Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
A |
T |
7: 119,181,975 (GRCm39) |
Y408F |
probably benign |
Het |
Adamts9 |
G |
T |
6: 92,857,661 (GRCm39) |
P876T |
probably benign |
Het |
Afap1l2 |
T |
A |
19: 56,906,462 (GRCm39) |
D479V |
probably damaging |
Het |
Aire |
T |
C |
10: 77,873,809 (GRCm39) |
E300G |
probably damaging |
Het |
Ampd3 |
A |
G |
7: 110,402,307 (GRCm39) |
E428G |
probably damaging |
Het |
Apaf1 |
A |
T |
10: 90,913,463 (GRCm39) |
Y153* |
probably null |
Het |
Arhgap10 |
T |
C |
8: 77,985,786 (GRCm39) |
T694A |
probably benign |
Het |
Arhgef39 |
A |
G |
4: 43,496,819 (GRCm39) |
|
probably null |
Het |
Arhgef5 |
T |
C |
6: 43,251,736 (GRCm39) |
V829A |
possibly damaging |
Het |
Arrdc4 |
A |
G |
7: 68,390,741 (GRCm39) |
M333T |
|
Het |
Boc |
G |
T |
16: 44,322,018 (GRCm39) |
R215S |
|
Het |
Capn2 |
G |
A |
1: 182,344,795 (GRCm39) |
A42V |
probably benign |
Het |
Ccdc136 |
T |
A |
6: 29,405,939 (GRCm39) |
M95K |
probably benign |
Het |
Ccdc183 |
A |
T |
2: 25,499,520 (GRCm39) |
Y438N |
probably benign |
Het |
Ccnf |
C |
A |
17: 24,468,367 (GRCm39) |
R10M |
probably damaging |
Het |
Cd19 |
A |
G |
7: 126,011,284 (GRCm39) |
F300S |
probably damaging |
Het |
Cdkl3 |
G |
T |
11: 51,895,816 (GRCm39) |
C21F |
probably damaging |
Het |
Celf2 |
C |
T |
2: 6,620,522 (GRCm39) |
R183Q |
probably damaging |
Het |
Clca3a1 |
T |
G |
3: 144,719,698 (GRCm39) |
D424A |
probably benign |
Het |
Clec3a |
A |
G |
8: 115,144,887 (GRCm39) |
D21G |
probably benign |
Het |
Clec4e |
T |
C |
6: 123,263,306 (GRCm39) |
N78S |
probably benign |
Het |
Clpb |
A |
T |
7: 101,313,399 (GRCm39) |
S128C |
possibly damaging |
Het |
Cntnap5a |
T |
A |
1: 116,369,985 (GRCm39) |
Y867* |
probably null |
Het |
Dgkg |
G |
C |
16: 22,385,194 (GRCm39) |
N437K |
|
Het |
Dnhd1 |
A |
G |
7: 105,335,773 (GRCm39) |
E1139G |
probably damaging |
Het |
Dnhd1 |
G |
A |
7: 105,344,134 (GRCm39) |
R1826H |
probably damaging |
Het |
Etl4 |
A |
G |
2: 20,811,052 (GRCm39) |
H1413R |
|
Het |
Fibp |
T |
A |
19: 5,513,850 (GRCm39) |
V271D |
possibly damaging |
Het |
Gabra4 |
G |
T |
5: 71,791,023 (GRCm39) |
T273K |
probably damaging |
Het |
Gan |
G |
A |
8: 117,914,219 (GRCm39) |
D206N |
probably damaging |
Het |
Gstz1 |
A |
T |
12: 87,206,923 (GRCm39) |
I106F |
probably damaging |
Het |
Hivep2 |
T |
G |
10: 14,006,546 (GRCm39) |
L1048R |
probably damaging |
Het |
Htr6 |
A |
T |
4: 138,801,750 (GRCm39) |
M108K |
probably damaging |
Het |
Hycc1 |
A |
C |
5: 24,170,255 (GRCm39) |
S365A |
probably benign |
Het |
Itgad |
A |
G |
7: 127,803,723 (GRCm39) |
E1134G |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 41,366,648 (GRCm39) |
G657S |
|
Het |
Lrp2 |
T |
C |
2: 69,307,423 (GRCm39) |
I2879V |
probably benign |
Het |
Lyst |
G |
T |
13: 13,852,587 (GRCm39) |
V2196L |
probably benign |
Het |
Mettl5 |
T |
A |
2: 69,711,717 (GRCm39) |
I50F |
possibly damaging |
Het |
Mmadhc |
A |
G |
2: 50,186,341 (GRCm39) |
|
probably benign |
Het |
Msantd1 |
G |
A |
5: 35,075,076 (GRCm39) |
W46* |
probably null |
Het |
Mto1 |
T |
C |
9: 78,364,712 (GRCm39) |
I317T |
probably damaging |
Het |
Myef2 |
T |
G |
2: 124,957,377 (GRCm39) |
D126A |
probably damaging |
Het |
Net1 |
A |
G |
13: 3,937,569 (GRCm39) |
|
probably null |
Het |
Nnmt |
A |
T |
9: 48,503,660 (GRCm39) |
M122K |
probably benign |
Het |
Nos1 |
A |
G |
5: 118,087,849 (GRCm39) |
K1371E |
probably benign |
Het |
Nrcam |
G |
C |
12: 44,636,931 (GRCm39) |
W1121C |
probably damaging |
Het |
Nt5c2 |
A |
G |
19: 46,877,409 (GRCm39) |
S511P |
|
Het |
Or10w1 |
C |
A |
19: 13,632,414 (GRCm39) |
A207E |
probably damaging |
Het |
Or1j17 |
G |
T |
2: 36,578,778 (GRCm39) |
V255F |
probably benign |
Het |
Or2k2 |
T |
C |
4: 58,785,585 (GRCm39) |
I46V |
possibly damaging |
Het |
Or4a73 |
A |
G |
2: 89,421,261 (GRCm39) |
F66S |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,790,860 (GRCm39) |
K66E |
probably damaging |
Het |
Paqr4 |
A |
G |
17: 23,956,656 (GRCm39) |
W236R |
probably damaging |
Het |
Parm1 |
A |
G |
5: 91,760,923 (GRCm39) |
Y265C |
probably damaging |
Het |
Pcbp2 |
T |
C |
15: 102,392,628 (GRCm39) |
Y178H |
probably damaging |
Het |
Pidd1 |
G |
A |
7: 141,021,678 (GRCm39) |
P261S |
probably damaging |
Het |
Pik3r6 |
T |
C |
11: 68,442,159 (GRCm39) |
V705A |
possibly damaging |
Het |
Pla2g15 |
G |
T |
8: 106,887,275 (GRCm39) |
V156F |
possibly damaging |
Het |
Prpf6 |
G |
A |
2: 181,289,137 (GRCm39) |
V609M |
possibly damaging |
Het |
Resf1 |
A |
G |
6: 149,226,965 (GRCm39) |
N4D |
possibly damaging |
Het |
Rprd2 |
A |
G |
3: 95,679,505 (GRCm39) |
V491A |
probably benign |
Het |
Rtp3 |
T |
A |
9: 110,818,600 (GRCm39) |
H27L |
probably damaging |
Het |
Sema5b |
G |
A |
16: 35,443,121 (GRCm39) |
R42Q |
possibly damaging |
Het |
Serpina3f |
A |
G |
12: 104,183,743 (GRCm39) |
K202E |
probably damaging |
Het |
Slc25a33 |
T |
G |
4: 149,833,767 (GRCm39) |
M168L |
probably benign |
Het |
Slc7a8 |
A |
G |
14: 54,964,341 (GRCm39) |
C371R |
probably damaging |
Het |
Smyd1 |
T |
C |
6: 71,192,808 (GRCm39) |
N467S |
probably benign |
Het |
Sptbn4 |
A |
G |
7: 27,107,807 (GRCm39) |
W872R |
probably damaging |
Het |
Syne1 |
A |
T |
10: 5,152,009 (GRCm39) |
I5766N |
probably damaging |
Het |
Syne2 |
A |
G |
12: 75,986,760 (GRCm39) |
S1699G |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,047 (GRCm39) |
D423G |
possibly damaging |
Het |
Tcf19 |
A |
T |
17: 35,825,792 (GRCm39) |
F122I |
probably damaging |
Het |
Tdpoz4 |
A |
T |
3: 93,704,221 (GRCm39) |
T173S |
probably benign |
Het |
Trappc8 |
T |
A |
18: 20,983,975 (GRCm39) |
H681L |
possibly damaging |
Het |
Tsks |
A |
G |
7: 44,605,931 (GRCm39) |
T466A |
possibly damaging |
Het |
Ubr1 |
T |
C |
2: 120,764,820 (GRCm39) |
I545V |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,159,024 (GRCm39) |
E1170G |
probably benign |
Het |
Usp29 |
A |
G |
7: 6,964,396 (GRCm39) |
R80G |
possibly damaging |
Het |
Utrn |
C |
T |
10: 12,282,225 (GRCm39) |
R3258H |
probably damaging |
Het |
Vmn1r13 |
T |
G |
6: 57,187,549 (GRCm39) |
V236G |
probably benign |
Het |
Vmn1r33 |
T |
A |
6: 66,589,002 (GRCm39) |
D184V |
probably damaging |
Het |
Vmn2r87 |
T |
C |
10: 130,315,794 (GRCm39) |
N91D |
probably damaging |
Het |
Wrn |
A |
G |
8: 33,774,644 (GRCm39) |
|
probably null |
Het |
Zan |
G |
A |
5: 137,461,636 (GRCm39) |
P1181L |
unknown |
Het |
Zbtb47 |
C |
A |
9: 121,591,990 (GRCm39) |
Y103* |
probably null |
Het |
Zfc3h1 |
C |
A |
10: 115,259,362 (GRCm39) |
L1645I |
possibly damaging |
Het |
Zfhx2 |
G |
T |
14: 55,302,191 (GRCm39) |
P1931Q |
probably damaging |
Het |
Zfp352 |
A |
G |
4: 90,113,128 (GRCm39) |
K423E |
probably benign |
Het |
Zfp574 |
T |
A |
7: 24,780,515 (GRCm39) |
H512Q |
|
Het |
Zfp7 |
G |
A |
15: 76,774,531 (GRCm39) |
R191H |
probably benign |
Het |
Zfp771 |
A |
T |
7: 126,844,301 (GRCm39) |
K46* |
probably null |
Het |
Zkscan8 |
T |
C |
13: 21,704,763 (GRCm39) |
E392G |
probably damaging |
Het |
|
Other mutations in Trim36 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01710:Trim36
|
APN |
18 |
46,321,455 (GRCm39) |
splice site |
probably benign |
|
IGL02728:Trim36
|
APN |
18 |
46,305,669 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03166:Trim36
|
APN |
18 |
46,345,388 (GRCm39) |
missense |
probably benign |
|
IGL03209:Trim36
|
APN |
18 |
46,300,575 (GRCm39) |
missense |
probably benign |
|
R0346:Trim36
|
UTSW |
18 |
46,332,776 (GRCm39) |
unclassified |
probably benign |
|
R0426:Trim36
|
UTSW |
18 |
46,305,592 (GRCm39) |
missense |
probably damaging |
0.97 |
R0463:Trim36
|
UTSW |
18 |
46,311,523 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0590:Trim36
|
UTSW |
18 |
46,305,643 (GRCm39) |
missense |
probably benign |
0.01 |
R0751:Trim36
|
UTSW |
18 |
46,329,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R1037:Trim36
|
UTSW |
18 |
46,329,385 (GRCm39) |
splice site |
probably benign |
|
R1184:Trim36
|
UTSW |
18 |
46,329,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Trim36
|
UTSW |
18 |
46,319,250 (GRCm39) |
nonsense |
probably null |
|
R1571:Trim36
|
UTSW |
18 |
46,305,562 (GRCm39) |
missense |
probably benign |
0.01 |
R1687:Trim36
|
UTSW |
18 |
46,321,724 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2057:Trim36
|
UTSW |
18 |
46,329,229 (GRCm39) |
missense |
probably benign |
0.02 |
R2103:Trim36
|
UTSW |
18 |
46,329,149 (GRCm39) |
missense |
probably benign |
|
R2127:Trim36
|
UTSW |
18 |
46,345,404 (GRCm39) |
missense |
probably benign |
0.27 |
R3853:Trim36
|
UTSW |
18 |
46,305,439 (GRCm39) |
splice site |
probably benign |
|
R4209:Trim36
|
UTSW |
18 |
46,329,191 (GRCm39) |
missense |
probably benign |
0.44 |
R4787:Trim36
|
UTSW |
18 |
46,305,599 (GRCm39) |
missense |
probably benign |
0.10 |
R4810:Trim36
|
UTSW |
18 |
46,305,536 (GRCm39) |
missense |
probably benign |
0.07 |
R4953:Trim36
|
UTSW |
18 |
46,329,245 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5107:Trim36
|
UTSW |
18 |
46,305,705 (GRCm39) |
missense |
probably benign |
|
R5320:Trim36
|
UTSW |
18 |
46,300,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Trim36
|
UTSW |
18 |
46,302,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R5823:Trim36
|
UTSW |
18 |
46,302,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R6619:Trim36
|
UTSW |
18 |
46,321,475 (GRCm39) |
missense |
probably damaging |
0.96 |
R7349:Trim36
|
UTSW |
18 |
46,302,495 (GRCm39) |
missense |
probably benign |
0.29 |
R7814:Trim36
|
UTSW |
18 |
46,300,691 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7853:Trim36
|
UTSW |
18 |
46,305,558 (GRCm39) |
missense |
probably benign |
0.14 |
R8008:Trim36
|
UTSW |
18 |
46,305,556 (GRCm39) |
missense |
probably benign |
0.34 |
R8294:Trim36
|
UTSW |
18 |
46,331,588 (GRCm39) |
missense |
probably benign |
0.02 |
R8735:Trim36
|
UTSW |
18 |
46,302,452 (GRCm39) |
missense |
probably benign |
0.10 |
R8899:Trim36
|
UTSW |
18 |
46,302,264 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9091:Trim36
|
UTSW |
18 |
46,300,580 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9106:Trim36
|
UTSW |
18 |
46,300,664 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9135:Trim36
|
UTSW |
18 |
46,302,410 (GRCm39) |
missense |
probably benign |
0.03 |
R9262:Trim36
|
UTSW |
18 |
46,300,506 (GRCm39) |
missense |
probably benign |
0.01 |
R9270:Trim36
|
UTSW |
18 |
46,300,580 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9505:Trim36
|
UTSW |
18 |
46,329,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R9587:Trim36
|
UTSW |
18 |
46,308,722 (GRCm39) |
missense |
probably benign |
0.06 |
R9763:Trim36
|
UTSW |
18 |
46,309,125 (GRCm39) |
missense |
probably benign |
0.42 |
|