Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
T |
C |
7: 43,147,273 (GRCm39) |
I320V |
possibly damaging |
Het |
Adat2 |
A |
G |
10: 13,429,020 (GRCm39) |
K4R |
probably benign |
Het |
Adgb |
G |
A |
10: 10,311,754 (GRCm39) |
L226F |
probably damaging |
Het |
Adgrb3 |
C |
T |
1: 25,137,978 (GRCm39) |
V1192I |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,446,750 (GRCm39) |
N71I |
possibly damaging |
Het |
Amigo2 |
T |
G |
15: 97,143,223 (GRCm39) |
T400P |
probably damaging |
Het |
Ankhd1 |
A |
T |
18: 36,789,826 (GRCm39) |
Q466L |
|
Het |
Auh |
T |
C |
13: 53,073,049 (GRCm39) |
I111V |
probably benign |
Het |
Brwd1 |
A |
G |
16: 95,835,039 (GRCm39) |
F942L |
probably damaging |
Het |
C1qtnf7 |
A |
G |
5: 43,773,486 (GRCm39) |
N262D |
probably damaging |
Het |
Cdh9 |
T |
A |
15: 16,856,316 (GRCm39) |
S785R |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,714,851 (GRCm39) |
T2046A |
possibly damaging |
Het |
Cep170b |
T |
C |
12: 112,711,099 (GRCm39) |
V1493A |
probably damaging |
Het |
Cep290 |
C |
T |
10: 100,328,543 (GRCm39) |
R111W |
probably benign |
Het |
Chd2 |
T |
A |
7: 73,091,390 (GRCm39) |
H1617L |
probably damaging |
Het |
Ciao3 |
C |
T |
17: 26,001,103 (GRCm39) |
P452S |
probably benign |
Het |
Clnk |
T |
C |
5: 38,864,041 (GRCm39) |
D404G |
probably damaging |
Het |
Col18a1 |
C |
T |
10: 76,902,839 (GRCm39) |
G795D |
probably damaging |
Het |
Csf3r |
T |
A |
4: 125,931,449 (GRCm39) |
Y477* |
probably null |
Het |
Dnah17 |
T |
A |
11: 118,001,373 (GRCm39) |
K857* |
probably null |
Het |
Dnah2 |
T |
G |
11: 69,326,130 (GRCm39) |
I3674L |
probably damaging |
Het |
Dnah6 |
A |
C |
6: 73,072,189 (GRCm39) |
I2431S |
possibly damaging |
Het |
Eml6 |
T |
A |
11: 29,752,501 (GRCm39) |
I971F |
possibly damaging |
Het |
Fancc |
T |
A |
13: 63,465,372 (GRCm39) |
|
probably null |
Het |
Gabrb2 |
A |
C |
11: 42,517,569 (GRCm39) |
K464Q |
probably benign |
Het |
Gbp4 |
T |
A |
5: 105,270,848 (GRCm39) |
D261V |
possibly damaging |
Het |
Gdf3 |
A |
G |
6: 122,583,875 (GRCm39) |
V164A |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,263,513 (GRCm39) |
D978G |
probably damaging |
Het |
Gm20730 |
C |
T |
6: 43,058,708 (GRCm39) |
G35R |
probably null |
Het |
Grin2b |
G |
A |
6: 135,900,362 (GRCm39) |
T173I |
probably damaging |
Het |
Gtf3c3 |
A |
T |
1: 54,462,731 (GRCm39) |
V344E |
possibly damaging |
Het |
Hsd3b5 |
A |
G |
3: 98,537,420 (GRCm39) |
I32T |
probably damaging |
Het |
Ido1 |
G |
C |
8: 25,083,204 (GRCm39) |
L74V |
probably damaging |
Het |
Igkv1-88 |
T |
A |
6: 68,839,357 (GRCm39) |
D85V |
probably damaging |
Het |
Il22ra1 |
A |
G |
4: 135,464,770 (GRCm39) |
I159V |
probably benign |
Het |
Iqgap1 |
A |
T |
7: 80,379,848 (GRCm39) |
F1175Y |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,401,094 (GRCm39) |
V531A |
probably benign |
Het |
Itga1 |
T |
A |
13: 115,133,458 (GRCm39) |
Q484L |
probably null |
Het |
Itga11 |
A |
T |
9: 62,651,300 (GRCm39) |
E281V |
probably benign |
Het |
Kpna3 |
T |
C |
14: 61,610,411 (GRCm39) |
N343S |
possibly damaging |
Het |
Larp1b |
A |
G |
3: 40,987,969 (GRCm39) |
K64E |
possibly damaging |
Het |
Larp1b |
A |
G |
3: 40,990,251 (GRCm39) |
N133S |
probably benign |
Het |
Lctl |
T |
A |
9: 64,029,392 (GRCm39) |
L161H |
probably damaging |
Het |
Mlip |
A |
G |
9: 77,137,765 (GRCm39) |
S381P |
probably damaging |
Het |
Mroh9 |
A |
G |
1: 162,873,601 (GRCm39) |
I518T |
probably benign |
Het |
Mst1r |
A |
G |
9: 107,797,211 (GRCm39) |
Q1360R |
probably benign |
Het |
Muc5b |
T |
A |
7: 141,418,629 (GRCm39) |
C3858* |
probably null |
Het |
Naip1 |
A |
T |
13: 100,562,284 (GRCm39) |
H960Q |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,791,786 (GRCm39) |
S1321T |
probably benign |
Het |
Nid2 |
C |
A |
14: 19,852,598 (GRCm39) |
T1102K |
probably damaging |
Het |
Nsmaf |
C |
T |
4: 6,408,563 (GRCm39) |
V739M |
probably damaging |
Het |
Or1o2 |
T |
G |
17: 37,542,341 (GRCm39) |
K307Q |
probably benign |
Het |
Or4k15 |
T |
G |
14: 50,364,446 (GRCm39) |
S137R |
probably benign |
Het |
Or5ar1 |
T |
A |
2: 85,672,001 (GRCm39) |
M45L |
probably benign |
Het |
Or5b110-ps1 |
A |
G |
19: 13,259,954 (GRCm39) |
I156T |
probably damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,862 (GRCm39) |
Q167R |
probably benign |
Het |
Osbpl9 |
G |
A |
4: 108,943,536 (GRCm39) |
P159S |
probably damaging |
Het |
Parpbp |
A |
G |
10: 87,929,499 (GRCm39) |
S450P |
probably damaging |
Het |
Pdgfrb |
A |
G |
18: 61,197,118 (GRCm39) |
T185A |
probably benign |
Het |
Pkd1 |
T |
C |
17: 24,812,476 (GRCm39) |
V3803A |
probably damaging |
Het |
Plau |
A |
T |
14: 20,889,534 (GRCm39) |
K200* |
probably null |
Het |
Plce1 |
A |
T |
19: 38,513,109 (GRCm39) |
Q136L |
probably benign |
Het |
Plekhd1 |
C |
T |
12: 80,769,219 (GRCm39) |
T493I |
probably benign |
Het |
Pofut1 |
T |
C |
2: 153,101,338 (GRCm39) |
S31P |
unknown |
Het |
Prlr |
T |
A |
15: 10,326,010 (GRCm39) |
I243N |
probably damaging |
Het |
Ptgis |
A |
G |
2: 167,065,908 (GRCm39) |
L174P |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,292,190 (GRCm39) |
I792K |
probably damaging |
Het |
Retreg3 |
C |
T |
11: 100,993,806 (GRCm39) |
S136N |
probably damaging |
Het |
Rigi |
T |
A |
4: 40,229,653 (GRCm39) |
I89F |
possibly damaging |
Het |
Rnf213 |
C |
T |
11: 119,358,123 (GRCm39) |
T4291M |
|
Het |
Rtn1 |
A |
G |
12: 72,350,917 (GRCm39) |
Y431H |
probably damaging |
Het |
Rwdd3 |
A |
G |
3: 120,965,253 (GRCm39) |
|
probably benign |
Het |
Scyl3 |
A |
T |
1: 163,777,907 (GRCm39) |
|
probably null |
Het |
Sh2b2 |
G |
T |
5: 136,248,511 (GRCm39) |
Q510K |
probably damaging |
Het |
Sh2b3 |
G |
A |
5: 121,956,763 (GRCm39) |
P333S |
probably benign |
Het |
Sirpd |
A |
G |
3: 15,385,545 (GRCm39) |
V119A |
probably damaging |
Het |
Slc27a6 |
A |
T |
18: 58,742,255 (GRCm39) |
N490Y |
probably damaging |
Het |
Slc45a1 |
C |
T |
4: 150,723,002 (GRCm39) |
R294Q |
probably benign |
Het |
Sorl1 |
A |
C |
9: 41,888,878 (GRCm39) |
I1974S |
possibly damaging |
Het |
Specc1l |
C |
A |
10: 75,099,120 (GRCm39) |
N857K |
probably benign |
Het |
Speg |
T |
C |
1: 75,405,886 (GRCm39) |
L3030P |
probably damaging |
Het |
Spsb1 |
A |
C |
4: 149,991,357 (GRCm39) |
D70E |
probably benign |
Het |
Srsf11 |
A |
G |
3: 157,722,062 (GRCm39) |
S270P |
unknown |
Het |
Ssr3 |
A |
C |
3: 65,295,213 (GRCm39) |
V100G |
probably damaging |
Het |
Synpo |
G |
A |
18: 60,737,547 (GRCm39) |
T133I |
probably damaging |
Het |
Tas2r120 |
T |
G |
6: 132,634,773 (GRCm39) |
V285G |
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,495,133 (GRCm39) |
V1187D |
probably damaging |
Het |
Tmed8 |
C |
A |
12: 87,228,162 (GRCm39) |
|
probably null |
Het |
Tmem51 |
G |
A |
4: 141,764,875 (GRCm39) |
T61M |
probably damaging |
Het |
Tonsl |
A |
T |
15: 76,514,807 (GRCm39) |
D1132E |
probably benign |
Het |
Tor1aip1 |
C |
T |
1: 155,883,330 (GRCm39) |
V358I |
possibly damaging |
Het |
Txlna |
A |
T |
4: 129,524,112 (GRCm39) |
M415K |
probably damaging |
Het |
Tyms |
T |
A |
5: 30,278,558 (GRCm39) |
|
probably benign |
Het |
Uggt2 |
G |
T |
14: 119,326,681 (GRCm39) |
L177I |
probably benign |
Het |
Uqcrh |
T |
C |
4: 115,927,076 (GRCm39) |
H74R |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,909,699 (GRCm39) |
S33T |
probably benign |
Het |
Zfp553 |
T |
A |
7: 126,835,188 (GRCm39) |
C248S |
probably damaging |
Het |
Zfp574 |
G |
A |
7: 24,780,001 (GRCm39) |
C341Y |
possibly damaging |
Het |
Zfp729b |
T |
C |
13: 67,739,617 (GRCm39) |
T883A |
possibly damaging |
Het |
Zfp738 |
T |
A |
13: 67,818,322 (GRCm39) |
K556N |
probably damaging |
Het |
|
Other mutations in Fam135b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Fam135b
|
APN |
15 |
71,322,343 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00565:Fam135b
|
APN |
15 |
71,343,361 (GRCm39) |
missense |
probably benign |
|
IGL00645:Fam135b
|
APN |
15 |
71,334,395 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00686:Fam135b
|
APN |
15 |
71,334,168 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00857:Fam135b
|
APN |
15 |
71,335,465 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01443:Fam135b
|
APN |
15 |
71,335,213 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01690:Fam135b
|
APN |
15 |
71,328,784 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01920:Fam135b
|
APN |
15 |
71,493,885 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01987:Fam135b
|
APN |
15 |
71,333,964 (GRCm39) |
missense |
probably benign |
|
IGL02154:Fam135b
|
APN |
15 |
71,320,559 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03107:Fam135b
|
APN |
15 |
71,335,410 (GRCm39) |
missense |
probably benign |
|
IGL03264:Fam135b
|
APN |
15 |
71,334,637 (GRCm39) |
missense |
probably benign |
|
IGL03055:Fam135b
|
UTSW |
15 |
71,493,883 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0010:Fam135b
|
UTSW |
15 |
71,493,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Fam135b
|
UTSW |
15 |
71,493,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Fam135b
|
UTSW |
15 |
71,317,886 (GRCm39) |
missense |
probably benign |
0.02 |
R0413:Fam135b
|
UTSW |
15 |
71,335,670 (GRCm39) |
missense |
probably benign |
0.45 |
R0524:Fam135b
|
UTSW |
15 |
71,334,133 (GRCm39) |
missense |
probably benign |
0.00 |
R0565:Fam135b
|
UTSW |
15 |
71,362,686 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0628:Fam135b
|
UTSW |
15 |
71,320,505 (GRCm39) |
splice site |
probably benign |
|
R1415:Fam135b
|
UTSW |
15 |
71,328,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R1462:Fam135b
|
UTSW |
15 |
71,493,845 (GRCm39) |
splice site |
probably benign |
|
R1701:Fam135b
|
UTSW |
15 |
71,331,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R1797:Fam135b
|
UTSW |
15 |
71,324,290 (GRCm39) |
missense |
probably benign |
0.41 |
R1807:Fam135b
|
UTSW |
15 |
71,335,761 (GRCm39) |
missense |
probably benign |
|
R1835:Fam135b
|
UTSW |
15 |
71,362,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Fam135b
|
UTSW |
15 |
71,404,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Fam135b
|
UTSW |
15 |
71,493,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R1998:Fam135b
|
UTSW |
15 |
71,324,253 (GRCm39) |
missense |
probably damaging |
0.98 |
R2076:Fam135b
|
UTSW |
15 |
71,350,092 (GRCm39) |
missense |
probably damaging |
0.99 |
R2518:Fam135b
|
UTSW |
15 |
71,335,760 (GRCm39) |
missense |
probably benign |
0.00 |
R3110:Fam135b
|
UTSW |
15 |
71,335,879 (GRCm39) |
missense |
probably benign |
0.05 |
R3112:Fam135b
|
UTSW |
15 |
71,335,879 (GRCm39) |
missense |
probably benign |
0.05 |
R3932:Fam135b
|
UTSW |
15 |
71,322,280 (GRCm39) |
missense |
probably benign |
0.29 |
R4361:Fam135b
|
UTSW |
15 |
71,362,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4397:Fam135b
|
UTSW |
15 |
71,320,525 (GRCm39) |
missense |
probably benign |
0.17 |
R4435:Fam135b
|
UTSW |
15 |
71,320,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R4645:Fam135b
|
UTSW |
15 |
71,334,189 (GRCm39) |
missense |
probably benign |
|
R4740:Fam135b
|
UTSW |
15 |
71,335,920 (GRCm39) |
missense |
probably benign |
0.01 |
R4748:Fam135b
|
UTSW |
15 |
71,335,904 (GRCm39) |
missense |
probably benign |
0.00 |
R4754:Fam135b
|
UTSW |
15 |
71,334,800 (GRCm39) |
missense |
probably benign |
0.01 |
R5044:Fam135b
|
UTSW |
15 |
71,334,560 (GRCm39) |
missense |
probably benign |
0.02 |
R5469:Fam135b
|
UTSW |
15 |
71,317,892 (GRCm39) |
missense |
probably benign |
0.16 |
R5617:Fam135b
|
UTSW |
15 |
71,493,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Fam135b
|
UTSW |
15 |
71,333,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R5778:Fam135b
|
UTSW |
15 |
71,350,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R5891:Fam135b
|
UTSW |
15 |
71,397,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Fam135b
|
UTSW |
15 |
71,334,744 (GRCm39) |
missense |
|
|
R5982:Fam135b
|
UTSW |
15 |
71,320,518 (GRCm39) |
critical splice donor site |
probably null |
|
R5987:Fam135b
|
UTSW |
15 |
71,362,697 (GRCm39) |
missense |
probably benign |
0.00 |
R6535:Fam135b
|
UTSW |
15 |
71,493,924 (GRCm39) |
missense |
probably damaging |
0.99 |
R6734:Fam135b
|
UTSW |
15 |
71,334,629 (GRCm39) |
missense |
probably benign |
0.02 |
R6887:Fam135b
|
UTSW |
15 |
71,335,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R7028:Fam135b
|
UTSW |
15 |
71,343,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7035:Fam135b
|
UTSW |
15 |
71,334,102 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7097:Fam135b
|
UTSW |
15 |
71,493,917 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7143:Fam135b
|
UTSW |
15 |
71,351,000 (GRCm39) |
missense |
probably benign |
0.44 |
R7414:Fam135b
|
UTSW |
15 |
71,350,105 (GRCm39) |
missense |
probably damaging |
0.97 |
R7439:Fam135b
|
UTSW |
15 |
71,335,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R7441:Fam135b
|
UTSW |
15 |
71,335,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R7545:Fam135b
|
UTSW |
15 |
71,322,359 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7642:Fam135b
|
UTSW |
15 |
71,350,991 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7649:Fam135b
|
UTSW |
15 |
71,334,429 (GRCm39) |
missense |
probably benign |
0.00 |
R7686:Fam135b
|
UTSW |
15 |
71,335,233 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7866:Fam135b
|
UTSW |
15 |
71,333,925 (GRCm39) |
missense |
probably benign |
0.00 |
R8006:Fam135b
|
UTSW |
15 |
71,334,183 (GRCm39) |
missense |
probably benign |
0.00 |
R8068:Fam135b
|
UTSW |
15 |
71,404,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8167:Fam135b
|
UTSW |
15 |
71,404,840 (GRCm39) |
missense |
probably null |
1.00 |
R8252:Fam135b
|
UTSW |
15 |
71,404,872 (GRCm39) |
missense |
probably benign |
0.10 |
R8548:Fam135b
|
UTSW |
15 |
71,334,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R8833:Fam135b
|
UTSW |
15 |
71,334,783 (GRCm39) |
missense |
probably benign |
0.04 |
R8955:Fam135b
|
UTSW |
15 |
71,334,063 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8961:Fam135b
|
UTSW |
15 |
71,404,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Fam135b
|
UTSW |
15 |
71,334,189 (GRCm39) |
missense |
probably benign |
0.00 |
R9149:Fam135b
|
UTSW |
15 |
71,334,744 (GRCm39) |
missense |
|
|
R9161:Fam135b
|
UTSW |
15 |
71,334,417 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9227:Fam135b
|
UTSW |
15 |
71,335,856 (GRCm39) |
missense |
probably benign |
0.28 |
R9230:Fam135b
|
UTSW |
15 |
71,335,856 (GRCm39) |
missense |
probably benign |
0.28 |
R9365:Fam135b
|
UTSW |
15 |
71,334,813 (GRCm39) |
missense |
probably benign |
0.00 |
R9622:Fam135b
|
UTSW |
15 |
71,397,686 (GRCm39) |
missense |
probably damaging |
0.98 |
R9758:Fam135b
|
UTSW |
15 |
71,324,199 (GRCm39) |
missense |
probably benign |
0.28 |
R9759:Fam135b
|
UTSW |
15 |
71,335,689 (GRCm39) |
missense |
probably benign |
0.44 |
T0722:Fam135b
|
UTSW |
15 |
71,335,734 (GRCm39) |
missense |
probably damaging |
1.00 |
T0975:Fam135b
|
UTSW |
15 |
71,335,734 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fam135b
|
UTSW |
15 |
71,493,925 (GRCm39) |
start codon destroyed |
probably null |
0.06 |
|