Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm1 |
A |
G |
7: 119,258,350 (GRCm39) |
E481G |
probably damaging |
Het |
Anks1b |
C |
T |
10: 89,912,928 (GRCm39) |
T351M |
probably damaging |
Het |
Arhgap45 |
T |
A |
10: 79,864,836 (GRCm39) |
M933K |
probably damaging |
Het |
Asph |
A |
C |
4: 9,542,314 (GRCm39) |
|
probably benign |
Het |
Bace2 |
T |
C |
16: 97,213,388 (GRCm39) |
|
probably null |
Het |
Cacna1b |
A |
G |
2: 24,496,540 (GRCm39) |
V125A |
probably benign |
Het |
Cbarp |
T |
C |
10: 79,967,603 (GRCm39) |
D539G |
probably damaging |
Het |
Ccdc59 |
A |
T |
10: 105,677,388 (GRCm39) |
K9M |
possibly damaging |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Cdr1 |
T |
G |
X: 60,228,968 (GRCm39) |
D66A |
unknown |
Het |
Cfap91 |
A |
T |
16: 38,131,400 (GRCm39) |
I471N |
possibly damaging |
Het |
Clca3a2 |
T |
A |
3: 144,519,679 (GRCm39) |
T232S |
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,519,882 (GRCm39) |
|
probably benign |
Het |
Col1a2 |
A |
T |
6: 4,520,788 (GRCm39) |
Q375L |
possibly damaging |
Het |
Cpd |
T |
C |
11: 76,702,685 (GRCm39) |
N561S |
probably damaging |
Het |
Csn1s1 |
A |
T |
5: 87,824,995 (GRCm39) |
Q221L |
possibly damaging |
Het |
Depdc5 |
G |
A |
5: 33,058,965 (GRCm39) |
|
probably null |
Het |
Dnah10 |
T |
C |
5: 124,896,476 (GRCm39) |
|
probably null |
Het |
Dsg2 |
T |
C |
18: 20,712,185 (GRCm39) |
F107S |
probably damaging |
Het |
Dthd1 |
A |
G |
5: 63,000,300 (GRCm39) |
I541V |
probably benign |
Het |
Eml6 |
G |
A |
11: 29,783,049 (GRCm39) |
|
probably benign |
Het |
Fermt2 |
A |
C |
14: 45,741,948 (GRCm39) |
|
probably null |
Het |
Gimap8 |
A |
T |
6: 48,635,730 (GRCm39) |
R498S |
possibly damaging |
Het |
Glis1 |
A |
G |
4: 107,489,488 (GRCm39) |
N692D |
possibly damaging |
Het |
Grtp1 |
G |
A |
8: 13,239,755 (GRCm39) |
|
probably benign |
Het |
Hecw1 |
G |
T |
13: 14,420,421 (GRCm39) |
Q1001K |
possibly damaging |
Het |
Hydin |
T |
C |
8: 111,130,927 (GRCm39) |
V606A |
possibly damaging |
Het |
Krt33b |
T |
A |
11: 99,914,835 (GRCm39) |
N388I |
probably benign |
Het |
Lipf |
T |
C |
19: 33,950,438 (GRCm39) |
Y277H |
probably damaging |
Het |
Lmod1 |
A |
G |
1: 135,291,654 (GRCm39) |
K170E |
probably benign |
Het |
Lrrtm1 |
A |
T |
6: 77,220,635 (GRCm39) |
M31L |
probably benign |
Het |
Man1c1 |
A |
G |
4: 134,430,263 (GRCm39) |
I173T |
possibly damaging |
Het |
Med17 |
T |
C |
9: 15,187,187 (GRCm39) |
K196E |
probably damaging |
Het |
Mmp25 |
T |
A |
17: 23,863,765 (GRCm39) |
I22F |
probably benign |
Het |
Nrg3 |
T |
A |
14: 38,092,965 (GRCm39) |
N540I |
possibly damaging |
Het |
Nsun5 |
C |
T |
5: 135,404,317 (GRCm39) |
Q375* |
probably null |
Het |
Or52ad1 |
T |
C |
7: 102,995,272 (GRCm39) |
M288V |
probably benign |
Het |
Or52r1c |
T |
A |
7: 102,735,548 (GRCm39) |
H269Q |
probably benign |
Het |
Pcdh1 |
G |
T |
18: 38,322,815 (GRCm39) |
A1006E |
probably benign |
Het |
Pdss1 |
T |
A |
2: 22,796,799 (GRCm39) |
|
probably null |
Het |
Plaa |
G |
A |
4: 94,457,696 (GRCm39) |
A758V |
probably damaging |
Het |
Prl6a1 |
T |
A |
13: 27,499,303 (GRCm39) |
W24R |
probably damaging |
Het |
Ptk7 |
T |
C |
17: 46,883,476 (GRCm39) |
H863R |
probably damaging |
Het |
Rbm10 |
T |
C |
X: 20,513,934 (GRCm39) |
L429P |
possibly damaging |
Het |
Rhou |
T |
C |
8: 124,387,880 (GRCm39) |
I204T |
possibly damaging |
Het |
Serpind1 |
G |
T |
16: 17,154,972 (GRCm39) |
M266I |
probably benign |
Het |
Sgcg |
A |
T |
14: 61,467,074 (GRCm39) |
F175L |
probably damaging |
Het |
Slc2a2 |
T |
G |
3: 28,772,920 (GRCm39) |
C238G |
probably damaging |
Het |
Slc39a8 |
A |
G |
3: 135,592,584 (GRCm39) |
M420V |
probably benign |
Het |
Slc7a9 |
C |
A |
7: 35,163,167 (GRCm39) |
Y457* |
probably null |
Het |
Smpd3 |
C |
T |
8: 106,991,452 (GRCm39) |
R367H |
probably damaging |
Het |
Sntb2 |
T |
C |
8: 107,662,729 (GRCm39) |
V99A |
probably benign |
Het |
Specc1l |
T |
G |
10: 75,094,965 (GRCm39) |
I796R |
probably damaging |
Het |
Stfa2l1 |
G |
T |
16: 35,980,316 (GRCm39) |
V29F |
probably damaging |
Het |
Synrg |
T |
C |
11: 83,885,180 (GRCm39) |
F455S |
probably damaging |
Het |
Tap2 |
T |
C |
17: 34,431,328 (GRCm39) |
V422A |
possibly damaging |
Het |
Tcf7 |
A |
T |
11: 52,173,610 (GRCm39) |
|
probably null |
Het |
Tcp10a |
A |
G |
17: 7,597,173 (GRCm39) |
Y110C |
probably damaging |
Het |
Thoc1 |
T |
A |
18: 9,959,255 (GRCm39) |
S43R |
probably damaging |
Het |
Tlr1 |
A |
G |
5: 65,083,251 (GRCm39) |
V442A |
probably damaging |
Het |
Tmub1 |
A |
G |
5: 24,650,922 (GRCm39) |
*261Q |
probably null |
Het |
Trpc3 |
G |
A |
3: 36,688,532 (GRCm39) |
R836* |
probably null |
Het |
Tsbp1 |
A |
T |
17: 34,640,836 (GRCm39) |
H57L |
possibly damaging |
Het |
Ube2u |
T |
C |
4: 100,381,495 (GRCm39) |
S185P |
possibly damaging |
Het |
Vamp5 |
A |
G |
6: 72,346,323 (GRCm39) |
V91A |
probably benign |
Het |
Vcp |
A |
G |
4: 42,980,846 (GRCm39) |
Y755H |
probably damaging |
Het |
Vmn1r35 |
A |
T |
6: 66,655,950 (GRCm39) |
M73K |
possibly damaging |
Het |
Vmn2r12 |
C |
T |
5: 109,239,397 (GRCm39) |
E389K |
probably damaging |
Het |
Wdfy3 |
A |
T |
5: 102,091,988 (GRCm39) |
F450L |
probably benign |
Het |
Xpo4 |
G |
T |
14: 57,841,897 (GRCm39) |
Q473K |
probably benign |
Het |
Xpo7 |
A |
G |
14: 70,909,130 (GRCm39) |
I797T |
probably damaging |
Het |
Xylt1 |
C |
A |
7: 117,234,011 (GRCm39) |
Q513K |
probably benign |
Het |
Zfp229 |
T |
C |
17: 21,964,484 (GRCm39) |
F238S |
probably damaging |
Het |
|
Other mutations in Cela3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Cela3b
|
APN |
4 |
137,150,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00708:Cela3b
|
APN |
4 |
137,149,280 (GRCm39) |
missense |
probably benign |
|
IGL01301:Cela3b
|
APN |
4 |
137,151,154 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01613:Cela3b
|
APN |
4 |
137,152,382 (GRCm39) |
missense |
possibly damaging |
0.66 |
ANU18:Cela3b
|
UTSW |
4 |
137,151,154 (GRCm39) |
critical splice donor site |
probably null |
|
R0669:Cela3b
|
UTSW |
4 |
137,155,841 (GRCm39) |
missense |
probably benign |
0.06 |
R2938:Cela3b
|
UTSW |
4 |
137,150,574 (GRCm39) |
missense |
probably benign |
0.01 |
R4327:Cela3b
|
UTSW |
4 |
137,151,242 (GRCm39) |
missense |
probably benign |
0.26 |
R4451:Cela3b
|
UTSW |
4 |
137,148,355 (GRCm39) |
utr 3 prime |
probably benign |
|
R5059:Cela3b
|
UTSW |
4 |
137,152,181 (GRCm39) |
missense |
probably benign |
0.00 |
R5707:Cela3b
|
UTSW |
4 |
137,152,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R7952:Cela3b
|
UTSW |
4 |
137,149,219 (GRCm39) |
missense |
probably benign |
0.27 |
R9045:Cela3b
|
UTSW |
4 |
137,152,110 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9339:Cela3b
|
UTSW |
4 |
137,152,355 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Cela3b
|
UTSW |
4 |
137,150,622 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Cela3b
|
UTSW |
4 |
137,150,621 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cela3b
|
UTSW |
4 |
137,155,795 (GRCm39) |
missense |
probably damaging |
0.99 |
|