Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi2 |
C |
T |
1: 60,489,251 (GRCm39) |
T291I |
probably benign |
Het |
Aox1 |
A |
C |
1: 58,088,625 (GRCm39) |
D137A |
possibly damaging |
Het |
Apbb2 |
T |
C |
5: 66,609,444 (GRCm39) |
K68E |
probably damaging |
Het |
Arf3 |
A |
T |
15: 98,638,933 (GRCm39) |
M108K |
probably benign |
Het |
Atg2b |
T |
A |
12: 105,583,388 (GRCm39) |
I2058F |
probably damaging |
Het |
Bhlhe40 |
C |
T |
6: 108,639,518 (GRCm39) |
L99F |
probably damaging |
Het |
Cd200l1 |
T |
C |
16: 45,238,271 (GRCm39) |
H294R |
probably benign |
Het |
Cyp2b10 |
G |
A |
7: 25,625,670 (GRCm39) |
R500H |
probably damaging |
Het |
Dlc1 |
C |
T |
8: 37,039,997 (GRCm39) |
E937K |
probably damaging |
Het |
Dll3 |
A |
T |
7: 27,995,793 (GRCm39) |
V336D |
possibly damaging |
Het |
Dync2h1 |
A |
G |
9: 7,037,727 (GRCm39) |
F3377L |
probably benign |
Het |
Eef1d |
A |
G |
15: 75,768,160 (GRCm39) |
Y561H |
probably damaging |
Het |
Efcab3 |
T |
G |
11: 104,911,352 (GRCm39) |
V4544G |
probably benign |
Het |
Epb41l1 |
C |
A |
2: 156,363,591 (GRCm39) |
T700K |
probably benign |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
Ephb2 |
C |
A |
4: 136,402,769 (GRCm39) |
G501C |
probably benign |
Het |
Erbb3 |
T |
C |
10: 128,406,030 (GRCm39) |
Y1129C |
probably damaging |
Het |
Fbn1 |
C |
T |
2: 125,212,726 (GRCm39) |
V799M |
possibly damaging |
Het |
Fbxo9 |
G |
A |
9: 77,991,933 (GRCm39) |
P353S |
probably benign |
Het |
Ggt1 |
T |
G |
10: 75,412,056 (GRCm39) |
V100G |
probably benign |
Het |
Gm45861 |
T |
C |
8: 28,032,531 (GRCm39) |
M885T |
unknown |
Het |
Grin2d |
A |
T |
7: 45,483,425 (GRCm39) |
Y917* |
probably null |
Het |
Hectd4 |
T |
A |
5: 121,415,819 (GRCm39) |
V540D |
possibly damaging |
Het |
Helz |
T |
A |
11: 107,495,079 (GRCm39) |
I351K |
probably damaging |
Het |
Ighv2-6-8 |
A |
G |
12: 113,759,980 (GRCm39) |
V43A |
probably damaging |
Het |
Igkv9-129 |
T |
A |
6: 67,817,106 (GRCm39) |
I70N |
probably damaging |
Het |
Il18 |
A |
T |
9: 50,489,178 (GRCm39) |
D69V |
probably damaging |
Het |
Kcnh7 |
T |
A |
2: 62,552,209 (GRCm39) |
E927D |
|
Het |
Kcnt2 |
T |
A |
1: 140,356,587 (GRCm39) |
V342E |
probably benign |
Het |
Khdc4 |
A |
G |
3: 88,607,286 (GRCm39) |
N330S |
probably benign |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Krt18 |
C |
G |
15: 101,937,962 (GRCm39) |
A153G |
probably damaging |
Het |
Lmntd2 |
A |
T |
7: 140,791,977 (GRCm39) |
|
probably benign |
Het |
Lrrc26 |
G |
T |
2: 25,180,286 (GRCm39) |
A96S |
probably benign |
Het |
Map3k11 |
A |
T |
19: 5,752,166 (GRCm39) |
S783C |
probably damaging |
Het |
Mib2 |
G |
A |
4: 155,740,729 (GRCm39) |
L632F |
possibly damaging |
Het |
Mical2 |
A |
C |
7: 111,910,661 (GRCm39) |
D277A |
possibly damaging |
Het |
Mtr |
A |
T |
13: 12,250,365 (GRCm39) |
F339L |
probably benign |
Het |
Musk |
T |
C |
4: 58,354,032 (GRCm39) |
F362L |
probably benign |
Het |
Ncor1 |
G |
A |
11: 62,233,871 (GRCm39) |
Q444* |
probably null |
Het |
Nek4 |
T |
C |
14: 30,685,924 (GRCm39) |
S279P |
|
Het |
Nell1 |
C |
T |
7: 50,210,543 (GRCm39) |
T348I |
unknown |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nrip1 |
T |
C |
16: 76,088,902 (GRCm39) |
H885R |
probably damaging |
Het |
Or13a19 |
G |
A |
7: 139,902,938 (GRCm39) |
G109R |
possibly damaging |
Het |
Or2a5 |
T |
A |
6: 42,874,201 (GRCm39) |
V272D |
|
Het |
Or2y12 |
C |
A |
11: 49,426,028 (GRCm39) |
N5K |
probably damaging |
Het |
Or6c69c |
T |
A |
10: 129,910,522 (GRCm39) |
V81D |
possibly damaging |
Het |
Or6d14 |
A |
G |
6: 116,534,255 (GRCm39) |
T290A |
possibly damaging |
Het |
Otog |
A |
G |
7: 45,959,571 (GRCm39) |
D720G |
probably damaging |
Het |
P3h3 |
C |
A |
6: 124,834,564 (GRCm39) |
Q29H |
possibly damaging |
Het |
Parn |
A |
G |
16: 13,466,281 (GRCm39) |
|
probably null |
Het |
Pcnt |
C |
A |
10: 76,245,407 (GRCm39) |
E1077* |
probably null |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pigb |
A |
G |
9: 72,929,576 (GRCm39) |
W336R |
probably damaging |
Het |
Pkdrej |
A |
T |
15: 85,700,538 (GRCm39) |
S1799R |
probably damaging |
Het |
Pnpla6 |
G |
T |
8: 3,567,401 (GRCm39) |
M86I |
possibly damaging |
Het |
Prickle2 |
T |
C |
6: 92,435,620 (GRCm39) |
K50E |
possibly damaging |
Het |
Psg21 |
A |
G |
7: 18,386,389 (GRCm39) |
V199A |
probably benign |
Het |
Reep3 |
T |
C |
10: 66,871,786 (GRCm39) |
|
probably null |
Het |
Reln |
T |
C |
5: 22,104,155 (GRCm39) |
D3272G |
probably damaging |
Het |
Rps6ka4 |
A |
G |
19: 6,808,667 (GRCm39) |
V526A |
possibly damaging |
Het |
Sel1l3 |
T |
C |
5: 53,280,771 (GRCm39) |
E911G |
probably damaging |
Het |
Serpinb6b |
C |
A |
13: 33,162,125 (GRCm39) |
A308E |
probably benign |
Het |
Slc26a4 |
A |
G |
12: 31,572,523 (GRCm39) |
V746A |
probably benign |
Het |
Slc4a3 |
T |
G |
1: 75,527,957 (GRCm39) |
M402R |
probably damaging |
Het |
Slc9b1 |
A |
T |
3: 135,078,900 (GRCm39) |
T186S |
possibly damaging |
Het |
Slk |
A |
G |
19: 47,608,712 (GRCm39) |
Q555R |
probably benign |
Het |
Smc2 |
T |
A |
4: 52,475,100 (GRCm39) |
D925E |
probably benign |
Het |
Stat5a |
A |
T |
11: 100,774,764 (GRCm39) |
T758S |
unknown |
Het |
Sulf1 |
A |
G |
1: 12,906,499 (GRCm39) |
S514G |
probably benign |
Het |
Tcp11l1 |
T |
A |
2: 104,536,853 (GRCm39) |
N4I |
probably damaging |
Het |
Tex2 |
A |
T |
11: 106,402,731 (GRCm39) |
I1047K |
unknown |
Het |
Tmem184b |
A |
G |
15: 79,261,264 (GRCm39) |
V114A |
possibly damaging |
Het |
Trmt11 |
A |
G |
10: 30,467,027 (GRCm39) |
V95A |
probably benign |
Het |
Trp53bp2 |
A |
G |
1: 182,268,433 (GRCm39) |
D169G |
possibly damaging |
Het |
Ttc41 |
T |
A |
10: 86,549,599 (GRCm39) |
N264K |
possibly damaging |
Het |
Uba2 |
A |
C |
7: 33,853,987 (GRCm39) |
S318R |
probably benign |
Het |
Wapl |
T |
A |
14: 34,451,139 (GRCm39) |
N724K |
probably damaging |
Het |
Wfdc9 |
T |
A |
2: 164,493,671 (GRCm39) |
I5F |
probably damaging |
Het |
Zan |
C |
T |
5: 137,406,563 (GRCm39) |
D3686N |
unknown |
Het |
Zfp618 |
A |
T |
4: 63,012,708 (GRCm39) |
Y140F |
probably benign |
Het |
Zfp790 |
A |
G |
7: 29,527,593 (GRCm39) |
T93A |
probably benign |
Het |
Zfp979 |
A |
C |
4: 147,697,984 (GRCm39) |
F242V |
probably benign |
Het |
|
Other mutations in Or6c208 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02162:Or6c208
|
APN |
10 |
129,223,973 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03096:Or6c208
|
APN |
10 |
129,224,318 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03365:Or6c208
|
APN |
10 |
129,224,108 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0645:Or6c208
|
UTSW |
10 |
129,224,162 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1104:Or6c208
|
UTSW |
10 |
129,224,090 (GRCm39) |
missense |
probably benign |
0.31 |
R1456:Or6c208
|
UTSW |
10 |
129,223,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R1487:Or6c208
|
UTSW |
10 |
129,224,209 (GRCm39) |
missense |
probably benign |
0.26 |
R1526:Or6c208
|
UTSW |
10 |
129,224,176 (GRCm39) |
missense |
probably benign |
0.01 |
R1860:Or6c208
|
UTSW |
10 |
129,223,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R1930:Or6c208
|
UTSW |
10 |
129,223,745 (GRCm39) |
missense |
probably benign |
|
R1931:Or6c208
|
UTSW |
10 |
129,223,745 (GRCm39) |
missense |
probably benign |
|
R4623:Or6c208
|
UTSW |
10 |
129,223,915 (GRCm39) |
missense |
probably benign |
0.11 |
R5385:Or6c208
|
UTSW |
10 |
129,223,633 (GRCm39) |
missense |
probably benign |
0.05 |
R5483:Or6c208
|
UTSW |
10 |
129,223,526 (GRCm39) |
missense |
probably benign |
0.02 |
R5780:Or6c208
|
UTSW |
10 |
129,223,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Or6c208
|
UTSW |
10 |
129,224,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R6956:Or6c208
|
UTSW |
10 |
129,224,166 (GRCm39) |
missense |
probably benign |
0.04 |
R7102:Or6c208
|
UTSW |
10 |
129,224,036 (GRCm39) |
missense |
probably damaging |
0.99 |
R7584:Or6c208
|
UTSW |
10 |
129,223,901 (GRCm39) |
missense |
probably damaging |
0.99 |
R7626:Or6c208
|
UTSW |
10 |
129,223,726 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8845:Or6c208
|
UTSW |
10 |
129,224,065 (GRCm39) |
missense |
probably damaging |
0.96 |
|