Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
T |
16: 4,653,453 (GRCm39) |
M1L |
unknown |
Het |
Abca13 |
T |
A |
11: 9,460,668 (GRCm39) |
I4226N |
probably damaging |
Het |
Ankrd10 |
C |
A |
8: 11,678,518 (GRCm39) |
E125* |
probably null |
Het |
Apob |
A |
T |
12: 8,059,009 (GRCm39) |
D2497V |
possibly damaging |
Het |
Arap1 |
G |
A |
7: 101,035,725 (GRCm39) |
W87* |
probably null |
Het |
Arhgef37 |
C |
T |
18: 61,640,277 (GRCm39) |
V261I |
probably benign |
Het |
Arl4a |
A |
C |
12: 40,086,472 (GRCm39) |
C92G |
probably benign |
Het |
Arrdc2 |
C |
T |
8: 71,289,501 (GRCm39) |
|
probably null |
Het |
Atg16l1 |
A |
C |
1: 87,706,704 (GRCm39) |
T355P |
probably damaging |
Het |
Card14 |
T |
G |
11: 119,224,435 (GRCm39) |
|
probably null |
Het |
Cd109 |
G |
A |
9: 78,564,801 (GRCm39) |
V249I |
probably benign |
Het |
Cdhr4 |
A |
G |
9: 107,873,453 (GRCm39) |
D395G |
probably damaging |
Het |
Celsr1 |
C |
A |
15: 85,822,207 (GRCm39) |
M1703I |
possibly damaging |
Het |
Cfap157 |
A |
G |
2: 32,669,752 (GRCm39) |
I277T |
probably benign |
Het |
Chst4 |
A |
G |
8: 110,757,095 (GRCm39) |
V173A |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,617,911 (GRCm39) |
N731D |
probably benign |
Het |
Col11a2 |
A |
G |
17: 34,278,936 (GRCm39) |
E1122G |
possibly damaging |
Het |
Csf1r |
C |
G |
18: 61,247,954 (GRCm39) |
P341A |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,297,215 (GRCm39) |
E253G |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,343,804 (GRCm39) |
D2829V |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,512,067 (GRCm39) |
N2998S |
probably damaging |
Het |
Ehbp1 |
C |
T |
11: 22,235,842 (GRCm39) |
|
probably benign |
Het |
Eprs1 |
A |
T |
1: 185,139,371 (GRCm39) |
K919* |
probably null |
Het |
Esp16 |
A |
T |
17: 39,850,821 (GRCm39) |
K67* |
probably null |
Het |
Fam83h |
C |
T |
15: 75,874,502 (GRCm39) |
R945H |
probably benign |
Het |
Flnb |
T |
A |
14: 7,869,822 (GRCm38) |
V195E |
probably damaging |
Het |
Gm3159 |
T |
C |
14: 4,398,567 (GRCm38) |
I86T |
probably damaging |
Het |
Gm4744 |
G |
A |
6: 40,926,281 (GRCm39) |
S103F |
|
Het |
Gvin2 |
A |
G |
7: 105,548,088 (GRCm39) |
S1655P |
probably benign |
Het |
Ift122 |
T |
A |
6: 115,887,292 (GRCm39) |
I713N |
probably benign |
Het |
Ilkap |
A |
G |
1: 91,306,266 (GRCm39) |
I105T |
probably damaging |
Het |
Isl1 |
G |
T |
13: 116,441,835 (GRCm39) |
H133N |
possibly damaging |
Het |
Jade1 |
T |
A |
3: 41,559,113 (GRCm39) |
L398Q |
possibly damaging |
Het |
Kcnh7 |
C |
T |
2: 62,681,003 (GRCm39) |
V195M |
probably benign |
Het |
Kif3a |
A |
T |
11: 53,489,627 (GRCm39) |
K669* |
probably null |
Het |
L3mbtl4 |
G |
A |
17: 68,937,239 (GRCm39) |
R420H |
probably damaging |
Het |
Mrgprb1 |
A |
T |
7: 48,097,321 (GRCm39) |
I197N |
probably damaging |
Het |
Mthfd1 |
A |
G |
12: 76,340,929 (GRCm39) |
T263A |
probably damaging |
Het |
Mtmr7 |
G |
A |
8: 41,059,927 (GRCm39) |
A62V |
possibly damaging |
Het |
Naxe |
A |
G |
3: 87,965,757 (GRCm39) |
|
probably benign |
Het |
Ndufs2 |
T |
C |
1: 171,068,677 (GRCm39) |
T51A |
probably benign |
Het |
Nlrc5 |
T |
A |
8: 95,249,848 (GRCm39) |
L1824Q |
probably damaging |
Het |
Notch1 |
A |
G |
2: 26,362,251 (GRCm39) |
V27A |
unknown |
Het |
Nucks1 |
A |
T |
1: 131,857,473 (GRCm39) |
M169L |
probably benign |
Het |
Or10ag53 |
T |
A |
2: 87,083,215 (GRCm39) |
D311E |
probably benign |
Het |
Or13p4 |
C |
T |
4: 118,547,229 (GRCm39) |
S140N |
probably benign |
Het |
Or4a80 |
T |
A |
2: 89,582,599 (GRCm39) |
Y191F |
probably benign |
Het |
Or4k45 |
T |
A |
2: 111,395,324 (GRCm39) |
H155L |
probably damaging |
Het |
Or51aa2 |
A |
T |
7: 103,187,479 (GRCm39) |
S321T |
probably benign |
Het |
Or52n20 |
G |
T |
7: 104,320,022 (GRCm39) |
V38L |
probably benign |
Het |
Or5w10 |
T |
A |
2: 87,375,114 (GRCm39) |
Y258F |
probably damaging |
Het |
Pcnt |
C |
T |
10: 76,239,457 (GRCm39) |
|
probably null |
Het |
Pdcd7 |
T |
C |
9: 65,254,039 (GRCm39) |
S206P |
probably benign |
Het |
Pdia4 |
A |
T |
6: 47,773,575 (GRCm39) |
Y591* |
probably null |
Het |
Pgap6 |
G |
T |
17: 26,340,931 (GRCm39) |
R678L |
probably damaging |
Het |
Plxna4 |
C |
T |
6: 32,192,647 (GRCm39) |
M771I |
probably benign |
Het |
Pramel47 |
C |
T |
5: 95,488,092 (GRCm39) |
H9Y |
possibly damaging |
Het |
Ptpn13 |
A |
G |
5: 103,712,031 (GRCm39) |
Y1643C |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,717,671 (GRCm39) |
I1906V |
probably benign |
Het |
Rab33b |
T |
A |
3: 51,391,795 (GRCm39) |
S15T |
probably benign |
Het |
Rasip1 |
A |
T |
7: 45,284,467 (GRCm39) |
M644L |
possibly damaging |
Het |
Rnf4 |
G |
A |
5: 34,506,035 (GRCm39) |
C55Y |
probably damaging |
Het |
Sel1l |
A |
T |
12: 91,780,735 (GRCm39) |
Y585* |
probably null |
Het |
Slc40a1 |
A |
T |
1: 45,950,576 (GRCm39) |
F292Y |
probably damaging |
Het |
Smarca4 |
G |
A |
9: 21,570,144 (GRCm39) |
D716N |
probably damaging |
Het |
Sp7 |
T |
A |
15: 102,266,837 (GRCm39) |
H323L |
possibly damaging |
Het |
Speer1m |
T |
C |
5: 11,971,489 (GRCm39) |
L147P |
probably damaging |
Het |
Sprtn |
A |
G |
8: 125,629,933 (GRCm39) |
S409G |
probably benign |
Het |
St3gal2 |
T |
G |
8: 111,688,853 (GRCm39) |
L131R |
probably damaging |
Het |
Tctn1 |
A |
G |
5: 122,399,552 (GRCm39) |
C91R |
probably damaging |
Het |
Tgm1 |
A |
T |
14: 55,937,754 (GRCm39) |
V785E |
probably damaging |
Het |
Topaz1 |
G |
T |
9: 122,579,573 (GRCm39) |
V828L |
probably benign |
Het |
Triobp |
C |
T |
15: 78,878,326 (GRCm39) |
H1750Y |
possibly damaging |
Het |
Ttc27 |
G |
A |
17: 75,050,047 (GRCm39) |
|
probably null |
Het |
Usp2 |
G |
A |
9: 43,987,350 (GRCm39) |
G216D |
possibly damaging |
Het |
Vmn2r99 |
A |
G |
17: 19,614,020 (GRCm39) |
D580G |
probably benign |
Het |
Wbp1l |
G |
A |
19: 46,640,988 (GRCm39) |
R106H |
possibly damaging |
Het |
Zmym2 |
G |
T |
14: 57,151,606 (GRCm39) |
C497F |
probably damaging |
Het |
|
Other mutations in Fam169a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01325:Fam169a
|
APN |
13 |
97,259,207 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01380:Fam169a
|
APN |
13 |
97,228,459 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01761:Fam169a
|
APN |
13 |
97,228,426 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02628:Fam169a
|
APN |
13 |
97,247,796 (GRCm39) |
splice site |
probably benign |
|
IGL02739:Fam169a
|
APN |
13 |
97,230,563 (GRCm39) |
splice site |
probably benign |
|
IGL03171:Fam169a
|
APN |
13 |
97,246,522 (GRCm39) |
splice site |
probably benign |
|
IGL03306:Fam169a
|
APN |
13 |
97,243,497 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03377:Fam169a
|
APN |
13 |
97,228,381 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02980:Fam169a
|
UTSW |
13 |
97,250,188 (GRCm39) |
critical splice donor site |
probably null |
|
R0282:Fam169a
|
UTSW |
13 |
97,234,223 (GRCm39) |
splice site |
probably benign |
|
R1319:Fam169a
|
UTSW |
13 |
97,234,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Fam169a
|
UTSW |
13 |
97,255,038 (GRCm39) |
missense |
probably benign |
0.01 |
R1468:Fam169a
|
UTSW |
13 |
97,255,038 (GRCm39) |
missense |
probably benign |
0.01 |
R2037:Fam169a
|
UTSW |
13 |
97,243,600 (GRCm39) |
missense |
probably benign |
0.37 |
R2380:Fam169a
|
UTSW |
13 |
97,255,043 (GRCm39) |
splice site |
probably benign |
|
R3805:Fam169a
|
UTSW |
13 |
97,234,192 (GRCm39) |
missense |
probably benign |
0.00 |
R4434:Fam169a
|
UTSW |
13 |
97,263,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4435:Fam169a
|
UTSW |
13 |
97,263,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Fam169a
|
UTSW |
13 |
97,263,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Fam169a
|
UTSW |
13 |
97,234,093 (GRCm39) |
missense |
probably benign |
0.02 |
R4896:Fam169a
|
UTSW |
13 |
97,234,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fam169a
|
UTSW |
13 |
97,234,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R5276:Fam169a
|
UTSW |
13 |
97,255,004 (GRCm39) |
missense |
probably benign |
0.01 |
R5370:Fam169a
|
UTSW |
13 |
97,243,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Fam169a
|
UTSW |
13 |
97,230,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Fam169a
|
UTSW |
13 |
97,230,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Fam169a
|
UTSW |
13 |
97,263,196 (GRCm39) |
nonsense |
probably null |
|
R8322:Fam169a
|
UTSW |
13 |
97,259,260 (GRCm39) |
missense |
probably benign |
0.00 |
R8698:Fam169a
|
UTSW |
13 |
97,243,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Fam169a
|
UTSW |
13 |
97,250,628 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9231:Fam169a
|
UTSW |
13 |
97,254,967 (GRCm39) |
missense |
probably benign |
0.08 |
R9479:Fam169a
|
UTSW |
13 |
97,250,695 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9479:Fam169a
|
UTSW |
13 |
97,246,543 (GRCm39) |
missense |
possibly damaging |
0.68 |
|