Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
T |
2: 151,314,062 (GRCm39) |
S539T |
possibly damaging |
Het |
Abcc6 |
C |
T |
7: 45,634,569 (GRCm39) |
R1136Q |
probably benign |
Het |
Abhd12b |
A |
C |
12: 70,213,708 (GRCm39) |
|
probably null |
Het |
Agk |
T |
G |
6: 40,334,050 (GRCm39) |
V98G |
possibly damaging |
Het |
Apbb2 |
A |
G |
5: 66,609,252 (GRCm39) |
S132P |
probably damaging |
Het |
Apc2 |
T |
C |
10: 80,142,046 (GRCm39) |
S322P |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,293,667 (GRCm39) |
V486A |
probably benign |
Het |
Asxl2 |
A |
G |
12: 3,507,200 (GRCm39) |
K131E |
probably damaging |
Het |
Atp13a4 |
A |
G |
16: 29,260,398 (GRCm39) |
V560A |
|
Het |
Bnc1 |
C |
T |
7: 81,623,719 (GRCm39) |
G503S |
probably damaging |
Het |
Bsn |
C |
A |
9: 107,987,704 (GRCm39) |
V2683F |
unknown |
Het |
Btbd7 |
A |
T |
12: 102,804,241 (GRCm39) |
N266K |
probably benign |
Het |
Ccdc121rt2 |
T |
C |
5: 112,597,681 (GRCm39) |
V76A |
probably benign |
Het |
Cdca7l |
G |
A |
12: 117,839,346 (GRCm39) |
D350N |
possibly damaging |
Het |
Cfap251 |
A |
G |
5: 123,411,913 (GRCm39) |
D515G |
probably benign |
Het |
Ciao2a |
A |
T |
9: 66,045,667 (GRCm39) |
N145I |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,696,171 (GRCm39) |
D3239V |
unknown |
Het |
Col9a1 |
T |
A |
1: 24,224,208 (GRCm39) |
I130N |
unknown |
Het |
Cr2 |
A |
G |
1: 194,840,913 (GRCm39) |
W460R |
probably damaging |
Het |
Cyb561d2 |
A |
G |
9: 107,417,583 (GRCm39) |
F56S |
probably damaging |
Het |
Dnaaf1 |
A |
G |
8: 120,302,194 (GRCm39) |
I32V |
probably benign |
Het |
Dnah11 |
T |
A |
12: 117,958,950 (GRCm39) |
T2978S |
possibly damaging |
Het |
Dsg2 |
T |
A |
18: 20,716,056 (GRCm39) |
D302E |
probably damaging |
Het |
Gimap8 |
C |
A |
6: 48,633,545 (GRCm39) |
Q455K |
probably benign |
Het |
Hps6 |
C |
G |
19: 45,994,141 (GRCm39) |
R693G |
possibly damaging |
Het |
Irx1 |
C |
T |
13: 72,107,635 (GRCm39) |
G349D |
probably damaging |
Het |
Itga8 |
C |
G |
2: 12,187,495 (GRCm39) |
G728A |
probably damaging |
Het |
Lcat |
T |
C |
8: 106,666,710 (GRCm39) |
T271A |
possibly damaging |
Het |
Mapkapk2 |
T |
C |
1: 130,983,679 (GRCm39) |
H308R |
probably damaging |
Het |
Mast1 |
A |
T |
8: 85,642,953 (GRCm39) |
N947K |
probably damaging |
Het |
Mpeg1 |
A |
T |
19: 12,440,419 (GRCm39) |
I626F |
probably damaging |
Het |
Mrtfa |
T |
C |
15: 80,902,274 (GRCm39) |
S349G |
possibly damaging |
Het |
Myh15 |
T |
C |
16: 49,015,900 (GRCm39) |
S1859P |
possibly damaging |
Het |
Nlrx1 |
A |
T |
9: 44,167,712 (GRCm39) |
D728E |
probably benign |
Het |
Or1j8 |
A |
G |
2: 36,192,387 (GRCm39) |
T279A |
probably benign |
Het |
Or8c19-ps1 |
G |
T |
9: 38,220,516 (GRCm39) |
V142F |
probably benign |
Het |
Pcdhb18 |
A |
T |
18: 37,624,562 (GRCm39) |
S631C |
probably damaging |
Het |
Pcdhga11 |
C |
A |
18: 37,890,364 (GRCm39) |
Y457* |
probably null |
Het |
Pcdhga5 |
T |
C |
18: 37,829,823 (GRCm39) |
I757T |
probably benign |
Het |
Pcgf5 |
G |
A |
19: 36,389,348 (GRCm39) |
|
probably benign |
Het |
Pdf |
A |
G |
8: 107,775,100 (GRCm39) |
V44A |
possibly damaging |
Het |
Pip4p1 |
T |
C |
14: 51,166,503 (GRCm39) |
T194A |
possibly damaging |
Het |
Prtg |
A |
T |
9: 72,819,583 (GRCm39) |
*1192L |
probably null |
Het |
Ptk7 |
A |
G |
17: 46,877,193 (GRCm39) |
F955S |
possibly damaging |
Het |
Rbp3 |
C |
A |
14: 33,684,492 (GRCm39) |
Q1174K |
possibly damaging |
Het |
Rufy1 |
T |
C |
11: 50,321,796 (GRCm39) |
D46G |
possibly damaging |
Het |
Sbf2 |
A |
G |
7: 109,948,202 (GRCm39) |
V1216A |
probably benign |
Het |
Serpina11 |
A |
G |
12: 103,952,722 (GRCm39) |
V18A |
unknown |
Het |
Serpinb6a |
T |
A |
13: 34,115,543 (GRCm39) |
N47I |
probably damaging |
Het |
Shc2 |
T |
C |
10: 79,456,924 (GRCm39) |
H564R |
probably damaging |
Het |
Sirt7 |
T |
A |
11: 120,514,888 (GRCm39) |
R115* |
probably null |
Het |
Slc22a14 |
A |
T |
9: 119,059,290 (GRCm39) |
|
probably benign |
Het |
Stra8 |
T |
A |
6: 34,912,581 (GRCm39) |
S331T |
probably damaging |
Het |
Tm9sf2 |
A |
G |
14: 122,380,883 (GRCm39) |
T324A |
probably benign |
Het |
Tmem268 |
T |
C |
4: 63,498,530 (GRCm39) |
S224P |
probably benign |
Het |
Tns1 |
T |
C |
1: 73,976,407 (GRCm39) |
D1147G |
probably damaging |
Het |
Tomm22 |
C |
T |
15: 79,555,311 (GRCm39) |
|
probably benign |
Het |
Top1 |
A |
G |
2: 160,556,158 (GRCm39) |
Y539C |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,009,552 (GRCm39) |
|
probably benign |
Het |
Trav3-1 |
T |
C |
14: 52,818,428 (GRCm39) |
V34A |
probably damaging |
Het |
Tspyl5 |
T |
C |
15: 33,687,238 (GRCm39) |
N236D |
possibly damaging |
Het |
Ttc41 |
A |
G |
10: 86,565,679 (GRCm39) |
D411G |
probably benign |
Het |
Vmn1r128 |
A |
T |
7: 21,083,922 (GRCm39) |
M209L |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,355,527 (GRCm39) |
D3429E |
probably benign |
Het |
Zfp418 |
A |
T |
7: 7,185,797 (GRCm39) |
T587S |
probably benign |
Het |
|
Other mutations in Faf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00519:Faf1
|
APN |
4 |
109,697,578 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00569:Faf1
|
APN |
4 |
109,819,077 (GRCm39) |
makesense |
probably null |
|
IGL01398:Faf1
|
APN |
4 |
109,593,793 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01640:Faf1
|
APN |
4 |
109,697,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01739:Faf1
|
APN |
4 |
109,534,278 (GRCm39) |
splice site |
probably benign |
|
IGL02265:Faf1
|
APN |
4 |
109,600,101 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02372:Faf1
|
APN |
4 |
109,792,779 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02999:Faf1
|
APN |
4 |
109,719,090 (GRCm39) |
missense |
probably benign |
0.01 |
R0058:Faf1
|
UTSW |
4 |
109,593,821 (GRCm39) |
missense |
probably benign |
0.00 |
R0058:Faf1
|
UTSW |
4 |
109,593,821 (GRCm39) |
missense |
probably benign |
0.00 |
R0098:Faf1
|
UTSW |
4 |
109,792,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0098:Faf1
|
UTSW |
4 |
109,792,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0183:Faf1
|
UTSW |
4 |
109,792,807 (GRCm39) |
missense |
probably benign |
|
R0463:Faf1
|
UTSW |
4 |
109,748,138 (GRCm39) |
missense |
probably benign |
0.02 |
R0505:Faf1
|
UTSW |
4 |
109,697,600 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0755:Faf1
|
UTSW |
4 |
109,819,036 (GRCm39) |
missense |
probably benign |
0.00 |
R1705:Faf1
|
UTSW |
4 |
109,534,199 (GRCm39) |
start gained |
probably benign |
|
R2061:Faf1
|
UTSW |
4 |
109,568,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Faf1
|
UTSW |
4 |
109,568,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Faf1
|
UTSW |
4 |
109,568,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R2696:Faf1
|
UTSW |
4 |
109,698,525 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3937:Faf1
|
UTSW |
4 |
109,614,889 (GRCm39) |
splice site |
probably benign |
|
R3939:Faf1
|
UTSW |
4 |
109,719,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4602:Faf1
|
UTSW |
4 |
109,584,625 (GRCm39) |
missense |
probably benign |
|
R4727:Faf1
|
UTSW |
4 |
109,697,564 (GRCm39) |
missense |
probably damaging |
0.96 |
R4860:Faf1
|
UTSW |
4 |
109,600,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R4860:Faf1
|
UTSW |
4 |
109,600,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R4896:Faf1
|
UTSW |
4 |
109,699,496 (GRCm39) |
missense |
probably benign |
0.02 |
R4913:Faf1
|
UTSW |
4 |
109,792,746 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5688:Faf1
|
UTSW |
4 |
109,652,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R5721:Faf1
|
UTSW |
4 |
109,792,863 (GRCm39) |
missense |
probably benign |
0.34 |
R5905:Faf1
|
UTSW |
4 |
109,748,126 (GRCm39) |
missense |
probably benign |
0.03 |
R6190:Faf1
|
UTSW |
4 |
109,719,012 (GRCm39) |
missense |
probably damaging |
0.97 |
R6364:Faf1
|
UTSW |
4 |
109,818,997 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6454:Faf1
|
UTSW |
4 |
109,699,531 (GRCm39) |
missense |
probably benign |
0.27 |
R6805:Faf1
|
UTSW |
4 |
109,719,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R7101:Faf1
|
UTSW |
4 |
109,783,153 (GRCm39) |
missense |
probably benign |
0.12 |
R7381:Faf1
|
UTSW |
4 |
109,719,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R7392:Faf1
|
UTSW |
4 |
109,652,040 (GRCm39) |
missense |
probably benign |
0.01 |
R7584:Faf1
|
UTSW |
4 |
109,783,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R7660:Faf1
|
UTSW |
4 |
109,719,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R7678:Faf1
|
UTSW |
4 |
109,687,061 (GRCm39) |
missense |
probably benign |
0.00 |
R7715:Faf1
|
UTSW |
4 |
109,568,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R7721:Faf1
|
UTSW |
4 |
109,593,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Faf1
|
UTSW |
4 |
109,698,550 (GRCm39) |
missense |
probably benign |
0.01 |
R9028:Faf1
|
UTSW |
4 |
109,748,105 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9646:Faf1
|
UTSW |
4 |
109,652,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R9700:Faf1
|
UTSW |
4 |
109,748,179 (GRCm39) |
missense |
possibly damaging |
0.48 |
Z1176:Faf1
|
UTSW |
4 |
109,697,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|