Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
G |
T |
16: 20,152,338 (GRCm39) |
Q1403K |
probably benign |
Het |
Adamts12 |
G |
A |
15: 11,241,548 (GRCm39) |
M373I |
probably damaging |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
Aire |
T |
C |
10: 77,879,314 (GRCm39) |
H15R |
probably damaging |
Het |
Aldh3b2 |
T |
C |
19: 4,027,572 (GRCm39) |
F38L |
probably damaging |
Het |
Alk |
A |
C |
17: 72,910,416 (GRCm39) |
C97G |
probably benign |
Het |
Ano8 |
T |
C |
8: 71,931,602 (GRCm39) |
|
probably benign |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Asgr2 |
G |
T |
11: 69,987,658 (GRCm39) |
R52L |
probably damaging |
Het |
Atp2a1 |
A |
G |
7: 126,058,780 (GRCm39) |
I145T |
possibly damaging |
Het |
Atrnl1 |
A |
G |
19: 57,703,134 (GRCm39) |
T1051A |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,362,315 (GRCm39) |
V424D |
possibly damaging |
Het |
Capn3 |
T |
C |
2: 120,327,494 (GRCm39) |
V574A |
probably benign |
Het |
Capzb |
C |
A |
4: 138,984,679 (GRCm39) |
D67E |
probably damaging |
Het |
Ccdc68 |
A |
T |
18: 70,089,062 (GRCm39) |
T202S |
probably benign |
Het |
Ccser2 |
T |
C |
14: 36,618,270 (GRCm39) |
K123R |
probably damaging |
Het |
Ccser2 |
T |
A |
14: 36,618,271 (GRCm39) |
K123* |
probably null |
Het |
Ces2h |
T |
C |
8: 105,744,473 (GRCm39) |
I316T |
probably benign |
Het |
Chd3 |
T |
G |
11: 69,255,523 (GRCm39) |
K122Q |
possibly damaging |
Het |
Col12a1 |
T |
C |
9: 79,580,279 (GRCm39) |
T1533A |
probably benign |
Het |
Cr2 |
T |
A |
1: 194,838,213 (GRCm39) |
K1084* |
probably null |
Het |
Ddx28 |
A |
G |
8: 106,737,314 (GRCm39) |
L248P |
probably benign |
Het |
Depdc5 |
A |
G |
5: 33,075,286 (GRCm39) |
E488G |
probably benign |
Het |
Dld |
T |
C |
12: 31,384,745 (GRCm39) |
T305A |
probably benign |
Het |
Dok5 |
T |
A |
2: 170,683,373 (GRCm39) |
F211L |
probably damaging |
Het |
Duox2 |
T |
C |
2: 122,117,532 (GRCm39) |
D934G |
probably benign |
Het |
Eif3a |
G |
A |
19: 60,755,236 (GRCm39) |
T982I |
unknown |
Het |
Erbb2 |
G |
T |
11: 98,326,161 (GRCm39) |
R979L |
probably benign |
Het |
Espl1 |
G |
T |
15: 102,206,964 (GRCm39) |
V143L |
possibly damaging |
Het |
Fanci |
T |
C |
7: 79,080,236 (GRCm39) |
L598P |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,147,473 (GRCm39) |
E3923V |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 24,903,550 (GRCm39) |
K95* |
probably null |
Het |
Gpr108 |
G |
T |
17: 57,543,217 (GRCm39) |
T484K |
probably damaging |
Het |
Hao1 |
T |
A |
2: 134,340,238 (GRCm39) |
N351I |
possibly damaging |
Het |
Hepacam |
A |
T |
9: 37,295,189 (GRCm39) |
N308I |
possibly damaging |
Het |
Herc2 |
T |
C |
7: 55,798,571 (GRCm39) |
|
probably null |
Het |
Hltf |
T |
C |
3: 20,130,685 (GRCm39) |
I301T |
probably benign |
Het |
Igsf10 |
A |
T |
3: 59,226,514 (GRCm39) |
N2386K |
probably damaging |
Het |
Ikbke |
G |
T |
1: 131,186,937 (GRCm39) |
T585K |
probably benign |
Het |
Iqgap3 |
A |
G |
3: 88,021,287 (GRCm39) |
T448A |
possibly damaging |
Het |
Kl |
T |
C |
5: 150,904,450 (GRCm39) |
S401P |
possibly damaging |
Het |
Lama4 |
T |
C |
10: 38,941,615 (GRCm39) |
V684A |
probably benign |
Het |
Lgals8 |
A |
T |
13: 12,469,824 (GRCm39) |
F45Y |
probably damaging |
Het |
Lgalsl |
G |
A |
11: 20,776,491 (GRCm39) |
R134C |
probably benign |
Het |
Lmcd1 |
T |
C |
6: 112,306,875 (GRCm39) |
V349A |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,618,718 (GRCm39) |
N119Y |
possibly damaging |
Het |
Lrrc73 |
T |
A |
17: 46,566,621 (GRCm39) |
I157N |
probably damaging |
Het |
Map3k8 |
A |
G |
18: 4,334,766 (GRCm39) |
Y293H |
probably damaging |
Het |
Mybphl |
A |
T |
3: 108,282,400 (GRCm39) |
|
probably null |
Het |
Naa12 |
T |
C |
18: 80,255,161 (GRCm39) |
S152P |
probably benign |
Het |
Ndrg1 |
A |
G |
15: 66,802,930 (GRCm39) |
M140T |
possibly damaging |
Het |
Or2n1e |
T |
A |
17: 38,585,997 (GRCm39) |
C112S |
possibly damaging |
Het |
Or8b38 |
A |
G |
9: 37,972,796 (GRCm39) |
Y60C |
probably damaging |
Het |
Pbx2 |
T |
C |
17: 34,812,951 (GRCm39) |
S76P |
possibly damaging |
Het |
Plcl2 |
T |
A |
17: 50,913,826 (GRCm39) |
S278R |
probably benign |
Het |
Polr3d |
A |
T |
14: 70,676,915 (GRCm39) |
L393* |
probably null |
Het |
Prmt6 |
T |
C |
3: 110,157,683 (GRCm39) |
Q202R |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Sag |
T |
A |
1: 87,759,662 (GRCm39) |
I300N |
probably damaging |
Het |
Sap25 |
T |
A |
5: 137,640,180 (GRCm39) |
|
probably null |
Het |
Scarb2 |
A |
G |
5: 92,608,695 (GRCm39) |
L177P |
probably damaging |
Het |
Sh3pxd2b |
A |
T |
11: 32,372,203 (GRCm39) |
N457Y |
possibly damaging |
Het |
Siae |
T |
A |
9: 37,542,902 (GRCm39) |
|
probably null |
Het |
Slc36a1 |
T |
C |
11: 55,119,150 (GRCm39) |
L375P |
probably damaging |
Het |
Smg8 |
A |
G |
11: 86,976,594 (GRCm39) |
V329A |
probably damaging |
Het |
Tas2r113 |
A |
T |
6: 132,870,695 (GRCm39) |
Y241F |
probably damaging |
Het |
Tm9sf3 |
T |
G |
19: 41,244,668 (GRCm39) |
S70R |
probably benign |
Het |
Tmem144 |
C |
T |
3: 79,732,594 (GRCm39) |
S228N |
probably damaging |
Het |
Tmem45a |
C |
A |
16: 56,642,701 (GRCm39) |
V157F |
possibly damaging |
Het |
Tpbg |
G |
T |
9: 85,726,429 (GRCm39) |
V133L |
probably damaging |
Het |
Trpv3 |
G |
A |
11: 73,186,209 (GRCm39) |
V667I |
possibly damaging |
Het |
Ube2c |
T |
C |
2: 164,613,241 (GRCm39) |
F53S |
probably damaging |
Het |
Vmn1r78 |
T |
A |
7: 11,887,250 (GRCm39) |
V287D |
probably damaging |
Het |
Vmn2r114 |
T |
A |
17: 23,527,035 (GRCm39) |
D499V |
probably benign |
Het |
Zpld2 |
C |
G |
4: 133,927,610 (GRCm39) |
C381S |
probably damaging |
Het |
Zpld2 |
T |
A |
4: 133,929,430 (GRCm39) |
T292S |
possibly damaging |
Het |
|
Other mutations in Arsk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00903:Arsk
|
APN |
13 |
76,246,487 (GRCm39) |
splice site |
probably null |
|
IGL02537:Arsk
|
APN |
13 |
76,223,025 (GRCm39) |
nonsense |
probably null |
|
IGL02691:Arsk
|
APN |
13 |
76,223,069 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03038:Arsk
|
APN |
13 |
76,213,632 (GRCm39) |
splice site |
probably benign |
|
PIT4480001:Arsk
|
UTSW |
13 |
76,210,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R0277:Arsk
|
UTSW |
13 |
76,223,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0900:Arsk
|
UTSW |
13 |
76,246,576 (GRCm39) |
unclassified |
probably benign |
|
R1441:Arsk
|
UTSW |
13 |
76,223,083 (GRCm39) |
missense |
probably benign |
0.01 |
R1923:Arsk
|
UTSW |
13 |
76,214,985 (GRCm39) |
splice site |
probably benign |
|
R2131:Arsk
|
UTSW |
13 |
76,239,931 (GRCm39) |
nonsense |
probably null |
|
R3723:Arsk
|
UTSW |
13 |
76,214,772 (GRCm39) |
missense |
probably damaging |
0.98 |
R4088:Arsk
|
UTSW |
13 |
76,246,533 (GRCm39) |
missense |
probably benign |
|
R4851:Arsk
|
UTSW |
13 |
76,213,398 (GRCm39) |
critical splice donor site |
probably null |
|
R5406:Arsk
|
UTSW |
13 |
76,242,066 (GRCm39) |
missense |
probably benign |
|
R5629:Arsk
|
UTSW |
13 |
76,242,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R5869:Arsk
|
UTSW |
13 |
76,239,903 (GRCm39) |
missense |
probably benign |
0.29 |
R6217:Arsk
|
UTSW |
13 |
76,239,935 (GRCm39) |
missense |
unknown |
|
R6552:Arsk
|
UTSW |
13 |
76,220,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R6560:Arsk
|
UTSW |
13 |
76,223,105 (GRCm39) |
missense |
probably benign |
0.33 |
R6726:Arsk
|
UTSW |
13 |
76,222,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R7421:Arsk
|
UTSW |
13 |
76,210,634 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8178:Arsk
|
UTSW |
13 |
76,239,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Arsk
|
UTSW |
13 |
76,220,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R8503:Arsk
|
UTSW |
13 |
76,239,830 (GRCm39) |
nonsense |
probably null |
|
R8743:Arsk
|
UTSW |
13 |
76,214,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R9517:Arsk
|
UTSW |
13 |
76,210,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Arsk
|
UTSW |
13 |
76,223,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Arsk
|
UTSW |
13 |
76,220,227 (GRCm39) |
missense |
probably damaging |
0.97 |
X0050:Arsk
|
UTSW |
13 |
76,213,399 (GRCm39) |
missense |
probably null |
0.78 |
X0066:Arsk
|
UTSW |
13 |
76,210,575 (GRCm39) |
missense |
probably benign |
0.02 |
Z1192:Arsk
|
UTSW |
13 |
76,246,637 (GRCm39) |
unclassified |
probably benign |
|
|