Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam34l |
T |
C |
8: 44,078,274 (GRCm39) |
H650R |
probably benign |
Het |
Adgrl2 |
T |
C |
3: 148,522,922 (GRCm39) |
Y1367C |
probably damaging |
Het |
Aqr |
A |
T |
2: 113,947,052 (GRCm39) |
C1043* |
probably null |
Het |
Arhgef17 |
A |
G |
7: 100,530,548 (GRCm39) |
S1413P |
probably damaging |
Het |
AU041133 |
A |
G |
10: 81,987,405 (GRCm39) |
T352A |
probably benign |
Het |
Bcl7a |
A |
G |
5: 123,489,958 (GRCm39) |
T41A |
probably damaging |
Het |
Btbd10 |
A |
T |
7: 112,921,967 (GRCm39) |
F298Y |
probably damaging |
Het |
Ccdc57 |
G |
A |
11: 120,764,528 (GRCm39) |
T749I |
probably benign |
Het |
Clcnkb |
T |
C |
4: 141,132,143 (GRCm39) |
N646S |
probably benign |
Het |
Dcst1 |
T |
C |
3: 89,257,667 (GRCm39) |
D701G |
probably benign |
Het |
Dnah14 |
C |
A |
1: 181,455,997 (GRCm39) |
T1001K |
possibly damaging |
Het |
Dnah8 |
G |
T |
17: 30,965,933 (GRCm39) |
G2422W |
probably damaging |
Het |
Dyrk2 |
A |
T |
10: 118,696,328 (GRCm39) |
I310N |
probably damaging |
Het |
Eif5b |
A |
T |
1: 38,089,320 (GRCm39) |
N1099Y |
probably damaging |
Het |
Elp2 |
T |
A |
18: 24,768,033 (GRCm39) |
N762K |
probably benign |
Het |
Esco2 |
A |
G |
14: 66,068,494 (GRCm39) |
V272A |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,910,564 (GRCm39) |
S1813A |
probably benign |
Het |
Igf2r |
A |
G |
17: 12,916,228 (GRCm39) |
V1710A |
probably damaging |
Het |
Iqgap3 |
GGAGAG |
GGAG |
3: 88,020,078 (GRCm39) |
|
probably null |
Het |
Kcnk5 |
T |
C |
14: 20,194,784 (GRCm39) |
T185A |
possibly damaging |
Het |
Litafd |
G |
A |
16: 8,501,173 (GRCm39) |
V10I |
unknown |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Nol4 |
A |
T |
18: 22,852,186 (GRCm39) |
C460S |
probably benign |
Het |
Ntaq1 |
C |
A |
15: 58,017,074 (GRCm39) |
P163Q |
probably damaging |
Het |
Or10g3b |
T |
A |
14: 52,587,270 (GRCm39) |
I78F |
possibly damaging |
Het |
Or4f14b |
T |
C |
2: 111,775,184 (GRCm39) |
I206V |
probably benign |
Het |
Ovch2 |
G |
A |
7: 107,389,315 (GRCm39) |
A371V |
probably benign |
Het |
Pcdhb4 |
A |
G |
18: 37,442,625 (GRCm39) |
D645G |
probably damaging |
Het |
Pcnt |
A |
C |
10: 76,269,851 (GRCm39) |
S207A |
possibly damaging |
Het |
Pex1 |
A |
T |
5: 3,685,505 (GRCm39) |
Q1211L |
probably benign |
Het |
Pnn |
A |
G |
12: 59,115,553 (GRCm39) |
E99G |
probably damaging |
Het |
Prkrip1 |
A |
T |
5: 136,218,478 (GRCm39) |
|
probably null |
Het |
Rnf133 |
A |
G |
6: 23,649,486 (GRCm39) |
F191L |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,438,848 (GRCm39) |
T1674A |
probably damaging |
Het |
Sdccag8 |
G |
A |
1: 176,839,501 (GRCm39) |
V682M |
probably damaging |
Het |
Spi1 |
T |
C |
2: 90,944,741 (GRCm39) |
L162P |
probably damaging |
Het |
Sptan1 |
C |
G |
2: 29,920,985 (GRCm39) |
N2432K |
probably damaging |
Het |
Stx2 |
A |
G |
5: 129,064,884 (GRCm39) |
V271A |
probably benign |
Het |
Sumf2 |
G |
A |
5: 129,878,867 (GRCm39) |
D68N |
probably damaging |
Het |
Tsc22d4 |
A |
G |
5: 137,760,855 (GRCm39) |
E92G |
possibly damaging |
Het |
Ube3c |
G |
T |
5: 29,792,316 (GRCm39) |
R37L |
probably benign |
Het |
Ubr5 |
A |
G |
15: 38,002,814 (GRCm39) |
S1446P |
probably damaging |
Het |
Veph1 |
T |
C |
3: 66,162,505 (GRCm39) |
N51S |
probably damaging |
Het |
Vmn1r82 |
T |
C |
7: 12,039,290 (GRCm39) |
F70L |
possibly damaging |
Het |
Vmn2r92 |
A |
G |
17: 18,389,084 (GRCm39) |
N466S |
probably damaging |
Het |
Vwf |
T |
A |
6: 125,634,164 (GRCm39) |
V2153D |
possibly damaging |
Het |
Yeats2 |
A |
G |
16: 19,998,344 (GRCm39) |
T300A |
probably benign |
Het |
Zc3h12d |
G |
T |
10: 7,715,735 (GRCm39) |
R46L |
probably damaging |
Het |
Zfp516 |
T |
C |
18: 82,973,916 (GRCm39) |
I38T |
probably damaging |
Het |
Zic5 |
G |
A |
14: 122,697,100 (GRCm39) |
T505I |
unknown |
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 |
R5537:Zpld1
|
UTSW |
16 |
55,054,003 (GRCm39) |
missense |
possibly damaging |
0.84 |
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 |
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 |
|