Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009J06Rik |
G |
A |
6: 40,945,138 (GRCm39) |
V206I |
probably damaging |
Het |
Abca8b |
A |
C |
11: 109,865,500 (GRCm39) |
M319R |
probably damaging |
Het |
Abcc6 |
T |
C |
7: 45,665,928 (GRCm39) |
R231G |
probably benign |
Het |
Acadm |
A |
G |
3: 153,635,209 (GRCm39) |
Y302H |
probably damaging |
Het |
Acox3 |
C |
A |
5: 35,760,352 (GRCm39) |
R423S |
probably damaging |
Het |
Adgrb3 |
A |
C |
1: 25,527,169 (GRCm39) |
M589R |
probably benign |
Het |
Adgrl2 |
A |
C |
3: 148,564,909 (GRCm39) |
F224V |
probably damaging |
Het |
Adm2 |
G |
C |
15: 89,208,282 (GRCm39) |
G74A |
probably damaging |
Het |
Aen |
T |
A |
7: 78,552,370 (GRCm39) |
V15E |
probably damaging |
Het |
Ankzf1 |
T |
A |
1: 75,169,160 (GRCm39) |
V22D |
possibly damaging |
Het |
Arap2 |
T |
A |
5: 62,763,498 (GRCm39) |
K1549* |
probably null |
Het |
Arhgef11 |
G |
A |
3: 87,620,324 (GRCm39) |
R430H |
probably benign |
Het |
Asb17 |
T |
G |
3: 153,550,148 (GRCm39) |
L60W |
probably damaging |
Het |
BC035044 |
T |
C |
6: 128,867,948 (GRCm39) |
|
probably benign |
Het |
Bltp2 |
A |
G |
11: 78,166,000 (GRCm39) |
T1422A |
probably benign |
Het |
Cacna2d1 |
A |
T |
5: 16,471,716 (GRCm39) |
M254L |
possibly damaging |
Het |
Celf6 |
T |
C |
9: 59,511,160 (GRCm39) |
|
probably benign |
Het |
Cemip2 |
G |
T |
19: 21,789,937 (GRCm39) |
A668S |
probably benign |
Het |
Coro2b |
C |
T |
9: 62,333,123 (GRCm39) |
V120I |
probably benign |
Het |
Cyp20a1 |
C |
A |
1: 60,415,353 (GRCm39) |
|
probably benign |
Het |
Cyp2c67 |
C |
A |
19: 39,631,708 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
A |
G |
9: 111,297,122 (GRCm39) |
H222R |
probably benign |
Het |
Deaf1 |
A |
G |
7: 140,904,060 (GRCm39) |
S109P |
possibly damaging |
Het |
Dlg5 |
T |
A |
14: 24,194,516 (GRCm39) |
D1675V |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,727,268 (GRCm39) |
V605E |
probably benign |
Het |
Dync2i1 |
T |
C |
12: 116,195,404 (GRCm39) |
|
probably benign |
Het |
Frem2 |
A |
T |
3: 53,479,876 (GRCm39) |
I1939N |
possibly damaging |
Het |
Fsip2 |
A |
T |
2: 82,811,931 (GRCm39) |
Y2750F |
possibly damaging |
Het |
Gpr39 |
T |
A |
1: 125,800,161 (GRCm39) |
I304N |
probably damaging |
Het |
Hdac7 |
G |
A |
15: 97,707,410 (GRCm39) |
|
probably benign |
Het |
Hipk1 |
T |
C |
3: 103,685,480 (GRCm39) |
H45R |
probably benign |
Het |
Hyal2 |
T |
C |
9: 107,447,386 (GRCm39) |
L13P |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,221,997 (GRCm39) |
R479W |
probably damaging |
Het |
Lilrb4b |
A |
G |
10: 51,357,517 (GRCm39) |
T118A |
probably damaging |
Het |
Lin7a |
C |
A |
10: 107,247,930 (GRCm39) |
F78L |
possibly damaging |
Het |
Lpin3 |
A |
G |
2: 160,737,310 (GRCm39) |
D119G |
possibly damaging |
Het |
Lrp2 |
G |
A |
2: 69,331,074 (GRCm39) |
R1661C |
probably damaging |
Het |
Lrrc45 |
A |
G |
11: 120,610,844 (GRCm39) |
K527E |
probably benign |
Het |
Map10 |
C |
T |
8: 126,397,611 (GRCm39) |
P335S |
probably benign |
Het |
Mast3 |
A |
G |
8: 71,244,955 (GRCm39) |
S2P |
possibly damaging |
Het |
Mbtps1 |
A |
G |
8: 120,268,808 (GRCm39) |
|
probably benign |
Het |
Mms22l |
T |
A |
4: 24,591,084 (GRCm39) |
N1018K |
probably benign |
Het |
Nckipsd |
C |
A |
9: 108,689,571 (GRCm39) |
A244D |
possibly damaging |
Het |
Nt5el |
A |
T |
13: 105,248,877 (GRCm39) |
R364* |
probably null |
Het |
Or12k5 |
C |
A |
2: 36,895,139 (GRCm39) |
L162F |
probably damaging |
Het |
Or1j1 |
A |
T |
2: 36,703,069 (GRCm39) |
F12I |
probably damaging |
Het |
Or4k44 |
A |
G |
2: 111,368,142 (GRCm39) |
V164A |
probably benign |
Het |
Or52j3 |
T |
A |
7: 102,836,421 (GRCm39) |
F204L |
probably benign |
Het |
Or8b12c |
T |
A |
9: 37,715,243 (GRCm39) |
I12N |
possibly damaging |
Het |
Pcx |
A |
T |
19: 4,652,251 (GRCm39) |
D112V |
probably damaging |
Het |
Phf14 |
G |
A |
6: 11,987,682 (GRCm39) |
|
probably null |
Het |
Pkd1l1 |
A |
G |
11: 8,851,200 (GRCm39) |
I744T |
probably damaging |
Het |
Ppip5k2 |
A |
G |
1: 97,668,607 (GRCm39) |
L560P |
probably damaging |
Het |
Psmd14 |
A |
T |
2: 61,615,874 (GRCm39) |
M248L |
probably benign |
Het |
Ryr1 |
T |
G |
7: 28,782,962 (GRCm39) |
E1884A |
possibly damaging |
Het |
Scn4b |
T |
A |
9: 45,061,727 (GRCm39) |
S204R |
probably damaging |
Het |
Slc12a1 |
A |
T |
2: 125,026,777 (GRCm39) |
M471L |
possibly damaging |
Het |
Slc17a5 |
A |
G |
9: 78,468,082 (GRCm39) |
V236A |
probably benign |
Het |
Sobp |
T |
C |
10: 42,897,720 (GRCm39) |
T622A |
probably damaging |
Het |
Spata31d1a |
G |
T |
13: 59,850,056 (GRCm39) |
R691S |
probably benign |
Het |
Speg |
A |
G |
1: 75,398,595 (GRCm39) |
E2014G |
probably damaging |
Het |
Steap4 |
A |
G |
5: 8,025,902 (GRCm39) |
|
probably benign |
Het |
Tas2r144 |
G |
A |
6: 42,192,537 (GRCm39) |
M92I |
probably benign |
Het |
Tbc1d5 |
T |
C |
17: 51,242,560 (GRCm39) |
Q179R |
probably benign |
Het |
Tcf25 |
T |
C |
8: 124,115,326 (GRCm39) |
Y188H |
probably benign |
Het |
Tmem200a |
G |
A |
10: 25,954,518 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
G |
A |
15: 72,897,816 (GRCm39) |
R377W |
probably damaging |
Het |
Tssk5 |
T |
C |
15: 76,256,409 (GRCm39) |
T337A |
probably benign |
Het |
Ttc23 |
T |
C |
7: 67,328,743 (GRCm39) |
V228A |
probably benign |
Het |
Tulp1 |
A |
T |
17: 28,581,645 (GRCm39) |
|
probably benign |
Het |
Uqcc3 |
A |
G |
19: 8,858,117 (GRCm39) |
F25L |
probably damaging |
Het |
Vmn2r1 |
G |
A |
3: 63,996,994 (GRCm39) |
G217S |
probably damaging |
Het |
Vmn2r120 |
C |
T |
17: 57,829,374 (GRCm39) |
E508K |
probably benign |
Het |
Wdfy3 |
C |
A |
5: 101,991,947 (GRCm39) |
V3451L |
probably benign |
Het |
Wdr19 |
G |
A |
5: 65,382,033 (GRCm39) |
V418I |
probably benign |
Het |
Xirp2 |
C |
T |
2: 67,338,383 (GRCm39) |
T208I |
probably benign |
Het |
Xpnpep1 |
A |
G |
19: 52,980,107 (GRCm39) |
V639A |
probably benign |
Het |
|
Other mutations in Adam7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00667:Adam7
|
APN |
14 |
68,759,387 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01418:Adam7
|
APN |
14 |
68,762,655 (GRCm39) |
missense |
probably benign |
|
IGL01934:Adam7
|
APN |
14 |
68,770,048 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02655:Adam7
|
APN |
14 |
68,754,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02669:Adam7
|
APN |
14 |
68,745,343 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4445001:Adam7
|
UTSW |
14 |
68,747,197 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0195:Adam7
|
UTSW |
14 |
68,765,076 (GRCm39) |
splice site |
probably benign |
|
R0277:Adam7
|
UTSW |
14 |
68,748,306 (GRCm39) |
splice site |
probably null |
|
R0362:Adam7
|
UTSW |
14 |
68,747,105 (GRCm39) |
splice site |
probably benign |
|
R0440:Adam7
|
UTSW |
14 |
68,748,305 (GRCm39) |
splice site |
probably null |
|
R0927:Adam7
|
UTSW |
14 |
68,754,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Adam7
|
UTSW |
14 |
68,752,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R1270:Adam7
|
UTSW |
14 |
68,765,118 (GRCm39) |
missense |
probably damaging |
0.98 |
R1299:Adam7
|
UTSW |
14 |
68,763,748 (GRCm39) |
splice site |
probably benign |
|
R1527:Adam7
|
UTSW |
14 |
68,738,970 (GRCm39) |
missense |
probably benign |
0.04 |
R1731:Adam7
|
UTSW |
14 |
68,762,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Adam7
|
UTSW |
14 |
68,735,899 (GRCm39) |
missense |
probably benign |
0.00 |
R1921:Adam7
|
UTSW |
14 |
68,750,074 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2062:Adam7
|
UTSW |
14 |
68,742,610 (GRCm39) |
missense |
probably benign |
0.09 |
R2156:Adam7
|
UTSW |
14 |
68,748,792 (GRCm39) |
missense |
probably benign |
0.02 |
R2353:Adam7
|
UTSW |
14 |
68,742,537 (GRCm39) |
missense |
probably benign |
0.01 |
R2697:Adam7
|
UTSW |
14 |
68,752,232 (GRCm39) |
nonsense |
probably null |
|
R4080:Adam7
|
UTSW |
14 |
68,757,988 (GRCm39) |
missense |
probably benign |
0.05 |
R4775:Adam7
|
UTSW |
14 |
68,745,361 (GRCm39) |
missense |
probably benign |
0.41 |
R5202:Adam7
|
UTSW |
14 |
68,745,305 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6006:Adam7
|
UTSW |
14 |
68,748,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6087:Adam7
|
UTSW |
14 |
68,748,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Adam7
|
UTSW |
14 |
68,742,546 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6417:Adam7
|
UTSW |
14 |
68,742,070 (GRCm39) |
missense |
probably benign |
0.37 |
R6672:Adam7
|
UTSW |
14 |
68,742,151 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6756:Adam7
|
UTSW |
14 |
68,762,728 (GRCm39) |
missense |
probably benign |
0.00 |
R6777:Adam7
|
UTSW |
14 |
68,762,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Adam7
|
UTSW |
14 |
68,771,100 (GRCm39) |
missense |
probably benign |
0.22 |
R7127:Adam7
|
UTSW |
14 |
68,752,218 (GRCm39) |
critical splice donor site |
probably null |
|
R7209:Adam7
|
UTSW |
14 |
68,767,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R7399:Adam7
|
UTSW |
14 |
68,741,915 (GRCm39) |
splice site |
probably null |
|
R7675:Adam7
|
UTSW |
14 |
68,737,302 (GRCm39) |
missense |
probably benign |
0.07 |
R7788:Adam7
|
UTSW |
14 |
68,750,094 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7868:Adam7
|
UTSW |
14 |
68,770,090 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8135:Adam7
|
UTSW |
14 |
68,754,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8281:Adam7
|
UTSW |
14 |
68,745,334 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8507:Adam7
|
UTSW |
14 |
68,763,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9049:Adam7
|
UTSW |
14 |
68,762,674 (GRCm39) |
missense |
probably benign |
0.01 |
R9240:Adam7
|
UTSW |
14 |
68,747,208 (GRCm39) |
missense |
probably benign |
0.02 |
R9429:Adam7
|
UTSW |
14 |
68,771,080 (GRCm39) |
missense |
probably null |
|
R9744:Adam7
|
UTSW |
14 |
68,742,583 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Adam7
|
UTSW |
14 |
68,765,150 (GRCm39) |
missense |
probably benign |
0.26 |
|