Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
T |
C |
17: 24,526,427 (GRCm39) |
Y619C |
probably damaging |
Het |
Adck1 |
A |
G |
12: 88,368,949 (GRCm39) |
|
probably null |
Het |
Agap3 |
A |
C |
5: 24,656,123 (GRCm39) |
|
probably null |
Het |
Ankib1 |
A |
T |
5: 3,782,566 (GRCm39) |
H354Q |
probably damaging |
Het |
Ankrd29 |
T |
G |
18: 12,387,679 (GRCm39) |
N301T |
probably benign |
Het |
Arhgef4 |
A |
G |
1: 34,846,356 (GRCm39) |
T379A |
probably damaging |
Het |
Arid1a |
A |
G |
4: 133,480,417 (GRCm39) |
V169A |
probably benign |
Het |
Bag2 |
T |
C |
1: 33,787,417 (GRCm39) |
|
probably null |
Het |
Bmt2 |
A |
C |
6: 13,628,686 (GRCm39) |
Y332* |
probably null |
Het |
Bpifb1 |
A |
T |
2: 154,053,501 (GRCm39) |
K248* |
probably null |
Het |
Caap1 |
C |
A |
4: 94,444,751 (GRCm39) |
|
probably null |
Het |
Calcr |
T |
A |
6: 3,692,576 (GRCm39) |
Y389F |
probably damaging |
Het |
Capn1 |
C |
T |
19: 6,043,946 (GRCm39) |
V562I |
probably benign |
Het |
Ccr1 |
T |
A |
9: 123,763,985 (GRCm39) |
T182S |
probably benign |
Het |
Ceacam15 |
T |
C |
7: 16,407,259 (GRCm39) |
D86G |
probably benign |
Het |
Cldnd1 |
C |
T |
16: 58,550,006 (GRCm39) |
T63I |
probably benign |
Het |
Col12a1 |
A |
T |
9: 79,559,368 (GRCm39) |
|
probably null |
Het |
Cystm1 |
A |
G |
18: 36,526,348 (GRCm39) |
|
probably benign |
Het |
Ddx55 |
T |
A |
5: 124,705,028 (GRCm39) |
Y428* |
probably null |
Het |
Ensa |
G |
A |
3: 95,538,745 (GRCm39) |
G118D |
probably benign |
Het |
Folh1 |
A |
T |
7: 86,372,482 (GRCm39) |
|
probably null |
Het |
Foxj2 |
C |
A |
6: 122,814,948 (GRCm39) |
P328Q |
probably damaging |
Het |
Fscn3 |
A |
G |
6: 28,435,627 (GRCm39) |
I417V |
probably damaging |
Het |
Galnt7 |
T |
C |
8: 57,995,761 (GRCm39) |
|
probably benign |
Het |
Gm11563 |
T |
A |
11: 99,549,246 (GRCm39) |
*169C |
probably null |
Het |
Hfm1 |
A |
T |
5: 107,049,709 (GRCm39) |
D417E |
possibly damaging |
Het |
Ighv15-2 |
A |
G |
12: 114,528,230 (GRCm39) |
S107P |
probably damaging |
Het |
Itsn2 |
A |
G |
12: 4,711,944 (GRCm39) |
D904G |
probably damaging |
Het |
Kif1b |
A |
T |
4: 149,322,339 (GRCm39) |
L860* |
probably null |
Het |
Krt79 |
T |
C |
15: 101,839,119 (GRCm39) |
E450G |
probably damaging |
Het |
Lama1 |
T |
C |
17: 68,045,775 (GRCm39) |
S227P |
probably damaging |
Het |
Lamp5 |
C |
A |
2: 135,902,786 (GRCm39) |
H168Q |
probably benign |
Het |
Lilra5 |
A |
T |
7: 4,245,076 (GRCm39) |
Q240L |
possibly damaging |
Het |
Lrp1 |
A |
T |
10: 127,385,813 (GRCm39) |
C3521S |
probably benign |
Het |
Mroh1 |
T |
A |
15: 76,292,730 (GRCm39) |
|
probably null |
Het |
Nlrp4g |
A |
T |
9: 124,349,515 (GRCm38) |
|
noncoding transcript |
Het |
Nr2f6 |
A |
T |
8: 71,831,179 (GRCm39) |
I70N |
probably benign |
Het |
Nr4a2 |
T |
A |
2: 57,000,163 (GRCm39) |
D311V |
probably damaging |
Het |
Odad2 |
G |
A |
18: 7,286,763 (GRCm39) |
T156M |
probably benign |
Het |
Or10w1 |
T |
A |
19: 13,632,750 (GRCm39) |
M319K |
probably benign |
Het |
Or10x4 |
T |
C |
1: 174,219,442 (GRCm39) |
L269P |
probably damaging |
Het |
Or52n20 |
T |
A |
7: 104,320,711 (GRCm39) |
F267L |
probably damaging |
Het |
Pcgf6 |
A |
G |
19: 47,036,545 (GRCm39) |
|
probably null |
Het |
Prc1 |
C |
A |
7: 79,962,911 (GRCm39) |
H131Q |
probably benign |
Het |
Ptprq |
C |
A |
10: 107,360,114 (GRCm39) |
R2187L |
probably damaging |
Het |
Rasl2-9 |
C |
A |
7: 5,128,702 (GRCm39) |
R76L |
possibly damaging |
Het |
Rdh16f1 |
A |
T |
10: 127,626,685 (GRCm39) |
Y246F |
probably benign |
Het |
Rit1 |
T |
C |
3: 88,624,982 (GRCm39) |
|
probably benign |
Het |
Sash1 |
A |
G |
10: 8,605,672 (GRCm39) |
V906A |
probably benign |
Het |
Scnn1b |
T |
C |
7: 121,501,509 (GRCm39) |
V108A |
probably benign |
Het |
Sema4f |
A |
T |
6: 82,895,265 (GRCm39) |
I356N |
probably damaging |
Het |
Shc4 |
A |
T |
2: 125,491,197 (GRCm39) |
L447Q |
probably damaging |
Het |
Slc24a1 |
T |
C |
9: 64,856,758 (GRCm39) |
M50V |
unknown |
Het |
Slc28a3 |
T |
A |
13: 58,722,077 (GRCm39) |
D269V |
possibly damaging |
Het |
Slc35e1 |
A |
G |
8: 73,246,166 (GRCm39) |
S89P |
possibly damaging |
Het |
Smpd5 |
T |
A |
15: 76,179,008 (GRCm39) |
H125Q |
probably benign |
Het |
Snapc2 |
A |
G |
8: 4,304,578 (GRCm39) |
T31A |
probably damaging |
Het |
Sox5 |
G |
C |
6: 143,779,214 (GRCm39) |
H606D |
possibly damaging |
Het |
Spag6 |
A |
G |
2: 18,742,107 (GRCm39) |
T367A |
possibly damaging |
Het |
Spag8 |
T |
C |
4: 43,651,636 (GRCm39) |
T413A |
probably damaging |
Het |
Sptlc3 |
G |
A |
2: 139,389,087 (GRCm39) |
G156R |
probably damaging |
Het |
Stx19 |
A |
G |
16: 62,642,783 (GRCm39) |
T200A |
probably benign |
Het |
Tas2r116 |
A |
G |
6: 132,832,668 (GRCm39) |
T90A |
probably benign |
Het |
Tasor2 |
G |
A |
13: 3,640,069 (GRCm39) |
T356I |
probably benign |
Het |
Tbl3 |
A |
G |
17: 24,924,304 (GRCm39) |
|
probably benign |
Het |
Tekt5 |
G |
T |
16: 10,213,058 (GRCm39) |
P76T |
probably damaging |
Het |
Tjp2 |
C |
T |
19: 24,074,030 (GRCm39) |
E1086K |
possibly damaging |
Het |
Topbp1 |
T |
C |
9: 103,200,770 (GRCm39) |
L601P |
probably damaging |
Het |
Trav16 |
T |
A |
14: 53,980,934 (GRCm39) |
M41K |
possibly damaging |
Het |
Trav6-5 |
C |
A |
14: 53,728,960 (GRCm39) |
N72K |
probably benign |
Het |
Trpm3 |
C |
G |
19: 22,692,659 (GRCm39) |
T250S |
possibly damaging |
Het |
Vps35 |
A |
T |
8: 85,987,891 (GRCm39) |
D753E |
probably benign |
Het |
Vstm2a |
A |
T |
11: 16,213,061 (GRCm39) |
N149Y |
probably damaging |
Het |
Vwa2 |
G |
T |
19: 56,895,318 (GRCm39) |
M497I |
probably benign |
Het |
Zfat |
C |
A |
15: 68,052,223 (GRCm39) |
V517L |
probably benign |
Het |
Zfp169 |
C |
A |
13: 48,643,708 (GRCm39) |
R473L |
possibly damaging |
Het |
Zfp672 |
T |
C |
11: 58,220,324 (GRCm39) |
|
probably benign |
Het |
Zranb1 |
T |
C |
7: 132,574,443 (GRCm39) |
V420A |
probably damaging |
Het |
|
Other mutations in Pcdhb6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Pcdhb6
|
APN |
18 |
37,467,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02123:Pcdhb6
|
APN |
18 |
37,468,873 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02491:Pcdhb6
|
APN |
18 |
37,468,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02496:Pcdhb6
|
APN |
18 |
37,468,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02608:Pcdhb6
|
APN |
18 |
37,467,747 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03130:Pcdhb6
|
APN |
18 |
37,468,640 (GRCm39) |
nonsense |
probably null |
|
IGL03144:Pcdhb6
|
APN |
18 |
37,467,459 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03189:Pcdhb6
|
APN |
18 |
37,469,205 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03203:Pcdhb6
|
APN |
18 |
37,467,585 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03388:Pcdhb6
|
APN |
18 |
37,469,190 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4445001:Pcdhb6
|
UTSW |
18 |
37,468,300 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0571:Pcdhb6
|
UTSW |
18 |
37,468,167 (GRCm39) |
missense |
probably benign |
0.01 |
R0734:Pcdhb6
|
UTSW |
18 |
37,468,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R1727:Pcdhb6
|
UTSW |
18 |
37,467,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Pcdhb6
|
UTSW |
18 |
37,468,633 (GRCm39) |
missense |
probably benign |
0.10 |
R2207:Pcdhb6
|
UTSW |
18 |
37,468,633 (GRCm39) |
missense |
probably benign |
0.10 |
R2303:Pcdhb6
|
UTSW |
18 |
37,469,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R2401:Pcdhb6
|
UTSW |
18 |
37,468,222 (GRCm39) |
missense |
probably benign |
0.35 |
R3409:Pcdhb6
|
UTSW |
18 |
37,468,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R3411:Pcdhb6
|
UTSW |
18 |
37,468,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R3625:Pcdhb6
|
UTSW |
18 |
37,469,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Pcdhb6
|
UTSW |
18 |
37,469,259 (GRCm39) |
missense |
probably benign |
0.01 |
R4821:Pcdhb6
|
UTSW |
18 |
37,467,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R5218:Pcdhb6
|
UTSW |
18 |
37,467,388 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5465:Pcdhb6
|
UTSW |
18 |
37,467,783 (GRCm39) |
missense |
probably damaging |
0.97 |
R5522:Pcdhb6
|
UTSW |
18 |
37,467,402 (GRCm39) |
missense |
probably benign |
|
R5556:Pcdhb6
|
UTSW |
18 |
37,467,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5703:Pcdhb6
|
UTSW |
18 |
37,467,753 (GRCm39) |
missense |
probably benign |
0.15 |
R6154:Pcdhb6
|
UTSW |
18 |
37,467,966 (GRCm39) |
missense |
probably benign |
0.00 |
R6256:Pcdhb6
|
UTSW |
18 |
37,468,978 (GRCm39) |
missense |
probably damaging |
0.98 |
R6304:Pcdhb6
|
UTSW |
18 |
37,468,974 (GRCm39) |
nonsense |
probably null |
|
R6528:Pcdhb6
|
UTSW |
18 |
37,467,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6883:Pcdhb6
|
UTSW |
18 |
37,468,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Pcdhb6
|
UTSW |
18 |
37,469,329 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7307:Pcdhb6
|
UTSW |
18 |
37,468,531 (GRCm39) |
missense |
probably benign |
|
R7313:Pcdhb6
|
UTSW |
18 |
37,468,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R7378:Pcdhb6
|
UTSW |
18 |
37,468,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R7555:Pcdhb6
|
UTSW |
18 |
37,468,332 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7606:Pcdhb6
|
UTSW |
18 |
37,468,659 (GRCm39) |
missense |
probably damaging |
0.99 |
R7701:Pcdhb6
|
UTSW |
18 |
37,467,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Pcdhb6
|
UTSW |
18 |
37,469,365 (GRCm39) |
missense |
probably benign |
0.05 |
R7905:Pcdhb6
|
UTSW |
18 |
37,467,607 (GRCm39) |
missense |
probably benign |
0.00 |
R7982:Pcdhb6
|
UTSW |
18 |
37,467,273 (GRCm39) |
nonsense |
probably null |
|
R8818:Pcdhb6
|
UTSW |
18 |
37,468,837 (GRCm39) |
missense |
probably benign |
0.06 |
R8917:Pcdhb6
|
UTSW |
18 |
37,468,431 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9397:Pcdhb6
|
UTSW |
18 |
37,469,353 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Pcdhb6
|
UTSW |
18 |
37,468,199 (GRCm39) |
missense |
probably damaging |
1.00 |
|