Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy1 |
T |
A |
11: 7,096,532 (GRCm39) |
L640Q |
probably damaging |
Het |
Afap1l1 |
T |
C |
18: 61,891,721 (GRCm39) |
E32G |
probably damaging |
Het |
Atp1a1 |
T |
A |
3: 101,489,411 (GRCm39) |
M734L |
probably benign |
Het |
B4galt6 |
T |
C |
18: 20,822,296 (GRCm39) |
D294G |
probably damaging |
Het |
Baz1a |
T |
G |
12: 54,941,133 (GRCm39) |
D1539A |
probably damaging |
Het |
Bmper |
T |
A |
9: 23,208,520 (GRCm39) |
S141T |
probably benign |
Het |
Camkv |
T |
C |
9: 107,822,545 (GRCm39) |
V20A |
probably damaging |
Het |
Chst8 |
A |
G |
7: 34,375,279 (GRCm39) |
Y187H |
probably damaging |
Het |
Coro1c |
A |
G |
5: 113,983,443 (GRCm39) |
Y362H |
probably damaging |
Het |
Csmd3 |
C |
A |
15: 47,499,846 (GRCm39) |
G3008* |
probably null |
Het |
Dnah17 |
T |
C |
11: 118,008,029 (GRCm39) |
|
probably benign |
Het |
Dnajb1 |
C |
T |
8: 84,335,135 (GRCm39) |
R59C |
possibly damaging |
Het |
Dpf1 |
A |
G |
7: 29,003,533 (GRCm39) |
K10E |
probably benign |
Het |
Eif5 |
T |
C |
12: 111,509,989 (GRCm39) |
L311P |
probably damaging |
Het |
Eqtn |
A |
G |
4: 94,795,825 (GRCm39) |
F251S |
probably damaging |
Het |
Fancg |
A |
G |
4: 43,002,998 (GRCm39) |
S620P |
probably benign |
Het |
Farp1 |
T |
C |
14: 121,494,169 (GRCm39) |
V550A |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,194,767 (GRCm39) |
T1091A |
probably damaging |
Het |
Fbxo33 |
A |
G |
12: 59,266,246 (GRCm39) |
|
probably benign |
Het |
Fndc5 |
A |
T |
4: 129,035,887 (GRCm39) |
I175F |
probably damaging |
Het |
Gtf2ird2 |
G |
C |
5: 134,246,310 (GRCm39) |
R856P |
probably benign |
Het |
Hc |
A |
T |
2: 34,881,077 (GRCm39) |
F1481I |
probably damaging |
Het |
Helz2 |
T |
A |
2: 180,876,862 (GRCm39) |
T1211S |
probably benign |
Het |
Hmcn2 |
G |
A |
2: 31,299,023 (GRCm39) |
V2790M |
probably damaging |
Het |
Ighv1-82 |
T |
C |
12: 115,916,297 (GRCm39) |
Y71C |
probably damaging |
Het |
Itgam |
A |
G |
7: 127,711,560 (GRCm39) |
D725G |
probably damaging |
Het |
Kif9 |
T |
C |
9: 110,350,371 (GRCm39) |
V754A |
probably benign |
Het |
Larp4b |
C |
A |
13: 9,186,945 (GRCm39) |
T91K |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,299,190 (GRCm39) |
E1948G |
possibly damaging |
Het |
Mllt6 |
G |
A |
11: 97,560,326 (GRCm39) |
S210N |
possibly damaging |
Het |
Mrgprb13 |
A |
T |
7: 47,961,496 (GRCm39) |
|
noncoding transcript |
Het |
Nlrc4 |
A |
T |
17: 74,755,078 (GRCm39) |
L46* |
probably null |
Het |
Or13c7c |
A |
G |
4: 43,836,010 (GRCm39) |
I160T |
probably benign |
Het |
Or7g21 |
A |
T |
9: 19,032,373 (GRCm39) |
T38S |
probably damaging |
Het |
Or8d1b |
T |
C |
9: 38,887,151 (GRCm39) |
Y60H |
possibly damaging |
Het |
Orm1 |
A |
G |
4: 63,264,230 (GRCm39) |
|
probably null |
Het |
Parva |
A |
T |
7: 112,178,927 (GRCm39) |
H311L |
probably benign |
Het |
Pramel25 |
A |
G |
4: 143,521,493 (GRCm39) |
I370V |
probably benign |
Het |
Proca1 |
C |
A |
11: 78,096,092 (GRCm39) |
S154R |
probably damaging |
Het |
R3hdm2 |
T |
C |
10: 127,307,771 (GRCm39) |
V344A |
probably damaging |
Het |
Rabep1 |
A |
T |
11: 70,799,247 (GRCm39) |
K293N |
probably damaging |
Het |
Ranbp6 |
A |
G |
19: 29,789,083 (GRCm39) |
V423A |
probably damaging |
Het |
Rnf20 |
T |
A |
4: 49,652,639 (GRCm39) |
Y711N |
possibly damaging |
Het |
Sf3b1 |
A |
T |
1: 55,042,309 (GRCm39) |
M498K |
possibly damaging |
Het |
Sin3a |
T |
C |
9: 57,018,272 (GRCm39) |
M897T |
probably benign |
Het |
Sp140 |
T |
A |
1: 85,538,549 (GRCm39) |
D95E |
possibly damaging |
Het |
Srbd1 |
A |
C |
17: 86,308,964 (GRCm39) |
I738S |
possibly damaging |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Het |
Svep1 |
A |
G |
4: 58,072,991 (GRCm39) |
V2106A |
possibly damaging |
Het |
Tasor2 |
T |
C |
13: 3,638,496 (GRCm39) |
R412G |
probably benign |
Het |
Trpc7 |
A |
G |
13: 56,952,363 (GRCm39) |
Y548H |
probably damaging |
Het |
Vmn1r170 |
A |
T |
7: 23,306,054 (GRCm39) |
H152L |
possibly damaging |
Het |
Zfp184 |
A |
G |
13: 22,144,051 (GRCm39) |
I586V |
probably damaging |
Het |
Zfp454 |
T |
C |
11: 50,774,629 (GRCm39) |
T15A |
probably damaging |
Het |
|
Other mutations in Tex47 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Tex47
|
APN |
5 |
7,355,468 (GRCm39) |
nonsense |
probably null |
|
IGL00673:Tex47
|
APN |
5 |
7,355,211 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4495001:Tex47
|
UTSW |
5 |
7,355,011 (GRCm39) |
missense |
probably benign |
0.34 |
R0648:Tex47
|
UTSW |
5 |
7,355,215 (GRCm39) |
missense |
probably benign |
0.04 |
R1911:Tex47
|
UTSW |
5 |
7,355,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R2163:Tex47
|
UTSW |
5 |
7,355,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R3690:Tex47
|
UTSW |
5 |
7,354,777 (GRCm39) |
intron |
probably benign |
|
R3762:Tex47
|
UTSW |
5 |
7,355,529 (GRCm39) |
missense |
probably benign |
0.01 |
R4423:Tex47
|
UTSW |
5 |
7,355,364 (GRCm39) |
missense |
probably benign |
0.10 |
R4424:Tex47
|
UTSW |
5 |
7,355,364 (GRCm39) |
missense |
probably benign |
0.10 |
R5107:Tex47
|
UTSW |
5 |
7,354,842 (GRCm39) |
missense |
probably benign |
0.01 |
R5589:Tex47
|
UTSW |
5 |
7,354,834 (GRCm39) |
missense |
probably benign |
|
R6265:Tex47
|
UTSW |
5 |
7,355,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R6325:Tex47
|
UTSW |
5 |
7,354,935 (GRCm39) |
nonsense |
probably null |
|
R6580:Tex47
|
UTSW |
5 |
7,355,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8390:Tex47
|
UTSW |
5 |
7,355,301 (GRCm39) |
missense |
probably benign |
0.00 |
R8889:Tex47
|
UTSW |
5 |
7,355,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R8892:Tex47
|
UTSW |
5 |
7,355,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R9416:Tex47
|
UTSW |
5 |
7,355,194 (GRCm39) |
missense |
possibly damaging |
0.48 |
|