Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd15 |
C |
T |
11: 77,406,236 (GRCm39) |
A71V |
probably damaging |
Het |
Ager |
A |
G |
17: 34,819,692 (GRCm39) |
E357G |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,378,797 (GRCm39) |
S2095P |
possibly damaging |
Het |
Ampd2 |
T |
C |
3: 107,987,653 (GRCm39) |
|
probably null |
Het |
Arrdc1 |
T |
C |
2: 24,815,807 (GRCm39) |
I398V |
probably benign |
Het |
Ash1l |
T |
C |
3: 88,959,372 (GRCm39) |
Y2250H |
probably damaging |
Het |
Brca2 |
G |
A |
5: 150,475,723 (GRCm39) |
A2478T |
probably damaging |
Het |
Btrc |
T |
A |
19: 45,501,821 (GRCm39) |
|
probably benign |
Het |
C8g |
C |
T |
2: 25,390,228 (GRCm39) |
A6T |
probably benign |
Het |
Ccdc121rt3 |
C |
T |
5: 112,502,630 (GRCm39) |
G358D |
probably benign |
Het |
Cdc123 |
T |
A |
2: 5,808,788 (GRCm39) |
|
probably null |
Het |
Cilp |
G |
A |
9: 65,186,997 (GRCm39) |
G1031S |
probably damaging |
Het |
Cldn5 |
G |
A |
16: 18,596,227 (GRCm39) |
G161D |
probably damaging |
Het |
Cndp2 |
G |
A |
18: 84,695,440 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
C |
A |
11: 101,071,186 (GRCm39) |
F366L |
probably damaging |
Het |
Corin |
C |
T |
5: 72,460,133 (GRCm39) |
|
probably null |
Het |
Ctdspl2 |
G |
A |
2: 121,834,410 (GRCm39) |
R332K |
probably benign |
Het |
Dido1 |
G |
A |
2: 180,304,121 (GRCm39) |
P1261L |
probably damaging |
Het |
Dop1a |
A |
T |
9: 86,430,225 (GRCm39) |
R2200* |
probably null |
Het |
Dtx3l |
G |
A |
16: 35,753,098 (GRCm39) |
L503F |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,044,029 (GRCm39) |
K259R |
probably benign |
Het |
Enpep |
T |
A |
3: 129,113,097 (GRCm39) |
T203S |
probably damaging |
Het |
Epha2 |
T |
A |
4: 141,049,358 (GRCm39) |
|
probably null |
Het |
Fam20b |
T |
C |
1: 156,513,758 (GRCm39) |
|
probably benign |
Het |
Fbln7 |
A |
G |
2: 128,719,349 (GRCm39) |
T49A |
probably benign |
Het |
Fgf14 |
T |
A |
14: 124,913,951 (GRCm39) |
K60M |
probably benign |
Het |
Fhad1 |
T |
C |
4: 141,712,822 (GRCm39) |
I206V |
probably benign |
Het |
Figla |
A |
G |
6: 85,997,764 (GRCm39) |
E164G |
probably benign |
Het |
Gimap4 |
C |
A |
6: 48,668,216 (GRCm39) |
Q196K |
probably benign |
Het |
Glcci1 |
C |
T |
6: 8,537,964 (GRCm39) |
T6I |
probably damaging |
Het |
Grk4 |
T |
C |
5: 34,852,094 (GRCm39) |
S113P |
probably benign |
Het |
Hectd3 |
G |
A |
4: 116,853,763 (GRCm39) |
E220K |
probably damaging |
Het |
Hecw1 |
A |
G |
13: 14,515,328 (GRCm39) |
|
probably null |
Het |
Helz2 |
G |
A |
2: 180,878,090 (GRCm39) |
P903S |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,307,447 (GRCm39) |
V3942A |
probably benign |
Het |
Irs1 |
G |
T |
1: 82,267,165 (GRCm39) |
H350Q |
probably benign |
Het |
Kdm1b |
G |
A |
13: 47,217,530 (GRCm39) |
E46K |
probably damaging |
Het |
Klf11 |
A |
G |
12: 24,705,304 (GRCm39) |
N253D |
probably damaging |
Het |
Klhl23 |
T |
C |
2: 69,664,232 (GRCm39) |
I527T |
probably damaging |
Het |
Lars1 |
G |
A |
18: 42,343,115 (GRCm39) |
R1101C |
probably damaging |
Het |
Lcn4 |
G |
A |
2: 26,558,588 (GRCm39) |
P166L |
probably damaging |
Het |
Letmd1 |
T |
A |
15: 100,370,423 (GRCm39) |
|
probably null |
Het |
Lilra6 |
T |
A |
7: 3,915,661 (GRCm39) |
D358V |
probably damaging |
Het |
Mmrn2 |
A |
G |
14: 34,097,642 (GRCm39) |
D24G |
probably benign |
Het |
Mroh2b |
G |
T |
15: 4,955,166 (GRCm39) |
D720Y |
probably damaging |
Het |
Mrps35 |
C |
T |
6: 146,957,482 (GRCm39) |
T169M |
probably damaging |
Het |
Muc4 |
G |
A |
16: 32,574,886 (GRCm39) |
G1157D |
probably benign |
Het |
Naga |
T |
A |
15: 82,218,989 (GRCm39) |
M237L |
probably null |
Het |
Nfu1 |
G |
A |
6: 86,997,791 (GRCm39) |
E225K |
probably damaging |
Het |
Nin |
A |
T |
12: 70,089,443 (GRCm39) |
L1324Q |
probably benign |
Het |
Oc90 |
T |
A |
15: 65,769,569 (GRCm39) |
Y96F |
probably damaging |
Het |
Or5b116 |
T |
C |
19: 13,423,023 (GRCm39) |
Y216H |
probably damaging |
Het |
Or5m11b |
T |
A |
2: 85,806,339 (GRCm39) |
F251I |
probably damaging |
Het |
Or6ae1 |
A |
G |
7: 139,742,116 (GRCm39) |
V249A |
probably damaging |
Het |
Or8c9 |
G |
A |
9: 38,241,427 (GRCm39) |
M181I |
possibly damaging |
Het |
Orc4 |
A |
T |
2: 48,799,506 (GRCm39) |
C324S |
possibly damaging |
Het |
Pals1 |
A |
G |
12: 78,876,501 (GRCm39) |
I482V |
probably benign |
Het |
Pdzrn4 |
T |
C |
15: 92,668,418 (GRCm39) |
S857P |
probably benign |
Het |
Plec |
C |
T |
15: 76,070,108 (GRCm39) |
E1000K |
possibly damaging |
Het |
Plvap |
A |
T |
8: 71,961,125 (GRCm39) |
V149D |
probably benign |
Het |
Pm20d2 |
A |
T |
4: 33,174,772 (GRCm39) |
N371K |
probably damaging |
Het |
Ppp2r5d |
A |
G |
17: 46,995,610 (GRCm39) |
Y480H |
probably benign |
Het |
Prkd1 |
A |
T |
12: 50,472,298 (GRCm39) |
V205E |
probably damaging |
Het |
R3hdm2 |
A |
G |
10: 127,312,559 (GRCm39) |
I434V |
probably benign |
Het |
Rel |
T |
A |
11: 23,695,546 (GRCm39) |
T246S |
probably damaging |
Het |
Rnf215 |
T |
A |
11: 4,086,719 (GRCm39) |
V172E |
probably damaging |
Het |
Scara3 |
T |
C |
14: 66,158,553 (GRCm39) |
D485G |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,321,169 (GRCm39) |
Y1308N |
probably damaging |
Het |
Sis |
A |
T |
3: 72,839,393 (GRCm39) |
D824E |
possibly damaging |
Het |
Slc27a4 |
T |
A |
2: 29,701,202 (GRCm39) |
V331E |
probably damaging |
Het |
Srebf1 |
C |
T |
11: 60,091,528 (GRCm39) |
R999H |
probably benign |
Het |
St3gal3 |
A |
C |
4: 117,964,859 (GRCm39) |
M1R |
probably null |
Het |
Tapbp |
C |
T |
17: 34,138,914 (GRCm39) |
|
probably null |
Het |
Tep1 |
A |
T |
14: 51,103,494 (GRCm39) |
N265K |
probably damaging |
Het |
Thoc2l |
T |
A |
5: 104,666,123 (GRCm39) |
I215N |
probably damaging |
Het |
Tln2 |
T |
A |
9: 67,203,696 (GRCm39) |
N470I |
probably damaging |
Het |
Trim43a |
G |
T |
9: 88,470,211 (GRCm39) |
W339L |
probably damaging |
Het |
Ttc22 |
T |
C |
4: 106,479,977 (GRCm39) |
F77S |
probably damaging |
Het |
Ttc8 |
A |
G |
12: 98,887,023 (GRCm39) |
E32G |
probably benign |
Het |
Uhmk1 |
A |
T |
1: 170,036,222 (GRCm39) |
|
probably null |
Het |
Usp17lc |
A |
G |
7: 103,068,148 (GRCm39) |
H481R |
possibly damaging |
Het |
Vamp8 |
G |
A |
6: 72,362,617 (GRCm39) |
T35M |
probably damaging |
Het |
Vill |
A |
G |
9: 118,894,654 (GRCm39) |
Y53C |
probably damaging |
Het |
Vmn1r222 |
A |
T |
13: 23,416,932 (GRCm39) |
S94T |
probably damaging |
Het |
Vmn2r93 |
A |
G |
17: 18,525,413 (GRCm39) |
Y357C |
possibly damaging |
Het |
Vps13c |
T |
A |
9: 67,800,394 (GRCm39) |
V536D |
possibly damaging |
Het |
Vrtn |
G |
A |
12: 84,696,855 (GRCm39) |
C535Y |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,367,388 (GRCm39) |
Y181C |
probably damaging |
Het |
Wfikkn2 |
G |
A |
11: 94,129,721 (GRCm39) |
T140I |
probably damaging |
Het |
Ykt6 |
T |
A |
11: 5,912,349 (GRCm39) |
F101I |
probably damaging |
Het |
Zfp277 |
C |
T |
12: 40,428,825 (GRCm39) |
G174D |
probably benign |
Het |
Zfp638 |
A |
G |
6: 83,955,047 (GRCm39) |
|
probably null |
Het |
Zzef1 |
C |
T |
11: 72,815,505 (GRCm39) |
P2942S |
probably damaging |
Het |
|
Other mutations in Or4a80 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01938:Or4a80
|
APN |
2 |
89,582,692 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02287:Or4a80
|
APN |
2 |
89,582,958 (GRCm39) |
nonsense |
probably null |
|
IGL03149:Or4a80
|
APN |
2 |
89,583,172 (GRCm39) |
splice site |
probably null |
|
R0017:Or4a80
|
UTSW |
2 |
89,582,365 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1466:Or4a80
|
UTSW |
2 |
89,582,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Or4a80
|
UTSW |
2 |
89,582,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R2008:Or4a80
|
UTSW |
2 |
89,582,417 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2484:Or4a80
|
UTSW |
2 |
89,582,578 (GRCm39) |
missense |
probably benign |
0.00 |
R5135:Or4a80
|
UTSW |
2 |
89,582,239 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5648:Or4a80
|
UTSW |
2 |
89,582,417 (GRCm39) |
missense |
probably damaging |
0.99 |
R6021:Or4a80
|
UTSW |
2 |
89,582,465 (GRCm39) |
missense |
probably benign |
0.13 |
R6952:Or4a80
|
UTSW |
2 |
89,582,971 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7039:Or4a80
|
UTSW |
2 |
89,583,095 (GRCm39) |
missense |
probably benign |
0.01 |
R7088:Or4a80
|
UTSW |
2 |
89,582,443 (GRCm39) |
missense |
probably benign |
0.01 |
R7443:Or4a80
|
UTSW |
2 |
89,582,285 (GRCm39) |
missense |
probably benign |
0.01 |
R7444:Or4a80
|
UTSW |
2 |
89,583,103 (GRCm39) |
missense |
probably benign |
0.01 |
R7538:Or4a80
|
UTSW |
2 |
89,582,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Or4a80
|
UTSW |
2 |
89,582,906 (GRCm39) |
missense |
probably benign |
0.32 |
R7818:Or4a80
|
UTSW |
2 |
89,582,288 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7964:Or4a80
|
UTSW |
2 |
89,583,158 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8358:Or4a80
|
UTSW |
2 |
89,582,423 (GRCm39) |
missense |
probably benign |
0.24 |
R8438:Or4a80
|
UTSW |
2 |
89,583,061 (GRCm39) |
missense |
probably damaging |
0.98 |
R8493:Or4a80
|
UTSW |
2 |
89,582,599 (GRCm39) |
missense |
probably benign |
0.06 |
R8724:Or4a80
|
UTSW |
2 |
89,582,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Or4a80
|
UTSW |
2 |
89,583,298 (GRCm39) |
start gained |
probably benign |
|
R9668:Or4a80
|
UTSW |
2 |
89,582,636 (GRCm39) |
missense |
probably benign |
|
|