Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
C |
7: 119,944,523 (GRCm39) |
V386A |
probably benign |
Het |
Adk |
G |
A |
14: 21,419,154 (GRCm39) |
A247T |
probably damaging |
Het |
Ankrd27 |
T |
A |
7: 35,291,231 (GRCm39) |
L9Q |
possibly damaging |
Het |
Atad2 |
A |
G |
15: 57,966,679 (GRCm39) |
L638P |
probably damaging |
Het |
Atf7ip |
T |
A |
6: 136,573,489 (GRCm39) |
D1009E |
probably benign |
Het |
Bend7 |
A |
T |
2: 4,749,133 (GRCm39) |
K83N |
probably damaging |
Het |
Bicc1 |
C |
T |
10: 70,781,146 (GRCm39) |
D562N |
possibly damaging |
Het |
Calcrl |
T |
A |
2: 84,181,549 (GRCm39) |
N200Y |
probably damaging |
Het |
Ccdc125 |
C |
A |
13: 100,814,453 (GRCm39) |
A11E |
possibly damaging |
Het |
Cd5l |
A |
G |
3: 87,273,258 (GRCm39) |
T76A |
probably benign |
Het |
Cdhr5 |
A |
T |
7: 140,853,644 (GRCm39) |
I2N |
probably damaging |
Het |
Cdk10 |
C |
T |
8: 123,957,353 (GRCm39) |
A230V |
probably damaging |
Het |
Cep128 |
T |
C |
12: 90,966,319 (GRCm39) |
|
probably benign |
Het |
Cep131 |
T |
C |
11: 119,966,982 (GRCm39) |
N186D |
probably damaging |
Het |
Cfhr4 |
T |
A |
1: 139,661,181 (GRCm39) |
D556V |
probably damaging |
Het |
Cog7 |
G |
T |
7: 121,570,604 (GRCm39) |
P168Q |
probably damaging |
Het |
Col28a1 |
T |
A |
6: 8,014,559 (GRCm39) |
M949L |
probably benign |
Het |
Coq8b |
T |
A |
7: 26,950,016 (GRCm39) |
M365K |
probably damaging |
Het |
Cpa1 |
A |
G |
6: 30,639,515 (GRCm39) |
E18G |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,411,542 (GRCm39) |
H2520R |
probably benign |
Het |
Cyp2c69 |
T |
C |
19: 39,866,038 (GRCm39) |
N185S |
probably benign |
Het |
Dpm1 |
G |
A |
2: 168,052,456 (GRCm39) |
T260I |
probably damaging |
Het |
Dtx3 |
A |
T |
10: 127,027,176 (GRCm39) |
|
probably null |
Het |
Eepd1 |
T |
C |
9: 25,500,756 (GRCm39) |
V401A |
possibly damaging |
Het |
Ehhadh |
A |
G |
16: 21,581,952 (GRCm39) |
S347P |
possibly damaging |
Het |
Elp3 |
A |
G |
14: 65,785,313 (GRCm39) |
|
probably null |
Het |
Enam |
C |
T |
5: 88,640,967 (GRCm39) |
Q210* |
probably null |
Het |
Epha1 |
C |
T |
6: 42,340,750 (GRCm39) |
R607H |
probably benign |
Het |
Erich6 |
A |
G |
3: 58,544,251 (GRCm39) |
I112T |
probably benign |
Het |
F830045P16Rik |
A |
G |
2: 129,302,470 (GRCm39) |
V374A |
possibly damaging |
Het |
Fam171a2 |
C |
A |
11: 102,329,511 (GRCm39) |
R416L |
possibly damaging |
Het |
Fbn1 |
T |
C |
2: 125,214,319 (GRCm39) |
N764S |
probably benign |
Het |
Fip1l1 |
C |
T |
5: 74,752,600 (GRCm39) |
T469I |
probably damaging |
Het |
Flad1 |
G |
A |
3: 89,313,217 (GRCm39) |
R342C |
probably damaging |
Het |
Fzd3 |
A |
G |
14: 65,477,269 (GRCm39) |
V95A |
probably benign |
Het |
Garem1 |
T |
C |
18: 21,280,950 (GRCm39) |
T469A |
probably benign |
Het |
Gm17093 |
A |
G |
14: 44,755,805 (GRCm39) |
Y24C |
unknown |
Het |
Grap2 |
T |
C |
15: 80,522,762 (GRCm39) |
V96A |
possibly damaging |
Het |
Greb1 |
A |
T |
12: 16,734,361 (GRCm39) |
|
probably null |
Het |
Grid2ip |
A |
T |
5: 143,374,530 (GRCm39) |
K913* |
probably null |
Het |
Gzmk |
T |
C |
13: 113,309,555 (GRCm39) |
D126G |
probably damaging |
Het |
Hibch |
A |
G |
1: 52,924,337 (GRCm39) |
I171V |
possibly damaging |
Het |
Hipk2 |
G |
T |
6: 38,795,339 (GRCm39) |
T310K |
possibly damaging |
Het |
Hk3 |
T |
C |
13: 55,154,231 (GRCm39) |
Y815C |
probably damaging |
Het |
Hps5 |
A |
T |
7: 46,437,778 (GRCm39) |
V99E |
probably damaging |
Het |
Hspg2 |
A |
G |
4: 137,268,977 (GRCm39) |
H2203R |
possibly damaging |
Het |
Il12rb2 |
A |
G |
6: 67,286,121 (GRCm39) |
V108A |
probably damaging |
Het |
Kdm2a |
A |
C |
19: 4,375,054 (GRCm39) |
S692R |
probably benign |
Het |
Kif13a |
T |
C |
13: 46,980,224 (GRCm39) |
K176R |
probably damaging |
Het |
Kif5b |
T |
C |
18: 6,216,869 (GRCm39) |
K485E |
probably damaging |
Het |
Ktn1 |
C |
T |
14: 47,963,413 (GRCm39) |
R1111* |
probably null |
Het |
Lrrc23 |
A |
T |
6: 124,755,152 (GRCm39) |
N128K |
probably benign |
Het |
Mad1l1 |
G |
A |
5: 140,286,017 (GRCm39) |
Q293* |
probably null |
Het |
Man1b1 |
A |
T |
2: 25,235,487 (GRCm39) |
I338F |
possibly damaging |
Het |
Marchf1 |
G |
T |
8: 66,921,015 (GRCm39) |
V225L |
probably damaging |
Het |
Matcap2 |
A |
T |
9: 22,335,673 (GRCm39) |
D97V |
probably damaging |
Het |
Mrpl3 |
A |
G |
9: 104,934,231 (GRCm39) |
D118G |
probably damaging |
Het |
Nomo1 |
A |
T |
7: 45,733,139 (GRCm39) |
Q1209L |
unknown |
Het |
Nrcam |
A |
G |
12: 44,620,802 (GRCm39) |
E949G |
probably damaging |
Het |
Olfm5 |
T |
G |
7: 103,803,572 (GRCm39) |
N297T |
probably damaging |
Het |
Or51h7 |
T |
A |
7: 102,591,453 (GRCm39) |
L110F |
probably damaging |
Het |
Pcdh7 |
A |
T |
5: 57,878,146 (GRCm39) |
N567I |
probably damaging |
Het |
Pkn1 |
A |
G |
8: 84,404,595 (GRCm39) |
L495P |
probably damaging |
Het |
Pkp1 |
T |
C |
1: 135,810,326 (GRCm39) |
S415G |
probably damaging |
Het |
Pou2f1 |
T |
A |
1: 165,744,492 (GRCm39) |
Q53L |
probably null |
Het |
Pramel26 |
G |
A |
4: 143,537,375 (GRCm39) |
Q319* |
probably null |
Het |
Prkce |
A |
G |
17: 86,937,511 (GRCm39) |
K648R |
probably benign |
Het |
Ptprh |
G |
A |
7: 4,576,429 (GRCm39) |
T277I |
possibly damaging |
Het |
Rpl31 |
C |
T |
1: 39,410,048 (GRCm39) |
R83C |
probably benign |
Het |
Rpusd3 |
G |
A |
6: 113,393,837 (GRCm39) |
Q194* |
probably null |
Het |
Sgsm1 |
T |
A |
5: 113,430,492 (GRCm39) |
N298Y |
probably damaging |
Het |
She |
G |
A |
3: 89,758,946 (GRCm39) |
G355D |
probably benign |
Het |
Shld2 |
A |
G |
14: 33,990,582 (GRCm39) |
V108A |
probably benign |
Het |
Snx11 |
C |
T |
11: 96,665,284 (GRCm39) |
E9K |
possibly damaging |
Het |
Soat1 |
C |
A |
1: 156,260,507 (GRCm39) |
A444S |
probably benign |
Het |
Sox6 |
T |
C |
7: 115,085,897 (GRCm39) |
Y690C |
probably damaging |
Het |
Spata13 |
T |
A |
14: 60,970,628 (GRCm39) |
F10I |
probably benign |
Het |
St18 |
C |
A |
1: 6,873,129 (GRCm39) |
T288K |
probably benign |
Het |
Tifa |
C |
T |
3: 127,590,235 (GRCm39) |
S2F |
probably damaging |
Het |
Tmem232 |
A |
T |
17: 65,737,883 (GRCm39) |
S392R |
probably benign |
Het |
Tmtc3 |
T |
C |
10: 100,302,082 (GRCm39) |
N289S |
probably damaging |
Het |
Tpo |
A |
G |
12: 30,142,633 (GRCm39) |
F697S |
probably damaging |
Het |
Trp53 |
A |
G |
11: 69,478,456 (GRCm39) |
T122A |
probably damaging |
Het |
Trps1 |
A |
C |
15: 50,690,712 (GRCm39) |
I10S |
probably benign |
Het |
Tubgcp5 |
C |
T |
7: 55,443,933 (GRCm39) |
|
probably benign |
Het |
Unc13c |
T |
G |
9: 73,839,354 (GRCm39) |
Y499S |
possibly damaging |
Het |
Unc45a |
C |
A |
7: 79,982,783 (GRCm39) |
D381Y |
probably damaging |
Het |
Upf1 |
G |
C |
8: 70,792,018 (GRCm39) |
H402Q |
probably benign |
Het |
Uroc1 |
A |
T |
6: 90,326,174 (GRCm39) |
I510F |
possibly damaging |
Het |
Usp15 |
A |
G |
10: 122,963,662 (GRCm39) |
F589L |
probably damaging |
Het |
Vmn2r76 |
T |
C |
7: 85,874,733 (GRCm39) |
Y748C |
probably damaging |
Het |
Wwp1 |
T |
C |
4: 19,662,143 (GRCm39) |
N151D |
probably benign |
Het |
Zbtb40 |
A |
T |
4: 136,728,527 (GRCm39) |
S439T |
probably benign |
Het |
Zbtb6 |
A |
T |
2: 37,318,728 (GRCm39) |
L400* |
probably null |
Het |
Zfp125 |
C |
T |
12: 20,949,961 (GRCm39) |
|
noncoding transcript |
Het |
Zmynd8 |
A |
C |
2: 165,681,954 (GRCm39) |
Y183* |
probably null |
Het |
Zpld2 |
A |
G |
4: 133,920,410 (GRCm39) |
V585A |
probably benign |
Het |
|
Other mutations in Il6st |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00515:Il6st
|
APN |
13 |
112,617,967 (GRCm39) |
splice site |
probably null |
|
IGL00571:Il6st
|
APN |
13 |
112,624,394 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01151:Il6st
|
APN |
13 |
112,630,185 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01336:Il6st
|
APN |
13 |
112,616,773 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01501:Il6st
|
APN |
13 |
112,616,593 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01512:Il6st
|
APN |
13 |
112,640,900 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01657:Il6st
|
APN |
13 |
112,618,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01863:Il6st
|
APN |
13 |
112,640,744 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01916:Il6st
|
APN |
13 |
112,616,606 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01978:Il6st
|
APN |
13 |
112,633,891 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02089:Il6st
|
APN |
13 |
112,631,774 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02752:Il6st
|
APN |
13 |
112,616,729 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02988:Il6st
|
UTSW |
13 |
112,635,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Il6st
|
UTSW |
13 |
112,637,682 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0550:Il6st
|
UTSW |
13 |
112,611,648 (GRCm39) |
splice site |
probably null |
|
R0606:Il6st
|
UTSW |
13 |
112,640,806 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1126:Il6st
|
UTSW |
13 |
112,640,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Il6st
|
UTSW |
13 |
112,617,998 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1581:Il6st
|
UTSW |
13 |
112,618,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R1632:Il6st
|
UTSW |
13 |
112,640,866 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1881:Il6st
|
UTSW |
13 |
112,640,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Il6st
|
UTSW |
13 |
112,635,423 (GRCm39) |
missense |
probably null |
0.94 |
R2043:Il6st
|
UTSW |
13 |
112,616,753 (GRCm39) |
missense |
probably benign |
0.00 |
R2128:Il6st
|
UTSW |
13 |
112,640,709 (GRCm39) |
missense |
probably benign |
0.01 |
R2137:Il6st
|
UTSW |
13 |
112,639,392 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3433:Il6st
|
UTSW |
13 |
112,640,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R3696:Il6st
|
UTSW |
13 |
112,640,916 (GRCm39) |
missense |
probably benign |
0.13 |
R3697:Il6st
|
UTSW |
13 |
112,640,916 (GRCm39) |
missense |
probably benign |
0.13 |
R3698:Il6st
|
UTSW |
13 |
112,640,916 (GRCm39) |
missense |
probably benign |
0.13 |
R4172:Il6st
|
UTSW |
13 |
112,631,861 (GRCm39) |
missense |
probably benign |
0.25 |
R4543:Il6st
|
UTSW |
13 |
112,617,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R4641:Il6st
|
UTSW |
13 |
112,625,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Il6st
|
UTSW |
13 |
112,637,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4922:Il6st
|
UTSW |
13 |
112,639,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R5088:Il6st
|
UTSW |
13 |
112,627,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R5104:Il6st
|
UTSW |
13 |
112,625,182 (GRCm39) |
missense |
probably benign |
0.02 |
R5853:Il6st
|
UTSW |
13 |
112,618,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6602:Il6st
|
UTSW |
13 |
112,640,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7082:Il6st
|
UTSW |
13 |
112,640,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R7101:Il6st
|
UTSW |
13 |
112,631,907 (GRCm39) |
critical splice donor site |
probably null |
|
R7192:Il6st
|
UTSW |
13 |
112,631,741 (GRCm39) |
missense |
probably benign |
0.00 |
R7273:Il6st
|
UTSW |
13 |
112,631,832 (GRCm39) |
missense |
probably benign |
0.37 |
R7330:Il6st
|
UTSW |
13 |
112,630,185 (GRCm39) |
missense |
probably benign |
0.00 |
R7427:Il6st
|
UTSW |
13 |
112,625,094 (GRCm39) |
missense |
probably benign |
0.01 |
R7770:Il6st
|
UTSW |
13 |
112,639,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R8086:Il6st
|
UTSW |
13 |
112,631,094 (GRCm39) |
splice site |
probably null |
|
R8307:Il6st
|
UTSW |
13 |
112,624,281 (GRCm39) |
missense |
probably benign |
0.16 |
R8831:Il6st
|
UTSW |
13 |
112,640,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R9041:Il6st
|
UTSW |
13 |
112,611,631 (GRCm39) |
missense |
probably benign |
0.00 |
R9189:Il6st
|
UTSW |
13 |
112,635,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R9316:Il6st
|
UTSW |
13 |
112,639,349 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9409:Il6st
|
UTSW |
13 |
112,640,872 (GRCm39) |
missense |
probably benign |
0.00 |
R9763:Il6st
|
UTSW |
13 |
112,627,051 (GRCm39) |
missense |
probably damaging |
1.00 |
U24488:Il6st
|
UTSW |
13 |
112,631,168 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Il6st
|
UTSW |
13 |
112,630,152 (GRCm39) |
missense |
probably benign |
0.01 |
|