Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa1b |
A |
G |
9: 118,985,728 (GRCm39) |
S66P |
possibly damaging |
Het |
Adh7 |
A |
T |
3: 137,929,825 (GRCm39) |
E167V |
probably damaging |
Het |
Ano6 |
T |
C |
15: 95,859,992 (GRCm39) |
S705P |
probably damaging |
Het |
Arpc1b |
T |
C |
5: 145,063,739 (GRCm39) |
V329A |
probably benign |
Het |
Btla |
C |
T |
16: 45,063,092 (GRCm39) |
H152Y |
probably benign |
Het |
Cadps |
T |
C |
14: 12,465,883 (GRCm38) |
E1009G |
probably damaging |
Het |
Cyp4a12a |
G |
T |
4: 115,159,221 (GRCm39) |
V164F |
probably damaging |
Het |
Duox1 |
G |
T |
2: 122,155,065 (GRCm39) |
|
probably null |
Het |
Fcgbpl1 |
A |
T |
7: 27,852,260 (GRCm39) |
H1261L |
possibly damaging |
Het |
Fmo6 |
A |
G |
1: 162,757,461 (GRCm39) |
I104T |
probably damaging |
Het |
Fnbp4 |
T |
C |
2: 90,576,172 (GRCm39) |
|
probably null |
Het |
Garem1 |
T |
C |
18: 21,262,769 (GRCm39) |
T682A |
probably benign |
Het |
Gm49358 |
A |
G |
10: 86,651,762 (GRCm39) |
E188G |
probably benign |
Het |
Gm5773 |
T |
C |
3: 93,681,162 (GRCm39) |
I278T |
probably benign |
Het |
Ifi27l2a |
A |
G |
12: 103,409,756 (GRCm39) |
|
probably benign |
Het |
Inpp5d |
A |
C |
1: 87,627,412 (GRCm39) |
K308T |
probably damaging |
Het |
Irf6 |
A |
T |
1: 192,849,774 (GRCm39) |
Y232F |
probably damaging |
Het |
Kcnmb4 |
T |
C |
10: 116,309,248 (GRCm39) |
Q60R |
probably benign |
Het |
Klri2 |
T |
C |
6: 129,709,985 (GRCm39) |
D205G |
probably benign |
Het |
Mcm9 |
A |
T |
10: 53,492,110 (GRCm39) |
W352R |
probably damaging |
Het |
Nat8 |
A |
G |
6: 85,807,650 (GRCm39) |
V161A |
possibly damaging |
Het |
Nlrp9c |
A |
T |
7: 26,077,556 (GRCm39) |
M742K |
probably benign |
Het |
Or10ag58 |
C |
A |
2: 87,265,623 (GRCm39) |
T264K |
probably damaging |
Het |
Or13j1 |
T |
C |
4: 43,705,723 (GRCm39) |
T282A |
possibly damaging |
Het |
Or5an10 |
C |
A |
19: 12,275,934 (GRCm39) |
Q187H |
probably damaging |
Het |
Pcdha11 |
A |
T |
18: 37,144,242 (GRCm39) |
D111V |
probably damaging |
Het |
Pcdhb6 |
A |
T |
18: 37,468,198 (GRCm39) |
D373V |
probably damaging |
Het |
Pcolce2 |
A |
T |
9: 95,560,396 (GRCm39) |
|
probably null |
Het |
Pik3cb |
T |
C |
9: 98,983,453 (GRCm39) |
M52V |
probably benign |
Het |
Pipox |
T |
C |
11: 77,774,729 (GRCm39) |
E118G |
probably benign |
Het |
Pou4f2 |
T |
C |
8: 79,162,307 (GRCm39) |
S99G |
probably benign |
Het |
Ptpn12 |
T |
A |
5: 21,260,711 (GRCm39) |
Q12L |
probably benign |
Het |
Sim2 |
G |
T |
16: 93,926,395 (GRCm39) |
A540S |
probably benign |
Het |
Smg1 |
A |
T |
7: 117,767,403 (GRCm39) |
|
probably benign |
Het |
Sntb1 |
A |
G |
15: 55,769,719 (GRCm39) |
V90A |
probably benign |
Het |
Spns2 |
T |
C |
11: 72,347,196 (GRCm39) |
|
probably null |
Het |
Syne1 |
G |
T |
10: 5,181,704 (GRCm39) |
C4210* |
probably null |
Het |
Tek |
T |
C |
4: 94,725,426 (GRCm39) |
I564T |
possibly damaging |
Het |
Tmem94 |
T |
G |
11: 115,687,287 (GRCm39) |
C1135W |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,937,493 (GRCm39) |
D3827E |
probably damaging |
Het |
Ttl |
A |
G |
2: 128,923,992 (GRCm39) |
D235G |
possibly damaging |
Het |
Tuba4a |
A |
G |
1: 75,194,066 (GRCm39) |
S5P |
probably damaging |
Het |
Uaca |
T |
A |
9: 60,777,173 (GRCm39) |
V518D |
probably damaging |
Het |
Unc80 |
A |
T |
1: 66,685,563 (GRCm39) |
Q2229L |
probably benign |
Het |
Unkl |
C |
T |
17: 25,449,307 (GRCm39) |
A78V |
probably damaging |
Het |
Uroc1 |
C |
T |
6: 90,315,574 (GRCm39) |
Q152* |
probably null |
Het |
Vmn2r51 |
G |
T |
7: 9,834,025 (GRCm39) |
Q338K |
possibly damaging |
Het |
Vps50 |
C |
T |
6: 3,498,513 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cttnbp2nl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01365:Cttnbp2nl
|
APN |
3 |
104,912,346 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01832:Cttnbp2nl
|
APN |
3 |
104,918,544 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02070:Cttnbp2nl
|
APN |
3 |
104,918,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Cttnbp2nl
|
UTSW |
3 |
104,913,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Cttnbp2nl
|
UTSW |
3 |
104,913,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R0132:Cttnbp2nl
|
UTSW |
3 |
104,913,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Cttnbp2nl
|
UTSW |
3 |
104,918,594 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3766:Cttnbp2nl
|
UTSW |
3 |
104,912,117 (GRCm39) |
missense |
probably benign |
0.27 |
R3964:Cttnbp2nl
|
UTSW |
3 |
104,913,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R4509:Cttnbp2nl
|
UTSW |
3 |
104,940,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Cttnbp2nl
|
UTSW |
3 |
104,913,191 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4820:Cttnbp2nl
|
UTSW |
3 |
104,918,640 (GRCm39) |
missense |
probably benign |
0.00 |
R5233:Cttnbp2nl
|
UTSW |
3 |
104,912,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R6230:Cttnbp2nl
|
UTSW |
3 |
104,918,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R6385:Cttnbp2nl
|
UTSW |
3 |
104,912,952 (GRCm39) |
missense |
probably benign |
0.41 |
R6551:Cttnbp2nl
|
UTSW |
3 |
104,912,433 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6685:Cttnbp2nl
|
UTSW |
3 |
104,912,814 (GRCm39) |
missense |
probably benign |
0.06 |
R7262:Cttnbp2nl
|
UTSW |
3 |
104,940,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R7509:Cttnbp2nl
|
UTSW |
3 |
104,940,046 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7619:Cttnbp2nl
|
UTSW |
3 |
104,912,076 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7978:Cttnbp2nl
|
UTSW |
3 |
104,915,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R8115:Cttnbp2nl
|
UTSW |
3 |
104,913,402 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Cttnbp2nl
|
UTSW |
3 |
104,912,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|