Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
A |
9: 124,056,687 (GRCm39) |
H100L |
probably benign |
Het |
Apaf1 |
A |
T |
10: 90,856,596 (GRCm39) |
H870Q |
probably damaging |
Het |
Aplf |
T |
C |
6: 87,623,068 (GRCm39) |
D358G |
probably damaging |
Het |
Atp10a |
A |
T |
7: 58,423,733 (GRCm39) |
S233C |
probably damaging |
Het |
Ccdc158 |
A |
T |
5: 92,814,579 (GRCm39) |
Y82* |
probably null |
Het |
Clba1 |
C |
T |
12: 112,773,217 (GRCm39) |
P70L |
possibly damaging |
Het |
Cubn |
T |
C |
2: 13,491,600 (GRCm39) |
D149G |
probably damaging |
Het |
Cyp4f14 |
T |
C |
17: 33,133,608 (GRCm39) |
T83A |
probably benign |
Het |
Endog |
A |
G |
2: 30,061,648 (GRCm39) |
|
probably benign |
Het |
Extl3 |
T |
C |
14: 65,304,246 (GRCm39) |
E721G |
probably benign |
Het |
Gatad1 |
T |
C |
5: 3,693,540 (GRCm39) |
R210G |
probably benign |
Het |
Gcn1 |
A |
G |
5: 115,751,518 (GRCm39) |
H2033R |
probably damaging |
Het |
Gm12830 |
T |
C |
4: 114,702,246 (GRCm39) |
M136T |
|
Het |
Gm6871 |
T |
C |
7: 41,196,202 (GRCm39) |
|
silent |
Het |
Hoxc4 |
T |
C |
15: 102,944,098 (GRCm39) |
S159P |
probably damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,880,611 (GRCm39) |
Q494L |
probably null |
Het |
Igfn1 |
T |
A |
1: 135,896,183 (GRCm39) |
N1461I |
probably damaging |
Het |
Il23r |
C |
A |
6: 67,400,352 (GRCm39) |
K659N |
probably damaging |
Het |
Map3k11 |
A |
G |
19: 5,740,755 (GRCm39) |
S161G |
possibly damaging |
Het |
Naip6 |
T |
A |
13: 100,452,773 (GRCm39) |
Q96L |
probably damaging |
Het |
Nup133 |
T |
C |
8: 124,642,057 (GRCm39) |
E802G |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,086,563 (GRCm39) |
S56F |
probably damaging |
Het |
Or10x4 |
T |
A |
1: 174,219,243 (GRCm39) |
S203T |
probably benign |
Het |
Or51a24 |
T |
C |
7: 103,734,002 (GRCm39) |
N95S |
probably benign |
Het |
Otop2 |
A |
T |
11: 115,220,152 (GRCm39) |
S331C |
possibly damaging |
Het |
Pira1 |
C |
G |
7: 3,740,319 (GRCm39) |
A301P |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,387,539 (GRCm39) |
R1818G |
possibly damaging |
Het |
Pms1 |
A |
T |
1: 53,228,590 (GRCm39) |
I886N |
probably damaging |
Het |
Pnpla6 |
A |
G |
8: 3,588,068 (GRCm39) |
Y1107C |
probably damaging |
Het |
Ppp3ca |
A |
G |
3: 136,611,062 (GRCm39) |
T362A |
probably damaging |
Het |
Rarb |
A |
G |
14: 16,574,942 (GRCm38) |
S25P |
possibly damaging |
Het |
Rnf121 |
A |
T |
7: 101,673,218 (GRCm39) |
|
probably null |
Het |
Sae1 |
T |
C |
7: 16,070,712 (GRCm39) |
Y266C |
probably damaging |
Het |
Scpep1 |
A |
T |
11: 88,838,031 (GRCm39) |
F85L |
probably damaging |
Het |
Shank1 |
T |
A |
7: 43,962,530 (GRCm39) |
|
probably null |
Het |
Slc40a1 |
T |
C |
1: 45,948,652 (GRCm39) |
K543E |
probably benign |
Het |
Slc9a9 |
A |
G |
9: 94,842,499 (GRCm39) |
Y350C |
probably damaging |
Het |
Sun2 |
G |
T |
15: 79,618,420 (GRCm39) |
Y246* |
probably null |
Het |
Tas1r2 |
T |
A |
4: 139,397,031 (GRCm39) |
I790N |
probably damaging |
Het |
Tmtc2 |
T |
C |
10: 105,158,863 (GRCm39) |
T577A |
probably benign |
Het |
Trim24 |
T |
G |
6: 37,896,427 (GRCm39) |
|
probably null |
Het |
Ttc12 |
A |
G |
9: 49,349,718 (GRCm39) |
V693A |
probably benign |
Het |
Zbtb22 |
A |
C |
17: 34,136,938 (GRCm39) |
D361A |
probably damaging |
Het |
Zfp276 |
T |
A |
8: 123,983,570 (GRCm39) |
C324* |
probably null |
Het |
Zfp536 |
A |
G |
7: 37,267,952 (GRCm39) |
L488P |
probably damaging |
Het |
|
Other mutations in Ift70a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02724:Ift70a2
|
APN |
2 |
75,806,682 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03269:Ift70a2
|
APN |
2 |
75,808,479 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0011:Ift70a2
|
UTSW |
2 |
75,806,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R0751:Ift70a2
|
UTSW |
2 |
75,808,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R0766:Ift70a2
|
UTSW |
2 |
75,806,676 (GRCm39) |
missense |
probably benign |
0.00 |
R0835:Ift70a2
|
UTSW |
2 |
75,808,494 (GRCm39) |
missense |
probably benign |
|
R1133:Ift70a2
|
UTSW |
2 |
75,807,727 (GRCm39) |
nonsense |
probably null |
|
R1212:Ift70a2
|
UTSW |
2 |
75,806,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312:Ift70a2
|
UTSW |
2 |
75,806,676 (GRCm39) |
missense |
probably benign |
0.00 |
R4780:Ift70a2
|
UTSW |
2 |
75,807,920 (GRCm39) |
missense |
probably benign |
0.19 |
R4799:Ift70a2
|
UTSW |
2 |
75,807,729 (GRCm39) |
missense |
probably benign |
0.01 |
R4847:Ift70a2
|
UTSW |
2 |
75,808,058 (GRCm39) |
missense |
probably benign |
0.03 |
R5176:Ift70a2
|
UTSW |
2 |
75,807,421 (GRCm39) |
missense |
probably benign |
|
R5390:Ift70a2
|
UTSW |
2 |
75,807,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5724:Ift70a2
|
UTSW |
2 |
75,808,074 (GRCm39) |
missense |
probably benign |
|
R6975:Ift70a2
|
UTSW |
2 |
75,808,004 (GRCm39) |
nonsense |
probably null |
|
R7028:Ift70a2
|
UTSW |
2 |
75,806,613 (GRCm39) |
nonsense |
probably null |
|
R7234:Ift70a2
|
UTSW |
2 |
75,806,540 (GRCm39) |
nonsense |
probably null |
|
R7246:Ift70a2
|
UTSW |
2 |
75,808,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Ift70a2
|
UTSW |
2 |
75,807,273 (GRCm39) |
missense |
probably benign |
0.04 |
R8073:Ift70a2
|
UTSW |
2 |
75,806,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R9038:Ift70a2
|
UTSW |
2 |
75,808,215 (GRCm39) |
missense |
probably benign |
0.09 |
R9278:Ift70a2
|
UTSW |
2 |
75,807,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9454:Ift70a2
|
UTSW |
2 |
75,806,812 (GRCm39) |
missense |
probably benign |
0.05 |
R9694:Ift70a2
|
UTSW |
2 |
75,807,691 (GRCm39) |
missense |
probably benign |
0.41 |
|