Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
T |
C |
6: 91,895,091 (GRCm39) |
V262A |
probably benign |
Het |
Abtb2 |
A |
G |
2: 103,397,349 (GRCm39) |
E93G |
possibly damaging |
Het |
Adam5 |
A |
C |
8: 25,232,172 (GRCm39) |
|
probably null |
Het |
Adam5 |
G |
A |
8: 25,271,619 (GRCm39) |
T596I |
probably damaging |
Het |
Adgrb2 |
T |
A |
4: 129,907,668 (GRCm39) |
Y1001N |
probably damaging |
Het |
Aox1 |
T |
G |
1: 58,344,544 (GRCm39) |
S546A |
probably benign |
Het |
Asic2 |
T |
C |
11: 81,464,280 (GRCm39) |
|
probably benign |
Het |
Cacna1g |
A |
G |
11: 94,350,177 (GRCm39) |
F556S |
possibly damaging |
Het |
Cbl |
A |
G |
9: 44,064,166 (GRCm39) |
V790A |
probably benign |
Het |
Cd300c2 |
A |
T |
11: 114,891,807 (GRCm39) |
C22* |
probably null |
Het |
Cdh11 |
C |
T |
8: 103,374,090 (GRCm39) |
|
probably null |
Het |
Ces2g |
C |
T |
8: 105,693,989 (GRCm39) |
Q442* |
probably null |
Het |
Cps1 |
A |
T |
1: 67,200,063 (GRCm39) |
T404S |
probably damaging |
Het |
Csf2rb2 |
A |
T |
15: 78,170,174 (GRCm39) |
|
probably null |
Het |
Csmd2 |
A |
G |
4: 128,346,318 (GRCm39) |
Y1526C |
probably benign |
Het |
Cyp2a12 |
C |
T |
7: 26,730,640 (GRCm39) |
Q202* |
probably null |
Het |
Cyp2c39 |
G |
A |
19: 39,502,020 (GRCm39) |
M136I |
probably benign |
Het |
Cyp2j13 |
G |
A |
4: 95,947,280 (GRCm39) |
T257I |
probably damaging |
Het |
Dnah8 |
T |
A |
17: 30,965,949 (GRCm39) |
L2427Q |
probably damaging |
Het |
Dop1b |
G |
T |
16: 93,560,318 (GRCm39) |
|
probably null |
Het |
Entrep1 |
A |
G |
19: 23,952,790 (GRCm39) |
S507P |
possibly damaging |
Het |
Epcam |
T |
C |
17: 87,951,049 (GRCm39) |
V212A |
possibly damaging |
Het |
Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
Flvcr2 |
T |
A |
12: 85,829,756 (GRCm39) |
V255D |
probably damaging |
Het |
Galc |
G |
T |
12: 98,197,731 (GRCm39) |
T326K |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gen1 |
A |
T |
12: 11,291,561 (GRCm39) |
Y808N |
probably benign |
Het |
Glis1 |
C |
T |
4: 107,476,761 (GRCm39) |
A306V |
probably damaging |
Het |
Gm10638 |
A |
G |
8: 87,473,028 (GRCm39) |
|
probably benign |
Het |
Gm12789 |
G |
A |
4: 101,846,182 (GRCm39) |
|
probably benign |
Het |
Gm27048 |
C |
T |
8: 81,661,228 (GRCm39) |
|
noncoding transcript |
Het |
Gm4204 |
T |
C |
1: 135,160,556 (GRCm39) |
|
noncoding transcript |
Het |
Gm904 |
A |
T |
13: 50,799,325 (GRCm39) |
I95F |
possibly damaging |
Het |
Gvin3 |
T |
G |
7: 106,197,793 (GRCm39) |
|
noncoding transcript |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Ints11 |
G |
A |
4: 155,972,887 (GRCm39) |
D526N |
probably benign |
Het |
Itfg2 |
A |
G |
6: 128,393,279 (GRCm39) |
|
probably benign |
Het |
Jund |
T |
C |
8: 71,152,254 (GRCm39) |
V183A |
probably damaging |
Het |
Kcnj8 |
A |
G |
6: 142,512,221 (GRCm39) |
S129P |
probably damaging |
Het |
Kcnq3 |
A |
G |
15: 65,867,259 (GRCm39) |
S795P |
probably damaging |
Het |
Lhx8 |
G |
T |
3: 154,035,925 (GRCm39) |
A22E |
probably benign |
Het |
Lrp8 |
A |
G |
4: 107,664,006 (GRCm39) |
|
probably benign |
Het |
Lvrn |
G |
T |
18: 47,026,768 (GRCm39) |
A789S |
probably damaging |
Het |
Lvrn |
T |
C |
18: 47,014,479 (GRCm39) |
S526P |
probably damaging |
Het |
Mga |
T |
A |
2: 119,794,535 (GRCm39) |
C2622S |
possibly damaging |
Het |
Mroh8 |
T |
C |
2: 157,070,647 (GRCm39) |
E568G |
probably benign |
Het |
Ms4a4b |
C |
A |
19: 11,440,503 (GRCm39) |
|
probably benign |
Het |
Muc2 |
T |
C |
7: 141,303,280 (GRCm39) |
F99S |
probably benign |
Het |
Myo5c |
T |
A |
9: 75,180,825 (GRCm39) |
I738N |
probably damaging |
Het |
Naip6 |
A |
C |
13: 100,433,477 (GRCm39) |
V1120G |
probably damaging |
Het |
Ncl |
T |
C |
1: 86,283,901 (GRCm39) |
T307A |
probably benign |
Het |
Npr1 |
A |
T |
3: 90,363,272 (GRCm39) |
D869E |
possibly damaging |
Het |
Nup93 |
A |
G |
8: 95,013,231 (GRCm39) |
T36A |
probably benign |
Het |
Olfml2b |
C |
A |
1: 170,489,947 (GRCm39) |
T189N |
probably damaging |
Het |
Or4c12b |
A |
G |
2: 89,647,312 (GRCm39) |
N208S |
possibly damaging |
Het |
Or8b9 |
T |
C |
9: 37,766,608 (GRCm39) |
F165L |
probably benign |
Het |
P4htm |
A |
C |
9: 108,456,427 (GRCm39) |
W458G |
probably damaging |
Het |
Pdzrn4 |
G |
T |
15: 92,668,638 (GRCm39) |
R930L |
probably damaging |
Het |
Pgam5 |
G |
A |
5: 110,408,301 (GRCm39) |
A240V |
probably damaging |
Het |
Prex2 |
T |
C |
1: 11,220,129 (GRCm39) |
|
probably benign |
Het |
Ptpru |
T |
G |
4: 131,515,693 (GRCm39) |
E897A |
probably damaging |
Het |
Rapgef2 |
A |
T |
3: 78,981,670 (GRCm39) |
N1256K |
probably benign |
Het |
Rhbdl3 |
A |
G |
11: 80,210,439 (GRCm39) |
E64G |
probably benign |
Het |
Sel1l3 |
A |
T |
5: 53,289,184 (GRCm39) |
L879Q |
probably damaging |
Het |
Siah1a |
G |
T |
8: 87,451,703 (GRCm39) |
D260E |
probably benign |
Het |
Skint6 |
T |
C |
4: 112,924,667 (GRCm39) |
I522V |
probably benign |
Het |
Slco4c1 |
G |
A |
1: 96,768,953 (GRCm39) |
P303L |
probably damaging |
Het |
Smok3c |
T |
C |
5: 138,062,813 (GRCm39) |
I100T |
probably damaging |
Het |
Snx24 |
C |
A |
18: 53,518,295 (GRCm39) |
Y141* |
probably null |
Het |
Tigit |
A |
G |
16: 43,469,594 (GRCm39) |
S166P |
probably damaging |
Het |
Tmem183a |
C |
T |
1: 134,275,904 (GRCm39) |
R324Q |
probably benign |
Het |
Tmie |
T |
C |
9: 110,696,001 (GRCm39) |
D130G |
possibly damaging |
Het |
Uggt1 |
G |
A |
1: 36,241,936 (GRCm39) |
R333* |
probably null |
Het |
Vmn2r111 |
T |
C |
17: 22,767,637 (GRCm39) |
N620S |
possibly damaging |
Het |
Vmn2r12 |
T |
A |
5: 109,240,852 (GRCm39) |
N87I |
probably damaging |
Het |
Vmn2r92 |
A |
G |
17: 18,404,605 (GRCm39) |
D583G |
probably benign |
Het |
Zdhhc17 |
T |
C |
10: 110,821,819 (GRCm39) |
D60G |
possibly damaging |
Het |
|
Other mutations in Bcl11b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Bcl11b
|
APN |
12 |
107,932,074 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02492:Bcl11b
|
APN |
12 |
107,881,945 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02559:Bcl11b
|
APN |
12 |
107,881,653 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02950:Bcl11b
|
APN |
12 |
107,956,065 (GRCm39) |
missense |
probably benign |
0.00 |
Acidophilus
|
UTSW |
12 |
107,883,562 (GRCm39) |
missense |
probably damaging |
1.00 |
Activia
|
UTSW |
12 |
107,969,402 (GRCm39) |
start codon destroyed |
probably benign |
0.21 |
hyphae
|
UTSW |
12 |
107,882,260 (GRCm39) |
missense |
probably benign |
0.01 |
R0055:Bcl11b
|
UTSW |
12 |
107,932,036 (GRCm39) |
missense |
probably benign |
0.02 |
R0762:Bcl11b
|
UTSW |
12 |
107,931,922 (GRCm39) |
intron |
probably benign |
|
R1549:Bcl11b
|
UTSW |
12 |
107,883,422 (GRCm39) |
missense |
probably damaging |
0.97 |
R1682:Bcl11b
|
UTSW |
12 |
107,882,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Bcl11b
|
UTSW |
12 |
107,881,910 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2495:Bcl11b
|
UTSW |
12 |
107,881,706 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3053:Bcl11b
|
UTSW |
12 |
107,882,260 (GRCm39) |
missense |
probably benign |
0.01 |
R4094:Bcl11b
|
UTSW |
12 |
107,883,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R4095:Bcl11b
|
UTSW |
12 |
107,883,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R4155:Bcl11b
|
UTSW |
12 |
107,883,684 (GRCm39) |
splice site |
probably null |
|
R4156:Bcl11b
|
UTSW |
12 |
107,883,684 (GRCm39) |
splice site |
probably null |
|
R4157:Bcl11b
|
UTSW |
12 |
107,883,684 (GRCm39) |
splice site |
probably null |
|
R4611:Bcl11b
|
UTSW |
12 |
107,882,789 (GRCm39) |
missense |
probably damaging |
0.97 |
R4906:Bcl11b
|
UTSW |
12 |
107,882,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Bcl11b
|
UTSW |
12 |
107,932,031 (GRCm39) |
nonsense |
probably null |
|
R5108:Bcl11b
|
UTSW |
12 |
107,931,985 (GRCm39) |
missense |
probably benign |
0.04 |
R5190:Bcl11b
|
UTSW |
12 |
107,955,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R6380:Bcl11b
|
UTSW |
12 |
107,969,360 (GRCm39) |
missense |
probably benign |
0.20 |
R6423:Bcl11b
|
UTSW |
12 |
107,881,678 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6792:Bcl11b
|
UTSW |
12 |
107,955,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:Bcl11b
|
UTSW |
12 |
107,882,851 (GRCm39) |
missense |
probably damaging |
0.99 |
R7074:Bcl11b
|
UTSW |
12 |
107,955,766 (GRCm39) |
missense |
probably benign |
0.01 |
R7371:Bcl11b
|
UTSW |
12 |
107,955,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Bcl11b
|
UTSW |
12 |
107,882,467 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7590:Bcl11b
|
UTSW |
12 |
107,969,402 (GRCm39) |
start codon destroyed |
probably benign |
0.21 |
R8005:Bcl11b
|
UTSW |
12 |
107,882,456 (GRCm39) |
missense |
probably benign |
|
R8131:Bcl11b
|
UTSW |
12 |
107,931,967 (GRCm39) |
missense |
probably benign |
|
R8783:Bcl11b
|
UTSW |
12 |
107,883,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8914:Bcl11b
|
UTSW |
12 |
107,883,163 (GRCm39) |
missense |
probably damaging |
0.98 |
R9281:Bcl11b
|
UTSW |
12 |
107,882,257 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9566:Bcl11b
|
UTSW |
12 |
107,881,784 (GRCm39) |
missense |
possibly damaging |
0.93 |
X0018:Bcl11b
|
UTSW |
12 |
107,955,948 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Bcl11b
|
UTSW |
12 |
107,883,136 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Bcl11b
|
UTSW |
12 |
107,955,999 (GRCm39) |
missense |
probably damaging |
0.99 |
|