Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
G |
3: 59,843,771 (GRCm39) |
H155R |
possibly damaging |
Het |
Abca13 |
G |
T |
11: 9,244,559 (GRCm39) |
V2141L |
probably benign |
Het |
Adam17 |
T |
C |
12: 21,390,459 (GRCm39) |
|
probably benign |
Het |
Adam3 |
A |
T |
8: 25,185,331 (GRCm39) |
C456S |
probably damaging |
Het |
Aldh4a1 |
G |
T |
4: 139,369,882 (GRCm39) |
|
probably benign |
Het |
Anapc4 |
A |
G |
5: 52,999,359 (GRCm39) |
|
probably benign |
Het |
Ank3 |
A |
T |
10: 69,718,198 (GRCm39) |
Q483L |
probably damaging |
Het |
Ankle2 |
A |
G |
5: 110,389,925 (GRCm39) |
|
probably benign |
Het |
Ankrd13b |
T |
A |
11: 77,364,114 (GRCm39) |
T150S |
possibly damaging |
Het |
Apeh |
A |
G |
9: 107,964,254 (GRCm39) |
M524T |
probably benign |
Het |
Arl14epl |
T |
A |
18: 47,059,484 (GRCm39) |
|
probably null |
Het |
Atg2a |
T |
C |
19: 6,302,569 (GRCm39) |
F964S |
possibly damaging |
Het |
Atg2b |
C |
T |
12: 105,583,412 (GRCm39) |
V2050M |
probably damaging |
Het |
Atp2b4 |
A |
T |
1: 133,659,956 (GRCm39) |
|
probably benign |
Het |
Bbof1 |
T |
A |
12: 84,477,045 (GRCm39) |
S512T |
probably benign |
Het |
Camta1 |
C |
A |
4: 151,159,597 (GRCm39) |
R1614L |
probably damaging |
Het |
Car10 |
T |
C |
11: 93,381,408 (GRCm39) |
Y100H |
probably damaging |
Het |
Ccdc81 |
T |
A |
7: 89,542,504 (GRCm39) |
E124V |
probably damaging |
Het |
Cd84 |
A |
G |
1: 171,700,494 (GRCm39) |
T204A |
probably benign |
Het |
Celf2 |
A |
G |
2: 6,608,987 (GRCm39) |
S178P |
probably damaging |
Het |
Chat |
G |
A |
14: 32,130,976 (GRCm39) |
T555M |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,834,111 (GRCm39) |
F917S |
probably damaging |
Het |
Chrna2 |
C |
A |
14: 66,386,553 (GRCm39) |
T233N |
probably damaging |
Het |
Cnpy2 |
T |
C |
10: 128,162,054 (GRCm39) |
V109A |
probably benign |
Het |
Col4a1 |
T |
C |
8: 11,258,333 (GRCm39) |
|
probably null |
Het |
Csmd1 |
C |
T |
8: 15,982,529 (GRCm39) |
V2713M |
possibly damaging |
Het |
Cuedc1 |
G |
A |
11: 88,074,231 (GRCm39) |
R255Q |
probably damaging |
Het |
Cxcl15 |
A |
T |
5: 90,945,897 (GRCm39) |
|
probably benign |
Het |
Dach1 |
A |
T |
14: 98,138,765 (GRCm39) |
H559Q |
possibly damaging |
Het |
Dele1 |
T |
C |
18: 38,387,124 (GRCm39) |
|
probably null |
Het |
Dennd4c |
C |
T |
4: 86,744,259 (GRCm39) |
T1367M |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,102,372 (GRCm39) |
Y365* |
probably null |
Het |
Dicer1 |
T |
C |
12: 104,669,100 (GRCm39) |
Y1194C |
possibly damaging |
Het |
Dmxl1 |
C |
G |
18: 50,024,534 (GRCm39) |
S1736* |
probably null |
Het |
Dnah7a |
C |
T |
1: 53,536,285 (GRCm39) |
R2586K |
probably benign |
Het |
Dnajb8 |
T |
C |
6: 88,199,467 (GRCm39) |
M1T |
probably null |
Het |
Dync2h1 |
G |
A |
9: 7,122,692 (GRCm39) |
P2088L |
probably benign |
Het |
Eftud2 |
T |
G |
11: 102,735,048 (GRCm39) |
H617P |
probably damaging |
Het |
Ephb1 |
A |
G |
9: 101,873,179 (GRCm39) |
|
probably benign |
Het |
Fam184a |
G |
T |
10: 53,574,975 (GRCm39) |
H155Q |
probably benign |
Het |
Firrm |
T |
C |
1: 163,799,412 (GRCm39) |
|
probably null |
Het |
Ganc |
G |
T |
2: 120,278,882 (GRCm39) |
E700* |
probably null |
Het |
Gm10912 |
A |
G |
2: 103,897,290 (GRCm39) |
|
probably benign |
Het |
Haus5 |
A |
T |
7: 30,358,492 (GRCm39) |
I294N |
probably damaging |
Het |
Hmgcr |
G |
T |
13: 96,796,651 (GRCm39) |
|
probably null |
Het |
Hr |
T |
A |
14: 70,799,352 (GRCm39) |
C641* |
probably null |
Het |
Itga10 |
A |
G |
3: 96,565,490 (GRCm39) |
N1038S |
probably damaging |
Het |
Itgb1bp1 |
T |
G |
12: 21,321,436 (GRCm39) |
Y172S |
probably damaging |
Het |
Kprp |
T |
C |
3: 92,732,030 (GRCm39) |
N340S |
probably damaging |
Het |
Kremen1 |
A |
G |
11: 5,165,447 (GRCm39) |
I41T |
probably damaging |
Het |
Krt6b |
A |
G |
15: 101,586,042 (GRCm39) |
|
probably benign |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Ldhd |
A |
G |
8: 112,356,309 (GRCm39) |
Y86H |
probably benign |
Het |
Lilra6 |
A |
T |
7: 3,915,784 (GRCm39) |
I76N |
possibly damaging |
Het |
Mak |
T |
C |
13: 41,199,743 (GRCm39) |
T299A |
probably benign |
Het |
Med25 |
A |
G |
7: 44,534,502 (GRCm39) |
|
probably null |
Het |
Mpg |
A |
T |
11: 32,180,039 (GRCm39) |
N189I |
probably damaging |
Het |
Mroh8 |
A |
G |
2: 157,071,838 (GRCm39) |
Y556H |
probably damaging |
Het |
Myh8 |
T |
A |
11: 67,175,333 (GRCm39) |
S294T |
probably benign |
Het |
Myom1 |
T |
A |
17: 71,391,312 (GRCm39) |
D842E |
probably benign |
Het |
Myorg |
A |
G |
4: 41,498,538 (GRCm39) |
F364S |
probably damaging |
Het |
Nat2 |
C |
T |
8: 67,953,982 (GRCm39) |
Q31* |
probably null |
Het |
Nf1 |
T |
A |
11: 79,329,595 (GRCm39) |
M653K |
probably benign |
Het |
Nhs |
C |
A |
X: 160,620,355 (GRCm39) |
R1467I |
probably damaging |
Het |
Npr2 |
A |
G |
4: 43,632,801 (GRCm39) |
E206G |
probably benign |
Het |
Nsd3 |
G |
A |
8: 26,168,732 (GRCm39) |
G629D |
possibly damaging |
Het |
Nwd1 |
G |
A |
8: 73,408,633 (GRCm39) |
C831Y |
probably damaging |
Het |
Or5t9 |
A |
G |
2: 86,659,950 (GRCm39) |
I285V |
probably benign |
Het |
P2ry14 |
A |
G |
3: 59,023,449 (GRCm39) |
S4P |
possibly damaging |
Het |
Parp4 |
A |
G |
14: 56,873,172 (GRCm39) |
|
probably benign |
Het |
Pate14 |
A |
T |
9: 36,549,873 (GRCm39) |
|
probably null |
Het |
Pclo |
A |
G |
5: 14,728,299 (GRCm39) |
|
probably benign |
Het |
Pclo |
T |
C |
5: 14,729,412 (GRCm39) |
|
probably benign |
Het |
Pcnt |
A |
T |
10: 76,240,429 (GRCm39) |
S1202T |
possibly damaging |
Het |
Pfkfb4 |
A |
G |
9: 108,856,825 (GRCm39) |
Y412C |
probably damaging |
Het |
Pgm2 |
T |
A |
5: 64,267,898 (GRCm39) |
V449D |
probably damaging |
Het |
Poldip3 |
T |
A |
15: 83,022,436 (GRCm39) |
D116V |
probably damaging |
Het |
Pom121 |
G |
T |
5: 135,410,686 (GRCm39) |
Q824K |
unknown |
Het |
Prkdc |
G |
T |
16: 15,649,146 (GRCm39) |
G3707* |
probably null |
Het |
Prr14l |
T |
C |
5: 33,001,560 (GRCm39) |
|
probably benign |
Het |
Ptbp2 |
T |
G |
3: 119,514,613 (GRCm39) |
I405L |
probably benign |
Het |
Rad21l |
A |
T |
2: 151,490,989 (GRCm39) |
|
probably benign |
Het |
Rbm6 |
G |
A |
9: 107,724,488 (GRCm39) |
Q488* |
probably null |
Het |
Rdh1 |
T |
A |
10: 127,600,652 (GRCm39) |
M225K |
probably benign |
Het |
Recql5 |
T |
C |
11: 115,819,209 (GRCm39) |
D119G |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Robo1 |
T |
C |
16: 72,810,013 (GRCm39) |
|
probably null |
Het |
Samd12 |
G |
A |
15: 53,723,567 (GRCm39) |
T42I |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,442,766 (GRCm39) |
M1494K |
probably damaging |
Het |
Sec31a |
G |
A |
5: 100,523,099 (GRCm39) |
P864L |
probably benign |
Het |
Senp2 |
T |
C |
16: 21,855,320 (GRCm39) |
V344A |
probably benign |
Het |
Serpina5 |
G |
A |
12: 104,069,621 (GRCm39) |
D278N |
probably benign |
Het |
Sh3tc1 |
A |
T |
5: 35,860,806 (GRCm39) |
V1017D |
probably damaging |
Het |
Sin3a |
T |
A |
9: 57,004,179 (GRCm39) |
Y310* |
probably null |
Het |
Slc25a32 |
T |
C |
15: 38,960,940 (GRCm39) |
T248A |
probably benign |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Slc4a10 |
G |
A |
2: 62,117,206 (GRCm39) |
V722M |
probably damaging |
Het |
Slco1a4 |
A |
G |
6: 141,776,586 (GRCm39) |
|
probably benign |
Het |
Smg6 |
T |
A |
11: 74,819,884 (GRCm39) |
Y52N |
probably damaging |
Het |
Sncb |
T |
G |
13: 54,913,400 (GRCm39) |
T33P |
probably damaging |
Het |
Spef2 |
A |
G |
15: 9,584,070 (GRCm39) |
|
probably null |
Het |
Spmip1 |
G |
T |
6: 29,478,169 (GRCm39) |
|
probably benign |
Het |
Sugp1 |
A |
G |
8: 70,512,013 (GRCm39) |
E203G |
probably damaging |
Het |
Suv39h2 |
A |
T |
2: 3,473,616 (GRCm39) |
C105S |
probably damaging |
Het |
Tlr1 |
A |
T |
5: 65,083,963 (GRCm39) |
F205I |
probably damaging |
Het |
Tnip1 |
A |
T |
11: 54,808,699 (GRCm39) |
M496K |
probably damaging |
Het |
Tnxb |
G |
A |
17: 34,937,219 (GRCm39) |
E2889K |
probably damaging |
Het |
Trim30b |
T |
A |
7: 104,015,010 (GRCm39) |
H126L |
possibly damaging |
Het |
Trpm7 |
A |
T |
2: 126,668,638 (GRCm39) |
Y759* |
probably null |
Het |
Ttc17 |
A |
G |
2: 94,153,465 (GRCm39) |
I1000T |
possibly damaging |
Het |
Ttc27 |
A |
T |
17: 75,025,710 (GRCm39) |
N61I |
probably benign |
Het |
Uba6 |
T |
C |
5: 86,260,609 (GRCm39) |
Y990C |
probably damaging |
Het |
Vav3 |
A |
G |
3: 109,571,756 (GRCm39) |
|
probably benign |
Het |
Vmn2r55 |
C |
T |
7: 12,404,945 (GRCm39) |
A153T |
possibly damaging |
Het |
Wars2 |
A |
G |
3: 99,123,865 (GRCm39) |
D242G |
probably damaging |
Het |
Xylt2 |
G |
A |
11: 94,560,762 (GRCm39) |
Q259* |
probably null |
Het |
Zfp27 |
G |
A |
7: 29,593,947 (GRCm39) |
P673S |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,378,309 (GRCm39) |
I1023T |
possibly damaging |
Het |
|
Other mutations in Or52r1c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01618:Or52r1c
|
APN |
7 |
102,735,582 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02113:Or52r1c
|
APN |
7 |
102,735,057 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02398:Or52r1c
|
APN |
7 |
102,735,313 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02718:Or52r1c
|
APN |
7 |
102,734,790 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02941:Or52r1c
|
APN |
7 |
102,735,528 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02942:Or52r1c
|
APN |
7 |
102,735,405 (GRCm39) |
missense |
probably benign |
0.07 |
R0496:Or52r1c
|
UTSW |
7 |
102,734,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R0646:Or52r1c
|
UTSW |
7 |
102,735,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R1652:Or52r1c
|
UTSW |
7 |
102,735,013 (GRCm39) |
missense |
probably benign |
0.04 |
R2312:Or52r1c
|
UTSW |
7 |
102,735,633 (GRCm39) |
missense |
probably damaging |
0.99 |
R2849:Or52r1c
|
UTSW |
7 |
102,735,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Or52r1c
|
UTSW |
7 |
102,735,548 (GRCm39) |
missense |
probably benign |
0.01 |
R3176:Or52r1c
|
UTSW |
7 |
102,734,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Or52r1c
|
UTSW |
7 |
102,734,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R3708:Or52r1c
|
UTSW |
7 |
102,735,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4737:Or52r1c
|
UTSW |
7 |
102,735,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Or52r1c
|
UTSW |
7 |
102,735,664 (GRCm39) |
missense |
probably benign |
0.00 |
R5172:Or52r1c
|
UTSW |
7 |
102,734,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R5849:Or52r1c
|
UTSW |
7 |
102,734,728 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R6294:Or52r1c
|
UTSW |
7 |
102,734,874 (GRCm39) |
missense |
probably benign |
0.01 |
R6846:Or52r1c
|
UTSW |
7 |
102,735,265 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6869:Or52r1c
|
UTSW |
7 |
102,735,075 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6936:Or52r1c
|
UTSW |
7 |
102,735,021 (GRCm39) |
missense |
probably damaging |
0.97 |
R7133:Or52r1c
|
UTSW |
7 |
102,735,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R7724:Or52r1c
|
UTSW |
7 |
102,735,470 (GRCm39) |
nonsense |
probably null |
|
R7772:Or52r1c
|
UTSW |
7 |
102,735,388 (GRCm39) |
missense |
probably benign |
0.23 |
R9341:Or52r1c
|
UTSW |
7 |
102,735,324 (GRCm39) |
nonsense |
probably null |
|
R9343:Or52r1c
|
UTSW |
7 |
102,735,324 (GRCm39) |
nonsense |
probably null |
|
R9718:Or52r1c
|
UTSW |
7 |
102,735,196 (GRCm39) |
missense |
probably benign |
0.00 |
R9752:Or52r1c
|
UTSW |
7 |
102,735,669 (GRCm39) |
missense |
probably benign |
0.03 |
|