Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c12 |
C |
T |
13: 4,320,155 (GRCm39) |
|
probably benign |
Het |
Ap3b1 |
T |
A |
13: 94,664,725 (GRCm39) |
M888K |
unknown |
Het |
Arhgap23 |
T |
A |
11: 97,391,641 (GRCm39) |
V223E |
probably damaging |
Het |
Atm |
C |
T |
9: 53,410,497 (GRCm39) |
W1028* |
probably null |
Het |
Atp7b |
A |
G |
8: 22,518,334 (GRCm39) |
V168A |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Caskin1 |
C |
T |
17: 24,723,774 (GRCm39) |
A854V |
probably benign |
Het |
Cdcp1 |
T |
C |
9: 123,019,027 (GRCm39) |
N84S |
probably benign |
Het |
Cdh20 |
T |
A |
1: 110,027,009 (GRCm39) |
I475N |
probably damaging |
Het |
Ciz1 |
A |
T |
2: 32,255,848 (GRCm39) |
Y107F |
probably benign |
Het |
Creb3l4 |
T |
C |
3: 90,145,199 (GRCm39) |
N318D |
probably benign |
Het |
Dmrt3 |
G |
A |
19: 25,588,550 (GRCm39) |
A130T |
probably benign |
Het |
Dmxl1 |
A |
T |
18: 50,088,937 (GRCm39) |
K2805N |
probably damaging |
Het |
Dusp15 |
T |
A |
2: 152,788,209 (GRCm39) |
I63F |
probably damaging |
Het |
Dync2h1 |
T |
C |
9: 7,035,063 (GRCm39) |
Q3462R |
probably benign |
Het |
Evpl |
A |
G |
11: 116,120,232 (GRCm39) |
C569R |
probably benign |
Het |
Fmnl3 |
A |
T |
15: 99,219,322 (GRCm39) |
M766K |
possibly damaging |
Het |
G6pc2 |
A |
G |
2: 69,057,140 (GRCm39) |
N262S |
probably damaging |
Het |
Galk1 |
A |
T |
11: 115,899,762 (GRCm39) |
L325Q |
probably damaging |
Het |
H3c3 |
T |
C |
13: 23,929,108 (GRCm39) |
I125V |
probably benign |
Het |
Hr |
G |
A |
14: 70,795,510 (GRCm39) |
G352R |
probably damaging |
Het |
Il12b |
A |
T |
11: 44,294,864 (GRCm39) |
M1L |
not run |
Het |
Lpar6 |
A |
T |
14: 73,476,950 (GRCm39) |
M304L |
probably benign |
Het |
Mpeg1 |
G |
A |
19: 12,439,291 (GRCm39) |
A250T |
probably benign |
Het |
Mtcl3 |
T |
C |
10: 29,072,721 (GRCm39) |
I671T |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,180,863 (GRCm39) |
K1221R |
probably benign |
Het |
Ogfrl1 |
T |
A |
1: 23,409,399 (GRCm39) |
I276F |
probably damaging |
Het |
Or4f62 |
A |
G |
2: 111,986,869 (GRCm39) |
D191G |
possibly damaging |
Het |
Or4x12-ps1 |
T |
C |
2: 89,916,631 (GRCm39) |
Y58C |
probably damaging |
Het |
Oxr1 |
A |
G |
15: 41,574,260 (GRCm39) |
N2S |
probably benign |
Het |
P3h3 |
G |
A |
6: 124,822,940 (GRCm39) |
R505C |
probably damaging |
Het |
Pcdhb16 |
A |
T |
18: 37,612,392 (GRCm39) |
I451F |
possibly damaging |
Het |
Pet117 |
C |
A |
2: 144,215,122 (GRCm39) |
D36E |
probably benign |
Het |
Prf1 |
T |
C |
10: 61,138,948 (GRCm39) |
V302A |
probably damaging |
Het |
Prkdc |
G |
A |
16: 15,601,029 (GRCm39) |
A2897T |
possibly damaging |
Het |
Prkra |
A |
G |
2: 76,460,879 (GRCm39) |
L273P |
probably damaging |
Het |
Prr30 |
T |
A |
14: 101,436,365 (GRCm39) |
T66S |
probably benign |
Het |
Slc29a4 |
A |
G |
5: 142,700,819 (GRCm39) |
Y188C |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,122,425 (GRCm39) |
K297* |
probably null |
Het |
Tcof1 |
G |
C |
18: 60,962,123 (GRCm39) |
A702G |
possibly damaging |
Het |
Tmem100 |
G |
A |
11: 89,926,574 (GRCm39) |
A134T |
probably damaging |
Het |
Tmem132c |
A |
G |
5: 127,437,003 (GRCm39) |
D164G |
possibly damaging |
Het |
Tnfsf18 |
A |
G |
1: 161,331,047 (GRCm39) |
T66A |
possibly damaging |
Het |
Ubr4 |
C |
T |
4: 139,129,935 (GRCm39) |
T685I |
probably damaging |
Het |
Uck1 |
T |
C |
2: 32,146,524 (GRCm39) |
Y185C |
|
Het |
Umod |
T |
A |
7: 119,070,639 (GRCm39) |
I418F |
probably benign |
Het |
Upp1 |
A |
T |
11: 9,079,561 (GRCm39) |
S41C |
probably damaging |
Het |
Vmn1r168 |
A |
T |
7: 23,240,428 (GRCm39) |
Y95F |
probably benign |
Het |
Vmn1r180 |
G |
T |
7: 23,652,415 (GRCm39) |
D193Y |
probably damaging |
Het |
Vmn2r11 |
A |
G |
5: 109,195,319 (GRCm39) |
V669A |
probably damaging |
Het |
Vmn2r55 |
T |
A |
7: 12,385,796 (GRCm39) |
Y728F |
probably damaging |
Het |
Vmn2r78 |
A |
G |
7: 86,603,513 (GRCm39) |
T564A |
possibly damaging |
Het |
Vps13d |
T |
A |
4: 144,865,183 (GRCm39) |
N2057I |
|
Het |
Wdfy3 |
C |
T |
5: 102,030,446 (GRCm39) |
R2354Q |
probably damaging |
Het |
Wdr77 |
T |
A |
3: 105,866,975 (GRCm39) |
C26S |
probably damaging |
Het |
Yif1b |
C |
T |
7: 28,946,690 (GRCm39) |
A267V |
probably benign |
Het |
Zfp316 |
A |
G |
5: 143,248,565 (GRCm39) |
V227A |
unknown |
Het |
Zfp600 |
T |
A |
4: 146,133,151 (GRCm39) |
H606Q |
unknown |
Het |
Zfp804a |
T |
C |
2: 82,087,919 (GRCm39) |
W583R |
probably benign |
Het |
Zfp961 |
T |
C |
8: 72,719,686 (GRCm39) |
W39R |
probably damaging |
Het |
Zfp990 |
T |
A |
4: 145,264,156 (GRCm39) |
C385S |
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 |
IGL02550:Or4k37
|
APN |
2 |
111,158,845 (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 |
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 |
|