Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
T |
A |
10: 29,097,902 (GRCm39) |
C100S |
probably damaging |
Het |
Abcc8 |
C |
T |
7: 45,800,204 (GRCm39) |
R526H |
probably damaging |
Het |
Acad10 |
G |
A |
5: 121,769,630 (GRCm39) |
P609S |
probably benign |
Het |
Acod1 |
A |
T |
14: 103,288,775 (GRCm39) |
D95V |
probably damaging |
Het |
Acsm5 |
A |
T |
7: 119,129,677 (GRCm39) |
I130F |
possibly damaging |
Het |
Ago4 |
A |
T |
4: 126,410,864 (GRCm39) |
D208E |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,250,881 (GRCm39) |
|
probably null |
Het |
Ankar |
A |
T |
1: 72,697,853 (GRCm39) |
I791K |
probably damaging |
Het |
Ano10 |
A |
G |
9: 122,088,011 (GRCm39) |
V364A |
probably damaging |
Het |
Arhgap9 |
T |
C |
10: 127,164,854 (GRCm39) |
|
probably null |
Het |
Arsi |
G |
A |
18: 61,049,666 (GRCm39) |
C183Y |
probably damaging |
Het |
Ascl2 |
T |
G |
7: 142,521,953 (GRCm39) |
E97A |
probably damaging |
Het |
Bcl2a1a |
C |
T |
9: 88,839,506 (GRCm39) |
R135W |
probably damaging |
Het |
Bms1 |
C |
T |
6: 118,368,114 (GRCm39) |
|
probably null |
Het |
Bysl |
T |
A |
17: 47,915,260 (GRCm39) |
T163S |
probably benign |
Het |
Card10 |
A |
G |
15: 78,664,473 (GRCm39) |
I821T |
probably benign |
Het |
Cc2d2a |
A |
T |
5: 43,892,737 (GRCm39) |
Q1433L |
probably damaging |
Het |
Ccz1 |
G |
T |
5: 143,949,815 (GRCm39) |
T70K |
probably damaging |
Het |
Cdc25c |
G |
C |
18: 34,871,292 (GRCm39) |
L275V |
probably damaging |
Het |
Cep164 |
A |
T |
9: 45,686,547 (GRCm39) |
L729Q |
probably damaging |
Het |
Clcn6 |
A |
G |
4: 148,101,951 (GRCm39) |
|
probably null |
Het |
Clcn7 |
T |
A |
17: 25,374,420 (GRCm39) |
V507E |
probably damaging |
Het |
Cracdl |
T |
C |
1: 37,664,381 (GRCm39) |
M506V |
probably benign |
Het |
Ctso |
A |
C |
3: 81,840,041 (GRCm39) |
T24P |
probably damaging |
Het |
Dis3l2 |
A |
T |
1: 86,917,980 (GRCm39) |
N543I |
probably benign |
Het |
Dnah12 |
A |
T |
14: 26,491,907 (GRCm39) |
Y1114F |
possibly damaging |
Het |
Emx1 |
A |
G |
6: 85,181,033 (GRCm39) |
D250G |
probably benign |
Het |
Epha4 |
G |
A |
1: 77,488,339 (GRCm39) |
A47V |
possibly damaging |
Het |
Fam149b |
A |
C |
14: 20,428,524 (GRCm39) |
N341T |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,782,001 (GRCm39) |
K62R |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,816,782 (GRCm39) |
S4172P |
probably benign |
Het |
Gbp3 |
A |
G |
3: 142,276,343 (GRCm39) |
R480G |
probably benign |
Het |
Get3 |
A |
G |
8: 85,746,395 (GRCm39) |
V151A |
possibly damaging |
Het |
Gja8 |
T |
G |
3: 96,827,033 (GRCm39) |
T210P |
probably damaging |
Het |
Gm5431 |
T |
A |
11: 48,779,536 (GRCm39) |
N740I |
probably benign |
Het |
Gm9930 |
T |
C |
10: 9,410,446 (GRCm39) |
|
noncoding transcript |
Het |
Gstt4 |
C |
T |
10: 75,650,959 (GRCm39) |
C221Y |
probably benign |
Het |
Gzmg |
A |
T |
14: 56,395,832 (GRCm39) |
D42E |
probably benign |
Het |
Hoxd12 |
G |
A |
2: 74,505,815 (GRCm39) |
A129T |
possibly damaging |
Het |
Hs2st1 |
G |
A |
3: 144,275,691 (GRCm39) |
|
probably benign |
Het |
Ifnlr1 |
G |
T |
4: 135,432,559 (GRCm39) |
D332Y |
probably damaging |
Het |
Igsf10 |
T |
C |
3: 59,239,287 (GRCm39) |
D298G |
probably damaging |
Het |
Irf1 |
T |
C |
11: 53,664,617 (GRCm39) |
V108A |
probably damaging |
Het |
Jsrp1 |
C |
G |
10: 80,648,140 (GRCm39) |
S36T |
probably benign |
Het |
Kcnq5 |
T |
A |
1: 21,576,006 (GRCm39) |
R233* |
probably null |
Het |
Kif7 |
T |
C |
7: 79,352,012 (GRCm39) |
K917E |
probably damaging |
Het |
Krt7 |
A |
C |
15: 101,310,538 (GRCm39) |
I62L |
probably benign |
Het |
Lifr |
A |
G |
15: 7,196,397 (GRCm39) |
T194A |
probably benign |
Het |
Ltbp2 |
T |
C |
12: 84,851,183 (GRCm39) |
|
probably null |
Het |
Maco1 |
A |
G |
4: 134,531,699 (GRCm39) |
S657P |
probably damaging |
Het |
Man2c1 |
A |
G |
9: 57,048,672 (GRCm39) |
|
probably null |
Het |
Met |
T |
C |
6: 17,491,966 (GRCm39) |
S243P |
probably damaging |
Het |
Mllt10 |
C |
A |
2: 18,069,935 (GRCm39) |
D30E |
possibly damaging |
Het |
Mre11a |
A |
C |
9: 14,707,065 (GRCm39) |
|
probably null |
Het |
Mroh9 |
A |
G |
1: 162,866,514 (GRCm39) |
S710P |
probably benign |
Het |
Mvk |
C |
A |
5: 114,588,459 (GRCm39) |
Y116* |
probably null |
Het |
Myh1 |
A |
G |
11: 67,096,423 (GRCm39) |
I301V |
probably benign |
Het |
Ncf1 |
T |
C |
5: 134,254,552 (GRCm39) |
D184G |
probably damaging |
Het |
Nxpe4 |
T |
C |
9: 48,304,533 (GRCm39) |
F207L |
probably damaging |
Het |
Or2ag18 |
G |
T |
7: 106,405,168 (GRCm39) |
P167H |
probably damaging |
Het |
Or2y1b |
T |
G |
11: 49,209,048 (GRCm39) |
L225R |
probably damaging |
Het |
Or4k51 |
T |
A |
2: 111,584,661 (GRCm39) |
N22K |
probably benign |
Het |
Or52b1 |
A |
T |
7: 104,978,817 (GRCm39) |
I194N |
probably damaging |
Het |
Or5b24 |
T |
A |
19: 12,912,537 (GRCm39) |
M145K |
possibly damaging |
Het |
Or5w14 |
T |
C |
2: 87,541,392 (GRCm39) |
N286S |
probably damaging |
Het |
Pcdh1 |
G |
A |
18: 38,332,532 (GRCm39) |
T296M |
possibly damaging |
Het |
Pcdh15 |
A |
G |
10: 74,481,828 (GRCm39) |
D391G |
possibly damaging |
Het |
Pcdha7 |
C |
A |
18: 37,107,786 (GRCm39) |
D270E |
probably damaging |
Het |
Pgam1 |
C |
A |
19: 41,904,315 (GRCm39) |
S137R |
probably damaging |
Het |
Pitpnm2 |
T |
C |
5: 124,274,389 (GRCm39) |
E240G |
probably damaging |
Het |
Plce1 |
T |
G |
19: 38,748,498 (GRCm39) |
I1729S |
probably damaging |
Het |
Plppr4 |
G |
T |
3: 117,125,355 (GRCm39) |
N161K |
probably damaging |
Het |
Pramel27 |
G |
A |
4: 143,578,561 (GRCm39) |
V274I |
probably benign |
Het |
Prkce |
T |
A |
17: 86,932,754 (GRCm39) |
I578N |
probably damaging |
Het |
Prss58 |
A |
C |
6: 40,874,734 (GRCm39) |
S36A |
probably damaging |
Het |
Ptprm |
T |
C |
17: 67,000,773 (GRCm39) |
H1128R |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,159,798 (GRCm39) |
Y178C |
probably benign |
Het |
Rubcn |
T |
C |
16: 32,667,624 (GRCm39) |
N179S |
probably damaging |
Het |
Sh3bp1 |
C |
T |
15: 78,795,706 (GRCm39) |
P612S |
probably damaging |
Het |
Sh3bp5 |
G |
A |
14: 31,133,586 (GRCm39) |
T82M |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,965,314 (GRCm39) |
Y974C |
probably damaging |
Het |
Slc9c1 |
T |
C |
16: 45,365,099 (GRCm39) |
I144T |
possibly damaging |
Het |
Slf2 |
T |
C |
19: 44,930,045 (GRCm39) |
I374T |
possibly damaging |
Het |
Snx13 |
A |
G |
12: 35,188,080 (GRCm39) |
D786G |
probably benign |
Het |
Spcs3 |
A |
G |
8: 54,976,389 (GRCm39) |
V151A |
possibly damaging |
Het |
Sstr2 |
A |
T |
11: 113,515,749 (GRCm39) |
I223F |
probably damaging |
Het |
Stac3 |
T |
C |
10: 127,339,787 (GRCm39) |
|
probably null |
Het |
Tas1r2 |
A |
G |
4: 139,387,162 (GRCm39) |
N207S |
probably damaging |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Tgm5 |
T |
C |
2: 120,907,429 (GRCm39) |
E98G |
possibly damaging |
Het |
Tktl2 |
A |
G |
8: 66,965,504 (GRCm39) |
E354G |
probably benign |
Het |
Tmem94 |
G |
A |
11: 115,682,787 (GRCm39) |
R608H |
probably damaging |
Het |
Tnrc6a |
G |
A |
7: 122,770,315 (GRCm39) |
V702I |
probably damaging |
Het |
Trappc10 |
A |
G |
10: 78,047,357 (GRCm39) |
S380P |
possibly damaging |
Het |
Trim24 |
G |
A |
6: 37,880,587 (GRCm39) |
|
probably null |
Het |
Ugt1a2 |
A |
G |
1: 88,128,846 (GRCm39) |
Y163C |
probably damaging |
Het |
Vmn1r215 |
A |
G |
13: 23,260,343 (GRCm39) |
I128V |
probably benign |
Het |
Vmn2r50 |
T |
A |
7: 9,781,640 (GRCm39) |
E368D |
possibly damaging |
Het |
Vmn2r59 |
T |
C |
7: 41,693,190 (GRCm39) |
N470S |
probably damaging |
Het |
Vps45 |
T |
C |
3: 95,948,757 (GRCm39) |
T333A |
probably benign |
Het |
Zbtb44 |
T |
A |
9: 30,965,539 (GRCm39) |
D316E |
probably damaging |
Het |
Zdhhc1 |
C |
T |
8: 106,210,190 (GRCm39) |
V76M |
probably benign |
Het |
Zfp235 |
T |
C |
7: 23,841,549 (GRCm39) |
F656S |
probably damaging |
Het |
|
Other mutations in Cchcr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00488:Cchcr1
|
APN |
17 |
35,839,469 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02723:Cchcr1
|
APN |
17 |
35,841,699 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02806:Cchcr1
|
APN |
17 |
35,836,153 (GRCm39) |
splice site |
probably benign |
|
IGL03055:Cchcr1
|
UTSW |
17 |
35,837,516 (GRCm39) |
missense |
probably benign |
0.33 |
R0569:Cchcr1
|
UTSW |
17 |
35,839,865 (GRCm39) |
critical splice donor site |
probably null |
|
R1438:Cchcr1
|
UTSW |
17 |
35,841,457 (GRCm39) |
critical splice donor site |
probably null |
|
R2055:Cchcr1
|
UTSW |
17 |
35,837,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R3910:Cchcr1
|
UTSW |
17 |
35,836,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R3911:Cchcr1
|
UTSW |
17 |
35,836,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Cchcr1
|
UTSW |
17 |
35,836,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5590:Cchcr1
|
UTSW |
17 |
35,837,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R5821:Cchcr1
|
UTSW |
17 |
35,839,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R5940:Cchcr1
|
UTSW |
17 |
35,835,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R5941:Cchcr1
|
UTSW |
17 |
35,835,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R6006:Cchcr1
|
UTSW |
17 |
35,835,597 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6114:Cchcr1
|
UTSW |
17 |
35,836,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R6146:Cchcr1
|
UTSW |
17 |
35,839,475 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6262:Cchcr1
|
UTSW |
17 |
35,841,413 (GRCm39) |
missense |
probably benign |
0.04 |
R6369:Cchcr1
|
UTSW |
17 |
35,839,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R6478:Cchcr1
|
UTSW |
17 |
35,835,600 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6827:Cchcr1
|
UTSW |
17 |
35,841,302 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6860:Cchcr1
|
UTSW |
17 |
35,840,015 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7109:Cchcr1
|
UTSW |
17 |
35,828,838 (GRCm39) |
critical splice donor site |
probably null |
|
R7276:Cchcr1
|
UTSW |
17 |
35,840,031 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7341:Cchcr1
|
UTSW |
17 |
35,837,610 (GRCm39) |
missense |
probably benign |
0.00 |
R7404:Cchcr1
|
UTSW |
17 |
35,835,693 (GRCm39) |
missense |
probably benign |
0.09 |
R7472:Cchcr1
|
UTSW |
17 |
35,839,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Cchcr1
|
UTSW |
17 |
35,837,383 (GRCm39) |
missense |
probably benign |
0.01 |
R8189:Cchcr1
|
UTSW |
17 |
35,837,563 (GRCm39) |
missense |
probably benign |
|
R9276:Cchcr1
|
UTSW |
17 |
35,841,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R9758:Cchcr1
|
UTSW |
17 |
35,839,285 (GRCm39) |
critical splice donor site |
probably null |
|
X0025:Cchcr1
|
UTSW |
17 |
35,837,573 (GRCm39) |
missense |
probably benign |
0.13 |
Z1177:Cchcr1
|
UTSW |
17 |
35,839,560 (GRCm39) |
missense |
probably damaging |
0.99 |
|