Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029J07Rik |
A |
T |
8: 45,970,468 (GRCm38) |
I69N |
probably damaging |
Het |
Aars2 |
T |
A |
17: 45,516,921 (GRCm38) |
D555E |
probably damaging |
Het |
Adgre1 |
C |
A |
17: 57,450,073 (GRCm38) |
Q777K |
possibly damaging |
Het |
Agpat4 |
G |
A |
17: 12,210,377 (GRCm38) |
|
probably null |
Het |
Ak7 |
G |
A |
12: 105,713,575 (GRCm38) |
V123M |
probably benign |
Het |
Ankle1 |
AT |
A |
8: 71,407,207 (GRCm38) |
|
probably benign |
Het |
Ankrd44 |
T |
G |
1: 54,766,748 (GRCm38) |
|
probably benign |
Het |
Aprt |
A |
T |
8: 122,575,415 (GRCm38) |
|
probably null |
Het |
Aptx |
T |
C |
4: 40,702,766 (GRCm38) |
|
probably null |
Het |
Arsi |
G |
A |
18: 60,916,651 (GRCm38) |
G202E |
probably benign |
Het |
AY358078 |
T |
A |
14: 51,826,075 (GRCm38) |
C393S |
possibly damaging |
Het |
Bbip1 |
T |
C |
19: 53,932,175 (GRCm38) |
M1V |
probably null |
Het |
Cacng7 |
T |
A |
7: 3,336,691 (GRCm38) |
M36K |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,084,827 (GRCm38) |
W156R |
probably damaging |
Het |
Casd1 |
G |
A |
6: 4,631,165 (GRCm38) |
|
probably null |
Het |
Casz1 |
T |
A |
4: 148,933,267 (GRCm38) |
Y338N |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,500,420 (GRCm38) |
N122S |
probably damaging |
Het |
Celf2 |
G |
T |
2: 6,586,020 (GRCm38) |
N279K |
possibly damaging |
Het |
Cit |
A |
G |
5: 115,994,087 (GRCm38) |
T1801A |
probably benign |
Het |
Cnot2 |
A |
G |
10: 116,499,418 (GRCm38) |
I275T |
probably damaging |
Het |
Ddx4 |
T |
C |
13: 112,612,060 (GRCm38) |
K435E |
probably damaging |
Het |
Dnajc6 |
T |
C |
4: 101,611,264 (GRCm38) |
F166L |
probably damaging |
Het |
Dst |
T |
C |
1: 34,169,856 (GRCm38) |
L820P |
probably damaging |
Het |
Dusp11 |
T |
A |
6: 85,950,055 (GRCm38) |
N193Y |
probably damaging |
Het |
Epb41l1 |
A |
T |
2: 156,509,261 (GRCm38) |
E418D |
possibly damaging |
Het |
Esyt2 |
T |
G |
12: 116,318,890 (GRCm38) |
N153K |
probably damaging |
Het |
Exoc6b |
T |
G |
6: 85,003,159 (GRCm38) |
|
probably benign |
Het |
Ezr |
C |
T |
17: 6,739,722 (GRCm38) |
E502K |
possibly damaging |
Het |
Fbxw11 |
T |
A |
11: 32,711,859 (GRCm38) |
Y66N |
possibly damaging |
Het |
Frem2 |
A |
G |
3: 53,547,807 (GRCm38) |
L2116S |
possibly damaging |
Het |
Fry |
T |
C |
5: 150,386,104 (GRCm38) |
L671P |
probably damaging |
Het |
Galnt7 |
A |
G |
8: 57,545,769 (GRCm38) |
I262T |
probably damaging |
Het |
Glp1r |
T |
C |
17: 30,931,247 (GRCm38) |
F381S |
probably benign |
Het |
Gm3867 |
T |
C |
9: 36,257,271 (GRCm38) |
|
noncoding transcript |
Het |
Gm5662 |
T |
C |
12: 88,271,774 (GRCm38) |
N72S |
probably benign |
Het |
Gm8741 |
G |
T |
17: 35,336,086 (GRCm38) |
|
noncoding transcript |
Het |
Golgb1 |
A |
G |
16: 36,918,625 (GRCm38) |
D2442G |
probably damaging |
Het |
Gp1bb |
A |
T |
16: 18,621,143 (GRCm38) |
L67Q |
probably damaging |
Het |
Gstm7 |
G |
A |
3: 107,926,919 (GRCm38) |
T206I |
possibly damaging |
Het |
Hist1h2bf |
A |
T |
13: 23,574,057 (GRCm38) |
V45E |
possibly damaging |
Het |
Hs3st5 |
A |
T |
10: 36,828,806 (GRCm38) |
D35V |
probably benign |
Het |
Hspa13 |
T |
C |
16: 75,761,302 (GRCm38) |
H125R |
probably benign |
Het |
Hspa1a |
T |
G |
17: 34,971,180 (GRCm38) |
H249P |
probably damaging |
Het |
Igkv10-95 |
A |
T |
6: 68,680,578 (GRCm38) |
Q6L |
probably damaging |
Het |
Il1rap |
T |
A |
16: 26,714,776 (GRCm38) |
L474H |
probably benign |
Het |
Ipo11 |
T |
A |
13: 106,879,737 (GRCm38) |
Y489F |
probably benign |
Het |
Itga5 |
A |
G |
15: 103,350,832 (GRCm38) |
Y723H |
probably damaging |
Het |
Itih2 |
T |
C |
2: 10,105,160 (GRCm38) |
N594S |
probably damaging |
Het |
Itk |
T |
A |
11: 46,336,515 (GRCm38) |
Q427L |
probably benign |
Het |
Kif26b |
A |
G |
1: 178,679,355 (GRCm38) |
Y332C |
probably damaging |
Het |
Kmt2c |
G |
A |
5: 25,354,384 (GRCm38) |
R1086W |
probably damaging |
Het |
Ktn1 |
T |
A |
14: 47,726,179 (GRCm38) |
|
probably benign |
Het |
Lars2 |
T |
A |
9: 123,418,693 (GRCm38) |
I305N |
probably damaging |
Het |
Lgmn |
G |
T |
12: 102,400,124 (GRCm38) |
|
probably benign |
Het |
Ltbp4 |
C |
T |
7: 27,306,700 (GRCm38) |
E1453K |
probably damaging |
Het |
Lypd8 |
G |
A |
11: 58,386,849 (GRCm38) |
M152I |
probably benign |
Het |
Man2a1 |
T |
A |
17: 64,712,459 (GRCm38) |
S773T |
probably benign |
Het |
Map2k6 |
T |
G |
11: 110,499,474 (GRCm38) |
L278R |
probably damaging |
Het |
Mbtps1 |
A |
T |
8: 119,535,347 (GRCm38) |
D354E |
probably damaging |
Het |
Mcpt9 |
C |
T |
14: 56,028,592 (GRCm38) |
V60M |
probably damaging |
Het |
Mical3 |
C |
A |
6: 120,934,838 (GRCm38) |
E1083* |
probably null |
Het |
Mms19 |
A |
G |
19: 41,945,496 (GRCm38) |
V811A |
possibly damaging |
Het |
Mrc2 |
G |
A |
11: 105,348,431 (GRCm38) |
|
probably null |
Het |
Mslnl |
G |
A |
17: 25,742,934 (GRCm38) |
V128M |
probably damaging |
Het |
Mtcl1 |
T |
A |
17: 66,377,887 (GRCm38) |
H520L |
probably benign |
Het |
Mymk |
A |
T |
2: 27,062,707 (GRCm38) |
F130I |
probably damaging |
Het |
Myo1f |
C |
T |
17: 33,582,332 (GRCm38) |
R333C |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,871,882 (GRCm38) |
H1640Q |
probably benign |
Het |
Nav1 |
A |
G |
1: 135,592,448 (GRCm38) |
|
probably benign |
Het |
Ncbp3 |
G |
T |
11: 73,079,018 (GRCm38) |
G564C |
probably damaging |
Het |
Ncoa4 |
A |
T |
14: 32,176,725 (GRCm38) |
I501L |
probably benign |
Het |
Ngp |
T |
A |
9: 110,420,815 (GRCm38) |
N60K |
possibly damaging |
Het |
Npc1l1 |
G |
T |
11: 6,228,215 (GRCm38) |
D398E |
probably damaging |
Het |
Nphs2 |
T |
A |
1: 156,326,131 (GRCm38) |
M264K |
probably damaging |
Het |
Olfr1193 |
G |
A |
2: 88,677,896 (GRCm38) |
V14I |
probably benign |
Het |
Olfr1193 |
T |
G |
2: 88,678,179 (GRCm38) |
V101G |
probably benign |
Het |
Olfr145 |
T |
A |
9: 37,898,326 (GRCm38) |
S307R |
probably benign |
Het |
Olfr58 |
T |
A |
9: 19,783,146 (GRCm38) |
Y4* |
probably null |
Het |
Patz1 |
A |
G |
11: 3,306,241 (GRCm38) |
Y509C |
probably damaging |
Het |
Pax8 |
G |
A |
2: 24,421,583 (GRCm38) |
P447S |
probably damaging |
Het |
Pde11a |
A |
G |
2: 76,158,333 (GRCm38) |
V488A |
probably benign |
Het |
Pex11g |
C |
T |
8: 3,465,899 (GRCm38) |
V45M |
probably benign |
Het |
Pik3ip1 |
T |
A |
11: 3,333,327 (GRCm38) |
S142R |
probably damaging |
Het |
Pitpnm2 |
C |
G |
5: 124,125,371 (GRCm38) |
A819P |
probably damaging |
Het |
Pla2g4e |
T |
G |
2: 120,186,382 (GRCm38) |
H226P |
possibly damaging |
Het |
Plin4 |
T |
A |
17: 56,105,418 (GRCm38) |
M538L |
probably benign |
Het |
Ppp3cb |
T |
C |
14: 20,520,646 (GRCm38) |
N339S |
possibly damaging |
Het |
Rev1 |
T |
C |
1: 38,053,649 (GRCm38) |
E1202G |
probably damaging |
Het |
Rngtt |
T |
A |
4: 33,339,133 (GRCm38) |
|
probably benign |
Het |
Serpinb12 |
T |
A |
1: 106,949,153 (GRCm38) |
D66E |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,255,307 (GRCm38) |
F958Y |
probably damaging |
Het |
Slc35e2 |
T |
C |
4: 155,617,649 (GRCm38) |
F290S |
probably benign |
Het |
Sorl1 |
C |
T |
9: 42,031,914 (GRCm38) |
V889M |
possibly damaging |
Het |
Sptlc3 |
G |
A |
2: 139,636,680 (GRCm38) |
V520I |
probably benign |
Het |
Stam |
A |
T |
2: 14,115,858 (GRCm38) |
H53L |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,192,935 (GRCm38) |
S497P |
probably damaging |
Het |
Tarbp1 |
A |
G |
8: 126,474,330 (GRCm38) |
Y246H |
probably damaging |
Het |
Tbx15 |
A |
G |
3: 99,352,367 (GRCm38) |
Y518C |
probably damaging |
Het |
Tdrd5 |
T |
A |
1: 156,284,374 (GRCm38) |
T479S |
probably benign |
Het |
Tescl |
T |
C |
7: 24,333,258 (GRCm38) |
E214G |
probably damaging |
Het |
Tex10 |
T |
C |
4: 48,452,946 (GRCm38) |
D671G |
probably benign |
Het |
Tmem132d |
A |
G |
5: 127,984,296 (GRCm38) |
V414A |
probably benign |
Het |
Tmem41b |
T |
A |
7: 109,974,734 (GRCm38) |
|
probably benign |
Het |
Tnfrsf18 |
A |
G |
4: 156,021,880 (GRCm38) |
|
probably benign |
Het |
Tulp4 |
T |
A |
17: 6,198,833 (GRCm38) |
D42E |
probably damaging |
Het |
Ubtd1 |
A |
G |
19: 42,033,664 (GRCm38) |
N125S |
probably damaging |
Het |
Ubxn4 |
T |
A |
1: 128,255,449 (GRCm38) |
F68I |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,776,271 (GRCm38) |
S958P |
probably benign |
Het |
Vash2 |
T |
C |
1: 190,960,301 (GRCm38) |
S226G |
probably benign |
Het |
Vmn2r120 |
C |
T |
17: 57,509,120 (GRCm38) |
G745E |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,837,693 (GRCm38) |
I593F |
probably benign |
Het |
Zfp398 |
T |
C |
6: 47,840,427 (GRCm38) |
L67P |
probably damaging |
Het |
Zfp607b |
T |
A |
7: 27,703,695 (GRCm38) |
H525Q |
probably damaging |
Het |
Zfp629 |
T |
C |
7: 127,612,320 (GRCm38) |
T106A |
probably benign |
Het |
Zfp980 |
G |
A |
4: 145,702,083 (GRCm38) |
G461S |
probably benign |
Het |
Zic5 |
T |
A |
14: 122,464,800 (GRCm38) |
D173V |
probably damaging |
Het |
Zranb2 |
G |
A |
3: 157,541,884 (GRCm38) |
|
probably benign |
Het |
|