Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
C |
A |
5: 77,025,396 (GRCm39) |
C961F |
probably damaging |
Het |
Abca16 |
A |
C |
7: 120,032,608 (GRCm39) |
D209A |
probably damaging |
Het |
Adamts14 |
T |
C |
10: 61,036,151 (GRCm39) |
I1047V |
probably benign |
Het |
Ak1 |
A |
G |
2: 32,520,282 (GRCm39) |
K27E |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,011,809 (GRCm39) |
D837E |
probably benign |
Het |
Arfgef3 |
T |
C |
10: 18,473,104 (GRCm39) |
Y1653C |
probably damaging |
Het |
Atad2 |
T |
G |
15: 57,970,264 (GRCm39) |
I446L |
probably benign |
Het |
Atp8b3 |
T |
G |
10: 80,365,912 (GRCm39) |
T313P |
possibly damaging |
Het |
Btg4 |
T |
C |
9: 51,028,489 (GRCm39) |
L72S |
probably damaging |
Het |
Canx |
A |
G |
11: 50,195,186 (GRCm39) |
I294T |
probably damaging |
Het |
Casp1 |
G |
A |
9: 5,303,663 (GRCm39) |
E250K |
probably benign |
Het |
Chchd10 |
T |
A |
10: 75,772,166 (GRCm39) |
S46T |
probably benign |
Het |
Col12a1 |
G |
T |
9: 79,585,563 (GRCm39) |
Y1271* |
probably null |
Het |
Col3a1 |
G |
A |
1: 45,381,395 (GRCm39) |
|
probably null |
Het |
Ctc1 |
A |
T |
11: 68,922,390 (GRCm39) |
T872S |
probably benign |
Het |
Cx3cl1 |
T |
C |
8: 95,507,048 (GRCm39) |
F351S |
probably damaging |
Het |
Cyb5r4 |
T |
A |
9: 86,937,867 (GRCm39) |
H295Q |
probably damaging |
Het |
Cyp2j7 |
T |
C |
4: 96,105,656 (GRCm39) |
T285A |
probably benign |
Het |
Dip2a |
G |
A |
10: 76,153,925 (GRCm39) |
T135M |
probably damaging |
Het |
Eif1ad18 |
T |
G |
12: 88,050,810 (GRCm39) |
I115S |
probably damaging |
Het |
Fgf10 |
A |
G |
13: 118,925,695 (GRCm39) |
E158G |
probably damaging |
Het |
Ftcd |
G |
T |
10: 76,417,403 (GRCm39) |
A281S |
probably benign |
Het |
Gpat4 |
A |
T |
8: 23,669,486 (GRCm39) |
M333K |
possibly damaging |
Het |
Gpcpd1 |
A |
G |
2: 132,376,673 (GRCm39) |
L541P |
probably damaging |
Het |
Grk5 |
T |
C |
19: 61,071,663 (GRCm39) |
Y408H |
probably damaging |
Het |
Hcrtr2 |
A |
G |
9: 76,153,627 (GRCm39) |
|
probably null |
Het |
Hsd17b13 |
T |
A |
5: 104,116,633 (GRCm39) |
N127I |
probably damaging |
Het |
Hspa4 |
T |
G |
11: 53,174,983 (GRCm39) |
D158A |
probably benign |
Het |
Ice2 |
G |
A |
9: 69,322,857 (GRCm39) |
A451T |
possibly damaging |
Het |
Inpp5e |
A |
T |
2: 26,298,169 (GRCm39) |
I144K |
possibly damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lrrc49 |
T |
C |
9: 60,495,060 (GRCm39) |
I652V |
possibly damaging |
Het |
Man1a |
A |
T |
10: 53,795,268 (GRCm39) |
W571R |
probably damaging |
Het |
Mecom |
A |
G |
3: 30,047,807 (GRCm39) |
S32P |
probably damaging |
Het |
Mrpl40 |
A |
G |
16: 18,691,224 (GRCm39) |
I162T |
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Mtmr12 |
T |
C |
15: 12,257,716 (GRCm39) |
W265R |
probably damaging |
Het |
Mup21 |
C |
T |
4: 62,067,663 (GRCm39) |
V79I |
probably benign |
Het |
Myh11 |
G |
A |
16: 14,086,967 (GRCm39) |
|
probably benign |
Het |
Myom3 |
T |
A |
4: 135,506,711 (GRCm39) |
F495I |
probably benign |
Het |
Ncoa7 |
A |
T |
10: 30,574,122 (GRCm39) |
|
probably benign |
Het |
Nisch |
T |
C |
14: 30,895,594 (GRCm39) |
Y45C |
probably damaging |
Het |
Nkain2 |
T |
A |
10: 32,766,435 (GRCm39) |
|
probably benign |
Het |
Or1ak2 |
A |
T |
2: 36,827,775 (GRCm39) |
I215F |
possibly damaging |
Het |
Or4k1 |
A |
G |
14: 50,377,629 (GRCm39) |
S156P |
probably damaging |
Het |
Pdcl |
A |
C |
2: 37,245,708 (GRCm39) |
H98Q |
probably damaging |
Het |
Pink1 |
A |
G |
4: 138,043,013 (GRCm39) |
V427A |
probably damaging |
Het |
Plce1 |
T |
C |
19: 38,769,067 (GRCm39) |
S2242P |
probably damaging |
Het |
Plrg1 |
C |
A |
3: 82,976,375 (GRCm39) |
|
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,702,803 (GRCm39) |
F586S |
possibly damaging |
Het |
Pnpla7 |
G |
A |
2: 24,930,985 (GRCm39) |
V867M |
possibly damaging |
Het |
Ppfia3 |
T |
A |
7: 45,001,631 (GRCm39) |
D427V |
possibly damaging |
Het |
Ppp6r3 |
A |
T |
19: 3,521,971 (GRCm39) |
|
probably benign |
Het |
Pros1 |
A |
T |
16: 62,723,881 (GRCm39) |
S210C |
probably damaging |
Het |
Ptk2b |
A |
G |
14: 66,395,841 (GRCm39) |
S839P |
probably benign |
Het |
Ptpre |
T |
C |
7: 135,280,046 (GRCm39) |
V570A |
possibly damaging |
Het |
Rbm48 |
C |
T |
5: 3,645,259 (GRCm39) |
A142T |
probably damaging |
Het |
Safb2 |
T |
C |
17: 56,883,909 (GRCm39) |
|
probably null |
Het |
Scnn1a |
A |
G |
6: 125,315,801 (GRCm39) |
E384G |
probably benign |
Het |
Sec23ip |
A |
G |
7: 128,354,575 (GRCm39) |
Y277C |
probably benign |
Het |
Slc25a29 |
G |
A |
12: 108,793,637 (GRCm39) |
T42M |
probably damaging |
Het |
Slc6a4 |
A |
T |
11: 76,905,990 (GRCm39) |
T264S |
probably benign |
Het |
Srgap3 |
A |
G |
6: 112,752,527 (GRCm39) |
M319T |
probably damaging |
Het |
Strn4 |
T |
A |
7: 16,572,207 (GRCm39) |
I640N |
probably damaging |
Het |
Tacc2 |
A |
G |
7: 130,225,475 (GRCm39) |
D739G |
probably benign |
Het |
Tlr6 |
T |
A |
5: 65,112,763 (GRCm39) |
D48V |
probably damaging |
Het |
Tmem125 |
T |
C |
4: 118,399,101 (GRCm39) |
D110G |
probably damaging |
Het |
Tmem198 |
A |
G |
1: 75,461,567 (GRCm39) |
D341G |
probably damaging |
Het |
Tnfaip3 |
A |
G |
10: 18,880,682 (GRCm39) |
F462L |
possibly damaging |
Het |
Tnrc6a |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
7: 122,761,669 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
A |
1: 188,410,486 (GRCm39) |
I2378N |
possibly damaging |
Het |
Usp47 |
A |
G |
7: 111,654,127 (GRCm39) |
T108A |
probably damaging |
Het |
Vmn1r236 |
T |
A |
17: 21,506,900 (GRCm39) |
I6K |
probably benign |
Het |
Vmn2r65 |
A |
T |
7: 84,595,505 (GRCm39) |
V393D |
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 |
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 |
R6960:Tigd4
|
UTSW |
3 |
84,501,423 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|