Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd15 |
C |
T |
11: 77,515,410 (GRCm38) |
A71V |
probably damaging |
Het |
Ager |
A |
G |
17: 34,600,718 (GRCm38) |
E357G |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,729,049 (GRCm38) |
S2095P |
possibly damaging |
Het |
Ampd2 |
T |
C |
3: 108,080,337 (GRCm38) |
|
probably null |
Het |
Arrdc1 |
T |
C |
2: 24,925,795 (GRCm38) |
I398V |
probably benign |
Het |
Ash1l |
T |
C |
3: 89,052,065 (GRCm38) |
Y2250H |
probably damaging |
Het |
BC005561 |
T |
A |
5: 104,518,257 (GRCm38) |
I215N |
probably damaging |
Het |
Brca2 |
G |
A |
5: 150,552,258 (GRCm38) |
A2478T |
probably damaging |
Het |
Btrc |
T |
A |
19: 45,513,382 (GRCm38) |
|
probably benign |
Het |
C8g |
C |
T |
2: 25,500,216 (GRCm38) |
A6T |
probably benign |
Het |
Cdc123 |
T |
A |
2: 5,803,977 (GRCm38) |
|
probably null |
Het |
Cilp |
G |
A |
9: 65,279,715 (GRCm38) |
G1031S |
probably damaging |
Het |
Cldn5 |
G |
A |
16: 18,777,477 (GRCm38) |
G161D |
probably damaging |
Het |
Cndp2 |
G |
A |
18: 84,677,315 (GRCm38) |
|
probably benign |
Het |
Cntnap1 |
C |
A |
11: 101,180,360 (GRCm38) |
F366L |
probably damaging |
Het |
Corin |
C |
T |
5: 72,302,790 (GRCm38) |
|
probably null |
Het |
Ctdspl2 |
G |
A |
2: 122,003,929 (GRCm38) |
R332K |
probably benign |
Het |
Dido1 |
G |
A |
2: 180,662,328 (GRCm38) |
P1261L |
probably damaging |
Het |
Dopey1 |
A |
T |
9: 86,548,172 (GRCm38) |
R2200* |
probably null |
Het |
Dtx3l |
G |
A |
16: 35,932,728 (GRCm38) |
L503F |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,067,047 (GRCm38) |
K259R |
probably benign |
Het |
Enpep |
T |
A |
3: 129,319,448 (GRCm38) |
T203S |
probably damaging |
Het |
Epha2 |
T |
A |
4: 141,322,047 (GRCm38) |
|
probably null |
Het |
Fam20b |
T |
C |
1: 156,686,188 (GRCm38) |
|
probably benign |
Het |
Fbln7 |
A |
G |
2: 128,877,429 (GRCm38) |
T49A |
probably benign |
Het |
Fgf14 |
T |
A |
14: 124,676,539 (GRCm38) |
K60M |
probably benign |
Het |
Fhad1 |
T |
C |
4: 141,985,511 (GRCm38) |
I206V |
probably benign |
Het |
Figla |
A |
G |
6: 86,020,782 (GRCm38) |
E164G |
probably benign |
Het |
Gimap4 |
C |
A |
6: 48,691,282 (GRCm38) |
Q196K |
probably benign |
Het |
Glcci1 |
C |
T |
6: 8,537,964 (GRCm38) |
T6I |
probably damaging |
Het |
Gm6583 |
C |
T |
5: 112,354,764 (GRCm38) |
G358D |
probably benign |
Het |
Grk4 |
T |
C |
5: 34,694,750 (GRCm38) |
S113P |
probably benign |
Het |
Hectd3 |
G |
A |
4: 116,996,566 (GRCm38) |
E220K |
probably damaging |
Het |
Hecw1 |
A |
G |
13: 14,340,743 (GRCm38) |
|
probably null |
Het |
Helz2 |
G |
A |
2: 181,236,297 (GRCm38) |
P903S |
probably damaging |
Het |
Hydin |
T |
C |
8: 110,580,815 (GRCm38) |
V3942A |
probably benign |
Het |
Irs1 |
G |
T |
1: 82,289,444 (GRCm38) |
H350Q |
probably benign |
Het |
Kdm1b |
G |
A |
13: 47,064,054 (GRCm38) |
E46K |
probably damaging |
Het |
Klf11 |
A |
G |
12: 24,655,305 (GRCm38) |
N253D |
probably damaging |
Het |
Klhl23 |
T |
C |
2: 69,833,888 (GRCm38) |
I527T |
probably damaging |
Het |
Lars |
G |
A |
18: 42,210,050 (GRCm38) |
R1101C |
probably damaging |
Het |
Lcn4 |
G |
A |
2: 26,668,576 (GRCm38) |
P166L |
probably damaging |
Het |
Letmd1 |
T |
A |
15: 100,472,542 (GRCm38) |
|
probably null |
Het |
Lilra6 |
T |
A |
7: 3,912,662 (GRCm38) |
D358V |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,375,685 (GRCm38) |
D24G |
probably benign |
Het |
Mpp5 |
A |
G |
12: 78,829,727 (GRCm38) |
I482V |
probably benign |
Het |
Mroh2b |
G |
T |
15: 4,925,684 (GRCm38) |
D720Y |
probably damaging |
Het |
Mrps35 |
C |
T |
6: 147,055,984 (GRCm38) |
T169M |
probably damaging |
Het |
Muc4 |
G |
A |
16: 32,753,595 (GRCm38) |
G1157D |
probably benign |
Het |
Naga |
T |
A |
15: 82,334,788 (GRCm38) |
M237L |
probably null |
Het |
Nfu1 |
G |
A |
6: 87,020,809 (GRCm38) |
E225K |
probably damaging |
Het |
Nin |
A |
T |
12: 70,042,669 (GRCm38) |
L1324Q |
probably benign |
Het |
Oc90 |
T |
A |
15: 65,897,720 (GRCm38) |
Y96F |
probably damaging |
Het |
Olfr1253 |
C |
T |
2: 89,752,267 (GRCm38) |
C187Y |
probably damaging |
Het |
Olfr1471 |
T |
C |
19: 13,445,659 (GRCm38) |
Y216H |
probably damaging |
Het |
Olfr25 |
G |
A |
9: 38,330,131 (GRCm38) |
M181I |
possibly damaging |
Het |
Olfr522 |
A |
G |
7: 140,162,203 (GRCm38) |
V249A |
probably damaging |
Het |
Orc4 |
A |
T |
2: 48,909,494 (GRCm38) |
C324S |
possibly damaging |
Het |
Pdzrn4 |
T |
C |
15: 92,770,537 (GRCm38) |
S857P |
probably benign |
Het |
Plec |
C |
T |
15: 76,185,908 (GRCm38) |
E1000K |
possibly damaging |
Het |
Plvap |
A |
T |
8: 71,508,481 (GRCm38) |
V149D |
probably benign |
Het |
Pm20d2 |
A |
T |
4: 33,174,772 (GRCm38) |
N371K |
probably damaging |
Het |
Ppp2r5d |
A |
G |
17: 46,684,684 (GRCm38) |
Y480H |
probably benign |
Het |
Prkd1 |
A |
T |
12: 50,425,515 (GRCm38) |
V205E |
probably damaging |
Het |
R3hdm2 |
A |
G |
10: 127,476,690 (GRCm38) |
I434V |
probably benign |
Het |
Rel |
T |
A |
11: 23,745,546 (GRCm38) |
T246S |
probably damaging |
Het |
Rnf215 |
T |
A |
11: 4,136,719 (GRCm38) |
V172E |
probably damaging |
Het |
Scara3 |
T |
C |
14: 65,921,104 (GRCm38) |
D485G |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,431,157 (GRCm38) |
Y1308N |
probably damaging |
Het |
Sis |
A |
T |
3: 72,932,060 (GRCm38) |
D824E |
possibly damaging |
Het |
Slc27a4 |
T |
A |
2: 29,811,190 (GRCm38) |
V331E |
probably damaging |
Het |
Srebf1 |
C |
T |
11: 60,200,702 (GRCm38) |
R999H |
probably benign |
Het |
St3gal3 |
A |
C |
4: 118,107,662 (GRCm38) |
M1R |
probably null |
Het |
Tapbp |
C |
T |
17: 33,919,940 (GRCm38) |
|
probably null |
Het |
Tep1 |
A |
T |
14: 50,866,037 (GRCm38) |
N265K |
probably damaging |
Het |
Tln2 |
T |
A |
9: 67,296,414 (GRCm38) |
N470I |
probably damaging |
Het |
Trim43a |
G |
T |
9: 88,588,158 (GRCm38) |
W339L |
probably damaging |
Het |
Ttc22 |
T |
C |
4: 106,622,780 (GRCm38) |
F77S |
probably damaging |
Het |
Ttc8 |
A |
G |
12: 98,920,764 (GRCm38) |
E32G |
probably benign |
Het |
Uhmk1 |
A |
T |
1: 170,208,653 (GRCm38) |
|
probably null |
Het |
Usp17lc |
A |
G |
7: 103,418,941 (GRCm38) |
H481R |
possibly damaging |
Het |
Vamp8 |
G |
A |
6: 72,385,634 (GRCm38) |
T35M |
probably damaging |
Het |
Vill |
A |
G |
9: 119,065,586 (GRCm38) |
Y53C |
probably damaging |
Het |
Vmn1r222 |
A |
T |
13: 23,232,762 (GRCm38) |
S94T |
probably damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,305,151 (GRCm38) |
Y357C |
possibly damaging |
Het |
Vps13c |
T |
A |
9: 67,893,112 (GRCm38) |
V536D |
possibly damaging |
Het |
Vrtn |
G |
A |
12: 84,650,081 (GRCm38) |
C535Y |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,768,165 (GRCm38) |
Y181C |
probably damaging |
Het |
Wfikkn2 |
G |
A |
11: 94,238,895 (GRCm38) |
T140I |
probably damaging |
Het |
Ykt6 |
T |
A |
11: 5,962,349 (GRCm38) |
F101I |
probably damaging |
Het |
Zfp277 |
C |
T |
12: 40,378,826 (GRCm38) |
G174D |
probably benign |
Het |
Zfp638 |
A |
G |
6: 83,978,065 (GRCm38) |
|
probably null |
Het |
Zzef1 |
C |
T |
11: 72,924,679 (GRCm38) |
P2942S |
probably damaging |
Het |
|
Other mutations in Olfr1029 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02020:Olfr1029
|
APN |
2 |
85,975,235 (GRCm38) |
utr 5 prime |
probably benign |
|
IGL02126:Olfr1029
|
APN |
2 |
85,976,173 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02584:Olfr1029
|
APN |
2 |
85,975,875 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL03410:Olfr1029
|
APN |
2 |
85,975,420 (GRCm38) |
missense |
probably damaging |
0.99 |
R1466:Olfr1029
|
UTSW |
2 |
85,975,995 (GRCm38) |
missense |
probably damaging |
1.00 |
R1466:Olfr1029
|
UTSW |
2 |
85,975,995 (GRCm38) |
missense |
probably damaging |
1.00 |
R1499:Olfr1029
|
UTSW |
2 |
85,976,028 (GRCm38) |
missense |
possibly damaging |
0.62 |
R2925:Olfr1029
|
UTSW |
2 |
85,975,781 (GRCm38) |
nonsense |
probably null |
|
R2970:Olfr1029
|
UTSW |
2 |
85,976,110 (GRCm38) |
missense |
possibly damaging |
0.75 |
R4571:Olfr1029
|
UTSW |
2 |
85,975,831 (GRCm38) |
missense |
probably damaging |
0.97 |
R5533:Olfr1029
|
UTSW |
2 |
85,975,453 (GRCm38) |
missense |
possibly damaging |
0.78 |
R5654:Olfr1029
|
UTSW |
2 |
85,976,156 (GRCm38) |
missense |
probably benign |
0.00 |
R5827:Olfr1029
|
UTSW |
2 |
85,975,306 (GRCm38) |
missense |
probably benign |
0.00 |
R5967:Olfr1029
|
UTSW |
2 |
85,976,191 (GRCm38) |
missense |
probably benign |
0.01 |
R6291:Olfr1029
|
UTSW |
2 |
85,975,582 (GRCm38) |
missense |
probably damaging |
1.00 |
R6735:Olfr1029
|
UTSW |
2 |
85,975,434 (GRCm38) |
missense |
possibly damaging |
0.81 |
R6897:Olfr1029
|
UTSW |
2 |
85,975,356 (GRCm38) |
missense |
possibly damaging |
0.45 |
R7053:Olfr1029
|
UTSW |
2 |
85,976,014 (GRCm38) |
missense |
possibly damaging |
0.64 |
R7163:Olfr1029
|
UTSW |
2 |
85,975,588 (GRCm38) |
missense |
probably damaging |
1.00 |
R7358:Olfr1029
|
UTSW |
2 |
85,975,436 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8047:Olfr1029
|
UTSW |
2 |
85,975,927 (GRCm38) |
missense |
possibly damaging |
0.52 |
R8271:Olfr1029
|
UTSW |
2 |
85,975,741 (GRCm38) |
missense |
probably benign |
0.40 |
R8271:Olfr1029
|
UTSW |
2 |
85,975,422 (GRCm38) |
missense |
probably damaging |
1.00 |
R8364:Olfr1029
|
UTSW |
2 |
85,976,014 (GRCm38) |
missense |
possibly damaging |
0.64 |
R9100:Olfr1029
|
UTSW |
2 |
85,975,752 (GRCm38) |
missense |
probably benign |
0.00 |
R9190:Olfr1029
|
UTSW |
2 |
85,975,540 (GRCm38) |
missense |
possibly damaging |
0.66 |
R9646:Olfr1029
|
UTSW |
2 |
85,976,102 (GRCm38) |
missense |
probably benign |
0.18 |
|