Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck5 |
G |
A |
15: 76,478,383 (GRCm39) |
D277N |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,670,288 (GRCm39) |
S2353T |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,743,371 (GRCm39) |
N43K |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,185,937 (GRCm39) |
I12T |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,741,363 (GRCm39) |
L903P |
probably damaging |
Het |
Ankhd1 |
T |
G |
18: 36,780,878 (GRCm39) |
S1977A |
probably benign |
Het |
Ap1m2 |
T |
C |
9: 21,216,983 (GRCm39) |
M118V |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,548,639 (GRCm39) |
K846R |
possibly damaging |
Het |
Aqr |
C |
A |
2: 113,971,396 (GRCm39) |
E480* |
probably null |
Het |
Arl6 |
G |
T |
16: 59,434,199 (GRCm39) |
Q182K |
probably benign |
Het |
Arpc2 |
A |
G |
1: 74,294,034 (GRCm39) |
K106E |
probably benign |
Het |
Atp8a1 |
A |
C |
5: 67,889,524 (GRCm39) |
F599V |
|
Het |
B3galt5 |
A |
T |
16: 96,117,203 (GRCm39) |
I279F |
probably damaging |
Het |
Calcoco2 |
G |
T |
11: 95,991,104 (GRCm39) |
A211D |
unknown |
Het |
Ccdc33 |
T |
C |
9: 57,993,855 (GRCm39) |
E342G |
possibly damaging |
Het |
Ccdc88a |
C |
A |
11: 29,405,484 (GRCm39) |
Q386K |
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,862,065 (GRCm39) |
K82E |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,503,575 (GRCm39) |
Y792N |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,658,254 (GRCm39) |
I653V |
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,812,649 (GRCm39) |
R2826W |
unknown |
Het |
D6Ertd527e |
A |
G |
6: 87,088,908 (GRCm39) |
N357S |
unknown |
Het |
Dmgdh |
T |
A |
13: 93,857,123 (GRCm39) |
N742K |
probably benign |
Het |
Dnai3 |
T |
C |
3: 145,748,594 (GRCm39) |
N840S |
probably benign |
Het |
Dnajc6 |
A |
G |
4: 101,475,821 (GRCm39) |
N565D |
probably benign |
Het |
Doc2g |
A |
G |
19: 4,054,390 (GRCm39) |
Y155C |
probably damaging |
Het |
Dot1l |
G |
A |
10: 80,624,361 (GRCm39) |
G943D |
probably damaging |
Het |
Dst |
T |
C |
1: 34,220,736 (GRCm39) |
V2180A |
probably benign |
Het |
Eftud2 |
A |
C |
11: 102,759,422 (GRCm39) |
Y160* |
probably null |
Het |
Ehd1 |
A |
T |
19: 6,331,262 (GRCm39) |
Q140L |
probably benign |
Het |
Etv3 |
T |
C |
3: 87,443,172 (GRCm39) |
V252A |
probably benign |
Het |
F11 |
A |
T |
8: 45,694,566 (GRCm39) |
C598* |
probably null |
Het |
Fancm |
T |
A |
12: 65,137,758 (GRCm39) |
N316K |
probably benign |
Het |
Flnc |
T |
C |
6: 29,457,214 (GRCm39) |
V2372A |
probably damaging |
Het |
Fry |
A |
G |
5: 150,282,488 (GRCm39) |
R338G |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,837,591 (GRCm39) |
T136A |
probably benign |
Het |
Golga7b |
T |
C |
19: 42,255,462 (GRCm39) |
V113A |
possibly damaging |
Het |
Gpn3 |
G |
T |
5: 122,520,306 (GRCm39) |
V102L |
|
Het |
Herc2 |
A |
G |
7: 55,820,338 (GRCm39) |
N2859S |
possibly damaging |
Het |
Hpd |
A |
T |
5: 123,318,948 (GRCm39) |
|
probably null |
Het |
Hspg2 |
C |
T |
4: 137,266,887 (GRCm39) |
T1964I |
probably benign |
Het |
Hydin |
A |
T |
8: 111,220,965 (GRCm39) |
T1454S |
probably benign |
Het |
Irgm2 |
A |
T |
11: 58,110,872 (GRCm39) |
T188S |
possibly damaging |
Het |
Jak3 |
A |
G |
8: 72,131,366 (GRCm39) |
D77G |
probably damaging |
Het |
Kcnj4 |
G |
T |
15: 79,369,220 (GRCm39) |
F253L |
possibly damaging |
Het |
Kidins220 |
T |
A |
12: 25,106,895 (GRCm39) |
D1358E |
probably benign |
Het |
Klf1 |
C |
A |
8: 85,630,061 (GRCm39) |
C295* |
probably null |
Het |
Kmt2a |
C |
T |
9: 44,760,102 (GRCm39) |
W582* |
probably null |
Het |
Lrig2 |
A |
G |
3: 104,371,556 (GRCm39) |
C716R |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,765,004 (GRCm39) |
D2941N |
|
Het |
Lrpprc |
A |
T |
17: 85,020,262 (GRCm39) |
V1141E |
probably damaging |
Het |
Mrgprx1 |
C |
T |
7: 47,671,273 (GRCm39) |
G158D |
probably benign |
Het |
Muc5b |
C |
A |
7: 141,409,279 (GRCm39) |
A1121D |
unknown |
Het |
Nf1 |
G |
T |
11: 79,334,733 (GRCm39) |
V852L |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,118,286 (GRCm39) |
E670G |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,784,601 (GRCm39) |
T101A |
probably benign |
Het |
Or10a49 |
T |
C |
7: 108,467,563 (GRCm39) |
Y266C |
probably damaging |
Het |
Or2t35 |
T |
A |
14: 14,407,963 (GRCm38) |
I245K |
probably benign |
Het |
Or5b123 |
G |
A |
19: 13,597,365 (GRCm39) |
V237I |
probably benign |
Het |
P2rx2 |
T |
C |
5: 110,488,172 (GRCm39) |
T461A |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,799,194 (GRCm39) |
T419I |
probably damaging |
Het |
Patz1 |
T |
C |
11: 3,244,562 (GRCm39) |
V481A |
unknown |
Het |
Pdlim5 |
A |
G |
3: 142,018,058 (GRCm39) |
L179P |
probably benign |
Het |
Pik3ap1 |
A |
T |
19: 41,296,967 (GRCm39) |
V461D |
probably damaging |
Het |
Polq |
T |
C |
16: 36,848,176 (GRCm39) |
V261A |
probably damaging |
Het |
Ppm1a |
G |
A |
12: 72,837,451 (GRCm39) |
V333M |
possibly damaging |
Het |
R3hcc1l |
T |
C |
19: 42,552,671 (GRCm39) |
L556P |
probably benign |
Het |
Rabggta |
G |
A |
14: 55,956,375 (GRCm39) |
Q365* |
probably null |
Het |
Ranbp9 |
T |
C |
13: 43,578,519 (GRCm39) |
T185A |
probably benign |
Het |
Rd3l |
T |
G |
12: 111,945,913 (GRCm39) |
N189H |
probably damaging |
Het |
Rnf17 |
A |
G |
14: 56,722,636 (GRCm39) |
T1066A |
probably damaging |
Het |
Rnf213 |
G |
A |
11: 119,332,794 (GRCm39) |
A2669T |
|
Het |
Ros1 |
T |
A |
10: 51,996,931 (GRCm39) |
H1268L |
probably benign |
Het |
Rps6ka4 |
G |
T |
19: 6,809,354 (GRCm39) |
S433R |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,759,092 (GRCm39) |
L3362P |
probably damaging |
Het |
Setd1b |
A |
T |
5: 123,298,046 (GRCm39) |
T1361S |
unknown |
Het |
Setd2 |
T |
C |
9: 110,377,570 (GRCm39) |
S462P |
probably damaging |
Het |
Sgsm3 |
A |
T |
15: 80,890,935 (GRCm39) |
Q132L |
probably benign |
Het |
Slx1b |
C |
A |
7: 126,291,698 (GRCm39) |
R122L |
probably damaging |
Het |
Sorbs2 |
A |
T |
8: 46,276,788 (GRCm39) |
T1167S |
probably benign |
Het |
Spdya |
A |
C |
17: 71,869,513 (GRCm39) |
T103P |
probably damaging |
Het |
Stfa2 |
A |
G |
16: 36,228,638 (GRCm39) |
S20P |
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,891,026 (GRCm39) |
T400A |
probably benign |
Het |
Tardbp |
A |
T |
4: 148,709,751 (GRCm39) |
D23E |
probably damaging |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tgm1 |
C |
T |
14: 55,948,441 (GRCm39) |
D237N |
probably benign |
Het |
Tmem198 |
A |
T |
1: 75,459,272 (GRCm39) |
I76F |
possibly damaging |
Het |
Trpv2 |
A |
T |
11: 62,475,385 (GRCm39) |
Y266F |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,569,845 (GRCm39) |
G27016E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,781,824 (GRCm39) |
E1074G |
unknown |
Het |
Unc5b |
A |
T |
10: 60,613,322 (GRCm39) |
W305R |
probably damaging |
Het |
Usp38 |
A |
G |
8: 81,741,164 (GRCm39) |
|
probably benign |
Het |
Vmn1r79 |
A |
G |
7: 11,910,582 (GRCm39) |
T155A |
probably benign |
Het |
Vwce |
G |
A |
19: 10,615,481 (GRCm39) |
V121I |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,865,961 (GRCm39) |
D530E |
probably benign |
Het |
Wnt4 |
A |
G |
4: 137,023,929 (GRCm39) |
T299A |
probably benign |
Het |
Yeats2 |
T |
A |
16: 20,047,491 (GRCm39) |
Y1284* |
probably null |
Het |
Zfp113 |
A |
T |
5: 138,148,888 (GRCm39) |
Y85* |
probably null |
Het |
Zfp184 |
A |
G |
13: 22,144,096 (GRCm39) |
T601A |
probably benign |
Het |
Zfp655 |
A |
G |
5: 145,180,442 (GRCm39) |
E100G |
probably damaging |
Het |
|
Other mutations in Tgs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01063:Tgs1
|
APN |
4 |
3,591,292 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01154:Tgs1
|
APN |
4 |
3,585,473 (GRCm39) |
nonsense |
probably null |
|
IGL01554:Tgs1
|
APN |
4 |
3,593,632 (GRCm39) |
missense |
probably null |
0.68 |
IGL01613:Tgs1
|
APN |
4 |
3,585,183 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02117:Tgs1
|
APN |
4 |
3,585,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02259:Tgs1
|
APN |
4 |
3,604,743 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02697:Tgs1
|
APN |
4 |
3,585,564 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02814:Tgs1
|
APN |
4 |
3,585,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02962:Tgs1
|
APN |
4 |
3,586,181 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03223:Tgs1
|
APN |
4 |
3,591,322 (GRCm39) |
splice site |
probably benign |
|
IGL03340:Tgs1
|
APN |
4 |
3,604,813 (GRCm39) |
missense |
probably benign |
0.44 |
K2124:Tgs1
|
UTSW |
4 |
3,595,547 (GRCm39) |
missense |
probably benign |
0.00 |
R0189:Tgs1
|
UTSW |
4 |
3,593,620 (GRCm39) |
missense |
probably benign |
0.08 |
R0708:Tgs1
|
UTSW |
4 |
3,586,152 (GRCm39) |
missense |
probably benign |
0.07 |
R1029:Tgs1
|
UTSW |
4 |
3,593,471 (GRCm39) |
missense |
probably damaging |
0.98 |
R1446:Tgs1
|
UTSW |
4 |
3,604,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Tgs1
|
UTSW |
4 |
3,585,964 (GRCm39) |
missense |
probably benign |
|
R1711:Tgs1
|
UTSW |
4 |
3,598,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R1889:Tgs1
|
UTSW |
4 |
3,614,928 (GRCm39) |
missense |
probably benign |
0.31 |
R2911:Tgs1
|
UTSW |
4 |
3,585,616 (GRCm39) |
missense |
probably benign |
0.00 |
R3695:Tgs1
|
UTSW |
4 |
3,604,949 (GRCm39) |
splice site |
probably null |
|
R4615:Tgs1
|
UTSW |
4 |
3,585,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Tgs1
|
UTSW |
4 |
3,586,170 (GRCm39) |
missense |
probably benign |
|
R6088:Tgs1
|
UTSW |
4 |
3,595,383 (GRCm39) |
missense |
probably benign |
0.06 |
R6442:Tgs1
|
UTSW |
4 |
3,604,760 (GRCm39) |
nonsense |
probably null |
|
R7542:Tgs1
|
UTSW |
4 |
3,595,439 (GRCm39) |
missense |
probably benign |
0.01 |
R7894:Tgs1
|
UTSW |
4 |
3,598,652 (GRCm39) |
missense |
probably benign |
0.10 |
R7966:Tgs1
|
UTSW |
4 |
3,586,215 (GRCm39) |
missense |
probably benign |
0.02 |
R7996:Tgs1
|
UTSW |
4 |
3,605,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R8202:Tgs1
|
UTSW |
4 |
3,586,097 (GRCm39) |
missense |
probably benign |
0.01 |
R8298:Tgs1
|
UTSW |
4 |
3,605,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R9006:Tgs1
|
UTSW |
4 |
3,595,427 (GRCm39) |
missense |
probably benign |
0.02 |
R9035:Tgs1
|
UTSW |
4 |
3,593,491 (GRCm39) |
missense |
probably benign |
0.01 |
R9052:Tgs1
|
UTSW |
4 |
3,585,166 (GRCm39) |
missense |
probably benign |
0.00 |
R9188:Tgs1
|
UTSW |
4 |
3,585,693 (GRCm39) |
missense |
probably benign |
0.13 |
R9378:Tgs1
|
UTSW |
4 |
3,595,475 (GRCm39) |
missense |
probably benign |
0.01 |
R9696:Tgs1
|
UTSW |
4 |
3,575,071 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9750:Tgs1
|
UTSW |
4 |
3,585,869 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Tgs1
|
UTSW |
4 |
3,585,912 (GRCm39) |
missense |
probably benign |
0.03 |
|