Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
T |
14: 32,383,001 (GRCm39) |
L988* |
probably null |
Het |
4930546C10Rik |
A |
G |
18: 69,083,106 (GRCm39) |
F36S |
unknown |
Het |
Acan |
C |
A |
7: 78,750,101 (GRCm39) |
T1624K |
possibly damaging |
Het |
Ambn |
T |
C |
5: 88,613,051 (GRCm39) |
|
probably null |
Het |
Ankrd24 |
T |
C |
10: 81,478,352 (GRCm39) |
I437T |
unknown |
Het |
Arl4d |
C |
T |
11: 101,557,827 (GRCm39) |
R118W |
probably damaging |
Het |
Atg2a |
A |
G |
19: 6,306,721 (GRCm39) |
|
probably benign |
Het |
Bcan |
T |
C |
3: 87,895,695 (GRCm39) |
T814A |
probably benign |
Het |
Brca2 |
T |
A |
5: 150,492,498 (GRCm39) |
M3171K |
possibly damaging |
Het |
Cd209a |
T |
A |
8: 3,798,739 (GRCm39) |
S23C |
probably damaging |
Het |
Chek2 |
A |
T |
5: 111,011,175 (GRCm39) |
K324N |
probably benign |
Het |
Col12a1 |
C |
T |
9: 79,599,577 (GRCm39) |
V859I |
probably benign |
Het |
Cyp7b1 |
C |
T |
3: 18,150,788 (GRCm39) |
R317H |
probably benign |
Het |
Dmxl2 |
A |
G |
9: 54,308,941 (GRCm39) |
S1937P |
probably benign |
Het |
Epb41l1 |
T |
G |
2: 156,335,869 (GRCm39) |
V11G |
probably damaging |
Het |
Ephb6 |
C |
T |
6: 41,590,293 (GRCm39) |
A15V |
probably benign |
Het |
Fat3 |
G |
A |
9: 15,858,822 (GRCm39) |
P3798L |
probably benign |
Het |
Foxd1 |
T |
A |
13: 98,491,596 (GRCm39) |
C157S |
probably damaging |
Het |
Gja10 |
T |
C |
4: 32,601,058 (GRCm39) |
Q442R |
probably benign |
Het |
Gm17019 |
A |
C |
5: 15,081,798 (GRCm39) |
M47R |
possibly damaging |
Het |
Gpr179 |
C |
A |
11: 97,242,329 (GRCm39) |
E172* |
probably null |
Het |
Grhl1 |
G |
A |
12: 24,634,945 (GRCm39) |
|
probably null |
Het |
Gtf2ird2 |
A |
T |
5: 134,226,106 (GRCm39) |
E184V |
probably benign |
Het |
Hace1 |
A |
G |
10: 45,576,766 (GRCm39) |
I813V |
probably benign |
Het |
Hk2 |
A |
T |
6: 82,715,379 (GRCm39) |
L385Q |
probably damaging |
Het |
Htt |
C |
T |
5: 34,976,376 (GRCm39) |
T726I |
probably benign |
Het |
Itga8 |
T |
C |
2: 12,145,206 (GRCm39) |
S916G |
probably benign |
Het |
Jag1 |
A |
T |
2: 136,935,175 (GRCm39) |
F396I |
probably damaging |
Het |
Kif16b |
A |
G |
2: 142,554,899 (GRCm39) |
M633T |
possibly damaging |
Het |
Klf5 |
T |
A |
14: 99,538,922 (GRCm39) |
F112I |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,128,610 (GRCm39) |
Q2989L |
|
Het |
Lrrc28 |
C |
A |
7: 67,278,042 (GRCm39) |
|
probably null |
Het |
Map4k5 |
T |
C |
12: 69,859,931 (GRCm39) |
T739A |
possibly damaging |
Het |
Mbd3l2 |
A |
T |
9: 18,355,914 (GRCm39) |
R80* |
probably null |
Het |
Mctp2 |
T |
C |
7: 71,752,904 (GRCm39) |
E783G |
probably damaging |
Het |
Mill2 |
A |
T |
7: 18,590,489 (GRCm39) |
M190L |
probably benign |
Het |
N4bp3 |
T |
C |
11: 51,535,256 (GRCm39) |
N311S |
probably benign |
Het |
Nanos2 |
A |
T |
7: 18,721,549 (GRCm39) |
D7V |
probably damaging |
Het |
Ndufs7 |
T |
A |
10: 80,089,619 (GRCm39) |
|
probably null |
Het |
Nexn |
T |
C |
3: 151,948,306 (GRCm39) |
N483S |
probably benign |
Het |
Nlrp1b |
T |
G |
11: 71,073,288 (GRCm39) |
E185A |
probably damaging |
Het |
Nop2 |
C |
A |
6: 125,114,118 (GRCm39) |
Q195K |
probably benign |
Het |
Or4a15 |
A |
G |
2: 89,192,957 (GRCm39) |
V272A |
possibly damaging |
Het |
Pde12 |
G |
A |
14: 26,390,577 (GRCm39) |
S44L |
probably benign |
Het |
Pde1c |
A |
T |
6: 56,114,371 (GRCm39) |
V514E |
probably damaging |
Het |
Pdzph1 |
A |
T |
17: 59,281,334 (GRCm39) |
V316D |
probably benign |
Het |
Prl3c1 |
A |
T |
13: 27,387,578 (GRCm39) |
I208F |
possibly damaging |
Het |
Raver2 |
G |
A |
4: 100,964,399 (GRCm39) |
|
probably null |
Het |
Rpl13a-ps1 |
T |
A |
19: 50,018,747 (GRCm39) |
H143L |
probably benign |
Het |
Septin14 |
A |
T |
5: 129,760,642 (GRCm39) |
I402K |
possibly damaging |
Het |
Sla2 |
T |
A |
2: 156,717,885 (GRCm39) |
Y129F |
possibly damaging |
Het |
Smarca2 |
TGCAGCAGCAGCAGCAGCA |
TGCAGCAGCAGCAGCA |
19: 26,608,358 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
G |
9: 41,911,567 (GRCm39) |
S1448P |
probably damaging |
Het |
Spast |
G |
A |
17: 74,695,273 (GRCm39) |
R604H |
probably damaging |
Het |
Speg |
G |
A |
1: 75,365,517 (GRCm39) |
G633S |
probably damaging |
Het |
Stxbp5l |
ATTTT |
ATTTTT |
16: 37,036,414 (GRCm39) |
|
probably null |
Het |
Syt11 |
T |
C |
3: 88,669,335 (GRCm39) |
M186V |
probably benign |
Het |
Tex26 |
C |
A |
5: 149,380,369 (GRCm39) |
N133K |
probably benign |
Het |
Tnfrsf17 |
T |
C |
16: 11,131,910 (GRCm39) |
C32R |
probably damaging |
Het |
Trem1 |
T |
A |
17: 48,544,374 (GRCm39) |
V133E |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,664,661 (GRCm39) |
M906K |
possibly damaging |
Het |
Ugt2b35 |
T |
A |
5: 87,159,189 (GRCm39) |
I461K |
possibly damaging |
Het |
Vmn2r77 |
T |
A |
7: 86,444,430 (GRCm39) |
C28S |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,979,137 (GRCm39) |
L425F |
probably damaging |
Het |
Zfp790 |
C |
T |
7: 29,522,525 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or4n4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01370:Or4n4
|
APN |
14 |
50,519,689 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01801:Or4n4
|
APN |
14 |
50,519,665 (GRCm39) |
missense |
probably benign |
|
IGL01992:Or4n4
|
APN |
14 |
50,518,798 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02137:Or4n4
|
APN |
14 |
50,519,135 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02494:Or4n4
|
APN |
14 |
50,519,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Or4n4
|
APN |
14 |
50,519,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Or4n4
|
UTSW |
14 |
50,518,801 (GRCm39) |
missense |
probably benign |
|
PIT4142001:Or4n4
|
UTSW |
14 |
50,518,784 (GRCm39) |
makesense |
probably null |
|
R0570:Or4n4
|
UTSW |
14 |
50,519,370 (GRCm39) |
missense |
probably benign |
0.00 |
R1570:Or4n4
|
UTSW |
14 |
50,518,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Or4n4
|
UTSW |
14 |
50,518,848 (GRCm39) |
nonsense |
probably null |
|
R2313:Or4n4
|
UTSW |
14 |
50,519,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R4594:Or4n4
|
UTSW |
14 |
50,519,140 (GRCm39) |
missense |
probably benign |
0.02 |
R6442:Or4n4
|
UTSW |
14 |
50,518,826 (GRCm39) |
missense |
probably damaging |
0.98 |
R6783:Or4n4
|
UTSW |
14 |
50,519,644 (GRCm39) |
missense |
probably benign |
|
R7334:Or4n4
|
UTSW |
14 |
50,519,036 (GRCm39) |
missense |
probably benign |
0.08 |
R7763:Or4n4
|
UTSW |
14 |
50,518,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R8207:Or4n4
|
UTSW |
14 |
50,519,036 (GRCm39) |
missense |
probably benign |
0.02 |
R8228:Or4n4
|
UTSW |
14 |
50,518,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Or4n4
|
UTSW |
14 |
50,519,236 (GRCm39) |
missense |
probably benign |
0.04 |
R8809:Or4n4
|
UTSW |
14 |
50,519,236 (GRCm39) |
missense |
probably benign |
0.04 |
R8962:Or4n4
|
UTSW |
14 |
50,518,816 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9800:Or4n4
|
UTSW |
14 |
50,519,701 (GRCm39) |
missense |
probably benign |
|
|