Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930578I06Rik |
C |
T |
14: 64,210,658 (GRCm39) |
R190H |
probably benign |
Het |
Acp6 |
T |
C |
3: 97,066,683 (GRCm39) |
|
probably null |
Het |
Adora3 |
T |
A |
3: 105,815,131 (GRCm39) |
Y148N |
probably damaging |
Het |
Ahnak2 |
G |
A |
12: 112,740,040 (GRCm39) |
S538L |
probably damaging |
Het |
Aox3 |
T |
G |
1: 58,215,646 (GRCm39) |
V1026G |
probably damaging |
Het |
Ap3d1 |
TTCTCTCTCTCTCTCTCT |
TTCTCTCTCTCTCTCT |
10: 80,548,612 (GRCm39) |
|
probably null |
Het |
Arhgef37 |
G |
A |
18: 61,627,996 (GRCm39) |
A649V |
probably benign |
Het |
Atp5f1a |
G |
A |
18: 77,869,015 (GRCm39) |
R413H |
possibly damaging |
Het |
Bace1 |
A |
T |
9: 45,766,109 (GRCm39) |
I179F |
probably damaging |
Het |
Brinp1 |
A |
G |
4: 68,717,123 (GRCm39) |
F242L |
probably damaging |
Het |
Brk1 |
T |
C |
6: 113,592,805 (GRCm39) |
Y63H |
possibly damaging |
Het |
Ccdc74a |
A |
G |
16: 17,466,736 (GRCm39) |
T148A |
probably benign |
Het |
Cenpc1 |
T |
A |
5: 86,193,180 (GRCm39) |
L236F |
probably damaging |
Het |
Col13a1 |
C |
T |
10: 61,698,439 (GRCm39) |
E541K |
unknown |
Het |
Copg1 |
T |
A |
6: 87,866,678 (GRCm39) |
C44S |
probably damaging |
Het |
D130043K22Rik |
A |
G |
13: 25,047,595 (GRCm39) |
E380G |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,404,460 (GRCm39) |
D2694G |
probably damaging |
Het |
Dgkd |
A |
T |
1: 87,844,560 (GRCm39) |
N242I |
possibly damaging |
Het |
Dnah2 |
C |
T |
11: 69,313,416 (GRCm39) |
V4248I |
probably damaging |
Het |
Dpy19l3 |
T |
A |
7: 35,411,607 (GRCm39) |
K376* |
probably null |
Het |
Eef1d |
A |
G |
15: 75,775,255 (GRCm39) |
S135P |
possibly damaging |
Het |
Epc2 |
T |
A |
2: 49,427,177 (GRCm39) |
S574T |
probably benign |
Het |
Eps15 |
G |
A |
4: 109,223,727 (GRCm39) |
|
probably benign |
Het |
Eps8 |
T |
C |
6: 137,455,967 (GRCm39) |
|
probably benign |
Het |
Exoc5 |
A |
T |
14: 49,289,839 (GRCm39) |
V13E |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,214,317 (GRCm39) |
C765S |
possibly damaging |
Het |
Fbxo5 |
A |
T |
10: 5,752,392 (GRCm39) |
C74S |
probably benign |
Het |
Fbxw9 |
T |
C |
8: 85,792,530 (GRCm39) |
S322P |
probably damaging |
Het |
Fmo5 |
T |
A |
3: 97,553,195 (GRCm39) |
I381N |
probably damaging |
Het |
Fmo6 |
T |
C |
1: 162,751,964 (GRCm39) |
D175G |
probably benign |
Het |
Gm7361 |
A |
G |
5: 26,467,008 (GRCm39) |
|
probably null |
Het |
Gm9961 |
G |
A |
16: 11,720,899 (GRCm39) |
|
probably benign |
Het |
Golga7b |
T |
A |
19: 42,255,405 (GRCm39) |
|
probably null |
Het |
Gorab |
T |
C |
1: 163,213,967 (GRCm39) |
E321G |
probably benign |
Het |
Gpx1 |
T |
A |
9: 108,216,594 (GRCm39) |
V28E |
probably benign |
Het |
H2-T15 |
T |
A |
17: 36,369,253 (GRCm39) |
|
probably benign |
Het |
H3c14 |
T |
C |
3: 96,154,575 (GRCm39) |
I125T |
probably damaging |
Het |
Hk1 |
T |
C |
10: 62,178,318 (GRCm39) |
S8G |
probably benign |
Het |
Iqsec1 |
C |
T |
6: 90,641,038 (GRCm39) |
R1026H |
probably damaging |
Het |
Kdm4b |
A |
T |
17: 56,660,091 (GRCm39) |
Y86F |
probably benign |
Het |
Kprp |
C |
T |
3: 92,731,829 (GRCm39) |
R407Q |
unknown |
Het |
Lamb1 |
C |
T |
12: 31,371,005 (GRCm39) |
T1400M |
probably benign |
Het |
Lcor |
G |
T |
19: 41,573,803 (GRCm39) |
A853S |
probably benign |
Het |
Lrriq3 |
T |
A |
3: 154,893,447 (GRCm39) |
Y383N |
possibly damaging |
Het |
Map3k21 |
T |
C |
8: 126,654,294 (GRCm39) |
I371T |
probably benign |
Het |
Mllt1 |
A |
T |
17: 57,212,819 (GRCm39) |
F105I |
probably damaging |
Het |
Nfatc2 |
A |
G |
2: 168,378,312 (GRCm39) |
M451T |
probably damaging |
Het |
Nfkbiz |
A |
C |
16: 55,638,787 (GRCm39) |
N224K |
probably damaging |
Het |
Nlrp4d |
A |
G |
7: 10,115,088 (GRCm39) |
V531A |
noncoding transcript |
Het |
Noc3l |
A |
G |
19: 38,778,081 (GRCm39) |
Y778H |
probably benign |
Het |
Nup98 |
C |
A |
7: 101,802,403 (GRCm39) |
A734S |
possibly damaging |
Het |
Or2ag18 |
T |
C |
7: 106,405,171 (GRCm39) |
Y166C |
probably damaging |
Het |
Or4k2 |
T |
A |
14: 50,424,039 (GRCm39) |
I212F |
probably damaging |
Het |
Or9g20 |
A |
G |
2: 85,630,033 (GRCm39) |
Y194H |
probably damaging |
Het |
Or9r7 |
T |
A |
10: 129,962,756 (GRCm39) |
R57* |
probably null |
Het |
Pate4 |
A |
T |
9: 35,519,535 (GRCm39) |
C52S |
probably damaging |
Het |
Pecr |
C |
A |
1: 72,316,490 (GRCm39) |
A72S |
probably benign |
Het |
Pomt1 |
A |
G |
2: 32,142,004 (GRCm39) |
N578S |
probably benign |
Het |
Ppm1a |
T |
C |
12: 72,830,738 (GRCm39) |
S88P |
probably benign |
Het |
Ppm1l |
T |
A |
3: 69,449,844 (GRCm39) |
|
probably benign |
Het |
Prdm13 |
A |
G |
4: 21,685,543 (GRCm39) |
S86P |
unknown |
Het |
Prph2 |
T |
C |
17: 47,221,848 (GRCm39) |
S76P |
probably benign |
Het |
Sarnp |
G |
A |
10: 128,669,212 (GRCm39) |
R23H |
probably damaging |
Het |
Septin1 |
T |
C |
7: 126,816,064 (GRCm39) |
|
probably benign |
Het |
Serpini1 |
T |
C |
3: 75,520,481 (GRCm39) |
I26T |
probably benign |
Het |
Setdb2 |
A |
G |
14: 59,646,715 (GRCm39) |
I616T |
probably benign |
Het |
Slc38a6 |
T |
A |
12: 73,390,424 (GRCm39) |
|
probably null |
Het |
Smg6 |
T |
C |
11: 74,820,988 (GRCm39) |
S420P |
possibly damaging |
Het |
Srp72 |
T |
A |
5: 77,132,009 (GRCm39) |
H229Q |
probably benign |
Het |
Ston2 |
A |
G |
12: 91,615,448 (GRCm39) |
V320A |
possibly damaging |
Het |
Stx3 |
A |
T |
19: 11,754,515 (GRCm39) |
I269N |
possibly damaging |
Het |
Tdg-ps |
A |
G |
15: 82,400,843 (GRCm39) |
|
noncoding transcript |
Het |
Tecpr1 |
T |
A |
5: 144,150,935 (GRCm39) |
N291I |
probably benign |
Het |
Tmem177 |
A |
G |
1: 119,838,553 (GRCm39) |
V42A |
probably benign |
Het |
Trim26 |
T |
A |
17: 37,168,886 (GRCm39) |
|
probably benign |
Het |
Ttc17 |
A |
G |
2: 94,196,980 (GRCm39) |
S456P |
probably benign |
Het |
Tubgcp6 |
T |
C |
15: 88,988,021 (GRCm39) |
Y984C |
probably benign |
Het |
Unc5cl |
A |
G |
17: 48,766,872 (GRCm39) |
E82G |
possibly damaging |
Het |
Uncx |
T |
C |
5: 139,529,875 (GRCm39) |
S43P |
probably damaging |
Het |
Vmn1r1 |
A |
G |
1: 181,985,332 (GRCm39) |
V111A |
probably benign |
Het |
Vmn1r168 |
A |
G |
7: 23,240,907 (GRCm39) |
I255V |
probably damaging |
Het |
Vwce |
A |
G |
19: 10,628,000 (GRCm39) |
T487A |
probably benign |
Het |
Xaf1 |
A |
G |
11: 72,197,682 (GRCm39) |
|
probably benign |
Het |
Zfp27 |
G |
T |
7: 29,594,261 (GRCm39) |
P568Q |
probably damaging |
Het |
Zfp382 |
A |
T |
7: 29,832,885 (GRCm39) |
I179F |
possibly damaging |
Het |
|
Other mutations in Slc2a10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Slc2a10
|
APN |
2 |
165,356,700 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01465:Slc2a10
|
APN |
2 |
165,359,597 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02565:Slc2a10
|
APN |
2 |
165,357,000 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02902:Slc2a10
|
APN |
2 |
165,360,142 (GRCm39) |
missense |
probably benign |
0.08 |
PIT4362001:Slc2a10
|
UTSW |
2 |
165,358,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1453:Slc2a10
|
UTSW |
2 |
165,359,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1677:Slc2a10
|
UTSW |
2 |
165,357,361 (GRCm39) |
missense |
probably benign |
0.04 |
R1850:Slc2a10
|
UTSW |
2 |
165,357,133 (GRCm39) |
missense |
probably benign |
0.00 |
R1920:Slc2a10
|
UTSW |
2 |
165,356,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Slc2a10
|
UTSW |
2 |
165,356,701 (GRCm39) |
nonsense |
probably null |
|
R3921:Slc2a10
|
UTSW |
2 |
165,357,521 (GRCm39) |
missense |
probably benign |
0.00 |
R4407:Slc2a10
|
UTSW |
2 |
165,356,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Slc2a10
|
UTSW |
2 |
165,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R4923:Slc2a10
|
UTSW |
2 |
165,356,676 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4935:Slc2a10
|
UTSW |
2 |
165,359,578 (GRCm39) |
missense |
probably benign |
0.05 |
R4954:Slc2a10
|
UTSW |
2 |
165,356,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R5681:Slc2a10
|
UTSW |
2 |
165,356,660 (GRCm39) |
missense |
probably benign |
0.00 |
R5782:Slc2a10
|
UTSW |
2 |
165,356,758 (GRCm39) |
nonsense |
probably null |
|
R6116:Slc2a10
|
UTSW |
2 |
165,359,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R6713:Slc2a10
|
UTSW |
2 |
165,357,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Slc2a10
|
UTSW |
2 |
165,357,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7237:Slc2a10
|
UTSW |
2 |
165,357,197 (GRCm39) |
missense |
probably benign |
|
R7568:Slc2a10
|
UTSW |
2 |
165,356,802 (GRCm39) |
missense |
probably damaging |
0.98 |
R8323:Slc2a10
|
UTSW |
2 |
165,356,671 (GRCm39) |
missense |
probably benign |
0.05 |
R8407:Slc2a10
|
UTSW |
2 |
165,356,787 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9147:Slc2a10
|
UTSW |
2 |
165,357,543 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9148:Slc2a10
|
UTSW |
2 |
165,357,543 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9632:Slc2a10
|
UTSW |
2 |
165,358,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|