Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
A |
G |
7: 130,959,389 (GRCm39) |
S150P |
probably damaging |
Het |
5530400C23Rik |
T |
G |
6: 133,270,174 (GRCm39) |
|
probably benign |
Het |
Ahctf1 |
A |
C |
1: 179,591,033 (GRCm39) |
|
probably null |
Het |
Ang5 |
T |
C |
14: 44,200,206 (GRCm39) |
V90A |
probably benign |
Het |
Ano9 |
C |
T |
7: 140,684,623 (GRCm39) |
G442R |
probably damaging |
Het |
Apaf1 |
G |
A |
10: 90,895,914 (GRCm39) |
T386I |
probably damaging |
Het |
Apob |
C |
A |
12: 8,056,440 (GRCm39) |
H1608N |
probably damaging |
Het |
Arhgap12 |
C |
A |
18: 6,064,433 (GRCm39) |
|
probably benign |
Het |
Asxl1 |
T |
A |
2: 153,241,824 (GRCm39) |
D791E |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,713,891 (GRCm39) |
V383A |
probably benign |
Het |
Btbd1 |
A |
C |
7: 81,465,754 (GRCm39) |
D197E |
probably damaging |
Het |
Camta2 |
T |
C |
11: 70,564,785 (GRCm39) |
I938V |
possibly damaging |
Het |
Ccn5 |
G |
A |
2: 163,667,233 (GRCm39) |
C78Y |
probably damaging |
Het |
Cdca7 |
C |
A |
2: 72,313,811 (GRCm39) |
A200D |
possibly damaging |
Het |
Cep104 |
A |
T |
4: 154,091,249 (GRCm39) |
Y923F |
possibly damaging |
Het |
Cep135 |
G |
C |
5: 76,769,152 (GRCm39) |
V601L |
probably benign |
Het |
Ces2b |
G |
A |
8: 105,562,542 (GRCm39) |
G291S |
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,638,639 (GRCm39) |
G1400D |
probably damaging |
Het |
Cyth2 |
T |
C |
7: 45,462,541 (GRCm39) |
E1G |
probably damaging |
Het |
Dand5 |
A |
T |
8: 85,542,921 (GRCm39) |
L185Q |
probably damaging |
Het |
Dck |
T |
C |
5: 88,929,080 (GRCm39) |
V253A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,586,396 (GRCm39) |
S650P |
probably damaging |
Het |
Dicer1 |
G |
A |
12: 104,673,123 (GRCm39) |
P799S |
probably damaging |
Het |
Dst |
C |
T |
1: 34,228,200 (GRCm39) |
P1606L |
probably damaging |
Het |
Eya2 |
G |
A |
2: 165,611,157 (GRCm39) |
C477Y |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,756,503 (GRCm39) |
N498K |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 58,290,217 (GRCm39) |
|
probably null |
Het |
Gda |
A |
T |
19: 21,411,667 (GRCm39) |
F44I |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,768,119 (GRCm39) |
R703C |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,736,633 (GRCm39) |
L1960Q |
probably damaging |
Het |
Gramd1b |
T |
C |
9: 40,219,651 (GRCm39) |
D341G |
probably damaging |
Het |
Grid2 |
G |
T |
6: 63,480,419 (GRCm39) |
A78S |
probably benign |
Het |
Hao2 |
A |
T |
3: 98,790,876 (GRCm39) |
|
probably benign |
Het |
Hook3 |
A |
G |
8: 26,609,014 (GRCm39) |
V10A |
probably benign |
Het |
Kif20a |
A |
G |
18: 34,762,262 (GRCm39) |
E425G |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,403,252 (GRCm39) |
D2107G |
probably benign |
Het |
Lrriq3 |
T |
C |
3: 154,893,373 (GRCm39) |
I358T |
possibly damaging |
Het |
Mad2l2 |
A |
G |
4: 148,225,381 (GRCm39) |
D17G |
possibly damaging |
Het |
Mastl |
G |
T |
2: 23,023,358 (GRCm39) |
T455K |
probably benign |
Het |
Mkln1 |
G |
T |
6: 31,409,862 (GRCm39) |
|
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,387,947 (GRCm39) |
Y16N |
possibly damaging |
Het |
Mmp24 |
C |
T |
2: 155,634,517 (GRCm39) |
A79V |
probably benign |
Het |
Mrps35 |
T |
A |
6: 146,972,232 (GRCm39) |
C292S |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,427,643 (GRCm39) |
F1435L |
possibly damaging |
Het |
Nars2 |
C |
T |
7: 96,689,130 (GRCm39) |
H351Y |
probably damaging |
Het |
Nat2 |
A |
T |
8: 67,953,919 (GRCm39) |
I10F |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Olfm5 |
A |
T |
7: 103,803,076 (GRCm39) |
Y462* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,591,986 (GRCm39) |
H87Y |
probably damaging |
Het |
Or1j12 |
C |
A |
2: 36,342,660 (GRCm39) |
A21E |
probably benign |
Het |
Or2w3 |
C |
A |
11: 58,556,986 (GRCm39) |
F200L |
probably damaging |
Het |
Or4c122 |
C |
A |
2: 89,079,742 (GRCm39) |
E87* |
probably null |
Het |
Or5p70 |
T |
A |
7: 107,994,438 (GRCm39) |
I37N |
probably damaging |
Het |
Or7g35 |
T |
C |
9: 19,496,600 (GRCm39) |
S256P |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,789,111 (GRCm39) |
I213N |
probably damaging |
Het |
Or8g20 |
A |
T |
9: 39,396,284 (GRCm39) |
F85L |
probably benign |
Het |
Otog |
A |
T |
7: 45,900,819 (GRCm39) |
|
probably benign |
Het |
Pdcd2l |
A |
T |
7: 33,892,232 (GRCm39) |
D212E |
possibly damaging |
Het |
Pex5 |
T |
C |
6: 124,381,596 (GRCm39) |
N213S |
probably benign |
Het |
Pkn3 |
C |
T |
2: 29,971,146 (GRCm39) |
P238S |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,536 (GRCm39) |
I45K |
probably damaging |
Het |
Prl2b1 |
A |
T |
13: 27,574,723 (GRCm39) |
|
probably null |
Het |
Ptprb |
A |
T |
10: 116,204,712 (GRCm39) |
I1849L |
possibly damaging |
Het |
Rasal3 |
G |
T |
17: 32,612,500 (GRCm39) |
S787Y |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,532,177 (GRCm39) |
D596E |
possibly damaging |
Het |
Sdhd |
A |
T |
9: 50,515,064 (GRCm39) |
V9D |
possibly damaging |
Het |
Serinc5 |
T |
C |
13: 92,844,565 (GRCm39) |
S436P |
probably damaging |
Het |
Slc27a1 |
C |
T |
8: 72,036,808 (GRCm39) |
P348L |
probably damaging |
Het |
Slc28a2b |
A |
T |
2: 122,344,879 (GRCm39) |
I162F |
probably damaging |
Het |
Smg1 |
G |
A |
7: 117,759,606 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
A |
T |
9: 41,955,196 (GRCm39) |
|
probably benign |
Het |
Sprtn |
T |
A |
8: 125,626,957 (GRCm39) |
H112Q |
probably damaging |
Het |
Tasor2 |
A |
T |
13: 3,626,054 (GRCm39) |
F1299I |
probably benign |
Het |
Tet2 |
A |
G |
3: 133,173,363 (GRCm39) |
M1633T |
probably benign |
Het |
Tet2 |
T |
A |
3: 133,173,486 (GRCm39) |
D1592V |
probably benign |
Het |
Tmem68 |
A |
T |
4: 3,569,667 (GRCm39) |
C8S |
probably damaging |
Het |
Tnrc6a |
T |
A |
7: 122,771,039 (GRCm39) |
I943N |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,844,069 (GRCm39) |
V191D |
probably damaging |
Het |
Tsc22d4 |
T |
C |
5: 137,760,917 (GRCm39) |
S113P |
probably damaging |
Het |
Ttc21b |
T |
C |
2: 66,069,914 (GRCm39) |
R250G |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,278,174 (GRCm39) |
Y721C |
probably damaging |
Het |
Ubtfl1 |
A |
T |
9: 18,320,660 (GRCm39) |
I63F |
probably damaging |
Het |
Ush1c |
G |
A |
7: 45,874,332 (GRCm39) |
P171S |
probably benign |
Het |
Utp20 |
A |
T |
10: 88,603,323 (GRCm39) |
N1843K |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,074,253 (GRCm39) |
Y285H |
probably damaging |
Het |
Virma |
A |
G |
4: 11,498,769 (GRCm39) |
D70G |
probably damaging |
Het |
Vmn2r102 |
T |
C |
17: 19,898,277 (GRCm39) |
F431L |
probably benign |
Het |
Wdr17 |
A |
G |
8: 55,114,530 (GRCm39) |
I662T |
probably damaging |
Het |
Wdr87-ps |
T |
A |
7: 29,232,690 (GRCm39) |
|
noncoding transcript |
Het |
Zfp160 |
G |
A |
17: 21,247,268 (GRCm39) |
R606H |
probably benign |
Het |
Zfp369 |
C |
T |
13: 65,444,248 (GRCm39) |
R464C |
probably damaging |
Het |
|
Other mutations in Or4e1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01596:Or4e1
|
APN |
14 |
52,700,822 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02601:Or4e1
|
APN |
14 |
52,700,802 (GRCm39) |
nonsense |
probably null |
|
IGL02635:Or4e1
|
APN |
14 |
52,701,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R0139:Or4e1
|
UTSW |
14 |
52,700,669 (GRCm39) |
missense |
probably damaging |
0.98 |
R0501:Or4e1
|
UTSW |
14 |
52,701,383 (GRCm39) |
start codon destroyed |
possibly damaging |
0.79 |
R0612:Or4e1
|
UTSW |
14 |
52,701,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1691:Or4e1
|
UTSW |
14 |
52,701,288 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4290:Or4e1
|
UTSW |
14 |
52,701,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Or4e1
|
UTSW |
14 |
52,701,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Or4e1
|
UTSW |
14 |
52,700,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R5073:Or4e1
|
UTSW |
14 |
52,701,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Or4e1
|
UTSW |
14 |
52,701,311 (GRCm39) |
missense |
probably benign |
0.00 |
R5384:Or4e1
|
UTSW |
14 |
52,700,714 (GRCm39) |
missense |
probably benign |
0.41 |
R5663:Or4e1
|
UTSW |
14 |
52,701,052 (GRCm39) |
missense |
probably benign |
0.12 |
R5861:Or4e1
|
UTSW |
14 |
52,700,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:Or4e1
|
UTSW |
14 |
52,701,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7040:Or4e1
|
UTSW |
14 |
52,700,932 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7216:Or4e1
|
UTSW |
14 |
52,700,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Or4e1
|
UTSW |
14 |
52,700,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R8310:Or4e1
|
UTSW |
14 |
52,701,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Or4e1
|
UTSW |
14 |
52,701,358 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8942:Or4e1
|
UTSW |
14 |
52,700,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R9185:Or4e1
|
UTSW |
14 |
52,700,984 (GRCm39) |
missense |
probably benign |
0.33 |
R9218:Or4e1
|
UTSW |
14 |
52,700,788 (GRCm39) |
missense |
probably damaging |
0.97 |
R9516:Or4e1
|
UTSW |
14 |
52,700,873 (GRCm39) |
missense |
probably benign |
0.02 |
|