Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
A |
G |
10: 87,066,066 (GRCm39) |
E249G |
possibly damaging |
Het |
2610028H24Rik |
A |
G |
10: 76,293,349 (GRCm39) |
M136V |
possibly damaging |
Het |
4930523C07Rik |
A |
T |
1: 159,902,945 (GRCm39) |
K72* |
probably null |
Het |
Abca6 |
A |
G |
11: 110,110,475 (GRCm39) |
I558T |
probably benign |
Het |
Acot10 |
T |
C |
15: 20,666,712 (GRCm39) |
T10A |
probably benign |
Het |
Adgrl4 |
T |
A |
3: 151,205,838 (GRCm39) |
D233E |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,705,199 (GRCm39) |
F1537Y |
probably damaging |
Het |
Aqp3 |
T |
A |
4: 41,098,061 (GRCm39) |
I17F |
probably benign |
Het |
Arap1 |
T |
A |
7: 101,058,527 (GRCm39) |
L1375H |
probably damaging |
Het |
Aspm |
T |
C |
1: 139,385,373 (GRCm39) |
V339A |
probably benign |
Het |
Atp13a3 |
G |
A |
16: 30,173,094 (GRCm39) |
A261V |
probably damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,640,142 (GRCm39) |
Y399H |
probably benign |
Het |
Cept1 |
A |
G |
3: 106,420,195 (GRCm39) |
V213A |
probably damaging |
Het |
Cit |
A |
G |
5: 116,123,566 (GRCm39) |
D1469G |
possibly damaging |
Het |
Cnga2 |
A |
G |
X: 71,051,394 (GRCm39) |
Y182C |
possibly damaging |
Het |
Cox20 |
A |
G |
1: 178,149,512 (GRCm39) |
I54V |
probably benign |
Het |
Dhx8 |
C |
A |
11: 101,629,235 (GRCm39) |
D261E |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,349,011 (GRCm39) |
I2486N |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,408,467 (GRCm39) |
Q3484R |
probably benign |
Het |
Drd1 |
T |
C |
13: 54,207,572 (GRCm39) |
Y207C |
probably damaging |
Het |
Dtl |
C |
T |
1: 191,290,222 (GRCm39) |
V222I |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,607,316 (GRCm39) |
Y2636H |
probably damaging |
Het |
Endog |
C |
A |
2: 30,062,048 (GRCm39) |
D154E |
probably benign |
Het |
Epc1 |
A |
T |
18: 6,462,954 (GRCm39) |
V14E |
probably damaging |
Het |
Ercc4 |
C |
A |
16: 12,965,798 (GRCm39) |
T810K |
probably damaging |
Het |
Fam43b |
T |
A |
4: 138,123,299 (GRCm39) |
N7I |
possibly damaging |
Het |
Fgd1 |
T |
C |
X: 149,869,213 (GRCm39) |
|
probably null |
Het |
Filip1 |
G |
T |
9: 79,726,612 (GRCm39) |
T669N |
probably damaging |
Het |
Fndc1 |
A |
G |
17: 7,997,497 (GRCm39) |
|
probably benign |
Het |
Foxk1 |
C |
A |
5: 142,420,943 (GRCm39) |
S189* |
probably null |
Het |
Gatm |
T |
C |
2: 122,431,017 (GRCm39) |
N274S |
probably damaging |
Het |
Gdf9 |
A |
G |
11: 53,328,334 (GRCm39) |
Y430C |
probably damaging |
Het |
Gga1 |
C |
T |
15: 78,772,648 (GRCm39) |
P260S |
probably damaging |
Het |
Gm11595 |
A |
T |
11: 99,663,327 (GRCm39) |
C118S |
unknown |
Het |
Gm382 |
G |
T |
X: 125,970,274 (GRCm39) |
V820L |
possibly damaging |
Het |
Gzmk |
T |
A |
13: 113,308,548 (GRCm39) |
I179F |
probably damaging |
Het |
Hsp90b1 |
T |
C |
10: 86,531,570 (GRCm39) |
D421G |
probably damaging |
Het |
Hus1 |
A |
G |
11: 8,956,011 (GRCm39) |
M174T |
probably damaging |
Het |
Ifngr2 |
T |
A |
16: 91,359,761 (GRCm39) |
Y289* |
probably null |
Het |
Il6st |
T |
A |
13: 112,640,709 (GRCm39) |
H828Q |
probably benign |
Het |
Impg2 |
T |
A |
16: 56,038,742 (GRCm39) |
Y127N |
probably damaging |
Het |
Irf3 |
T |
A |
7: 44,651,168 (GRCm39) |
W345R |
probably damaging |
Het |
Kif1b |
G |
A |
4: 149,272,097 (GRCm39) |
S1568L |
possibly damaging |
Het |
Klhl42 |
A |
G |
6: 147,003,251 (GRCm39) |
T342A |
probably benign |
Het |
Kndc1 |
G |
T |
7: 139,510,025 (GRCm39) |
R1289L |
probably damaging |
Het |
Knl1 |
A |
T |
2: 118,902,300 (GRCm39) |
T1334S |
possibly damaging |
Het |
L3mbtl3 |
G |
T |
10: 26,189,766 (GRCm39) |
D499E |
unknown |
Het |
Ldhd |
T |
A |
8: 112,353,680 (GRCm39) |
M478L |
probably benign |
Het |
Loxl4 |
C |
G |
19: 42,592,402 (GRCm39) |
E385D |
probably damaging |
Het |
Lrriq1 |
G |
A |
10: 103,050,718 (GRCm39) |
T678I |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,386,567 (GRCm39) |
I1017F |
probably benign |
Het |
Madcam1 |
A |
G |
10: 79,501,406 (GRCm39) |
E157G |
possibly damaging |
Het |
Mamdc4 |
T |
C |
2: 25,459,270 (GRCm39) |
D195G |
probably damaging |
Het |
Mctp1 |
A |
G |
13: 76,972,941 (GRCm39) |
D648G |
probably damaging |
Het |
Mycbp2 |
T |
C |
14: 103,438,666 (GRCm39) |
M2072V |
probably benign |
Het |
Nck1 |
A |
G |
9: 100,379,600 (GRCm39) |
|
probably null |
Het |
Ndufaf4 |
G |
T |
4: 24,898,608 (GRCm39) |
D55Y |
probably damaging |
Het |
Nek11 |
A |
T |
9: 105,177,560 (GRCm39) |
D230E |
probably benign |
Het |
Nit2 |
T |
C |
16: 56,981,559 (GRCm39) |
K67E |
possibly damaging |
Het |
Or12j2 |
C |
T |
7: 139,916,342 (GRCm39) |
T189M |
probably damaging |
Het |
Or5ae1 |
T |
C |
7: 84,565,701 (GRCm39) |
F238S |
probably damaging |
Het |
Or6a2 |
T |
C |
7: 106,600,455 (GRCm39) |
D204G |
probably damaging |
Het |
Or6c1 |
A |
T |
10: 129,518,401 (GRCm39) |
V69E |
possibly damaging |
Het |
Pakap |
A |
G |
4: 57,854,890 (GRCm39) |
Y134C |
probably benign |
Het |
Pccb |
G |
C |
9: 100,867,884 (GRCm39) |
D347E |
probably damaging |
Het |
Plcl1 |
T |
A |
1: 55,736,997 (GRCm39) |
F779L |
probably damaging |
Het |
Prune2 |
C |
A |
19: 17,099,786 (GRCm39) |
D1763E |
probably benign |
Het |
Pwwp2a |
A |
G |
11: 43,596,145 (GRCm39) |
S437G |
probably benign |
Het |
Rabgap1l |
A |
T |
1: 160,566,527 (GRCm39) |
D90E |
probably benign |
Het |
Rapgef4 |
T |
A |
2: 72,056,897 (GRCm39) |
I552N |
possibly damaging |
Het |
Scn7a |
A |
T |
2: 66,528,330 (GRCm39) |
I720K |
probably damaging |
Het |
Scn9a |
T |
A |
2: 66,356,998 (GRCm39) |
N1101I |
probably damaging |
Het |
Siglec1 |
A |
T |
2: 130,922,417 (GRCm39) |
Y553N |
probably damaging |
Het |
Slc22a23 |
A |
G |
13: 34,387,953 (GRCm39) |
L381P |
possibly damaging |
Het |
Slc7a11 |
T |
A |
3: 50,338,558 (GRCm39) |
T284S |
probably damaging |
Het |
Slc8a2 |
T |
A |
7: 15,874,417 (GRCm39) |
|
probably null |
Het |
Stimate |
T |
C |
14: 30,588,581 (GRCm39) |
Y103H |
probably damaging |
Het |
Stox1 |
T |
C |
10: 62,500,314 (GRCm39) |
T749A |
probably benign |
Het |
Tg |
A |
G |
15: 66,566,743 (GRCm39) |
I1264V |
probably benign |
Het |
Top2a |
A |
C |
11: 98,900,633 (GRCm39) |
V609G |
probably damaging |
Het |
Trmt44 |
G |
A |
5: 35,732,176 (GRCm39) |
P72S |
probably benign |
Het |
Ttll3 |
G |
C |
6: 113,389,895 (GRCm39) |
S760T |
probably benign |
Het |
Ttn |
T |
C |
2: 76,579,022 (GRCm39) |
D23957G |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,664,241 (GRCm39) |
|
probably benign |
Het |
Ubxn1 |
T |
G |
19: 8,849,434 (GRCm39) |
V59G |
probably benign |
Het |
Ubxn4 |
T |
C |
1: 128,172,247 (GRCm39) |
S14P |
probably benign |
Het |
Uso1 |
T |
A |
5: 92,343,229 (GRCm39) |
M771K |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,649,917 (GRCm39) |
F431S |
probably damaging |
Het |
Vmn1r206 |
T |
C |
13: 22,804,782 (GRCm39) |
S142G |
probably benign |
Het |
Vmn2r19 |
A |
G |
6: 123,285,289 (GRCm39) |
|
probably null |
Het |
Vps36 |
G |
T |
8: 22,708,305 (GRCm39) |
|
probably null |
Het |
Wnt3 |
A |
G |
11: 103,703,474 (GRCm39) |
H319R |
possibly damaging |
Het |
Zbtb26 |
G |
T |
2: 37,326,563 (GRCm39) |
Q158K |
probably benign |
Het |
Zfp648 |
T |
C |
1: 154,080,353 (GRCm39) |
S171P |
probably benign |
Het |
|
Other mutations in Snx29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00733:Snx29
|
APN |
16 |
11,221,366 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02207:Snx29
|
APN |
16 |
11,556,216 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Snx29
|
UTSW |
16 |
11,221,488 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4810001:Snx29
|
UTSW |
16 |
11,218,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Snx29
|
UTSW |
16 |
11,478,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Snx29
|
UTSW |
16 |
11,478,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Snx29
|
UTSW |
16 |
11,556,237 (GRCm39) |
missense |
probably benign |
0.01 |
R0506:Snx29
|
UTSW |
16 |
11,213,167 (GRCm39) |
missense |
probably benign |
0.15 |
R0621:Snx29
|
UTSW |
16 |
11,223,651 (GRCm39) |
splice site |
probably null |
|
R0975:Snx29
|
UTSW |
16 |
11,165,735 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1225:Snx29
|
UTSW |
16 |
11,238,550 (GRCm39) |
intron |
probably benign |
|
R1406:Snx29
|
UTSW |
16 |
11,217,657 (GRCm39) |
missense |
probably benign |
0.38 |
R1406:Snx29
|
UTSW |
16 |
11,217,657 (GRCm39) |
missense |
probably benign |
0.38 |
R1452:Snx29
|
UTSW |
16 |
11,449,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1515:Snx29
|
UTSW |
16 |
11,217,701 (GRCm39) |
critical splice donor site |
probably null |
|
R1874:Snx29
|
UTSW |
16 |
11,185,545 (GRCm39) |
missense |
probably benign |
0.01 |
R1953:Snx29
|
UTSW |
16 |
11,217,647 (GRCm39) |
nonsense |
probably null |
|
R1978:Snx29
|
UTSW |
16 |
11,185,588 (GRCm39) |
missense |
probably benign |
0.23 |
R2054:Snx29
|
UTSW |
16 |
11,449,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R2105:Snx29
|
UTSW |
16 |
11,328,898 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2152:Snx29
|
UTSW |
16 |
11,218,707 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2912:Snx29
|
UTSW |
16 |
11,265,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R2913:Snx29
|
UTSW |
16 |
11,265,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R2914:Snx29
|
UTSW |
16 |
11,265,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R4468:Snx29
|
UTSW |
16 |
11,238,565 (GRCm39) |
splice site |
probably null |
|
R4469:Snx29
|
UTSW |
16 |
11,238,565 (GRCm39) |
splice site |
probably null |
|
R4612:Snx29
|
UTSW |
16 |
11,265,359 (GRCm39) |
missense |
probably damaging |
0.99 |
R4744:Snx29
|
UTSW |
16 |
11,167,773 (GRCm39) |
nonsense |
probably null |
|
R4798:Snx29
|
UTSW |
16 |
11,238,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Snx29
|
UTSW |
16 |
11,221,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R5165:Snx29
|
UTSW |
16 |
11,238,639 (GRCm39) |
missense |
probably damaging |
0.98 |
R5207:Snx29
|
UTSW |
16 |
11,556,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5235:Snx29
|
UTSW |
16 |
11,231,110 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5274:Snx29
|
UTSW |
16 |
11,556,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Snx29
|
UTSW |
16 |
11,217,688 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5462:Snx29
|
UTSW |
16 |
11,328,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5655:Snx29
|
UTSW |
16 |
11,573,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R6036:Snx29
|
UTSW |
16 |
11,556,301 (GRCm39) |
splice site |
probably null |
|
R6036:Snx29
|
UTSW |
16 |
11,556,301 (GRCm39) |
splice site |
probably null |
|
R6326:Snx29
|
UTSW |
16 |
11,221,430 (GRCm39) |
missense |
probably benign |
|
R6576:Snx29
|
UTSW |
16 |
11,532,920 (GRCm39) |
critical splice donor site |
probably null |
|
R7406:Snx29
|
UTSW |
16 |
11,573,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R7552:Snx29
|
UTSW |
16 |
11,238,649 (GRCm39) |
critical splice donor site |
probably null |
|
R7555:Snx29
|
UTSW |
16 |
11,218,806 (GRCm39) |
missense |
probably benign |
0.02 |
R7736:Snx29
|
UTSW |
16 |
11,185,588 (GRCm39) |
missense |
probably benign |
0.23 |
R7962:Snx29
|
UTSW |
16 |
11,231,221 (GRCm39) |
critical splice donor site |
probably null |
|
R8101:Snx29
|
UTSW |
16 |
11,389,580 (GRCm39) |
missense |
probably benign |
0.16 |
R8415:Snx29
|
UTSW |
16 |
11,265,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R8549:Snx29
|
UTSW |
16 |
11,532,920 (GRCm39) |
critical splice donor site |
probably null |
|
R9010:Snx29
|
UTSW |
16 |
11,449,391 (GRCm39) |
missense |
probably benign |
0.00 |
R9091:Snx29
|
UTSW |
16 |
11,213,155 (GRCm39) |
missense |
probably benign |
0.33 |
R9099:Snx29
|
UTSW |
16 |
11,478,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R9176:Snx29
|
UTSW |
16 |
11,236,728 (GRCm39) |
missense |
probably benign |
|
R9258:Snx29
|
UTSW |
16 |
11,532,799 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9270:Snx29
|
UTSW |
16 |
11,213,155 (GRCm39) |
missense |
probably benign |
0.33 |
R9672:Snx29
|
UTSW |
16 |
11,478,515 (GRCm39) |
missense |
probably benign |
0.00 |
R9778:Snx29
|
UTSW |
16 |
11,223,609 (GRCm39) |
missense |
possibly damaging |
0.90 |
|