Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd11 |
G |
A |
5: 135,038,654 (GRCm39) |
C30Y |
probably benign |
Het |
Akr1c20 |
C |
T |
13: 4,562,671 (GRCm39) |
V95M |
probably damaging |
Het |
Ano7 |
A |
G |
1: 93,322,195 (GRCm39) |
D401G |
probably benign |
Het |
Arhgef10l |
G |
A |
4: 140,305,616 (GRCm39) |
T176I |
possibly damaging |
Het |
Armc2 |
A |
C |
10: 41,842,792 (GRCm39) |
V337G |
probably damaging |
Het |
Atp6v0d2 |
T |
A |
4: 19,922,400 (GRCm39) |
Y33F |
probably benign |
Het |
Banp |
A |
G |
8: 122,747,291 (GRCm39) |
S447G |
probably benign |
Het |
Car8 |
T |
A |
4: 8,238,860 (GRCm39) |
Y32F |
possibly damaging |
Het |
Ccdc188 |
C |
T |
16: 18,036,539 (GRCm39) |
P124S |
probably damaging |
Het |
Cdc23 |
A |
T |
18: 34,780,072 (GRCm39) |
D85E |
probably benign |
Het |
Cnot6l |
T |
C |
5: 96,242,084 (GRCm39) |
E213G |
possibly damaging |
Het |
Cntnap4 |
A |
G |
8: 113,484,113 (GRCm39) |
T389A |
probably benign |
Het |
Cramp1 |
A |
T |
17: 25,202,196 (GRCm39) |
C429S |
probably damaging |
Het |
Crygn |
T |
C |
5: 24,961,072 (GRCm39) |
H78R |
probably benign |
Het |
D630003M21Rik |
T |
A |
2: 158,059,588 (GRCm39) |
D104V |
probably damaging |
Het |
Dcaf10 |
T |
G |
4: 45,348,196 (GRCm39) |
H217Q |
probably damaging |
Het |
Dmrtb1 |
C |
T |
4: 107,541,179 (GRCm39) |
V61M |
probably benign |
Het |
Dnai1 |
A |
G |
4: 41,605,823 (GRCm39) |
E271G |
probably benign |
Het |
Efr3a |
G |
A |
15: 65,701,679 (GRCm39) |
V198I |
probably benign |
Het |
Emsy |
G |
A |
7: 98,289,060 (GRCm39) |
T79M |
probably damaging |
Het |
Ergic1 |
A |
G |
17: 26,853,449 (GRCm39) |
D145G |
probably damaging |
Het |
Fah |
A |
G |
7: 84,244,686 (GRCm39) |
V229A |
probably damaging |
Het |
Fam76a |
G |
A |
4: 132,629,342 (GRCm39) |
T270I |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,055,353 (GRCm39) |
M4191L |
probably benign |
Het |
Fbxl22 |
G |
T |
9: 66,418,999 (GRCm39) |
R213S |
probably benign |
Het |
Fktn |
T |
C |
4: 53,734,859 (GRCm39) |
F127L |
probably benign |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
A |
T |
4: 46,734,096 (GRCm39) |
S541T |
probably benign |
Het |
Gm7489 |
A |
G |
15: 53,749,402 (GRCm39) |
H158R |
unknown |
Het |
Greb1l |
G |
C |
18: 10,542,056 (GRCm39) |
E1268Q |
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,482,848 (GRCm39) |
D126G |
probably damaging |
Het |
Ikzf3 |
T |
A |
11: 98,409,525 (GRCm39) |
T13S |
probably benign |
Het |
Il23r |
T |
C |
6: 67,400,846 (GRCm39) |
T495A |
probably benign |
Het |
Insyn2b |
A |
G |
11: 34,353,034 (GRCm39) |
T359A |
probably benign |
Het |
Irf5 |
A |
G |
6: 29,535,461 (GRCm39) |
T230A |
probably benign |
Het |
Itga2b |
A |
T |
11: 102,348,108 (GRCm39) |
I831N |
probably damaging |
Het |
Itgb4 |
A |
G |
11: 115,891,087 (GRCm39) |
D1168G |
probably damaging |
Het |
Kcnma1 |
G |
T |
14: 23,440,991 (GRCm39) |
P605Q |
probably benign |
Het |
Larp7 |
A |
T |
3: 127,337,916 (GRCm39) |
M381K |
possibly damaging |
Het |
Lfng |
G |
A |
5: 140,598,588 (GRCm39) |
G269D |
probably benign |
Het |
Liph |
T |
C |
16: 21,780,986 (GRCm39) |
I335V |
probably benign |
Het |
Map2k2 |
A |
T |
10: 80,954,040 (GRCm39) |
I169F |
possibly damaging |
Het |
Mmrn1 |
T |
A |
6: 60,964,044 (GRCm39) |
|
probably null |
Het |
Nod2 |
A |
G |
8: 89,387,425 (GRCm39) |
|
probably null |
Het |
Or51ag1 |
A |
C |
7: 103,155,586 (GRCm39) |
L189R |
probably damaging |
Het |
Or5b101 |
T |
A |
19: 13,005,360 (GRCm39) |
Y111F |
probably benign |
Het |
Or9s23 |
T |
C |
1: 92,501,219 (GRCm39) |
F109L |
probably benign |
Het |
Pcdh20 |
G |
T |
14: 88,707,143 (GRCm39) |
F52L |
probably null |
Het |
Pkhd1 |
A |
T |
1: 20,573,223 (GRCm39) |
N1894K |
probably damaging |
Het |
Pla2r1 |
T |
A |
2: 60,334,536 (GRCm39) |
D412V |
possibly damaging |
Het |
Pole |
T |
G |
5: 110,465,663 (GRCm39) |
M1197R |
probably benign |
Het |
Ppp2r5d |
A |
T |
17: 46,995,472 (GRCm39) |
M497K |
probably benign |
Het |
Rbm45 |
G |
T |
2: 76,206,797 (GRCm39) |
V270F |
possibly damaging |
Het |
Ros1 |
A |
T |
10: 52,020,957 (GRCm39) |
F673I |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,691,048 (GRCm39) |
L1113* |
probably null |
Het |
Scn4a |
A |
G |
11: 106,212,841 (GRCm39) |
I1388T |
probably benign |
Het |
Sema3c |
G |
A |
5: 17,899,845 (GRCm39) |
V446I |
probably damaging |
Het |
Six4 |
T |
C |
12: 73,159,408 (GRCm39) |
Y176C |
probably damaging |
Het |
Slc35a5 |
T |
A |
16: 44,964,570 (GRCm39) |
K221M |
possibly damaging |
Het |
Slc6a19 |
A |
G |
13: 73,841,182 (GRCm39) |
I76T |
probably damaging |
Het |
Slfn4 |
A |
G |
11: 83,077,419 (GRCm39) |
D69G |
probably damaging |
Het |
Smc6 |
T |
C |
12: 11,367,844 (GRCm39) |
F1085L |
probably benign |
Het |
Spatc1l |
A |
G |
10: 76,398,224 (GRCm39) |
S9G |
probably benign |
Het |
Stx8 |
T |
A |
11: 68,000,106 (GRCm39) |
I182N |
probably damaging |
Het |
Sult2a8 |
A |
T |
7: 14,147,596 (GRCm39) |
C232S |
probably benign |
Het |
Susd4 |
G |
A |
1: 182,686,070 (GRCm39) |
A207T |
probably benign |
Het |
Svep1 |
G |
A |
4: 58,054,539 (GRCm39) |
P3350S |
probably benign |
Het |
Tbx20 |
A |
T |
9: 24,685,108 (GRCm39) |
S12T |
probably damaging |
Het |
Tfrc |
A |
G |
16: 32,437,985 (GRCm39) |
K346R |
probably benign |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Umodl1 |
A |
T |
17: 31,192,666 (GRCm39) |
|
probably null |
Het |
Vmn1r201 |
T |
C |
13: 22,659,538 (GRCm39) |
F251L |
possibly damaging |
Het |
Vmn1r230 |
A |
G |
17: 21,066,933 (GRCm39) |
T41A |
probably benign |
Het |
Vmn2r20 |
A |
G |
6: 123,362,882 (GRCm39) |
L634P |
probably damaging |
Het |
Vmn2r81 |
A |
T |
10: 79,129,664 (GRCm39) |
R852W |
probably damaging |
Het |
Wdr41 |
A |
T |
13: 95,151,701 (GRCm39) |
N287I |
probably benign |
Het |
Zfp202 |
A |
G |
9: 40,121,758 (GRCm39) |
D285G |
possibly damaging |
Het |
|
Other mutations in Pom121l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02104:Pom121l2
|
APN |
13 |
22,166,445 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02223:Pom121l2
|
APN |
13 |
22,166,265 (GRCm39) |
missense |
probably benign |
0.01 |
R0401:Pom121l2
|
UTSW |
13 |
22,166,395 (GRCm39) |
missense |
probably benign |
0.01 |
R0402:Pom121l2
|
UTSW |
13 |
22,172,649 (GRCm39) |
splice site |
probably benign |
|
R0437:Pom121l2
|
UTSW |
13 |
22,167,375 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0575:Pom121l2
|
UTSW |
13 |
22,168,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R0605:Pom121l2
|
UTSW |
13 |
22,166,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0892:Pom121l2
|
UTSW |
13 |
22,166,644 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0992:Pom121l2
|
UTSW |
13 |
22,166,929 (GRCm39) |
missense |
probably benign |
0.01 |
R1259:Pom121l2
|
UTSW |
13 |
22,166,297 (GRCm39) |
nonsense |
probably null |
|
R1564:Pom121l2
|
UTSW |
13 |
22,167,523 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1603:Pom121l2
|
UTSW |
13 |
22,167,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Pom121l2
|
UTSW |
13 |
22,167,954 (GRCm39) |
missense |
probably benign |
0.03 |
R1970:Pom121l2
|
UTSW |
13 |
22,167,642 (GRCm39) |
missense |
probably damaging |
0.98 |
R2018:Pom121l2
|
UTSW |
13 |
22,166,904 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2180:Pom121l2
|
UTSW |
13 |
22,166,145 (GRCm39) |
missense |
probably benign |
0.08 |
R2277:Pom121l2
|
UTSW |
13 |
22,168,417 (GRCm39) |
missense |
probably benign |
|
R2365:Pom121l2
|
UTSW |
13 |
22,167,954 (GRCm39) |
missense |
probably benign |
0.20 |
R3951:Pom121l2
|
UTSW |
13 |
22,166,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R4371:Pom121l2
|
UTSW |
13 |
22,166,409 (GRCm39) |
missense |
probably benign |
0.01 |
R4574:Pom121l2
|
UTSW |
13 |
22,168,572 (GRCm39) |
missense |
probably benign |
0.02 |
R4593:Pom121l2
|
UTSW |
13 |
22,168,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Pom121l2
|
UTSW |
13 |
22,167,984 (GRCm39) |
missense |
probably benign |
0.02 |
R5320:Pom121l2
|
UTSW |
13 |
22,166,015 (GRCm39) |
nonsense |
probably null |
|
R5661:Pom121l2
|
UTSW |
13 |
22,168,425 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5662:Pom121l2
|
UTSW |
13 |
22,166,358 (GRCm39) |
missense |
probably benign |
0.01 |
R5908:Pom121l2
|
UTSW |
13 |
22,165,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R5980:Pom121l2
|
UTSW |
13 |
22,167,546 (GRCm39) |
missense |
probably damaging |
0.96 |
R6145:Pom121l2
|
UTSW |
13 |
22,166,472 (GRCm39) |
nonsense |
probably null |
|
R6160:Pom121l2
|
UTSW |
13 |
22,167,838 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6327:Pom121l2
|
UTSW |
13 |
22,166,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6504:Pom121l2
|
UTSW |
13 |
22,167,631 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6745:Pom121l2
|
UTSW |
13 |
22,167,868 (GRCm39) |
missense |
probably benign |
0.00 |
R6750:Pom121l2
|
UTSW |
13 |
22,166,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Pom121l2
|
UTSW |
13 |
22,165,939 (GRCm39) |
missense |
probably damaging |
0.99 |
R6796:Pom121l2
|
UTSW |
13 |
22,167,694 (GRCm39) |
missense |
probably benign |
0.09 |
R6984:Pom121l2
|
UTSW |
13 |
22,166,191 (GRCm39) |
missense |
probably benign |
0.33 |
R7284:Pom121l2
|
UTSW |
13 |
22,166,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Pom121l2
|
UTSW |
13 |
22,168,502 (GRCm39) |
missense |
probably benign |
0.16 |
R7568:Pom121l2
|
UTSW |
13 |
22,166,796 (GRCm39) |
missense |
probably benign |
0.03 |
R7624:Pom121l2
|
UTSW |
13 |
22,167,699 (GRCm39) |
missense |
probably damaging |
0.97 |
R7956:Pom121l2
|
UTSW |
13 |
22,167,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Pom121l2
|
UTSW |
13 |
22,166,544 (GRCm39) |
missense |
probably benign |
0.00 |
R8506:Pom121l2
|
UTSW |
13 |
22,167,789 (GRCm39) |
missense |
probably benign |
0.04 |
R9167:Pom121l2
|
UTSW |
13 |
22,167,160 (GRCm39) |
missense |
probably damaging |
0.97 |
R9313:Pom121l2
|
UTSW |
13 |
22,168,506 (GRCm39) |
missense |
probably benign |
0.09 |
R9332:Pom121l2
|
UTSW |
13 |
22,165,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R9463:Pom121l2
|
UTSW |
13 |
22,168,402 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Pom121l2
|
UTSW |
13 |
22,172,656 (GRCm39) |
critical splice acceptor site |
probably null |
|
|