Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atxn1l |
T |
C |
8: 110,459,312 (GRCm39) |
R317G |
probably benign |
Het |
B130006D01Rik |
T |
A |
11: 95,616,992 (GRCm39) |
|
probably benign |
Het |
Brinp2 |
T |
C |
1: 158,074,379 (GRCm39) |
T581A |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,548,540 (GRCm39) |
I1179N |
probably damaging |
Het |
Cacnb3 |
A |
G |
15: 98,541,301 (GRCm39) |
D434G |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,847,341 (GRCm39) |
T423A |
possibly damaging |
Het |
Chkb |
C |
T |
15: 89,311,986 (GRCm39) |
|
probably benign |
Het |
Cit |
T |
C |
5: 116,071,913 (GRCm39) |
Y623H |
probably benign |
Het |
Clstn3 |
G |
A |
6: 124,408,559 (GRCm39) |
R918C |
possibly damaging |
Het |
Dnah2 |
T |
A |
11: 69,406,906 (GRCm39) |
M200L |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,838,506 (GRCm39) |
H3097L |
probably benign |
Het |
Dst |
T |
A |
1: 34,314,401 (GRCm39) |
L4217H |
probably damaging |
Het |
Fam107b |
T |
A |
2: 3,779,565 (GRCm39) |
L80Q |
probably damaging |
Het |
Fgfr1 |
T |
A |
8: 26,045,595 (GRCm39) |
C55S |
probably damaging |
Het |
Igkv4-71 |
C |
A |
6: 69,220,264 (GRCm39) |
G78* |
probably null |
Het |
Igsf10 |
A |
G |
3: 59,237,452 (GRCm39) |
S910P |
probably benign |
Het |
Ikzf3 |
T |
C |
11: 98,407,718 (GRCm39) |
D41G |
probably damaging |
Het |
Larp1 |
T |
A |
11: 57,933,648 (GRCm39) |
I358N |
possibly damaging |
Het |
Marchf5 |
C |
T |
19: 37,188,067 (GRCm39) |
|
probably benign |
Het |
Mpdz |
T |
C |
4: 81,287,895 (GRCm39) |
T455A |
probably damaging |
Het |
Myo1b |
A |
G |
1: 51,815,510 (GRCm39) |
V612A |
possibly damaging |
Het |
Nipbl |
T |
C |
15: 8,380,023 (GRCm39) |
D923G |
probably benign |
Het |
Nlrp4b |
T |
C |
7: 10,448,918 (GRCm39) |
F7L |
probably damaging |
Het |
Nynrin |
T |
A |
14: 56,109,502 (GRCm39) |
N1536K |
possibly damaging |
Het |
Or10d5 |
T |
A |
9: 39,861,921 (GRCm39) |
T49S |
probably benign |
Het |
Or13a22 |
A |
G |
7: 140,072,751 (GRCm39) |
N67D |
probably damaging |
Het |
Or4c107 |
T |
C |
2: 88,788,885 (GRCm39) |
V25A |
probably benign |
Het |
Pclo |
T |
C |
5: 14,589,647 (GRCm39) |
V649A |
unknown |
Het |
Pom121 |
A |
G |
5: 135,421,389 (GRCm39) |
|
probably benign |
Het |
Ptcd2 |
A |
T |
13: 99,466,521 (GRCm39) |
I224N |
possibly damaging |
Het |
Rsrp1 |
C |
T |
4: 134,651,290 (GRCm39) |
P18L |
unknown |
Het |
Sash1 |
A |
T |
10: 8,605,422 (GRCm39) |
N989K |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,546,219 (GRCm39) |
H927Q |
probably benign |
Het |
Selenoi |
G |
T |
5: 30,461,222 (GRCm39) |
V128F |
probably damaging |
Het |
Slc25a42 |
T |
C |
8: 70,642,092 (GRCm39) |
I117V |
probably benign |
Het |
Spata1 |
A |
G |
3: 146,195,558 (GRCm39) |
|
probably benign |
Het |
Sptlc3 |
A |
T |
2: 139,431,615 (GRCm39) |
Y379F |
possibly damaging |
Het |
Tent4a |
A |
T |
13: 69,648,678 (GRCm39) |
S693T |
probably benign |
Het |
Tinag |
C |
T |
9: 76,952,885 (GRCm39) |
R33K |
probably benign |
Het |
Trappc8 |
T |
C |
18: 20,968,061 (GRCm39) |
D1092G |
probably benign |
Het |
Xntrpc |
A |
G |
7: 101,722,401 (GRCm39) |
E22G |
probably damaging |
Het |
Zbtb7b |
A |
G |
3: 89,287,278 (GRCm39) |
M397T |
possibly damaging |
Het |
Zgpat |
A |
G |
2: 181,020,682 (GRCm39) |
D285G |
probably benign |
Het |
|
Other mutations in Npas4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01865:Npas4
|
APN |
19 |
5,035,819 (GRCm39) |
nonsense |
probably null |
|
IGL02746:Npas4
|
APN |
19 |
5,036,695 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03061:Npas4
|
APN |
19 |
5,036,365 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03340:Npas4
|
APN |
19 |
5,035,094 (GRCm39) |
utr 3 prime |
probably benign |
|
R0879:Npas4
|
UTSW |
19 |
5,036,944 (GRCm39) |
missense |
probably benign |
|
R0920:Npas4
|
UTSW |
19 |
5,036,344 (GRCm39) |
nonsense |
probably null |
|
R1751:Npas4
|
UTSW |
19 |
5,038,211 (GRCm39) |
missense |
probably benign |
0.05 |
R1767:Npas4
|
UTSW |
19 |
5,038,211 (GRCm39) |
missense |
probably benign |
0.05 |
R2066:Npas4
|
UTSW |
19 |
5,037,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R2201:Npas4
|
UTSW |
19 |
5,037,392 (GRCm39) |
missense |
probably benign |
0.06 |
R3973:Npas4
|
UTSW |
19 |
5,036,579 (GRCm39) |
missense |
probably benign |
|
R4117:Npas4
|
UTSW |
19 |
5,037,391 (GRCm39) |
missense |
probably damaging |
0.99 |
R4846:Npas4
|
UTSW |
19 |
5,036,805 (GRCm39) |
missense |
probably benign |
0.34 |
R5007:Npas4
|
UTSW |
19 |
5,039,684 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6155:Npas4
|
UTSW |
19 |
5,036,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6255:Npas4
|
UTSW |
19 |
5,036,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Npas4
|
UTSW |
19 |
5,036,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Npas4
|
UTSW |
19 |
5,036,108 (GRCm39) |
missense |
probably benign |
|
R8864:Npas4
|
UTSW |
19 |
5,038,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Npas4
|
UTSW |
19 |
5,038,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R9573:Npas4
|
UTSW |
19 |
5,035,837 (GRCm39) |
missense |
probably benign |
0.19 |
Z1177:Npas4
|
UTSW |
19 |
5,036,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|