Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
G |
A |
2: 151,315,459 (GRCm39) |
S73F |
possibly damaging |
Het |
4932414N04Rik |
A |
T |
2: 68,578,712 (GRCm39) |
*753L |
probably null |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Adam19 |
T |
C |
11: 46,027,142 (GRCm39) |
S592P |
probably benign |
Het |
Adamtsl3 |
A |
G |
7: 82,206,447 (GRCm39) |
K843R |
possibly damaging |
Het |
Ap2a2 |
A |
T |
7: 141,184,855 (GRCm39) |
T213S |
probably benign |
Het |
Asb5 |
A |
G |
8: 55,038,974 (GRCm39) |
E280G |
probably benign |
Het |
Becn1 |
T |
C |
11: 101,179,778 (GRCm39) |
D403G |
probably damaging |
Het |
Ccr7 |
G |
T |
11: 99,036,315 (GRCm39) |
N202K |
probably benign |
Het |
Cd36 |
T |
C |
5: 18,019,790 (GRCm39) |
T104A |
possibly damaging |
Het |
Cnot4 |
C |
T |
6: 35,028,464 (GRCm39) |
W384* |
probably null |
Het |
Col15a1 |
G |
A |
4: 47,312,087 (GRCm39) |
V1301M |
probably damaging |
Het |
Dock2 |
C |
A |
11: 34,204,391 (GRCm39) |
A1384S |
probably benign |
Het |
Ehbp1l1 |
T |
C |
19: 5,758,698 (GRCm39) |
E1648G |
possibly damaging |
Het |
Fbn1 |
G |
T |
2: 125,163,661 (GRCm39) |
A2065E |
possibly damaging |
Het |
Fras1 |
A |
G |
5: 96,884,880 (GRCm39) |
Y2586C |
probably damaging |
Het |
Galm |
T |
A |
17: 80,457,568 (GRCm39) |
Y28* |
probably null |
Het |
Ggt7 |
A |
G |
2: 155,332,919 (GRCm39) |
V648A |
possibly damaging |
Het |
Gm17067 |
T |
A |
7: 42,357,839 (GRCm39) |
D221V |
probably damaging |
Het |
Gpr3 |
T |
C |
4: 132,937,805 (GRCm39) |
N289S |
probably damaging |
Het |
Ighv11-2 |
A |
G |
12: 114,012,277 (GRCm39) |
|
probably benign |
Het |
Ighv11-2 |
G |
A |
12: 114,012,099 (GRCm39) |
L39F |
probably damaging |
Het |
Ipo9 |
G |
A |
1: 135,329,983 (GRCm39) |
L486F |
probably damaging |
Het |
Jak2 |
T |
A |
19: 29,275,739 (GRCm39) |
N726K |
probably benign |
Het |
Map4 |
T |
C |
9: 109,881,768 (GRCm39) |
S211P |
possibly damaging |
Het |
Mlh1 |
A |
T |
9: 111,081,946 (GRCm39) |
L259Q |
probably damaging |
Het |
Naa25 |
A |
G |
5: 121,558,558 (GRCm39) |
E300G |
probably benign |
Het |
Or8g34 |
A |
T |
9: 39,373,326 (GRCm39) |
M200L |
probably benign |
Het |
Or8g54 |
T |
A |
9: 39,707,490 (GRCm39) |
V273E |
possibly damaging |
Het |
Parva |
G |
A |
7: 112,166,972 (GRCm39) |
V182I |
probably benign |
Het |
Pcdhgb4 |
T |
C |
18: 37,854,697 (GRCm39) |
I364T |
probably damaging |
Het |
Pdik1l |
A |
G |
4: 134,011,580 (GRCm39) |
S164P |
probably damaging |
Het |
Pfas |
A |
T |
11: 68,881,871 (GRCm39) |
I938N |
probably benign |
Het |
Plscr1l1 |
G |
A |
9: 92,234,721 (GRCm39) |
C152Y |
possibly damaging |
Het |
Prdm4 |
TCTCCTCCT |
TCTCCT |
10: 85,728,987 (GRCm39) |
|
probably null |
Het |
Prob1 |
C |
T |
18: 35,787,079 (GRCm39) |
V392M |
possibly damaging |
Het |
Rasgrf1 |
T |
C |
9: 89,793,624 (GRCm39) |
S134P |
possibly damaging |
Het |
Rorb |
T |
A |
19: 18,955,301 (GRCm39) |
Y20F |
probably damaging |
Het |
Rsph9 |
G |
T |
17: 46,445,909 (GRCm39) |
D220E |
probably damaging |
Het |
Safb2 |
C |
A |
17: 56,882,630 (GRCm39) |
K334N |
possibly damaging |
Het |
Sall3 |
T |
C |
18: 81,016,027 (GRCm39) |
T634A |
probably benign |
Het |
Scaf1 |
A |
G |
7: 44,657,007 (GRCm39) |
|
probably benign |
Het |
Slco1a5 |
T |
A |
6: 142,221,255 (GRCm39) |
|
probably benign |
Het |
Spata21 |
C |
T |
4: 140,824,210 (GRCm39) |
R158C |
probably benign |
Het |
Srrm2 |
G |
A |
17: 24,038,311 (GRCm39) |
|
probably benign |
Het |
Stk38l |
C |
A |
6: 146,659,998 (GRCm39) |
T10N |
probably benign |
Het |
Supv3l1 |
G |
A |
10: 62,266,371 (GRCm39) |
P602S |
possibly damaging |
Het |
Timm44 |
C |
T |
8: 4,316,769 (GRCm39) |
|
probably null |
Het |
Tll2 |
T |
A |
19: 41,093,420 (GRCm39) |
R465S |
possibly damaging |
Het |
Tmem151b |
A |
G |
17: 45,856,526 (GRCm39) |
S305P |
probably damaging |
Het |
Utrn |
T |
C |
10: 12,625,839 (GRCm39) |
D114G |
probably damaging |
Het |
Vmn2r109 |
A |
T |
17: 20,760,933 (GRCm39) |
M808K |
possibly damaging |
Het |
Washc2 |
T |
A |
6: 116,225,056 (GRCm39) |
D801E |
possibly damaging |
Het |
Xkr4 |
T |
C |
1: 3,286,751 (GRCm39) |
I480V |
probably benign |
Het |
Zfp507 |
G |
T |
7: 35,475,663 (GRCm39) |
S58* |
probably null |
Het |
Zfp768 |
T |
A |
7: 126,943,804 (GRCm39) |
D108V |
possibly damaging |
Het |
|
Other mutations in Tmem104 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00501:Tmem104
|
APN |
11 |
115,134,763 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02948:Tmem104
|
APN |
11 |
115,088,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03010:Tmem104
|
APN |
11 |
115,134,360 (GRCm39) |
missense |
probably benign |
0.01 |
R0107:Tmem104
|
UTSW |
11 |
115,093,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Tmem104
|
UTSW |
11 |
115,092,134 (GRCm39) |
splice site |
probably benign |
|
R0534:Tmem104
|
UTSW |
11 |
115,091,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2034:Tmem104
|
UTSW |
11 |
115,134,373 (GRCm39) |
missense |
probably benign |
0.42 |
R2037:Tmem104
|
UTSW |
11 |
115,092,221 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4095:Tmem104
|
UTSW |
11 |
115,134,749 (GRCm39) |
nonsense |
probably null |
|
R4640:Tmem104
|
UTSW |
11 |
115,134,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R4981:Tmem104
|
UTSW |
11 |
115,095,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Tmem104
|
UTSW |
11 |
115,134,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Tmem104
|
UTSW |
11 |
115,092,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R5522:Tmem104
|
UTSW |
11 |
115,079,149 (GRCm39) |
critical splice donor site |
probably null |
|
R6025:Tmem104
|
UTSW |
11 |
115,096,349 (GRCm39) |
nonsense |
probably null |
|
R6247:Tmem104
|
UTSW |
11 |
115,134,819 (GRCm39) |
missense |
probably benign |
|
R6522:Tmem104
|
UTSW |
11 |
115,134,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7962:Tmem104
|
UTSW |
11 |
115,134,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R7980:Tmem104
|
UTSW |
11 |
115,134,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R8323:Tmem104
|
UTSW |
11 |
115,134,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8552:Tmem104
|
UTSW |
11 |
115,088,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9012:Tmem104
|
UTSW |
11 |
115,092,144 (GRCm39) |
missense |
probably benign |
0.01 |
R9363:Tmem104
|
UTSW |
11 |
115,134,691 (GRCm39) |
missense |
probably benign |
0.14 |
R9507:Tmem104
|
UTSW |
11 |
115,091,699 (GRCm39) |
missense |
probably damaging |
1.00 |
|