Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810062G17Rik |
T |
C |
3: 36,530,356 (GRCm39) |
S25P |
unknown |
Het |
4921539E11Rik |
A |
G |
4: 103,092,678 (GRCm39) |
I268T |
unknown |
Het |
4930507D05Rik |
T |
A |
10: 62,285,581 (GRCm39) |
C102S |
unknown |
Het |
Abca14 |
T |
A |
7: 119,888,739 (GRCm39) |
Y1228* |
probably null |
Het |
Abca17 |
T |
C |
17: 24,517,934 (GRCm39) |
I792V |
probably benign |
Het |
Abca6 |
C |
A |
11: 110,102,589 (GRCm39) |
L878F |
probably benign |
Het |
Adk |
C |
A |
14: 21,126,386 (GRCm39) |
T4N |
probably benign |
Het |
Ankrd40cl |
G |
A |
11: 94,175,560 (GRCm39) |
S65N |
probably benign |
Het |
Atg2b |
A |
T |
12: 105,611,140 (GRCm39) |
F1264I |
probably damaging |
Het |
Atl3 |
T |
G |
19: 7,507,921 (GRCm39) |
S358A |
probably benign |
Het |
Atp8a2 |
T |
A |
14: 60,271,187 (GRCm39) |
Y248F |
probably damaging |
Het |
Bcas3 |
T |
C |
11: 85,474,749 (GRCm39) |
V785A |
probably damaging |
Het |
Cckar |
C |
T |
5: 53,860,201 (GRCm39) |
|
probably null |
Het |
Cdc42se2 |
A |
G |
11: 54,614,417 (GRCm39) |
F47L |
probably benign |
Het |
Cfap58 |
T |
C |
19: 47,963,992 (GRCm39) |
L540P |
probably damaging |
Het |
Copg1 |
A |
G |
6: 87,868,957 (GRCm39) |
E117G |
probably benign |
Het |
Cstpp1 |
T |
C |
2: 91,112,099 (GRCm39) |
Q250R |
probably benign |
Het |
Cul2 |
C |
T |
18: 3,431,560 (GRCm39) |
T655M |
probably damaging |
Het |
Ddi2 |
T |
C |
4: 141,412,429 (GRCm39) |
Q161R |
probably benign |
Het |
Dffb |
T |
C |
4: 154,059,121 (GRCm39) |
Y52C |
probably damaging |
Het |
Dll1 |
T |
C |
17: 15,591,198 (GRCm39) |
Q249R |
probably benign |
Het |
Dnmt3a |
T |
A |
12: 3,957,701 (GRCm39) |
I894N |
probably damaging |
Het |
Fshr |
G |
A |
17: 89,293,265 (GRCm39) |
T471I |
probably damaging |
Het |
Gabpb1 |
C |
T |
2: 126,500,488 (GRCm39) |
V4I |
probably benign |
Het |
Gbp9 |
T |
C |
5: 105,231,542 (GRCm39) |
Q348R |
probably damaging |
Het |
Gm21149 |
G |
A |
5: 15,677,110 (GRCm39) |
S248F |
unknown |
Het |
Gpr152 |
C |
A |
19: 4,192,640 (GRCm39) |
H60Q |
probably benign |
Het |
Hdac9 |
A |
G |
12: 34,362,602 (GRCm39) |
S612P |
probably benign |
Het |
Hhipl2 |
A |
G |
1: 183,199,747 (GRCm39) |
D102G |
possibly damaging |
Het |
Hspa9 |
A |
G |
18: 35,073,294 (GRCm39) |
V530A |
possibly damaging |
Het |
Igfbp7 |
T |
C |
5: 77,549,384 (GRCm39) |
N173S |
unknown |
Het |
Ighv1-75 |
A |
G |
12: 115,797,791 (GRCm39) |
S44P |
possibly damaging |
Het |
Iqgap3 |
C |
A |
3: 88,016,176 (GRCm39) |
F986L |
probably damaging |
Het |
Itgax |
G |
T |
7: 127,735,500 (GRCm39) |
G523W |
probably damaging |
Het |
Itih3 |
A |
G |
14: 30,637,587 (GRCm39) |
|
probably null |
Het |
Kcnb2 |
T |
C |
1: 15,780,523 (GRCm39) |
I465T |
probably benign |
Het |
Kmt2b |
A |
G |
7: 30,279,228 (GRCm39) |
V1478A |
probably damaging |
Het |
Ky |
A |
T |
9: 102,419,411 (GRCm39) |
I473F |
probably damaging |
Het |
Lbr |
A |
G |
1: 181,666,034 (GRCm39) |
V25A |
probably damaging |
Het |
Ldlr |
A |
G |
9: 21,657,135 (GRCm39) |
T751A |
probably benign |
Het |
Lrrtm4 |
A |
G |
6: 80,786,154 (GRCm39) |
E587G |
probably damaging |
Het |
Lvrn |
A |
C |
18: 47,006,847 (GRCm39) |
|
probably null |
Het |
Mast2 |
A |
T |
4: 116,173,044 (GRCm39) |
C594S |
probably damaging |
Het |
Mast4 |
A |
G |
13: 102,910,711 (GRCm39) |
V644A |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,842,604 (GRCm39) |
Y293H |
probably damaging |
Het |
Mthfd2 |
A |
T |
6: 83,283,665 (GRCm39) |
V339E |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,590,644 (GRCm39) |
I881F |
|
Het |
Myo7a |
A |
G |
7: 97,743,536 (GRCm39) |
S372P |
possibly damaging |
Het |
Nbea |
T |
A |
3: 55,693,879 (GRCm39) |
K2180* |
probably null |
Het |
Neb |
T |
C |
2: 52,101,507 (GRCm39) |
D4621G |
probably damaging |
Het |
Nefh |
C |
T |
11: 4,890,042 (GRCm39) |
S859N |
probably benign |
Het |
Nek2 |
T |
A |
1: 191,563,289 (GRCm39) |
H384Q |
possibly damaging |
Het |
Nfkb2 |
A |
G |
19: 46,298,782 (GRCm39) |
E645G |
probably benign |
Het |
Nin |
G |
T |
12: 70,149,468 (GRCm39) |
P47Q |
|
Het |
Nit1 |
C |
A |
1: 171,171,307 (GRCm39) |
K178N |
probably benign |
Het |
Nrap |
C |
A |
19: 56,317,452 (GRCm39) |
K1433N |
probably damaging |
Het |
Nrap |
T |
C |
19: 56,317,453 (GRCm39) |
K1433R |
probably benign |
Het |
Nup85 |
A |
G |
11: 115,457,463 (GRCm39) |
Y55C |
possibly damaging |
Het |
Or2a14 |
G |
T |
6: 43,130,469 (GRCm39) |
V77F |
possibly damaging |
Het |
Pde1b |
A |
G |
15: 103,411,985 (GRCm39) |
K29E |
probably benign |
Het |
Pheta2 |
G |
T |
15: 82,227,537 (GRCm39) |
D19Y |
probably damaging |
Het |
Pheta2 |
C |
G |
15: 82,227,535 (GRCm39) |
A18G |
probably damaging |
Het |
Pik3cg |
A |
T |
12: 32,226,687 (GRCm39) |
Y1067N |
probably benign |
Het |
Pkd1l1 |
C |
T |
11: 8,799,016 (GRCm39) |
G2249S |
probably damaging |
Het |
Plppr4 |
T |
A |
3: 117,121,976 (GRCm39) |
T201S |
possibly damaging |
Het |
Polr1e |
A |
G |
4: 45,018,678 (GRCm39) |
T3A |
probably benign |
Het |
Polr1has |
A |
T |
17: 37,275,249 (GRCm39) |
R7S |
probably benign |
Het |
Pou6f2 |
G |
T |
13: 18,414,389 (GRCm39) |
Q129K |
unknown |
Het |
Ppil4 |
T |
A |
10: 7,675,341 (GRCm39) |
D163E |
probably benign |
Het |
Pradc1 |
A |
G |
6: 85,424,952 (GRCm39) |
F82L |
probably benign |
Het |
Psd3 |
T |
C |
8: 68,194,414 (GRCm39) |
K784R |
probably null |
Het |
Ptgs1 |
C |
A |
2: 36,141,204 (GRCm39) |
S550R |
probably damaging |
Het |
Pxylp1 |
A |
G |
9: 96,711,030 (GRCm39) |
L153P |
probably damaging |
Het |
Rgs10 |
A |
C |
7: 127,975,729 (GRCm39) |
F146C |
probably damaging |
Het |
Rimbp2 |
G |
A |
5: 128,874,875 (GRCm39) |
P239S |
probably damaging |
Het |
Rp1 |
A |
G |
1: 4,112,255 (GRCm39) |
Y1199H |
unknown |
Het |
Rrp12 |
A |
T |
19: 41,857,231 (GRCm39) |
M1181K |
probably benign |
Het |
Rundc3b |
T |
C |
5: 8,570,982 (GRCm39) |
N279S |
probably benign |
Het |
Sbf2 |
G |
T |
7: 110,027,514 (GRCm39) |
P494Q |
probably damaging |
Het |
Scnn1b |
A |
G |
7: 121,509,693 (GRCm39) |
T281A |
probably benign |
Het |
Scube2 |
A |
T |
7: 109,430,971 (GRCm39) |
N409K |
probably damaging |
Het |
Serpina3m |
A |
C |
12: 104,359,008 (GRCm39) |
D340A |
probably damaging |
Het |
Sez6 |
G |
A |
11: 77,865,121 (GRCm39) |
E623K |
possibly damaging |
Het |
Sgpp2 |
T |
C |
1: 78,367,200 (GRCm39) |
I111T |
probably benign |
Het |
Shprh |
C |
T |
10: 11,038,574 (GRCm39) |
T443I |
possibly damaging |
Het |
Sis |
T |
A |
3: 72,799,074 (GRCm39) |
Y1726F |
possibly damaging |
Het |
Slc17a9 |
T |
C |
2: 180,374,321 (GRCm39) |
L129P |
probably damaging |
Het |
Slc4a4 |
T |
A |
5: 89,188,205 (GRCm39) |
|
probably null |
Het |
Slco3a1 |
T |
C |
7: 73,952,957 (GRCm39) |
E534G |
possibly damaging |
Het |
Smok2b |
A |
T |
17: 13,454,052 (GRCm39) |
I71F |
possibly damaging |
Het |
Tmbim7 |
A |
T |
5: 3,711,809 (GRCm39) |
H18L |
probably damaging |
Het |
Tmem151a |
A |
T |
19: 5,131,876 (GRCm39) |
Y443* |
probably null |
Het |
Tnks1bp1 |
T |
G |
2: 84,902,125 (GRCm39) |
S1674A |
probably benign |
Het |
Trappc11 |
T |
A |
8: 47,946,348 (GRCm39) |
I1095F |
probably damaging |
Het |
Trim11 |
A |
G |
11: 58,872,864 (GRCm39) |
R183G |
possibly damaging |
Het |
Trim29 |
A |
G |
9: 43,231,797 (GRCm39) |
D348G |
probably benign |
Het |
Ttc28 |
A |
T |
5: 111,433,637 (GRCm39) |
S2224C |
probably damaging |
Het |
Vps13d |
C |
T |
4: 144,875,915 (GRCm39) |
V1537M |
|
Het |
Zfp1005 |
T |
A |
2: 150,110,305 (GRCm39) |
C332S |
possibly damaging |
Het |
Zfp184 |
A |
G |
13: 22,143,665 (GRCm39) |
D457G |
possibly damaging |
Het |
|
Other mutations in Slc1a5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Slc1a5
|
APN |
7 |
16,520,804 (GRCm39) |
nonsense |
probably null |
|
IGL01295:Slc1a5
|
APN |
7 |
16,529,787 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02388:Slc1a5
|
APN |
7 |
16,519,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02863:Slc1a5
|
APN |
7 |
16,527,646 (GRCm39) |
missense |
probably benign |
|
IGL03149:Slc1a5
|
APN |
7 |
16,523,745 (GRCm39) |
missense |
probably damaging |
0.96 |
R0001:Slc1a5
|
UTSW |
7 |
16,527,562 (GRCm39) |
splice site |
probably null |
|
R0368:Slc1a5
|
UTSW |
7 |
16,516,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Slc1a5
|
UTSW |
7 |
16,520,829 (GRCm39) |
missense |
probably benign |
|
R1430:Slc1a5
|
UTSW |
7 |
16,516,328 (GRCm39) |
missense |
probably benign |
0.00 |
R1769:Slc1a5
|
UTSW |
7 |
16,531,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4058:Slc1a5
|
UTSW |
7 |
16,529,778 (GRCm39) |
missense |
probably damaging |
0.98 |
R4944:Slc1a5
|
UTSW |
7 |
16,531,668 (GRCm39) |
utr 3 prime |
probably benign |
|
R5220:Slc1a5
|
UTSW |
7 |
16,527,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Slc1a5
|
UTSW |
7 |
16,529,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R5986:Slc1a5
|
UTSW |
7 |
16,516,151 (GRCm39) |
missense |
probably benign |
0.26 |
R7171:Slc1a5
|
UTSW |
7 |
16,531,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R7270:Slc1a5
|
UTSW |
7 |
16,519,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Slc1a5
|
UTSW |
7 |
16,530,085 (GRCm39) |
critical splice donor site |
probably null |
|
R7630:Slc1a5
|
UTSW |
7 |
16,529,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Slc1a5
|
UTSW |
7 |
16,527,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R7944:Slc1a5
|
UTSW |
7 |
16,523,807 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7945:Slc1a5
|
UTSW |
7 |
16,523,807 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8221:Slc1a5
|
UTSW |
7 |
16,515,902 (GRCm39) |
missense |
probably benign |
0.05 |
Z1088:Slc1a5
|
UTSW |
7 |
16,531,594 (GRCm39) |
missense |
probably damaging |
1.00 |
|