Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,396,304 (GRCm39) |
S103N |
probably benign |
Het |
Ace |
A |
G |
11: 105,863,299 (GRCm39) |
D358G |
possibly damaging |
Het |
Acvr2b |
A |
T |
9: 119,257,116 (GRCm39) |
H115L |
probably damaging |
Het |
Adam15 |
G |
A |
3: 89,254,742 (GRCm39) |
T106I |
possibly damaging |
Het |
Adamts16 |
A |
G |
13: 70,883,948 (GRCm39) |
C1076R |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,092,481 (GRCm39) |
Y614C |
probably damaging |
Het |
Adhfe1 |
A |
T |
1: 9,627,276 (GRCm39) |
H225L |
probably benign |
Het |
Aff3 |
A |
G |
1: 38,220,397 (GRCm39) |
I1171T |
probably damaging |
Het |
Agps |
T |
A |
2: 75,697,182 (GRCm39) |
M334K |
probably damaging |
Het |
Akr1e1 |
A |
G |
13: 4,652,678 (GRCm39) |
|
probably null |
Het |
Als2cl |
G |
A |
9: 110,718,191 (GRCm39) |
V311M |
probably benign |
Het |
Amdhd1 |
A |
T |
10: 93,375,813 (GRCm39) |
L7H |
probably damaging |
Het |
Apba1 |
A |
T |
19: 23,870,782 (GRCm39) |
I205F |
probably damaging |
Het |
Arhgap26 |
A |
T |
18: 39,244,917 (GRCm39) |
E187D |
possibly damaging |
Het |
Ash1l |
A |
T |
3: 88,914,530 (GRCm39) |
H1720L |
probably benign |
Het |
Atp9a |
T |
C |
2: 168,575,988 (GRCm39) |
|
probably benign |
Het |
Bcl7c |
G |
A |
7: 127,307,695 (GRCm39) |
A2V |
probably damaging |
Het |
Catsperg1 |
G |
C |
7: 28,909,912 (GRCm39) |
P72R |
probably benign |
Het |
Ccdc103 |
G |
A |
11: 102,774,922 (GRCm39) |
G174R |
probably benign |
Het |
Ccdc171 |
A |
T |
4: 83,612,512 (GRCm39) |
K976M |
probably damaging |
Het |
Ceacam1 |
T |
C |
7: 25,173,360 (GRCm39) |
N276S |
possibly damaging |
Het |
Cep152 |
T |
C |
2: 125,463,127 (GRCm39) |
E18G |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,461,803 (GRCm39) |
N91S |
probably damaging |
Het |
Cers3 |
T |
C |
7: 66,393,442 (GRCm39) |
L17P |
probably benign |
Het |
Cpsf3 |
A |
G |
12: 21,356,844 (GRCm39) |
N489S |
possibly damaging |
Het |
Cramp1 |
A |
G |
17: 25,187,920 (GRCm39) |
S1225P |
probably damaging |
Het |
Dck |
G |
A |
5: 88,913,166 (GRCm39) |
G18R |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,387,914 (GRCm39) |
E3124D |
probably benign |
Het |
Dync2i2 |
T |
A |
2: 29,923,953 (GRCm39) |
T191S |
probably benign |
Het |
Fam135b |
A |
G |
15: 71,334,744 (GRCm39) |
S817P |
|
Het |
Fsip2 |
T |
C |
2: 82,812,374 (GRCm39) |
Y2898H |
possibly damaging |
Het |
Fzr1 |
T |
C |
10: 81,205,249 (GRCm39) |
H249R |
probably benign |
Het |
Gbp10 |
T |
G |
5: 105,366,861 (GRCm39) |
Q457P |
probably damaging |
Het |
Gin1 |
G |
C |
1: 97,710,819 (GRCm39) |
L167F |
probably damaging |
Het |
Gm14226 |
A |
T |
2: 154,866,843 (GRCm39) |
I267F |
probably damaging |
Het |
Gmnc |
A |
G |
16: 26,781,642 (GRCm39) |
|
probably null |
Het |
Hectd2 |
A |
T |
19: 36,576,402 (GRCm39) |
I311F |
probably damaging |
Het |
Heg1 |
A |
G |
16: 33,558,961 (GRCm39) |
K1085E |
probably benign |
Het |
Hmbs |
G |
A |
9: 44,252,983 (GRCm39) |
Q34* |
probably null |
Het |
Hyal6 |
T |
A |
6: 24,734,151 (GRCm39) |
M28K |
probably benign |
Het |
Ifi27l2a |
T |
C |
12: 103,405,678 (GRCm39) |
V141A |
possibly damaging |
Het |
Ift122 |
T |
A |
6: 115,867,492 (GRCm39) |
I414N |
probably damaging |
Het |
Iglv2 |
A |
T |
16: 19,079,434 (GRCm39) |
V23E |
probably damaging |
Het |
Itgax |
A |
T |
7: 127,730,641 (GRCm39) |
I120L |
probably benign |
Het |
Kifc3 |
A |
G |
8: 95,853,317 (GRCm39) |
I13T |
probably benign |
Het |
Lmod3 |
T |
C |
6: 97,224,625 (GRCm39) |
N399D |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,365,326 (GRCm39) |
I3145K |
probably benign |
Het |
Map2k5 |
A |
C |
9: 63,201,006 (GRCm39) |
I209S |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,141,388 (GRCm39) |
E117G |
probably damaging |
Het |
Milr1 |
A |
G |
11: 106,652,105 (GRCm39) |
H172R |
probably benign |
Het |
Myod1 |
A |
C |
7: 46,026,593 (GRCm39) |
D166A |
|
Het |
Neb |
C |
T |
2: 52,100,878 (GRCm39) |
V4647M |
possibly damaging |
Het |
Nek1 |
A |
T |
8: 61,574,055 (GRCm39) |
D1101V |
probably damaging |
Het |
Nlrp2 |
A |
T |
7: 5,330,572 (GRCm39) |
V608D |
probably benign |
Het |
Noc3l |
G |
A |
19: 38,800,835 (GRCm39) |
Q216* |
probably null |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nup160 |
T |
A |
2: 90,552,585 (GRCm39) |
|
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Oat |
C |
T |
7: 132,166,006 (GRCm39) |
S193N |
probably benign |
Het |
Oma1 |
A |
G |
4: 103,182,214 (GRCm39) |
|
probably null |
Het |
Or12e13 |
G |
T |
2: 87,663,523 (GRCm39) |
G47* |
probably null |
Het |
Or1e16 |
T |
A |
11: 73,286,853 (GRCm39) |
|
probably benign |
Het |
Or1j15 |
T |
G |
2: 36,458,988 (GRCm39) |
F126C |
probably benign |
Het |
Or6c206 |
A |
G |
10: 129,097,184 (GRCm39) |
Y118C |
probably damaging |
Het |
Or6c216 |
A |
G |
10: 129,678,482 (GRCm39) |
V143A |
probably damaging |
Het |
Os9 |
A |
G |
10: 126,933,918 (GRCm39) |
S500P |
possibly damaging |
Het |
Osbpl11 |
A |
T |
16: 33,047,660 (GRCm39) |
N541I |
|
Het |
Pcnx4 |
A |
G |
12: 72,613,671 (GRCm39) |
I539V |
probably benign |
Het |
Ppfia3 |
T |
A |
7: 44,999,717 (GRCm39) |
|
probably null |
Het |
Ppp1r3a |
T |
C |
6: 14,722,098 (GRCm39) |
K275E |
probably benign |
Het |
Pten |
A |
G |
19: 32,769,972 (GRCm39) |
N63S |
probably benign |
Het |
Rptor |
A |
G |
11: 119,777,896 (GRCm39) |
N1020S |
probably benign |
Het |
Sall2 |
C |
A |
14: 52,550,673 (GRCm39) |
D841Y |
possibly damaging |
Het |
Sbno1 |
T |
A |
5: 124,519,762 (GRCm39) |
H1172L |
probably benign |
Het |
Scaf4 |
A |
T |
16: 90,027,054 (GRCm39) |
L921Q |
probably damaging |
Het |
Sec22c |
C |
A |
9: 121,524,750 (GRCm39) |
R11L |
probably damaging |
Het |
Skint6 |
T |
A |
4: 113,034,173 (GRCm39) |
D318V |
probably damaging |
Het |
Slc22a28 |
T |
C |
19: 8,049,205 (GRCm39) |
N348S |
probably benign |
Het |
Slc44a2 |
G |
T |
9: 21,253,305 (GRCm39) |
K77N |
possibly damaging |
Het |
Smc1b |
C |
T |
15: 84,950,431 (GRCm39) |
V1198I |
probably benign |
Het |
Spef2 |
A |
T |
15: 9,717,568 (GRCm39) |
M316K |
probably damaging |
Het |
Stra8 |
T |
C |
6: 34,911,016 (GRCm39) |
Y215H |
probably damaging |
Het |
Sv2a |
G |
T |
3: 96,097,010 (GRCm39) |
R445L |
probably benign |
Het |
Sycp1 |
A |
C |
3: 102,758,944 (GRCm39) |
L771R |
probably damaging |
Het |
Tchp |
A |
T |
5: 114,859,184 (GRCm39) |
R493* |
probably null |
Het |
Ttc13 |
G |
A |
8: 125,410,039 (GRCm39) |
A391V |
probably benign |
Het |
Unc13b |
C |
T |
4: 43,176,186 (GRCm39) |
T2338I |
unknown |
Het |
Wac |
A |
G |
18: 7,921,592 (GRCm39) |
D576G |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,222,688 (GRCm39) |
N559S |
probably benign |
Het |
Zscan20 |
A |
T |
4: 128,481,914 (GRCm39) |
S583T |
probably benign |
Het |
|
Other mutations in Eogt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00911:Eogt
|
APN |
6 |
97,096,961 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01292:Eogt
|
APN |
6 |
97,120,988 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02332:Eogt
|
APN |
6 |
97,102,566 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Eogt
|
APN |
6 |
97,120,934 (GRCm39) |
missense |
possibly damaging |
0.83 |
disappointment
|
UTSW |
6 |
97,120,926 (GRCm39) |
missense |
probably benign |
0.00 |
lovelorn
|
UTSW |
6 |
97,090,875 (GRCm39) |
missense |
probably damaging |
1.00 |
mournful
|
UTSW |
6 |
97,095,915 (GRCm39) |
splice site |
probably null |
|
predawn
|
UTSW |
6 |
97,112,245 (GRCm39) |
splice site |
probably benign |
|
Underachiever
|
UTSW |
6 |
97,097,162 (GRCm39) |
missense |
probably benign |
0.01 |
R0019:Eogt
|
UTSW |
6 |
97,111,234 (GRCm39) |
unclassified |
probably benign |
|
R0112:Eogt
|
UTSW |
6 |
97,112,245 (GRCm39) |
splice site |
probably benign |
|
R0325:Eogt
|
UTSW |
6 |
97,090,916 (GRCm39) |
missense |
probably damaging |
0.99 |
R0497:Eogt
|
UTSW |
6 |
97,112,194 (GRCm39) |
missense |
probably benign |
0.00 |
R0730:Eogt
|
UTSW |
6 |
97,092,970 (GRCm39) |
nonsense |
probably null |
|
R1730:Eogt
|
UTSW |
6 |
97,090,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Eogt
|
UTSW |
6 |
97,090,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Eogt
|
UTSW |
6 |
97,108,337 (GRCm39) |
missense |
probably benign |
0.02 |
R2279:Eogt
|
UTSW |
6 |
97,111,262 (GRCm39) |
missense |
probably benign |
0.28 |
R2679:Eogt
|
UTSW |
6 |
97,097,761 (GRCm39) |
missense |
probably benign |
0.01 |
R2993:Eogt
|
UTSW |
6 |
97,095,915 (GRCm39) |
splice site |
probably null |
|
R3176:Eogt
|
UTSW |
6 |
97,108,355 (GRCm39) |
missense |
probably benign |
0.21 |
R3276:Eogt
|
UTSW |
6 |
97,108,355 (GRCm39) |
missense |
probably benign |
0.21 |
R3876:Eogt
|
UTSW |
6 |
97,097,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R3940:Eogt
|
UTSW |
6 |
97,090,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Eogt
|
UTSW |
6 |
97,111,265 (GRCm39) |
missense |
probably benign |
0.00 |
R4704:Eogt
|
UTSW |
6 |
97,090,813 (GRCm39) |
missense |
probably damaging |
0.99 |
R4849:Eogt
|
UTSW |
6 |
97,093,016 (GRCm39) |
missense |
probably damaging |
0.99 |
R4867:Eogt
|
UTSW |
6 |
97,097,108 (GRCm39) |
intron |
probably benign |
|
R4905:Eogt
|
UTSW |
6 |
97,119,792 (GRCm39) |
missense |
probably benign |
0.01 |
R5120:Eogt
|
UTSW |
6 |
97,111,276 (GRCm39) |
missense |
probably benign |
|
R5143:Eogt
|
UTSW |
6 |
97,102,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Eogt
|
UTSW |
6 |
97,092,996 (GRCm39) |
missense |
probably benign |
0.01 |
R6351:Eogt
|
UTSW |
6 |
97,097,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6418:Eogt
|
UTSW |
6 |
97,122,353 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6498:Eogt
|
UTSW |
6 |
97,112,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6950:Eogt
|
UTSW |
6 |
97,111,343 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7114:Eogt
|
UTSW |
6 |
97,092,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7185:Eogt
|
UTSW |
6 |
97,097,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Eogt
|
UTSW |
6 |
97,089,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Eogt
|
UTSW |
6 |
97,096,944 (GRCm39) |
missense |
probably damaging |
0.98 |
R7467:Eogt
|
UTSW |
6 |
97,119,794 (GRCm39) |
missense |
probably benign |
0.01 |
R7526:Eogt
|
UTSW |
6 |
97,090,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R7672:Eogt
|
UTSW |
6 |
97,090,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R7851:Eogt
|
UTSW |
6 |
97,097,162 (GRCm39) |
missense |
probably benign |
0.01 |
R7956:Eogt
|
UTSW |
6 |
97,120,926 (GRCm39) |
missense |
probably benign |
0.00 |
R8021:Eogt
|
UTSW |
6 |
97,111,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R8475:Eogt
|
UTSW |
6 |
97,122,327 (GRCm39) |
nonsense |
probably null |
|
R8508:Eogt
|
UTSW |
6 |
97,120,959 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8550:Eogt
|
UTSW |
6 |
97,089,033 (GRCm39) |
missense |
probably benign |
0.20 |
R8854:Eogt
|
UTSW |
6 |
97,108,359 (GRCm39) |
nonsense |
probably null |
|
R9258:Eogt
|
UTSW |
6 |
97,089,043 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9500:Eogt
|
UTSW |
6 |
97,096,992 (GRCm39) |
missense |
probably benign |
0.03 |
|