A |
9: 92,482,801 (GRCm39) |
W456R |
probably damaging |
Het |
Pmpcb |
T |
C |
5: 21,961,832 (GRCm39) |
V450A |
probably benign |
Het |
Poln |
G |
A |
5: 34,286,871 (GRCm39) |
T99I |
possibly damaging |
Het |
Prg2 |
A |
G |
2: 84,812,404 (GRCm39) |
D38G |
possibly damaging |
Het |
Psmd7 |
A |
C |
8: 108,310,831 (GRCm39) |
Y138D |
probably damaging |
Het |
Ptprk |
T |
A |
10: 28,139,504 (GRCm39) |
Y76* |
probably null |
Het |
Ranbp2 |
T |
A |
10: 58,328,414 (GRCm39) |
V2810E |
probably damaging |
Het |
Rgma |
A |
T |
7: 73,067,648 (GRCm39) |
H411L |
probably damaging |
Het |
Sapcd1 |
T |
C |
17: 35,246,814 (GRCm39) |
T25A |
probably damaging |
Het |
Serpinb6e |
T |
C |
13: 34,024,977 (GRCm39) |
I105V |
possibly damaging |
Het |
Serpinb9f |
A |
T |
13: 33,513,396 (GRCm39) |
T158S |
probably benign |
Het |
Sirpb1b |
T |
A |
3: 15,613,843 (GRCm39) |
T80S |
probably benign |
Het |
Skint6 |
A |
T |
4: 113,049,869 (GRCm39) |
S265R |
possibly damaging |
Het |
Slc23a2 |
A |
T |
2: 131,902,629 (GRCm39) |
F524L |
probably benign |
Het |
Slc2a13 |
C |
A |
15: 91,234,302 (GRCm39) |
G345C |
probably damaging |
Het |
Sp110 |
A |
G |
1: 85,511,231 (GRCm39) |
|
probably null |
Het |
Srcin1 |
A |
G |
11: 97,439,803 (GRCm39) |
V109A |
probably benign |
Het |
Tfcp2l1 |
A |
G |
1: 118,560,118 (GRCm39) |
N70S |
probably damaging |
Het |
Tmem30c |
T |
A |
16: 57,090,553 (GRCm39) |
H218L |
probably benign |
Het |
Tmprss11d |
G |
A |
5: 86,486,680 (GRCm39) |
T70I |
probably damaging |
Het |
Tnpo2 |
A |
T |
8: 85,765,114 (GRCm39) |
Q32L |
probably benign |
Het |
Trav16n |
A |
C |
14: 53,588,867 (GRCm39) |
T48P |
probably damaging |
Het |
Ufc1 |
A |
G |
1: 171,117,095 (GRCm39) |
Y110H |
probably damaging |
Het |
Wars2 |
A |
G |
3: 99,123,888 (GRCm39) |
K250E |
probably damaging |
Het |
Wdfy4 |
G |
T |
14: 32,869,049 (GRCm39) |
N326K |
probably benign |
Het |
Xirp2 |
A |
T |
2: 67,341,557 (GRCm39) |
E1266V |
probably damaging |
Het |
Zfp423 |
A |
C |
8: 88,507,857 (GRCm39) |
L829R |
probably damaging |
Het |
Zfp735 |
A |
G |
11: 73,603,029 (GRCm39) |
K658E |
possibly damaging |
Het |
Zscan12 |
T |
A |
13: 21,547,847 (GRCm39) |
C10S |
possibly damaging |
Het |
Zswim3 |
T |
A |
2: 164,662,687 (GRCm39) |
M389K |
probably damaging |
Het |
|
Other mutations in Fam169a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Fam169a
|
APN |
13 |
97,259,207 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01380:Fam169a
|
APN |
13 |
97,228,459 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01761:Fam169a
|
APN |
13 |
97,228,426 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02628:Fam169a
|
APN |
13 |
97,247,796 (GRCm39) |
splice site |
probably benign |
|
IGL02739:Fam169a
|
APN |
13 |
97,230,563 (GRCm39) |
splice site |
probably benign |
|
IGL03171:Fam169a
|
APN |
13 |
97,246,522 (GRCm39) |
splice site |
probably benign |
|
IGL03306:Fam169a
|
APN |
13 |
97,243,497 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03377:Fam169a
|
APN |
13 |
97,228,381 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02980:Fam169a
|
UTSW |
13 |
97,250,188 (GRCm39) |
critical splice donor site |
probably null |
|
R0282:Fam169a
|
UTSW |
13 |
97,234,223 (GRCm39) |
splice site |
probably benign |
|
R1319:Fam169a
|
UTSW |
13 |
97,234,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Fam169a
|
UTSW |
13 |
97,255,038 (GRCm39) |
missense |
probably benign |
0.01 |
R1468:Fam169a
|
UTSW |
13 |
97,255,038 (GRCm39) |
missense |
probably benign |
0.01 |
R2037:Fam169a
|
UTSW |
13 |
97,243,600 (GRCm39) |
missense |
probably benign |
0.37 |
R2380:Fam169a
|
UTSW |
13 |
97,255,043 (GRCm39) |
splice site |
probably benign |
|
R3805:Fam169a
|
UTSW |
13 |
97,234,192 (GRCm39) |
missense |
probably benign |
0.00 |
R4434:Fam169a
|
UTSW |
13 |
97,263,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4435:Fam169a
|
UTSW |
13 |
97,263,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Fam169a
|
UTSW |
13 |
97,263,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Fam169a
|
UTSW |
13 |
97,234,093 (GRCm39) |
missense |
probably benign |
0.02 |
R4896:Fam169a
|
UTSW |
13 |
97,234,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fam169a
|
UTSW |
13 |
97,234,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5276:Fam169a
|
UTSW |
13 |
97,255,004 (GRCm39) |
missense |
probably benign |
0.01 |
R5370:Fam169a
|
UTSW |
13 |
97,243,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Fam169a
|
UTSW |
13 |
97,230,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Fam169a
|
UTSW |
13 |
97,230,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Fam169a
|
UTSW |
13 |
97,263,196 (GRCm39) |
nonsense |
probably null |
|
R8322:Fam169a
|
UTSW |
13 |
97,259,260 (GRCm39) |
missense |
probably benign |
0.00 |
R8493:Fam169a
|
UTSW |
13 |
97,259,367 (GRCm39) |
missense |
probably benign |
0.00 |
R8698:Fam169a
|
UTSW |
13 |
97,243,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Fam169a
|
UTSW |
13 |
97,254,967 (GRCm39) |
missense |
probably benign |
0.08 |
R9479:Fam169a
|
UTSW |
13 |
97,250,695 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9479:Fam169a
|
UTSW |
13 |
97,246,543 (GRCm39) |
missense |
possibly damaging |
0.68 |
|