Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
G |
A |
13: 60,992,948 (GRCm39) |
P244S |
probably damaging |
Het |
Acoxl |
A |
T |
2: 127,852,085 (GRCm39) |
Q129L |
probably damaging |
Het |
Akna |
T |
C |
4: 63,316,268 (GRCm39) |
T32A |
probably benign |
Het |
Alox15 |
C |
T |
11: 70,235,645 (GRCm39) |
|
probably null |
Het |
Antxrl |
T |
C |
14: 33,787,864 (GRCm39) |
S296P |
probably damaging |
Het |
Arrb2 |
G |
T |
11: 70,328,142 (GRCm39) |
G52* |
probably null |
Het |
Bltp2 |
T |
C |
11: 78,179,105 (GRCm39) |
F2091S |
probably benign |
Het |
Capn2 |
A |
T |
1: 182,309,045 (GRCm39) |
I499N |
probably damaging |
Het |
Cfhr4 |
T |
A |
1: 139,629,719 (GRCm39) |
D683V |
possibly damaging |
Het |
Cspg4b |
T |
A |
13: 113,504,686 (GRCm39) |
D396E |
probably benign |
Het |
Cubn |
T |
A |
2: 13,326,066 (GRCm39) |
I2700F |
probably damaging |
Het |
Cypt4 |
A |
T |
9: 24,536,965 (GRCm39) |
N152Y |
probably benign |
Het |
Dmxl2 |
T |
C |
9: 54,316,467 (GRCm39) |
N1640D |
probably damaging |
Het |
Dnah7b |
A |
T |
1: 46,379,377 (GRCm39) |
N3704Y |
possibly damaging |
Het |
Dnah9 |
A |
G |
11: 65,963,565 (GRCm39) |
|
probably null |
Het |
Elac2 |
G |
A |
11: 64,890,265 (GRCm39) |
|
probably null |
Het |
Erich3 |
A |
T |
3: 154,433,029 (GRCm39) |
|
probably null |
Het |
Espnl |
T |
C |
1: 91,270,351 (GRCm39) |
V386A |
probably damaging |
Het |
Fbxl6 |
T |
A |
15: 76,422,898 (GRCm39) |
|
probably benign |
Het |
Fdps |
A |
C |
3: 89,008,068 (GRCm39) |
F17V |
probably damaging |
Het |
Gigyf2 |
T |
C |
1: 87,346,898 (GRCm39) |
I576T |
possibly damaging |
Het |
Gm20939 |
A |
G |
17: 95,184,657 (GRCm39) |
E435G |
possibly damaging |
Het |
Hivep1 |
G |
A |
13: 42,310,852 (GRCm39) |
V1031I |
probably damaging |
Het |
Hydin |
T |
G |
8: 111,324,603 (GRCm39) |
S4655A |
probably benign |
Het |
Ifrd1 |
T |
A |
12: 40,273,157 (GRCm39) |
|
probably benign |
Het |
Iqgap1 |
G |
T |
7: 80,378,729 (GRCm39) |
T1219K |
possibly damaging |
Het |
Lmtk3 |
G |
A |
7: 45,443,233 (GRCm39) |
E639K |
possibly damaging |
Het |
Map3k5 |
A |
G |
10: 20,017,326 (GRCm39) |
*1373W |
probably null |
Het |
Mia2 |
G |
A |
12: 59,235,332 (GRCm39) |
|
probably null |
Het |
Micu2 |
T |
C |
14: 58,156,896 (GRCm39) |
D313G |
possibly damaging |
Het |
Mrgpra4 |
A |
G |
7: 47,631,371 (GRCm39) |
S77P |
probably damaging |
Het |
Mrpl51 |
T |
C |
6: 125,169,367 (GRCm39) |
V17A |
probably benign |
Het |
Neurod4 |
A |
T |
10: 130,106,661 (GRCm39) |
Y204* |
probably null |
Het |
Or2n1 |
A |
G |
17: 38,486,013 (GRCm39) |
I13V |
probably benign |
Het |
Or56a42-ps1 |
A |
T |
7: 104,776,217 (GRCm39) |
V97E |
probably benign |
Het |
Or5p67 |
G |
A |
7: 107,922,460 (GRCm39) |
T141I |
probably benign |
Het |
Or6c66b |
A |
T |
10: 129,377,132 (GRCm39) |
H242L |
probably damaging |
Het |
Pate2 |
T |
C |
9: 35,596,941 (GRCm39) |
|
probably benign |
Het |
Pcdhgb8 |
G |
A |
18: 37,896,580 (GRCm39) |
R550Q |
probably benign |
Het |
Phldb3 |
T |
C |
7: 24,323,577 (GRCm39) |
L437P |
possibly damaging |
Het |
Pianp |
C |
A |
6: 124,978,565 (GRCm39) |
P257T |
possibly damaging |
Het |
Rbbp6 |
T |
A |
7: 122,584,287 (GRCm39) |
H140Q |
possibly damaging |
Het |
Rfx2 |
A |
G |
17: 57,087,804 (GRCm39) |
I529T |
probably damaging |
Het |
Rnf113a1 |
A |
C |
X: 36,455,840 (GRCm39) |
T266P |
probably benign |
Het |
Rp1l1 |
T |
C |
14: 64,268,599 (GRCm39) |
I1395T |
possibly damaging |
Het |
Rps6ka2 |
A |
C |
17: 7,519,035 (GRCm39) |
K186Q |
probably damaging |
Het |
Rsf1 |
CGGC |
CGGCGGCGGGGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Rtel1 |
C |
A |
2: 180,964,256 (GRCm39) |
T85N |
probably benign |
Het |
Rtn4rl2 |
T |
C |
2: 84,710,967 (GRCm39) |
N99S |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,723,741 (GRCm39) |
G4106D |
possibly damaging |
Het |
Scgb2b24 |
A |
G |
7: 33,437,894 (GRCm39) |
V71A |
probably benign |
Het |
Sgip1 |
A |
G |
4: 102,778,225 (GRCm39) |
|
probably benign |
Het |
Slc12a4 |
G |
A |
8: 106,676,371 (GRCm39) |
T515I |
probably damaging |
Het |
Spag1 |
C |
T |
15: 36,197,895 (GRCm39) |
R286* |
probably null |
Het |
Strbp |
C |
T |
2: 37,515,228 (GRCm39) |
R266Q |
probably damaging |
Het |
Strn |
G |
T |
17: 78,977,787 (GRCm39) |
|
probably benign |
Het |
Thnsl2 |
C |
A |
6: 71,118,264 (GRCm39) |
V55L |
probably benign |
Het |
Tmem178b |
A |
T |
6: 40,231,858 (GRCm39) |
Q164L |
unknown |
Het |
Tmprss6 |
C |
T |
15: 78,324,457 (GRCm39) |
R786H |
probably damaging |
Het |
Ttc21a |
T |
A |
9: 119,770,268 (GRCm39) |
L113Q |
possibly damaging |
Het |
Ttc21b |
T |
C |
2: 66,038,994 (GRCm39) |
|
probably null |
Het |
Vmn2r51 |
T |
C |
7: 9,832,191 (GRCm39) |
D465G |
probably damaging |
Het |
Vmp1 |
A |
C |
11: 86,556,913 (GRCm39) |
|
probably null |
Het |
Wdcp |
T |
C |
12: 4,901,358 (GRCm39) |
F405L |
probably damaging |
Het |
Zfhx3 |
A |
T |
8: 109,676,149 (GRCm39) |
T2400S |
probably benign |
Het |
Zfp27 |
T |
C |
7: 29,593,860 (GRCm39) |
T702A |
probably benign |
Het |
Zfp87 |
T |
C |
13: 74,520,080 (GRCm39) |
S333G |
probably benign |
Het |
|
Other mutations in 9130023H24Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01294:9130023H24Rik
|
APN |
7 |
127,836,291 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01865:9130023H24Rik
|
APN |
7 |
127,836,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R0319:9130023H24Rik
|
UTSW |
7 |
127,836,362 (GRCm39) |
missense |
probably benign |
|
R1376:9130023H24Rik
|
UTSW |
7 |
127,836,182 (GRCm39) |
missense |
probably benign |
0.17 |
R1376:9130023H24Rik
|
UTSW |
7 |
127,836,182 (GRCm39) |
missense |
probably benign |
0.17 |
R2373:9130023H24Rik
|
UTSW |
7 |
127,836,487 (GRCm39) |
missense |
probably benign |
0.13 |
R4751:9130023H24Rik
|
UTSW |
7 |
127,836,258 (GRCm39) |
missense |
probably benign |
0.00 |
R5543:9130023H24Rik
|
UTSW |
7 |
127,836,353 (GRCm39) |
missense |
probably benign |
|
R5577:9130023H24Rik
|
UTSW |
7 |
127,835,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:9130023H24Rik
|
UTSW |
7 |
127,835,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:9130023H24Rik
|
UTSW |
7 |
127,835,664 (GRCm39) |
missense |
probably benign |
0.01 |
R7040:9130023H24Rik
|
UTSW |
7 |
127,835,897 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7529:9130023H24Rik
|
UTSW |
7 |
127,836,336 (GRCm39) |
nonsense |
probably null |
|
R7672:9130023H24Rik
|
UTSW |
7 |
127,836,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R8863:9130023H24Rik
|
UTSW |
7 |
127,836,123 (GRCm39) |
missense |
possibly damaging |
0.50 |
|