Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
T |
C |
4: 53,072,924 (GRCm39) |
D1170G |
probably benign |
Het |
Ak7 |
A |
T |
12: 105,676,503 (GRCm39) |
T68S |
probably benign |
Het |
Arhgap12 |
A |
T |
18: 6,111,901 (GRCm39) |
N26K |
probably damaging |
Het |
B3galt1 |
A |
T |
2: 67,949,033 (GRCm39) |
E249D |
probably damaging |
Het |
Catsper4 |
T |
A |
4: 133,954,648 (GRCm39) |
M1L |
probably benign |
Het |
Cc2d2b |
T |
C |
19: 40,773,506 (GRCm39) |
V523A |
possibly damaging |
Het |
Ccn4 |
C |
T |
15: 66,791,047 (GRCm39) |
T283M |
probably benign |
Het |
Cyp11a1 |
T |
C |
9: 57,925,659 (GRCm39) |
F98S |
probably damaging |
Het |
Cyp2d26 |
T |
C |
15: 82,674,446 (GRCm39) |
S479G |
probably damaging |
Het |
Dclre1a |
T |
G |
19: 56,531,141 (GRCm39) |
Y735S |
probably damaging |
Het |
Dio2 |
C |
T |
12: 90,696,671 (GRCm39) |
G106R |
probably damaging |
Het |
Efcab12 |
T |
C |
6: 115,815,273 (GRCm39) |
|
probably benign |
Het |
Ehhadh |
C |
A |
16: 21,581,028 (GRCm39) |
V655L |
probably benign |
Het |
Ercc2 |
G |
A |
7: 19,127,615 (GRCm39) |
R379Q |
probably damaging |
Het |
Fabp4 |
A |
G |
3: 10,273,537 (GRCm39) |
V12A |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,223,980 (GRCm39) |
I590V |
probably benign |
Het |
Grm8 |
C |
A |
6: 27,981,281 (GRCm39) |
V210L |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,625,065 (GRCm39) |
D359G |
probably damaging |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,136,749 (GRCm39) |
Y1493N |
probably benign |
Het |
Lyst |
A |
G |
13: 13,808,663 (GRCm39) |
N111S |
probably benign |
Het |
Lyz2 |
G |
C |
10: 117,114,607 (GRCm39) |
I107M |
possibly damaging |
Het |
Mgat5 |
A |
T |
1: 127,248,371 (GRCm39) |
D91V |
possibly damaging |
Het |
Mical3 |
T |
A |
6: 120,935,504 (GRCm39) |
D1674V |
probably damaging |
Het |
Myom2 |
G |
A |
8: 15,167,741 (GRCm39) |
A1109T |
probably null |
Het |
Naa16 |
A |
G |
14: 79,596,911 (GRCm39) |
Y358H |
possibly damaging |
Het |
Nktr |
T |
A |
9: 121,571,758 (GRCm39) |
H226Q |
probably damaging |
Het |
Ocln |
T |
G |
13: 100,635,380 (GRCm39) |
K503T |
possibly damaging |
Het |
Olfm4 |
T |
C |
14: 80,258,754 (GRCm39) |
L301S |
probably damaging |
Het |
Or4f4b |
G |
A |
2: 111,314,071 (GRCm39) |
V127I |
possibly damaging |
Het |
Or6c74 |
T |
C |
10: 129,869,972 (GRCm39) |
L159P |
probably benign |
Het |
Paqr4 |
G |
A |
17: 23,956,697 (GRCm39) |
A222V |
probably benign |
Het |
Pcdhb13 |
A |
G |
18: 37,576,509 (GRCm39) |
T296A |
probably benign |
Het |
Phka2 |
G |
A |
X: 159,316,044 (GRCm39) |
V230I |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,474,707 (GRCm39) |
V309A |
probably damaging |
Het |
Ptger4 |
T |
C |
15: 5,264,196 (GRCm39) |
R462G |
probably benign |
Het |
Ptprc |
C |
T |
1: 138,006,183 (GRCm39) |
|
probably null |
Het |
Rabggta |
A |
C |
14: 55,959,299 (GRCm39) |
|
probably null |
Het |
Rnf25 |
A |
G |
1: 74,634,403 (GRCm39) |
S207P |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Rtf1 |
A |
G |
2: 119,541,559 (GRCm39) |
Q264R |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,816,129 (GRCm39) |
V619A |
probably benign |
Het |
Serpinb6d |
A |
G |
13: 33,855,181 (GRCm39) |
N285S |
probably benign |
Het |
Slamf6 |
A |
G |
1: 171,745,320 (GRCm39) |
M16V |
probably damaging |
Het |
Slc22a23 |
A |
G |
13: 34,528,140 (GRCm39) |
|
probably null |
Het |
Slc23a2 |
T |
C |
2: 131,933,173 (GRCm39) |
D95G |
probably damaging |
Het |
Smc3 |
T |
C |
19: 53,617,802 (GRCm39) |
Y600H |
probably damaging |
Het |
Tarbp1 |
G |
A |
8: 127,155,778 (GRCm39) |
T1320M |
possibly damaging |
Het |
Tjp1 |
A |
T |
7: 64,952,763 (GRCm39) |
F1444I |
possibly damaging |
Het |
Tstd3 |
A |
T |
4: 21,767,118 (GRCm39) |
M1K |
probably null |
Het |
Zbtb46 |
T |
C |
2: 181,065,217 (GRCm39) |
D311G |
probably damaging |
Het |
|
Other mutations in Tigd4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01791:Tigd4
|
APN |
3 |
84,502,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R0080:Tigd4
|
UTSW |
3 |
84,501,452 (GRCm39) |
missense |
probably benign |
0.19 |
R0320:Tigd4
|
UTSW |
3 |
84,502,481 (GRCm39) |
missense |
probably benign |
|
R0347:Tigd4
|
UTSW |
3 |
84,501,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Tigd4
|
UTSW |
3 |
84,502,394 (GRCm39) |
missense |
probably benign |
0.00 |
R1876:Tigd4
|
UTSW |
3 |
84,501,242 (GRCm39) |
nonsense |
probably null |
|
R2142:Tigd4
|
UTSW |
3 |
84,501,670 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2258:Tigd4
|
UTSW |
3 |
84,501,600 (GRCm39) |
missense |
probably benign |
0.00 |
R2519:Tigd4
|
UTSW |
3 |
84,501,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R2866:Tigd4
|
UTSW |
3 |
84,501,259 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2867:Tigd4
|
UTSW |
3 |
84,501,259 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2867:Tigd4
|
UTSW |
3 |
84,501,259 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3974:Tigd4
|
UTSW |
3 |
84,502,585 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4094:Tigd4
|
UTSW |
3 |
84,501,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Tigd4
|
UTSW |
3 |
84,502,460 (GRCm39) |
missense |
probably benign |
0.03 |
R5155:Tigd4
|
UTSW |
3 |
84,501,970 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5878:Tigd4
|
UTSW |
3 |
84,501,749 (GRCm39) |
missense |
probably benign |
0.09 |
R6174:Tigd4
|
UTSW |
3 |
84,502,574 (GRCm39) |
missense |
probably benign |
0.02 |
R7414:Tigd4
|
UTSW |
3 |
84,501,128 (GRCm39) |
missense |
probably benign |
0.37 |
R7445:Tigd4
|
UTSW |
3 |
84,502,471 (GRCm39) |
missense |
probably benign |
0.01 |
R7696:Tigd4
|
UTSW |
3 |
84,502,224 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7810:Tigd4
|
UTSW |
3 |
84,502,310 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8016:Tigd4
|
UTSW |
3 |
84,501,971 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8489:Tigd4
|
UTSW |
3 |
84,502,526 (GRCm39) |
missense |
probably benign |
|
R8745:Tigd4
|
UTSW |
3 |
84,501,874 (GRCm39) |
missense |
probably benign |
0.03 |
R8872:Tigd4
|
UTSW |
3 |
84,501,547 (GRCm39) |
missense |
probably benign |
|
X0023:Tigd4
|
UTSW |
3 |
84,501,164 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Tigd4
|
UTSW |
3 |
84,501,785 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tigd4
|
UTSW |
3 |
84,501,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|