Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
C |
G |
4: 129,901,624 (GRCm39) |
P416R |
probably damaging |
Het |
Adgre1 |
A |
G |
17: 57,709,742 (GRCm39) |
D133G |
unknown |
Het |
Alpl |
A |
C |
4: 137,476,887 (GRCm39) |
|
probably null |
Het |
Ankrd65 |
T |
C |
4: 155,875,133 (GRCm39) |
|
probably benign |
Het |
Baalc |
A |
T |
15: 38,797,480 (GRCm39) |
|
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,070,820 (GRCm39) |
T204A |
probably benign |
Het |
Bud31 |
A |
G |
5: 145,083,265 (GRCm39) |
Y77C |
probably damaging |
Het |
Calhm6 |
G |
A |
10: 34,003,647 (GRCm39) |
R87* |
probably null |
Het |
Capsl |
A |
G |
15: 9,461,930 (GRCm39) |
|
probably benign |
Het |
Ccna1 |
A |
G |
3: 54,956,004 (GRCm39) |
V116A |
probably damaging |
Het |
Cdc42bpa |
C |
A |
1: 179,928,755 (GRCm39) |
H723N |
probably benign |
Het |
CK137956 |
C |
T |
4: 127,845,093 (GRCm39) |
V217I |
probably benign |
Het |
Cog5 |
A |
G |
12: 31,919,460 (GRCm39) |
T540A |
probably damaging |
Het |
Cps1 |
T |
C |
1: 67,196,995 (GRCm39) |
W349R |
probably damaging |
Het |
Crispld2 |
G |
T |
8: 120,752,806 (GRCm39) |
V285L |
probably benign |
Het |
Crtc2 |
T |
A |
3: 90,170,804 (GRCm39) |
F626I |
probably damaging |
Het |
Daam1 |
G |
A |
12: 71,991,154 (GRCm39) |
R256H |
unknown |
Het |
Dhx38 |
G |
T |
8: 110,288,576 (GRCm39) |
|
probably benign |
Het |
Dok4 |
G |
A |
8: 95,591,764 (GRCm39) |
A324V |
probably benign |
Het |
Dscam |
T |
C |
16: 96,626,982 (GRCm39) |
|
probably null |
Het |
Dusp16 |
A |
T |
6: 134,695,365 (GRCm39) |
S489T |
probably benign |
Het |
Ecpas |
A |
G |
4: 58,864,418 (GRCm39) |
W288R |
probably damaging |
Het |
Erbin |
A |
T |
13: 103,970,866 (GRCm39) |
Y917N |
probably damaging |
Het |
F13b |
A |
T |
1: 139,450,297 (GRCm39) |
|
probably null |
Het |
Fdx1 |
C |
A |
9: 51,874,725 (GRCm39) |
A15S |
probably benign |
Het |
Ffar4 |
A |
T |
19: 38,085,630 (GRCm39) |
Q19L |
probably benign |
Het |
Folh1 |
A |
C |
7: 86,395,400 (GRCm39) |
V344G |
probably damaging |
Het |
Fscb |
T |
A |
12: 64,520,292 (GRCm39) |
E391D |
possibly damaging |
Het |
Gigyf2 |
G |
A |
1: 87,368,568 (GRCm39) |
G1083R |
probably damaging |
Het |
Gm14403 |
C |
A |
2: 177,200,359 (GRCm39) |
H102N |
probably benign |
Het |
Gm4847 |
A |
G |
1: 166,457,961 (GRCm39) |
F464S |
probably damaging |
Het |
Gpam |
A |
T |
19: 55,084,611 (GRCm39) |
M56K |
possibly damaging |
Het |
Gpr165 |
T |
A |
X: 95,760,778 (GRCm39) |
F352I |
probably damaging |
Het |
Grik2 |
T |
G |
10: 48,977,260 (GRCm39) |
I891L |
probably damaging |
Het |
Gsr |
T |
C |
8: 34,171,603 (GRCm39) |
|
probably benign |
Het |
Hhla1 |
A |
G |
15: 65,808,140 (GRCm39) |
F302L |
probably benign |
Het |
Impg1 |
T |
C |
9: 80,252,590 (GRCm39) |
D453G |
possibly damaging |
Het |
Inpp5d |
T |
A |
1: 87,625,872 (GRCm39) |
V495E |
possibly damaging |
Het |
Iqca1l |
A |
T |
5: 24,759,626 (GRCm39) |
L48Q |
probably damaging |
Het |
Iqce |
A |
T |
5: 140,660,990 (GRCm39) |
L450H |
probably damaging |
Het |
Itfg2 |
A |
G |
6: 128,390,486 (GRCm39) |
|
probably null |
Het |
Kif13a |
A |
G |
13: 46,966,218 (GRCm39) |
V400A |
possibly damaging |
Het |
Kif7 |
T |
C |
7: 79,363,629 (GRCm39) |
Y93C |
probably damaging |
Het |
Krt33a |
A |
G |
11: 99,906,909 (GRCm39) |
V22A |
probably benign |
Het |
Lct |
T |
C |
1: 128,228,319 (GRCm39) |
D1058G |
probably damaging |
Het |
Lrp6 |
G |
T |
6: 134,457,481 (GRCm39) |
D774E |
possibly damaging |
Het |
Lrrc9 |
T |
A |
12: 72,525,537 (GRCm39) |
S828R |
possibly damaging |
Het |
Ly75 |
A |
G |
2: 60,138,620 (GRCm39) |
W1416R |
probably damaging |
Het |
Mdh2 |
T |
C |
5: 135,819,004 (GRCm39) |
I320T |
possibly damaging |
Het |
Med13l |
T |
A |
5: 118,876,560 (GRCm39) |
V912E |
probably damaging |
Het |
Mgarp |
T |
C |
3: 51,296,456 (GRCm39) |
D182G |
possibly damaging |
Het |
Mllt10 |
T |
C |
2: 18,151,698 (GRCm39) |
|
probably benign |
Het |
Mmp28 |
G |
A |
11: 83,334,629 (GRCm39) |
A375V |
probably damaging |
Het |
Mrps23 |
T |
A |
11: 88,101,511 (GRCm39) |
H133Q |
probably benign |
Het |
Msh6 |
T |
C |
17: 88,282,679 (GRCm39) |
S35P |
probably benign |
Het |
Myo3a |
A |
G |
2: 22,328,447 (GRCm39) |
D347G |
possibly damaging |
Het |
Npc1l1 |
T |
C |
11: 6,173,040 (GRCm39) |
K800E |
possibly damaging |
Het |
Or2ag13 |
A |
T |
7: 106,473,084 (GRCm39) |
Y123N |
probably damaging |
Het |
Or51ai2 |
T |
C |
7: 103,586,971 (GRCm39) |
I128T |
probably benign |
Het |
Or5i1 |
T |
G |
2: 87,613,166 (GRCm39) |
I94S |
probably damaging |
Het |
Or5m9 |
T |
C |
2: 85,876,931 (GRCm39) |
V35A |
probably benign |
Het |
Or5m9 |
T |
C |
2: 85,877,278 (GRCm39) |
F151L |
possibly damaging |
Het |
Or5t7 |
G |
A |
2: 86,506,834 (GRCm39) |
P281L |
probably damaging |
Het |
Or6p1 |
T |
A |
1: 174,258,129 (GRCm39) |
I45N |
possibly damaging |
Het |
Osmr |
A |
C |
15: 6,853,999 (GRCm39) |
W570G |
probably damaging |
Het |
Otol1 |
A |
T |
3: 69,935,117 (GRCm39) |
I370F |
probably damaging |
Het |
Pank2 |
A |
G |
2: 131,122,180 (GRCm39) |
Y235C |
probably damaging |
Het |
Pias2 |
T |
C |
18: 77,193,581 (GRCm39) |
S187P |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,383,086 (GRCm39) |
N1115S |
probably benign |
Het |
Pld1 |
G |
T |
3: 28,163,966 (GRCm39) |
A800S |
probably damaging |
Het |
Prex2 |
T |
C |
1: 11,256,857 (GRCm39) |
|
probably benign |
Het |
Ptpn3 |
T |
C |
4: 57,194,304 (GRCm39) |
Q908R |
probably benign |
Het |
Rab3gap2 |
T |
A |
1: 184,984,589 (GRCm39) |
|
probably benign |
Het |
Rbm24 |
A |
T |
13: 46,573,826 (GRCm39) |
N82Y |
probably damaging |
Het |
Rpl27 |
T |
C |
11: 101,336,081 (GRCm39) |
V47A |
possibly damaging |
Het |
Serpina1f |
A |
G |
12: 103,659,826 (GRCm39) |
V152A |
possibly damaging |
Het |
Serpina5 |
A |
G |
12: 104,068,392 (GRCm39) |
Y151C |
probably damaging |
Het |
Serpinb7 |
A |
G |
1: 107,379,737 (GRCm39) |
*381W |
probably null |
Het |
Sh2b2 |
A |
G |
5: 136,261,117 (GRCm39) |
F33S |
probably damaging |
Het |
Slc22a2 |
A |
C |
17: 12,834,159 (GRCm39) |
I476L |
probably benign |
Het |
Slc6a12 |
A |
T |
6: 121,332,331 (GRCm39) |
I222F |
probably benign |
Het |
Smim26 |
G |
A |
2: 144,437,033 (GRCm39) |
D61N |
probably damaging |
Het |
Soat1 |
A |
T |
1: 156,268,924 (GRCm39) |
Y209N |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,902,667 (GRCm39) |
H1630R |
probably null |
Het |
Sptlc2 |
A |
T |
12: 87,393,580 (GRCm39) |
|
probably null |
Het |
Strn3 |
G |
A |
12: 51,657,187 (GRCm39) |
T642I |
probably damaging |
Het |
Syce1l |
T |
A |
8: 114,380,700 (GRCm39) |
D137E |
possibly damaging |
Het |
Syne2 |
T |
C |
12: 76,028,837 (GRCm39) |
|
probably null |
Het |
Tcf25 |
C |
A |
8: 124,108,203 (GRCm39) |
P86Q |
probably benign |
Het |
Tmem19 |
A |
T |
10: 115,197,715 (GRCm39) |
Y43* |
probably null |
Het |
Tmem30b |
T |
C |
12: 73,592,942 (GRCm39) |
N58D |
probably benign |
Het |
Tnn |
A |
C |
1: 159,948,327 (GRCm39) |
I795M |
probably damaging |
Het |
Tnpo1 |
A |
G |
13: 98,991,954 (GRCm39) |
Y641H |
probably damaging |
Het |
Tra2a |
A |
T |
6: 49,227,889 (GRCm39) |
|
probably benign |
Het |
Trappc8 |
A |
T |
18: 20,999,243 (GRCm39) |
F295I |
probably benign |
Het |
Vmn2r101 |
T |
A |
17: 19,809,245 (GRCm39) |
W125R |
probably damaging |
Het |
Vps8 |
C |
A |
16: 21,261,107 (GRCm39) |
F82L |
probably damaging |
Het |
Ythdf2 |
A |
T |
4: 131,931,779 (GRCm39) |
S460R |
probably damaging |
Het |
|
Other mutations in Cfap161 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01827:Cfap161
|
APN |
7 |
83,442,648 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01999:Cfap161
|
APN |
7 |
83,440,899 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02291:Cfap161
|
APN |
7 |
83,440,847 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02444:Cfap161
|
APN |
7 |
83,425,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Cfap161
|
UTSW |
7 |
83,442,484 (GRCm39) |
missense |
probably null |
0.01 |
R1599:Cfap161
|
UTSW |
7 |
83,425,287 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1828:Cfap161
|
UTSW |
7 |
83,440,932 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2117:Cfap161
|
UTSW |
7 |
83,425,184 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2262:Cfap161
|
UTSW |
7 |
83,442,580 (GRCm39) |
missense |
probably benign |
0.37 |
R3618:Cfap161
|
UTSW |
7 |
83,429,390 (GRCm39) |
nonsense |
probably null |
|
R4015:Cfap161
|
UTSW |
7 |
83,429,479 (GRCm39) |
missense |
probably benign |
0.01 |
R5821:Cfap161
|
UTSW |
7 |
83,425,188 (GRCm39) |
missense |
probably benign |
0.38 |
R6477:Cfap161
|
UTSW |
7 |
83,443,230 (GRCm39) |
nonsense |
probably null |
|
R6478:Cfap161
|
UTSW |
7 |
83,442,484 (GRCm39) |
missense |
probably benign |
0.00 |
R7108:Cfap161
|
UTSW |
7 |
83,442,518 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7203:Cfap161
|
UTSW |
7 |
83,425,258 (GRCm39) |
missense |
probably damaging |
0.97 |
R7582:Cfap161
|
UTSW |
7 |
83,426,290 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8714:Cfap161
|
UTSW |
7 |
83,442,482 (GRCm39) |
missense |
probably benign |
0.11 |
R8762:Cfap161
|
UTSW |
7 |
83,443,282 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9587:Cfap161
|
UTSW |
7 |
83,440,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Cfap161
|
UTSW |
7 |
83,442,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9702:Cfap161
|
UTSW |
7 |
83,442,652 (GRCm39) |
missense |
probably benign |
0.00 |
|