Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
A |
G |
19: 43,797,101 (GRCm39) |
K491E |
probably benign |
Het |
Abcd3 |
T |
C |
3: 121,569,117 (GRCm39) |
I374V |
probably benign |
Het |
Adam34 |
G |
A |
8: 44,104,439 (GRCm39) |
T402I |
probably benign |
Het |
Angptl7 |
G |
T |
4: 148,581,790 (GRCm39) |
H199N |
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,621,840 (GRCm39) |
C671R |
possibly damaging |
Het |
Anxa7 |
G |
A |
14: 20,521,495 (GRCm39) |
P67L |
unknown |
Het |
Ap3d1 |
T |
A |
10: 80,547,952 (GRCm39) |
Q913H |
probably benign |
Het |
Arhgef37 |
A |
G |
18: 61,656,948 (GRCm39) |
I39T |
probably damaging |
Het |
Armh4 |
G |
A |
14: 50,008,024 (GRCm39) |
T483I |
probably damaging |
Het |
C3ar1 |
T |
A |
6: 122,828,044 (GRCm39) |
T58S |
probably damaging |
Het |
Caap1 |
A |
T |
4: 94,389,332 (GRCm39) |
L334Q |
probably damaging |
Het |
Ccr1 |
A |
T |
9: 123,763,882 (GRCm39) |
I216K |
probably damaging |
Het |
Cdh9 |
T |
A |
15: 16,831,162 (GRCm39) |
|
probably null |
Het |
Cept1 |
A |
G |
3: 106,411,921 (GRCm39) |
F351S |
possibly damaging |
Het |
Cfap61 |
A |
G |
2: 145,791,879 (GRCm39) |
D112G |
possibly damaging |
Het |
Cul9 |
T |
A |
17: 46,839,528 (GRCm39) |
S817C |
possibly damaging |
Het |
Dido1 |
A |
G |
2: 180,303,195 (GRCm39) |
S1570P |
probably benign |
Het |
Disc1 |
A |
G |
8: 125,814,754 (GRCm39) |
D206G |
probably damaging |
Het |
Dock5 |
T |
A |
14: 68,083,439 (GRCm39) |
R157* |
probably null |
Het |
Dpp6 |
A |
G |
5: 27,926,140 (GRCm39) |
D738G |
probably damaging |
Het |
F10 |
G |
T |
8: 13,095,086 (GRCm39) |
W81L |
probably damaging |
Het |
Fam217a |
T |
C |
13: 35,095,147 (GRCm39) |
D356G |
probably damaging |
Het |
Fes |
T |
C |
7: 80,031,473 (GRCm39) |
E467G |
probably damaging |
Het |
Fignl2 |
A |
T |
15: 100,951,339 (GRCm39) |
D314E |
unknown |
Het |
Foxh1 |
T |
C |
15: 76,552,719 (GRCm39) |
|
probably benign |
Het |
Gdpd5 |
T |
C |
7: 99,109,199 (GRCm39) |
L573P |
probably benign |
Het |
Gigyf1 |
T |
A |
5: 137,523,469 (GRCm39) |
S934T |
probably damaging |
Het |
Gm7356 |
C |
T |
17: 14,221,937 (GRCm39) |
V31I |
probably benign |
Het |
Hoatz |
A |
G |
9: 51,011,298 (GRCm39) |
|
probably null |
Het |
Hoxa2 |
C |
A |
6: 52,140,517 (GRCm39) |
K156N |
probably damaging |
Het |
Ifi203 |
G |
A |
1: 173,756,857 (GRCm39) |
|
probably benign |
Het |
Il5ra |
A |
T |
6: 106,692,604 (GRCm39) |
D380E |
possibly damaging |
Het |
Ino80c |
C |
A |
18: 24,254,865 (GRCm39) |
|
probably benign |
Het |
Kif18a |
T |
A |
2: 109,163,966 (GRCm39) |
W772R |
probably benign |
Het |
Lipo3 |
G |
T |
19: 33,557,880 (GRCm39) |
Q171K |
probably damaging |
Het |
Mga |
A |
T |
2: 119,794,709 (GRCm39) |
T2798S |
probably damaging |
Het |
Msantd5l |
A |
G |
11: 51,145,249 (GRCm39) |
S113P |
probably damaging |
Het |
Mybpc1 |
T |
A |
10: 88,394,437 (GRCm39) |
T297S |
probably benign |
Het |
Myh7 |
T |
G |
14: 55,228,440 (GRCm39) |
Q222P |
probably benign |
Het |
N4bp2l2 |
T |
C |
5: 150,585,362 (GRCm39) |
D206G |
probably benign |
Het |
Nacc2 |
G |
C |
2: 25,952,216 (GRCm39) |
T380S |
probably benign |
Het |
Niban3 |
T |
A |
8: 72,060,307 (GRCm39) |
|
probably benign |
Het |
Nkpd1 |
T |
A |
7: 19,255,875 (GRCm39) |
D186E |
probably damaging |
Het |
Nol10 |
A |
T |
12: 17,466,863 (GRCm39) |
E581V |
probably benign |
Het |
Ntrk1 |
A |
T |
3: 87,693,366 (GRCm39) |
N255K |
possibly damaging |
Het |
Nudt5 |
T |
G |
2: 5,869,228 (GRCm39) |
D151E |
probably benign |
Het |
Obscn |
A |
T |
11: 58,892,858 (GRCm39) |
L6796Q |
probably benign |
Het |
Or10p21 |
C |
T |
10: 128,847,802 (GRCm39) |
A216V |
probably benign |
Het |
Or4k2 |
A |
G |
14: 50,423,999 (GRCm39) |
I225T |
possibly damaging |
Het |
Oxct2b |
A |
G |
4: 123,010,838 (GRCm39) |
T253A |
probably benign |
Het |
Patl1 |
G |
A |
19: 11,891,725 (GRCm39) |
C10Y |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,310,427 (GRCm39) |
R1905G |
possibly damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,402,312 (GRCm39) |
E2228G |
possibly damaging |
Het |
Plcg1 |
A |
G |
2: 160,589,986 (GRCm39) |
K135E |
probably benign |
Het |
Proz |
A |
G |
8: 13,115,319 (GRCm39) |
T112A |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,099,199 (GRCm39) |
N1568D |
probably benign |
Het |
Rbm4 |
A |
G |
19: 4,837,539 (GRCm39) |
V431A |
probably benign |
Het |
Rgs19 |
G |
T |
2: 181,333,058 (GRCm39) |
C40* |
probably null |
Het |
Rimbp3 |
T |
A |
16: 17,030,884 (GRCm39) |
I1436K |
probably benign |
Het |
Rnps1 |
T |
A |
17: 24,641,176 (GRCm39) |
M192K |
probably damaging |
Het |
Rrad |
C |
T |
8: 105,355,222 (GRCm39) |
R262Q |
possibly damaging |
Het |
Slc17a9 |
G |
A |
2: 180,380,210 (GRCm39) |
V318I |
probably benign |
Het |
Slc5a12 |
A |
G |
2: 110,467,455 (GRCm39) |
I412V |
probably damaging |
Het |
Smc4 |
T |
A |
3: 68,925,491 (GRCm39) |
N329K |
probably benign |
Het |
St3gal4 |
G |
A |
9: 34,964,723 (GRCm39) |
R165W |
probably damaging |
Het |
Strbp |
G |
A |
2: 37,493,949 (GRCm39) |
R375* |
probably null |
Het |
Tacc2 |
A |
G |
7: 130,228,367 (GRCm39) |
N1684S |
possibly damaging |
Het |
Tet1 |
A |
T |
10: 62,676,063 (GRCm39) |
L671* |
probably null |
Het |
Tex2 |
C |
A |
11: 106,458,144 (GRCm39) |
E429* |
probably null |
Het |
Tgm4 |
T |
C |
9: 122,869,541 (GRCm39) |
I40T |
possibly damaging |
Het |
Tmem132d |
C |
T |
5: 127,869,676 (GRCm39) |
D553N |
probably damaging |
Het |
Tnks |
A |
T |
8: 35,320,501 (GRCm39) |
Y723* |
probably null |
Het |
Tnks1bp1 |
A |
T |
2: 84,894,320 (GRCm39) |
T1416S |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,904,646 (GRCm39) |
L1137Q |
probably damaging |
Het |
Tor4a |
A |
C |
2: 25,085,202 (GRCm39) |
C68G |
probably damaging |
Het |
Tubb2b |
A |
C |
13: 34,312,445 (GRCm39) |
V116G |
probably damaging |
Het |
Upb1 |
T |
A |
10: 75,250,827 (GRCm39) |
S99T |
probably benign |
Het |
Vmn1r31 |
T |
A |
6: 58,449,083 (GRCm39) |
I261F |
unknown |
Het |
Vmn1r53 |
T |
C |
6: 90,200,571 (GRCm39) |
Y251C |
probably benign |
Het |
Vmn2r58 |
T |
C |
7: 41,513,981 (GRCm39) |
R221G |
|
Het |
Vmn2r88 |
A |
T |
14: 51,655,983 (GRCm39) |
I740F |
possibly damaging |
Het |
Zfp644 |
C |
T |
5: 106,783,503 (GRCm39) |
G1015R |
probably damaging |
Het |
Zfy1 |
T |
C |
Y: 738,726 (GRCm39) |
D160G |
unknown |
Het |
Zscan25 |
T |
A |
5: 145,223,200 (GRCm39) |
V156E |
probably damaging |
Het |
Zyg11b |
A |
T |
4: 108,109,356 (GRCm39) |
F443I |
|
Het |
|
Other mutations in Enpep |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00791:Enpep
|
APN |
3 |
129,125,731 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01895:Enpep
|
APN |
3 |
129,063,983 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02193:Enpep
|
APN |
3 |
129,075,336 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02215:Enpep
|
APN |
3 |
129,063,926 (GRCm39) |
splice site |
probably benign |
|
IGL02511:Enpep
|
APN |
3 |
129,115,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02579:Enpep
|
APN |
3 |
129,077,739 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02634:Enpep
|
APN |
3 |
129,103,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03034:Enpep
|
APN |
3 |
129,092,599 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03214:Enpep
|
APN |
3 |
129,086,896 (GRCm39) |
missense |
probably benign |
|
IGL03401:Enpep
|
APN |
3 |
129,106,269 (GRCm39) |
missense |
probably benign |
0.01 |
P0041:Enpep
|
UTSW |
3 |
129,125,847 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0371:Enpep
|
UTSW |
3 |
129,077,516 (GRCm39) |
critical splice donor site |
probably null |
|
R0479:Enpep
|
UTSW |
3 |
129,106,323 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1036:Enpep
|
UTSW |
3 |
129,077,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R1466:Enpep
|
UTSW |
3 |
129,113,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Enpep
|
UTSW |
3 |
129,113,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Enpep
|
UTSW |
3 |
129,113,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Enpep
|
UTSW |
3 |
129,074,172 (GRCm39) |
missense |
probably benign |
0.14 |
R2101:Enpep
|
UTSW |
3 |
129,092,587 (GRCm39) |
missense |
probably benign |
0.00 |
R2153:Enpep
|
UTSW |
3 |
129,074,231 (GRCm39) |
missense |
probably damaging |
0.99 |
R2474:Enpep
|
UTSW |
3 |
129,077,807 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3618:Enpep
|
UTSW |
3 |
129,077,807 (GRCm39) |
missense |
possibly damaging |
0.77 |
R3619:Enpep
|
UTSW |
3 |
129,077,807 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4275:Enpep
|
UTSW |
3 |
129,125,927 (GRCm39) |
missense |
probably benign |
0.02 |
R4291:Enpep
|
UTSW |
3 |
129,063,966 (GRCm39) |
nonsense |
probably null |
|
R4438:Enpep
|
UTSW |
3 |
129,077,740 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4570:Enpep
|
UTSW |
3 |
129,075,197 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4678:Enpep
|
UTSW |
3 |
129,097,362 (GRCm39) |
critical splice donor site |
probably null |
|
R4679:Enpep
|
UTSW |
3 |
129,097,362 (GRCm39) |
critical splice donor site |
probably null |
|
R4748:Enpep
|
UTSW |
3 |
129,125,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4878:Enpep
|
UTSW |
3 |
129,070,420 (GRCm39) |
missense |
probably benign |
0.17 |
R4954:Enpep
|
UTSW |
3 |
129,077,829 (GRCm39) |
missense |
probably damaging |
0.98 |
R5074:Enpep
|
UTSW |
3 |
129,097,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R5261:Enpep
|
UTSW |
3 |
129,099,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Enpep
|
UTSW |
3 |
129,074,159 (GRCm39) |
missense |
probably benign |
0.30 |
R5661:Enpep
|
UTSW |
3 |
129,070,406 (GRCm39) |
missense |
probably damaging |
0.98 |
R5687:Enpep
|
UTSW |
3 |
129,092,743 (GRCm39) |
splice site |
probably null |
|
R5695:Enpep
|
UTSW |
3 |
129,102,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5697:Enpep
|
UTSW |
3 |
129,102,772 (GRCm39) |
missense |
probably benign |
|
R5889:Enpep
|
UTSW |
3 |
129,106,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:Enpep
|
UTSW |
3 |
129,106,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5968:Enpep
|
UTSW |
3 |
129,074,587 (GRCm39) |
missense |
probably benign |
|
R5976:Enpep
|
UTSW |
3 |
129,092,773 (GRCm39) |
missense |
probably damaging |
0.97 |
R6151:Enpep
|
UTSW |
3 |
129,126,067 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6367:Enpep
|
UTSW |
3 |
129,125,730 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6468:Enpep
|
UTSW |
3 |
129,125,509 (GRCm39) |
critical splice donor site |
probably null |
|
R6484:Enpep
|
UTSW |
3 |
129,115,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R6938:Enpep
|
UTSW |
3 |
129,092,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R6989:Enpep
|
UTSW |
3 |
129,074,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7073:Enpep
|
UTSW |
3 |
129,106,319 (GRCm39) |
nonsense |
probably null |
|
R7258:Enpep
|
UTSW |
3 |
129,125,724 (GRCm39) |
missense |
probably benign |
0.01 |
R7452:Enpep
|
UTSW |
3 |
129,065,052 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7576:Enpep
|
UTSW |
3 |
129,077,740 (GRCm39) |
missense |
probably benign |
0.03 |
R7684:Enpep
|
UTSW |
3 |
129,115,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7697:Enpep
|
UTSW |
3 |
129,102,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8050:Enpep
|
UTSW |
3 |
129,099,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8080:Enpep
|
UTSW |
3 |
129,092,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R8318:Enpep
|
UTSW |
3 |
129,063,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Enpep
|
UTSW |
3 |
129,102,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8474:Enpep
|
UTSW |
3 |
129,113,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R8532:Enpep
|
UTSW |
3 |
129,070,302 (GRCm39) |
nonsense |
probably null |
|
R8826:Enpep
|
UTSW |
3 |
129,065,067 (GRCm39) |
missense |
probably damaging |
0.97 |
R8884:Enpep
|
UTSW |
3 |
129,115,052 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8937:Enpep
|
UTSW |
3 |
129,115,007 (GRCm39) |
critical splice donor site |
probably null |
|
R8959:Enpep
|
UTSW |
3 |
129,113,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R9348:Enpep
|
UTSW |
3 |
129,102,772 (GRCm39) |
missense |
probably benign |
0.03 |
R9375:Enpep
|
UTSW |
3 |
129,125,529 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Enpep
|
UTSW |
3 |
129,070,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|