Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,771,237 (GRCm39) |
L142P |
probably benign |
Het |
Abca13 |
A |
T |
11: 9,241,126 (GRCm39) |
R996S |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,151,017 (GRCm39) |
F558L |
possibly damaging |
Het |
Acp7 |
T |
A |
7: 28,330,307 (GRCm39) |
D2V |
unknown |
Het |
Acvr1c |
T |
C |
2: 58,174,948 (GRCm39) |
D280G |
probably damaging |
Het |
Atp8a1 |
A |
G |
5: 67,781,380 (GRCm39) |
S1124P |
|
Het |
B4galnt1 |
A |
T |
10: 127,003,657 (GRCm39) |
T207S |
probably benign |
Het |
C2cd4d |
C |
A |
3: 94,271,445 (GRCm39) |
T237N |
probably benign |
Het |
C8b |
T |
C |
4: 104,637,824 (GRCm39) |
C99R |
probably damaging |
Het |
Ccnk |
C |
A |
12: 108,159,964 (GRCm39) |
Q149K |
possibly damaging |
Het |
Chfr |
A |
G |
5: 110,288,226 (GRCm39) |
D47G |
probably benign |
Het |
Chid1 |
A |
T |
7: 141,109,401 (GRCm39) |
|
probably null |
Het |
Cibar2 |
T |
A |
8: 120,895,342 (GRCm39) |
T187S |
possibly damaging |
Het |
Cmya5 |
T |
A |
13: 93,232,208 (GRCm39) |
E960V |
probably damaging |
Het |
Col18a1 |
A |
G |
10: 76,932,118 (GRCm39) |
S112P |
unknown |
Het |
Cps1 |
G |
A |
1: 67,210,080 (GRCm39) |
V637I |
probably damaging |
Het |
Crispld1 |
A |
G |
1: 17,823,102 (GRCm39) |
T390A |
probably benign |
Het |
Cyp2c54 |
A |
T |
19: 40,058,697 (GRCm39) |
L245* |
probably null |
Het |
Ddr2 |
G |
T |
1: 169,812,530 (GRCm39) |
T654K |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,868,855 (GRCm39) |
|
probably null |
Het |
Elavl4 |
C |
T |
4: 110,068,622 (GRCm39) |
|
probably null |
Het |
Emilin1 |
T |
C |
5: 31,078,004 (GRCm39) |
V921A |
probably benign |
Het |
Evpl |
T |
A |
11: 116,113,939 (GRCm39) |
E1250D |
probably damaging |
Het |
Fam228a |
C |
T |
12: 4,782,790 (GRCm39) |
G101E |
probably benign |
Het |
Gemin4 |
T |
C |
11: 76,102,932 (GRCm39) |
T610A |
probably damaging |
Het |
Glis1 |
T |
C |
4: 107,292,880 (GRCm39) |
M1T |
probably null |
Het |
Gm14399 |
C |
T |
2: 174,972,252 (GRCm39) |
|
probably benign |
Het |
Gorasp2 |
C |
T |
2: 70,509,849 (GRCm39) |
T170I |
probably damaging |
Het |
Gpr37 |
A |
G |
6: 25,669,341 (GRCm39) |
V501A |
possibly damaging |
Het |
Grik4 |
T |
A |
9: 42,533,356 (GRCm39) |
Q388L |
probably benign |
Het |
Hspg2 |
T |
A |
4: 137,278,436 (GRCm39) |
D3035E |
probably damaging |
Het |
Htr4 |
A |
T |
18: 62,545,247 (GRCm39) |
N11Y |
probably benign |
Het |
Itgb2l |
A |
G |
16: 96,230,243 (GRCm39) |
S356P |
probably damaging |
Het |
Klk1b22 |
A |
G |
7: 43,764,173 (GRCm39) |
N34D |
probably benign |
Het |
Lmcd1 |
A |
G |
6: 112,287,500 (GRCm39) |
D62G |
possibly damaging |
Het |
Lrp2 |
C |
T |
2: 69,316,696 (GRCm39) |
G2095E |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,334,536 (GRCm39) |
E4407V |
possibly damaging |
Het |
Mcm5 |
T |
C |
8: 75,851,487 (GRCm39) |
F631L |
probably benign |
Het |
Mov10l1 |
A |
G |
15: 88,878,071 (GRCm39) |
S170G |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,411,239 (GRCm39) |
D1395V |
unknown |
Het |
Muc6 |
G |
A |
7: 141,226,842 (GRCm39) |
T1395M |
probably benign |
Het |
Myh15 |
A |
G |
16: 48,911,468 (GRCm39) |
D300G |
probably damaging |
Het |
Naa80 |
T |
C |
9: 107,460,498 (GRCm39) |
L131P |
probably damaging |
Het |
Ndst4 |
A |
G |
3: 125,231,952 (GRCm39) |
T174A |
probably benign |
Het |
Nr2c2 |
G |
A |
6: 92,136,359 (GRCm39) |
V400I |
probably damaging |
Het |
Or1l4 |
T |
C |
2: 37,092,092 (GRCm39) |
Y280H |
probably damaging |
Het |
Or1l4b |
G |
T |
2: 37,037,021 (GRCm39) |
V266L |
probably benign |
Het |
Or51aa2 |
A |
T |
7: 103,187,935 (GRCm39) |
Y169N |
probably benign |
Het |
Or52m1 |
T |
C |
7: 102,290,190 (GRCm39) |
S246P |
probably damaging |
Het |
Or6b1 |
G |
A |
6: 42,811,330 (GRCm39) |
|
probably null |
Het |
Or6c5c |
T |
A |
10: 129,298,620 (GRCm39) |
I25N |
probably damaging |
Het |
Parn |
T |
C |
16: 13,443,927 (GRCm39) |
|
probably null |
Het |
Pfkl |
T |
C |
10: 77,827,857 (GRCm39) |
T468A |
probably damaging |
Het |
Pi16 |
C |
A |
17: 29,538,208 (GRCm39) |
P7Q |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,768,340 (GRCm39) |
I2205T |
possibly damaging |
Het |
Prss16 |
A |
T |
13: 22,187,317 (GRCm39) |
N442K |
probably damaging |
Het |
Pus7 |
A |
G |
5: 23,957,342 (GRCm39) |
S370P |
probably damaging |
Het |
Ripk3 |
G |
T |
14: 56,024,741 (GRCm39) |
Y210* |
probably null |
Het |
Rps6ka2 |
C |
A |
17: 7,539,034 (GRCm39) |
F317L |
probably damaging |
Het |
Slc13a3 |
G |
A |
2: 165,287,448 (GRCm39) |
R169W |
possibly damaging |
Het |
Slc6a21 |
T |
A |
7: 44,931,904 (GRCm39) |
I256N |
possibly damaging |
Het |
Slc6a9 |
G |
A |
4: 117,725,303 (GRCm39) |
R589Q |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 15,875,077 (GRCm39) |
S442P |
probably damaging |
Het |
Snupn |
T |
A |
9: 56,890,028 (GRCm39) |
M283K |
probably damaging |
Het |
Steap3 |
A |
T |
1: 120,162,087 (GRCm39) |
M395K |
probably damaging |
Het |
Sv2b |
G |
A |
7: 74,797,402 (GRCm39) |
P331S |
probably damaging |
Het |
Tlr1 |
A |
G |
5: 65,084,115 (GRCm39) |
V154A |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,835,382 (GRCm39) |
S1580P |
probably damaging |
Het |
Tmem51 |
TCCCC |
TCCC |
4: 141,764,996 (GRCm39) |
|
probably null |
Het |
Trav14d-3-dv8 |
G |
A |
14: 53,316,218 (GRCm39) |
R26H |
probably benign |
Het |
Trp53 |
C |
T |
11: 69,482,081 (GRCm39) |
L365F |
probably benign |
Het |
Trp53bp1 |
A |
T |
2: 121,029,516 (GRCm39) |
I1838N |
probably damaging |
Het |
Ugt1a5 |
A |
T |
1: 88,094,608 (GRCm39) |
K279* |
probably null |
Het |
Unc80 |
A |
G |
1: 66,591,368 (GRCm39) |
E1141G |
possibly damaging |
Het |
Vti1b |
T |
C |
12: 79,213,153 (GRCm39) |
D49G |
probably benign |
Het |
Wnt10a |
A |
T |
1: 74,832,641 (GRCm39) |
H78L |
possibly damaging |
Het |
Zfp869 |
G |
A |
8: 70,159,128 (GRCm39) |
H482Y |
probably damaging |
Het |
Zfyve1 |
A |
G |
12: 83,598,314 (GRCm39) |
V638A |
probably damaging |
Het |
|
Other mutations in Nek5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Nek5
|
APN |
8 |
22,601,199 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01418:Nek5
|
APN |
8 |
22,585,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01485:Nek5
|
APN |
8 |
22,573,385 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01640:Nek5
|
APN |
8 |
22,610,856 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01894:Nek5
|
APN |
8 |
22,603,835 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Nek5
|
APN |
8 |
22,586,842 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02332:Nek5
|
APN |
8 |
22,585,277 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02718:Nek5
|
APN |
8 |
22,587,479 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03203:Nek5
|
APN |
8 |
22,608,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03325:Nek5
|
APN |
8 |
22,569,158 (GRCm39) |
missense |
probably benign |
|
R0257:Nek5
|
UTSW |
8 |
22,613,688 (GRCm39) |
intron |
probably benign |
|
R0522:Nek5
|
UTSW |
8 |
22,578,813 (GRCm39) |
splice site |
probably benign |
|
R0525:Nek5
|
UTSW |
8 |
22,569,093 (GRCm39) |
unclassified |
probably benign |
|
R1476:Nek5
|
UTSW |
8 |
22,586,747 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1483:Nek5
|
UTSW |
8 |
22,586,806 (GRCm39) |
missense |
probably benign |
0.30 |
R1764:Nek5
|
UTSW |
8 |
22,599,928 (GRCm39) |
missense |
probably damaging |
0.98 |
R1892:Nek5
|
UTSW |
8 |
22,597,745 (GRCm39) |
missense |
probably benign |
0.11 |
R1989:Nek5
|
UTSW |
8 |
22,601,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Nek5
|
UTSW |
8 |
22,603,648 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4114:Nek5
|
UTSW |
8 |
22,601,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4116:Nek5
|
UTSW |
8 |
22,601,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Nek5
|
UTSW |
8 |
22,573,443 (GRCm39) |
missense |
probably damaging |
0.99 |
R4952:Nek5
|
UTSW |
8 |
22,569,104 (GRCm39) |
missense |
probably benign |
0.00 |
R4952:Nek5
|
UTSW |
8 |
22,586,815 (GRCm39) |
missense |
probably benign |
0.00 |
R5185:Nek5
|
UTSW |
8 |
22,573,397 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5816:Nek5
|
UTSW |
8 |
22,586,752 (GRCm39) |
missense |
probably benign |
0.02 |
R5884:Nek5
|
UTSW |
8 |
22,578,817 (GRCm39) |
critical splice donor site |
probably null |
|
R6009:Nek5
|
UTSW |
8 |
22,610,838 (GRCm39) |
missense |
probably benign |
0.00 |
R6279:Nek5
|
UTSW |
8 |
22,597,737 (GRCm39) |
missense |
probably benign |
|
R6300:Nek5
|
UTSW |
8 |
22,597,737 (GRCm39) |
missense |
probably benign |
|
R6437:Nek5
|
UTSW |
8 |
22,575,476 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7034:Nek5
|
UTSW |
8 |
22,597,739 (GRCm39) |
missense |
probably benign |
0.00 |
R7036:Nek5
|
UTSW |
8 |
22,597,739 (GRCm39) |
missense |
probably benign |
0.00 |
R7436:Nek5
|
UTSW |
8 |
22,598,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Nek5
|
UTSW |
8 |
22,580,533 (GRCm39) |
missense |
probably benign |
0.12 |
R7827:Nek5
|
UTSW |
8 |
22,573,403 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8057:Nek5
|
UTSW |
8 |
22,578,922 (GRCm39) |
missense |
probably benign |
0.21 |
R8350:Nek5
|
UTSW |
8 |
22,603,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R8847:Nek5
|
UTSW |
8 |
22,613,595 (GRCm39) |
missense |
probably benign |
0.01 |
R8888:Nek5
|
UTSW |
8 |
22,580,495 (GRCm39) |
critical splice donor site |
probably null |
|
R8933:Nek5
|
UTSW |
8 |
22,610,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Nek5
|
UTSW |
8 |
22,601,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9353:Nek5
|
UTSW |
8 |
22,563,961 (GRCm39) |
missense |
probably benign |
0.00 |
R9574:Nek5
|
UTSW |
8 |
22,564,040 (GRCm39) |
missense |
probably benign |
0.00 |
R9745:Nek5
|
UTSW |
8 |
22,573,479 (GRCm39) |
missense |
probably benign |
0.04 |
X0012:Nek5
|
UTSW |
8 |
22,585,264 (GRCm39) |
missense |
possibly damaging |
0.92 |
|