Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 9,005,485 (GRCm39) |
I1123F |
probably damaging |
Het |
Acsl3 |
C |
T |
1: 78,684,073 (GRCm39) |
R702C |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,604,892 (GRCm39) |
E1031G |
probably damaging |
Het |
Ankle2 |
T |
C |
5: 110,397,361 (GRCm39) |
S536P |
probably damaging |
Het |
Arfgef2 |
G |
T |
2: 166,698,513 (GRCm39) |
|
probably null |
Het |
Bahd1 |
G |
T |
2: 118,746,461 (GRCm39) |
D27Y |
probably damaging |
Het |
Brinp2 |
C |
T |
1: 158,082,583 (GRCm39) |
V246I |
probably damaging |
Het |
Ccdc187 |
C |
A |
2: 26,166,237 (GRCm39) |
A731S |
probably benign |
Het |
Cdc37l1 |
T |
A |
19: 28,972,518 (GRCm39) |
N70K |
probably damaging |
Het |
Cdk5r1 |
A |
G |
11: 80,368,825 (GRCm39) |
Y164C |
probably damaging |
Het |
Clrn3 |
A |
T |
7: 135,115,791 (GRCm39) |
H186Q |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,606,872 (GRCm39) |
T517I |
probably damaging |
Het |
Crhr1 |
T |
A |
11: 104,054,682 (GRCm39) |
N98K |
possibly damaging |
Het |
Dst |
C |
T |
1: 34,228,959 (GRCm39) |
S2362L |
probably benign |
Het |
Eapp |
G |
A |
12: 54,738,844 (GRCm39) |
T98I |
probably benign |
Het |
Iqsec3 |
T |
C |
6: 121,389,603 (GRCm39) |
|
probably benign |
Het |
Kctd12 |
A |
G |
14: 103,219,713 (GRCm39) |
V55A |
probably benign |
Het |
Kmt2d |
G |
A |
15: 98,749,990 (GRCm39) |
|
probably benign |
Het |
Lgr5 |
T |
C |
10: 115,292,594 (GRCm39) |
D432G |
probably benign |
Het |
Mrgprx1 |
T |
A |
7: 47,670,898 (GRCm39) |
H283L |
probably benign |
Het |
Nlrp4e |
T |
C |
7: 23,019,914 (GRCm39) |
F134L |
probably benign |
Het |
Or1e34 |
T |
C |
11: 73,778,523 (GRCm39) |
K225R |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,393 (GRCm39) |
M136K |
probably damaging |
Het |
Or5m5 |
T |
A |
2: 85,814,570 (GRCm39) |
Y129N |
possibly damaging |
Het |
Or8b43 |
T |
A |
9: 38,360,538 (GRCm39) |
Y123* |
probably null |
Het |
Pfkp |
C |
A |
13: 6,669,278 (GRCm39) |
W235L |
probably damaging |
Het |
Prom1 |
C |
T |
5: 44,158,118 (GRCm39) |
|
probably null |
Het |
Psma5-ps |
A |
G |
10: 85,149,913 (GRCm39) |
|
noncoding transcript |
Het |
Rab14 |
A |
T |
2: 35,082,649 (GRCm39) |
F12L |
possibly damaging |
Het |
Rnf40 |
T |
A |
7: 127,195,261 (GRCm39) |
I429N |
probably benign |
Het |
S100pbp |
G |
A |
4: 129,075,981 (GRCm39) |
P115S |
probably benign |
Het |
Scarf1 |
G |
A |
11: 75,416,357 (GRCm39) |
A600T |
probably damaging |
Het |
Slc6a5 |
T |
C |
7: 49,609,059 (GRCm39) |
F755L |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,367,023 (GRCm39) |
I510F |
probably benign |
Het |
Spag16 |
T |
C |
1: 69,866,175 (GRCm39) |
S5P |
probably benign |
Het |
Tex15 |
A |
G |
8: 34,061,641 (GRCm39) |
Y631C |
probably damaging |
Het |
Tmem182 |
A |
T |
1: 40,894,069 (GRCm39) |
I195F |
probably benign |
Het |
Tox |
A |
G |
4: 6,697,510 (GRCm39) |
L431P |
probably damaging |
Het |
Tprn |
G |
A |
2: 25,153,369 (GRCm39) |
A224T |
probably benign |
Het |
Tsg101 |
T |
C |
7: 46,540,876 (GRCm39) |
K294E |
probably benign |
Het |
Tubb2a |
C |
A |
13: 34,259,434 (GRCm39) |
V119L |
probably benign |
Het |
Vps37d |
C |
T |
5: 135,103,256 (GRCm39) |
E129K |
possibly damaging |
Het |
Zfp974 |
TAATCTGTCTCCAAATCTG |
TAATCTG |
7: 27,611,671 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zpld1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01360:Zpld1
|
APN |
16 |
55,046,748 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01380:Zpld1
|
APN |
16 |
55,072,133 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02089:Zpld1
|
APN |
16 |
55,071,974 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03350:Zpld1
|
APN |
16 |
55,061,692 (GRCm39) |
splice site |
probably benign |
|
whirl
|
UTSW |
16 |
55,053,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Zpld1
|
UTSW |
16 |
55,071,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Zpld1
|
UTSW |
16 |
55,068,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R1500:Zpld1
|
UTSW |
16 |
55,053,935 (GRCm39) |
missense |
probably damaging |
0.97 |
R3712:Zpld1
|
UTSW |
16 |
55,046,799 (GRCm39) |
nonsense |
probably null |
|
R4096:Zpld1
|
UTSW |
16 |
55,053,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4835:Zpld1
|
UTSW |
16 |
55,068,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R5153:Zpld1
|
UTSW |
16 |
55,067,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5412:Zpld1
|
UTSW |
16 |
55,052,646 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5527:Zpld1
|
UTSW |
16 |
55,046,725 (GRCm39) |
missense |
probably benign |
0.06 |
R6167:Zpld1
|
UTSW |
16 |
55,053,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Zpld1
|
UTSW |
16 |
55,053,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Zpld1
|
UTSW |
16 |
55,052,603 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6877:Zpld1
|
UTSW |
16 |
55,072,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R7165:Zpld1
|
UTSW |
16 |
55,052,594 (GRCm39) |
missense |
probably benign |
0.03 |
R7382:Zpld1
|
UTSW |
16 |
55,067,046 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7423:Zpld1
|
UTSW |
16 |
55,054,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R8217:Zpld1
|
UTSW |
16 |
55,047,295 (GRCm39) |
critical splice donor site |
probably null |
|
R8377:Zpld1
|
UTSW |
16 |
55,067,017 (GRCm39) |
missense |
probably benign |
0.04 |
R9076:Zpld1
|
UTSW |
16 |
55,061,764 (GRCm39) |
missense |
probably benign |
0.32 |
R9564:Zpld1
|
UTSW |
16 |
55,061,701 (GRCm39) |
nonsense |
probably null |
|
Z1176:Zpld1
|
UTSW |
16 |
55,072,128 (GRCm39) |
missense |
probably damaging |
1.00 |
|