Other mutations in this stock |
Total: 116 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
C |
T |
10: 28,862,225 (GRCm39) |
V22I |
probably benign |
Het |
Abca8a |
A |
T |
11: 109,929,225 (GRCm39) |
V1296D |
possibly damaging |
Het |
Abca8b |
C |
T |
11: 109,831,687 (GRCm39) |
S1328N |
probably damaging |
Het |
Adcy1 |
G |
A |
11: 7,111,914 (GRCm39) |
M926I |
probably damaging |
Het |
Aff4 |
G |
T |
11: 53,291,102 (GRCm39) |
M687I |
possibly damaging |
Het |
Agbl2 |
T |
A |
2: 90,638,322 (GRCm39) |
Y636N |
possibly damaging |
Het |
Agtr1a |
A |
T |
13: 30,565,567 (GRCm39) |
I211F |
probably damaging |
Het |
Alkbh8 |
T |
G |
9: 3,385,147 (GRCm39) |
S480A |
possibly damaging |
Het |
Ankrd13b |
A |
T |
11: 77,368,370 (GRCm39) |
V84E |
probably damaging |
Het |
Ap3b1 |
C |
T |
13: 94,664,704 (GRCm39) |
T881I |
unknown |
Het |
Apbb1 |
A |
C |
7: 105,208,453 (GRCm39) |
D617E |
probably damaging |
Het |
Apobec4 |
A |
G |
1: 152,633,033 (GRCm39) |
R354G |
probably benign |
Het |
Brdt |
T |
G |
5: 107,496,483 (GRCm39) |
C198W |
possibly damaging |
Het |
Cacna1b |
G |
T |
2: 24,569,370 (GRCm39) |
H851Q |
possibly damaging |
Het |
Car2 |
G |
T |
3: 14,963,115 (GRCm39) |
V217F |
possibly damaging |
Het |
Ccdc24 |
A |
C |
4: 117,727,077 (GRCm39) |
|
probably benign |
Het |
Chodl |
C |
A |
16: 78,738,203 (GRCm39) |
A57E |
probably damaging |
Het |
Clgn |
G |
T |
8: 84,136,167 (GRCm39) |
C185F |
probably damaging |
Het |
Cltc |
G |
T |
11: 86,596,068 (GRCm39) |
N1223K |
probably damaging |
Het |
Cnot10 |
T |
C |
9: 114,458,161 (GRCm39) |
N115S |
probably damaging |
Het |
Col12a1 |
T |
C |
9: 79,606,603 (GRCm39) |
R607G |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,690,651 (GRCm39) |
V835A |
probably benign |
Het |
Cplane2 |
C |
T |
4: 140,947,177 (GRCm39) |
P186L |
probably benign |
Het |
Csmd3 |
G |
C |
15: 48,485,447 (GRCm39) |
L153V |
probably damaging |
Het |
Ctr9 |
A |
G |
7: 110,643,209 (GRCm39) |
H527R |
probably benign |
Het |
Cwc22 |
G |
A |
2: 77,759,787 (GRCm39) |
R87W |
probably damaging |
Het |
D930020B18Rik |
T |
A |
10: 121,505,106 (GRCm39) |
N107K |
probably benign |
Het |
Dgkg |
C |
A |
16: 22,388,921 (GRCm39) |
V418L |
probably benign |
Het |
Dhx40 |
A |
G |
11: 86,691,789 (GRCm39) |
|
probably null |
Het |
Diaph1 |
A |
T |
18: 37,989,004 (GRCm39) |
M910K |
probably damaging |
Het |
Diras2 |
T |
A |
13: 52,661,711 (GRCm39) |
M199L |
possibly damaging |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dock5 |
T |
A |
14: 68,015,052 (GRCm39) |
Q1302H |
probably benign |
Het |
Dync1i2 |
T |
C |
2: 71,058,967 (GRCm39) |
S90P |
probably benign |
Het |
E2f8 |
A |
T |
7: 48,516,943 (GRCm39) |
V812E |
probably damaging |
Het |
Egfem1 |
C |
A |
3: 29,744,323 (GRCm39) |
Q521K |
probably damaging |
Het |
Fbxl18 |
A |
T |
5: 142,864,475 (GRCm39) |
C699* |
probably null |
Het |
Fgf3 |
C |
T |
7: 144,392,520 (GRCm39) |
R26* |
probably null |
Het |
Fpr-rs7 |
T |
G |
17: 20,334,365 (GRCm39) |
I42L |
probably benign |
Het |
Gm3159 |
T |
A |
14: 4,398,582 (GRCm38) |
M91K |
probably damaging |
Het |
Gprin3 |
A |
G |
6: 59,330,877 (GRCm39) |
S477P |
possibly damaging |
Het |
Grm8 |
A |
T |
6: 27,761,203 (GRCm39) |
|
probably null |
Het |
Hepacam2 |
A |
T |
6: 3,466,142 (GRCm39) |
D420E |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,485,529 (GRCm39) |
W4358R |
probably benign |
Het |
Ifna6 |
G |
A |
4: 88,745,956 (GRCm39) |
A102T |
probably benign |
Het |
Ighv2-2 |
T |
C |
12: 113,552,142 (GRCm39) |
Q32R |
probably benign |
Het |
Igkv1-131 |
T |
A |
6: 67,743,242 (GRCm39) |
Q47L |
possibly damaging |
Het |
Il16 |
T |
C |
7: 83,323,761 (GRCm39) |
E263G |
probably damaging |
Het |
Kansl1 |
A |
T |
11: 104,225,974 (GRCm39) |
C981S |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,410,298 (GRCm39) |
F1483I |
probably damaging |
Het |
Ltf |
T |
C |
9: 110,849,980 (GRCm39) |
M1T |
probably null |
Het |
Ly75 |
C |
T |
2: 60,129,426 (GRCm39) |
R1653H |
probably benign |
Het |
Macrod2 |
T |
C |
2: 142,018,587 (GRCm39) |
F240S |
probably damaging |
Het |
Mansc4 |
A |
T |
6: 146,983,047 (GRCm39) |
M130K |
probably benign |
Het |
Mccc1 |
C |
T |
3: 36,044,197 (GRCm39) |
|
probably null |
Het |
Mink1 |
G |
T |
11: 70,495,991 (GRCm39) |
R75L |
possibly damaging |
Het |
Mst1 |
A |
G |
9: 107,958,485 (GRCm39) |
D65G |
probably damaging |
Het |
Myo9b |
C |
T |
8: 71,796,330 (GRCm39) |
A857V |
probably damaging |
Het |
Ndufa4 |
A |
G |
6: 11,900,574 (GRCm39) |
V70A |
probably benign |
Het |
Npat |
T |
A |
9: 53,466,400 (GRCm39) |
S230T |
probably benign |
Het |
Nr1d1 |
A |
G |
11: 98,662,134 (GRCm39) |
Y167H |
probably damaging |
Het |
Oca2 |
A |
G |
7: 56,064,210 (GRCm39) |
D735G |
probably damaging |
Het |
Odr4 |
G |
A |
1: 150,250,588 (GRCm39) |
L319F |
probably damaging |
Het |
Or2a7 |
T |
C |
6: 43,151,265 (GRCm39) |
V115A |
probably benign |
Het |
Or2b2 |
C |
T |
13: 21,887,393 (GRCm39) |
T74I |
probably benign |
Het |
Or2y13 |
A |
G |
11: 49,414,771 (GRCm39) |
T74A |
probably damaging |
Het |
Or7g20 |
T |
A |
9: 18,946,854 (GRCm39) |
I145N |
possibly damaging |
Het |
Otop1 |
A |
G |
5: 38,457,507 (GRCm39) |
Y422C |
probably damaging |
Het |
Pde4dip |
G |
A |
3: 97,748,964 (GRCm39) |
R126* |
probably null |
Het |
Pdp2 |
C |
T |
8: 105,321,320 (GRCm39) |
P390S |
probably damaging |
Het |
Pds5b |
A |
T |
5: 150,639,926 (GRCm39) |
T14S |
possibly damaging |
Het |
Pfkp |
T |
C |
13: 6,638,631 (GRCm39) |
E580G |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,250,767 (GRCm39) |
L212Q |
possibly damaging |
Het |
Piezo2 |
G |
C |
18: 63,250,768 (GRCm39) |
L444V |
probably benign |
Het |
Pla2g4d |
T |
A |
2: 120,109,429 (GRCm39) |
T207S |
possibly damaging |
Het |
Plk2 |
C |
A |
13: 110,535,591 (GRCm39) |
T471K |
possibly damaging |
Het |
Potefam1 |
T |
C |
2: 111,041,910 (GRCm39) |
T342A |
probably benign |
Het |
Potegl |
T |
A |
2: 23,102,730 (GRCm39) |
L156Q |
probably damaging |
Het |
Ppp1r3g |
G |
A |
13: 36,153,245 (GRCm39) |
E222K |
probably damaging |
Het |
Pramel28 |
A |
T |
4: 143,691,708 (GRCm39) |
D338E |
possibly damaging |
Het |
Prkcg |
A |
G |
7: 3,371,974 (GRCm39) |
D480G |
probably damaging |
Het |
Pxdc1 |
T |
A |
13: 34,836,178 (GRCm39) |
T81S |
probably benign |
Het |
Rnf150 |
A |
T |
8: 83,730,228 (GRCm39) |
K253* |
probably null |
Het |
Sae1 |
T |
C |
7: 16,104,387 (GRCm39) |
|
probably null |
Het |
Scin |
C |
T |
12: 40,113,258 (GRCm39) |
D538N |
probably damaging |
Het |
Serpinb3c |
C |
A |
1: 107,199,533 (GRCm39) |
K329N |
probably damaging |
Het |
Sgo2b |
T |
A |
8: 64,380,008 (GRCm39) |
K941N |
possibly damaging |
Het |
Six1 |
C |
T |
12: 73,093,058 (GRCm39) |
S48N |
possibly damaging |
Het |
Slc39a8 |
G |
A |
3: 135,590,449 (GRCm39) |
G381R |
probably damaging |
Het |
Slc9b1 |
A |
G |
3: 135,063,320 (GRCm39) |
K35E |
unknown |
Het |
Srek1 |
C |
T |
13: 103,895,752 (GRCm39) |
A274T |
probably damaging |
Het |
Steap2 |
A |
T |
5: 5,727,497 (GRCm39) |
Y279* |
probably null |
Het |
Svil |
T |
A |
18: 5,046,823 (GRCm39) |
L110* |
probably null |
Het |
Syncrip |
T |
C |
9: 88,338,762 (GRCm39) |
|
probably benign |
Het |
Tcf20 |
A |
G |
15: 82,737,443 (GRCm39) |
I1336T |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,155,451 (GRCm39) |
K36* |
probably null |
Het |
Tenm2 |
A |
G |
11: 36,032,510 (GRCm39) |
V670A |
probably damaging |
Het |
Thbd |
G |
A |
2: 148,249,286 (GRCm39) |
T194I |
probably damaging |
Het |
Tm9sf2 |
A |
T |
14: 122,389,374 (GRCm39) |
|
probably null |
Het |
Tmtc4 |
A |
T |
14: 123,187,911 (GRCm39) |
I225N |
probably damaging |
Het |
Tpp1 |
C |
T |
7: 105,396,743 (GRCm39) |
V425M |
probably damaging |
Het |
Trbc2 |
T |
A |
6: 41,524,746 (GRCm39) |
Y144* |
probably null |
Het |
Trps1 |
T |
C |
15: 50,709,504 (GRCm39) |
D282G |
probably damaging |
Het |
Tsc22d4 |
T |
A |
5: 137,745,404 (GRCm39) |
S9R |
probably damaging |
Het |
Upp1 |
T |
A |
11: 9,086,025 (GRCm39) |
D287E |
probably benign |
Het |
Uso1 |
A |
C |
5: 92,349,158 (GRCm39) |
Q916H |
probably damaging |
Het |
Uty |
T |
A |
Y: 1,134,902 (GRCm39) |
Y884F |
probably damaging |
Het |
Vmn1r222 |
T |
C |
13: 23,416,950 (GRCm39) |
R88G |
probably damaging |
Het |
Vmn1r79 |
T |
C |
7: 11,910,928 (GRCm39) |
V270A |
possibly damaging |
Het |
Zbtb22 |
T |
C |
17: 34,136,709 (GRCm39) |
S285P |
probably benign |
Het |
Zfp385a |
A |
G |
15: 103,226,492 (GRCm39) |
V82A |
probably damaging |
Het |
Zfp59 |
T |
C |
7: 27,553,594 (GRCm39) |
F349L |
probably benign |
Het |
Zfp780b |
T |
G |
7: 27,662,224 (GRCm39) |
H777P |
probably benign |
Het |
Zfp82 |
T |
C |
7: 29,756,549 (GRCm39) |
T178A |
probably benign |
Het |
Zfp850 |
T |
C |
7: 27,688,513 (GRCm39) |
Y565C |
probably damaging |
Het |
Zfp957 |
A |
G |
14: 79,450,207 (GRCm39) |
Y531H |
probably damaging |
Het |
|
Other mutations in Man1c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00835:Man1c1
|
APN |
4 |
134,291,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02237:Man1c1
|
APN |
4 |
134,311,609 (GRCm39) |
critical splice donor site |
probably null |
|
R0201:Man1c1
|
UTSW |
4 |
134,367,709 (GRCm39) |
splice site |
probably null |
|
R0390:Man1c1
|
UTSW |
4 |
134,305,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Man1c1
|
UTSW |
4 |
134,296,379 (GRCm39) |
nonsense |
probably null |
|
R1108:Man1c1
|
UTSW |
4 |
134,291,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Man1c1
|
UTSW |
4 |
134,308,100 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1914:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R2171:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Man1c1
|
UTSW |
4 |
134,430,263 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2938:Man1c1
|
UTSW |
4 |
134,430,263 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2971:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R3806:Man1c1
|
UTSW |
4 |
134,430,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R3977:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Man1c1
|
UTSW |
4 |
134,320,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R4065:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4066:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4067:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4209:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4210:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4290:Man1c1
|
UTSW |
4 |
134,291,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Man1c1
|
UTSW |
4 |
134,430,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Man1c1
|
UTSW |
4 |
134,430,500 (GRCm39) |
missense |
probably benign |
0.27 |
R4766:Man1c1
|
UTSW |
4 |
134,430,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R5226:Man1c1
|
UTSW |
4 |
134,305,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R5637:Man1c1
|
UTSW |
4 |
134,318,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R5939:Man1c1
|
UTSW |
4 |
134,293,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R7251:Man1c1
|
UTSW |
4 |
134,308,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:Man1c1
|
UTSW |
4 |
134,291,814 (GRCm39) |
critical splice donor site |
probably null |
|
R8551:Man1c1
|
UTSW |
4 |
134,430,326 (GRCm39) |
nonsense |
probably null |
|
R8745:Man1c1
|
UTSW |
4 |
134,303,295 (GRCm39) |
missense |
probably damaging |
0.96 |
R9116:Man1c1
|
UTSW |
4 |
134,311,705 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9272:Man1c1
|
UTSW |
4 |
134,291,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R9406:Man1c1
|
UTSW |
4 |
134,303,318 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Man1c1
|
UTSW |
4 |
134,303,318 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Man1c1
|
UTSW |
4 |
134,430,683 (GRCm39) |
missense |
possibly damaging |
0.74 |
X0063:Man1c1
|
UTSW |
4 |
134,303,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|