Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abce1 |
G |
A |
8: 80,425,982 (GRCm39) |
P265L |
probably benign |
Het |
Adam20 |
A |
G |
8: 41,249,101 (GRCm39) |
T404A |
probably benign |
Het |
Ascc3 |
A |
G |
10: 50,643,554 (GRCm39) |
D1835G |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,590,220 (GRCm39) |
|
probably null |
Het |
Bard1 |
A |
T |
1: 71,106,297 (GRCm39) |
N443K |
probably damaging |
Het |
Btnl1 |
A |
G |
17: 34,604,647 (GRCm39) |
D476G |
possibly damaging |
Het |
C2cd3 |
A |
T |
7: 100,067,711 (GRCm39) |
I487F |
|
Het |
Cadm4 |
A |
G |
7: 24,203,030 (GRCm39) |
E384G |
possibly damaging |
Het |
Camsap3 |
A |
G |
8: 3,648,075 (GRCm39) |
K128E |
probably benign |
Het |
Casz1 |
C |
T |
4: 149,027,492 (GRCm39) |
P1005S |
probably damaging |
Het |
Cd38 |
C |
A |
5: 44,058,790 (GRCm39) |
L135M |
probably damaging |
Het |
Cdk20 |
A |
G |
13: 64,585,734 (GRCm39) |
E244G |
probably benign |
Het |
Cfap54 |
A |
T |
10: 92,714,378 (GRCm39) |
V2667D |
unknown |
Het |
Col11a1 |
A |
G |
3: 114,012,435 (GRCm39) |
K1792E |
unknown |
Het |
Cpne9 |
A |
T |
6: 113,272,003 (GRCm39) |
D377V |
probably benign |
Het |
Csmd1 |
A |
T |
8: 15,982,550 (GRCm39) |
C2706S |
probably damaging |
Het |
Ctnnbl1 |
T |
C |
2: 157,651,391 (GRCm39) |
V222A |
probably benign |
Het |
Frmpd2 |
T |
C |
14: 33,227,452 (GRCm39) |
S277P |
probably benign |
Het |
Herc2 |
C |
T |
7: 55,734,884 (GRCm39) |
T158I |
probably benign |
Het |
Hoxa4 |
G |
T |
6: 52,167,537 (GRCm39) |
H215N |
possibly damaging |
Het |
Hpd |
G |
T |
5: 123,312,443 (GRCm39) |
Q309K |
probably benign |
Het |
Il20ra |
A |
G |
10: 19,626,452 (GRCm39) |
T159A |
probably damaging |
Het |
Ints10 |
T |
A |
8: 69,255,638 (GRCm39) |
Y209* |
probably null |
Het |
Ints2 |
A |
G |
11: 86,103,486 (GRCm39) |
I1190T |
probably damaging |
Het |
Jhy |
A |
G |
9: 40,872,188 (GRCm39) |
V107A |
probably null |
Het |
Kdm4d |
C |
T |
9: 14,374,532 (GRCm39) |
R442H |
probably damaging |
Het |
Kifbp |
T |
C |
10: 62,413,756 (GRCm39) |
Y134C |
probably benign |
Het |
Klb |
A |
T |
5: 65,540,958 (GRCm39) |
H1017L |
probably benign |
Het |
Kndc1 |
T |
A |
7: 139,481,285 (GRCm39) |
|
probably null |
Het |
Krtap4-1 |
GGCAGCAGGGGCTGCAGCAAGGGCTGCAGCAGGGGC |
GGCAGCAGGGGCTGCAGCAAGGGCTGCAGCAGGGGCTGCAGCAAGGGCTGCAGCAGGGGC |
11: 99,518,660 (GRCm39) |
|
probably benign |
Het |
Lrrn3 |
T |
C |
12: 41,503,047 (GRCm39) |
I423M |
probably damaging |
Het |
Magi2 |
T |
G |
5: 20,596,365 (GRCm39) |
F274L |
probably damaging |
Het |
Magi2 |
T |
A |
5: 20,596,392 (GRCm39) |
D283E |
probably benign |
Het |
Map3k19 |
A |
C |
1: 127,751,492 (GRCm39) |
S620A |
probably damaging |
Het |
Meis2 |
C |
T |
2: 115,697,369 (GRCm39) |
M388I |
probably benign |
Het |
Ms4a3 |
G |
C |
19: 11,615,613 (GRCm39) |
H54Q |
probably benign |
Het |
Nfe2l1 |
A |
T |
11: 96,710,585 (GRCm39) |
M548K |
possibly damaging |
Het |
Ninl |
C |
T |
2: 150,792,234 (GRCm39) |
C763Y |
probably benign |
Het |
Numa1 |
T |
C |
7: 101,650,834 (GRCm39) |
F1522L |
probably benign |
Het |
Or13a25 |
T |
A |
7: 140,247,680 (GRCm39) |
I153N |
possibly damaging |
Het |
Or2bd2 |
T |
C |
7: 6,441,922 (GRCm39) |
|
probably benign |
Het |
Pcdhgc3 |
G |
A |
18: 37,939,916 (GRCm39) |
V106I |
probably benign |
Het |
Phf3 |
A |
G |
1: 30,863,552 (GRCm39) |
V152A |
unknown |
Het |
Pira1 |
A |
G |
7: 3,738,838 (GRCm39) |
S590P |
probably damaging |
Het |
Plcg2 |
A |
T |
8: 118,284,057 (GRCm39) |
D118V |
probably damaging |
Het |
Pnpla1 |
A |
G |
17: 29,097,443 (GRCm39) |
D203G |
probably damaging |
Het |
Ppip5k2 |
A |
T |
1: 97,672,888 (GRCm39) |
M474K |
probably benign |
Het |
Ppp1r12b |
T |
C |
1: 134,814,280 (GRCm39) |
E341G |
possibly damaging |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rrs1 |
C |
T |
1: 9,615,645 (GRCm39) |
|
probably benign |
Het |
Scaf11 |
T |
C |
15: 96,318,592 (GRCm39) |
N324S |
probably damaging |
Het |
Spaca1 |
T |
A |
4: 34,042,157 (GRCm39) |
|
probably null |
Het |
Sun3 |
G |
T |
11: 8,979,346 (GRCm39) |
D118E |
probably benign |
Het |
Svop |
C |
T |
5: 114,180,992 (GRCm39) |
V215I |
probably benign |
Het |
Tbc1d15 |
A |
T |
10: 115,045,474 (GRCm39) |
C497S |
probably damaging |
Het |
Tdrd6 |
A |
T |
17: 43,937,064 (GRCm39) |
I1328N |
probably damaging |
Het |
Tuba8 |
T |
A |
6: 121,198,381 (GRCm39) |
D116E |
probably benign |
Het |
Ube2z |
A |
G |
11: 95,949,200 (GRCm39) |
I213T |
possibly damaging |
Het |
Ubqln4 |
G |
A |
3: 88,462,797 (GRCm39) |
|
probably null |
Het |
Vps13a |
A |
G |
19: 16,631,718 (GRCm39) |
I2639T |
possibly damaging |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp94 |
A |
T |
7: 24,003,166 (GRCm39) |
V92E |
probably benign |
Het |
|
Other mutations in Anp32a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00655:Anp32a
|
APN |
9 |
62,278,994 (GRCm39) |
splice site |
probably benign |
|
IGL01799:Anp32a
|
APN |
9 |
62,279,092 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02066:Anp32a
|
APN |
9 |
62,284,615 (GRCm39) |
unclassified |
probably benign |
|
IGL02536:Anp32a
|
APN |
9 |
62,279,110 (GRCm39) |
missense |
probably damaging |
0.98 |
R1608:Anp32a
|
UTSW |
9 |
62,279,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R2149:Anp32a
|
UTSW |
9 |
62,279,084 (GRCm39) |
missense |
probably benign |
0.19 |
R5287:Anp32a
|
UTSW |
9 |
62,249,275 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5381:Anp32a
|
UTSW |
9 |
62,279,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R5403:Anp32a
|
UTSW |
9 |
62,249,275 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5427:Anp32a
|
UTSW |
9 |
62,284,598 (GRCm39) |
unclassified |
probably benign |
|
R6856:Anp32a
|
UTSW |
9 |
62,279,397 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6906:Anp32a
|
UTSW |
9 |
62,284,851 (GRCm39) |
unclassified |
probably benign |
|
R7949:Anp32a
|
UTSW |
9 |
62,280,948 (GRCm39) |
missense |
unknown |
|
R9501:Anp32a
|
UTSW |
9 |
62,282,019 (GRCm39) |
missense |
unknown |
|
|