Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadl |
A |
G |
1: 66,884,325 (GRCm39) |
|
probably null |
Het |
Acer3 |
G |
A |
7: 97,873,185 (GRCm39) |
T171I |
probably benign |
Het |
Acsm2 |
C |
T |
7: 119,172,507 (GRCm39) |
P117S |
probably damaging |
Het |
Anxa2 |
A |
G |
9: 69,374,588 (GRCm39) |
S22G |
probably benign |
Het |
Arrb2 |
T |
C |
11: 70,327,696 (GRCm39) |
I120T |
probably damaging |
Het |
Atp11a |
G |
T |
8: 12,866,997 (GRCm39) |
K141N |
possibly damaging |
Het |
Casd1 |
T |
C |
6: 4,642,009 (GRCm39) |
V762A |
probably benign |
Het |
Ccdc61 |
A |
T |
7: 18,627,227 (GRCm39) |
S48T |
probably benign |
Het |
Cntn2 |
T |
C |
1: 132,456,801 (GRCm39) |
M82V |
probably null |
Het |
Cobll1 |
A |
G |
2: 64,938,207 (GRCm39) |
S359P |
probably damaging |
Het |
Ctnnbl1 |
C |
A |
2: 157,726,055 (GRCm39) |
D465E |
probably benign |
Het |
Def6 |
A |
T |
17: 28,447,235 (GRCm39) |
E622V |
probably benign |
Het |
Dmgdh |
T |
C |
13: 93,854,083 (GRCm39) |
Y678H |
probably damaging |
Het |
Dock9 |
A |
T |
14: 121,935,724 (GRCm39) |
M1K |
probably null |
Het |
Esyt1 |
T |
C |
10: 128,357,962 (GRCm39) |
K216E |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,156,017 (GRCm39) |
D545G |
probably benign |
Het |
Galnt12 |
A |
T |
4: 47,104,126 (GRCm39) |
D128V |
possibly damaging |
Het |
Gm1110 |
C |
T |
9: 26,793,130 (GRCm39) |
V549I |
probably benign |
Het |
Gm7361 |
A |
G |
5: 26,466,120 (GRCm39) |
I161V |
possibly damaging |
Het |
Gsn |
T |
C |
2: 35,172,619 (GRCm39) |
|
probably benign |
Het |
Gvin3 |
A |
T |
7: 106,200,846 (GRCm39) |
|
noncoding transcript |
Het |
Il16 |
T |
A |
7: 83,323,704 (GRCm39) |
Q282L |
possibly damaging |
Het |
Il3ra |
A |
G |
14: 14,348,055 (GRCm38) |
D67G |
probably benign |
Het |
Insrr |
T |
C |
3: 87,711,805 (GRCm39) |
L515P |
probably damaging |
Het |
Jhy |
A |
G |
9: 40,828,466 (GRCm39) |
F480S |
probably benign |
Het |
Klc4 |
C |
A |
17: 46,947,836 (GRCm39) |
|
probably null |
Het |
Klhl12 |
G |
T |
1: 134,395,443 (GRCm39) |
C135F |
possibly damaging |
Het |
Ly6m |
T |
G |
15: 74,752,604 (GRCm39) |
H24P |
probably damaging |
Het |
Mboat7 |
G |
T |
7: 3,686,905 (GRCm39) |
|
probably null |
Het |
Myo1f |
G |
A |
17: 33,807,116 (GRCm39) |
D522N |
probably damaging |
Het |
Myo1f |
A |
G |
17: 33,799,124 (GRCm39) |
|
probably benign |
Het |
Nbea |
C |
A |
3: 55,926,835 (GRCm39) |
M789I |
probably damaging |
Het |
Ncapd2 |
T |
C |
6: 125,154,410 (GRCm39) |
D602G |
probably benign |
Het |
Ncaph2 |
A |
T |
15: 89,254,064 (GRCm39) |
K344* |
probably null |
Het |
Nek2 |
A |
G |
1: 191,554,371 (GRCm39) |
Y70C |
probably damaging |
Het |
Or2t1 |
T |
C |
14: 14,328,423 (GRCm38) |
L104P |
possibly damaging |
Het |
Or4k35 |
T |
A |
2: 111,100,349 (GRCm39) |
D121V |
probably damaging |
Het |
Or5ak22 |
G |
A |
2: 85,230,166 (GRCm39) |
A237V |
probably damaging |
Het |
Or7e166 |
C |
A |
9: 19,624,343 (GRCm39) |
F73L |
possibly damaging |
Het |
Or8g35 |
T |
A |
9: 39,381,842 (GRCm39) |
Y60F |
probably benign |
Het |
Plcb3 |
T |
A |
19: 6,937,544 (GRCm39) |
K625* |
probably null |
Het |
Plrg1 |
T |
C |
3: 82,968,430 (GRCm39) |
|
probably null |
Het |
Ptpn12 |
A |
G |
5: 21,203,137 (GRCm39) |
V547A |
probably benign |
Het |
Ralgapb |
A |
G |
2: 158,290,331 (GRCm39) |
D748G |
probably damaging |
Het |
Rcbtb2 |
A |
G |
14: 73,399,459 (GRCm39) |
E41G |
probably damaging |
Het |
Rela |
G |
T |
19: 5,691,534 (GRCm39) |
R236L |
possibly damaging |
Het |
Rps6kc1 |
A |
G |
1: 190,604,059 (GRCm39) |
S188P |
probably damaging |
Het |
Sipa1l1 |
A |
T |
12: 82,487,723 (GRCm39) |
K1666* |
probably null |
Het |
Slco1a1 |
C |
T |
6: 141,889,191 (GRCm39) |
M40I |
probably benign |
Het |
Smarca4 |
C |
A |
9: 21,597,418 (GRCm39) |
P1391Q |
probably benign |
Het |
Stra6 |
A |
G |
9: 58,057,366 (GRCm39) |
N392S |
possibly damaging |
Het |
Syt4 |
A |
G |
18: 31,577,246 (GRCm39) |
I36T |
probably damaging |
Het |
Tgfbr2 |
A |
T |
9: 115,939,197 (GRCm39) |
M235K |
probably benign |
Het |
Tmem87a |
T |
A |
2: 120,204,966 (GRCm39) |
|
probably null |
Het |
Tmf1 |
T |
C |
6: 97,135,522 (GRCm39) |
D918G |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,412,535 (GRCm39) |
Y312C |
probably damaging |
Het |
Usp47 |
C |
T |
7: 111,703,561 (GRCm39) |
R1178C |
probably damaging |
Het |
Vmn2r95 |
T |
A |
17: 18,671,994 (GRCm39) |
I577N |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,572,242 (GRCm39) |
V953A |
probably benign |
Het |
Wasl |
A |
G |
6: 24,633,883 (GRCm39) |
F127S |
probably damaging |
Het |
Wdr1 |
C |
T |
5: 38,698,206 (GRCm39) |
V192I |
probably damaging |
Het |
Wnt9a |
C |
T |
11: 59,221,744 (GRCm39) |
T214I |
probably damaging |
Het |
Xpo5 |
A |
G |
17: 46,540,255 (GRCm39) |
D693G |
probably benign |
Het |
Zan |
A |
G |
5: 137,385,301 (GRCm39) |
L5044P |
unknown |
Het |
Zhx3 |
T |
C |
2: 160,623,216 (GRCm39) |
N317S |
probably damaging |
Het |
|
Other mutations in Or4k37 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02426:Or4k37
|
APN |
2 |
111,158,920 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02553:Or4k37
|
APN |
2 |
111,159,333 (GRCm39) |
missense |
probably benign |
|
IGL02719:Or4k37
|
APN |
2 |
111,159,590 (GRCm39) |
nonsense |
probably null |
|
IGL02750:Or4k37
|
APN |
2 |
111,159,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02873:Or4k37
|
APN |
2 |
111,159,217 (GRCm39) |
missense |
probably benign |
|
IGL03252:Or4k37
|
APN |
2 |
111,159,125 (GRCm39) |
nonsense |
probably null |
|
IGL03375:Or4k37
|
APN |
2 |
111,159,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Or4k37
|
UTSW |
2 |
111,158,870 (GRCm39) |
nonsense |
probably null |
|
R0368:Or4k37
|
UTSW |
2 |
111,159,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R0497:Or4k37
|
UTSW |
2 |
111,159,175 (GRCm39) |
missense |
probably benign |
0.00 |
R0505:Or4k37
|
UTSW |
2 |
111,159,673 (GRCm39) |
missense |
probably benign |
0.00 |
R1557:Or4k37
|
UTSW |
2 |
111,158,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Or4k37
|
UTSW |
2 |
111,159,306 (GRCm39) |
missense |
probably benign |
0.02 |
R1691:Or4k37
|
UTSW |
2 |
111,159,198 (GRCm39) |
missense |
probably benign |
0.03 |
R2286:Or4k37
|
UTSW |
2 |
111,159,252 (GRCm39) |
missense |
probably benign |
0.01 |
R4230:Or4k37
|
UTSW |
2 |
111,159,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4274:Or4k37
|
UTSW |
2 |
111,159,160 (GRCm39) |
missense |
probably damaging |
0.98 |
R4305:Or4k37
|
UTSW |
2 |
111,159,643 (GRCm39) |
missense |
probably null |
0.82 |
R4495:Or4k37
|
UTSW |
2 |
111,159,365 (GRCm39) |
missense |
probably benign |
0.08 |
R5307:Or4k37
|
UTSW |
2 |
111,158,741 (GRCm39) |
splice site |
probably null |
|
R6115:Or4k37
|
UTSW |
2 |
111,159,558 (GRCm39) |
missense |
probably benign |
0.03 |
R6615:Or4k37
|
UTSW |
2 |
111,159,457 (GRCm39) |
missense |
probably benign |
0.00 |
R7169:Or4k37
|
UTSW |
2 |
111,158,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7601:Or4k37
|
UTSW |
2 |
111,159,565 (GRCm39) |
missense |
probably benign |
0.12 |
R8267:Or4k37
|
UTSW |
2 |
111,159,160 (GRCm39) |
missense |
probably benign |
0.22 |
R8447:Or4k37
|
UTSW |
2 |
111,159,307 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8749:Or4k37
|
UTSW |
2 |
111,158,817 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8795:Or4k37
|
UTSW |
2 |
111,158,881 (GRCm39) |
nonsense |
probably null |
|
R9269:Or4k37
|
UTSW |
2 |
111,159,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R9598:Or4k37
|
UTSW |
2 |
111,159,633 (GRCm39) |
nonsense |
probably null |
|
R9679:Or4k37
|
UTSW |
2 |
111,159,345 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Or4k37
|
UTSW |
2 |
111,159,170 (GRCm39) |
missense |
probably benign |
0.03 |
|