Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
C |
A |
11: 109,960,635 (GRCm39) |
A628S |
probably damaging |
Het |
Abca9 |
T |
C |
11: 110,036,405 (GRCm39) |
N568S |
probably damaging |
Het |
Ada |
C |
T |
2: 163,574,814 (GRCm39) |
A108T |
possibly damaging |
Het |
Adam6a |
T |
A |
12: 113,508,069 (GRCm39) |
D147E |
possibly damaging |
Het |
Ampd1 |
A |
T |
3: 103,006,154 (GRCm39) |
T655S |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,327,139 (GRCm39) |
F680S |
probably damaging |
Het |
Asap1 |
G |
A |
15: 63,991,869 (GRCm39) |
T783I |
probably benign |
Het |
Astn1 |
T |
A |
1: 158,329,923 (GRCm39) |
N259K |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,886,673 (GRCm39) |
V667A |
probably damaging |
Het |
Brat1 |
G |
A |
5: 140,698,382 (GRCm39) |
V185I |
probably benign |
Het |
Btnl6 |
T |
C |
17: 34,732,620 (GRCm39) |
Y318C |
probably damaging |
Het |
Caskin2 |
G |
A |
11: 115,694,522 (GRCm39) |
P360S |
probably benign |
Het |
Ccdc121rt3 |
T |
C |
5: 112,503,642 (GRCm39) |
T21A |
probably benign |
Het |
Cd68 |
T |
A |
11: 69,555,754 (GRCm39) |
|
probably benign |
Het |
Cdca2 |
T |
C |
14: 67,952,355 (GRCm39) |
|
probably benign |
Het |
Cdk6 |
G |
A |
5: 3,523,217 (GRCm39) |
M212I |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,481,159 (GRCm39) |
F302Y |
probably damaging |
Het |
Celsr2 |
T |
C |
3: 108,301,055 (GRCm39) |
E2746G |
possibly damaging |
Het |
Clec4a4 |
G |
A |
6: 122,989,703 (GRCm39) |
V115I |
probably benign |
Het |
Clip3 |
C |
A |
7: 29,998,307 (GRCm39) |
A251E |
possibly damaging |
Het |
Cmah |
T |
C |
13: 24,623,180 (GRCm39) |
L350P |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,370,103 (GRCm39) |
R907* |
probably null |
Het |
Cntnap5b |
T |
C |
1: 99,999,814 (GRCm39) |
Y191H |
probably benign |
Het |
Col4a4 |
A |
T |
1: 82,458,207 (GRCm39) |
C1122* |
probably null |
Het |
Coq5 |
A |
G |
5: 115,433,842 (GRCm39) |
|
probably benign |
Het |
Cpxcr1 |
A |
G |
X: 115,387,136 (GRCm39) |
K16E |
possibly damaging |
Het |
Dclk3 |
T |
C |
9: 111,298,304 (GRCm39) |
I616T |
probably benign |
Het |
Dhrs3 |
A |
T |
4: 144,646,057 (GRCm39) |
T122S |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,210,596 (GRCm39) |
I502V |
probably benign |
Het |
Dscaml1 |
G |
T |
9: 45,596,519 (GRCm39) |
G788W |
probably damaging |
Het |
Dusp10 |
C |
T |
1: 183,769,645 (GRCm39) |
|
probably null |
Het |
Ehbp1l1 |
C |
A |
19: 5,769,112 (GRCm39) |
L730F |
possibly damaging |
Het |
Eif2ak1 |
C |
T |
5: 143,808,785 (GRCm39) |
H75Y |
probably damaging |
Het |
Evi2a |
T |
C |
11: 79,418,398 (GRCm39) |
T71A |
probably benign |
Het |
Fam184a |
A |
T |
10: 53,511,461 (GRCm39) |
S1073T |
probably damaging |
Het |
Fam227a |
T |
C |
15: 79,499,582 (GRCm39) |
Y591C |
probably damaging |
Het |
Fam83a |
C |
T |
15: 57,873,272 (GRCm39) |
T367M |
probably benign |
Het |
Fam83g |
A |
G |
11: 61,593,819 (GRCm39) |
D451G |
probably damaging |
Het |
Fbn1 |
A |
G |
2: 125,203,185 (GRCm39) |
F1213L |
possibly damaging |
Het |
Fcgbp |
G |
A |
7: 27,791,273 (GRCm39) |
V845I |
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,766,942 (GRCm39) |
E342K |
probably benign |
Het |
Gm6632 |
T |
G |
5: 59,211,679 (GRCm39) |
|
noncoding transcript |
Het |
Gnl3 |
A |
T |
14: 30,738,418 (GRCm39) |
|
probably benign |
Het |
Hhipl1 |
C |
T |
12: 108,277,996 (GRCm39) |
T108I |
probably damaging |
Het |
Hs2st1 |
A |
T |
3: 144,141,256 (GRCm39) |
F271I |
possibly damaging |
Het |
Ido1 |
T |
C |
8: 25,074,462 (GRCm39) |
S303G |
probably damaging |
Het |
Ints2 |
C |
T |
11: 86,117,607 (GRCm39) |
R705H |
probably damaging |
Het |
Kcnc2 |
A |
G |
10: 112,292,305 (GRCm39) |
K49E |
probably damaging |
Het |
Kif3b |
T |
A |
2: 153,162,235 (GRCm39) |
V482E |
probably damaging |
Het |
Ldlrad2 |
G |
A |
4: 137,299,525 (GRCm39) |
P100S |
probably benign |
Het |
Lrba |
G |
T |
3: 86,687,573 (GRCm39) |
|
probably benign |
Het |
Lsm11 |
A |
T |
11: 45,824,730 (GRCm39) |
W266R |
probably benign |
Het |
Mob3a |
A |
T |
10: 80,522,988 (GRCm39) |
M215K |
probably benign |
Het |
Mterf1b |
T |
G |
5: 4,247,163 (GRCm39) |
L268R |
probably damaging |
Het |
Mvk |
T |
C |
5: 114,598,157 (GRCm39) |
F365L |
probably damaging |
Het |
Myo16 |
T |
A |
8: 10,552,796 (GRCm39) |
F945I |
probably damaging |
Het |
Myo1f |
G |
T |
17: 33,813,001 (GRCm39) |
K602N |
possibly damaging |
Het |
Nr2c2ap |
A |
T |
8: 70,585,765 (GRCm39) |
M108L |
probably benign |
Het |
Ofcc1 |
C |
T |
13: 40,362,305 (GRCm39) |
G206R |
probably benign |
Het |
Ogfrl1 |
A |
G |
1: 23,414,890 (GRCm39) |
F206L |
probably damaging |
Het |
Ola1 |
A |
T |
2: 72,987,188 (GRCm39) |
I148N |
probably damaging |
Het |
Or14c46 |
G |
T |
7: 85,918,270 (GRCm39) |
H242Q |
probably damaging |
Het |
Or4d10b |
T |
A |
19: 12,036,844 (GRCm39) |
T91S |
probably benign |
Het |
Or51f1d |
A |
G |
7: 102,701,288 (GRCm39) |
Y261C |
probably damaging |
Het |
Or6c2 |
A |
T |
10: 129,362,824 (GRCm39) |
M243L |
probably benign |
Het |
Or9m2 |
A |
G |
2: 87,821,334 (GRCm39) |
N293S |
probably damaging |
Het |
Otof |
A |
G |
5: 30,536,876 (GRCm39) |
|
probably null |
Het |
Pah |
G |
T |
10: 87,414,175 (GRCm39) |
K341N |
probably damaging |
Het |
Pfdn5 |
T |
A |
15: 102,236,946 (GRCm39) |
|
probably null |
Het |
Piezo2 |
A |
G |
18: 63,216,202 (GRCm39) |
C960R |
probably damaging |
Het |
Pitx2 |
T |
C |
3: 129,012,488 (GRCm39) |
V306A |
probably damaging |
Het |
Pkd1l2 |
C |
A |
8: 117,792,236 (GRCm39) |
|
probably benign |
Het |
Plekho1 |
T |
C |
3: 95,896,878 (GRCm39) |
E197G |
probably damaging |
Het |
Polr2i |
A |
G |
7: 29,932,227 (GRCm39) |
N34S |
probably damaging |
Het |
Psph |
A |
T |
5: 129,848,614 (GRCm39) |
D22E |
probably damaging |
Het |
Ptprs |
C |
A |
17: 56,731,128 (GRCm39) |
A687S |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,788,265 (GRCm39) |
K606R |
probably benign |
Het |
Rigi |
A |
G |
4: 40,208,868 (GRCm39) |
V703A |
possibly damaging |
Het |
Rims1 |
A |
G |
1: 22,577,362 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
C |
T |
11: 119,328,576 (GRCm39) |
P2002L |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,740,307 (GRCm39) |
C555S |
probably damaging |
Het |
Sftpd |
C |
A |
14: 40,894,384 (GRCm39) |
G345V |
probably damaging |
Het |
Slc41a1 |
T |
A |
1: 131,774,319 (GRCm39) |
M462K |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,264,990 (GRCm39) |
E676G |
probably damaging |
Het |
Sox6 |
T |
A |
7: 115,300,926 (GRCm39) |
|
probably benign |
Het |
Spdye4b |
G |
A |
5: 143,181,472 (GRCm39) |
R109Q |
probably damaging |
Het |
Spef1l |
C |
A |
7: 139,556,555 (GRCm39) |
R144L |
probably benign |
Het |
Spink8 |
A |
T |
9: 109,649,706 (GRCm39) |
I63L |
probably damaging |
Het |
St3gal3 |
A |
G |
4: 117,871,983 (GRCm39) |
L73P |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,871,818 (GRCm39) |
L1247P |
probably benign |
Het |
Tat |
A |
G |
8: 110,718,195 (GRCm39) |
R27G |
probably benign |
Het |
Tcerg1l |
C |
T |
7: 137,881,804 (GRCm39) |
R295H |
probably damaging |
Het |
Tfrc |
T |
C |
16: 32,445,467 (GRCm39) |
V596A |
probably damaging |
Het |
Tgfb3 |
C |
T |
12: 86,116,120 (GRCm39) |
|
probably null |
Het |
Tmed5 |
A |
T |
5: 108,280,248 (GRCm39) |
S15T |
probably benign |
Het |
Tph1 |
A |
T |
7: 46,303,286 (GRCm39) |
S231T |
probably benign |
Het |
Trim30d |
G |
A |
7: 104,121,701 (GRCm39) |
S198L |
probably damaging |
Het |
Trpm6 |
T |
C |
19: 18,773,859 (GRCm39) |
M412T |
probably benign |
Het |
Ttn |
G |
T |
2: 76,612,589 (GRCm39) |
D15417E |
probably benign |
Het |
U2surp |
A |
G |
9: 95,375,251 (GRCm39) |
I157T |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,156,890 (GRCm39) |
D2305G |
probably damaging |
Het |
Uvssa |
A |
G |
5: 33,546,165 (GRCm39) |
K179E |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,359,436 (GRCm39) |
F230S |
probably damaging |
Het |
Xirp2 |
A |
G |
2: 67,355,411 (GRCm39) |
K3391E |
probably benign |
Het |
Xpo7 |
T |
A |
14: 70,936,473 (GRCm39) |
H170L |
probably benign |
Het |
Zrsr2-ps1 |
T |
C |
11: 22,924,404 (GRCm39) |
W393R |
probably benign |
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 |
R0639:Foxn1
|
UTSW |
11 |
78,261,970 (GRCm39) |
missense |
possibly damaging |
0.67 |
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 |
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 |
|