Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930453N24Rik |
A |
G |
16: 64,586,821 (GRCm39) |
V301A |
probably benign |
Het |
Agbl3 |
T |
C |
6: 34,823,834 (GRCm39) |
L833P |
probably damaging |
Het |
Amph |
T |
C |
13: 19,326,168 (GRCm39) |
S633P |
probably damaging |
Het |
Aspscr1 |
T |
C |
11: 120,577,505 (GRCm39) |
V60A |
probably benign |
Het |
Atp13a3 |
C |
A |
16: 30,173,064 (GRCm39) |
C271F |
possibly damaging |
Het |
B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
BC051019 |
C |
T |
7: 109,317,202 (GRCm39) |
W163* |
probably null |
Het |
Capza1 |
T |
C |
3: 104,732,427 (GRCm39) |
E245G |
probably damaging |
Het |
Cd81 |
G |
T |
7: 142,619,030 (GRCm39) |
C18F |
probably damaging |
Het |
Cfap45 |
G |
T |
1: 172,366,056 (GRCm39) |
R303L |
probably benign |
Het |
Commd9 |
T |
C |
2: 101,725,499 (GRCm39) |
V24A |
possibly damaging |
Het |
Dennd4a |
A |
G |
9: 64,819,174 (GRCm39) |
N1742D |
possibly damaging |
Het |
Dgat1 |
G |
T |
15: 76,388,371 (GRCm39) |
A182D |
possibly damaging |
Het |
Dlg4 |
T |
C |
11: 69,917,909 (GRCm39) |
L64P |
probably benign |
Het |
Dna2 |
A |
G |
10: 62,792,768 (GRCm39) |
D261G |
probably damaging |
Het |
Epb41l4b |
C |
T |
4: 57,024,337 (GRCm39) |
|
probably null |
Het |
Fam13c |
T |
C |
10: 70,390,338 (GRCm39) |
L533P |
probably damaging |
Het |
Fjx1 |
T |
C |
2: 102,281,066 (GRCm39) |
T290A |
possibly damaging |
Het |
Hid1 |
C |
T |
11: 115,247,565 (GRCm39) |
E278K |
probably damaging |
Het |
Hsd3b7 |
T |
C |
7: 127,400,717 (GRCm39) |
I57T |
probably damaging |
Het |
Igfn1 |
A |
G |
1: 135,897,494 (GRCm39) |
V1024A |
probably benign |
Het |
Klhl32 |
T |
C |
4: 24,792,781 (GRCm39) |
T14A |
probably damaging |
Het |
Krt23 |
T |
C |
11: 99,376,614 (GRCm39) |
T181A |
probably benign |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lrrc36 |
A |
G |
8: 106,154,428 (GRCm39) |
E33G |
probably damaging |
Het |
Mettl13 |
G |
T |
1: 162,373,755 (GRCm39) |
H165Q |
probably damaging |
Het |
Mocos |
G |
A |
18: 24,812,447 (GRCm39) |
G447D |
probably damaging |
Het |
Ngef |
T |
A |
1: 87,413,953 (GRCm39) |
K399N |
probably damaging |
Het |
Ntrk1 |
A |
G |
3: 87,688,786 (GRCm39) |
L589P |
probably damaging |
Het |
Or4c104 |
C |
T |
2: 88,586,795 (GRCm39) |
V75I |
probably benign |
Het |
Pcdha2 |
A |
G |
18: 37,072,935 (GRCm39) |
S189G |
probably benign |
Het |
Peg10 |
T |
G |
6: 4,756,427 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
C |
T |
15: 44,414,156 (GRCm39) |
H2808Y |
probably benign |
Het |
Plekhg1 |
A |
G |
10: 3,907,087 (GRCm39) |
D668G |
probably damaging |
Het |
Ptcd2 |
A |
G |
13: 99,481,084 (GRCm39) |
C32R |
probably damaging |
Het |
Rgs8 |
A |
G |
1: 153,566,742 (GRCm39) |
T98A |
probably null |
Het |
Rhoh |
G |
A |
5: 66,049,931 (GRCm39) |
S67N |
probably benign |
Het |
Rnd3 |
A |
G |
2: 51,038,760 (GRCm39) |
F43L |
probably damaging |
Het |
Runx1 |
A |
G |
16: 92,441,134 (GRCm39) |
V225A |
probably benign |
Het |
Runx1t1 |
T |
C |
4: 13,889,769 (GRCm39) |
V566A |
probably benign |
Het |
Sall2 |
A |
G |
14: 52,552,028 (GRCm39) |
I387T |
probably damaging |
Het |
Sec14l1 |
T |
A |
11: 117,040,024 (GRCm39) |
V384D |
possibly damaging |
Het |
Sh3rf3 |
T |
C |
10: 58,919,355 (GRCm39) |
C491R |
probably damaging |
Het |
Slc22a27 |
T |
A |
19: 7,856,973 (GRCm39) |
|
probably benign |
Het |
Spire1 |
A |
G |
18: 67,678,783 (GRCm39) |
S53P |
probably damaging |
Het |
Tmco3 |
A |
G |
8: 13,370,848 (GRCm39) |
R671G |
probably benign |
Het |
Tmpo |
A |
G |
10: 90,998,123 (GRCm39) |
S555P |
probably benign |
Het |
Tnip1 |
A |
G |
11: 54,802,395 (GRCm39) |
S638P |
probably benign |
Het |
Tspan8 |
C |
T |
10: 115,671,187 (GRCm39) |
R115* |
probably null |
Het |
Txnrd1 |
A |
G |
10: 82,721,114 (GRCm39) |
E510G |
probably benign |
Het |
Ucp3 |
T |
C |
7: 100,131,871 (GRCm39) |
Y241H |
probably damaging |
Het |
Vmn2r96 |
A |
G |
17: 18,818,339 (GRCm39) |
I831V |
probably benign |
Het |
Zan |
T |
C |
5: 137,435,082 (GRCm39) |
I2104V |
unknown |
Het |
Zfp619 |
A |
C |
7: 39,184,823 (GRCm39) |
R284S |
probably benign |
Het |
Zfp715 |
T |
C |
7: 42,951,155 (GRCm39) |
M48V |
probably benign |
Het |
|
Other mutations in Itgae |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00424:Itgae
|
APN |
11 |
73,036,461 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00472:Itgae
|
APN |
11 |
73,004,520 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00821:Itgae
|
APN |
11 |
73,013,974 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01625:Itgae
|
APN |
11 |
73,010,263 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01639:Itgae
|
APN |
11 |
73,010,204 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Itgae
|
APN |
11 |
73,002,585 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01911:Itgae
|
APN |
11 |
73,006,963 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01949:Itgae
|
APN |
11 |
73,009,010 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02149:Itgae
|
APN |
11 |
72,994,720 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02179:Itgae
|
APN |
11 |
73,024,844 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02231:Itgae
|
APN |
11 |
72,981,448 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02292:Itgae
|
APN |
11 |
73,009,361 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02378:Itgae
|
APN |
11 |
73,008,947 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02525:Itgae
|
APN |
11 |
73,021,777 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02576:Itgae
|
APN |
11 |
73,009,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02729:Itgae
|
APN |
11 |
73,009,029 (GRCm39) |
splice site |
probably benign |
|
IGL02859:Itgae
|
APN |
11 |
73,005,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Itgae
|
APN |
11 |
73,016,136 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03107:Itgae
|
APN |
11 |
73,004,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03264:Itgae
|
APN |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03272:Itgae
|
APN |
11 |
73,024,680 (GRCm39) |
splice site |
probably null |
|
IGL03352:Itgae
|
APN |
11 |
73,022,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0134:Itgae
|
UTSW |
11 |
73,002,168 (GRCm39) |
missense |
probably benign |
0.00 |
R0225:Itgae
|
UTSW |
11 |
73,002,168 (GRCm39) |
missense |
probably benign |
0.00 |
R0320:Itgae
|
UTSW |
11 |
73,021,825 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0344:Itgae
|
UTSW |
11 |
73,008,973 (GRCm39) |
missense |
probably benign |
0.13 |
R0403:Itgae
|
UTSW |
11 |
73,014,009 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0631:Itgae
|
UTSW |
11 |
73,005,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:Itgae
|
UTSW |
11 |
73,020,032 (GRCm39) |
missense |
probably benign |
0.02 |
R0836:Itgae
|
UTSW |
11 |
73,020,032 (GRCm39) |
missense |
probably benign |
0.02 |
R0973:Itgae
|
UTSW |
11 |
73,029,335 (GRCm39) |
nonsense |
probably null |
|
R1231:Itgae
|
UTSW |
11 |
73,010,205 (GRCm39) |
missense |
probably benign |
0.02 |
R1389:Itgae
|
UTSW |
11 |
73,016,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R1433:Itgae
|
UTSW |
11 |
73,006,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Itgae
|
UTSW |
11 |
73,036,431 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1833:Itgae
|
UTSW |
11 |
73,007,988 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1914:Itgae
|
UTSW |
11 |
73,009,469 (GRCm39) |
splice site |
probably benign |
|
R1915:Itgae
|
UTSW |
11 |
73,009,469 (GRCm39) |
splice site |
probably benign |
|
R2061:Itgae
|
UTSW |
11 |
73,009,448 (GRCm39) |
missense |
probably benign |
0.00 |
R2380:Itgae
|
UTSW |
11 |
73,036,395 (GRCm39) |
missense |
probably benign |
0.00 |
R2435:Itgae
|
UTSW |
11 |
73,012,763 (GRCm39) |
nonsense |
probably null |
|
R2680:Itgae
|
UTSW |
11 |
73,005,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R2886:Itgae
|
UTSW |
11 |
73,031,513 (GRCm39) |
missense |
probably benign |
0.04 |
R3873:Itgae
|
UTSW |
11 |
73,004,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Itgae
|
UTSW |
11 |
73,006,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R4010:Itgae
|
UTSW |
11 |
73,002,165 (GRCm39) |
missense |
probably benign |
0.00 |
R4212:Itgae
|
UTSW |
11 |
73,010,178 (GRCm39) |
missense |
probably benign |
|
R4213:Itgae
|
UTSW |
11 |
73,010,178 (GRCm39) |
missense |
probably benign |
|
R4691:Itgae
|
UTSW |
11 |
73,010,345 (GRCm39) |
nonsense |
probably null |
|
R4736:Itgae
|
UTSW |
11 |
73,005,706 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5152:Itgae
|
UTSW |
11 |
73,021,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R5201:Itgae
|
UTSW |
11 |
73,001,382 (GRCm39) |
missense |
probably benign |
0.00 |
R5307:Itgae
|
UTSW |
11 |
73,036,464 (GRCm39) |
missense |
probably benign |
0.00 |
R5362:Itgae
|
UTSW |
11 |
73,002,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5448:Itgae
|
UTSW |
11 |
73,024,734 (GRCm39) |
critical splice donor site |
probably null |
|
R5645:Itgae
|
UTSW |
11 |
73,020,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5672:Itgae
|
UTSW |
11 |
73,036,377 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6079:Itgae
|
UTSW |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6138:Itgae
|
UTSW |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6226:Itgae
|
UTSW |
11 |
73,031,583 (GRCm39) |
missense |
probably benign |
0.11 |
R6244:Itgae
|
UTSW |
11 |
73,036,427 (GRCm39) |
missense |
probably damaging |
0.96 |
R6326:Itgae
|
UTSW |
11 |
73,022,519 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6332:Itgae
|
UTSW |
11 |
73,002,228 (GRCm39) |
splice site |
probably null |
|
R6502:Itgae
|
UTSW |
11 |
73,036,418 (GRCm39) |
missense |
probably benign |
0.10 |
R6825:Itgae
|
UTSW |
11 |
73,009,322 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7016:Itgae
|
UTSW |
11 |
73,010,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R7020:Itgae
|
UTSW |
11 |
73,002,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7069:Itgae
|
UTSW |
11 |
73,006,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R7132:Itgae
|
UTSW |
11 |
73,002,184 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7473:Itgae
|
UTSW |
11 |
73,031,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7599:Itgae
|
UTSW |
11 |
73,012,786 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7637:Itgae
|
UTSW |
11 |
73,004,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Itgae
|
UTSW |
11 |
73,014,095 (GRCm39) |
critical splice donor site |
probably null |
|
R7829:Itgae
|
UTSW |
11 |
73,029,618 (GRCm39) |
missense |
probably benign |
|
R7860:Itgae
|
UTSW |
11 |
73,011,099 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7978:Itgae
|
UTSW |
11 |
73,024,913 (GRCm39) |
missense |
probably damaging |
0.98 |
R8197:Itgae
|
UTSW |
11 |
73,011,210 (GRCm39) |
missense |
probably benign |
|
R8911:Itgae
|
UTSW |
11 |
73,004,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Itgae
|
UTSW |
11 |
73,016,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9284:Itgae
|
UTSW |
11 |
73,012,752 (GRCm39) |
missense |
probably benign |
0.25 |
R9355:Itgae
|
UTSW |
11 |
73,006,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R9414:Itgae
|
UTSW |
11 |
73,002,629 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9595:Itgae
|
UTSW |
11 |
73,016,182 (GRCm39) |
missense |
probably damaging |
0.99 |
R9618:Itgae
|
UTSW |
11 |
73,011,171 (GRCm39) |
missense |
possibly damaging |
0.78 |
U15987:Itgae
|
UTSW |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0024:Itgae
|
UTSW |
11 |
73,002,202 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1186:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1186:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1186:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1187:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1187:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1188:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1188:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1188:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1188:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1189:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1189:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1189:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1189:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1189:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1190:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1190:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1191:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1191:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1191:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1191:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1192:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1192:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1192:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1192:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
|