Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
A |
T |
8: 60,969,102 (GRCm39) |
M116L |
probably benign |
Het |
Adam25 |
A |
G |
8: 41,207,883 (GRCm39) |
D383G |
probably benign |
Het |
Adam26b |
T |
A |
8: 43,974,034 (GRCm39) |
M323L |
probably benign |
Het |
Adgrf3 |
T |
C |
5: 30,407,245 (GRCm39) |
H227R |
probably benign |
Het |
Antxr1 |
G |
A |
6: 87,114,273 (GRCm39) |
T498I |
probably benign |
Het |
Arg1 |
T |
A |
10: 24,791,627 (GRCm39) |
T285S |
possibly damaging |
Het |
Arhgdig |
T |
C |
17: 26,418,365 (GRCm39) |
D206G |
probably damaging |
Het |
Asb10 |
C |
A |
5: 24,745,875 (GRCm39) |
C17F |
possibly damaging |
Het |
Atg2b |
T |
C |
12: 105,618,379 (GRCm39) |
D891G |
probably damaging |
Het |
Cacna1h |
A |
T |
17: 25,611,083 (GRCm39) |
S572T |
possibly damaging |
Het |
Cenpj |
T |
C |
14: 56,780,257 (GRCm39) |
T985A |
probably benign |
Het |
Cfap65 |
G |
T |
1: 74,941,593 (GRCm39) |
N1780K |
probably damaging |
Het |
Cyp26c1 |
T |
C |
19: 37,681,447 (GRCm39) |
Y417H |
probably damaging |
Het |
Dnajb13 |
G |
T |
7: 100,152,393 (GRCm39) |
Q308K |
probably benign |
Het |
Fam107b |
T |
C |
2: 3,771,777 (GRCm39) |
S3P |
possibly damaging |
Het |
Gm3127 |
A |
G |
14: 15,425,787 (GRCm39) |
N64S |
probably damaging |
Het |
Gm4847 |
A |
C |
1: 166,460,249 (GRCm39) |
N412K |
probably benign |
Het |
Gtf3c3 |
A |
T |
1: 54,458,800 (GRCm39) |
|
probably null |
Het |
Guf1 |
T |
C |
5: 69,721,887 (GRCm39) |
S349P |
probably damaging |
Het |
Hvcn1 |
A |
G |
5: 122,371,586 (GRCm39) |
Y42C |
probably damaging |
Het |
Insm1 |
A |
G |
2: 146,065,027 (GRCm39) |
Y281C |
probably damaging |
Het |
Lrrc71 |
A |
G |
3: 87,650,281 (GRCm39) |
I264T |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 103,036,462 (GRCm39) |
N897S |
probably damaging |
Het |
Mtmr6 |
T |
A |
14: 60,533,596 (GRCm39) |
F375I |
probably damaging |
Het |
Mtor |
G |
C |
4: 148,536,807 (GRCm39) |
S27T |
possibly damaging |
Het |
Mylk4 |
T |
A |
13: 32,892,891 (GRCm39) |
K387N |
possibly damaging |
Het |
Nadk2 |
T |
G |
15: 9,092,935 (GRCm39) |
D247E |
probably benign |
Het |
Nfya |
T |
C |
17: 48,699,445 (GRCm39) |
T213A |
probably damaging |
Het |
Nlrp1a |
A |
G |
11: 70,990,354 (GRCm39) |
V1067A |
probably benign |
Het |
Nrbp2 |
C |
T |
15: 75,959,257 (GRCm39) |
R206Q |
possibly damaging |
Het |
Oas2 |
A |
G |
5: 120,871,293 (GRCm39) |
V722A |
probably benign |
Het |
Odad4 |
G |
A |
11: 100,452,731 (GRCm39) |
|
probably null |
Het |
Pcdhb2 |
G |
T |
18: 37,428,000 (GRCm39) |
|
probably benign |
Het |
Pdpr |
T |
A |
8: 111,852,317 (GRCm39) |
H561Q |
probably damaging |
Het |
Plcz1 |
A |
G |
6: 139,961,853 (GRCm39) |
F233L |
probably damaging |
Het |
Ppp1r3d |
A |
G |
2: 178,055,165 (GRCm39) |
I279T |
probably damaging |
Het |
Psg17 |
A |
G |
7: 18,548,416 (GRCm39) |
Y452H |
probably damaging |
Het |
Reg4 |
T |
C |
3: 98,140,428 (GRCm39) |
|
probably null |
Het |
Rint1 |
A |
G |
5: 24,010,477 (GRCm39) |
T229A |
probably benign |
Het |
Robo1 |
T |
G |
16: 72,839,866 (GRCm39) |
|
probably null |
Het |
Slc22a26 |
A |
C |
19: 7,779,952 (GRCm39) |
|
probably null |
Het |
Slc22a7 |
C |
T |
17: 46,749,156 (GRCm39) |
A54T |
probably benign |
Het |
Slc52a3 |
C |
A |
2: 151,846,534 (GRCm39) |
T165N |
possibly damaging |
Het |
Slc7a11 |
C |
T |
3: 50,378,486 (GRCm39) |
|
probably null |
Het |
Smap2 |
T |
C |
4: 120,873,996 (GRCm39) |
N18S |
probably benign |
Het |
Spag6l |
T |
C |
16: 16,595,278 (GRCm39) |
E369G |
probably damaging |
Het |
Tars3 |
T |
A |
7: 65,325,760 (GRCm39) |
Y445N |
probably damaging |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tmprss7 |
C |
T |
16: 45,483,637 (GRCm39) |
G579D |
probably benign |
Het |
Tpi1 |
T |
A |
6: 124,789,817 (GRCm39) |
K109* |
probably null |
Het |
Ttn |
T |
C |
2: 76,628,856 (GRCm39) |
E14466G |
possibly damaging |
Het |
Usp40 |
A |
T |
1: 87,890,152 (GRCm39) |
C903* |
probably null |
Het |
Vinac1 |
T |
A |
2: 128,880,192 (GRCm39) |
D578V |
|
Het |
Vmn2r104 |
T |
A |
17: 20,261,971 (GRCm39) |
L386F |
possibly damaging |
Het |
Vmn2r54 |
G |
A |
7: 12,349,630 (GRCm39) |
P651S |
probably damaging |
Het |
Wnk4 |
C |
A |
11: 101,153,721 (GRCm39) |
T261K |
probably damaging |
Het |
Wnt2b |
T |
C |
3: 104,854,432 (GRCm39) |
Y342C |
probably damaging |
Het |
Zbtb8b |
A |
G |
4: 129,326,755 (GRCm39) |
Y137H |
probably damaging |
Het |
|
Other mutations in Or4c108 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01812:Or4c108
|
APN |
2 |
88,803,868 (GRCm39) |
nonsense |
probably null |
|
IGL02685:Or4c108
|
APN |
2 |
88,803,365 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0240:Or4c108
|
UTSW |
2 |
88,803,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Or4c108
|
UTSW |
2 |
88,803,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Or4c108
|
UTSW |
2 |
88,804,109 (GRCm39) |
missense |
probably benign |
0.00 |
R1845:Or4c108
|
UTSW |
2 |
88,803,482 (GRCm39) |
missense |
probably benign |
0.22 |
R1868:Or4c108
|
UTSW |
2 |
88,804,128 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1953:Or4c108
|
UTSW |
2 |
88,804,224 (GRCm39) |
nonsense |
probably null |
|
R4205:Or4c108
|
UTSW |
2 |
88,803,482 (GRCm39) |
missense |
probably benign |
0.22 |
R4751:Or4c108
|
UTSW |
2 |
88,803,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R4895:Or4c108
|
UTSW |
2 |
88,804,055 (GRCm39) |
missense |
probably benign |
0.39 |
R4937:Or4c108
|
UTSW |
2 |
88,803,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R5621:Or4c108
|
UTSW |
2 |
88,803,810 (GRCm39) |
missense |
probably benign |
0.00 |
R5678:Or4c108
|
UTSW |
2 |
88,803,317 (GRCm39) |
nonsense |
probably null |
|
R5938:Or4c108
|
UTSW |
2 |
88,803,357 (GRCm39) |
missense |
probably benign |
0.00 |
R6021:Or4c108
|
UTSW |
2 |
88,803,376 (GRCm39) |
nonsense |
probably null |
|
R6180:Or4c108
|
UTSW |
2 |
88,804,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R6724:Or4c108
|
UTSW |
2 |
88,803,612 (GRCm39) |
missense |
probably benign |
0.02 |
R6873:Or4c108
|
UTSW |
2 |
88,803,768 (GRCm39) |
missense |
probably benign |
|
R6893:Or4c108
|
UTSW |
2 |
88,804,143 (GRCm39) |
missense |
probably benign |
0.00 |
R7221:Or4c108
|
UTSW |
2 |
88,803,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R8233:Or4c108
|
UTSW |
2 |
88,804,082 (GRCm39) |
missense |
probably benign |
|
R8262:Or4c108
|
UTSW |
2 |
88,803,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R8979:Or4c108
|
UTSW |
2 |
88,804,173 (GRCm39) |
missense |
probably benign |
0.00 |
R9136:Or4c108
|
UTSW |
2 |
88,804,113 (GRCm39) |
missense |
probably benign |
0.00 |
R9696:Or4c108
|
UTSW |
2 |
88,803,615 (GRCm39) |
missense |
probably benign |
0.05 |
R9726:Or4c108
|
UTSW |
2 |
88,804,221 (GRCm39) |
missense |
probably benign |
|
|