Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,203,335 (GRCm39) |
E414G |
probably benign |
Het |
Abca12 |
C |
A |
1: 71,302,647 (GRCm39) |
V2191L |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,217,508 (GRCm39) |
T317A |
possibly damaging |
Het |
Acap3 |
T |
G |
4: 155,990,082 (GRCm39) |
L750R |
probably damaging |
Het |
Anapc7 |
T |
A |
5: 122,581,889 (GRCm39) |
S511T |
probably benign |
Het |
Anp32a |
T |
A |
9: 62,279,084 (GRCm39) |
F46Y |
probably benign |
Het |
Anxa2 |
TCCC |
TCC |
9: 69,397,036 (GRCm39) |
|
probably null |
Het |
Arfgef1 |
C |
T |
1: 10,270,103 (GRCm39) |
A349T |
probably benign |
Het |
Arid2 |
T |
C |
15: 96,268,716 (GRCm39) |
I943T |
probably damaging |
Het |
Armh4 |
T |
C |
14: 49,989,028 (GRCm39) |
D647G |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
Btnl6 |
T |
C |
17: 34,733,321 (GRCm39) |
N218S |
possibly damaging |
Het |
Capn11 |
T |
C |
17: 45,944,033 (GRCm39) |
|
probably null |
Het |
Clcnkb |
C |
T |
4: 141,135,328 (GRCm39) |
G470D |
probably damaging |
Het |
Clic6 |
T |
A |
16: 92,296,095 (GRCm39) |
S252T |
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,155,383 (GRCm39) |
K318E |
possibly damaging |
Het |
Col5a3 |
A |
T |
9: 20,682,566 (GRCm39) |
V1626D |
unknown |
Het |
Col6a4 |
C |
A |
9: 105,954,128 (GRCm39) |
A404S |
probably benign |
Het |
Cyp2j5 |
G |
T |
4: 96,529,577 (GRCm39) |
H265N |
possibly damaging |
Het |
Dennd3 |
A |
T |
15: 73,426,909 (GRCm39) |
H762L |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,179,472 (GRCm39) |
|
probably null |
Het |
Emilin2 |
T |
C |
17: 71,580,987 (GRCm39) |
S580G |
probably benign |
Het |
Fbn2 |
C |
A |
18: 58,235,397 (GRCm39) |
|
probably null |
Het |
Gfm1 |
T |
C |
3: 67,381,893 (GRCm39) |
L693P |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,279,716 (GRCm39) |
Y375H |
probably damaging |
Het |
Gpha2 |
A |
G |
19: 6,277,012 (GRCm39) |
T38A |
probably damaging |
Het |
Gtf2h3 |
T |
C |
5: 124,737,848 (GRCm39) |
|
probably benign |
Het |
Hmgxb3 |
T |
C |
18: 61,290,746 (GRCm39) |
T376A |
probably benign |
Het |
Hspa12b |
A |
G |
2: 130,984,977 (GRCm39) |
D416G |
probably damaging |
Het |
Immt |
C |
T |
6: 71,821,659 (GRCm39) |
R28* |
probably null |
Het |
Iqgap1 |
T |
C |
7: 80,412,308 (GRCm39) |
Y180C |
probably damaging |
Het |
Kcnq3 |
T |
A |
15: 65,895,578 (GRCm39) |
D322V |
probably damaging |
Het |
Kifc2 |
C |
A |
15: 76,546,421 (GRCm39) |
L268I |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,080,860 (GRCm39) |
M1296T |
possibly damaging |
Het |
Lipk |
A |
G |
19: 33,999,017 (GRCm39) |
N104S |
possibly damaging |
Het |
Lrrc14b |
T |
A |
13: 74,511,876 (GRCm39) |
N68I |
possibly damaging |
Het |
Lrrc28 |
A |
T |
7: 67,181,430 (GRCm39) |
D268E |
probably damaging |
Het |
Ly6c2 |
T |
C |
15: 74,980,392 (GRCm39) |
*132W |
probably null |
Het |
Msh6 |
A |
G |
17: 88,293,516 (GRCm39) |
E757G |
probably damaging |
Het |
Mtss2 |
T |
C |
8: 111,453,015 (GRCm39) |
V47A |
possibly damaging |
Het |
Muc2 |
CGTG |
CGTGTG |
7: 141,699,185 (GRCm38) |
|
probably null |
Het |
Nalcn |
A |
T |
14: 123,607,429 (GRCm39) |
I680N |
probably benign |
Het |
Nup214 |
C |
T |
2: 31,924,478 (GRCm39) |
S1669F |
probably damaging |
Het |
Odr4 |
A |
T |
1: 150,264,310 (GRCm39) |
N66K |
probably benign |
Het |
Oosp2 |
A |
T |
19: 11,626,978 (GRCm39) |
L17* |
probably null |
Het |
Or10a5 |
A |
T |
7: 106,635,545 (GRCm39) |
Y61F |
possibly damaging |
Het |
Or13a28 |
C |
T |
7: 140,217,965 (GRCm39) |
T117M |
probably damaging |
Het |
Or8b48 |
T |
C |
9: 38,492,804 (GRCm39) |
V77A |
probably benign |
Het |
Or9i2 |
A |
C |
19: 13,815,946 (GRCm39) |
V197G |
probably damaging |
Het |
Pacc1 |
T |
G |
1: 191,077,306 (GRCm39) |
F210V |
probably benign |
Het |
Parvb |
A |
G |
15: 84,116,369 (GRCm39) |
K33E |
possibly damaging |
Het |
Pde4dip |
T |
A |
3: 97,700,152 (GRCm39) |
Q300L |
possibly damaging |
Het |
Phf2 |
T |
C |
13: 48,958,165 (GRCm39) |
K950E |
unknown |
Het |
Pira2 |
G |
A |
7: 3,847,170 (GRCm39) |
P124L |
probably damaging |
Het |
Plpp4 |
C |
T |
7: 128,981,095 (GRCm39) |
T157I |
probably benign |
Het |
Polrmt |
G |
A |
10: 79,576,109 (GRCm39) |
Q545* |
probably null |
Het |
Ptprs |
A |
G |
17: 56,724,706 (GRCm39) |
F1511L |
probably damaging |
Het |
Sbno1 |
T |
C |
5: 124,540,182 (GRCm39) |
|
probably null |
Het |
Setd1a |
T |
A |
7: 127,385,690 (GRCm39) |
V256D |
possibly damaging |
Het |
Slamf1 |
T |
C |
1: 171,594,840 (GRCm39) |
S16P |
probably damaging |
Het |
Slc16a14 |
T |
C |
1: 84,885,120 (GRCm39) |
D473G |
probably damaging |
Het |
Slc8a2 |
A |
T |
7: 15,893,089 (GRCm39) |
H917L |
probably damaging |
Het |
Sorbs2 |
A |
C |
8: 46,248,480 (GRCm39) |
D442A |
probably damaging |
Het |
Srp68 |
G |
T |
11: 116,151,693 (GRCm39) |
T301K |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,700,904 (GRCm39) |
C457* |
probably null |
Het |
Stk31 |
T |
G |
6: 49,416,152 (GRCm39) |
S652R |
possibly damaging |
Het |
Stra6 |
T |
G |
9: 58,059,822 (GRCm39) |
S594R |
probably benign |
Het |
Tbc1d9 |
G |
A |
8: 83,998,078 (GRCm39) |
E1212K |
probably damaging |
Het |
Thada |
C |
T |
17: 84,749,192 (GRCm39) |
R593Q |
probably damaging |
Het |
Tmem131 |
C |
A |
1: 36,851,690 (GRCm39) |
V938L |
probably benign |
Het |
Tmem132c |
T |
A |
5: 127,540,026 (GRCm39) |
W351R |
probably damaging |
Het |
Trim10 |
C |
T |
17: 37,187,906 (GRCm39) |
A374V |
probably benign |
Het |
Try10 |
T |
C |
6: 41,333,495 (GRCm39) |
V80A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,559,707 (GRCm39) |
T29565A |
possibly damaging |
Het |
Uggt2 |
G |
T |
14: 119,312,757 (GRCm39) |
Q351K |
probably benign |
Het |
Vmn1r120 |
A |
T |
7: 20,786,889 (GRCm39) |
V274D |
probably damaging |
Het |
Vmn1r62 |
A |
T |
7: 5,678,358 (GRCm39) |
H13L |
probably benign |
Het |
Vmn2r101 |
C |
T |
17: 19,809,225 (GRCm39) |
T118I |
probably benign |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Vps51 |
A |
G |
19: 6,118,164 (GRCm39) |
V777A |
probably benign |
Het |
Wnt5a |
A |
G |
14: 28,235,274 (GRCm39) |
Y86C |
probably damaging |
Het |
Xpa |
T |
C |
4: 46,183,189 (GRCm39) |
E200G |
probably damaging |
Het |
Zc3h12a |
C |
T |
4: 125,020,435 (GRCm39) |
R136K |
possibly damaging |
Het |
Zc3hav1 |
T |
C |
6: 38,313,472 (GRCm39) |
H191R |
probably damaging |
Het |
Zfp804a |
A |
G |
2: 82,089,008 (GRCm39) |
T946A |
probably benign |
Het |
|