Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
C |
T |
14: 70,393,907 (GRCm39) |
V243I |
probably benign |
Het |
Acadvl |
C |
T |
11: 69,902,010 (GRCm39) |
G485S |
probably benign |
Het |
Acap3 |
T |
A |
4: 155,986,908 (GRCm39) |
|
probably benign |
Het |
Adamts19 |
A |
G |
18: 59,023,356 (GRCm39) |
I250M |
probably damaging |
Het |
Amacr |
T |
A |
15: 10,983,496 (GRCm39) |
I102N |
probably damaging |
Het |
Apob |
A |
G |
12: 8,065,741 (GRCm39) |
T4237A |
probably benign |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
Bicd1 |
A |
T |
6: 149,420,752 (GRCm39) |
|
probably benign |
Het |
Caskin2 |
T |
A |
11: 115,698,125 (GRCm39) |
E49V |
probably damaging |
Het |
Cemip |
T |
A |
7: 83,622,449 (GRCm39) |
I577F |
probably benign |
Het |
Chrnb1 |
T |
C |
11: 69,686,501 (GRCm39) |
S40G |
possibly damaging |
Het |
Ctif |
C |
T |
18: 75,654,632 (GRCm39) |
C298Y |
probably benign |
Het |
Cul9 |
A |
C |
17: 46,840,977 (GRCm39) |
H764Q |
probably benign |
Het |
Cwf19l2 |
T |
A |
9: 3,458,839 (GRCm39) |
C763S |
probably damaging |
Het |
Dhx57 |
A |
T |
17: 80,549,596 (GRCm39) |
|
probably null |
Het |
Dnaaf10 |
T |
A |
11: 17,177,165 (GRCm39) |
N174K |
probably damaging |
Het |
Dnhd1 |
G |
A |
7: 105,353,171 (GRCm39) |
D2775N |
probably benign |
Het |
Enpp1 |
A |
T |
10: 24,537,833 (GRCm39) |
M384K |
possibly damaging |
Het |
Fat2 |
T |
C |
11: 55,202,144 (GRCm39) |
N310S |
probably benign |
Het |
Fbxw7 |
A |
T |
3: 84,874,814 (GRCm39) |
Y232F |
possibly damaging |
Het |
Fcamr |
T |
A |
1: 130,740,423 (GRCm39) |
S281T |
possibly damaging |
Het |
Gm10762 |
C |
T |
2: 128,809,106 (GRCm39) |
W81* |
probably null |
Het |
Gm5592 |
A |
G |
7: 40,805,314 (GRCm39) |
|
probably benign |
Het |
Gm5745 |
T |
C |
9: 73,082,980 (GRCm39) |
|
noncoding transcript |
Het |
Gm6185 |
G |
C |
1: 161,040,824 (GRCm39) |
|
noncoding transcript |
Het |
Hid1 |
T |
A |
11: 115,246,125 (GRCm39) |
N382Y |
probably damaging |
Het |
Hoxa10 |
A |
T |
6: 52,209,569 (GRCm39) |
F68I |
probably damaging |
Het |
Ift88 |
T |
A |
14: 57,679,326 (GRCm39) |
|
probably null |
Het |
Ighg2b |
A |
T |
12: 113,270,011 (GRCm39) |
*336R |
probably null |
Het |
Ighv7-2 |
A |
C |
12: 113,875,892 (GRCm39) |
L37R |
probably damaging |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Kcnn3 |
G |
C |
3: 89,574,596 (GRCm39) |
V703L |
possibly damaging |
Het |
Kiz |
C |
A |
2: 146,732,989 (GRCm39) |
S388R |
probably damaging |
Het |
Klhl20 |
G |
A |
1: 160,921,333 (GRCm39) |
Q41* |
probably null |
Het |
Krt31 |
T |
C |
11: 99,938,610 (GRCm39) |
I328V |
possibly damaging |
Het |
Lama4 |
A |
T |
10: 38,909,049 (GRCm39) |
I330L |
probably benign |
Het |
Lipo2 |
A |
T |
19: 33,723,151 (GRCm39) |
S213T |
probably benign |
Het |
Lrsam1 |
A |
T |
2: 32,816,804 (GRCm39) |
I723N |
probably damaging |
Het |
Man2b2 |
G |
A |
5: 36,972,865 (GRCm39) |
R550W |
probably damaging |
Het |
Map4k5 |
A |
T |
12: 69,888,758 (GRCm39) |
L224* |
probably null |
Het |
Mast3 |
A |
G |
8: 71,233,010 (GRCm39) |
S1101P |
probably damaging |
Het |
Mertk |
A |
G |
2: 128,643,225 (GRCm39) |
S875G |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,972,354 (GRCm39) |
M302V |
probably benign |
Het |
Mrgpra3 |
T |
A |
7: 47,239,716 (GRCm39) |
H70L |
possibly damaging |
Het |
Myh3 |
T |
A |
11: 66,979,836 (GRCm39) |
S592T |
probably benign |
Het |
Nbeal2 |
T |
C |
9: 110,465,383 (GRCm39) |
I451V |
possibly damaging |
Het |
Nup155 |
T |
A |
15: 8,158,010 (GRCm39) |
V489D |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,913,159 (GRCm39) |
T6300S |
probably benign |
Het |
Oprm1 |
A |
G |
10: 6,779,036 (GRCm39) |
I146V |
probably damaging |
Het |
Or1ad1 |
T |
A |
11: 50,875,910 (GRCm39) |
C127* |
probably null |
Het |
Or1j4 |
A |
G |
2: 36,740,888 (GRCm39) |
M277V |
probably benign |
Het |
Or4k44 |
G |
T |
2: 111,367,797 (GRCm39) |
T279K |
probably damaging |
Het |
Or5ae1 |
A |
C |
7: 84,565,634 (GRCm39) |
I216L |
possibly damaging |
Het |
Otub1 |
A |
T |
19: 7,181,794 (GRCm39) |
D27E |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,492,131 (GRCm39) |
V243A |
probably benign |
Het |
Pla2g12b |
G |
A |
10: 59,252,336 (GRCm39) |
|
probably null |
Het |
Plekha8 |
A |
G |
6: 54,601,546 (GRCm39) |
D321G |
probably damaging |
Het |
Pprc1 |
T |
C |
19: 46,059,795 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
G |
16: 15,468,576 (GRCm39) |
D129G |
possibly damaging |
Het |
Rbms3 |
C |
T |
9: 116,773,441 (GRCm39) |
|
probably benign |
Het |
Rictor |
T |
A |
15: 6,821,161 (GRCm39) |
V1495D |
probably benign |
Het |
Rpl31-ps21 |
T |
C |
5: 21,324,507 (GRCm39) |
|
noncoding transcript |
Het |
Ryr3 |
A |
T |
2: 112,483,090 (GRCm39) |
I4219N |
probably damaging |
Het |
Sbf2 |
G |
A |
7: 109,977,146 (GRCm39) |
|
probably benign |
Het |
Scn10a |
C |
T |
9: 119,467,738 (GRCm39) |
A801T |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,314,093 (GRCm39) |
Y1866F |
possibly damaging |
Het |
Sec1 |
A |
C |
7: 45,328,727 (GRCm39) |
Y107D |
probably damaging |
Het |
Sema6d |
C |
T |
2: 124,504,214 (GRCm39) |
T619M |
possibly damaging |
Het |
Sh2b3 |
C |
A |
5: 121,966,618 (GRCm39) |
|
probably benign |
Het |
Slc2a4 |
A |
G |
11: 69,837,413 (GRCm39) |
V44A |
probably damaging |
Het |
Slc5a12 |
T |
C |
2: 110,452,085 (GRCm39) |
I326T |
possibly damaging |
Het |
Smarca5 |
T |
C |
8: 81,435,309 (GRCm39) |
|
probably null |
Het |
Smarcd2 |
A |
G |
11: 106,157,357 (GRCm39) |
|
probably null |
Het |
Snrpa1 |
A |
T |
7: 65,719,321 (GRCm39) |
|
probably benign |
Het |
Sptbn5 |
T |
G |
2: 119,898,449 (GRCm39) |
K470Q |
probably benign |
Het |
Stard9 |
T |
G |
2: 120,526,422 (GRCm39) |
V893G |
possibly damaging |
Het |
Stx8 |
T |
G |
11: 67,864,099 (GRCm39) |
V53G |
possibly damaging |
Het |
Sv2c |
A |
T |
13: 96,122,457 (GRCm39) |
W440R |
probably damaging |
Het |
Tcstv2a |
A |
T |
13: 120,725,686 (GRCm39) |
T117S |
probably damaging |
Het |
Tmprss7 |
C |
T |
16: 45,483,679 (GRCm39) |
C565Y |
probably damaging |
Het |
Trafd1 |
A |
T |
5: 121,516,561 (GRCm39) |
L109H |
probably damaging |
Het |
Trpv4 |
A |
G |
5: 114,768,083 (GRCm39) |
I422T |
possibly damaging |
Het |
Usp24 |
T |
A |
4: 106,273,244 (GRCm39) |
Y2210N |
probably damaging |
Het |
Vmn1r236 |
A |
T |
17: 21,507,202 (GRCm39) |
N107Y |
probably damaging |
Het |
Vmn2r13 |
A |
T |
5: 109,321,938 (GRCm39) |
I253K |
probably damaging |
Het |
Vmn2r2 |
T |
A |
3: 64,041,960 (GRCm39) |
I252F |
probably damaging |
Het |
Vsig8 |
A |
G |
1: 172,387,205 (GRCm39) |
D27G |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,575,411 (GRCm39) |
Y908* |
probably null |
Het |
Wnk1 |
A |
T |
6: 119,939,399 (GRCm39) |
S1113T |
probably benign |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfp691 |
G |
T |
4: 119,027,764 (GRCm39) |
T156K |
probably damaging |
Het |
Zfp791 |
A |
T |
8: 85,837,035 (GRCm39) |
D276E |
probably benign |
Het |
|
Other mutations in Tmem181a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02071:Tmem181a
|
APN |
17 |
6,347,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Tmem181a
|
APN |
17 |
6,348,494 (GRCm39) |
missense |
probably damaging |
1.00 |
a_team
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
abraham
|
UTSW |
17 |
6,340,874 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4651001:Tmem181a
|
UTSW |
17 |
6,351,170 (GRCm39) |
missense |
probably benign |
|
R1966:Tmem181a
|
UTSW |
17 |
6,353,501 (GRCm39) |
missense |
probably benign |
|
R2139:Tmem181a
|
UTSW |
17 |
6,348,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R2323:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R2324:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3001:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3002:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3003:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3034:Tmem181a
|
UTSW |
17 |
6,330,901 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3425:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3426:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3427:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3428:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3499:Tmem181a
|
UTSW |
17 |
6,330,894 (GRCm39) |
nonsense |
probably null |
|
R3683:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R3893:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4226:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4227:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4428:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4429:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4430:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4465:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4466:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4467:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4496:Tmem181a
|
UTSW |
17 |
6,346,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R4728:Tmem181a
|
UTSW |
17 |
6,340,874 (GRCm39) |
missense |
probably benign |
0.03 |
R5301:Tmem181a
|
UTSW |
17 |
6,346,070 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5991:Tmem181a
|
UTSW |
17 |
6,339,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Tmem181a
|
UTSW |
17 |
6,330,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6222:Tmem181a
|
UTSW |
17 |
6,351,192 (GRCm39) |
missense |
probably benign |
0.29 |
R7131:Tmem181a
|
UTSW |
17 |
6,348,247 (GRCm39) |
missense |
probably damaging |
0.98 |
R7231:Tmem181a
|
UTSW |
17 |
6,348,195 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7374:Tmem181a
|
UTSW |
17 |
6,354,533 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7437:Tmem181a
|
UTSW |
17 |
6,353,540 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7592:Tmem181a
|
UTSW |
17 |
6,339,295 (GRCm39) |
missense |
probably benign |
0.00 |
R8175:Tmem181a
|
UTSW |
17 |
6,346,075 (GRCm39) |
missense |
probably benign |
0.00 |
R8327:Tmem181a
|
UTSW |
17 |
6,351,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R8385:Tmem181a
|
UTSW |
17 |
6,339,274 (GRCm39) |
missense |
probably benign |
0.10 |
R9144:Tmem181a
|
UTSW |
17 |
6,346,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9221:Tmem181a
|
UTSW |
17 |
6,307,265 (GRCm39) |
missense |
probably damaging |
0.99 |
R9327:Tmem181a
|
UTSW |
17 |
6,346,048 (GRCm39) |
missense |
possibly damaging |
0.94 |
RF010:Tmem181a
|
UTSW |
17 |
6,330,978 (GRCm39) |
critical splice donor site |
probably null |
|
|