Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
C |
T |
1: 183,765,702 (GRCm39) |
S119N |
probably benign |
Het |
4930503L19Rik |
T |
A |
18: 70,600,997 (GRCm39) |
|
probably null |
Het |
Adam18 |
T |
C |
8: 25,137,869 (GRCm39) |
T324A |
probably benign |
Het |
Adamts20 |
T |
A |
15: 94,184,252 (GRCm39) |
Q1517L |
probably benign |
Het |
AI429214 |
A |
G |
8: 37,461,473 (GRCm39) |
Q207R |
probably benign |
Het |
Arhgef7 |
A |
G |
8: 11,869,659 (GRCm39) |
T432A |
possibly damaging |
Het |
Atad2b |
A |
G |
12: 5,081,784 (GRCm39) |
N1231S |
probably benign |
Het |
Atp13a1 |
T |
C |
8: 70,254,794 (GRCm39) |
|
probably null |
Het |
Atp6v0a1 |
T |
A |
11: 100,946,317 (GRCm39) |
L770* |
probably null |
Het |
Atp8b3 |
T |
C |
10: 80,370,032 (GRCm39) |
N127S |
probably damaging |
Het |
B3gnt5 |
T |
A |
16: 19,588,760 (GRCm39) |
D326E |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,872,856 (GRCm39) |
S372T |
probably damaging |
Het |
Btbd9 |
T |
A |
17: 30,518,607 (GRCm39) |
D451V |
probably damaging |
Het |
Cd46 |
T |
C |
1: 194,724,300 (GRCm39) |
*366W |
probably null |
Het |
Cdcp3 |
T |
C |
7: 130,839,911 (GRCm39) |
L611P |
probably damaging |
Het |
Cdh18 |
T |
A |
15: 23,474,081 (GRCm39) |
D650E |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,185,767 (GRCm39) |
V248E |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,436,819 (GRCm39) |
S574P |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,128,412 (GRCm39) |
S858P |
probably damaging |
Het |
Cib4 |
T |
C |
5: 30,645,938 (GRCm39) |
D110G |
probably damaging |
Het |
Col9a2 |
T |
A |
4: 120,896,985 (GRCm39) |
|
probably null |
Het |
Csmd2 |
A |
T |
4: 128,389,981 (GRCm39) |
I2239F |
possibly damaging |
Het |
Csmd3 |
C |
A |
15: 47,522,485 (GRCm39) |
G2728V |
probably damaging |
Het |
Cxcl1 |
A |
T |
5: 91,039,626 (GRCm39) |
K85* |
probably null |
Het |
Cyp2d11 |
A |
G |
15: 82,273,730 (GRCm39) |
L416P |
possibly damaging |
Het |
Daam1 |
A |
C |
12: 71,962,558 (GRCm39) |
K90T |
unknown |
Het |
Depdc5 |
T |
A |
5: 33,144,310 (GRCm39) |
M1435K |
possibly damaging |
Het |
Dip2c |
G |
A |
13: 9,626,944 (GRCm39) |
A632T |
probably damaging |
Het |
Dld |
A |
T |
12: 31,384,053 (GRCm39) |
I350N |
probably damaging |
Het |
Dmtf1 |
T |
A |
5: 9,177,987 (GRCm39) |
I391F |
possibly damaging |
Het |
Dnah14 |
T |
C |
1: 181,579,710 (GRCm39) |
V3081A |
probably damaging |
Het |
Efemp1 |
A |
G |
11: 28,804,538 (GRCm39) |
E22G |
probably damaging |
Het |
Ephb6 |
A |
G |
6: 41,591,038 (GRCm39) |
D65G |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,807,436 (GRCm39) |
T1252S |
probably benign |
Het |
Gm4847 |
A |
G |
1: 166,457,824 (GRCm39) |
S510P |
probably benign |
Het |
Golga4 |
T |
C |
9: 118,366,341 (GRCm39) |
I365T |
probably damaging |
Het |
Gp2 |
A |
T |
7: 119,053,766 (GRCm39) |
L65Q |
probably damaging |
Het |
Ibtk |
T |
C |
9: 85,625,630 (GRCm39) |
Y40C |
probably damaging |
Het |
Ice1 |
C |
A |
13: 70,750,546 (GRCm39) |
V1847L |
probably benign |
Het |
Ift172 |
C |
T |
5: 31,422,699 (GRCm39) |
R917H |
probably benign |
Het |
Itgae |
C |
T |
11: 73,029,335 (GRCm39) |
Q1037* |
probably null |
Het |
Kbtbd7 |
A |
G |
14: 79,664,870 (GRCm39) |
E234G |
possibly damaging |
Het |
Khsrp |
T |
C |
17: 57,332,576 (GRCm39) |
T235A |
probably benign |
Het |
Klk13 |
T |
C |
7: 43,370,582 (GRCm39) |
|
probably null |
Het |
Lrfn5 |
G |
A |
12: 61,890,223 (GRCm39) |
G504D |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,369,793 (GRCm39) |
V91A |
possibly damaging |
Het |
Map6 |
G |
A |
7: 98,985,950 (GRCm39) |
G821D |
possibly damaging |
Het |
Mark1 |
A |
C |
1: 184,653,801 (GRCm39) |
V167G |
probably damaging |
Het |
Mrgprf |
T |
A |
7: 144,861,993 (GRCm39) |
L185Q |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,634,645 (GRCm39) |
V2422D |
probably damaging |
Het |
Myh13 |
T |
A |
11: 67,223,346 (GRCm39) |
I222N |
probably damaging |
Het |
Myh7b |
G |
A |
2: 155,462,347 (GRCm39) |
C350Y |
probably benign |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Olfm3 |
C |
A |
3: 114,895,635 (GRCm39) |
S172R |
probably benign |
Het |
Or13e8 |
A |
G |
4: 43,696,706 (GRCm39) |
S156P |
probably damaging |
Het |
Or1j14 |
A |
G |
2: 36,418,020 (GRCm39) |
I199V |
probably benign |
Het |
Or4c1 |
A |
T |
2: 89,133,528 (GRCm39) |
I136N |
probably damaging |
Het |
Or5d40 |
A |
T |
2: 88,015,322 (GRCm39) |
T34S |
probably benign |
Het |
Or8b48 |
T |
A |
9: 38,492,579 (GRCm39) |
V2D |
possibly damaging |
Het |
Pacs1 |
A |
T |
19: 5,193,857 (GRCm39) |
D557E |
probably damaging |
Het |
Pde1c |
A |
G |
6: 56,338,800 (GRCm39) |
F11L |
probably benign |
Het |
Phactr2 |
T |
C |
10: 13,122,883 (GRCm39) |
D343G |
possibly damaging |
Het |
Piezo2 |
T |
C |
18: 63,148,873 (GRCm39) |
Y2659C |
probably damaging |
Het |
Pkd2l2 |
A |
G |
18: 34,561,305 (GRCm39) |
T438A |
probably damaging |
Het |
Pld2 |
T |
C |
11: 70,447,907 (GRCm39) |
W857R |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 108,931,210 (GRCm39) |
V410A |
possibly damaging |
Het |
Pramel26 |
T |
C |
4: 143,538,428 (GRCm39) |
Y181C |
probably damaging |
Het |
Ptger2 |
A |
G |
14: 45,226,957 (GRCm39) |
Y179C |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rcan1 |
A |
T |
16: 92,190,408 (GRCm39) |
M177K |
probably benign |
Het |
Rilpl1 |
A |
G |
5: 124,639,951 (GRCm39) |
I122T |
possibly damaging |
Het |
Rilpl1 |
A |
G |
5: 124,639,934 (GRCm39) |
S156P |
probably benign |
Het |
Rims4 |
C |
T |
2: 163,705,849 (GRCm39) |
V262M |
possibly damaging |
Het |
Rpa1 |
C |
T |
11: 75,203,799 (GRCm39) |
|
probably null |
Het |
Saxo2 |
A |
G |
7: 82,284,078 (GRCm39) |
V260A |
probably benign |
Het |
Sel1l |
T |
C |
12: 91,791,634 (GRCm39) |
Y309C |
probably damaging |
Het |
Setd1b |
GCCCCCCC |
GCCCCCCCCCCCCC |
5: 123,298,766 (GRCm39) |
|
probably benign |
Het |
Slc33a1 |
A |
G |
3: 63,850,725 (GRCm39) |
F533S |
probably benign |
Het |
Slc38a4 |
C |
T |
15: 96,903,739 (GRCm39) |
V421M |
probably benign |
Het |
Snx14 |
A |
G |
9: 88,282,774 (GRCm39) |
|
probably null |
Het |
Spef2 |
A |
G |
15: 9,716,482 (GRCm39) |
F368S |
probably damaging |
Het |
Sri |
A |
T |
5: 8,109,381 (GRCm39) |
Q55L |
probably damaging |
Het |
Stkld1 |
A |
T |
2: 26,841,462 (GRCm39) |
Q469L |
probably benign |
Het |
Tm9sf1 |
T |
C |
14: 55,880,392 (GRCm39) |
T2A |
possibly damaging |
Het |
Tmco5 |
A |
G |
2: 116,713,699 (GRCm39) |
T122A |
probably benign |
Het |
Tmem59l |
G |
A |
8: 70,938,710 (GRCm39) |
P124S |
possibly damaging |
Het |
Tmem81 |
G |
A |
1: 132,435,662 (GRCm39) |
R156Q |
probably damaging |
Het |
Trpv6 |
T |
A |
6: 41,602,122 (GRCm39) |
T396S |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,228,276 (GRCm39) |
Y780* |
probably null |
Het |
Utp25 |
A |
T |
1: 192,797,011 (GRCm39) |
N573K |
probably damaging |
Het |
Vmn1r120 |
A |
G |
7: 20,786,941 (GRCm39) |
C257R |
probably damaging |
Het |
Vmn2r53 |
A |
G |
7: 12,335,319 (GRCm39) |
F114L |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,619,969 (GRCm39) |
E1549G |
probably damaging |
Het |
Zfp626 |
G |
A |
7: 27,517,907 (GRCm39) |
R296H |
probably damaging |
Het |
|
Other mutations in Stat4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Stat4
|
APN |
1 |
52,142,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00482:Stat4
|
APN |
1 |
52,113,856 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01395:Stat4
|
APN |
1 |
52,051,033 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01533:Stat4
|
APN |
1 |
52,137,578 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01943:Stat4
|
APN |
1 |
52,136,014 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02114:Stat4
|
APN |
1 |
52,142,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Stat4
|
APN |
1 |
52,053,029 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02601:Stat4
|
APN |
1 |
52,137,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Stat4
|
UTSW |
1 |
52,107,939 (GRCm39) |
missense |
probably benign |
0.01 |
R0243:Stat4
|
UTSW |
1 |
52,051,016 (GRCm39) |
missense |
probably benign |
0.22 |
R0329:Stat4
|
UTSW |
1 |
52,130,029 (GRCm39) |
intron |
probably benign |
|
R1144:Stat4
|
UTSW |
1 |
52,123,288 (GRCm39) |
splice site |
probably benign |
|
R1187:Stat4
|
UTSW |
1 |
52,115,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1331:Stat4
|
UTSW |
1 |
52,053,086 (GRCm39) |
missense |
probably benign |
0.20 |
R1401:Stat4
|
UTSW |
1 |
52,111,106 (GRCm39) |
splice site |
probably benign |
|
R1529:Stat4
|
UTSW |
1 |
52,050,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Stat4
|
UTSW |
1 |
52,146,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R2213:Stat4
|
UTSW |
1 |
52,053,014 (GRCm39) |
missense |
probably damaging |
0.98 |
R3003:Stat4
|
UTSW |
1 |
52,142,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Stat4
|
UTSW |
1 |
52,052,981 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3789:Stat4
|
UTSW |
1 |
52,050,955 (GRCm39) |
missense |
probably benign |
0.07 |
R3919:Stat4
|
UTSW |
1 |
52,135,981 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4320:Stat4
|
UTSW |
1 |
52,113,866 (GRCm39) |
missense |
probably benign |
|
R4373:Stat4
|
UTSW |
1 |
52,111,100 (GRCm39) |
critical splice donor site |
probably null |
|
R5024:Stat4
|
UTSW |
1 |
52,121,729 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5103:Stat4
|
UTSW |
1 |
52,111,054 (GRCm39) |
missense |
probably damaging |
0.97 |
R5206:Stat4
|
UTSW |
1 |
52,144,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R5944:Stat4
|
UTSW |
1 |
52,113,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R5961:Stat4
|
UTSW |
1 |
52,104,543 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6001:Stat4
|
UTSW |
1 |
52,136,026 (GRCm39) |
missense |
probably damaging |
0.96 |
R6161:Stat4
|
UTSW |
1 |
52,113,836 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6262:Stat4
|
UTSW |
1 |
52,141,360 (GRCm39) |
missense |
probably null |
1.00 |
R6701:Stat4
|
UTSW |
1 |
52,142,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R6767:Stat4
|
UTSW |
1 |
52,115,742 (GRCm39) |
missense |
probably benign |
0.00 |
R6989:Stat4
|
UTSW |
1 |
52,107,974 (GRCm39) |
missense |
probably benign |
0.09 |
R7507:Stat4
|
UTSW |
1 |
52,117,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Stat4
|
UTSW |
1 |
52,110,868 (GRCm39) |
splice site |
probably null |
|
R7546:Stat4
|
UTSW |
1 |
52,137,622 (GRCm39) |
missense |
probably damaging |
0.98 |
R7616:Stat4
|
UTSW |
1 |
52,053,037 (GRCm39) |
nonsense |
probably null |
|
R7751:Stat4
|
UTSW |
1 |
52,121,711 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8052:Stat4
|
UTSW |
1 |
52,118,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R8311:Stat4
|
UTSW |
1 |
52,142,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R8419:Stat4
|
UTSW |
1 |
52,137,637 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8679:Stat4
|
UTSW |
1 |
52,118,991 (GRCm39) |
missense |
probably null |
1.00 |
R8699:Stat4
|
UTSW |
1 |
52,111,096 (GRCm39) |
missense |
probably benign |
|
R8738:Stat4
|
UTSW |
1 |
52,115,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8921:Stat4
|
UTSW |
1 |
52,144,892 (GRCm39) |
missense |
probably benign |
0.39 |
R9013:Stat4
|
UTSW |
1 |
52,050,957 (GRCm39) |
missense |
probably benign |
0.00 |
R9237:Stat4
|
UTSW |
1 |
52,146,073 (GRCm39) |
missense |
probably benign |
|
R9729:Stat4
|
UTSW |
1 |
52,141,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9767:Stat4
|
UTSW |
1 |
52,141,653 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Stat4
|
UTSW |
1 |
52,137,644 (GRCm39) |
missense |
probably null |
1.00 |
Z1177:Stat4
|
UTSW |
1 |
52,123,258 (GRCm39) |
nonsense |
probably null |
|
|