Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,243,459 (GRCm39) |
V1774A |
probably damaging |
Het |
Adam34 |
G |
A |
8: 44,105,288 (GRCm39) |
P119L |
probably benign |
Het |
Ap3b2 |
T |
C |
7: 81,113,429 (GRCm39) |
|
probably null |
Het |
Arfip2 |
G |
A |
7: 105,286,430 (GRCm39) |
T124M |
probably damaging |
Het |
Arhgef26 |
T |
C |
3: 62,330,965 (GRCm39) |
S560P |
probably damaging |
Het |
Bcl11a |
A |
T |
11: 24,122,697 (GRCm39) |
|
probably null |
Het |
Cab39 |
A |
G |
1: 85,776,881 (GRCm39) |
E322G |
probably damaging |
Het |
Cad |
C |
A |
5: 31,229,665 (GRCm39) |
P1382Q |
probably benign |
Het |
Cc2d2a |
T |
C |
5: 43,864,243 (GRCm39) |
|
probably null |
Het |
Cela2a |
A |
T |
4: 141,549,011 (GRCm39) |
|
probably null |
Het |
Cert1 |
C |
T |
13: 96,770,629 (GRCm39) |
R487* |
probably null |
Het |
Ces1e |
A |
C |
8: 93,950,667 (GRCm39) |
I38S |
probably benign |
Het |
Ces1f |
A |
T |
8: 93,990,019 (GRCm39) |
F364I |
probably benign |
Het |
Cnpy4 |
C |
T |
5: 138,191,074 (GRCm39) |
Q217* |
probably null |
Het |
Crlf1 |
A |
G |
8: 70,951,249 (GRCm39) |
T43A |
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,173,816 (GRCm39) |
M707K |
probably damaging |
Het |
Ets2 |
G |
A |
16: 95,513,193 (GRCm39) |
S123N |
probably damaging |
Het |
Fry |
T |
C |
5: 150,394,933 (GRCm39) |
F304S |
probably damaging |
Het |
Gadd45gip1 |
G |
A |
8: 85,560,745 (GRCm39) |
R120H |
probably benign |
Het |
Gbf1 |
A |
G |
19: 46,242,459 (GRCm39) |
T96A |
probably benign |
Het |
Ggn |
T |
A |
7: 28,870,515 (GRCm39) |
M1K |
probably null |
Het |
Gm5239 |
A |
G |
18: 35,669,969 (GRCm39) |
T112A |
probably benign |
Het |
Insyn2b |
C |
A |
11: 34,352,826 (GRCm39) |
D289E |
possibly damaging |
Het |
Kifbp |
A |
T |
10: 62,413,861 (GRCm39) |
|
probably null |
Het |
Lrrc15 |
A |
T |
16: 30,092,561 (GRCm39) |
H259Q |
probably benign |
Het |
Lysmd4 |
A |
G |
7: 66,876,045 (GRCm39) |
Y236C |
probably damaging |
Het |
Med29 |
T |
C |
7: 28,086,284 (GRCm39) |
T175A |
possibly damaging |
Het |
Mfsd12 |
G |
T |
10: 81,193,633 (GRCm39) |
D68Y |
probably damaging |
Het |
Myh1 |
T |
C |
11: 67,108,338 (GRCm39) |
L1308P |
probably damaging |
Het |
Nphp4 |
T |
A |
4: 152,636,388 (GRCm39) |
|
probably null |
Het |
Or8g30 |
A |
G |
9: 39,230,757 (GRCm39) |
I51T |
probably benign |
Het |
Pdhx |
A |
G |
2: 102,858,625 (GRCm39) |
V393A |
probably benign |
Het |
Pgm5 |
A |
G |
19: 24,801,763 (GRCm39) |
I155T |
possibly damaging |
Het |
Pgr |
A |
T |
9: 8,965,023 (GRCm39) |
I889F |
probably benign |
Het |
Phactr4 |
T |
A |
4: 132,114,241 (GRCm39) |
K51I |
probably damaging |
Het |
Pum2 |
T |
A |
12: 8,778,754 (GRCm39) |
I468K |
possibly damaging |
Het |
Rab11a |
A |
G |
9: 64,632,835 (GRCm39) |
S24P |
probably damaging |
Het |
Rasef |
T |
C |
4: 73,666,799 (GRCm39) |
Q160R |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,813,772 (GRCm39) |
D339G |
probably benign |
Het |
Recql5 |
A |
G |
11: 115,785,499 (GRCm39) |
S666P |
probably benign |
Het |
Rfc1 |
A |
T |
5: 65,453,395 (GRCm39) |
|
probably null |
Het |
Scarb1 |
A |
G |
5: 125,366,756 (GRCm39) |
V59A |
probably damaging |
Het |
Slc2a4 |
C |
T |
11: 69,837,182 (GRCm39) |
V85M |
probably damaging |
Het |
Slc6a12 |
A |
G |
6: 121,335,584 (GRCm39) |
I291V |
possibly damaging |
Het |
Slco3a1 |
A |
C |
7: 74,154,174 (GRCm39) |
Y104D |
probably damaging |
Het |
Suz12 |
T |
A |
11: 79,889,904 (GRCm39) |
D13E |
probably damaging |
Het |
Tlr1 |
G |
T |
5: 65,083,310 (GRCm39) |
C422* |
probably null |
Het |
Tmco1 |
T |
C |
1: 167,153,462 (GRCm39) |
V114A |
probably damaging |
Het |
Trpa1 |
T |
C |
1: 14,951,856 (GRCm39) |
T948A |
probably benign |
Het |
Tub |
A |
T |
7: 108,620,134 (GRCm39) |
N93Y |
probably damaging |
Het |
Ufsp2 |
G |
A |
8: 46,445,270 (GRCm39) |
|
probably null |
Het |
Veph1 |
T |
C |
3: 66,079,396 (GRCm39) |
D373G |
probably benign |
Het |
Vmn1r206 |
A |
G |
13: 22,805,130 (GRCm39) |
S26P |
possibly damaging |
Het |
Vmn2r1 |
T |
C |
3: 63,989,240 (GRCm39) |
S60P |
possibly damaging |
Het |
Wdcp |
A |
G |
12: 4,901,583 (GRCm39) |
S480G |
probably benign |
Het |
Wnk4 |
T |
C |
11: 101,159,630 (GRCm39) |
S612P |
probably benign |
Het |
Zfp503 |
T |
C |
14: 22,036,527 (GRCm39) |
K130E |
probably benign |
Het |
Zkscan16 |
G |
A |
4: 58,957,602 (GRCm39) |
C628Y |
possibly damaging |
Het |
|
Other mutations in Chgb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01601:Chgb
|
APN |
2 |
132,635,411 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03031:Chgb
|
APN |
2 |
132,635,434 (GRCm39) |
missense |
probably benign |
0.03 |
R0513:Chgb
|
UTSW |
2 |
132,627,897 (GRCm39) |
splice site |
probably benign |
|
R0607:Chgb
|
UTSW |
2 |
132,635,255 (GRCm39) |
missense |
probably benign |
|
R1177:Chgb
|
UTSW |
2 |
132,635,390 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1468:Chgb
|
UTSW |
2 |
132,634,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Chgb
|
UTSW |
2 |
132,634,720 (GRCm39) |
missense |
probably benign |
0.00 |
R1595:Chgb
|
UTSW |
2 |
132,635,657 (GRCm39) |
missense |
probably benign |
0.22 |
R1994:Chgb
|
UTSW |
2 |
132,628,418 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3861:Chgb
|
UTSW |
2 |
132,635,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R4074:Chgb
|
UTSW |
2 |
132,635,847 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4354:Chgb
|
UTSW |
2 |
132,635,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:Chgb
|
UTSW |
2 |
132,635,219 (GRCm39) |
missense |
probably benign |
0.27 |
R4983:Chgb
|
UTSW |
2 |
132,635,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R5426:Chgb
|
UTSW |
2 |
132,635,453 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5711:Chgb
|
UTSW |
2 |
132,634,618 (GRCm39) |
missense |
probably benign |
0.00 |
R5946:Chgb
|
UTSW |
2 |
132,634,516 (GRCm39) |
missense |
probably benign |
|
R7116:Chgb
|
UTSW |
2 |
132,623,237 (GRCm39) |
start gained |
probably benign |
|
R8978:Chgb
|
UTSW |
2 |
132,634,498 (GRCm39) |
missense |
probably benign |
0.00 |
R9033:Chgb
|
UTSW |
2 |
132,634,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R9428:Chgb
|
UTSW |
2 |
132,635,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|