Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahi1 |
T |
C |
10: 20,876,465 (GRCm39) |
I792T |
probably benign |
Het |
Anks1b |
T |
A |
10: 90,759,379 (GRCm39) |
|
probably null |
Het |
Ano3 |
T |
G |
2: 110,693,232 (GRCm39) |
D122A |
probably benign |
Het |
Atp12a |
T |
C |
14: 56,610,801 (GRCm39) |
V315A |
probably benign |
Het |
B230104I21Rik |
G |
T |
4: 154,433,986 (GRCm39) |
G57* |
probably null |
Het |
Bpifb2 |
A |
G |
2: 153,733,050 (GRCm39) |
K378E |
probably damaging |
Het |
Cdk5rap2 |
T |
C |
4: 70,161,830 (GRCm39) |
|
probably benign |
Het |
Ceacam23 |
A |
G |
7: 17,651,369 (GRCm39) |
D840G |
possibly damaging |
Het |
Cflar |
A |
G |
1: 58,791,927 (GRCm39) |
D410G |
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,102,049 (GRCm39) |
V345A |
probably benign |
Het |
Cnga1 |
C |
T |
5: 72,776,404 (GRCm39) |
V20I |
possibly damaging |
Het |
Ddx50 |
T |
A |
10: 62,476,596 (GRCm39) |
K226* |
probably null |
Het |
Dnah5 |
T |
C |
15: 28,448,513 (GRCm39) |
V4192A |
possibly damaging |
Het |
Dnah8 |
G |
A |
17: 30,875,659 (GRCm39) |
D494N |
probably benign |
Het |
Dock7 |
A |
T |
4: 98,879,660 (GRCm39) |
C965S |
probably benign |
Het |
Dst |
C |
T |
1: 34,334,370 (GRCm39) |
A5083V |
probably damaging |
Het |
E130208F15Rik |
T |
C |
7: 30,021,726 (GRCm39) |
Q10R |
probably damaging |
Het |
Fbxw15 |
T |
C |
9: 109,384,741 (GRCm39) |
|
probably null |
Het |
Fxr2 |
A |
G |
11: 69,543,511 (GRCm39) |
N671D |
probably damaging |
Het |
Gbp7 |
A |
G |
3: 142,252,303 (GRCm39) |
T629A |
probably benign |
Het |
Grm1 |
T |
C |
10: 10,565,092 (GRCm39) |
Y1072C |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,244,685 (GRCm39) |
E714V |
possibly damaging |
Het |
Hsd17b13 |
T |
A |
5: 104,113,730 (GRCm39) |
E205D |
probably benign |
Het |
Igf2bp3 |
A |
G |
6: 49,094,084 (GRCm39) |
|
probably benign |
Het |
Il2ra |
A |
G |
2: 11,689,248 (GRCm39) |
H259R |
probably benign |
Het |
Klk15 |
G |
T |
7: 43,588,247 (GRCm39) |
R185L |
probably benign |
Het |
Map3k11 |
T |
G |
19: 5,745,937 (GRCm39) |
|
probably null |
Het |
Morn3 |
A |
G |
5: 123,179,166 (GRCm39) |
W95R |
probably damaging |
Het |
Nipbl |
A |
G |
15: 8,364,328 (GRCm39) |
|
probably null |
Het |
Nrap |
A |
T |
19: 56,329,006 (GRCm39) |
V1145D |
possibly damaging |
Het |
Or1e35 |
A |
G |
11: 73,797,755 (GRCm39) |
S188P |
probably damaging |
Het |
Or9k2 |
T |
A |
10: 129,998,542 (GRCm39) |
I218F |
probably benign |
Het |
Pdcd11 |
A |
G |
19: 47,093,198 (GRCm39) |
N492S |
possibly damaging |
Het |
Ptgfr |
C |
T |
3: 151,540,738 (GRCm39) |
V257I |
probably damaging |
Het |
Racgap1 |
T |
C |
15: 99,521,509 (GRCm39) |
E549G |
possibly damaging |
Het |
Rfx3 |
T |
C |
19: 27,808,165 (GRCm39) |
T193A |
probably damaging |
Het |
Rplp0 |
T |
A |
5: 115,699,489 (GRCm39) |
I149N |
probably benign |
Het |
Samd7 |
T |
G |
3: 30,810,883 (GRCm39) |
I300S |
probably benign |
Het |
Scpep1 |
A |
G |
11: 88,825,402 (GRCm39) |
|
probably null |
Het |
Senp6 |
T |
C |
9: 80,049,352 (GRCm39) |
|
probably benign |
Het |
Serpinb2 |
G |
T |
1: 107,447,446 (GRCm39) |
G78V |
probably damaging |
Het |
Sesn1 |
T |
C |
10: 41,687,189 (GRCm39) |
S58P |
probably benign |
Het |
Skic3 |
A |
G |
13: 76,259,938 (GRCm39) |
|
probably null |
Het |
Spg11 |
T |
C |
2: 121,928,680 (GRCm39) |
D591G |
possibly damaging |
Het |
Spire2 |
A |
C |
8: 124,080,833 (GRCm39) |
S26R |
probably damaging |
Het |
Strip2 |
T |
A |
6: 29,956,957 (GRCm39) |
|
probably benign |
Het |
Ttn |
G |
A |
2: 76,697,519 (GRCm39) |
|
probably benign |
Het |
Vmn2r77 |
A |
G |
7: 86,460,924 (GRCm39) |
Y750C |
probably damaging |
Het |
Wnt11 |
T |
A |
7: 98,488,383 (GRCm39) |
Y23* |
probably null |
Het |
Zbp1 |
T |
A |
2: 173,052,340 (GRCm39) |
D272V |
probably benign |
Het |
|
Other mutations in Or2l13b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01635:Or2l13b
|
APN |
16 |
19,348,845 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02139:Or2l13b
|
APN |
16 |
19,349,640 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02347:Or2l13b
|
APN |
16 |
19,349,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Or2l13b
|
APN |
16 |
19,349,667 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R0542:Or2l13b
|
UTSW |
16 |
19,348,732 (GRCm39) |
makesense |
probably null |
|
R1496:Or2l13b
|
UTSW |
16 |
19,349,133 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1707:Or2l13b
|
UTSW |
16 |
19,348,927 (GRCm39) |
missense |
probably benign |
0.18 |
R2006:Or2l13b
|
UTSW |
16 |
19,349,455 (GRCm39) |
missense |
probably benign |
0.02 |
R2220:Or2l13b
|
UTSW |
16 |
19,348,895 (GRCm39) |
nonsense |
probably null |
|
R3734:Or2l13b
|
UTSW |
16 |
19,349,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R4134:Or2l13b
|
UTSW |
16 |
19,349,452 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4135:Or2l13b
|
UTSW |
16 |
19,349,452 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4538:Or2l13b
|
UTSW |
16 |
19,349,381 (GRCm39) |
nonsense |
probably null |
|
R4631:Or2l13b
|
UTSW |
16 |
19,348,891 (GRCm39) |
nonsense |
probably null |
|
R4633:Or2l13b
|
UTSW |
16 |
19,349,034 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4872:Or2l13b
|
UTSW |
16 |
19,349,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R4910:Or2l13b
|
UTSW |
16 |
19,348,768 (GRCm39) |
missense |
probably benign |
0.03 |
R4945:Or2l13b
|
UTSW |
16 |
19,349,307 (GRCm39) |
missense |
probably benign |
0.03 |
R5345:Or2l13b
|
UTSW |
16 |
19,349,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Or2l13b
|
UTSW |
16 |
19,349,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R7074:Or2l13b
|
UTSW |
16 |
19,348,855 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7439:Or2l13b
|
UTSW |
16 |
19,349,650 (GRCm39) |
missense |
probably benign |
0.03 |
R7723:Or2l13b
|
UTSW |
16 |
19,349,358 (GRCm39) |
nonsense |
probably null |
|
R7860:Or2l13b
|
UTSW |
16 |
19,349,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Or2l13b
|
UTSW |
16 |
19,349,536 (GRCm39) |
missense |
|
|
R9515:Or2l13b
|
UTSW |
16 |
19,349,026 (GRCm39) |
missense |
probably benign |
0.00 |
|