Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16b |
A |
T |
2: 181,135,209 (GRCm39) |
D37V |
possibly damaging |
Het |
Ankhd1 |
A |
G |
18: 36,765,258 (GRCm39) |
D87G |
|
Het |
Ankrd31 |
A |
G |
13: 97,015,479 (GRCm39) |
S1583G |
probably damaging |
Het |
Ankub1 |
T |
C |
3: 57,599,938 (GRCm39) |
|
probably benign |
Het |
Apba3 |
A |
G |
10: 81,107,067 (GRCm39) |
D264G |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,880,560 (GRCm39) |
M508K |
probably benign |
Het |
Asap1 |
G |
A |
15: 64,002,099 (GRCm39) |
T404M |
probably damaging |
Het |
Cnot3 |
A |
T |
7: 3,648,479 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
AGTGT |
AGT |
7: 55,577,937 (GRCm39) |
|
probably null |
Het |
Cyp3a57 |
A |
G |
5: 145,307,795 (GRCm39) |
I184V |
probably benign |
Het |
D130052B06Rik |
GTCTACACTGTCCTGCACAGGTGACCCATCTACCCCGTCCTATCCTGGCGACCCATCTACACTGTCCTG |
GTCTACACTGTCCTG |
11: 33,573,355 (GRCm39) |
|
probably null |
Het |
Dab1 |
T |
A |
4: 104,570,987 (GRCm39) |
D210E |
|
Het |
Elavl1 |
G |
A |
8: 4,375,199 (GRCm39) |
|
probably benign |
Het |
Emilin1 |
C |
T |
5: 31,074,433 (GRCm39) |
Q225* |
probably null |
Het |
Eml6 |
G |
T |
11: 29,727,258 (GRCm39) |
A1288E |
probably benign |
Het |
Eno1 |
T |
C |
4: 150,329,796 (GRCm39) |
|
probably null |
Het |
Eprs1 |
C |
T |
1: 185,111,898 (GRCm39) |
R303C |
probably damaging |
Het |
Eps15l1 |
G |
A |
8: 73,126,878 (GRCm39) |
A651V |
probably benign |
Het |
Etl4 |
A |
T |
2: 20,714,368 (GRCm39) |
I156F |
probably damaging |
Het |
Faim2 |
A |
T |
15: 99,411,814 (GRCm39) |
I171N |
probably damaging |
Het |
Fam135a |
T |
A |
1: 24,069,939 (GRCm39) |
N381I |
probably damaging |
Het |
Fhip1a |
G |
T |
3: 85,637,831 (GRCm39) |
P156Q |
probably damaging |
Het |
Gabrg3 |
T |
A |
7: 56,384,833 (GRCm39) |
M243L |
probably benign |
Het |
Garin2 |
A |
G |
12: 78,761,809 (GRCm39) |
K158E |
possibly damaging |
Het |
Gm5134 |
A |
G |
10: 75,836,233 (GRCm39) |
I405V |
probably damaging |
Het |
Gm9376 |
A |
T |
14: 118,504,768 (GRCm39) |
K67* |
probably null |
Het |
Grm8 |
A |
T |
6: 27,761,354 (GRCm39) |
I290K |
possibly damaging |
Het |
Hao1 |
T |
A |
2: 134,390,121 (GRCm39) |
M73L |
probably benign |
Het |
Herc1 |
A |
G |
9: 66,369,150 (GRCm39) |
D452G |
|
Het |
Idh3b |
C |
A |
2: 130,123,413 (GRCm39) |
K192N |
possibly damaging |
Het |
Igkv6-23 |
A |
G |
6: 70,237,553 (GRCm39) |
S63P |
probably benign |
Het |
Itgb2 |
A |
C |
10: 77,384,398 (GRCm39) |
D173A |
probably damaging |
Het |
Jmjd8 |
A |
T |
17: 26,049,301 (GRCm39) |
T255S |
probably benign |
Het |
Lamc3 |
A |
C |
2: 31,820,714 (GRCm39) |
E1243A |
probably benign |
Het |
Map1a |
A |
G |
2: 121,129,939 (GRCm39) |
T252A |
probably damaging |
Het |
Mrgpra1 |
C |
A |
7: 46,985,203 (GRCm39) |
A159S |
probably benign |
Het |
Ndst3 |
T |
C |
3: 123,395,131 (GRCm39) |
I500V |
possibly damaging |
Het |
Nhsl1 |
A |
G |
10: 18,407,434 (GRCm39) |
T1523A |
possibly damaging |
Het |
Nr2f1 |
A |
G |
13: 78,343,298 (GRCm39) |
I322T |
probably damaging |
Het |
Nup210 |
T |
C |
6: 91,064,948 (GRCm39) |
E184G |
probably damaging |
Het |
Obsl1 |
C |
T |
1: 75,470,590 (GRCm39) |
W1022* |
probably null |
Het |
Or2l13 |
T |
A |
16: 19,306,449 (GRCm39) |
I287N |
probably damaging |
Het |
Or4a77 |
T |
A |
2: 89,486,846 (GRCm39) |
H313L |
probably benign |
Het |
Or52p2 |
G |
T |
7: 102,237,162 (GRCm39) |
Q263K |
possibly damaging |
Het |
Or5p51 |
A |
T |
7: 107,444,572 (GRCm39) |
Y123N |
probably damaging |
Het |
Or6c1 |
A |
T |
10: 129,518,149 (GRCm39) |
I153N |
probably damaging |
Het |
Or6c65 |
T |
A |
10: 129,603,720 (GRCm39) |
Y118* |
probably null |
Het |
Otulinl |
A |
G |
15: 27,658,319 (GRCm39) |
C184R |
probably benign |
Het |
Oxr1 |
C |
T |
15: 41,677,004 (GRCm39) |
P187L |
not run |
Het |
Parp8 |
A |
G |
13: 117,031,461 (GRCm39) |
L417P |
possibly damaging |
Het |
Pdia6 |
A |
G |
12: 17,324,509 (GRCm39) |
Q120R |
probably benign |
Het |
Ppp3cc |
T |
C |
14: 70,478,252 (GRCm39) |
N290S |
probably benign |
Het |
Prdm5 |
C |
A |
6: 65,808,244 (GRCm39) |
S63R |
possibly damaging |
Het |
Prr14l |
T |
C |
5: 32,988,445 (GRCm39) |
D350G |
probably benign |
Het |
Pwwp2a |
T |
C |
11: 43,607,878 (GRCm39) |
L497S |
probably damaging |
Het |
R3hdm2 |
A |
G |
10: 127,312,547 (GRCm39) |
N430D |
probably benign |
Het |
Rad51ap2 |
A |
G |
12: 11,507,344 (GRCm39) |
N422S |
possibly damaging |
Het |
Rbbp8 |
G |
A |
18: 11,805,638 (GRCm39) |
|
probably null |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCAGCGGCGGC |
7: 97,229,125 (GRCm39) |
|
probably benign |
Het |
Slc22a6 |
G |
A |
19: 8,599,522 (GRCm39) |
|
probably null |
Het |
Slc28a3 |
T |
A |
13: 58,714,045 (GRCm39) |
E440V |
possibly damaging |
Het |
Slc30a5 |
A |
T |
13: 100,947,932 (GRCm39) |
I482K |
probably damaging |
Het |
Slco1a1 |
A |
T |
6: 141,870,223 (GRCm39) |
F305Y |
probably damaging |
Het |
Slco1a8 |
G |
A |
6: 141,938,220 (GRCm39) |
A253V |
probably damaging |
Het |
Slco4c1 |
T |
C |
1: 96,756,690 (GRCm39) |
N544S |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,459,647 (GRCm39) |
I656N |
probably damaging |
Het |
Spata31h1 |
A |
T |
10: 82,120,953 (GRCm39) |
I4019K |
probably benign |
Het |
Taok1 |
A |
T |
11: 77,432,500 (GRCm39) |
L771* |
probably null |
Het |
Tmem231 |
T |
C |
8: 112,641,927 (GRCm39) |
D209G |
possibly damaging |
Het |
Tmem25 |
A |
G |
9: 44,706,705 (GRCm39) |
|
probably null |
Het |
Tmem79 |
T |
C |
3: 88,240,718 (GRCm39) |
T77A |
probably benign |
Het |
Topbp1 |
A |
T |
9: 103,205,836 (GRCm39) |
T825S |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,853,455 (GRCm39) |
Q1825L |
probably benign |
Het |
Uba1y |
T |
A |
Y: 821,348 (GRCm39) |
D110E |
probably damaging |
Het |
Utrn |
A |
T |
10: 12,261,280 (GRCm39) |
N3422K |
probably benign |
Het |
Vmn1r219 |
A |
T |
13: 23,347,314 (GRCm39) |
M168L |
probably benign |
Het |
Vmn2r62 |
T |
C |
7: 42,414,235 (GRCm39) |
H736R |
possibly damaging |
Het |
Wdr1 |
T |
C |
5: 38,697,435 (GRCm39) |
H291R |
possibly damaging |
Het |
Zan |
T |
C |
5: 137,413,401 (GRCm39) |
T3177A |
unknown |
Het |
Zbtb21 |
T |
C |
16: 97,752,495 (GRCm39) |
H596R |
possibly damaging |
Het |
|
Other mutations in Cxxc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01477:Cxxc1
|
APN |
18 |
74,352,985 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02250:Cxxc1
|
APN |
18 |
74,352,240 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02640:Cxxc1
|
APN |
18 |
74,354,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02802:Cxxc1
|
UTSW |
18 |
74,352,481 (GRCm39) |
nonsense |
probably null |
|
P0018:Cxxc1
|
UTSW |
18 |
74,353,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R0534:Cxxc1
|
UTSW |
18 |
74,351,962 (GRCm39) |
missense |
probably benign |
0.00 |
R0557:Cxxc1
|
UTSW |
18 |
74,351,845 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0576:Cxxc1
|
UTSW |
18 |
74,353,256 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0673:Cxxc1
|
UTSW |
18 |
74,351,984 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1539:Cxxc1
|
UTSW |
18 |
74,352,278 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1714:Cxxc1
|
UTSW |
18 |
74,352,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R4763:Cxxc1
|
UTSW |
18 |
74,352,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R5252:Cxxc1
|
UTSW |
18 |
74,353,022 (GRCm39) |
missense |
probably benign |
0.30 |
R5890:Cxxc1
|
UTSW |
18 |
74,354,237 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6908:Cxxc1
|
UTSW |
18 |
74,353,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Cxxc1
|
UTSW |
18 |
74,353,678 (GRCm39) |
critical splice donor site |
probably null |
|
R7404:Cxxc1
|
UTSW |
18 |
74,352,278 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7708:Cxxc1
|
UTSW |
18 |
74,349,314 (GRCm39) |
start gained |
probably benign |
|
R7790:Cxxc1
|
UTSW |
18 |
74,350,855 (GRCm39) |
missense |
probably damaging |
0.99 |
R7956:Cxxc1
|
UTSW |
18 |
74,352,054 (GRCm39) |
splice site |
probably null |
|
R8183:Cxxc1
|
UTSW |
18 |
74,353,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R8337:Cxxc1
|
UTSW |
18 |
74,353,910 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8673:Cxxc1
|
UTSW |
18 |
74,351,915 (GRCm39) |
missense |
probably benign |
0.04 |
R8735:Cxxc1
|
UTSW |
18 |
74,350,331 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8799:Cxxc1
|
UTSW |
18 |
74,354,128 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9122:Cxxc1
|
UTSW |
18 |
74,350,246 (GRCm39) |
missense |
probably benign |
|
R9607:Cxxc1
|
UTSW |
18 |
74,353,479 (GRCm39) |
critical splice donor site |
probably null |
|
R9624:Cxxc1
|
UTSW |
18 |
74,352,512 (GRCm39) |
missense |
possibly damaging |
0.73 |
T0975:Cxxc1
|
UTSW |
18 |
74,353,992 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Cxxc1
|
UTSW |
18 |
74,351,872 (GRCm39) |
missense |
probably benign |
|
|