Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600014C23Rik |
C |
T |
17: 46,043,999 (GRCm39) |
W86* |
probably null |
Het |
Acadl |
T |
C |
1: 66,896,567 (GRCm39) |
H75R |
probably benign |
Het |
Adamtsl1 |
T |
C |
4: 86,195,380 (GRCm39) |
F599S |
probably damaging |
Het |
Adrb3 |
T |
C |
8: 27,718,293 (GRCm39) |
N52S |
probably damaging |
Het |
Agbl3 |
T |
A |
6: 34,776,640 (GRCm39) |
L377Q |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,110,318 (GRCm39) |
L3007P |
probably damaging |
Het |
Amer3 |
T |
A |
1: 34,626,902 (GRCm39) |
Y380* |
probably null |
Het |
Ankrd13d |
A |
T |
19: 4,323,047 (GRCm39) |
|
probably null |
Het |
Ap4m1 |
T |
A |
5: 138,174,501 (GRCm39) |
C235S |
probably benign |
Het |
Arhgap29 |
T |
C |
3: 121,801,290 (GRCm39) |
F675S |
probably damaging |
Het |
Asah2 |
C |
A |
19: 31,986,039 (GRCm39) |
V544F |
probably damaging |
Het |
Ash2l |
A |
G |
8: 26,313,319 (GRCm39) |
I389T |
possibly damaging |
Het |
Bend5 |
T |
C |
4: 111,290,495 (GRCm39) |
S164P |
probably benign |
Het |
Cacna1d |
A |
G |
14: 29,893,251 (GRCm39) |
|
probably null |
Het |
Cdc25b |
A |
G |
2: 131,039,182 (GRCm39) |
N516D |
probably benign |
Het |
Cdc27 |
A |
G |
11: 104,422,560 (GRCm39) |
Y125H |
probably damaging |
Het |
Cdk5r2 |
C |
T |
1: 74,894,995 (GRCm39) |
L247F |
probably damaging |
Het |
Cenpf |
C |
A |
1: 189,390,259 (GRCm39) |
G1191V |
probably benign |
Het |
Cops4 |
C |
T |
5: 100,685,326 (GRCm39) |
T293I |
possibly damaging |
Het |
Csmd3 |
A |
G |
15: 47,777,336 (GRCm39) |
L1294P |
probably damaging |
Het |
Dclre1a |
T |
C |
19: 56,526,872 (GRCm39) |
Y848C |
probably damaging |
Het |
Disp2 |
A |
T |
2: 118,621,325 (GRCm39) |
I686F |
possibly damaging |
Het |
Dnah6 |
T |
A |
6: 72,999,395 (GRCm39) |
Y4012F |
probably benign |
Het |
Dnajc11 |
C |
G |
4: 152,054,393 (GRCm39) |
R200G |
probably damaging |
Het |
Dnhd1 |
A |
T |
7: 105,345,671 (GRCm39) |
D2272V |
possibly damaging |
Het |
Elane |
A |
C |
10: 79,722,183 (GRCm39) |
R5S |
possibly damaging |
Het |
Entpd7 |
G |
A |
19: 43,679,533 (GRCm39) |
V29M |
probably benign |
Het |
Fanca |
A |
G |
8: 124,016,098 (GRCm39) |
|
probably null |
Het |
Fgl1 |
G |
T |
8: 41,644,661 (GRCm39) |
T281K |
probably benign |
Het |
Flii |
T |
C |
11: 60,613,823 (GRCm39) |
|
probably null |
Het |
Fzd7 |
T |
A |
1: 59,523,719 (GRCm39) |
M534K |
probably damaging |
Het |
Galnt5 |
A |
G |
2: 57,889,407 (GRCm39) |
T336A |
probably benign |
Het |
Gli3 |
G |
A |
13: 15,899,300 (GRCm39) |
D896N |
probably damaging |
Het |
Gsx1 |
G |
T |
5: 147,126,756 (GRCm39) |
W193L |
probably damaging |
Het |
Gtpbp3 |
A |
T |
8: 71,945,379 (GRCm39) |
I485F |
probably damaging |
Het |
H2-M11 |
A |
G |
17: 36,858,283 (GRCm39) |
T26A |
probably benign |
Het |
Igfbp7 |
T |
C |
5: 77,499,827 (GRCm39) |
D243G |
probably damaging |
Het |
Il31ra |
A |
T |
13: 112,662,377 (GRCm39) |
D477E |
possibly damaging |
Het |
Inmt |
A |
C |
6: 55,148,212 (GRCm39) |
V139G |
probably damaging |
Het |
Inpp5j |
T |
A |
11: 3,451,147 (GRCm39) |
M501L |
probably benign |
Het |
Itsn2 |
T |
C |
12: 4,762,556 (GRCm39) |
F1579L |
probably damaging |
Het |
Kat2b |
C |
A |
17: 53,874,566 (GRCm39) |
A70E |
probably benign |
Het |
Klhl20 |
T |
C |
1: 160,921,281 (GRCm39) |
E58G |
probably damaging |
Het |
Krt79 |
A |
T |
15: 101,839,983 (GRCm39) |
Y337* |
probably null |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Letm1 |
T |
C |
5: 33,926,770 (GRCm39) |
I176V |
possibly damaging |
Het |
Lingo3 |
C |
A |
10: 80,671,618 (GRCm39) |
R104L |
probably benign |
Het |
Lrig3 |
T |
G |
10: 125,846,090 (GRCm39) |
C840G |
probably damaging |
Het |
Lrrc9 |
A |
G |
12: 72,533,062 (GRCm39) |
N977S |
probably damaging |
Het |
Lrrk2 |
T |
A |
15: 91,657,199 (GRCm39) |
M1831K |
probably benign |
Het |
Mn1 |
A |
T |
5: 111,567,182 (GRCm39) |
D384V |
probably damaging |
Het |
Morc3 |
C |
A |
16: 93,650,738 (GRCm39) |
H319Q |
probably damaging |
Het |
Morn1 |
T |
C |
4: 155,173,960 (GRCm39) |
F56L |
possibly damaging |
Het |
Mrpl53 |
G |
T |
6: 83,086,392 (GRCm39) |
V64L |
probably damaging |
Het |
Myo15a |
T |
A |
11: 60,370,162 (GRCm39) |
V974D |
probably benign |
Het |
Neb |
A |
G |
2: 52,146,136 (GRCm39) |
V2947A |
possibly damaging |
Het |
Nfasc |
A |
C |
1: 132,531,554 (GRCm39) |
N737K |
probably damaging |
Het |
Nlk |
T |
C |
11: 78,463,103 (GRCm39) |
D464G |
possibly damaging |
Het |
Nlrc4 |
C |
T |
17: 74,733,958 (GRCm39) |
R985K |
probably benign |
Het |
Nsun6 |
T |
C |
2: 15,001,147 (GRCm39) |
K470E |
probably benign |
Het |
Nup85 |
T |
G |
11: 115,455,357 (GRCm39) |
M1R |
probably null |
Het |
Or8b39 |
G |
A |
9: 37,996,666 (GRCm39) |
C178Y |
probably damaging |
Het |
Otop1 |
T |
C |
5: 38,445,292 (GRCm39) |
V150A |
possibly damaging |
Het |
Pclo |
C |
T |
5: 14,731,763 (GRCm39) |
R296* |
probably null |
Het |
Pdzd2 |
A |
T |
15: 12,458,144 (GRCm39) |
C240S |
possibly damaging |
Het |
Plekhg5 |
A |
G |
4: 152,198,577 (GRCm39) |
T922A |
probably benign |
Het |
Plekhm2 |
A |
C |
4: 141,369,381 (GRCm39) |
L101R |
probably damaging |
Het |
Plscr3 |
T |
A |
11: 69,738,820 (GRCm39) |
C161S |
probably benign |
Het |
Prr14l |
C |
T |
5: 32,986,259 (GRCm39) |
D1079N |
probably benign |
Het |
Ptpru |
A |
T |
4: 131,498,490 (GRCm39) |
V1377E |
possibly damaging |
Het |
Rab37 |
C |
A |
11: 115,049,528 (GRCm39) |
D112E |
probably benign |
Het |
Raet1e |
T |
A |
10: 22,050,274 (GRCm39) |
I19N |
probably damaging |
Het |
Rassf5 |
T |
C |
1: 131,172,803 (GRCm39) |
Y22C |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,416,721 (GRCm39) |
T1464A |
probably benign |
Het |
Safb |
T |
A |
17: 56,908,092 (GRCm39) |
|
probably benign |
Het |
Scarf2 |
A |
G |
16: 17,624,369 (GRCm39) |
|
probably null |
Het |
Scart2 |
A |
G |
7: 139,827,872 (GRCm39) |
N27D |
probably benign |
Het |
Sh3d19 |
T |
C |
3: 86,014,280 (GRCm39) |
S415P |
probably benign |
Het |
Slc26a9 |
T |
A |
1: 131,691,542 (GRCm39) |
L595Q |
probably damaging |
Het |
Slc4a8 |
T |
C |
15: 100,694,431 (GRCm39) |
Y470H |
probably damaging |
Het |
Slitrk3 |
T |
C |
3: 72,956,982 (GRCm39) |
N597D |
probably benign |
Het |
Spata31 |
T |
A |
13: 65,070,027 (GRCm39) |
V725E |
probably benign |
Het |
Spink12 |
T |
A |
18: 44,240,831 (GRCm39) |
C72* |
probably null |
Het |
Spink5 |
T |
A |
18: 44,146,042 (GRCm39) |
|
probably null |
Het |
Stk40 |
C |
A |
4: 126,012,125 (GRCm39) |
S9* |
probably null |
Het |
Sypl1 |
A |
T |
12: 33,015,420 (GRCm39) |
T40S |
probably damaging |
Het |
Tbc1d8 |
C |
T |
1: 39,430,290 (GRCm39) |
E438K |
probably benign |
Het |
Tdrd7 |
A |
G |
4: 45,989,102 (GRCm39) |
T111A |
probably benign |
Het |
Tg |
A |
T |
15: 66,613,333 (GRCm39) |
|
probably null |
Het |
Tlr5 |
T |
A |
1: 182,801,454 (GRCm39) |
W253R |
probably damaging |
Het |
Tmprss11c |
C |
T |
5: 86,383,328 (GRCm39) |
C353Y |
probably damaging |
Het |
Tnfrsf8 |
T |
A |
4: 145,014,597 (GRCm39) |
M271L |
probably benign |
Het |
Toe1 |
T |
C |
4: 116,663,947 (GRCm39) |
N21S |
probably benign |
Het |
Tpp2 |
T |
C |
1: 44,014,607 (GRCm39) |
F649L |
probably benign |
Het |
Ttll1 |
G |
A |
15: 83,386,426 (GRCm39) |
Q60* |
probably null |
Het |
Vcp |
C |
T |
4: 42,982,565 (GRCm39) |
R709Q |
probably benign |
Het |
Vmn1r119 |
T |
A |
7: 20,745,593 (GRCm39) |
H263L |
possibly damaging |
Het |
Vmn1r195 |
C |
A |
13: 22,463,111 (GRCm39) |
Q194K |
probably damaging |
Het |
Vmn1r33 |
T |
C |
6: 66,588,783 (GRCm39) |
Y257C |
probably damaging |
Het |
Vmn2r15 |
A |
G |
5: 109,440,881 (GRCm39) |
F326L |
probably benign |
Het |
Wbp11 |
A |
T |
6: 136,793,108 (GRCm39) |
|
probably benign |
Het |
Wwp2 |
T |
G |
8: 108,244,578 (GRCm39) |
V250G |
probably benign |
Het |
Xpnpep3 |
T |
C |
15: 81,315,038 (GRCm39) |
V246A |
probably benign |
Het |
Zcchc14 |
G |
A |
8: 122,332,188 (GRCm39) |
R419* |
probably null |
Het |
|
Other mutations in Foxn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00900:Foxn1
|
APN |
11 |
78,262,109 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01391:Foxn1
|
APN |
11 |
78,252,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01737:Foxn1
|
APN |
11 |
78,251,732 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02669:Foxn1
|
APN |
11 |
78,261,986 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03276:Foxn1
|
APN |
11 |
78,261,950 (GRCm39) |
missense |
probably benign |
0.16 |
Nudnik
|
UTSW |
11 |
78,252,438 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0200:Foxn1
|
UTSW |
11 |
78,251,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:Foxn1
|
UTSW |
11 |
78,249,825 (GRCm39) |
missense |
probably benign |
0.01 |
R1112:Foxn1
|
UTSW |
11 |
78,261,856 (GRCm39) |
missense |
probably benign |
0.29 |
R1167:Foxn1
|
UTSW |
11 |
78,249,892 (GRCm39) |
missense |
probably damaging |
0.99 |
R1251:Foxn1
|
UTSW |
11 |
78,249,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R1474:Foxn1
|
UTSW |
11 |
78,251,933 (GRCm39) |
missense |
probably benign |
|
R1506:Foxn1
|
UTSW |
11 |
78,256,761 (GRCm39) |
splice site |
probably benign |
|
R1616:Foxn1
|
UTSW |
11 |
78,249,692 (GRCm39) |
missense |
probably benign |
0.00 |
R1795:Foxn1
|
UTSW |
11 |
78,262,051 (GRCm39) |
missense |
probably benign |
0.01 |
R1905:Foxn1
|
UTSW |
11 |
78,262,636 (GRCm39) |
splice site |
probably null |
|
R1906:Foxn1
|
UTSW |
11 |
78,262,636 (GRCm39) |
splice site |
probably null |
|
R1975:Foxn1
|
UTSW |
11 |
78,256,763 (GRCm39) |
splice site |
probably benign |
|
R1976:Foxn1
|
UTSW |
11 |
78,256,763 (GRCm39) |
splice site |
probably benign |
|
R2206:Foxn1
|
UTSW |
11 |
78,249,630 (GRCm39) |
missense |
probably benign |
0.02 |
R2207:Foxn1
|
UTSW |
11 |
78,249,630 (GRCm39) |
missense |
probably benign |
0.02 |
R2988:Foxn1
|
UTSW |
11 |
78,249,603 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2989:Foxn1
|
UTSW |
11 |
78,249,603 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5015:Foxn1
|
UTSW |
11 |
78,261,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5140:Foxn1
|
UTSW |
11 |
78,252,459 (GRCm39) |
missense |
probably benign |
0.18 |
R5533:Foxn1
|
UTSW |
11 |
78,256,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R6712:Foxn1
|
UTSW |
11 |
78,252,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R6852:Foxn1
|
UTSW |
11 |
78,251,786 (GRCm39) |
missense |
probably benign |
0.00 |
R7176:Foxn1
|
UTSW |
11 |
78,251,693 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7331:Foxn1
|
UTSW |
11 |
78,249,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R7515:Foxn1
|
UTSW |
11 |
78,261,970 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7562:Foxn1
|
UTSW |
11 |
78,261,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R7657:Foxn1
|
UTSW |
11 |
78,256,790 (GRCm39) |
missense |
probably benign |
0.29 |
R8838:Foxn1
|
UTSW |
11 |
78,252,438 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9255:Foxn1
|
UTSW |
11 |
78,252,399 (GRCm39) |
nonsense |
probably null |
|
R9512:Foxn1
|
UTSW |
11 |
78,262,035 (GRCm39) |
missense |
|
|
X0067:Foxn1
|
UTSW |
11 |
78,252,368 (GRCm39) |
missense |
probably damaging |
1.00 |
|