Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
T |
C |
6: 91,926,926 (GRCm39) |
V862A |
probably benign |
Het |
A2m |
A |
T |
6: 121,645,512 (GRCm39) |
K1019M |
probably damaging |
Het |
Acot6 |
G |
T |
12: 84,147,789 (GRCm39) |
W15L |
possibly damaging |
Het |
Adam32 |
CCAGCAGCAGCAGCAGCAG |
CCAGCAGCAGCAGCAG |
8: 25,438,769 (GRCm39) |
|
probably benign |
Het |
Adnp |
C |
A |
2: 168,026,580 (GRCm39) |
Q238H |
possibly damaging |
Het |
Akap7 |
T |
C |
10: 25,047,053 (GRCm39) |
Y281C |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,605,387 (GRCm39) |
E1085G |
probably damaging |
Het |
Arhgef38 |
A |
T |
3: 132,837,924 (GRCm39) |
S669T |
unknown |
Het |
Atp8b2 |
A |
T |
3: 89,865,927 (GRCm39) |
S50R |
possibly damaging |
Het |
Atp8b5 |
T |
C |
4: 43,372,630 (GRCm39) |
I1090T |
probably benign |
Het |
Ccdc198 |
A |
T |
14: 49,473,367 (GRCm39) |
H129Q |
probably benign |
Het |
Chrna4 |
G |
A |
2: 180,670,602 (GRCm39) |
R385C |
probably damaging |
Het |
Col4a1 |
T |
A |
8: 11,267,446 (GRCm39) |
I1105F |
probably damaging |
Het |
Crybg2 |
G |
A |
4: 133,792,620 (GRCm39) |
R85Q |
probably benign |
Het |
Cspg4 |
T |
A |
9: 56,798,287 (GRCm39) |
L1434Q |
|
Het |
Cyp3a13 |
T |
C |
5: 137,919,758 (GRCm39) |
N6S |
probably benign |
Het |
Dnase2b |
A |
T |
3: 146,299,326 (GRCm39) |
Y42* |
probably null |
Het |
F11r |
A |
G |
1: 171,289,376 (GRCm39) |
E233G |
probably damaging |
Het |
Fip1l1 |
T |
C |
5: 74,747,703 (GRCm39) |
I390T |
possibly damaging |
Het |
Fiz1 |
G |
A |
7: 5,011,280 (GRCm39) |
R413C |
probably damaging |
Het |
Fus |
G |
A |
7: 127,580,440 (GRCm39) |
G450E |
unknown |
Het |
Gm11569 |
C |
A |
11: 99,689,267 (GRCm39) |
C144F |
unknown |
Het |
Gm7298 |
A |
T |
6: 121,756,436 (GRCm39) |
Y1027F |
probably damaging |
Het |
Grik5 |
C |
A |
7: 24,758,403 (GRCm39) |
W340L |
probably damaging |
Het |
H1f2 |
A |
G |
13: 23,923,373 (GRCm39) |
K181R |
unknown |
Het |
Hectd4 |
G |
A |
5: 121,391,967 (GRCm39) |
R77H |
|
Het |
Ift81 |
C |
A |
5: 122,689,122 (GRCm39) |
V665L |
probably benign |
Het |
Ints2 |
A |
G |
11: 86,125,524 (GRCm39) |
F559L |
probably damaging |
Het |
Kdm8 |
G |
A |
7: 125,054,296 (GRCm39) |
V176I |
probably benign |
Het |
Keap1 |
A |
T |
9: 21,142,121 (GRCm39) |
Y584* |
probably null |
Het |
Klra1 |
T |
C |
6: 130,357,607 (GRCm39) |
T7A |
|
Het |
Lmo7 |
T |
A |
14: 102,122,743 (GRCm39) |
W311R |
probably damaging |
Het |
Lrp6 |
A |
G |
6: 134,518,855 (GRCm39) |
V70A |
probably damaging |
Het |
Luc7l3 |
A |
T |
11: 94,190,793 (GRCm39) |
S174T |
unknown |
Het |
Madd |
T |
C |
2: 90,998,162 (GRCm39) |
T653A |
probably damaging |
Het |
Mlph |
G |
T |
1: 90,855,716 (GRCm39) |
G41V |
probably damaging |
Het |
Mov10l1 |
A |
G |
15: 88,896,118 (GRCm39) |
E654G |
possibly damaging |
Het |
Mpp3 |
T |
C |
11: 101,911,328 (GRCm39) |
I165V |
|
Het |
Mrgpra2a |
T |
G |
7: 47,076,394 (GRCm39) |
Y288S |
probably damaging |
Het |
Mroh9 |
T |
A |
1: 162,890,030 (GRCm39) |
M236L |
|
Het |
Muc5b |
A |
C |
7: 141,417,974 (GRCm39) |
K3640T |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,253,318 (GRCm39) |
I1485V |
probably benign |
Het |
Nf2 |
A |
T |
11: 4,744,873 (GRCm39) |
F285L |
probably damaging |
Het |
Nfx1 |
T |
A |
4: 40,990,845 (GRCm39) |
C471S |
probably damaging |
Het |
Nsd1 |
C |
T |
13: 55,361,253 (GRCm39) |
R74W |
probably damaging |
Het |
Nudt16l1 |
A |
T |
16: 4,758,281 (GRCm39) |
*212C |
probably null |
Het |
Oaf |
T |
C |
9: 43,133,992 (GRCm39) |
Y243C |
probably damaging |
Het |
Or51e1 |
T |
C |
7: 102,358,541 (GRCm39) |
V25A |
probably benign |
Het |
Or7g30 |
T |
A |
9: 19,352,531 (GRCm39) |
F107L |
probably benign |
Het |
Or7h8 |
A |
G |
9: 20,124,173 (GRCm39) |
H176R |
possibly damaging |
Het |
Or8b36 |
T |
A |
9: 37,937,690 (GRCm39) |
L196* |
probably null |
Het |
Parp9 |
T |
C |
16: 35,768,543 (GRCm39) |
I241T |
probably damaging |
Het |
Phlpp2 |
G |
T |
8: 110,666,590 (GRCm39) |
A1040S |
possibly damaging |
Het |
Pon2 |
A |
T |
6: 5,265,391 (GRCm39) |
V332E |
possibly damaging |
Het |
Ptprc |
A |
G |
1: 138,016,302 (GRCm39) |
V544A |
probably damaging |
Het |
Rfx6 |
A |
G |
10: 51,597,600 (GRCm39) |
S446G |
probably benign |
Het |
Rnf103 |
T |
A |
6: 71,487,099 (GRCm39) |
C577S |
probably benign |
Het |
Ros1 |
T |
G |
10: 51,922,301 (GRCm39) |
E2278D |
possibly damaging |
Het |
Rpl37 |
A |
G |
15: 5,147,109 (GRCm39) |
S50G |
probably benign |
Het |
Rrad |
C |
T |
8: 105,355,343 (GRCm39) |
V222M |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,769,283 (GRCm39) |
T2770A |
probably benign |
Het |
Secisbp2l |
G |
A |
2: 125,617,623 (GRCm39) |
P18L |
probably damaging |
Het |
Septin2 |
T |
A |
1: 93,429,310 (GRCm39) |
W260R |
probably damaging |
Het |
Slc35c2 |
A |
G |
2: 165,122,797 (GRCm39) |
M117T |
probably benign |
Het |
Slc44a5 |
A |
G |
3: 153,953,373 (GRCm39) |
T252A |
probably benign |
Het |
Speer4f2 |
T |
A |
5: 17,581,610 (GRCm39) |
L184Q |
|
Het |
Sphkap |
C |
G |
1: 83,234,982 (GRCm39) |
V1615L |
probably damaging |
Het |
Sult2a3 |
C |
T |
7: 13,806,981 (GRCm39) |
V234I |
probably benign |
Het |
Tanc1 |
T |
C |
2: 59,630,132 (GRCm39) |
L704P |
probably damaging |
Het |
Tas2r126 |
T |
C |
6: 42,412,174 (GRCm39) |
S236P |
probably benign |
Het |
Tnik |
A |
G |
3: 28,704,235 (GRCm39) |
I1020V |
probably damaging |
Het |
Tomm5 |
T |
C |
4: 45,106,724 (GRCm39) |
Q64R |
unknown |
Het |
Ttll13 |
A |
G |
7: 79,897,182 (GRCm39) |
E16G |
probably benign |
Het |
Vmn1r21 |
C |
A |
6: 57,821,348 (GRCm39) |
C32F |
probably benign |
Het |
Vmn2r51 |
T |
A |
7: 9,839,480 (GRCm39) |
D36V |
probably damaging |
Het |
Vmn2r63 |
C |
T |
7: 42,576,413 (GRCm39) |
D467N |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,625,850 (GRCm39) |
N454S |
possibly damaging |
Het |
Wfdc1 |
A |
C |
8: 120,406,116 (GRCm39) |
D77A |
|
Het |
Yme1l1 |
T |
A |
2: 23,077,815 (GRCm39) |
I419N |
probably damaging |
Het |
Zfp106 |
G |
A |
2: 120,364,812 (GRCm39) |
Q555* |
probably null |
Het |
Zfp773 |
A |
C |
7: 7,138,302 (GRCm39) |
M111R |
probably damaging |
Het |
Zmat3 |
G |
A |
3: 32,397,767 (GRCm39) |
A165V |
possibly damaging |
Het |
|
Other mutations in Or6c3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01669:Or6c3
|
APN |
10 |
129,309,080 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02393:Or6c3
|
APN |
10 |
129,309,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03010:Or6c3
|
APN |
10 |
129,308,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03325:Or6c3
|
APN |
10 |
129,309,474 (GRCm39) |
missense |
probably benign |
0.02 |
R1298:Or6c3
|
UTSW |
10 |
129,308,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R2215:Or6c3
|
UTSW |
10 |
129,309,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R5482:Or6c3
|
UTSW |
10 |
129,308,947 (GRCm39) |
missense |
probably benign |
0.31 |
R5699:Or6c3
|
UTSW |
10 |
129,308,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R5794:Or6c3
|
UTSW |
10 |
129,309,295 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6436:Or6c3
|
UTSW |
10 |
129,308,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R6480:Or6c3
|
UTSW |
10 |
129,308,590 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6884:Or6c3
|
UTSW |
10 |
129,309,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Or6c3
|
UTSW |
10 |
129,308,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Or6c3
|
UTSW |
10 |
129,309,061 (GRCm39) |
missense |
probably benign |
0.07 |
R8207:Or6c3
|
UTSW |
10 |
129,308,953 (GRCm39) |
missense |
probably benign |
0.09 |
R8777:Or6c3
|
UTSW |
10 |
129,309,374 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8777-TAIL:Or6c3
|
UTSW |
10 |
129,309,374 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8998:Or6c3
|
UTSW |
10 |
129,309,386 (GRCm39) |
missense |
probably benign |
0.36 |
R8999:Or6c3
|
UTSW |
10 |
129,309,386 (GRCm39) |
missense |
probably benign |
0.36 |
Z1176:Or6c3
|
UTSW |
10 |
129,309,484 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Or6c3
|
UTSW |
10 |
129,308,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|