Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat1 |
T |
C |
8: 112,709,128 (GRCm39) |
K232E |
probably benign |
Het |
Apba1 |
T |
C |
19: 23,871,326 (GRCm39) |
M386T |
probably damaging |
Het |
Appl2 |
G |
T |
10: 83,444,601 (GRCm39) |
F472L |
possibly damaging |
Het |
Atxn2 |
T |
C |
5: 121,941,140 (GRCm39) |
Y56H |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,647,368 (GRCm39) |
Y809C |
probably damaging |
Het |
Canx |
C |
T |
11: 50,201,694 (GRCm39) |
V59I |
probably benign |
Het |
Catsperb |
T |
C |
12: 101,560,478 (GRCm39) |
L823P |
probably damaging |
Het |
Crb3 |
T |
C |
17: 57,372,090 (GRCm39) |
S46P |
probably benign |
Het |
Daam1 |
G |
A |
12: 72,036,601 (GRCm39) |
R1058H |
probably damaging |
Het |
Ehd1 |
T |
A |
19: 6,348,502 (GRCm39) |
D493E |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,768,907 (GRCm39) |
Q746L |
probably damaging |
Het |
Epg5 |
T |
A |
18: 77,992,287 (GRCm39) |
M328K |
probably benign |
Het |
Flt4 |
T |
A |
11: 49,515,555 (GRCm39) |
S48T |
probably benign |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably null |
Het |
Gm7535 |
A |
G |
17: 18,131,936 (GRCm39) |
|
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Hmcn2 |
A |
T |
2: 31,240,586 (GRCm39) |
T494S |
probably benign |
Het |
Hydin |
G |
A |
8: 111,145,138 (GRCm39) |
V830I |
probably benign |
Het |
Map3k6 |
T |
A |
4: 132,973,983 (GRCm39) |
H487Q |
possibly damaging |
Het |
Myh14 |
G |
A |
7: 44,283,800 (GRCm39) |
P735S |
probably damaging |
Het |
Nfkb2 |
T |
C |
19: 46,296,163 (GRCm39) |
|
probably null |
Het |
Nlrp4c |
T |
C |
7: 6,076,113 (GRCm39) |
V671A |
probably benign |
Het |
Nsrp1 |
A |
T |
11: 76,936,587 (GRCm39) |
Y536* |
probably null |
Het |
Or4c112 |
G |
T |
2: 88,853,770 (GRCm39) |
H192Q |
probably benign |
Het |
Pak5 |
A |
G |
2: 135,958,123 (GRCm39) |
S322P |
probably damaging |
Het |
Pank2 |
A |
G |
2: 131,124,601 (GRCm39) |
|
probably null |
Het |
Phf6 |
A |
T |
X: 52,031,525 (GRCm39) |
I272F |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,480,056 (GRCm39) |
L1409P |
probably damaging |
Het |
Polr2a |
A |
G |
11: 69,633,511 (GRCm39) |
|
probably null |
Het |
Pp2d1 |
C |
A |
17: 53,822,482 (GRCm39) |
V195L |
probably benign |
Het |
Psma1 |
C |
T |
7: 113,864,173 (GRCm39) |
E227K |
unknown |
Het |
Ptger1 |
C |
T |
8: 84,395,357 (GRCm39) |
T278I |
probably benign |
Het |
Slc20a2 |
C |
A |
8: 23,050,532 (GRCm39) |
S250R |
probably benign |
Het |
Slc27a2 |
A |
G |
2: 126,409,672 (GRCm39) |
T285A |
probably damaging |
Het |
Slc47a2 |
T |
C |
11: 61,204,497 (GRCm39) |
T285A |
probably benign |
Het |
Slf1 |
T |
A |
13: 77,194,825 (GRCm39) |
|
probably null |
Het |
Tiam2 |
A |
G |
17: 3,465,389 (GRCm39) |
T373A |
probably benign |
Het |
Timd2 |
T |
A |
11: 46,577,844 (GRCm39) |
I96L |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Trpm2 |
T |
A |
10: 77,777,016 (GRCm39) |
D427V |
probably damaging |
Het |
Vax2 |
A |
T |
6: 83,714,871 (GRCm39) |
Y262F |
probably damaging |
Het |
Virma |
T |
C |
4: 11,544,924 (GRCm39) |
S1628P |
probably damaging |
Het |
Zan |
C |
A |
5: 137,408,568 (GRCm39) |
|
probably benign |
Het |
Zbtb22 |
T |
G |
17: 34,136,939 (GRCm39) |
D361E |
probably damaging |
Het |
Zfp27 |
A |
G |
7: 29,595,536 (GRCm39) |
L143P |
possibly damaging |
Het |
|
Other mutations in Tmem64 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00341:Tmem64
|
APN |
4 |
15,266,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02407:Tmem64
|
APN |
4 |
15,266,584 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4151001:Tmem64
|
UTSW |
4 |
15,283,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0257:Tmem64
|
UTSW |
4 |
15,266,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Tmem64
|
UTSW |
4 |
15,266,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R2218:Tmem64
|
UTSW |
4 |
15,266,658 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2571:Tmem64
|
UTSW |
4 |
15,266,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Tmem64
|
UTSW |
4 |
15,281,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5707:Tmem64
|
UTSW |
4 |
15,266,288 (GRCm39) |
missense |
probably damaging |
0.98 |
R7219:Tmem64
|
UTSW |
4 |
15,266,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Tmem64
|
UTSW |
4 |
15,266,176 (GRCm39) |
missense |
probably benign |
0.00 |
R8967:Tmem64
|
UTSW |
4 |
15,266,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R9086:Tmem64
|
UTSW |
4 |
15,266,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R9093:Tmem64
|
UTSW |
4 |
15,266,391 (GRCm39) |
missense |
probably benign |
0.35 |
|