Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030452D12Rik |
A |
G |
8: 107,233,822 (GRCm39) |
|
probably benign |
Het |
Acap3 |
C |
A |
4: 155,986,785 (GRCm39) |
S347* |
probably null |
Het |
Acvr1 |
G |
A |
2: 58,390,507 (GRCm39) |
P19L |
probably benign |
Het |
Add2 |
G |
T |
6: 86,081,611 (GRCm39) |
E366* |
probably null |
Het |
Ankrd28 |
C |
A |
14: 31,470,695 (GRCm39) |
A153S |
probably damaging |
Het |
Anxa8 |
A |
T |
14: 33,816,727 (GRCm39) |
I206F |
probably damaging |
Het |
Arhgef4 |
G |
A |
1: 34,771,403 (GRCm39) |
E1237K |
probably damaging |
Het |
Arid1a |
C |
T |
4: 133,416,416 (GRCm39) |
A1120T |
unknown |
Het |
Atad5 |
T |
C |
11: 79,997,247 (GRCm39) |
V857A |
probably damaging |
Het |
Atp2a3 |
T |
A |
11: 72,868,058 (GRCm39) |
|
probably null |
Het |
Atxn1l |
C |
T |
8: 110,459,027 (GRCm39) |
V412I |
possibly damaging |
Het |
Card11 |
A |
G |
5: 140,866,125 (GRCm39) |
S923P |
probably benign |
Het |
Cars1 |
C |
A |
7: 143,146,362 (GRCm39) |
E21* |
probably null |
Het |
Ccdc115 |
A |
G |
1: 34,476,702 (GRCm39) |
|
probably benign |
Het |
Ccnj |
T |
A |
19: 40,833,508 (GRCm39) |
|
probably null |
Het |
Cds2 |
C |
T |
2: 132,140,399 (GRCm39) |
T182I |
probably damaging |
Het |
Ceacam14 |
A |
G |
7: 17,549,248 (GRCm39) |
H213R |
probably benign |
Het |
Cfap44 |
A |
T |
16: 44,252,308 (GRCm39) |
M806L |
probably benign |
Het |
Chd8 |
A |
T |
14: 52,452,044 (GRCm39) |
I1317K |
probably damaging |
Het |
Cherp |
A |
T |
8: 73,215,366 (GRCm39) |
|
probably benign |
Het |
Creb5 |
C |
G |
6: 53,581,527 (GRCm39) |
T30S |
possibly damaging |
Het |
Csf2ra |
A |
G |
19: 61,215,333 (GRCm39) |
M94T |
probably benign |
Het |
Cyp2b19 |
A |
C |
7: 26,466,187 (GRCm39) |
D330A |
probably benign |
Het |
Ddost |
G |
A |
4: 138,037,499 (GRCm39) |
V188M |
possibly damaging |
Het |
Dnah7a |
A |
T |
1: 53,644,978 (GRCm39) |
D1019E |
probably benign |
Het |
Dtx1 |
A |
T |
5: 120,833,057 (GRCm39) |
I127N |
possibly damaging |
Het |
Dyrk2 |
T |
C |
10: 118,704,668 (GRCm39) |
T3A |
possibly damaging |
Het |
Elovl5 |
C |
T |
9: 77,868,193 (GRCm39) |
T35M |
probably damaging |
Het |
Emc7 |
T |
C |
2: 112,297,314 (GRCm39) |
|
probably benign |
Het |
Erp27 |
T |
C |
6: 136,886,487 (GRCm39) |
Y182C |
probably damaging |
Het |
Exoc2 |
T |
A |
13: 31,070,310 (GRCm39) |
|
probably benign |
Het |
F5 |
A |
C |
1: 164,012,676 (GRCm39) |
D530A |
probably damaging |
Het |
Fbxo41 |
A |
G |
6: 85,455,164 (GRCm39) |
S614P |
probably damaging |
Het |
Fmn1 |
T |
A |
2: 113,467,124 (GRCm39) |
Y1342N |
possibly damaging |
Het |
Gpr22 |
T |
A |
12: 31,758,793 (GRCm39) |
D443V |
possibly damaging |
Het |
Il17rd |
T |
A |
14: 26,813,888 (GRCm39) |
W56R |
probably damaging |
Het |
Itga2b |
A |
T |
11: 102,356,779 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
T |
C |
10: 67,091,261 (GRCm39) |
M2514T |
probably benign |
Het |
Klk1b9 |
T |
C |
7: 43,443,675 (GRCm39) |
|
probably benign |
Het |
Krr1 |
T |
C |
10: 111,811,503 (GRCm39) |
Y66H |
probably damaging |
Het |
Lamb2 |
T |
C |
9: 108,363,553 (GRCm39) |
|
probably benign |
Het |
Lgals3bp |
A |
T |
11: 118,284,290 (GRCm39) |
Y430N |
probably benign |
Het |
Lrp10 |
T |
C |
14: 54,705,036 (GRCm39) |
V113A |
probably benign |
Het |
Mgam |
A |
G |
6: 40,736,024 (GRCm39) |
Y841C |
probably damaging |
Het |
Nisch |
T |
A |
14: 30,899,421 (GRCm39) |
|
probably benign |
Het |
Nlrp4d |
G |
A |
7: 10,112,219 (GRCm39) |
T650I |
probably benign |
Het |
Or4f61 |
T |
A |
2: 111,922,981 (GRCm39) |
K22* |
probably null |
Het |
Or5p78 |
C |
T |
7: 108,211,577 (GRCm39) |
T21I |
possibly damaging |
Het |
Parp4 |
A |
G |
14: 56,886,300 (GRCm39) |
D1793G |
unknown |
Het |
Pcm1 |
A |
G |
8: 41,778,942 (GRCm39) |
D1850G |
probably benign |
Het |
Pgap2 |
G |
A |
7: 101,885,669 (GRCm39) |
A145T |
probably damaging |
Het |
Phc1 |
G |
A |
6: 122,299,995 (GRCm39) |
A583V |
probably damaging |
Het |
Plcd3 |
G |
A |
11: 102,962,085 (GRCm39) |
|
probably benign |
Het |
Ppm1m |
T |
A |
9: 106,074,501 (GRCm39) |
Q214L |
probably damaging |
Het |
Prkg2 |
A |
G |
5: 99,145,379 (GRCm39) |
|
probably benign |
Het |
Prss3l |
A |
G |
6: 41,422,271 (GRCm39) |
Y45H |
probably benign |
Het |
Rasal3 |
T |
C |
17: 32,614,791 (GRCm39) |
|
probably benign |
Het |
Rfc1 |
A |
T |
5: 65,421,640 (GRCm39) |
D1086E |
probably benign |
Het |
Rnf145 |
T |
A |
11: 44,452,587 (GRCm39) |
L522H |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,382,168 (GRCm39) |
|
probably null |
Het |
Sik1 |
C |
A |
17: 32,068,055 (GRCm39) |
V377F |
possibly damaging |
Het |
Slc44a4 |
T |
C |
17: 35,147,071 (GRCm39) |
I367T |
possibly damaging |
Het |
Slfn3 |
A |
G |
11: 83,103,954 (GRCm39) |
D275G |
possibly damaging |
Het |
Smarcad1 |
A |
T |
6: 65,051,806 (GRCm39) |
N313I |
possibly damaging |
Het |
Smc4 |
A |
T |
3: 68,915,361 (GRCm39) |
K138* |
probably null |
Het |
Smg6 |
T |
A |
11: 74,821,039 (GRCm39) |
S437T |
probably benign |
Het |
Spaca9 |
G |
T |
2: 28,586,005 (GRCm39) |
Q20K |
probably damaging |
Het |
Spatc1 |
T |
G |
15: 76,152,493 (GRCm39) |
I41S |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,096,385 (GRCm39) |
T5S |
possibly damaging |
Het |
St3gal1 |
C |
A |
15: 66,981,504 (GRCm39) |
|
probably benign |
Het |
Stat5a |
C |
A |
11: 100,753,961 (GRCm39) |
T97K |
probably benign |
Het |
Stat5b |
A |
T |
11: 100,689,156 (GRCm39) |
I246N |
probably benign |
Het |
Supt6 |
G |
T |
11: 78,117,829 (GRCm39) |
D462E |
probably damaging |
Het |
Swi5 |
A |
T |
2: 32,171,836 (GRCm39) |
|
probably benign |
Het |
Syne1 |
A |
T |
10: 5,355,435 (GRCm39) |
V375E |
probably damaging |
Het |
Tcp1 |
T |
C |
17: 13,143,239 (GRCm39) |
F516S |
probably benign |
Het |
Tdrd7 |
A |
T |
4: 45,965,488 (GRCm39) |
|
probably benign |
Het |
Tgfbr3 |
A |
T |
5: 107,288,289 (GRCm39) |
N457K |
probably benign |
Het |
Tmem209 |
A |
G |
6: 30,487,380 (GRCm39) |
M500T |
probably damaging |
Het |
Tmem44 |
C |
T |
16: 30,336,281 (GRCm39) |
|
probably benign |
Het |
Ttc21a |
T |
A |
9: 119,768,220 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,701,454 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,666,347 (GRCm39) |
I88F |
possibly damaging |
Het |
Ube2w |
T |
C |
1: 16,672,479 (GRCm39) |
|
probably benign |
Het |
Ufc1 |
C |
T |
1: 171,117,527 (GRCm39) |
|
probably benign |
Het |
Uhmk1 |
A |
G |
1: 170,039,971 (GRCm39) |
M132T |
possibly damaging |
Het |
Usp29 |
A |
G |
7: 6,966,181 (GRCm39) |
N675D |
possibly damaging |
Het |
Vmn1r23 |
A |
G |
6: 57,903,469 (GRCm39) |
V103A |
possibly damaging |
Het |
Wdr59 |
G |
T |
8: 112,248,604 (GRCm39) |
R4S |
possibly damaging |
Het |
Zc3hav1 |
T |
A |
6: 38,284,372 (GRCm39) |
E914D |
probably benign |
Het |
|
Other mutations in Fam149a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Fam149a
|
APN |
8 |
45,792,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00229:Fam149a
|
APN |
8 |
45,804,823 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01089:Fam149a
|
APN |
8 |
45,801,564 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01578:Fam149a
|
APN |
8 |
45,803,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03095:Fam149a
|
APN |
8 |
45,794,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Fam149a
|
APN |
8 |
45,801,580 (GRCm39) |
missense |
possibly damaging |
0.78 |
guangxi
|
UTSW |
8 |
45,834,778 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Fam149a
|
UTSW |
8 |
45,804,743 (GRCm39) |
missense |
probably benign |
0.00 |
R0111:Fam149a
|
UTSW |
8 |
45,794,183 (GRCm39) |
splice site |
probably benign |
|
R0113:Fam149a
|
UTSW |
8 |
45,794,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R0604:Fam149a
|
UTSW |
8 |
45,798,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1441:Fam149a
|
UTSW |
8 |
45,808,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Fam149a
|
UTSW |
8 |
45,792,411 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1861:Fam149a
|
UTSW |
8 |
45,792,399 (GRCm39) |
nonsense |
probably null |
|
R1981:Fam149a
|
UTSW |
8 |
45,834,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Fam149a
|
UTSW |
8 |
45,806,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Fam149a
|
UTSW |
8 |
45,794,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R3807:Fam149a
|
UTSW |
8 |
45,834,647 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4176:Fam149a
|
UTSW |
8 |
45,794,321 (GRCm39) |
missense |
probably benign |
0.41 |
R4913:Fam149a
|
UTSW |
8 |
45,806,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Fam149a
|
UTSW |
8 |
45,803,472 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5172:Fam149a
|
UTSW |
8 |
45,797,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R5436:Fam149a
|
UTSW |
8 |
45,801,508 (GRCm39) |
missense |
probably benign |
0.21 |
R6060:Fam149a
|
UTSW |
8 |
45,811,799 (GRCm39) |
intron |
probably benign |
|
R6426:Fam149a
|
UTSW |
8 |
45,834,611 (GRCm39) |
missense |
probably benign |
|
R6590:Fam149a
|
UTSW |
8 |
45,802,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6596:Fam149a
|
UTSW |
8 |
45,834,667 (GRCm39) |
missense |
probably benign |
0.25 |
R6690:Fam149a
|
UTSW |
8 |
45,802,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6730:Fam149a
|
UTSW |
8 |
45,834,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Fam149a
|
UTSW |
8 |
45,834,478 (GRCm39) |
missense |
probably benign |
|
R6916:Fam149a
|
UTSW |
8 |
45,803,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Fam149a
|
UTSW |
8 |
45,803,582 (GRCm39) |
missense |
probably benign |
0.08 |
R7219:Fam149a
|
UTSW |
8 |
45,803,600 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7352:Fam149a
|
UTSW |
8 |
45,794,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R7454:Fam149a
|
UTSW |
8 |
45,801,583 (GRCm39) |
missense |
probably benign |
0.29 |
R7591:Fam149a
|
UTSW |
8 |
45,803,472 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7788:Fam149a
|
UTSW |
8 |
45,834,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Fam149a
|
UTSW |
8 |
45,811,678 (GRCm39) |
missense |
|
|
R7915:Fam149a
|
UTSW |
8 |
45,794,280 (GRCm39) |
missense |
probably benign |
|
R8036:Fam149a
|
UTSW |
8 |
45,802,048 (GRCm39) |
missense |
probably benign |
0.00 |
R8181:Fam149a
|
UTSW |
8 |
45,834,755 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8239:Fam149a
|
UTSW |
8 |
45,803,490 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8246:Fam149a
|
UTSW |
8 |
45,834,655 (GRCm39) |
missense |
probably benign |
0.00 |
R8532:Fam149a
|
UTSW |
8 |
45,801,991 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8856:Fam149a
|
UTSW |
8 |
45,834,611 (GRCm39) |
missense |
|
|
R8986:Fam149a
|
UTSW |
8 |
45,811,837 (GRCm39) |
missense |
|
|
R9448:Fam149a
|
UTSW |
8 |
45,792,411 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9704:Fam149a
|
UTSW |
8 |
45,795,502 (GRCm39) |
missense |
probably benign |
0.24 |
R9794:Fam149a
|
UTSW |
8 |
45,834,449 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1176:Fam149a
|
UTSW |
8 |
45,795,495 (GRCm39) |
missense |
possibly damaging |
0.92 |
|