Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts6 |
T |
A |
13: 104,581,440 (GRCm39) |
C852S |
probably damaging |
Het |
Arf1 |
A |
G |
11: 59,104,186 (GRCm39) |
V43A |
probably damaging |
Het |
Arhgef26 |
T |
A |
3: 62,340,000 (GRCm39) |
M674K |
probably benign |
Het |
Asb1 |
A |
C |
1: 91,482,531 (GRCm39) |
K314N |
probably damaging |
Het |
Aste1 |
T |
C |
9: 105,274,294 (GRCm39) |
F178S |
probably damaging |
Het |
Avl9 |
T |
C |
6: 56,720,441 (GRCm39) |
F493S |
probably damaging |
Het |
BC024139 |
T |
C |
15: 76,009,422 (GRCm39) |
Y220C |
probably benign |
Het |
Ccdc60 |
T |
C |
5: 116,328,185 (GRCm39) |
E93G |
probably damaging |
Het |
Cep112 |
A |
G |
11: 108,377,779 (GRCm39) |
H295R |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,255,628 (GRCm39) |
K87E |
possibly damaging |
Het |
Chordc1 |
G |
T |
9: 18,223,789 (GRCm39) |
|
probably null |
Het |
Ciita |
A |
T |
16: 10,319,742 (GRCm39) |
D55V |
probably damaging |
Het |
Cklf |
T |
C |
8: 104,988,125 (GRCm39) |
V86A |
probably damaging |
Het |
Clock |
T |
A |
5: 76,393,376 (GRCm39) |
N189I |
possibly damaging |
Het |
Dnah14 |
T |
C |
1: 181,444,205 (GRCm39) |
|
probably null |
Het |
Dpep3 |
C |
G |
8: 106,700,245 (GRCm39) |
C487S |
probably benign |
Het |
Dtwd2 |
A |
G |
18: 49,856,799 (GRCm39) |
F163L |
probably benign |
Het |
Eln |
C |
T |
5: 134,735,456 (GRCm39) |
V776M |
unknown |
Het |
Fanci |
T |
A |
7: 79,055,971 (GRCm39) |
M201K |
possibly damaging |
Het |
Frmd4a |
A |
G |
2: 4,608,372 (GRCm39) |
T747A |
probably damaging |
Het |
Galnt9 |
T |
A |
5: 110,767,108 (GRCm39) |
C526* |
probably null |
Het |
Garnl3 |
T |
C |
2: 32,895,080 (GRCm39) |
E663G |
probably damaging |
Het |
Gdpd5 |
T |
C |
7: 99,100,945 (GRCm39) |
S247P |
probably damaging |
Het |
Gm4846 |
C |
T |
1: 166,322,142 (GRCm39) |
D142N |
probably damaging |
Het |
Kbtbd2 |
T |
A |
6: 56,756,917 (GRCm39) |
E273V |
probably damaging |
Het |
Klk1b11 |
A |
G |
7: 43,648,428 (GRCm39) |
E145G |
possibly damaging |
Het |
Mmp1a |
G |
T |
9: 7,475,364 (GRCm39) |
V378F |
possibly damaging |
Het |
Mon2 |
G |
T |
10: 122,872,016 (GRCm39) |
S336* |
probably null |
Het |
Mrgprh |
T |
A |
17: 13,095,917 (GRCm39) |
N52K |
probably damaging |
Het |
Myo9a |
T |
C |
9: 59,772,922 (GRCm39) |
F985L |
probably benign |
Het |
Nek3 |
T |
C |
8: 22,638,677 (GRCm39) |
N207S |
probably benign |
Het |
Nkpd1 |
A |
G |
7: 19,258,009 (GRCm39) |
D596G |
probably damaging |
Het |
Oc90 |
C |
A |
15: 65,761,557 (GRCm39) |
E154* |
probably null |
Het |
Or8b101 |
T |
A |
9: 38,020,426 (GRCm39) |
M143K |
possibly damaging |
Het |
Or8b3 |
C |
A |
9: 38,315,047 (GRCm39) |
Y292* |
probably null |
Het |
Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,358,874 (GRCm39) |
Y361C |
probably damaging |
Het |
Polr2h |
T |
C |
16: 20,539,285 (GRCm39) |
Y90H |
possibly damaging |
Het |
Potefam1 |
T |
A |
2: 111,020,699 (GRCm39) |
R136S |
unknown |
Het |
Ppp1r26 |
A |
G |
2: 28,343,649 (GRCm39) |
N1093S |
probably benign |
Het |
Prex1 |
G |
T |
2: 166,417,669 (GRCm39) |
R1313S |
probably damaging |
Het |
Ptprh |
A |
T |
7: 4,583,911 (GRCm39) |
V227E |
probably damaging |
Het |
Pycr2 |
A |
G |
1: 180,733,473 (GRCm39) |
D58G |
probably benign |
Het |
Rad54b |
G |
T |
4: 11,609,321 (GRCm39) |
E591* |
probably null |
Het |
Rptor |
T |
C |
11: 119,494,765 (GRCm39) |
S44P |
probably benign |
Het |
Safb2 |
T |
A |
17: 56,882,602 (GRCm39) |
T344S |
probably benign |
Het |
Samd9l |
T |
C |
6: 3,376,856 (GRCm39) |
E135G |
probably benign |
Het |
Sec23a |
A |
T |
12: 59,048,708 (GRCm39) |
I167N |
probably damaging |
Het |
Shoc2 |
C |
T |
19: 54,016,231 (GRCm39) |
T415I |
probably benign |
Het |
Sobp |
T |
C |
10: 42,898,374 (GRCm39) |
I404V |
probably benign |
Het |
Ssbp4 |
G |
T |
8: 71,052,395 (GRCm39) |
L147I |
probably benign |
Het |
Sspo |
G |
A |
6: 48,440,869 (GRCm39) |
R1777H |
possibly damaging |
Het |
Syt14 |
A |
G |
1: 192,612,814 (GRCm39) |
V379A |
probably damaging |
Het |
Tcf19 |
A |
G |
17: 35,825,899 (GRCm39) |
V86A |
probably damaging |
Het |
Tfap2a |
T |
A |
13: 40,870,875 (GRCm39) |
I338F |
possibly damaging |
Het |
Tmco6 |
C |
A |
18: 36,872,384 (GRCm39) |
N365K |
probably damaging |
Het |
Tmub2 |
G |
A |
11: 102,178,475 (GRCm39) |
R164K |
|
Het |
Togaram1 |
A |
G |
12: 65,065,906 (GRCm39) |
I1637V |
possibly damaging |
Het |
Wdr49 |
A |
C |
3: 75,205,419 (GRCm39) |
S666A |
probably benign |
Het |
Ybx1 |
T |
A |
4: 119,138,794 (GRCm39) |
Y236F |
possibly damaging |
Het |
Zfhx3 |
T |
A |
8: 109,676,756 (GRCm39) |
I2602N |
probably benign |
Het |
|
Other mutations in Tat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00555:Tat
|
APN |
8 |
110,725,417 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02686:Tat
|
APN |
8 |
110,723,481 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03217:Tat
|
APN |
8 |
110,721,818 (GRCm39) |
missense |
probably benign |
|
R0494:Tat
|
UTSW |
8 |
110,718,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Tat
|
UTSW |
8 |
110,718,270 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1473:Tat
|
UTSW |
8 |
110,723,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Tat
|
UTSW |
8 |
110,718,195 (GRCm39) |
missense |
probably benign |
0.00 |
R1749:Tat
|
UTSW |
8 |
110,722,846 (GRCm39) |
missense |
probably damaging |
0.97 |
R1791:Tat
|
UTSW |
8 |
110,718,261 (GRCm39) |
missense |
probably benign |
0.17 |
R2157:Tat
|
UTSW |
8 |
110,724,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Tat
|
UTSW |
8 |
110,722,842 (GRCm39) |
missense |
probably benign |
0.05 |
R5149:Tat
|
UTSW |
8 |
110,723,450 (GRCm39) |
missense |
probably benign |
0.35 |
R5256:Tat
|
UTSW |
8 |
110,724,966 (GRCm39) |
missense |
probably benign |
0.44 |
R5873:Tat
|
UTSW |
8 |
110,718,581 (GRCm39) |
critical splice donor site |
probably null |
|
R7197:Tat
|
UTSW |
8 |
110,723,459 (GRCm39) |
missense |
probably benign |
0.09 |
R7397:Tat
|
UTSW |
8 |
110,724,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Tat
|
UTSW |
8 |
110,718,242 (GRCm39) |
missense |
probably benign |
0.00 |
R8950:Tat
|
UTSW |
8 |
110,718,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Tat
|
UTSW |
8 |
110,725,031 (GRCm39) |
unclassified |
probably benign |
|
R9329:Tat
|
UTSW |
8 |
110,723,510 (GRCm39) |
missense |
probably benign |
0.00 |
R9436:Tat
|
UTSW |
8 |
110,718,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R9441:Tat
|
UTSW |
8 |
110,720,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R9536:Tat
|
UTSW |
8 |
110,722,711 (GRCm39) |
missense |
probably benign |
|
|