Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
A |
17: 9,220,728 (GRCm39) |
V409E |
probably damaging |
Het |
1700086D15Rik |
A |
G |
11: 65,043,393 (GRCm39) |
|
probably benign |
Het |
Apba1 |
A |
G |
19: 23,914,945 (GRCm39) |
N715S |
possibly damaging |
Het |
Arfgef3 |
G |
T |
10: 18,476,238 (GRCm39) |
A1527D |
probably damaging |
Het |
Cmtm2a |
G |
T |
8: 105,010,501 (GRCm39) |
P133T |
probably damaging |
Het |
Cyp2d9 |
T |
C |
15: 82,340,900 (GRCm39) |
V483A |
probably benign |
Het |
Dclre1b |
T |
A |
3: 103,715,456 (GRCm39) |
D14V |
probably damaging |
Het |
Dock5 |
T |
C |
14: 68,083,535 (GRCm39) |
I125V |
probably benign |
Het |
Fat4 |
T |
C |
3: 38,945,325 (GRCm39) |
V1406A |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,183,315 (GRCm39) |
F1790S |
possibly damaging |
Het |
Gm4787 |
A |
T |
12: 81,425,948 (GRCm39) |
M70K |
probably damaging |
Het |
Gulp1 |
A |
T |
1: 44,747,777 (GRCm39) |
D10V |
probably damaging |
Het |
Hagh |
T |
C |
17: 25,079,916 (GRCm39) |
|
probably benign |
Het |
Htt |
A |
G |
5: 34,956,789 (GRCm39) |
E206G |
probably damaging |
Het |
Hyou1 |
A |
G |
9: 44,299,355 (GRCm39) |
E682G |
probably benign |
Het |
Ift56 |
T |
C |
6: 38,362,435 (GRCm39) |
L70P |
probably damaging |
Het |
Igkv4-59 |
G |
T |
6: 69,415,450 (GRCm39) |
A35E |
probably damaging |
Het |
Krt78 |
A |
G |
15: 101,862,421 (GRCm39) |
V80A |
probably damaging |
Het |
Lars2 |
G |
A |
9: 123,247,841 (GRCm39) |
A333T |
possibly damaging |
Het |
Lrrc4 |
G |
A |
6: 28,830,515 (GRCm39) |
R367W |
probably damaging |
Het |
Med1 |
A |
T |
11: 98,080,009 (GRCm39) |
M44K |
possibly damaging |
Het |
Mep1a |
T |
A |
17: 43,788,986 (GRCm39) |
|
probably null |
Het |
Mmrn1 |
A |
G |
6: 60,952,819 (GRCm39) |
I367V |
probably benign |
Het |
Myo18a |
T |
C |
11: 77,738,830 (GRCm39) |
L1677P |
probably damaging |
Het |
Neb |
T |
C |
2: 52,209,717 (GRCm39) |
T246A |
probably benign |
Het |
Nkiras1 |
A |
G |
14: 18,280,073 (GRCm38) |
R155G |
probably benign |
Het |
Nrip1 |
T |
C |
16: 76,089,379 (GRCm39) |
N726S |
probably benign |
Het |
Nyap2 |
A |
G |
1: 81,219,156 (GRCm39) |
T393A |
possibly damaging |
Het |
Oprm1 |
A |
T |
10: 6,780,051 (GRCm39) |
I238F |
probably damaging |
Het |
Or4b1b |
A |
G |
2: 90,112,557 (GRCm39) |
Y121H |
probably damaging |
Het |
Or4b1d |
G |
A |
2: 89,969,489 (GRCm39) |
|
probably benign |
Het |
Or5m11b |
T |
A |
2: 85,805,764 (GRCm39) |
M59K |
probably damaging |
Het |
Pcnx2 |
T |
A |
8: 126,613,779 (GRCm39) |
E557D |
probably damaging |
Het |
Pole |
A |
G |
5: 110,472,425 (GRCm39) |
I1563V |
probably benign |
Het |
Pramel21 |
C |
A |
4: 143,341,851 (GRCm39) |
H93Q |
probably benign |
Het |
Prdx3 |
T |
G |
19: 60,859,848 (GRCm39) |
|
probably benign |
Het |
Rgsl1 |
C |
T |
1: 153,669,501 (GRCm39) |
R295K |
probably null |
Het |
Rhbdl2 |
T |
A |
4: 123,723,463 (GRCm39) |
L289* |
probably null |
Het |
Rnps1 |
A |
G |
17: 24,640,835 (GRCm39) |
|
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,395,823 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,603,033 (GRCm39) |
Y4518N |
probably damaging |
Het |
Scyl3 |
A |
G |
1: 163,772,436 (GRCm39) |
N296S |
probably damaging |
Het |
Sipa1l3 |
G |
A |
7: 29,047,964 (GRCm39) |
T1308M |
probably damaging |
Het |
Slc39a9 |
A |
G |
12: 80,691,662 (GRCm39) |
D3G |
probably damaging |
Het |
Slc4a9 |
A |
G |
18: 36,662,740 (GRCm39) |
E165G |
probably benign |
Het |
Slc6a3 |
A |
T |
13: 73,686,776 (GRCm39) |
I48F |
probably benign |
Het |
Stxbp3 |
C |
T |
3: 108,709,476 (GRCm39) |
C354Y |
probably damaging |
Het |
Terb1 |
C |
A |
8: 105,199,674 (GRCm39) |
|
probably benign |
Het |
Tfrc |
G |
A |
16: 32,443,649 (GRCm39) |
|
probably null |
Het |
Toporsl |
A |
C |
4: 52,611,134 (GRCm39) |
R342S |
probably benign |
Het |
Ube2d3 |
T |
A |
3: 135,170,978 (GRCm39) |
W141R |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,910,486 (GRCm39) |
V3417L |
probably benign |
Het |
|
Other mutations in Dok3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01837:Dok3
|
APN |
13 |
55,671,383 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Dok3
|
APN |
13 |
55,672,183 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02218:Dok3
|
APN |
13 |
55,671,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02656:Dok3
|
APN |
13 |
55,676,293 (GRCm39) |
missense |
probably damaging |
0.97 |
R0601:Dok3
|
UTSW |
13 |
55,672,076 (GRCm39) |
missense |
probably benign |
0.16 |
R1306:Dok3
|
UTSW |
13 |
55,675,261 (GRCm39) |
nonsense |
probably null |
|
R1749:Dok3
|
UTSW |
13 |
55,672,168 (GRCm39) |
frame shift |
probably null |
|
R3684:Dok3
|
UTSW |
13 |
55,672,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Dok3
|
UTSW |
13 |
55,671,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Dok3
|
UTSW |
13 |
55,671,389 (GRCm39) |
missense |
probably benign |
0.00 |
R7021:Dok3
|
UTSW |
13 |
55,672,097 (GRCm39) |
missense |
probably benign |
0.00 |
R7526:Dok3
|
UTSW |
13 |
55,675,306 (GRCm39) |
missense |
probably benign |
0.03 |
R8379:Dok3
|
UTSW |
13 |
55,671,833 (GRCm39) |
missense |
probably benign |
|
R8983:Dok3
|
UTSW |
13 |
55,671,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Dok3
|
UTSW |
13 |
55,672,186 (GRCm39) |
missense |
probably benign |
0.14 |
R9585:Dok3
|
UTSW |
13 |
55,672,057 (GRCm39) |
missense |
probably damaging |
1.00 |
|