Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519G04Rik |
T |
C |
5: 115,017,617 (GRCm39) |
S143P |
possibly damaging |
Het |
4933427D14Rik |
T |
C |
11: 72,066,365 (GRCm39) |
K614E |
probably damaging |
Het |
Aatk |
A |
G |
11: 119,906,948 (GRCm39) |
M155T |
possibly damaging |
Het |
Acvr2b |
T |
C |
9: 119,260,328 (GRCm39) |
L333P |
probably damaging |
Het |
Adam22 |
T |
C |
5: 8,128,699 (GRCm39) |
E865G |
probably damaging |
Het |
Add2 |
A |
G |
6: 86,087,870 (GRCm39) |
S358G |
probably damaging |
Het |
Agap2 |
T |
C |
10: 126,926,072 (GRCm39) |
|
probably null |
Het |
Alkbh8 |
G |
A |
9: 3,344,604 (GRCm39) |
W49* |
probably null |
Het |
AU015228 |
A |
T |
2: 129,942,549 (GRCm39) |
|
noncoding transcript |
Het |
Bank1 |
G |
T |
3: 135,953,450 (GRCm39) |
R102S |
probably benign |
Het |
Brap |
T |
A |
5: 121,800,193 (GRCm39) |
D27E |
probably damaging |
Het |
Cyb5r2 |
G |
T |
7: 107,349,484 (GRCm39) |
H276N |
possibly damaging |
Het |
Dhh |
A |
G |
15: 98,792,139 (GRCm39) |
F290L |
possibly damaging |
Het |
Dhrs7 |
T |
A |
12: 72,699,025 (GRCm39) |
N319I |
possibly damaging |
Het |
Ebpl |
A |
G |
14: 61,597,682 (GRCm39) |
V53A |
probably damaging |
Het |
Eif3j2 |
TGCCGCCGCCGCCGCCGCCGCCGCCGCC |
TGCCGCCGCCGCCGCCGCCGCCGCC |
18: 43,610,782 (GRCm39) |
|
probably benign |
Het |
Etnk1 |
A |
C |
6: 143,132,319 (GRCm39) |
N220T |
probably damaging |
Het |
F11r |
T |
A |
1: 171,288,166 (GRCm39) |
V64D |
probably benign |
Het |
Fam171a1 |
T |
C |
2: 3,225,946 (GRCm39) |
S360P |
probably damaging |
Het |
Fignl1 |
A |
G |
11: 11,751,585 (GRCm39) |
M490T |
probably damaging |
Het |
Fpr-rs7 |
A |
T |
17: 20,334,265 (GRCm39) |
M75K |
probably benign |
Het |
Fzd7 |
T |
A |
1: 59,523,595 (GRCm39) |
F493I |
possibly damaging |
Het |
Galnt14 |
G |
T |
17: 73,814,828 (GRCm39) |
P412T |
probably damaging |
Het |
Gcg |
T |
A |
2: 62,308,975 (GRCm39) |
S60C |
probably damaging |
Het |
Ggt1 |
A |
G |
10: 75,421,733 (GRCm39) |
K527E |
probably benign |
Het |
Gm16551 |
T |
A |
9: 74,758,153 (GRCm39) |
|
noncoding transcript |
Het |
Gm9972 |
A |
G |
11: 42,927,517 (GRCm39) |
K55E |
unknown |
Het |
Gpr141 |
T |
A |
13: 19,935,884 (GRCm39) |
D297V |
probably benign |
Het |
Grin2b |
G |
A |
6: 135,755,697 (GRCm39) |
S539L |
probably damaging |
Het |
Hhipl1 |
A |
T |
12: 108,286,238 (GRCm39) |
N515I |
possibly damaging |
Het |
Hmcn1 |
T |
G |
1: 150,453,363 (GRCm39) |
E5317D |
probably damaging |
Het |
Hsf5 |
T |
A |
11: 87,513,617 (GRCm39) |
N227K |
probably benign |
Het |
Igfn1 |
A |
T |
1: 135,910,196 (GRCm39) |
D129E |
probably benign |
Het |
Invs |
T |
C |
4: 48,397,609 (GRCm39) |
F339L |
probably damaging |
Het |
Jak2 |
T |
A |
19: 29,239,656 (GRCm39) |
S17T |
probably benign |
Het |
Mdga2 |
T |
A |
12: 66,844,501 (GRCm39) |
I166F |
probably benign |
Het |
Nck1 |
T |
C |
9: 100,388,797 (GRCm39) |
I6V |
probably benign |
Het |
Neb |
T |
C |
2: 52,040,589 (GRCm39) |
D6624G |
probably benign |
Het |
Nmur2 |
A |
G |
11: 55,931,661 (GRCm39) |
Y17H |
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,964,310 (GRCm39) |
L1298P |
probably damaging |
Het |
Ocel1 |
A |
G |
8: 71,825,397 (GRCm39) |
E161G |
probably damaging |
Het |
Or1j16 |
A |
T |
2: 36,530,991 (GRCm39) |
|
probably null |
Het |
Pabpc2 |
A |
G |
18: 39,907,881 (GRCm39) |
Y382C |
probably benign |
Het |
Panx1 |
A |
G |
9: 14,921,594 (GRCm39) |
|
probably benign |
Het |
Pdhx |
A |
T |
2: 102,872,641 (GRCm39) |
V147D |
probably benign |
Het |
Pigz |
A |
T |
16: 31,764,151 (GRCm39) |
H403L |
probably damaging |
Het |
Pilra |
T |
C |
5: 137,833,769 (GRCm39) |
|
probably null |
Het |
Rbm47 |
T |
C |
5: 66,184,036 (GRCm39) |
D189G |
probably damaging |
Het |
Rhobtb2 |
A |
G |
14: 70,031,451 (GRCm39) |
L558P |
probably damaging |
Het |
Scarf2 |
G |
A |
16: 17,621,380 (GRCm39) |
R322H |
probably damaging |
Het |
Sirt2 |
T |
C |
7: 28,476,438 (GRCm39) |
F26L |
probably damaging |
Het |
Slc1a1 |
A |
T |
19: 28,871,925 (GRCm39) |
T133S |
probably benign |
Het |
Slc1a2 |
A |
G |
2: 102,568,214 (GRCm39) |
I84V |
probably benign |
Het |
Slc28a2b |
A |
T |
2: 122,353,286 (GRCm39) |
K489* |
probably null |
Het |
Slc6a9 |
A |
T |
4: 117,725,092 (GRCm39) |
Q562L |
probably benign |
Het |
Snx29 |
C |
T |
16: 11,167,773 (GRCm39) |
Q25* |
probably null |
Het |
St6galnac6 |
A |
G |
2: 32,508,555 (GRCm39) |
I231V |
probably damaging |
Het |
Stard9 |
A |
G |
2: 120,526,604 (GRCm39) |
T954A |
probably benign |
Het |
Sufu |
A |
G |
19: 46,472,069 (GRCm39) |
M443V |
possibly damaging |
Het |
Sv2b |
T |
C |
7: 74,856,266 (GRCm39) |
D8G |
probably benign |
Het |
Tapbpl |
G |
A |
6: 125,205,248 (GRCm39) |
R233W |
probably damaging |
Het |
Tex10 |
A |
G |
4: 48,469,990 (GRCm39) |
L25S |
probably benign |
Het |
Trp53bp1 |
A |
T |
2: 121,041,794 (GRCm39) |
V1254D |
probably damaging |
Het |
Ugt3a1 |
T |
A |
15: 9,310,639 (GRCm39) |
I307N |
probably benign |
Het |
Unc13c |
T |
C |
9: 73,839,126 (GRCm39) |
D575G |
probably damaging |
Het |
Usf2 |
A |
T |
7: 30,654,197 (GRCm39) |
D166E |
probably damaging |
Het |
Usp25 |
T |
A |
16: 76,911,877 (GRCm39) |
L969M |
probably damaging |
Het |
Usp32 |
G |
A |
11: 84,885,219 (GRCm39) |
P1276L |
probably damaging |
Het |
Vmn2r8 |
T |
A |
5: 108,956,447 (GRCm39) |
E58D |
probably benign |
Het |
Zfp462 |
G |
T |
4: 55,011,598 (GRCm39) |
C40F |
probably damaging |
Het |
|
Other mutations in Septin3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01843:Septin3
|
APN |
15 |
82,163,814 (GRCm39) |
unclassified |
probably benign |
|
IGL01979:Septin3
|
APN |
15 |
82,168,593 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03118:Septin3
|
APN |
15 |
82,168,715 (GRCm39) |
splice site |
probably null |
|
R0478:Septin3
|
UTSW |
15 |
82,175,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R0556:Septin3
|
UTSW |
15 |
82,167,966 (GRCm39) |
unclassified |
probably benign |
|
R3804:Septin3
|
UTSW |
15 |
82,170,630 (GRCm39) |
splice site |
probably benign |
|
R3876:Septin3
|
UTSW |
15 |
82,170,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R4589:Septin3
|
UTSW |
15 |
82,170,092 (GRCm39) |
missense |
probably damaging |
0.99 |
R5954:Septin3
|
UTSW |
15 |
82,174,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Septin3
|
UTSW |
15 |
82,163,804 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7257:Septin3
|
UTSW |
15 |
82,173,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R7475:Septin3
|
UTSW |
15 |
82,170,657 (GRCm39) |
missense |
probably benign |
0.00 |
R7641:Septin3
|
UTSW |
15 |
82,174,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7754:Septin3
|
UTSW |
15 |
82,174,974 (GRCm39) |
missense |
probably benign |
0.03 |
R7895:Septin3
|
UTSW |
15 |
82,170,020 (GRCm39) |
missense |
probably benign |
0.00 |
R7991:Septin3
|
UTSW |
15 |
82,170,654 (GRCm39) |
missense |
probably benign |
0.39 |
R9328:Septin3
|
UTSW |
15 |
82,173,439 (GRCm39) |
missense |
probably damaging |
0.99 |
R9347:Septin3
|
UTSW |
15 |
82,167,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R9368:Septin3
|
UTSW |
15 |
82,163,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R9456:Septin3
|
UTSW |
15 |
82,167,352 (GRCm39) |
missense |
probably benign |
0.19 |
R9646:Septin3
|
UTSW |
15 |
82,170,088 (GRCm39) |
missense |
probably benign |
0.01 |
RF020:Septin3
|
UTSW |
15 |
82,168,662 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Septin3
|
UTSW |
15 |
82,163,705 (GRCm39) |
missense |
probably benign |
0.03 |
|