Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110032F04Rik |
T |
A |
3: 68,777,345 (GRCm39) |
I102N |
probably damaging |
Het |
2610008E11Rik |
A |
T |
10: 78,903,406 (GRCm39) |
C303* |
probably null |
Het |
A430033K04Rik |
T |
A |
5: 138,644,547 (GRCm39) |
V144D |
possibly damaging |
Het |
Adamts13 |
T |
A |
2: 26,883,024 (GRCm39) |
M858K |
probably benign |
Het |
Ankrd29 |
T |
C |
18: 12,408,760 (GRCm39) |
|
probably benign |
Het |
Apc |
T |
A |
18: 34,450,710 (GRCm39) |
S2535R |
probably damaging |
Het |
C1s1 |
T |
C |
6: 124,517,758 (GRCm39) |
D74G |
probably damaging |
Het |
Cacnb2 |
G |
A |
2: 14,972,773 (GRCm39) |
G227S |
possibly damaging |
Het |
Cbs |
T |
C |
17: 31,844,889 (GRCm39) |
D137G |
probably damaging |
Het |
Ccdc136 |
A |
G |
6: 29,418,070 (GRCm39) |
E846G |
probably damaging |
Het |
Cd6 |
A |
T |
19: 10,776,855 (GRCm39) |
S57T |
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,273,119 (GRCm39) |
|
probably benign |
Het |
Ctsj |
T |
C |
13: 61,149,249 (GRCm39) |
Y264C |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,429,463 (GRCm39) |
N915K |
probably damaging |
Het |
Dst |
T |
C |
1: 34,228,149 (GRCm39) |
L1914P |
probably damaging |
Het |
E2f2 |
A |
T |
4: 135,908,595 (GRCm39) |
|
probably null |
Het |
Edc4 |
T |
C |
8: 106,612,478 (GRCm39) |
L172P |
probably damaging |
Het |
Epb41l5 |
A |
T |
1: 119,570,319 (GRCm39) |
L23H |
probably damaging |
Het |
Fbxo2 |
A |
G |
4: 148,250,166 (GRCm39) |
E232G |
probably damaging |
Het |
Fmn1 |
A |
C |
2: 113,271,973 (GRCm39) |
N114H |
unknown |
Het |
Foxj1 |
T |
G |
11: 116,225,236 (GRCm39) |
I44L |
probably damaging |
Het |
Foxp1 |
TTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGTTGCTGCTGCTGTTGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGTTGCTGCTGCTGTTGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGTTGCTGCTGCTG |
6: 99,052,866 (GRCm39) |
|
probably benign |
Het |
Foxp2 |
A |
T |
6: 15,286,711 (GRCm39) |
Q67L |
possibly damaging |
Het |
Fuz |
C |
T |
7: 44,549,710 (GRCm39) |
P396L |
probably damaging |
Het |
Galntl5 |
A |
T |
5: 25,415,353 (GRCm39) |
I295L |
possibly damaging |
Het |
Gjd4 |
T |
A |
18: 9,280,095 (GRCm39) |
T328S |
probably benign |
Het |
Gramd1a |
A |
T |
7: 30,837,606 (GRCm39) |
|
probably benign |
Het |
Gzmb |
T |
C |
14: 56,496,964 (GRCm39) |
Y219C |
possibly damaging |
Het |
Hs3st5 |
A |
T |
10: 36,708,917 (GRCm39) |
I151F |
probably damaging |
Het |
Ighv4-1 |
A |
T |
12: 113,912,000 (GRCm39) |
D84E |
possibly damaging |
Het |
Il31ra |
C |
T |
13: 112,670,276 (GRCm39) |
E371K |
probably benign |
Het |
Imp4 |
G |
T |
1: 34,482,473 (GRCm39) |
V71L |
probably benign |
Het |
Itgax |
A |
G |
7: 127,747,913 (GRCm39) |
T1068A |
possibly damaging |
Het |
Klhl24 |
C |
T |
16: 19,936,690 (GRCm39) |
R433C |
probably damaging |
Het |
Larp4b |
C |
A |
13: 9,186,819 (GRCm39) |
P49Q |
possibly damaging |
Het |
Macc1 |
T |
C |
12: 119,414,091 (GRCm39) |
S756P |
possibly damaging |
Het |
Mael |
A |
G |
1: 166,029,259 (GRCm39) |
V388A |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,339,130 (GRCm39) |
T556A |
probably benign |
Het |
Mettl6 |
T |
C |
14: 31,204,855 (GRCm39) |
D189G |
probably damaging |
Het |
Moxd2 |
C |
A |
6: 40,860,978 (GRCm39) |
C271F |
probably damaging |
Het |
Ncor1 |
A |
T |
11: 62,224,672 (GRCm39) |
Y863N |
probably damaging |
Het |
Ndst4 |
C |
T |
3: 125,231,722 (GRCm39) |
A97V |
probably damaging |
Het |
Nherf4 |
A |
G |
9: 44,160,676 (GRCm39) |
C240R |
probably damaging |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nup160 |
A |
G |
2: 90,533,489 (GRCm39) |
D646G |
probably damaging |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Or1j19 |
A |
G |
2: 36,676,938 (GRCm39) |
T134A |
probably benign |
Het |
Or1p1 |
A |
C |
11: 74,180,169 (GRCm39) |
Q232H |
probably damaging |
Het |
Or5c1 |
T |
C |
2: 37,222,017 (GRCm39) |
L86P |
possibly damaging |
Het |
Or7h8 |
T |
A |
9: 20,124,358 (GRCm39) |
F238I |
probably damaging |
Het |
Or8k24 |
A |
G |
2: 86,216,324 (GRCm39) |
V146A |
probably benign |
Het |
Pabpc6 |
C |
T |
17: 9,886,937 (GRCm39) |
S538N |
probably benign |
Het |
Pcdhga1 |
C |
A |
18: 37,796,433 (GRCm39) |
A479D |
possibly damaging |
Het |
Pdgfd |
A |
T |
9: 6,333,328 (GRCm39) |
D172V |
probably benign |
Het |
Pfpl |
A |
T |
19: 12,405,804 (GRCm39) |
E18D |
possibly damaging |
Het |
Pih1d2 |
T |
A |
9: 50,532,321 (GRCm39) |
D126E |
possibly damaging |
Het |
Ppp1r13b |
T |
C |
12: 111,800,268 (GRCm39) |
H626R |
probably benign |
Het |
Ppp6r3 |
A |
T |
19: 3,543,974 (GRCm39) |
V347D |
probably damaging |
Het |
Ptpra |
T |
A |
2: 30,328,255 (GRCm39) |
M192K |
probably damaging |
Het |
Ptpra |
G |
T |
2: 30,328,256 (GRCm39) |
M192I |
probably benign |
Het |
Ptprj |
G |
A |
2: 90,288,562 (GRCm39) |
S801L |
probably benign |
Het |
Rasd2 |
C |
T |
8: 75,948,847 (GRCm39) |
R258* |
probably null |
Het |
Rfx3 |
A |
T |
19: 27,878,207 (GRCm39) |
V30E |
possibly damaging |
Het |
Rgs2 |
A |
G |
1: 143,877,925 (GRCm39) |
S124P |
probably damaging |
Het |
Ros1 |
A |
G |
10: 51,927,039 (GRCm39) |
F2215L |
probably benign |
Het |
Rph3a |
T |
C |
5: 121,086,880 (GRCm39) |
N440S |
possibly damaging |
Het |
Sacs |
T |
C |
14: 61,450,137 (GRCm39) |
V4061A |
possibly damaging |
Het |
Scgb1b3 |
G |
A |
7: 31,075,051 (GRCm39) |
V7M |
unknown |
Het |
Scn7a |
T |
C |
2: 66,514,507 (GRCm39) |
D1089G |
possibly damaging |
Het |
Sdk2 |
C |
T |
11: 113,714,226 (GRCm39) |
R1582Q |
probably benign |
Het |
Sdr16c5 |
T |
C |
4: 3,996,200 (GRCm39) |
M298V |
probably benign |
Het |
Sebox |
A |
G |
11: 78,395,222 (GRCm39) |
D188G |
possibly damaging |
Het |
Serpinf2 |
A |
T |
11: 75,323,418 (GRCm39) |
F429L |
probably damaging |
Het |
Six4 |
A |
C |
12: 73,155,681 (GRCm39) |
S429A |
probably benign |
Het |
Slc2a10 |
A |
T |
2: 165,357,543 (GRCm39) |
H401L |
possibly damaging |
Het |
Ssbp2 |
T |
C |
13: 91,842,141 (GRCm39) |
S321P |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,937,158 (GRCm39) |
E252G |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,084,172 (GRCm39) |
I1178T |
probably damaging |
Het |
Tafa5 |
T |
C |
15: 87,428,775 (GRCm39) |
I28T |
probably benign |
Het |
Tbc1d10a |
G |
T |
11: 4,136,835 (GRCm39) |
R16L |
unknown |
Het |
Tmem132b |
C |
A |
5: 125,864,167 (GRCm39) |
Q758K |
probably damaging |
Het |
Tnrc6a |
T |
G |
7: 122,785,667 (GRCm39) |
|
probably benign |
Het |
Tril |
A |
G |
6: 53,795,137 (GRCm39) |
L695P |
probably damaging |
Het |
Tspan3 |
A |
T |
9: 56,043,960 (GRCm39) |
Y243* |
probably null |
Het |
Ufl1 |
A |
T |
4: 25,278,712 (GRCm39) |
|
probably benign |
Het |
Utp4 |
A |
T |
8: 107,621,310 (GRCm39) |
N29I |
possibly damaging |
Het |
Vmn1r176 |
C |
T |
7: 23,534,785 (GRCm39) |
G123S |
probably benign |
Het |
Vmn1r225 |
T |
A |
17: 20,722,577 (GRCm39) |
M6K |
possibly damaging |
Het |
Vmn1r229 |
T |
C |
17: 21,034,758 (GRCm39) |
M1T |
probably null |
Het |
Vmn2r80 |
A |
T |
10: 79,030,687 (GRCm39) |
I838F |
probably damaging |
Het |
Vmn2r98 |
T |
A |
17: 19,286,383 (GRCm39) |
W294R |
probably benign |
Het |
Wnk1 |
A |
G |
6: 119,925,631 (GRCm39) |
S1527P |
unknown |
Het |
Zdhhc17 |
A |
T |
10: 110,785,503 (GRCm39) |
S436R |
possibly damaging |
Het |
Zfp12 |
T |
C |
5: 143,230,389 (GRCm39) |
S271P |
probably damaging |
Het |
Zfp330 |
T |
C |
8: 83,491,063 (GRCm39) |
Y249C |
|
Het |
Zfp444 |
A |
G |
7: 6,192,678 (GRCm39) |
H232R |
probably damaging |
Het |
|
Other mutations in Hspa12a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01419:Hspa12a
|
APN |
19 |
58,816,681 (GRCm39) |
splice site |
probably null |
|
IGL01516:Hspa12a
|
APN |
19 |
58,816,108 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01766:Hspa12a
|
APN |
19 |
58,787,899 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01986:Hspa12a
|
APN |
19 |
58,787,834 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02138:Hspa12a
|
APN |
19 |
58,816,730 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02170:Hspa12a
|
APN |
19 |
58,793,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02576:Hspa12a
|
APN |
19 |
58,787,842 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02623:Hspa12a
|
APN |
19 |
58,797,983 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02890:Hspa12a
|
APN |
19 |
58,809,431 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03209:Hspa12a
|
APN |
19 |
58,810,493 (GRCm39) |
splice site |
probably null |
|
IGL03343:Hspa12a
|
APN |
19 |
58,787,828 (GRCm39) |
missense |
probably benign |
0.00 |
R0040:Hspa12a
|
UTSW |
19 |
58,788,056 (GRCm39) |
missense |
probably benign |
0.10 |
R0090:Hspa12a
|
UTSW |
19 |
58,787,941 (GRCm39) |
missense |
probably benign |
0.00 |
R2139:Hspa12a
|
UTSW |
19 |
58,787,914 (GRCm39) |
missense |
probably benign |
|
R4031:Hspa12a
|
UTSW |
19 |
58,789,289 (GRCm39) |
missense |
probably benign |
0.17 |
R4686:Hspa12a
|
UTSW |
19 |
58,788,181 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4914:Hspa12a
|
UTSW |
19 |
58,787,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R5046:Hspa12a
|
UTSW |
19 |
58,787,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Hspa12a
|
UTSW |
19 |
58,788,092 (GRCm39) |
missense |
probably benign |
0.11 |
R5615:Hspa12a
|
UTSW |
19 |
58,793,082 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5781:Hspa12a
|
UTSW |
19 |
58,810,518 (GRCm39) |
missense |
probably damaging |
0.99 |
R6777:Hspa12a
|
UTSW |
19 |
58,810,519 (GRCm39) |
missense |
probably benign |
0.03 |
R6954:Hspa12a
|
UTSW |
19 |
58,788,124 (GRCm39) |
missense |
probably benign |
0.05 |
R7038:Hspa12a
|
UTSW |
19 |
58,793,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:Hspa12a
|
UTSW |
19 |
58,810,594 (GRCm39) |
missense |
probably benign |
0.07 |
R7249:Hspa12a
|
UTSW |
19 |
58,793,865 (GRCm39) |
missense |
probably benign |
0.27 |
R7677:Hspa12a
|
UTSW |
19 |
58,849,317 (GRCm39) |
missense |
probably benign |
0.01 |
R8110:Hspa12a
|
UTSW |
19 |
58,809,445 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8830:Hspa12a
|
UTSW |
19 |
58,793,895 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8955:Hspa12a
|
UTSW |
19 |
58,788,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Hspa12a
|
UTSW |
19 |
58,787,903 (GRCm39) |
nonsense |
probably null |
|
R9056:Hspa12a
|
UTSW |
19 |
58,813,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Hspa12a
|
UTSW |
19 |
58,793,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9157:Hspa12a
|
UTSW |
19 |
58,789,292 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9316:Hspa12a
|
UTSW |
19 |
58,793,079 (GRCm39) |
missense |
probably benign |
0.22 |
R9329:Hspa12a
|
UTSW |
19 |
58,789,298 (GRCm39) |
missense |
probably benign |
0.01 |
R9370:Hspa12a
|
UTSW |
19 |
58,813,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Hspa12a
|
UTSW |
19 |
58,797,891 (GRCm39) |
missense |
probably benign |
0.03 |
|