Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg4 |
T |
A |
9: 44,186,666 (GRCm39) |
M493L |
probably benign |
Het |
Abtb2 |
G |
A |
2: 103,539,629 (GRCm39) |
V665I |
probably benign |
Het |
Adamtsl1 |
C |
G |
4: 86,260,840 (GRCm39) |
S1017W |
probably damaging |
Het |
Aebp1 |
A |
G |
11: 5,821,469 (GRCm39) |
T623A |
possibly damaging |
Het |
Alox5 |
A |
G |
6: 116,390,741 (GRCm39) |
F470S |
probably damaging |
Het |
Angpt2 |
T |
C |
8: 18,755,855 (GRCm39) |
E204G |
probably benign |
Het |
Apip |
A |
G |
2: 102,919,838 (GRCm39) |
E138G |
probably damaging |
Het |
Apob |
C |
T |
12: 8,039,207 (GRCm39) |
T466M |
probably benign |
Het |
Atp2b3 |
GACAACA |
GACA |
X: 72,588,729 (GRCm39) |
|
probably benign |
Het |
Atxn7l3 |
A |
T |
11: 102,185,340 (GRCm39) |
D56E |
probably benign |
Het |
Cacna1s |
C |
T |
1: 136,026,289 (GRCm39) |
A1092V |
probably damaging |
Het |
Calr3 |
A |
G |
8: 73,181,044 (GRCm39) |
F183L |
probably damaging |
Het |
Cd300lb |
T |
A |
11: 114,816,877 (GRCm39) |
D55V |
probably benign |
Het |
Chid1 |
A |
C |
7: 141,108,384 (GRCm39) |
V145G |
probably damaging |
Het |
Chst15 |
T |
C |
7: 131,871,855 (GRCm39) |
N142S |
probably damaging |
Het |
Cnot4 |
C |
T |
6: 35,028,389 (GRCm39) |
R409Q |
probably damaging |
Het |
Cope |
T |
G |
8: 70,765,411 (GRCm39) |
I287S |
possibly damaging |
Het |
Cpd |
A |
T |
11: 76,731,212 (GRCm39) |
|
probably null |
Het |
Cux1 |
G |
T |
5: 136,337,133 (GRCm39) |
T785K |
probably benign |
Het |
Dennd2b |
A |
G |
7: 109,156,562 (GRCm39) |
S63P |
probably damaging |
Het |
Dthd1 |
T |
C |
5: 62,979,383 (GRCm39) |
S348P |
probably damaging |
Het |
Eno3 |
G |
T |
11: 70,551,903 (GRCm39) |
E64* |
probably null |
Het |
Entpd1 |
T |
A |
19: 40,713,507 (GRCm39) |
Y184* |
probably null |
Het |
Erv3 |
A |
T |
2: 131,698,083 (GRCm39) |
M92K |
probably benign |
Het |
Flg2 |
T |
A |
3: 93,110,445 (GRCm39) |
H824Q |
unknown |
Het |
Fndc9 |
G |
A |
11: 46,128,930 (GRCm39) |
G150S |
probably benign |
Het |
Gdap1 |
G |
A |
1: 17,217,169 (GRCm39) |
V43I |
possibly damaging |
Het |
Ifi213 |
C |
A |
1: 173,417,229 (GRCm39) |
L394F |
probably damaging |
Het |
Ift88 |
A |
G |
14: 57,668,085 (GRCm39) |
T29A |
possibly damaging |
Het |
Kdm4c |
A |
T |
4: 74,252,063 (GRCm39) |
I437L |
probably benign |
Het |
Kras |
T |
A |
6: 145,177,977 (GRCm39) |
E98D |
probably benign |
Het |
Lcorl |
C |
A |
5: 45,891,543 (GRCm39) |
R353I |
possibly damaging |
Het |
Lrrc4c |
A |
G |
2: 97,460,921 (GRCm39) |
I516V |
probably benign |
Het |
Lrrc51 |
T |
C |
7: 101,564,803 (GRCm39) |
D85G |
probably damaging |
Het |
Lypd6b |
G |
A |
2: 49,837,504 (GRCm39) |
A159T |
probably damaging |
Het |
Magel2 |
G |
A |
7: 62,030,188 (GRCm39) |
V1031I |
unknown |
Het |
Man1c1 |
A |
T |
4: 134,308,100 (GRCm39) |
N338K |
probably benign |
Het |
Mdn1 |
C |
A |
4: 32,739,977 (GRCm39) |
Q3744K |
probably damaging |
Het |
Micu3 |
G |
T |
8: 40,788,893 (GRCm39) |
A135S |
possibly damaging |
Het |
Muc4 |
T |
C |
16: 32,569,167 (GRCm39) |
S76P |
possibly damaging |
Het |
Nin |
T |
G |
12: 70,061,547 (GRCm39) |
T2106P |
probably benign |
Het |
Nlrp4e |
T |
C |
7: 23,021,268 (GRCm39) |
I585T |
probably benign |
Het |
Npy1r |
C |
T |
8: 67,156,847 (GRCm39) |
A89V |
probably benign |
Het |
Or4c115 |
G |
A |
2: 88,927,944 (GRCm39) |
A109V |
probably benign |
Het |
Or52ae7 |
T |
A |
7: 103,119,249 (GRCm39) |
M1K |
probably null |
Het |
Or52n3 |
T |
A |
7: 104,530,515 (GRCm39) |
Y200* |
probably null |
Het |
Or5w13 |
A |
T |
2: 87,523,872 (GRCm39) |
M118K |
probably damaging |
Het |
Parp14 |
T |
G |
16: 35,677,008 (GRCm39) |
T987P |
possibly damaging |
Het |
Pde7b |
A |
T |
10: 20,423,867 (GRCm39) |
V3E |
probably damaging |
Het |
Pdlim7 |
G |
T |
13: 55,656,107 (GRCm39) |
Y104* |
probably null |
Het |
Pgm2l1 |
A |
G |
7: 99,910,932 (GRCm39) |
K292R |
probably benign |
Het |
Plec |
T |
C |
15: 76,072,401 (GRCm39) |
E728G |
probably damaging |
Het |
Plppr4 |
T |
C |
3: 117,129,152 (GRCm39) |
Y105C |
probably damaging |
Het |
Polr1c |
A |
T |
17: 46,558,821 (GRCm39) |
N23K |
possibly damaging |
Het |
Ppp5c |
A |
T |
7: 16,743,861 (GRCm39) |
M191K |
probably damaging |
Het |
Prkca |
T |
C |
11: 107,869,142 (GRCm39) |
D57G |
probably damaging |
Het |
Prkcb |
A |
G |
7: 122,143,854 (GRCm39) |
|
probably null |
Het |
Prl6a1 |
A |
T |
13: 27,502,911 (GRCm39) |
Q169L |
probably null |
Het |
Prl6a1 |
C |
A |
13: 27,502,910 (GRCm39) |
Q169K |
possibly damaging |
Het |
Psmd14 |
G |
A |
2: 61,591,335 (GRCm39) |
R46H |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ramp2 |
A |
G |
11: 101,138,408 (GRCm39) |
T22A |
probably benign |
Het |
Rbm19 |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
5: 120,278,345 (GRCm39) |
|
probably benign |
Het |
Rbm25 |
A |
T |
12: 83,715,219 (GRCm39) |
E463D |
possibly damaging |
Het |
Retnlb |
A |
G |
16: 48,637,678 (GRCm39) |
I35V |
probably benign |
Het |
Sestd1 |
A |
G |
2: 77,071,976 (GRCm39) |
Y49H |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,431,306 (GRCm39) |
I2378N |
probably damaging |
Het |
Slc26a1 |
A |
T |
5: 108,819,740 (GRCm39) |
C486* |
probably null |
Het |
Spef2 |
T |
A |
15: 9,667,316 (GRCm39) |
I791F |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,650,798 (GRCm39) |
T1726A |
possibly damaging |
Het |
Stk38l |
T |
A |
6: 146,673,129 (GRCm39) |
M296K |
probably benign |
Het |
Taf5 |
T |
C |
19: 47,070,285 (GRCm39) |
F624L |
probably damaging |
Het |
Tmem30c |
G |
T |
16: 57,086,855 (GRCm39) |
T316K |
probably damaging |
Het |
Trpm2 |
A |
G |
10: 77,778,839 (GRCm39) |
S376P |
possibly damaging |
Het |
Vmn2r82 |
A |
T |
10: 79,214,702 (GRCm39) |
L228F |
probably damaging |
Het |
Zfp607b |
G |
A |
7: 27,398,087 (GRCm39) |
C57Y |
possibly damaging |
Het |
Zfp983 |
A |
G |
17: 21,881,269 (GRCm39) |
H399R |
probably damaging |
Het |
Zfp984 |
A |
T |
4: 147,840,002 (GRCm39) |
M283K |
probably benign |
Het |
|
Other mutations in Or11g27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01128:Or11g27
|
APN |
14 |
50,771,406 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01551:Or11g27
|
APN |
14 |
50,771,618 (GRCm39) |
missense |
probably benign |
|
IGL02024:Or11g27
|
APN |
14 |
50,771,307 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02867:Or11g27
|
APN |
14 |
50,770,970 (GRCm39) |
missense |
probably benign |
|
IGL02889:Or11g27
|
APN |
14 |
50,770,970 (GRCm39) |
missense |
probably benign |
|
IGL03195:Or11g27
|
APN |
14 |
50,770,877 (GRCm39) |
missense |
probably benign |
|
IGL03296:Or11g27
|
APN |
14 |
50,771,402 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0049:Or11g27
|
UTSW |
14 |
50,771,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Or11g27
|
UTSW |
14 |
50,771,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Or11g27
|
UTSW |
14 |
50,771,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R0556:Or11g27
|
UTSW |
14 |
50,771,381 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0661:Or11g27
|
UTSW |
14 |
50,771,552 (GRCm39) |
missense |
probably benign |
|
R0759:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0761:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0894:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1109:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1110:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1312:Or11g27
|
UTSW |
14 |
50,771,652 (GRCm39) |
missense |
probably benign |
|
R1446:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1470:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1470:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1502:Or11g27
|
UTSW |
14 |
50,771,234 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1529:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1624:Or11g27
|
UTSW |
14 |
50,771,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R1646:Or11g27
|
UTSW |
14 |
50,771,040 (GRCm39) |
missense |
probably benign |
0.01 |
R1687:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1795:Or11g27
|
UTSW |
14 |
50,771,159 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2011:Or11g27
|
UTSW |
14 |
50,771,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Or11g27
|
UTSW |
14 |
50,771,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R2697:Or11g27
|
UTSW |
14 |
50,771,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Or11g27
|
UTSW |
14 |
50,770,897 (GRCm39) |
missense |
probably benign |
0.19 |
R2858:Or11g27
|
UTSW |
14 |
50,770,897 (GRCm39) |
missense |
probably benign |
0.19 |
R3906:Or11g27
|
UTSW |
14 |
50,771,211 (GRCm39) |
missense |
probably benign |
0.03 |
R4327:Or11g27
|
UTSW |
14 |
50,770,971 (GRCm39) |
missense |
probably benign |
0.05 |
R4355:Or11g27
|
UTSW |
14 |
50,771,216 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4663:Or11g27
|
UTSW |
14 |
50,771,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Or11g27
|
UTSW |
14 |
50,771,804 (GRCm39) |
makesense |
probably null |
|
R5964:Or11g27
|
UTSW |
14 |
50,771,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R6148:Or11g27
|
UTSW |
14 |
50,771,778 (GRCm39) |
missense |
probably benign |
0.00 |
R6167:Or11g27
|
UTSW |
14 |
50,771,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Or11g27
|
UTSW |
14 |
50,771,711 (GRCm39) |
missense |
probably benign |
0.02 |
R6616:Or11g27
|
UTSW |
14 |
50,771,364 (GRCm39) |
missense |
probably benign |
0.43 |
R6910:Or11g27
|
UTSW |
14 |
50,771,330 (GRCm39) |
missense |
probably benign |
0.31 |
R7076:Or11g27
|
UTSW |
14 |
50,771,278 (GRCm39) |
nonsense |
probably null |
|
R7483:Or11g27
|
UTSW |
14 |
50,771,472 (GRCm39) |
missense |
probably benign |
0.06 |
R7574:Or11g27
|
UTSW |
14 |
50,771,770 (GRCm39) |
missense |
probably benign |
0.01 |
R7731:Or11g27
|
UTSW |
14 |
50,771,141 (GRCm39) |
missense |
probably damaging |
0.99 |
R8691:Or11g27
|
UTSW |
14 |
50,770,910 (GRCm39) |
missense |
probably benign |
0.01 |
R9072:Or11g27
|
UTSW |
14 |
50,771,211 (GRCm39) |
missense |
probably benign |
0.03 |
R9073:Or11g27
|
UTSW |
14 |
50,771,211 (GRCm39) |
missense |
probably benign |
0.03 |
R9321:Or11g27
|
UTSW |
14 |
50,771,471 (GRCm39) |
missense |
probably benign |
0.01 |
R9478:Or11g27
|
UTSW |
14 |
50,771,051 (GRCm39) |
missense |
probably benign |
0.01 |
R9557:Or11g27
|
UTSW |
14 |
50,771,552 (GRCm39) |
missense |
probably benign |
|
|