Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
G |
1: 71,359,123 (GRCm39) |
D561A |
probably benign |
Het |
Adgrg1 |
T |
C |
8: 95,731,965 (GRCm39) |
F204S |
probably benign |
Het |
Apoa2 |
T |
C |
1: 171,053,741 (GRCm39) |
L72P |
probably damaging |
Het |
Arhgef10 |
A |
T |
8: 15,030,583 (GRCm39) |
K987* |
probably null |
Het |
Arrb1 |
A |
G |
7: 99,188,981 (GRCm39) |
D9G |
unknown |
Het |
Asph |
A |
G |
4: 9,621,930 (GRCm39) |
S192P |
possibly damaging |
Het |
Bcas1 |
G |
A |
2: 170,229,084 (GRCm39) |
T309M |
possibly damaging |
Het |
Bcat2 |
C |
T |
7: 45,234,617 (GRCm39) |
T166M |
possibly damaging |
Het |
Bmp5 |
A |
T |
9: 75,801,072 (GRCm39) |
I401L |
probably damaging |
Het |
Bpifb9b |
G |
A |
2: 154,154,025 (GRCm39) |
G261R |
probably benign |
Het |
Cd53 |
T |
A |
3: 106,675,252 (GRCm39) |
Y106F |
probably benign |
Het |
Cdhr3 |
T |
A |
12: 33,103,519 (GRCm39) |
D366V |
probably benign |
Het |
Ceacam10 |
G |
C |
7: 24,480,636 (GRCm39) |
V256L |
unknown |
Het |
Cilp2 |
A |
G |
8: 70,334,071 (GRCm39) |
Y976H |
probably damaging |
Het |
Cklf |
A |
G |
8: 104,988,187 (GRCm39) |
T107A |
possibly damaging |
Het |
Dhx16 |
T |
A |
17: 36,192,568 (GRCm39) |
W167R |
possibly damaging |
Het |
Dkk2 |
T |
G |
3: 131,883,775 (GRCm39) |
L225R |
probably damaging |
Het |
Dmbt1 |
A |
T |
7: 130,718,625 (GRCm39) |
D1782V |
unknown |
Het |
Ebag9 |
A |
T |
15: 44,491,800 (GRCm39) |
D64V |
probably damaging |
Het |
Eif3j2 |
T |
C |
18: 43,610,382 (GRCm39) |
N144D |
possibly damaging |
Het |
Elp1 |
T |
C |
4: 56,776,920 (GRCm39) |
T626A |
possibly damaging |
Het |
Foxk2 |
A |
T |
11: 121,190,473 (GRCm39) |
Q538L |
possibly damaging |
Het |
Fpgt |
T |
G |
3: 154,792,747 (GRCm39) |
I427L |
probably benign |
Het |
Ganc |
A |
T |
2: 120,264,295 (GRCm39) |
N416I |
possibly damaging |
Het |
Gata6 |
A |
G |
18: 11,084,379 (GRCm39) |
Y556C |
probably damaging |
Het |
Gga2 |
A |
T |
7: 121,589,747 (GRCm39) |
V534E |
probably damaging |
Het |
Gm7324 |
T |
A |
14: 43,952,256 (GRCm39) |
S300T |
possibly damaging |
Het |
Gprc6a |
A |
C |
10: 51,491,549 (GRCm39) |
N733K |
possibly damaging |
Het |
Hivep3 |
C |
T |
4: 119,952,740 (GRCm39) |
T352I |
possibly damaging |
Het |
Ift88 |
T |
G |
14: 57,683,121 (GRCm39) |
V266G |
probably benign |
Het |
Ip6k1 |
G |
T |
9: 107,922,891 (GRCm39) |
G341V |
probably damaging |
Het |
Itga3 |
G |
T |
11: 94,967,029 (GRCm39) |
A45E |
probably damaging |
Het |
Kctd14 |
T |
A |
7: 97,107,147 (GRCm39) |
L134Q |
probably damaging |
Het |
Lats1 |
C |
A |
10: 7,578,128 (GRCm39) |
N417K |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,388,285 (GRCm39) |
H2380R |
unknown |
Het |
Lrrc4c |
A |
G |
2: 97,460,705 (GRCm39) |
T444A |
probably benign |
Het |
M1ap |
T |
C |
6: 82,982,565 (GRCm39) |
I283T |
probably benign |
Het |
Mapre2 |
T |
C |
18: 24,011,012 (GRCm39) |
S207P |
probably benign |
Het |
Moxd1 |
T |
C |
10: 24,158,608 (GRCm39) |
F421L |
probably damaging |
Het |
Nos2 |
T |
A |
11: 78,813,192 (GRCm39) |
C33* |
probably null |
Het |
Or14j4 |
A |
T |
17: 37,921,303 (GRCm39) |
L113H |
probably damaging |
Het |
Or1j16 |
A |
T |
2: 36,530,197 (GRCm39) |
I49F |
probably damaging |
Het |
Or5g26 |
T |
C |
2: 85,494,758 (GRCm39) |
T7A |
probably damaging |
Het |
Otud4 |
T |
C |
8: 80,382,394 (GRCm39) |
I201T |
possibly damaging |
Het |
Pank4 |
T |
C |
4: 155,054,204 (GRCm39) |
Y128H |
probably benign |
Het |
Phf11 |
C |
T |
14: 59,488,594 (GRCm39) |
D68N |
probably benign |
Het |
Pitpnm2 |
A |
G |
5: 124,261,093 (GRCm39) |
V1027A |
possibly damaging |
Het |
Plcb3 |
A |
G |
19: 6,946,991 (GRCm39) |
V8A |
probably benign |
Het |
Por |
A |
G |
5: 135,759,976 (GRCm39) |
E221G |
probably damaging |
Het |
Prokr2 |
A |
T |
2: 132,223,500 (GRCm39) |
L14* |
probably null |
Het |
Ptgis |
A |
G |
2: 167,033,891 (GRCm39) |
F459S |
unknown |
Het |
Ptpru |
T |
C |
4: 131,515,693 (GRCm39) |
E887G |
probably damaging |
Het |
Qrich2 |
GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG |
GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG |
11: 116,348,367 (GRCm39) |
|
probably benign |
Het |
Slc18a1 |
A |
G |
8: 69,518,206 (GRCm39) |
|
probably null |
Het |
Slc27a3 |
A |
G |
3: 90,296,740 (GRCm39) |
S120P |
probably benign |
Het |
Slc2a12 |
T |
A |
10: 22,540,717 (GRCm39) |
Y191N |
probably damaging |
Het |
Syncrip |
A |
G |
9: 88,343,721 (GRCm39) |
|
probably null |
Het |
Taar4 |
T |
A |
10: 23,836,897 (GRCm39) |
V169E |
probably damaging |
Het |
Tas1r1 |
C |
T |
4: 152,116,923 (GRCm39) |
G237D |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,117,571 (GRCm39) |
K30E |
probably damaging |
Het |
Tmem131l |
A |
T |
3: 83,847,875 (GRCm39) |
L330Q |
probably damaging |
Het |
Tmem67 |
A |
G |
4: 12,053,455 (GRCm39) |
F698L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,739,574 (GRCm39) |
Q3701L |
unknown |
Het |
Vmn2r17 |
G |
A |
5: 109,600,757 (GRCm39) |
R685K |
probably benign |
Het |
Ylpm1 |
C |
A |
12: 85,059,757 (GRCm39) |
A321E |
unknown |
Het |
Zdbf2 |
T |
A |
1: 63,347,166 (GRCm39) |
Y1848* |
probably null |
Het |
Zfand2b |
T |
A |
1: 75,146,176 (GRCm39) |
N61K |
probably null |
Het |
Zfp867 |
C |
T |
11: 59,354,016 (GRCm39) |
A438T |
probably damaging |
Het |
Zkscan14 |
G |
A |
5: 145,132,319 (GRCm39) |
T404I |
probably benign |
Het |
Zrsr2-ps1 |
C |
T |
11: 22,923,510 (GRCm39) |
Q95* |
probably null |
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 |
R2128:Snx29
|
UTSW |
16 |
11,218,835 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
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 |
|