Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,846,503 (GRCm39) |
S652P |
probably damaging |
Het |
Acsl6 |
G |
A |
11: 54,214,833 (GRCm39) |
G75S |
probably damaging |
Het |
Adamts7 |
A |
T |
9: 90,062,729 (GRCm39) |
K394N |
probably damaging |
Het |
Ahdc1 |
A |
G |
4: 132,793,220 (GRCm39) |
E1487G |
possibly damaging |
Het |
Aknad1 |
A |
G |
3: 108,664,609 (GRCm39) |
D406G |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,717,421 (GRCm39) |
T201A |
possibly damaging |
Het |
Ankrd2 |
C |
A |
19: 42,032,558 (GRCm39) |
A273E |
probably damaging |
Het |
Ankrd26 |
T |
A |
6: 118,500,843 (GRCm39) |
H876L |
possibly damaging |
Het |
Arhgap35 |
A |
T |
7: 16,231,950 (GRCm39) |
|
probably null |
Het |
Bag6 |
G |
A |
17: 35,363,583 (GRCm39) |
G751R |
probably damaging |
Het |
Brat1 |
G |
A |
5: 140,690,888 (GRCm39) |
|
probably benign |
Het |
Cacna1h |
C |
T |
17: 25,599,234 (GRCm39) |
A1742T |
probably damaging |
Het |
Catsperg1 |
G |
A |
7: 28,884,671 (GRCm39) |
Q922* |
probably null |
Het |
Cfap221 |
T |
G |
1: 119,863,834 (GRCm39) |
Y570S |
possibly damaging |
Het |
Cfap45 |
T |
C |
1: 172,359,728 (GRCm39) |
V76A |
probably benign |
Het |
Chil3 |
T |
C |
3: 106,071,562 (GRCm39) |
D34G |
probably benign |
Het |
Cpa1 |
A |
G |
6: 30,641,818 (GRCm39) |
D214G |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,693,070 (GRCm39) |
Y739H |
probably damaging |
Het |
Cttnbp2 |
T |
G |
6: 18,408,693 (GRCm39) |
D976A |
probably benign |
Het |
Dhrs7 |
A |
T |
12: 72,703,144 (GRCm39) |
V188E |
probably damaging |
Het |
Dpp9 |
A |
C |
17: 56,506,287 (GRCm39) |
I411S |
possibly damaging |
Het |
Elapor1 |
C |
T |
3: 108,382,359 (GRCm39) |
G270E |
probably damaging |
Het |
Fitm2 |
G |
A |
2: 163,314,516 (GRCm39) |
|
probably benign |
Het |
Flnc |
C |
T |
6: 29,459,507 (GRCm39) |
P2536S |
probably damaging |
Het |
Gm6370 |
T |
A |
5: 146,430,539 (GRCm39) |
D241E |
probably benign |
Het |
Gpatch1 |
C |
A |
7: 34,991,197 (GRCm39) |
D616Y |
probably damaging |
Het |
Gpc3 |
T |
A |
X: 51,486,083 (GRCm39) |
I344F |
probably damaging |
Het |
Hmgcs2 |
T |
A |
3: 98,198,499 (GRCm39) |
I134N |
probably damaging |
Het |
Hoxb3 |
T |
A |
11: 96,236,494 (GRCm39) |
S191T |
probably benign |
Het |
Ifit1bl1 |
C |
T |
19: 34,571,741 (GRCm39) |
E239K |
probably benign |
Het |
Ints8 |
A |
T |
4: 11,225,712 (GRCm39) |
M615K |
possibly damaging |
Het |
Irak1 |
G |
A |
X: 73,060,744 (GRCm39) |
T193I |
probably damaging |
Het |
Megf8 |
C |
T |
7: 25,041,173 (GRCm39) |
T1134I |
probably benign |
Het |
Mtrex |
T |
C |
13: 113,035,424 (GRCm39) |
I510V |
probably benign |
Het |
Nipsnap1 |
C |
A |
11: 4,839,974 (GRCm39) |
H232N |
possibly damaging |
Het |
Nme4 |
A |
T |
17: 26,311,114 (GRCm39) |
H150Q |
possibly damaging |
Het |
Nudt5 |
A |
T |
2: 5,860,794 (GRCm39) |
I22F |
possibly damaging |
Het |
P2rx7 |
T |
A |
5: 122,819,164 (GRCm39) |
Y529N |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pofut1 |
T |
A |
2: 153,103,167 (GRCm39) |
M267K |
probably damaging |
Het |
Rad54l2 |
T |
C |
9: 106,594,997 (GRCm39) |
D320G |
probably damaging |
Het |
Rdm1 |
C |
A |
11: 101,525,629 (GRCm39) |
A225E |
probably damaging |
Het |
Samm50 |
G |
A |
15: 84,086,515 (GRCm39) |
A245T |
probably benign |
Het |
Scfd2 |
A |
T |
5: 74,386,028 (GRCm39) |
M597K |
possibly damaging |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Ssh3 |
A |
G |
19: 4,319,101 (GRCm39) |
L3P |
probably damaging |
Het |
Stoml2 |
G |
T |
4: 43,030,243 (GRCm39) |
Y119* |
probably null |
Het |
Tbc1d31 |
A |
G |
15: 57,816,916 (GRCm39) |
D717G |
probably benign |
Het |
Timd5 |
A |
G |
11: 46,419,394 (GRCm39) |
N70S |
probably benign |
Het |
Tma7 |
C |
A |
9: 108,911,294 (GRCm39) |
|
probably benign |
Het |
Tmc1 |
A |
T |
19: 20,918,269 (GRCm39) |
L2M |
probably benign |
Het |
Tmem39b |
A |
C |
4: 129,587,716 (GRCm39) |
S32A |
probably benign |
Het |
Tnfsf14 |
T |
C |
17: 57,497,638 (GRCm39) |
D198G |
possibly damaging |
Het |
Tns3 |
T |
C |
11: 8,481,719 (GRCm39) |
Y211C |
probably damaging |
Het |
Ttc21b |
C |
T |
2: 66,065,467 (GRCm39) |
G436S |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,681,907 (GRCm39) |
|
probably benign |
Het |
Ube3b |
G |
A |
5: 114,527,135 (GRCm39) |
V118M |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,335,147 (GRCm39) |
T1210A |
probably damaging |
Het |
Vmn1r23 |
T |
C |
6: 57,903,604 (GRCm39) |
D58G |
probably benign |
Het |
Vmn2r104 |
A |
T |
17: 20,250,083 (GRCm39) |
N729K |
probably benign |
Het |
Wdr62 |
T |
A |
7: 29,957,574 (GRCm39) |
|
probably null |
Het |
Ywhah |
A |
G |
5: 33,184,484 (GRCm39) |
N229S |
probably damaging |
Het |
Zbtb47 |
A |
G |
9: 121,591,703 (GRCm39) |
T8A |
possibly damaging |
Het |
Zfyve27 |
C |
A |
19: 42,171,885 (GRCm39) |
A139D |
probably damaging |
Het |
Zmat1 |
A |
G |
X: 133,873,861 (GRCm39) |
L476P |
possibly damaging |
Het |
Zswim4 |
G |
T |
8: 84,952,498 (GRCm39) |
T488N |
possibly damaging |
Het |
|
Other mutations in 9930111J21Rik2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1986:9930111J21Rik2
|
UTSW |
11 |
48,910,119 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2023:9930111J21Rik2
|
UTSW |
11 |
48,911,144 (GRCm39) |
missense |
probably benign |
0.01 |
R2202:9930111J21Rik2
|
UTSW |
11 |
48,910,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R2337:9930111J21Rik2
|
UTSW |
11 |
48,911,131 (GRCm39) |
missense |
probably benign |
0.01 |
R3709:9930111J21Rik2
|
UTSW |
11 |
48,910,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:9930111J21Rik2
|
UTSW |
11 |
48,910,363 (GRCm39) |
missense |
probably damaging |
0.96 |
R3738:9930111J21Rik2
|
UTSW |
11 |
48,910,108 (GRCm39) |
nonsense |
probably null |
|
R3739:9930111J21Rik2
|
UTSW |
11 |
48,910,108 (GRCm39) |
nonsense |
probably null |
|
R4034:9930111J21Rik2
|
UTSW |
11 |
48,910,108 (GRCm39) |
nonsense |
probably null |
|
R5413:9930111J21Rik2
|
UTSW |
11 |
48,911,204 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5595:9930111J21Rik2
|
UTSW |
11 |
48,910,538 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5611:9930111J21Rik2
|
UTSW |
11 |
48,910,828 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5651:9930111J21Rik2
|
UTSW |
11 |
48,910,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R5715:9930111J21Rik2
|
UTSW |
11 |
48,910,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:9930111J21Rik2
|
UTSW |
11 |
48,910,088 (GRCm39) |
splice site |
probably null |
|
R6218:9930111J21Rik2
|
UTSW |
11 |
48,910,134 (GRCm39) |
missense |
probably benign |
0.06 |
R6536:9930111J21Rik2
|
UTSW |
11 |
48,910,550 (GRCm39) |
missense |
probably benign |
0.03 |
R7186:9930111J21Rik2
|
UTSW |
11 |
48,910,100 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7891:9930111J21Rik2
|
UTSW |
11 |
48,910,543 (GRCm39) |
missense |
probably benign |
0.11 |
R8056:9930111J21Rik2
|
UTSW |
11 |
48,910,909 (GRCm39) |
missense |
probably benign |
0.40 |
R8419:9930111J21Rik2
|
UTSW |
11 |
48,910,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R8726:9930111J21Rik2
|
UTSW |
11 |
48,910,507 (GRCm39) |
missense |
probably damaging |
1.00 |
|