Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
A |
T |
11: 72,049,851 (GRCm39) |
|
probably benign |
Het |
A830018L16Rik |
A |
T |
1: 11,484,706 (GRCm39) |
|
probably benign |
Het |
Acox1 |
C |
T |
11: 116,066,040 (GRCm39) |
R454H |
probably damaging |
Het |
Acte1 |
G |
T |
7: 143,434,902 (GRCm39) |
|
probably null |
Het |
Adam18 |
A |
G |
8: 25,164,703 (GRCm39) |
L4P |
probably damaging |
Het |
AI182371 |
A |
C |
2: 34,990,622 (GRCm39) |
L25R |
probably damaging |
Het |
Ankrd12 |
A |
C |
17: 66,277,195 (GRCm39) |
Y2026* |
probably null |
Het |
Atad5 |
C |
T |
11: 79,986,524 (GRCm39) |
T537M |
possibly damaging |
Het |
Atosa |
A |
G |
9: 74,911,562 (GRCm39) |
Y11C |
probably damaging |
Het |
Avil |
G |
T |
10: 126,846,455 (GRCm39) |
G420V |
probably damaging |
Het |
Bche |
A |
T |
3: 73,608,008 (GRCm39) |
F473I |
probably damaging |
Het |
Borcs5 |
T |
C |
6: 134,621,437 (GRCm39) |
|
probably null |
Het |
C4b |
T |
C |
17: 34,961,913 (GRCm39) |
Q111R |
probably benign |
Het |
Carmil2 |
T |
A |
8: 106,417,437 (GRCm39) |
I565N |
probably damaging |
Het |
Cd74 |
T |
C |
18: 60,943,127 (GRCm39) |
M155T |
probably damaging |
Het |
Chrnd |
G |
T |
1: 87,119,997 (GRCm39) |
R105L |
probably damaging |
Het |
Clpp |
G |
T |
17: 57,300,553 (GRCm39) |
E217* |
probably null |
Het |
Cpq |
T |
A |
15: 33,594,269 (GRCm39) |
Y427N |
probably damaging |
Het |
Crxos |
G |
A |
7: 15,636,900 (GRCm39) |
E54K |
possibly damaging |
Het |
Dcaf13 |
A |
G |
15: 39,001,612 (GRCm39) |
R307G |
possibly damaging |
Het |
Ddx55 |
A |
G |
5: 124,706,788 (GRCm39) |
D595G |
probably damaging |
Het |
Dld |
T |
A |
12: 31,390,868 (GRCm39) |
I193F |
possibly damaging |
Het |
Dnah11 |
T |
G |
12: 118,091,381 (GRCm39) |
E917A |
possibly damaging |
Het |
Dnai2 |
T |
A |
11: 114,641,302 (GRCm39) |
Y376N |
possibly damaging |
Het |
Dock7 |
A |
G |
4: 98,829,243 (GRCm39) |
Y2078H |
probably damaging |
Het |
Dusp4 |
A |
T |
8: 35,274,941 (GRCm39) |
N20I |
probably benign |
Het |
Dzank1 |
A |
G |
2: 144,333,729 (GRCm39) |
L367P |
probably benign |
Het |
Eea1 |
T |
A |
10: 95,832,822 (GRCm39) |
D222E |
probably damaging |
Het |
Erich3 |
G |
C |
3: 154,462,692 (GRCm39) |
R742S |
|
Het |
Erich6 |
C |
T |
3: 58,537,275 (GRCm39) |
M246I |
probably benign |
Het |
Galnt16 |
T |
G |
12: 80,623,314 (GRCm39) |
I158S |
probably damaging |
Het |
Gm28363 |
A |
G |
1: 117,655,080 (GRCm39) |
T100A |
possibly damaging |
Het |
Gm8257 |
A |
T |
14: 44,893,849 (GRCm39) |
Y36N |
probably damaging |
Het |
Gmpr2 |
T |
C |
14: 55,913,149 (GRCm39) |
V142A |
possibly damaging |
Het |
Grid2ip |
T |
C |
5: 143,366,260 (GRCm39) |
|
probably null |
Het |
Hamp2 |
A |
G |
7: 30,622,001 (GRCm39) |
F63L |
possibly damaging |
Het |
Hmga2 |
T |
C |
10: 120,309,159 (GRCm39) |
K66E |
probably damaging |
Het |
Hspa1a |
T |
C |
17: 35,190,019 (GRCm39) |
T295A |
probably benign |
Het |
Ift74 |
G |
A |
4: 94,510,128 (GRCm39) |
G53D |
probably damaging |
Het |
Ighv6-7 |
T |
C |
12: 114,419,703 (GRCm39) |
M1V |
probably null |
Het |
Kif7 |
G |
A |
7: 79,360,005 (GRCm39) |
R411C |
probably damaging |
Het |
Klhl30 |
T |
A |
1: 91,287,174 (GRCm39) |
Y487N |
probably damaging |
Het |
Kras |
T |
C |
6: 145,170,853 (GRCm39) |
E174G |
probably benign |
Het |
Krt84 |
T |
C |
15: 101,437,183 (GRCm39) |
I327V |
probably benign |
Het |
Lamb3 |
T |
A |
1: 193,014,525 (GRCm39) |
C561* |
probably null |
Het |
Lmbrd1 |
A |
G |
1: 24,767,407 (GRCm39) |
|
probably benign |
Het |
Lmnb1 |
T |
A |
18: 56,876,331 (GRCm39) |
S480T |
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,341,348 (GRCm39) |
G944D |
probably damaging |
Het |
Mta3 |
G |
A |
17: 84,083,146 (GRCm39) |
E280K |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,421,115 (GRCm39) |
I4236F |
|
Het |
Myh9 |
T |
C |
15: 77,655,432 (GRCm39) |
T1175A |
probably benign |
Het |
Myt1l |
T |
A |
12: 29,861,564 (GRCm39) |
D115E |
unknown |
Het |
Naa25 |
A |
G |
5: 121,552,573 (GRCm39) |
N167D |
probably benign |
Het |
Ncam1 |
G |
A |
9: 49,431,493 (GRCm39) |
P648L |
probably damaging |
Het |
Or2t26 |
T |
C |
11: 49,039,266 (GRCm39) |
Y61H |
probably damaging |
Het |
Or2t44 |
A |
T |
11: 58,677,519 (GRCm39) |
D153V |
probably damaging |
Het |
P3h3 |
G |
T |
6: 124,832,196 (GRCm39) |
A230E |
possibly damaging |
Het |
Pacs2 |
A |
G |
12: 113,020,476 (GRCm39) |
E253G |
probably damaging |
Het |
Pbld1 |
A |
T |
10: 62,901,648 (GRCm39) |
D57V |
probably benign |
Het |
Pcsk5 |
T |
C |
19: 17,452,275 (GRCm39) |
T1077A |
probably damaging |
Het |
Pou4f2 |
T |
A |
8: 79,161,932 (GRCm39) |
M224L |
|
Het |
Ppcdc |
C |
T |
9: 57,342,265 (GRCm39) |
R19H |
probably benign |
Het |
Ppp1r10 |
T |
A |
17: 36,241,018 (GRCm39) |
M640K |
probably benign |
Het |
Prdx6 |
A |
T |
1: 161,069,432 (GRCm39) |
|
probably benign |
Het |
Rab40b |
A |
G |
11: 121,250,384 (GRCm39) |
|
probably null |
Het |
Rassf9 |
T |
A |
10: 102,381,329 (GRCm39) |
M237K |
probably benign |
Het |
Rbbp8nl |
G |
T |
2: 179,919,769 (GRCm39) |
Y604* |
probably null |
Het |
Reep2 |
G |
T |
18: 34,975,929 (GRCm39) |
W42L |
possibly damaging |
Het |
Serpinb6e |
A |
T |
13: 34,017,261 (GRCm39) |
M253K |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,623,927 (GRCm39) |
Q304R |
probably damaging |
Het |
Slk |
T |
C |
19: 47,600,057 (GRCm39) |
M120T |
probably damaging |
Het |
Spata31e5 |
T |
C |
1: 28,816,155 (GRCm39) |
I626V |
probably benign |
Het |
Sphkap |
T |
A |
1: 83,256,927 (GRCm39) |
H274L |
probably benign |
Het |
Stc1 |
T |
G |
14: 69,269,884 (GRCm39) |
F155V |
possibly damaging |
Het |
Tbc1d12 |
A |
G |
19: 38,899,510 (GRCm39) |
T477A |
probably damaging |
Het |
Tmem19 |
T |
A |
10: 115,183,671 (GRCm39) |
I54F |
possibly damaging |
Het |
Tmem62 |
G |
A |
2: 120,817,316 (GRCm39) |
|
probably null |
Het |
Ttc6 |
A |
T |
12: 57,689,826 (GRCm39) |
R505S |
|
Het |
Ttn |
G |
T |
2: 76,623,184 (GRCm39) |
R15418S |
probably damaging |
Het |
Ugt2a3 |
C |
A |
5: 87,473,417 (GRCm39) |
C500F |
possibly damaging |
Het |
Ugt2b35 |
T |
C |
5: 87,149,310 (GRCm39) |
F187S |
probably benign |
Het |
Ung |
T |
A |
5: 114,269,456 (GRCm39) |
I56N |
probably damaging |
Het |
Vmn1r17 |
G |
T |
6: 57,338,142 (GRCm39) |
F25L |
probably benign |
Het |
Vmn1r29 |
C |
A |
6: 58,284,274 (GRCm39) |
|
probably benign |
Het |
Vps26c |
T |
A |
16: 94,302,481 (GRCm39) |
I242F |
probably benign |
Het |
Wdhd1 |
T |
C |
14: 47,504,470 (GRCm39) |
D368G |
probably benign |
Het |
Wdr3 |
A |
T |
3: 100,057,259 (GRCm39) |
I448N |
probably damaging |
Het |
Wdr47 |
T |
A |
3: 108,550,480 (GRCm39) |
M835K |
possibly damaging |
Het |
Wt1 |
G |
A |
2: 104,957,584 (GRCm39) |
G10D |
possibly damaging |
Het |
Zdhhc19 |
G |
A |
16: 32,316,500 (GRCm39) |
G85D |
probably damaging |
Het |
|
Other mutations in Ints4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00765:Ints4
|
APN |
7 |
97,184,412 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01736:Ints4
|
APN |
7 |
97,175,849 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01862:Ints4
|
APN |
7 |
97,190,360 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02277:Ints4
|
APN |
7 |
97,136,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02396:Ints4
|
APN |
7 |
97,187,107 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02661:Ints4
|
APN |
7 |
97,144,912 (GRCm39) |
missense |
probably benign |
|
IGL02750:Ints4
|
APN |
7 |
97,166,964 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03108:Ints4
|
APN |
7 |
97,140,137 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0332:Ints4
|
UTSW |
7 |
97,166,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R0449:Ints4
|
UTSW |
7 |
97,178,430 (GRCm39) |
missense |
probably damaging |
0.97 |
R1065:Ints4
|
UTSW |
7 |
97,157,099 (GRCm39) |
critical splice donor site |
probably null |
|
R1722:Ints4
|
UTSW |
7 |
97,162,786 (GRCm39) |
missense |
probably benign |
0.24 |
R2060:Ints4
|
UTSW |
7 |
97,150,970 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2211:Ints4
|
UTSW |
7 |
97,158,957 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3731:Ints4
|
UTSW |
7 |
97,155,308 (GRCm39) |
missense |
probably benign |
0.18 |
R3881:Ints4
|
UTSW |
7 |
97,165,464 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4089:Ints4
|
UTSW |
7 |
97,178,462 (GRCm39) |
nonsense |
probably null |
|
R4192:Ints4
|
UTSW |
7 |
97,156,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R4479:Ints4
|
UTSW |
7 |
97,134,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4980:Ints4
|
UTSW |
7 |
97,151,057 (GRCm39) |
critical splice donor site |
probably null |
|
R5029:Ints4
|
UTSW |
7 |
97,158,981 (GRCm39) |
missense |
probably benign |
0.06 |
R5306:Ints4
|
UTSW |
7 |
97,158,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Ints4
|
UTSW |
7 |
97,158,790 (GRCm39) |
splice site |
probably null |
|
R6317:Ints4
|
UTSW |
7 |
97,178,425 (GRCm39) |
nonsense |
probably null |
|
R6961:Ints4
|
UTSW |
7 |
97,190,397 (GRCm39) |
makesense |
probably null |
|
R7026:Ints4
|
UTSW |
7 |
97,168,361 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7156:Ints4
|
UTSW |
7 |
97,184,493 (GRCm39) |
critical splice donor site |
probably null |
|
R7205:Ints4
|
UTSW |
7 |
97,184,433 (GRCm39) |
nonsense |
probably null |
|
R7234:Ints4
|
UTSW |
7 |
97,179,507 (GRCm39) |
missense |
probably benign |
0.00 |
R7418:Ints4
|
UTSW |
7 |
97,140,179 (GRCm39) |
missense |
probably benign |
0.03 |
R7423:Ints4
|
UTSW |
7 |
97,156,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R7462:Ints4
|
UTSW |
7 |
97,155,335 (GRCm39) |
missense |
probably benign |
0.11 |
R7658:Ints4
|
UTSW |
7 |
97,178,460 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7947:Ints4
|
UTSW |
7 |
97,148,792 (GRCm39) |
missense |
probably benign |
|
R8114:Ints4
|
UTSW |
7 |
97,165,732 (GRCm39) |
splice site |
probably null |
|
R8426:Ints4
|
UTSW |
7 |
97,150,239 (GRCm39) |
nonsense |
probably null |
|
R8765:Ints4
|
UTSW |
7 |
97,151,016 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8777:Ints4
|
UTSW |
7 |
97,134,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777-TAIL:Ints4
|
UTSW |
7 |
97,134,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Ints4
|
UTSW |
7 |
97,190,276 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9057:Ints4
|
UTSW |
7 |
97,158,987 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9315:Ints4
|
UTSW |
7 |
97,156,840 (GRCm39) |
intron |
probably benign |
|
|