Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
G |
T |
4: 144,344,592 (GRCm39) |
A123S |
probably benign |
Het |
Adamts20 |
A |
C |
15: 94,243,871 (GRCm39) |
C619G |
probably damaging |
Het |
Ahcyl1 |
C |
A |
3: 107,575,604 (GRCm39) |
V394L |
probably benign |
Het |
Ankrd17 |
A |
C |
5: 90,386,825 (GRCm39) |
L2378V |
possibly damaging |
Het |
B3gnt3 |
T |
C |
8: 72,145,357 (GRCm39) |
Y337C |
probably damaging |
Het |
Bcl10 |
A |
G |
3: 145,630,266 (GRCm39) |
K18R |
possibly damaging |
Het |
Calcr |
G |
A |
6: 3,707,499 (GRCm39) |
A267V |
probably benign |
Het |
Ces1d |
C |
T |
8: 93,901,695 (GRCm39) |
G425S |
probably benign |
Het |
Col1a1 |
G |
T |
11: 94,838,505 (GRCm39) |
R899L |
unknown |
Het |
Commd1 |
C |
T |
11: 22,906,532 (GRCm39) |
R168H |
possibly damaging |
Het |
Cps1 |
T |
C |
1: 67,213,640 (GRCm39) |
S791P |
possibly damaging |
Het |
Ctsj |
T |
A |
13: 61,151,884 (GRCm39) |
I58F |
probably damaging |
Het |
Cyp2j5 |
T |
A |
4: 96,529,656 (GRCm39) |
K238N |
probably benign |
Het |
Dlgap4 |
A |
G |
2: 156,547,802 (GRCm39) |
D423G |
probably benign |
Het |
Eef1ece2 |
T |
A |
16: 20,463,010 (GRCm39) |
|
probably null |
Het |
Egln1 |
T |
C |
8: 125,675,256 (GRCm39) |
N180D |
probably benign |
Het |
Ehd1 |
T |
C |
19: 6,327,225 (GRCm39) |
F74S |
probably damaging |
Het |
Ext1 |
G |
A |
15: 52,970,881 (GRCm39) |
A350V |
probably damaging |
Het |
Fam186b |
T |
A |
15: 99,178,628 (GRCm39) |
I233F |
probably damaging |
Het |
Fam193a |
T |
G |
5: 34,597,473 (GRCm39) |
N91K |
probably benign |
Het |
Far1 |
T |
A |
7: 113,153,355 (GRCm39) |
N329K |
probably damaging |
Het |
Fhad1 |
A |
G |
4: 141,637,134 (GRCm39) |
S1111P |
probably damaging |
Het |
Fhl2 |
A |
G |
1: 43,180,984 (GRCm39) |
S69P |
probably damaging |
Het |
Flg2 |
C |
A |
3: 93,128,054 (GRCm39) |
P2322Q |
unknown |
Het |
Flvcr1 |
A |
G |
1: 190,757,843 (GRCm39) |
Y108H |
probably damaging |
Het |
Fos |
T |
A |
12: 85,522,792 (GRCm39) |
S235T |
probably benign |
Het |
Foxf1 |
T |
A |
8: 121,811,438 (GRCm39) |
S101T |
probably damaging |
Het |
Gfer |
C |
A |
17: 24,913,259 (GRCm39) |
D198Y |
probably damaging |
Het |
Ggps1 |
T |
C |
13: 14,229,034 (GRCm39) |
I50V |
probably benign |
Het |
Gkn2 |
A |
G |
6: 87,355,255 (GRCm39) |
T155A |
probably benign |
Het |
Gna12 |
C |
T |
5: 140,746,449 (GRCm39) |
C332Y |
probably damaging |
Het |
Hc |
T |
A |
2: 34,900,045 (GRCm39) |
Y1096F |
probably damaging |
Het |
Hoxa3 |
G |
A |
6: 52,147,267 (GRCm39) |
|
probably benign |
Het |
Hsd17b8 |
T |
G |
17: 34,246,411 (GRCm39) |
D117A |
probably benign |
Het |
Ifi206 |
A |
T |
1: 173,299,100 (GRCm39) |
Y835* |
probably null |
Het |
Ighv13-2 |
T |
G |
12: 114,321,544 (GRCm39) |
E65A |
probably damaging |
Het |
Kif5a |
A |
T |
10: 127,071,537 (GRCm39) |
Y770* |
probably null |
Het |
Lfng |
A |
G |
5: 140,593,384 (GRCm39) |
S72G |
probably benign |
Het |
Lipo2 |
C |
T |
19: 33,737,344 (GRCm39) |
|
probably benign |
Het |
Lnpep |
C |
T |
17: 17,783,109 (GRCm39) |
S564N |
probably benign |
Het |
Mfhas1 |
T |
A |
8: 36,057,025 (GRCm39) |
L500* |
probably null |
Het |
Mllt6 |
G |
A |
11: 97,561,142 (GRCm39) |
V277I |
probably benign |
Het |
Mroh5 |
C |
T |
15: 73,663,189 (GRCm39) |
D192N |
probably benign |
Het |
Myo1f |
T |
A |
17: 33,795,672 (GRCm39) |
V106D |
probably damaging |
Het |
Mypn |
T |
A |
10: 62,981,652 (GRCm39) |
I643F |
probably benign |
Het |
Nup188 |
A |
G |
2: 30,213,575 (GRCm39) |
N669D |
possibly damaging |
Het |
Or14j5 |
C |
G |
17: 38,161,714 (GRCm39) |
T77R |
probably damaging |
Het |
Or2r11 |
A |
T |
6: 42,437,573 (GRCm39) |
C127S |
probably damaging |
Het |
Or5g26 |
T |
C |
2: 85,494,689 (GRCm39) |
T30A |
probably benign |
Het |
Or8s8 |
T |
C |
15: 98,354,866 (GRCm39) |
V225A |
probably benign |
Het |
Osbpl10 |
A |
G |
9: 115,036,726 (GRCm39) |
T241A |
probably damaging |
Het |
Peg3 |
C |
T |
7: 6,711,839 (GRCm39) |
E1128K |
possibly damaging |
Het |
Plch1 |
C |
A |
3: 63,681,068 (GRCm39) |
M186I |
probably benign |
Het |
Pon3 |
A |
C |
6: 5,236,911 (GRCm39) |
L152R |
probably damaging |
Het |
Prr36 |
G |
A |
8: 4,263,905 (GRCm39) |
P587L |
unknown |
Het |
Psma2 |
T |
A |
13: 14,799,832 (GRCm39) |
I192N |
probably damaging |
Het |
Rbm11 |
T |
C |
16: 75,389,923 (GRCm39) |
F30L |
probably damaging |
Het |
Rpap3 |
G |
A |
15: 97,576,299 (GRCm39) |
A622V |
possibly damaging |
Het |
Scgb2b11 |
T |
A |
7: 31,908,807 (GRCm39) |
N98Y |
probably damaging |
Het |
Siglec1 |
A |
G |
2: 130,923,212 (GRCm39) |
L511P |
probably damaging |
Het |
Sirpb1c |
C |
T |
3: 15,887,156 (GRCm39) |
V228M |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,460,605 (GRCm39) |
Y804N |
probably damaging |
Het |
Sult6b2 |
T |
C |
6: 142,747,524 (GRCm39) |
D75G |
not run |
Het |
Sycp3 |
A |
C |
10: 88,302,368 (GRCm39) |
K119N |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,078,278 (GRCm39) |
L4703P |
probably damaging |
Het |
Tex12 |
C |
G |
9: 50,470,523 (GRCm39) |
L20F |
possibly damaging |
Het |
Them5 |
T |
A |
3: 94,250,603 (GRCm39) |
Y55* |
probably null |
Het |
Tmem43 |
A |
T |
6: 91,458,968 (GRCm39) |
D213V |
probably benign |
Het |
Tnfrsf10b |
A |
C |
14: 70,005,239 (GRCm39) |
Q44P |
unknown |
Het |
Trbv2 |
A |
T |
6: 41,024,836 (GRCm39) |
Q84L |
probably benign |
Het |
Trim2 |
C |
T |
3: 84,212,537 (GRCm39) |
|
probably benign |
Het |
Trim36 |
A |
G |
18: 46,305,558 (GRCm39) |
V475A |
probably benign |
Het |
Ttbk1 |
C |
A |
17: 46,758,269 (GRCm39) |
E788D |
probably benign |
Het |
Ttn |
T |
C |
2: 76,543,626 (GRCm39) |
D33120G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,576,256 (GRCm39) |
N24879I |
probably damaging |
Het |
Ube4a |
T |
A |
9: 44,864,308 (GRCm39) |
Q76L |
probably benign |
Het |
Vmn2r27 |
T |
A |
6: 124,168,980 (GRCm39) |
I717F |
probably damaging |
Het |
Vmn2r45 |
T |
C |
7: 8,485,987 (GRCm39) |
K434E |
possibly damaging |
Het |
Vta1 |
T |
C |
10: 14,531,461 (GRCm39) |
T305A |
probably damaging |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in 4921509C19Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01098:4921509C19Rik
|
APN |
2 |
151,315,453 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02117:4921509C19Rik
|
APN |
2 |
151,315,466 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02432:4921509C19Rik
|
APN |
2 |
151,314,481 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03025:4921509C19Rik
|
APN |
2 |
151,315,405 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0321:4921509C19Rik
|
UTSW |
2 |
151,314,620 (GRCm39) |
missense |
probably benign |
0.01 |
R0961:4921509C19Rik
|
UTSW |
2 |
151,314,686 (GRCm39) |
missense |
probably benign |
0.01 |
R1272:4921509C19Rik
|
UTSW |
2 |
151,313,977 (GRCm39) |
missense |
probably damaging |
0.98 |
R1455:4921509C19Rik
|
UTSW |
2 |
151,314,824 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3177:4921509C19Rik
|
UTSW |
2 |
151,314,020 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3277:4921509C19Rik
|
UTSW |
2 |
151,314,020 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4206:4921509C19Rik
|
UTSW |
2 |
151,315,435 (GRCm39) |
missense |
probably benign |
0.44 |
R4655:4921509C19Rik
|
UTSW |
2 |
151,314,778 (GRCm39) |
missense |
probably benign |
0.03 |
R4680:4921509C19Rik
|
UTSW |
2 |
151,315,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:4921509C19Rik
|
UTSW |
2 |
151,313,791 (GRCm39) |
missense |
unknown |
|
R4702:4921509C19Rik
|
UTSW |
2 |
151,314,509 (GRCm39) |
missense |
probably benign |
0.00 |
R4867:4921509C19Rik
|
UTSW |
2 |
151,314,742 (GRCm39) |
nonsense |
probably null |
|
R4962:4921509C19Rik
|
UTSW |
2 |
151,314,728 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5117:4921509C19Rik
|
UTSW |
2 |
151,314,460 (GRCm39) |
missense |
probably benign |
0.00 |
R5484:4921509C19Rik
|
UTSW |
2 |
151,313,851 (GRCm39) |
missense |
probably benign |
|
R5602:4921509C19Rik
|
UTSW |
2 |
151,315,459 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6374:4921509C19Rik
|
UTSW |
2 |
151,314,800 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6894:4921509C19Rik
|
UTSW |
2 |
151,315,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R7079:4921509C19Rik
|
UTSW |
2 |
151,315,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R7109:4921509C19Rik
|
UTSW |
2 |
151,315,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:4921509C19Rik
|
UTSW |
2 |
151,315,489 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7441:4921509C19Rik
|
UTSW |
2 |
151,314,845 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7845:4921509C19Rik
|
UTSW |
2 |
151,314,229 (GRCm39) |
missense |
probably damaging |
0.96 |
R8773:4921509C19Rik
|
UTSW |
2 |
151,314,062 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8805:4921509C19Rik
|
UTSW |
2 |
151,313,285 (GRCm39) |
splice site |
probably benign |
|
R8983:4921509C19Rik
|
UTSW |
2 |
151,313,272 (GRCm39) |
missense |
unknown |
|
R9257:4921509C19Rik
|
UTSW |
2 |
151,315,627 (GRCm39) |
missense |
probably benign |
0.05 |
R9566:4921509C19Rik
|
UTSW |
2 |
151,314,226 (GRCm39) |
missense |
probably benign |
0.13 |
|