Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
T |
C |
16: 20,367,796 (GRCm39) |
S52P |
possibly damaging |
Het |
Adamts19 |
G |
T |
18: 59,181,881 (GRCm39) |
G1107C |
probably damaging |
Het |
Afap1 |
A |
T |
5: 36,131,830 (GRCm39) |
T386S |
probably benign |
Het |
Alg12 |
T |
C |
15: 88,695,503 (GRCm39) |
Y331C |
probably null |
Het |
Aste1 |
T |
A |
9: 105,274,255 (GRCm39) |
I165N |
probably damaging |
Het |
Atp13a5 |
A |
G |
16: 29,167,805 (GRCm39) |
I118T |
probably damaging |
Het |
AW551984 |
A |
G |
9: 39,510,651 (GRCm39) |
V228A |
probably damaging |
Het |
Cachd1 |
A |
G |
4: 100,816,668 (GRCm39) |
Y357C |
possibly damaging |
Het |
Cacul1 |
T |
A |
19: 60,551,673 (GRCm39) |
H183L |
possibly damaging |
Het |
Casp16 |
T |
A |
17: 23,772,348 (GRCm39) |
I39F |
probably damaging |
Het |
Chd7 |
G |
T |
4: 8,839,529 (GRCm39) |
C1355F |
probably damaging |
Het |
Csnk1a1 |
A |
G |
18: 61,713,610 (GRCm39) |
|
probably null |
Het |
Ctif |
G |
A |
18: 75,698,115 (GRCm39) |
H182Y |
possibly damaging |
Het |
Cubn |
C |
T |
2: 13,329,971 (GRCm39) |
V2637I |
probably benign |
Het |
Dlx1 |
T |
A |
2: 71,360,652 (GRCm39) |
|
probably null |
Het |
Dsp |
A |
G |
13: 38,376,457 (GRCm39) |
N1414S |
possibly damaging |
Het |
Erich6 |
A |
T |
3: 58,544,449 (GRCm39) |
L46* |
probably null |
Het |
Fcho2 |
G |
A |
13: 98,862,282 (GRCm39) |
R804* |
probably null |
Het |
Gas7 |
T |
A |
11: 67,543,734 (GRCm39) |
I114N |
probably benign |
Het |
Gpr137b |
T |
C |
13: 13,533,929 (GRCm39) |
T376A |
probably benign |
Het |
H2-T24 |
T |
C |
17: 36,328,229 (GRCm39) |
M85V |
probably benign |
Het |
Klk1b16 |
T |
A |
7: 43,790,185 (GRCm39) |
C152S |
probably damaging |
Het |
Magt1 |
C |
T |
X: 105,040,501 (GRCm39) |
A100T |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,301,855 (GRCm39) |
K1060E |
possibly damaging |
Het |
Nif3l1 |
A |
T |
1: 58,491,288 (GRCm39) |
T213S |
probably benign |
Het |
Oasl1 |
T |
A |
5: 115,075,465 (GRCm39) |
F508L |
probably benign |
Het |
Or10ak8 |
A |
T |
4: 118,773,723 (GRCm39) |
*314R |
probably null |
Het |
Or2a25 |
T |
C |
6: 42,888,976 (GRCm39) |
V173A |
possibly damaging |
Het |
Or4a80 |
C |
T |
2: 89,582,423 (GRCm39) |
V250I |
probably benign |
Het |
Or5b122 |
T |
C |
19: 13,562,764 (GRCm39) |
L32P |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,348,522 (GRCm39) |
D95G |
probably benign |
Het |
Ptprr |
T |
C |
10: 115,884,180 (GRCm39) |
I79T |
probably benign |
Het |
Resf1 |
C |
T |
6: 149,228,076 (GRCm39) |
T374I |
probably damaging |
Het |
Rhbg |
T |
A |
3: 88,152,525 (GRCm39) |
N340Y |
probably damaging |
Het |
Sash1 |
C |
A |
10: 8,605,745 (GRCm39) |
V882L |
probably benign |
Het |
Sharpin |
C |
T |
15: 76,232,197 (GRCm39) |
V220I |
probably damaging |
Het |
Slc22a22 |
T |
A |
15: 57,108,243 (GRCm39) |
D524V |
probably damaging |
Het |
Slc43a3 |
T |
C |
2: 84,780,860 (GRCm39) |
Y362H |
probably benign |
Het |
Slc4a3 |
T |
A |
1: 75,530,359 (GRCm39) |
D687E |
probably damaging |
Het |
Slco1a5 |
A |
G |
6: 142,208,411 (GRCm39) |
S127P |
probably benign |
Het |
Spg11 |
T |
C |
2: 121,910,739 (GRCm39) |
I1213V |
possibly damaging |
Het |
Synj2 |
T |
A |
17: 6,074,080 (GRCm39) |
Y813* |
probably null |
Het |
Tbc1d10a |
T |
C |
11: 4,155,837 (GRCm39) |
M131T |
probably damaging |
Het |
Tnfrsf19 |
C |
A |
14: 61,208,634 (GRCm39) |
V296F |
probably benign |
Het |
Trim45 |
T |
C |
3: 100,834,634 (GRCm39) |
V439A |
probably damaging |
Het |
Trim54 |
A |
G |
5: 31,294,338 (GRCm39) |
T325A |
probably benign |
Het |
Usp40 |
T |
C |
1: 87,908,770 (GRCm39) |
E577G |
possibly damaging |
Het |
Uts2r |
T |
A |
11: 121,051,345 (GRCm39) |
Y70N |
probably damaging |
Het |
Vmn1r72 |
T |
G |
7: 11,404,310 (GRCm39) |
D46A |
probably damaging |
Het |
Zfc3h1 |
T |
C |
10: 115,240,198 (GRCm39) |
V577A |
probably benign |
Het |
Zfp987 |
T |
G |
4: 146,061,343 (GRCm39) |
H258Q |
probably damaging |
Het |
|
Other mutations in Lrrc31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03110:Lrrc31
|
APN |
3 |
30,733,415 (GRCm39) |
missense |
probably benign |
0.04 |
R0285:Lrrc31
|
UTSW |
3 |
30,739,097 (GRCm39) |
missense |
probably benign |
0.02 |
R0348:Lrrc31
|
UTSW |
3 |
30,743,377 (GRCm39) |
missense |
probably benign |
0.14 |
R0418:Lrrc31
|
UTSW |
3 |
30,743,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R0453:Lrrc31
|
UTSW |
3 |
30,741,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:Lrrc31
|
UTSW |
3 |
30,739,184 (GRCm39) |
splice site |
probably benign |
|
R2243:Lrrc31
|
UTSW |
3 |
30,739,179 (GRCm39) |
splice site |
probably benign |
|
R2248:Lrrc31
|
UTSW |
3 |
30,744,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4093:Lrrc31
|
UTSW |
3 |
30,749,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R4781:Lrrc31
|
UTSW |
3 |
30,741,526 (GRCm39) |
intron |
probably benign |
|
R4805:Lrrc31
|
UTSW |
3 |
30,745,446 (GRCm39) |
nonsense |
probably null |
|
R4835:Lrrc31
|
UTSW |
3 |
30,733,306 (GRCm39) |
missense |
probably damaging |
0.97 |
R4893:Lrrc31
|
UTSW |
3 |
30,733,446 (GRCm39) |
missense |
probably benign |
0.02 |
R4936:Lrrc31
|
UTSW |
3 |
30,743,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R5063:Lrrc31
|
UTSW |
3 |
30,744,085 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5135:Lrrc31
|
UTSW |
3 |
30,739,039 (GRCm39) |
nonsense |
probably null |
|
R5527:Lrrc31
|
UTSW |
3 |
30,745,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R5607:Lrrc31
|
UTSW |
3 |
30,743,994 (GRCm39) |
splice site |
probably null |
|
R5608:Lrrc31
|
UTSW |
3 |
30,743,994 (GRCm39) |
splice site |
probably null |
|
R5611:Lrrc31
|
UTSW |
3 |
30,745,304 (GRCm39) |
critical splice donor site |
probably null |
|
R5865:Lrrc31
|
UTSW |
3 |
30,733,289 (GRCm39) |
missense |
probably benign |
0.01 |
R6001:Lrrc31
|
UTSW |
3 |
30,745,318 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7583:Lrrc31
|
UTSW |
3 |
30,745,248 (GRCm39) |
splice site |
probably null |
|
R8812:Lrrc31
|
UTSW |
3 |
30,733,328 (GRCm39) |
missense |
probably benign |
0.37 |
R8955:Lrrc31
|
UTSW |
3 |
30,733,267 (GRCm39) |
missense |
probably benign |
0.00 |
R9072:Lrrc31
|
UTSW |
3 |
30,753,859 (GRCm39) |
missense |
probably benign |
0.00 |
R9073:Lrrc31
|
UTSW |
3 |
30,753,859 (GRCm39) |
missense |
probably benign |
0.00 |
R9682:Lrrc31
|
UTSW |
3 |
30,743,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R9691:Lrrc31
|
UTSW |
3 |
30,741,617 (GRCm39) |
missense |
probably damaging |
0.99 |
R9702:Lrrc31
|
UTSW |
3 |
30,735,226 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Lrrc31
|
UTSW |
3 |
30,743,428 (GRCm39) |
missense |
possibly damaging |
0.77 |
|