Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
A |
G |
6: 146,854,499 (GRCm39) |
V181A |
probably damaging |
Het |
Abca16 |
T |
A |
7: 120,076,993 (GRCm39) |
D686E |
probably benign |
Het |
Abca8a |
C |
A |
11: 109,953,908 (GRCm39) |
C844F |
probably damaging |
Het |
Acd |
G |
A |
8: 106,424,952 (GRCm39) |
P396L |
probably damaging |
Het |
Adamtsl3 |
A |
G |
7: 82,189,753 (GRCm39) |
Y659C |
probably damaging |
Het |
Ankfn1 |
C |
T |
11: 89,413,875 (GRCm39) |
V167M |
probably benign |
Het |
Ankrd13c |
T |
A |
3: 157,700,358 (GRCm39) |
L393Q |
possibly damaging |
Het |
Arid1b |
G |
A |
17: 5,386,879 (GRCm39) |
G1391D |
possibly damaging |
Het |
Arid5b |
T |
A |
10: 67,937,882 (GRCm39) |
D415V |
probably damaging |
Het |
Arl13b |
G |
T |
16: 62,647,774 (GRCm39) |
H45N |
probably benign |
Het |
Atp13a4 |
A |
T |
16: 29,268,797 (GRCm39) |
I519N |
|
Het |
Atrnl1 |
T |
C |
19: 57,643,420 (GRCm39) |
I436T |
probably benign |
Het |
Bbx |
A |
G |
16: 50,022,935 (GRCm39) |
I675T |
probably damaging |
Het |
Bcas1 |
A |
T |
2: 170,190,040 (GRCm39) |
V619E |
probably damaging |
Het |
Cad |
T |
C |
5: 31,218,576 (GRCm39) |
V501A |
possibly damaging |
Het |
Car8 |
T |
A |
4: 8,169,686 (GRCm39) |
N274I |
probably damaging |
Het |
Ccdc3 |
A |
G |
2: 5,146,143 (GRCm39) |
Q159R |
probably damaging |
Het |
Ccdc7b |
A |
T |
8: 129,893,459 (GRCm39) |
E95D |
possibly damaging |
Het |
Cdh12 |
G |
T |
15: 21,492,801 (GRCm39) |
|
probably benign |
Het |
Col11a1 |
G |
T |
3: 113,901,948 (GRCm39) |
G548* |
probably null |
Het |
Cpb2 |
A |
G |
14: 75,520,803 (GRCm39) |
E406G |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,747,132 (GRCm39) |
S1723G |
probably benign |
Het |
Ctu2 |
T |
C |
8: 123,206,045 (GRCm39) |
V262A |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,311,404 (GRCm39) |
N1772K |
possibly damaging |
Het |
Dock3 |
A |
T |
9: 106,774,569 (GRCm39) |
M62K |
probably benign |
Het |
Dok7 |
G |
A |
5: 35,214,239 (GRCm39) |
|
probably benign |
Het |
E2f3 |
A |
G |
13: 30,102,629 (GRCm39) |
Y211H |
probably damaging |
Het |
Elapor2 |
T |
C |
5: 9,460,699 (GRCm39) |
Y207H |
probably damaging |
Het |
Fam53c |
T |
A |
18: 34,895,774 (GRCm39) |
S25R |
probably damaging |
Het |
Fhod3 |
T |
G |
18: 25,030,681 (GRCm39) |
|
probably benign |
Het |
Foxp4 |
A |
G |
17: 48,180,033 (GRCm39) |
Y623H |
unknown |
Het |
Ggt1 |
A |
T |
10: 75,421,749 (GRCm39) |
H532L |
probably benign |
Het |
Gm10775 |
A |
C |
13: 65,407,770 (GRCm39) |
T24P |
unknown |
Het |
Hinfp |
A |
G |
9: 44,213,872 (GRCm39) |
S2P |
probably benign |
Het |
Hs3st4 |
A |
G |
7: 123,582,749 (GRCm39) |
T116A |
probably benign |
Het |
Ighv5-9-1 |
A |
T |
12: 113,699,818 (GRCm39) |
I98N |
probably damaging |
Het |
Ipo11 |
A |
T |
13: 107,046,713 (GRCm39) |
Y171N |
probably benign |
Het |
Jph1 |
C |
A |
1: 17,161,838 (GRCm39) |
A275S |
probably damaging |
Het |
Kcnh6 |
C |
G |
11: 105,924,860 (GRCm39) |
H941Q |
possibly damaging |
Het |
Kcnh7 |
A |
T |
2: 62,618,097 (GRCm39) |
I464K |
probably damaging |
Het |
Lrp8 |
C |
A |
4: 107,717,158 (GRCm39) |
P603T |
probably benign |
Het |
Mdm4 |
A |
T |
1: 132,929,169 (GRCm39) |
I176K |
possibly damaging |
Het |
Mpo |
T |
C |
11: 87,686,693 (GRCm39) |
V139A |
probably benign |
Het |
Niban3 |
A |
C |
8: 72,055,520 (GRCm39) |
D310A |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nup98 |
C |
A |
7: 101,788,037 (GRCm39) |
R1011L |
probably benign |
Het |
Or1f12 |
A |
G |
13: 21,721,864 (GRCm39) |
S89P |
possibly damaging |
Het |
Or4k51 |
G |
A |
2: 111,584,965 (GRCm39) |
V124M |
probably damaging |
Het |
Or9g4b |
A |
T |
2: 85,616,088 (GRCm39) |
I78L |
probably benign |
Het |
Pcdh7 |
A |
G |
5: 57,878,779 (GRCm39) |
D778G |
possibly damaging |
Het |
Pcdhb12 |
T |
C |
18: 37,570,675 (GRCm39) |
F607S |
probably damaging |
Het |
Pcolce |
A |
G |
5: 137,606,333 (GRCm39) |
F157L |
probably benign |
Het |
Pogk |
T |
C |
1: 166,226,780 (GRCm39) |
Y457C |
probably damaging |
Het |
Ppp1r21 |
G |
A |
17: 88,866,086 (GRCm39) |
E323K |
possibly damaging |
Het |
Prkn |
T |
A |
17: 11,456,527 (GRCm39) |
V117E |
probably damaging |
Het |
Prr12 |
A |
C |
7: 44,692,811 (GRCm39) |
F1574V |
probably damaging |
Het |
Rasl2-9 |
A |
T |
7: 5,128,448 (GRCm39) |
F161I |
probably damaging |
Het |
Rb1 |
A |
G |
14: 73,517,602 (GRCm39) |
I268T |
possibly damaging |
Het |
Rin3 |
A |
T |
12: 102,335,691 (GRCm39) |
D534V |
probably damaging |
Het |
Scn5a |
C |
T |
9: 119,315,717 (GRCm39) |
G1664S |
probably damaging |
Het |
Sin3b |
T |
C |
8: 73,471,168 (GRCm39) |
S372P |
probably benign |
Het |
Snx32 |
T |
A |
19: 5,548,485 (GRCm39) |
H65L |
probably damaging |
Het |
Spidr |
T |
A |
16: 15,855,544 (GRCm39) |
I324F |
probably damaging |
Het |
Stab1 |
A |
T |
14: 30,867,298 (GRCm39) |
F1687L |
probably benign |
Het |
Taar6 |
T |
C |
10: 23,860,903 (GRCm39) |
I214M |
probably benign |
Het |
Vmn2r105 |
T |
A |
17: 20,447,685 (GRCm39) |
N380Y |
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 |
R5677:Man1c1
|
UTSW |
4 |
134,296,371 (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 |
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 |
|