Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,775,677 (GRCm39) |
V1622D |
probably damaging |
Het |
Acadsb |
C |
T |
7: 131,033,763 (GRCm39) |
T260I |
probably damaging |
Het |
Acap2 |
A |
T |
16: 30,955,392 (GRCm39) |
V161E |
probably damaging |
Het |
Alk |
T |
C |
17: 72,181,190 (GRCm39) |
T1367A |
probably damaging |
Het |
Atg2a |
A |
C |
19: 6,291,905 (GRCm39) |
H27P |
probably damaging |
Het |
Atp2c1 |
C |
T |
9: 105,336,858 (GRCm39) |
|
probably null |
Het |
C1s1 |
T |
G |
6: 124,508,362 (GRCm39) |
K542N |
probably damaging |
Het |
Camk1d |
A |
G |
2: 5,303,901 (GRCm39) |
S351P |
probably benign |
Het |
Carf |
C |
A |
1: 60,148,558 (GRCm39) |
Q85K |
possibly damaging |
Het |
Caskin2 |
T |
C |
11: 115,698,683 (GRCm39) |
N43S |
probably damaging |
Het |
Cd40 |
T |
C |
2: 164,905,465 (GRCm39) |
C161R |
probably damaging |
Het |
Cdh19 |
A |
G |
1: 110,877,111 (GRCm39) |
F76S |
probably damaging |
Het |
Cdkl1 |
T |
C |
12: 69,794,100 (GRCm39) |
N346D |
probably benign |
Het |
Cdon |
A |
G |
9: 35,381,230 (GRCm39) |
D540G |
probably benign |
Het |
Cep164 |
T |
A |
9: 45,691,060 (GRCm39) |
E379V |
probably damaging |
Het |
Clock |
T |
C |
5: 76,377,256 (GRCm39) |
N681S |
probably benign |
Het |
Col15a1 |
G |
C |
4: 47,288,200 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
T |
G |
9: 105,808,152 (GRCm39) |
K965N |
unknown |
Het |
Dctn4 |
T |
A |
18: 60,659,304 (GRCm39) |
M1K |
probably null |
Het |
Dhx30 |
T |
C |
9: 109,915,750 (GRCm39) |
D741G |
probably damaging |
Het |
Dhx37 |
A |
G |
5: 125,507,958 (GRCm39) |
V104A |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,571,255 (GRCm39) |
K2788R |
possibly damaging |
Het |
Egfr |
T |
A |
11: 16,855,410 (GRCm39) |
D898E |
probably damaging |
Het |
Eif2ak4 |
G |
C |
2: 118,271,701 (GRCm39) |
|
probably null |
Het |
Eif6 |
A |
G |
2: 155,665,852 (GRCm39) |
L101P |
probably damaging |
Het |
Etaa1 |
A |
T |
11: 17,896,419 (GRCm39) |
V566E |
probably damaging |
Het |
Far2 |
C |
T |
6: 148,060,418 (GRCm39) |
T257I |
probably benign |
Het |
Fuca2 |
G |
A |
10: 13,390,563 (GRCm39) |
W453* |
probably null |
Het |
Galntl6 |
A |
T |
8: 58,310,590 (GRCm39) |
Y370* |
probably null |
Het |
Gcn1 |
T |
C |
5: 115,719,867 (GRCm39) |
V374A |
probably benign |
Het |
Hjv |
T |
C |
3: 96,435,881 (GRCm39) |
F380L |
probably benign |
Het |
Hycc2 |
T |
C |
1: 58,591,361 (GRCm39) |
D94G |
probably damaging |
Het |
Ifi202b |
A |
T |
1: 173,804,949 (GRCm39) |
M1K |
probably null |
Het |
Lama4 |
A |
G |
10: 38,950,688 (GRCm39) |
Y997C |
probably damaging |
Het |
Lepr |
T |
A |
4: 101,602,798 (GRCm39) |
C195* |
probably null |
Het |
Lrrc37 |
T |
A |
11: 103,508,263 (GRCm39) |
H1235L |
unknown |
Het |
Lrrc73 |
T |
C |
17: 46,565,535 (GRCm39) |
S89P |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,367,582 (GRCm39) |
E2393G |
probably damaging |
Het |
Mdga2 |
T |
A |
12: 66,517,481 (GRCm39) |
T118S |
possibly damaging |
Het |
Msantd5f3 |
T |
C |
4: 73,575,373 (GRCm39) |
S351P |
probably damaging |
Het |
Mtf2 |
A |
G |
5: 108,234,949 (GRCm39) |
K124R |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,399,075 (GRCm39) |
Y339H |
unknown |
Het |
Nes |
G |
A |
3: 87,887,012 (GRCm39) |
G1757E |
probably damaging |
Het |
Nfatc4 |
A |
T |
14: 56,064,685 (GRCm39) |
I391F |
probably damaging |
Het |
Nup93 |
A |
T |
8: 94,954,371 (GRCm39) |
I23F |
probably benign |
Het |
Or5h17 |
T |
G |
16: 58,820,083 (GRCm39) |
F12V |
probably damaging |
Het |
Or6y1 |
A |
C |
1: 174,276,923 (GRCm39) |
T245P |
probably damaging |
Het |
Or7g16 |
G |
T |
9: 18,726,742 (GRCm39) |
Q283K |
probably damaging |
Het |
Or9i14 |
A |
T |
19: 13,792,388 (GRCm39) |
C189S |
probably damaging |
Het |
Pak5 |
A |
C |
2: 135,943,126 (GRCm39) |
M338R |
probably benign |
Het |
Papola |
A |
G |
12: 105,766,032 (GRCm39) |
E44G |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,479,455 (GRCm39) |
E522V |
probably benign |
Het |
Peli2 |
A |
G |
14: 48,518,927 (GRCm39) |
E225G |
probably benign |
Het |
Pla2g1b |
T |
G |
5: 115,612,595 (GRCm39) |
I117S |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,943,469 (GRCm39) |
Q1246K |
probably benign |
Het |
Pole |
A |
G |
5: 110,480,288 (GRCm39) |
E1953G |
probably benign |
Het |
Pus7l |
T |
C |
15: 94,431,445 (GRCm39) |
I395V |
probably benign |
Het |
Shisa7 |
T |
G |
7: 4,837,333 (GRCm39) |
D244A |
probably damaging |
Het |
Slco3a1 |
T |
C |
7: 73,952,946 (GRCm39) |
T538A |
probably benign |
Het |
Syk |
T |
A |
13: 52,766,480 (GRCm39) |
N188K |
probably benign |
Het |
Tcf20 |
A |
G |
15: 82,740,705 (GRCm39) |
S249P |
probably benign |
Het |
Tmem25 |
T |
C |
9: 44,709,529 (GRCm39) |
T91A |
possibly damaging |
Het |
Trank1 |
T |
C |
9: 111,221,579 (GRCm39) |
V2772A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,596,447 (GRCm39) |
Y20155* |
probably null |
Het |
Uchl4 |
C |
T |
9: 64,142,986 (GRCm39) |
H156Y |
probably benign |
Het |
Ulbp1 |
A |
T |
10: 7,396,392 (GRCm39) |
L295Q |
unknown |
Het |
Vwf |
G |
A |
6: 125,581,254 (GRCm39) |
A631T |
|
Het |
Zfp810 |
C |
T |
9: 22,189,936 (GRCm39) |
C324Y |
probably damaging |
Het |
Zswim8 |
T |
C |
14: 20,761,908 (GRCm39) |
L227P |
probably damaging |
Het |
|
Other mutations in Or4a27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01109:Or4a27
|
APN |
2 |
88,559,409 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01515:Or4a27
|
APN |
2 |
88,559,352 (GRCm39) |
missense |
probably benign |
|
IGL01822:Or4a27
|
APN |
2 |
88,559,136 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02060:Or4a27
|
APN |
2 |
88,559,907 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02466:Or4a27
|
APN |
2 |
88,559,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02698:Or4a27
|
APN |
2 |
88,559,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R0336:Or4a27
|
UTSW |
2 |
88,559,498 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1037:Or4a27
|
UTSW |
2 |
88,559,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Or4a27
|
UTSW |
2 |
88,559,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R1674:Or4a27
|
UTSW |
2 |
88,559,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R1801:Or4a27
|
UTSW |
2 |
88,559,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1860:Or4a27
|
UTSW |
2 |
88,559,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Or4a27
|
UTSW |
2 |
88,559,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Or4a27
|
UTSW |
2 |
88,559,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R2308:Or4a27
|
UTSW |
2 |
88,559,428 (GRCm39) |
missense |
probably damaging |
0.97 |
R2411:Or4a27
|
UTSW |
2 |
88,559,741 (GRCm39) |
missense |
probably benign |
0.06 |
R4707:Or4a27
|
UTSW |
2 |
88,559,056 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5000:Or4a27
|
UTSW |
2 |
88,559,910 (GRCm39) |
missense |
probably damaging |
0.96 |
R5157:Or4a27
|
UTSW |
2 |
88,559,892 (GRCm39) |
missense |
probably benign |
|
R6000:Or4a27
|
UTSW |
2 |
88,559,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6021:Or4a27
|
UTSW |
2 |
88,559,294 (GRCm39) |
nonsense |
probably null |
|
R6389:Or4a27
|
UTSW |
2 |
88,559,016 (GRCm39) |
missense |
probably benign |
0.00 |
R6636:Or4a27
|
UTSW |
2 |
88,559,185 (GRCm39) |
missense |
probably benign |
0.01 |
R6637:Or4a27
|
UTSW |
2 |
88,559,185 (GRCm39) |
missense |
probably benign |
0.01 |
R6979:Or4a27
|
UTSW |
2 |
88,559,528 (GRCm39) |
missense |
probably benign |
0.03 |
R7618:Or4a27
|
UTSW |
2 |
88,559,180 (GRCm39) |
nonsense |
probably null |
|
R8382:Or4a27
|
UTSW |
2 |
88,559,857 (GRCm39) |
missense |
probably damaging |
0.98 |
R9293:Or4a27
|
UTSW |
2 |
88,559,799 (GRCm39) |
missense |
probably benign |
0.00 |
R9404:Or4a27
|
UTSW |
2 |
88,559,551 (GRCm39) |
missense |
probably benign |
|
R9660:Or4a27
|
UTSW |
2 |
88,559,142 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Or4a27
|
UTSW |
2 |
88,559,725 (GRCm39) |
missense |
probably damaging |
1.00 |
|