Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
T |
C |
10: 87,000,931 (GRCm39) |
L41P |
probably damaging |
Het |
3110082I17Rik |
A |
G |
5: 139,349,875 (GRCm39) |
V58A |
possibly damaging |
Het |
4932415M13Rik |
A |
T |
17: 54,031,374 (GRCm39) |
|
noncoding transcript |
Het |
Aldh1a7 |
C |
T |
19: 20,679,607 (GRCm39) |
V390M |
probably damaging |
Het |
Alg14 |
A |
G |
3: 121,092,259 (GRCm39) |
H34R |
probably damaging |
Het |
Ankrd27 |
A |
G |
7: 35,307,772 (GRCm39) |
N337S |
probably damaging |
Het |
Apoa2 |
T |
A |
1: 171,052,948 (GRCm39) |
|
probably benign |
Het |
Arl2 |
T |
G |
19: 6,186,052 (GRCm39) |
K126T |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,721,762 (GRCm39) |
W2072R |
probably benign |
Het |
Astl |
T |
C |
2: 127,184,339 (GRCm39) |
F21L |
probably benign |
Het |
Asxl3 |
A |
G |
18: 22,649,097 (GRCm39) |
D362G |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,172,333 (GRCm39) |
H2094Q |
probably benign |
Het |
Cacna2d4 |
C |
T |
6: 119,284,247 (GRCm39) |
R745W |
probably damaging |
Het |
Ccdc85a |
T |
A |
11: 28,533,296 (GRCm39) |
I83F |
probably damaging |
Het |
Ccnt2 |
T |
A |
1: 127,730,131 (GRCm39) |
M336K |
probably benign |
Het |
Cd226 |
A |
C |
18: 89,225,144 (GRCm39) |
|
probably benign |
Het |
Ceacam23 |
C |
A |
7: 17,638,906 (GRCm39) |
A301E |
possibly damaging |
Het |
Ces1f |
A |
T |
8: 93,996,652 (GRCm39) |
S214T |
probably damaging |
Het |
Clip1 |
T |
C |
5: 123,768,784 (GRCm39) |
D605G |
probably benign |
Het |
Col26a1 |
A |
G |
5: 136,794,154 (GRCm39) |
|
probably null |
Het |
Crtc1 |
A |
G |
8: 70,845,663 (GRCm39) |
V306A |
probably benign |
Het |
D130043K22Rik |
G |
A |
13: 25,047,563 (GRCm39) |
|
probably benign |
Het |
D17H6S53E |
A |
T |
17: 35,346,385 (GRCm39) |
|
probably null |
Het |
Dnah11 |
G |
A |
12: 118,160,397 (GRCm39) |
A111V |
probably benign |
Het |
Dyrk2 |
T |
C |
10: 118,697,027 (GRCm39) |
H77R |
probably benign |
Het |
Epha3 |
A |
G |
16: 63,423,882 (GRCm39) |
|
probably benign |
Het |
Epn2 |
T |
C |
11: 61,410,317 (GRCm39) |
N611S |
probably benign |
Het |
Erich6 |
A |
C |
3: 58,526,365 (GRCm39) |
|
probably benign |
Het |
Fam217b |
T |
C |
2: 178,062,782 (GRCm39) |
S249P |
probably benign |
Het |
Fam219b |
A |
G |
9: 57,445,299 (GRCm39) |
|
probably benign |
Het |
Fryl |
A |
T |
5: 73,246,424 (GRCm39) |
|
probably benign |
Het |
Ftdc2 |
G |
A |
16: 58,455,886 (GRCm39) |
S129L |
probably damaging |
Het |
Gm14496 |
T |
C |
2: 181,638,059 (GRCm39) |
W378R |
probably damaging |
Het |
Gm57858 |
A |
G |
3: 36,074,362 (GRCm39) |
|
probably benign |
Het |
Gm8674 |
A |
T |
13: 50,058,611 (GRCm39) |
|
noncoding transcript |
Het |
Grap |
T |
A |
11: 61,551,065 (GRCm39) |
D32E |
possibly damaging |
Het |
Grk2 |
C |
A |
19: 4,339,385 (GRCm39) |
L428F |
probably damaging |
Het |
Grm8 |
T |
A |
6: 27,363,178 (GRCm39) |
E779V |
probably damaging |
Het |
Hipk1 |
A |
G |
3: 103,661,612 (GRCm39) |
S670P |
probably damaging |
Het |
Ilrun |
A |
T |
17: 28,005,112 (GRCm39) |
S148R |
probably damaging |
Het |
Itgae |
A |
T |
11: 73,020,032 (GRCm39) |
M845L |
probably benign |
Het |
Itih1 |
A |
T |
14: 30,663,512 (GRCm39) |
V164E |
probably damaging |
Het |
Itpka |
T |
A |
2: 119,581,312 (GRCm39) |
N448K |
probably damaging |
Het |
Jak3 |
A |
C |
8: 72,136,622 (GRCm39) |
N643T |
probably damaging |
Het |
Lrfn5 |
A |
C |
12: 61,886,454 (GRCm39) |
T81P |
probably damaging |
Het |
Lrrc45 |
T |
A |
11: 120,609,019 (GRCm39) |
|
probably null |
Het |
Marchf6 |
T |
C |
15: 31,480,437 (GRCm39) |
Y562C |
probably benign |
Het |
Mcrs1 |
T |
C |
15: 99,141,330 (GRCm39) |
|
probably benign |
Het |
Meis1 |
G |
A |
11: 18,831,767 (GRCm39) |
H424Y |
possibly damaging |
Het |
Mst1r |
A |
G |
9: 107,791,975 (GRCm39) |
N837S |
probably benign |
Het |
Mst1r |
G |
A |
9: 107,790,366 (GRCm39) |
V660I |
probably benign |
Het |
Mthfd2l |
T |
C |
5: 91,094,801 (GRCm39) |
V90A |
probably damaging |
Het |
Mtnr1a |
A |
T |
8: 45,540,974 (GRCm39) |
I312F |
probably benign |
Het |
Or10g3b |
T |
C |
14: 52,586,835 (GRCm39) |
I223V |
probably benign |
Het |
Or51g1 |
C |
A |
7: 102,634,043 (GRCm39) |
L109F |
possibly damaging |
Het |
Or8b12b |
T |
C |
9: 37,684,372 (GRCm39) |
V139A |
probably benign |
Het |
Otog |
C |
T |
7: 45,918,786 (GRCm39) |
T954I |
possibly damaging |
Het |
Pdcd6 |
A |
G |
13: 74,464,443 (GRCm39) |
|
probably benign |
Het |
Phlpp2 |
A |
G |
8: 110,663,738 (GRCm39) |
T926A |
probably damaging |
Het |
Plec |
GGCAGCAG |
GGCAGCAGCAG |
15: 76,066,107 (GRCm39) |
|
probably benign |
Het |
Plekha5 |
T |
A |
6: 140,535,360 (GRCm39) |
|
probably benign |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Pramel23 |
A |
T |
4: 143,425,056 (GRCm39) |
M129K |
probably benign |
Het |
Rab27b |
T |
C |
18: 70,120,112 (GRCm39) |
|
probably benign |
Het |
Rapsn |
T |
C |
2: 90,867,153 (GRCm39) |
Y152H |
probably damaging |
Het |
Rasd1 |
A |
T |
11: 59,855,379 (GRCm39) |
F85I |
probably damaging |
Het |
Rgs1 |
A |
T |
1: 144,123,671 (GRCm39) |
S85T |
probably damaging |
Het |
Samd9l |
T |
C |
6: 3,372,725 (GRCm39) |
E1512G |
possibly damaging |
Het |
Sgsm1 |
C |
T |
5: 113,427,050 (GRCm39) |
A127T |
probably benign |
Het |
Shc1 |
A |
G |
3: 89,330,276 (GRCm39) |
D70G |
probably damaging |
Het |
Slc26a1 |
T |
A |
5: 108,821,389 (GRCm39) |
T167S |
probably benign |
Het |
Slc26a7 |
A |
T |
4: 14,593,873 (GRCm39) |
Y81N |
probably damaging |
Het |
Slc2a12 |
T |
C |
10: 22,577,915 (GRCm39) |
|
probably benign |
Het |
Slc30a7 |
T |
A |
3: 115,783,789 (GRCm39) |
|
probably null |
Het |
Slc44a5 |
T |
C |
3: 153,971,111 (GRCm39) |
S654P |
probably damaging |
Het |
Stard9 |
T |
G |
2: 120,527,480 (GRCm39) |
S1246A |
possibly damaging |
Het |
Stxbp5 |
A |
T |
10: 9,740,843 (GRCm39) |
S116R |
probably damaging |
Het |
Syvn1 |
C |
T |
19: 6,102,483 (GRCm39) |
P517L |
probably benign |
Het |
Tas2r105 |
T |
C |
6: 131,664,393 (GRCm39) |
I12V |
probably benign |
Het |
Tas2r121 |
A |
G |
6: 132,677,325 (GRCm39) |
S216P |
probably damaging |
Het |
Tcof1 |
T |
C |
18: 60,978,904 (GRCm39) |
D48G |
probably damaging |
Het |
Tgm3 |
C |
T |
2: 129,868,602 (GRCm39) |
|
probably benign |
Het |
Tle2 |
T |
C |
10: 81,424,781 (GRCm39) |
F667L |
probably damaging |
Het |
Tnfaip3 |
C |
A |
10: 18,878,697 (GRCm39) |
A704S |
probably benign |
Het |
Trabd2b |
A |
G |
4: 114,437,519 (GRCm39) |
Q232R |
probably benign |
Het |
Ttc28 |
T |
A |
5: 111,378,947 (GRCm39) |
I1144N |
probably damaging |
Het |
Ucp3 |
T |
A |
7: 100,128,748 (GRCm39) |
C25* |
probably null |
Het |
Ugt3a1 |
A |
G |
15: 9,370,236 (GRCm39) |
D460G |
probably damaging |
Het |
Urb1 |
T |
C |
16: 90,592,336 (GRCm39) |
D308G |
possibly damaging |
Het |
Ush1g |
G |
T |
11: 115,209,694 (GRCm39) |
R167S |
possibly damaging |
Het |
Vav3 |
A |
G |
3: 109,554,995 (GRCm39) |
N81S |
possibly damaging |
Het |
Vmn2r108 |
A |
T |
17: 20,691,721 (GRCm39) |
D267E |
probably benign |
Het |
Zng1 |
A |
G |
19: 24,918,203 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Pramel18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02430:Pramel18
|
APN |
4 |
101,767,477 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02683:Pramel18
|
APN |
4 |
101,767,551 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03403:Pramel18
|
APN |
4 |
101,767,125 (GRCm39) |
missense |
probably benign |
0.40 |
R1054:Pramel18
|
UTSW |
4 |
101,766,361 (GRCm39) |
missense |
probably benign |
0.00 |
R1953:Pramel18
|
UTSW |
4 |
101,767,312 (GRCm39) |
missense |
probably benign |
|
R2216:Pramel18
|
UTSW |
4 |
101,767,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3747:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3750:Pramel18
|
UTSW |
4 |
101,767,073 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4931:Pramel18
|
UTSW |
4 |
101,766,367 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5102:Pramel18
|
UTSW |
4 |
101,766,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Pramel18
|
UTSW |
4 |
101,767,317 (GRCm39) |
missense |
probably benign |
0.00 |
R5822:Pramel18
|
UTSW |
4 |
101,767,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Pramel18
|
UTSW |
4 |
101,767,189 (GRCm39) |
missense |
probably benign |
|
R6904:Pramel18
|
UTSW |
4 |
101,767,291 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7544:Pramel18
|
UTSW |
4 |
101,768,599 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7768:Pramel18
|
UTSW |
4 |
101,769,010 (GRCm39) |
missense |
probably benign |
|
R8342:Pramel18
|
UTSW |
4 |
101,767,581 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Pramel18
|
UTSW |
4 |
101,768,935 (GRCm39) |
missense |
probably benign |
0.09 |
Z1088:Pramel18
|
UTSW |
4 |
101,766,315 (GRCm39) |
splice site |
probably null |
|
Z1088:Pramel18
|
UTSW |
4 |
101,767,383 (GRCm39) |
missense |
probably benign |
0.00 |
|