Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
C |
7: 120,032,832 (GRCm39) |
|
probably benign |
Het |
Ace2 |
A |
T |
X: 162,939,524 (GRCm39) |
M123L |
possibly damaging |
Het |
Acvr1c |
A |
T |
2: 58,173,517 (GRCm39) |
N248K |
probably damaging |
Het |
Adam24 |
A |
T |
8: 41,134,400 (GRCm39) |
R623* |
probably null |
Het |
Agbl2 |
T |
A |
2: 90,641,626 (GRCm39) |
L752Q |
probably damaging |
Het |
Ankrd26 |
A |
T |
6: 118,488,654 (GRCm39) |
F1335Y |
probably damaging |
Het |
Ankrd34a |
A |
G |
3: 96,505,992 (GRCm39) |
S399G |
probably benign |
Het |
Aoc1l3 |
A |
T |
6: 48,967,007 (GRCm39) |
K652* |
probably null |
Het |
Ap3d1 |
G |
A |
10: 80,545,607 (GRCm39) |
P1041S |
probably benign |
Het |
Arid3b |
A |
T |
9: 57,703,431 (GRCm39) |
M466K |
possibly damaging |
Het |
Arsj |
T |
C |
3: 126,231,995 (GRCm39) |
I247T |
probably damaging |
Het |
AU016765 |
G |
A |
17: 64,826,873 (GRCm39) |
|
noncoding transcript |
Het |
Azin2 |
C |
T |
4: 128,844,577 (GRCm39) |
|
probably null |
Het |
Bcat2 |
T |
C |
7: 45,237,792 (GRCm39) |
Y313H |
possibly damaging |
Het |
Cables2 |
A |
G |
2: 179,901,873 (GRCm39) |
V465A |
probably damaging |
Het |
Ccdc60 |
G |
A |
5: 116,264,224 (GRCm39) |
H517Y |
probably damaging |
Het |
Cd55b |
A |
T |
1: 130,345,843 (GRCm39) |
|
probably null |
Het |
Cdc40 |
G |
A |
10: 40,759,067 (GRCm39) |
|
probably benign |
Het |
Cdh20 |
G |
A |
1: 109,976,754 (GRCm39) |
V140I |
probably benign |
Het |
Cdhr18 |
A |
T |
14: 13,828,582 (GRCm38) |
M726K |
probably null |
Het |
Cfi |
T |
C |
3: 129,652,477 (GRCm39) |
|
probably benign |
Het |
Chit1 |
G |
A |
1: 134,073,156 (GRCm39) |
|
probably null |
Het |
Chn1 |
A |
G |
2: 73,455,245 (GRCm39) |
C39R |
probably damaging |
Het |
Ciao1 |
A |
G |
2: 127,088,380 (GRCm39) |
S148P |
possibly damaging |
Het |
Clmn |
G |
A |
12: 104,756,361 (GRCm39) |
T163I |
probably damaging |
Het |
Cngb1 |
C |
A |
8: 96,026,320 (GRCm39) |
G154W |
probably damaging |
Het |
Col19a1 |
A |
T |
1: 24,303,831 (GRCm39) |
C1117* |
probably null |
Het |
Cplane1 |
T |
A |
15: 8,263,336 (GRCm39) |
S2496R |
probably damaging |
Het |
Cyp2d10 |
T |
A |
15: 82,289,495 (GRCm39) |
I206F |
probably benign |
Het |
Ddrgk1 |
G |
T |
2: 130,505,480 (GRCm39) |
|
probably benign |
Het |
Ddx18 |
A |
T |
1: 121,482,953 (GRCm39) |
V611D |
probably damaging |
Het |
Dnah8 |
A |
T |
17: 30,950,181 (GRCm39) |
H2000L |
probably damaging |
Het |
Duox1 |
T |
C |
2: 122,156,465 (GRCm39) |
V464A |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,139,159 (GRCm39) |
|
probably null |
Het |
Eif4enif1 |
A |
G |
11: 3,193,279 (GRCm39) |
H857R |
probably damaging |
Het |
Elmo2 |
A |
G |
2: 165,133,970 (GRCm39) |
|
probably benign |
Het |
Fam171b |
CCAGCAGCAGCAGCAGCAGCAGC |
CCAGCAGCAGCAGCAGCAGC |
2: 83,643,218 (GRCm39) |
|
probably benign |
Het |
Glrx |
A |
G |
13: 75,988,256 (GRCm39) |
I57V |
probably benign |
Het |
Golm1 |
A |
T |
13: 59,790,051 (GRCm39) |
|
probably benign |
Het |
Grm3 |
G |
A |
5: 9,561,682 (GRCm39) |
R723W |
probably damaging |
Het |
Gsta3 |
G |
A |
1: 21,327,601 (GRCm39) |
R45Q |
probably benign |
Het |
Gtf3c3 |
A |
C |
1: 54,468,117 (GRCm39) |
|
probably benign |
Het |
Hk3 |
C |
T |
13: 55,159,204 (GRCm39) |
V451I |
probably damaging |
Het |
Hoxa10 |
C |
A |
6: 52,211,350 (GRCm39) |
G189C |
possibly damaging |
Het |
Hs3st3b1 |
T |
C |
11: 63,780,569 (GRCm39) |
D186G |
probably benign |
Het |
Hscb |
G |
T |
5: 110,983,926 (GRCm39) |
H63N |
probably benign |
Het |
Itpr3 |
A |
G |
17: 27,330,191 (GRCm39) |
E1603G |
probably damaging |
Het |
Ivl |
T |
A |
3: 92,480,056 (GRCm39) |
H3L |
probably benign |
Het |
Klhl26 |
C |
A |
8: 70,904,911 (GRCm39) |
R252L |
probably damaging |
Het |
Krt31 |
T |
A |
11: 99,939,069 (GRCm39) |
T251S |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,832,714 (GRCm39) |
N1646S |
probably benign |
Het |
Lhx3 |
T |
C |
2: 26,093,974 (GRCm39) |
D83G |
probably benign |
Het |
Lss |
C |
A |
10: 76,381,296 (GRCm39) |
N427K |
possibly damaging |
Het |
Mettl24 |
G |
A |
10: 40,613,722 (GRCm39) |
A154T |
probably benign |
Het |
Mgat4a |
A |
T |
1: 37,575,118 (GRCm39) |
|
probably null |
Het |
Moxd2 |
C |
T |
6: 40,860,466 (GRCm39) |
R326Q |
probably damaging |
Het |
Mpdz |
G |
A |
4: 81,279,680 (GRCm39) |
A669V |
probably benign |
Het |
Msra |
G |
A |
14: 64,522,505 (GRCm39) |
|
probably benign |
Het |
Muc13 |
A |
T |
16: 33,628,281 (GRCm39) |
T344S |
probably benign |
Het |
Myo3b |
T |
C |
2: 70,088,419 (GRCm39) |
I866T |
probably benign |
Het |
Nbea |
T |
C |
3: 55,860,521 (GRCm39) |
S1852G |
possibly damaging |
Het |
Ncf2 |
A |
G |
1: 152,709,815 (GRCm39) |
|
probably benign |
Het |
Nfyc |
C |
A |
4: 120,630,861 (GRCm39) |
|
probably benign |
Het |
Nop2 |
T |
C |
6: 125,111,597 (GRCm39) |
V110A |
probably benign |
Het |
Nrg2 |
C |
A |
18: 36,329,897 (GRCm39) |
|
probably benign |
Het |
Nrl |
A |
G |
14: 55,759,892 (GRCm39) |
Y12H |
probably damaging |
Het |
Nrxn3 |
T |
C |
12: 89,227,151 (GRCm39) |
V635A |
probably damaging |
Het |
Or4d11 |
A |
C |
19: 12,013,275 (GRCm39) |
V277G |
probably benign |
Het |
Or6b2b |
T |
A |
1: 92,419,457 (GRCm39) |
T7S |
probably benign |
Het |
Or8k41 |
T |
A |
2: 86,313,703 (GRCm39) |
K128* |
probably null |
Het |
Or9g8 |
T |
A |
2: 85,607,515 (GRCm39) |
S196T |
probably benign |
Het |
Papolg |
A |
T |
11: 23,817,279 (GRCm39) |
N639K |
probably benign |
Het |
Paqr4 |
T |
C |
17: 23,956,638 (GRCm39) |
I242V |
probably damaging |
Het |
Pramel6 |
A |
T |
2: 87,339,076 (GRCm39) |
K92M |
probably damaging |
Het |
Prg4 |
T |
C |
1: 150,331,774 (GRCm39) |
T300A |
possibly damaging |
Het |
Ptprb |
A |
T |
10: 116,155,515 (GRCm39) |
|
probably benign |
Het |
Rab28 |
A |
T |
5: 41,783,133 (GRCm39) |
S216T |
probably benign |
Het |
Rrp1b |
A |
T |
17: 32,275,819 (GRCm39) |
R455S |
possibly damaging |
Het |
Sash1 |
A |
T |
10: 8,605,696 (GRCm39) |
M898K |
probably benign |
Het |
Scn8a |
C |
T |
15: 100,868,085 (GRCm39) |
T310I |
probably benign |
Het |
Secisbp2l |
C |
A |
2: 125,582,259 (GRCm39) |
D1066Y |
probably damaging |
Het |
Sipa1l2 |
A |
G |
8: 126,206,887 (GRCm39) |
|
probably benign |
Het |
Slc12a1 |
A |
G |
2: 125,036,113 (GRCm39) |
T662A |
probably benign |
Het |
Slc12a4 |
T |
C |
8: 106,672,669 (GRCm39) |
I749V |
probably benign |
Het |
Slc22a27 |
A |
G |
19: 7,887,092 (GRCm39) |
S266P |
probably damaging |
Het |
Slc25a14 |
G |
A |
X: 47,740,840 (GRCm39) |
V210I |
probably benign |
Het |
Slit1 |
T |
A |
19: 41,619,215 (GRCm39) |
N762I |
probably damaging |
Het |
Spata31d1b |
C |
A |
13: 59,865,835 (GRCm39) |
D994E |
possibly damaging |
Het |
Sphk1 |
A |
G |
11: 116,426,676 (GRCm39) |
I204V |
probably benign |
Het |
Srsf6 |
C |
T |
2: 162,776,403 (GRCm39) |
|
probably benign |
Het |
Tet2 |
T |
C |
3: 133,194,399 (GRCm39) |
T12A |
possibly damaging |
Het |
Tgfbi |
A |
T |
13: 56,762,127 (GRCm39) |
Q70L |
possibly damaging |
Het |
Tnrc6c |
A |
G |
11: 117,646,849 (GRCm39) |
D1450G |
possibly damaging |
Het |
Tra2b |
A |
G |
16: 22,073,795 (GRCm39) |
|
probably benign |
Het |
Trit1 |
T |
C |
4: 122,948,033 (GRCm39) |
I451T |
probably benign |
Het |
Trnau1ap |
A |
G |
4: 132,049,114 (GRCm39) |
Y30H |
probably damaging |
Het |
Ttc34 |
G |
A |
4: 154,950,139 (GRCm39) |
A1031T |
possibly damaging |
Het |
Ubiad1 |
A |
G |
4: 148,528,468 (GRCm39) |
L147P |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,683,758 (GRCm39) |
D4979G |
probably null |
Het |
Usp50 |
C |
T |
2: 126,619,943 (GRCm39) |
R123Q |
probably benign |
Het |
Vmn2r117 |
A |
T |
17: 23,696,454 (GRCm39) |
Y318N |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,228,047 (GRCm39) |
T304I |
probably null |
Het |
Wipf2 |
C |
T |
11: 98,783,236 (GRCm39) |
R221* |
probably null |
Het |
Ythdf3 |
A |
G |
3: 16,259,256 (GRCm39) |
N468D |
possibly damaging |
Het |
Zbtb17 |
T |
C |
4: 141,192,859 (GRCm39) |
I486T |
possibly damaging |
Het |
Zfp3 |
T |
C |
11: 70,662,202 (GRCm39) |
S54P |
probably benign |
Het |
Zscan10 |
A |
T |
17: 23,828,826 (GRCm39) |
H379L |
probably damaging |
Het |
|
Other mutations in Tlr9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00864:Tlr9
|
APN |
9 |
106,102,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01764:Tlr9
|
APN |
9 |
106,103,004 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02077:Tlr9
|
APN |
9 |
106,102,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02232:Tlr9
|
APN |
9 |
106,102,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Tlr9
|
APN |
9 |
106,101,929 (GRCm39) |
nonsense |
probably null |
|
Asura
|
UTSW |
9 |
106,101,846 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg1
|
UTSW |
9 |
106,102,206 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg11
|
UTSW |
9 |
106,101,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg2
|
UTSW |
9 |
106,103,664 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg3
|
UTSW |
9 |
106,101,351 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg5
|
UTSW |
9 |
106,101,888 (GRCm39) |
missense |
probably damaging |
1.00 |
Cpg6
|
UTSW |
9 |
106,103,792 (GRCm39) |
missense |
probably damaging |
1.00 |
cpg7
|
UTSW |
9 |
106,102,548 (GRCm39) |
missense |
probably benign |
0.00 |
Meager
|
UTSW |
9 |
106,101,338 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4498001:Tlr9
|
UTSW |
9 |
106,100,721 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Tlr9
|
UTSW |
9 |
106,102,164 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0058:Tlr9
|
UTSW |
9 |
106,102,164 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0071:Tlr9
|
UTSW |
9 |
106,100,777 (GRCm39) |
missense |
probably benign |
|
R0071:Tlr9
|
UTSW |
9 |
106,100,777 (GRCm39) |
missense |
probably benign |
|
R0126:Tlr9
|
UTSW |
9 |
106,102,881 (GRCm39) |
missense |
probably benign |
0.01 |
R0165:Tlr9
|
UTSW |
9 |
106,103,286 (GRCm39) |
missense |
probably benign |
0.10 |
R0534:Tlr9
|
UTSW |
9 |
106,102,086 (GRCm39) |
missense |
probably benign |
0.01 |
R0585:Tlr9
|
UTSW |
9 |
106,102,275 (GRCm39) |
missense |
probably benign |
0.01 |
R1527:Tlr9
|
UTSW |
9 |
106,100,949 (GRCm39) |
missense |
probably benign |
0.09 |
R1712:Tlr9
|
UTSW |
9 |
106,101,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1817:Tlr9
|
UTSW |
9 |
106,102,142 (GRCm39) |
missense |
probably benign |
|
R2117:Tlr9
|
UTSW |
9 |
106,102,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Tlr9
|
UTSW |
9 |
106,101,140 (GRCm39) |
missense |
probably benign |
0.05 |
R3700:Tlr9
|
UTSW |
9 |
106,101,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Tlr9
|
UTSW |
9 |
106,101,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R4608:Tlr9
|
UTSW |
9 |
106,102,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R4612:Tlr9
|
UTSW |
9 |
106,101,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Tlr9
|
UTSW |
9 |
106,101,876 (GRCm39) |
missense |
probably benign |
|
R5173:Tlr9
|
UTSW |
9 |
106,103,151 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5472:Tlr9
|
UTSW |
9 |
106,101,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5572:Tlr9
|
UTSW |
9 |
106,102,836 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5618:Tlr9
|
UTSW |
9 |
106,101,938 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5820:Tlr9
|
UTSW |
9 |
106,099,906 (GRCm39) |
critical splice donor site |
probably null |
|
R6393:Tlr9
|
UTSW |
9 |
106,102,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Tlr9
|
UTSW |
9 |
106,102,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Tlr9
|
UTSW |
9 |
106,101,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R7385:Tlr9
|
UTSW |
9 |
106,102,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Tlr9
|
UTSW |
9 |
106,101,729 (GRCm39) |
missense |
probably benign |
0.00 |
R7561:Tlr9
|
UTSW |
9 |
106,103,148 (GRCm39) |
missense |
probably benign |
0.00 |
R8889:Tlr9
|
UTSW |
9 |
106,099,834 (GRCm39) |
start gained |
probably benign |
|
R8892:Tlr9
|
UTSW |
9 |
106,099,834 (GRCm39) |
start gained |
probably benign |
|
R8926:Tlr9
|
UTSW |
9 |
106,103,213 (GRCm39) |
missense |
probably benign |
|
R9221:Tlr9
|
UTSW |
9 |
106,101,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R9228:Tlr9
|
UTSW |
9 |
106,102,752 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9581:Tlr9
|
UTSW |
9 |
106,101,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Tlr9
|
UTSW |
9 |
106,100,721 (GRCm39) |
missense |
probably benign |
0.00 |
R9697:Tlr9
|
UTSW |
9 |
106,100,723 (GRCm39) |
nonsense |
probably null |
|
R9788:Tlr9
|
UTSW |
9 |
106,101,006 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tlr9
|
UTSW |
9 |
106,100,862 (GRCm39) |
missense |
probably benign |
0.03 |
|