Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
A |
G |
19: 43,806,477 (GRCm39) |
K764E |
probably damaging |
Het |
Abcg2 |
T |
C |
6: 58,667,525 (GRCm39) |
V129A |
probably benign |
Het |
Adgrf5 |
A |
G |
17: 43,739,477 (GRCm39) |
Y72C |
possibly damaging |
Het |
Ago1 |
C |
T |
4: 126,337,021 (GRCm39) |
R228H |
probably damaging |
Het |
Ano1 |
A |
G |
7: 144,201,789 (GRCm39) |
V334A |
probably damaging |
Het |
Apob |
A |
T |
12: 8,052,164 (GRCm39) |
R1202* |
probably null |
Het |
Arfgap3 |
G |
T |
15: 83,194,501 (GRCm39) |
D389E |
probably benign |
Het |
Atf6b |
A |
T |
17: 34,867,549 (GRCm39) |
|
probably null |
Het |
Atoh8 |
T |
C |
6: 72,212,112 (GRCm39) |
K13E |
probably damaging |
Het |
Bicral |
G |
T |
17: 47,135,814 (GRCm39) |
N465K |
possibly damaging |
Het |
Bves |
T |
A |
10: 45,219,231 (GRCm39) |
Y110N |
probably damaging |
Het |
C4b |
A |
G |
17: 34,947,594 (GRCm39) |
Y1695H |
probably damaging |
Het |
Cage1 |
A |
G |
13: 38,207,356 (GRCm39) |
V163A |
probably benign |
Het |
Canx |
T |
C |
11: 50,195,252 (GRCm39) |
N272S |
probably damaging |
Het |
Caskin1 |
G |
T |
17: 24,715,433 (GRCm39) |
G93V |
probably damaging |
Het |
Cd34 |
T |
C |
1: 194,641,450 (GRCm39) |
V292A |
probably damaging |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdh16 |
C |
A |
8: 105,348,597 (GRCm39) |
G144* |
probably null |
Het |
Chaf1b |
T |
A |
16: 93,691,795 (GRCm39) |
H280Q |
probably damaging |
Het |
Chpf2 |
G |
A |
5: 24,796,220 (GRCm39) |
G389R |
probably damaging |
Het |
Crb1 |
T |
C |
1: 139,242,488 (GRCm39) |
Y330C |
probably damaging |
Het |
Cux2 |
A |
T |
5: 122,007,567 (GRCm39) |
V698E |
probably benign |
Het |
Dhtkd1 |
A |
G |
2: 5,947,430 (GRCm39) |
V18A |
unknown |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Enpp1 |
C |
G |
10: 24,536,090 (GRCm39) |
A437P |
probably damaging |
Het |
Fat2 |
C |
T |
11: 55,172,686 (GRCm39) |
V2676I |
possibly damaging |
Het |
Fzd2 |
A |
G |
11: 102,496,759 (GRCm39) |
D401G |
probably damaging |
Het |
Gnai3 |
C |
T |
3: 108,019,812 (GRCm39) |
V233I |
probably benign |
Het |
Golim4 |
T |
A |
3: 75,802,194 (GRCm39) |
D366V |
possibly damaging |
Het |
Grin1 |
T |
A |
2: 25,206,832 (GRCm39) |
T110S |
probably damaging |
Het |
Grin2a |
A |
G |
16: 9,487,608 (GRCm39) |
V430A |
probably benign |
Het |
Gstp3 |
G |
A |
19: 4,109,282 (GRCm39) |
T5I |
probably damaging |
Het |
Il17rb |
T |
A |
14: 29,719,111 (GRCm39) |
M324L |
probably benign |
Het |
Jmy |
A |
G |
13: 93,596,211 (GRCm39) |
Y473H |
probably damaging |
Het |
Khdc1b |
A |
G |
1: 21,454,534 (GRCm39) |
D79G |
probably benign |
Het |
Kremen2 |
T |
C |
17: 23,961,691 (GRCm39) |
E272G |
possibly damaging |
Het |
Lmo7 |
G |
C |
14: 102,124,614 (GRCm39) |
A358P |
probably damaging |
Het |
Mdh1b |
T |
C |
1: 63,760,741 (GRCm39) |
I107V |
probably benign |
Het |
Mlkl |
T |
C |
8: 112,060,242 (GRCm39) |
Q48R |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,079,665 (GRCm39) |
|
probably null |
Het |
Naip1 |
T |
A |
13: 100,562,081 (GRCm39) |
Q1028L |
probably damaging |
Het |
Ncald |
T |
A |
15: 37,397,423 (GRCm39) |
I86F |
possibly damaging |
Het |
Nid1 |
A |
C |
13: 13,675,058 (GRCm39) |
H926P |
probably benign |
Het |
Nlrp9a |
T |
A |
7: 26,256,787 (GRCm39) |
I46K |
possibly damaging |
Het |
Or1p1 |
A |
G |
11: 74,179,652 (GRCm39) |
Y60C |
probably damaging |
Het |
Or9r3 |
A |
T |
10: 129,947,859 (GRCm39) |
S267T |
probably benign |
Het |
Pak1 |
T |
A |
7: 97,557,004 (GRCm39) |
|
probably null |
Het |
Parpbp |
T |
A |
10: 87,960,824 (GRCm39) |
M221L |
probably benign |
Het |
Pde12 |
T |
C |
14: 26,390,035 (GRCm39) |
I225V |
probably benign |
Het |
Phf19 |
G |
T |
2: 34,789,620 (GRCm39) |
R367S |
probably benign |
Het |
Plcl2 |
A |
G |
17: 50,975,139 (GRCm39) |
|
probably null |
Het |
Plxnb1 |
A |
T |
9: 108,938,294 (GRCm39) |
I1283F |
possibly damaging |
Het |
Pramel6 |
T |
A |
2: 87,339,059 (GRCm39) |
N86K |
possibly damaging |
Het |
Prkdc |
A |
G |
16: 15,545,469 (GRCm39) |
T1862A |
probably benign |
Het |
Prpf40a |
A |
T |
2: 53,034,851 (GRCm39) |
I779K |
probably damaging |
Het |
Prss3b |
G |
A |
6: 41,009,315 (GRCm39) |
T173I |
probably benign |
Het |
Ptpn20 |
A |
T |
14: 33,352,942 (GRCm39) |
E227V |
probably damaging |
Het |
Rad54b |
C |
T |
4: 11,606,088 (GRCm39) |
R499C |
probably benign |
Het |
Rarg |
C |
A |
15: 102,147,939 (GRCm39) |
A291S |
probably damaging |
Het |
Rnf169 |
A |
T |
7: 99,574,615 (GRCm39) |
L660Q |
probably damaging |
Het |
Scn4a |
A |
G |
11: 106,226,550 (GRCm39) |
V670A |
probably damaging |
Het |
Serpinb9c |
A |
T |
13: 33,340,854 (GRCm39) |
C81* |
probably null |
Het |
Sik1 |
A |
G |
17: 32,067,771 (GRCm39) |
S435P |
probably benign |
Het |
Slc35g2 |
G |
A |
9: 100,435,329 (GRCm39) |
A114V |
probably damaging |
Het |
Slc7a14 |
A |
T |
3: 31,291,645 (GRCm39) |
V211E |
probably damaging |
Het |
Snrpn |
A |
T |
7: 59,637,204 (GRCm39) |
H37Q |
possibly damaging |
Het |
Spock3 |
T |
A |
8: 63,698,204 (GRCm39) |
C185* |
probably null |
Het |
Tbc1d4 |
A |
G |
14: 101,714,591 (GRCm39) |
S627P |
probably damaging |
Het |
Tgoln1 |
T |
C |
6: 72,592,653 (GRCm39) |
T276A |
probably benign |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tnpo2 |
T |
C |
8: 85,776,742 (GRCm39) |
L483P |
probably damaging |
Het |
Tpte |
T |
A |
8: 22,808,355 (GRCm39) |
D163E |
probably benign |
Het |
Trim36 |
A |
T |
18: 46,329,229 (GRCm39) |
D70E |
probably benign |
Het |
Umodl1 |
G |
A |
17: 31,227,740 (GRCm39) |
|
probably null |
Het |
Wdr90 |
T |
C |
17: 26,074,173 (GRCm39) |
T691A |
probably benign |
Het |
Zdhhc8 |
A |
G |
16: 18,046,210 (GRCm39) |
S118P |
probably damaging |
Het |
Zfp438 |
T |
C |
18: 5,214,085 (GRCm39) |
E291G |
probably benign |
Het |
Zfp879 |
C |
T |
11: 50,723,428 (GRCm39) |
E543K |
probably benign |
Het |
|
Other mutations in Gcm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01312:Gcm2
|
APN |
13 |
41,256,607 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01476:Gcm2
|
APN |
13 |
41,259,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02034:Gcm2
|
APN |
13 |
41,259,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02186:Gcm2
|
APN |
13 |
41,258,125 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02456:Gcm2
|
APN |
13 |
41,256,477 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03142:Gcm2
|
APN |
13 |
41,256,711 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03184:Gcm2
|
APN |
13 |
41,258,888 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Gcm2
|
UTSW |
13 |
41,256,315 (GRCm39) |
missense |
probably benign |
0.01 |
R0227:Gcm2
|
UTSW |
13 |
41,259,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R1061:Gcm2
|
UTSW |
13 |
41,259,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Gcm2
|
UTSW |
13 |
41,259,367 (GRCm39) |
missense |
probably benign |
0.19 |
R2058:Gcm2
|
UTSW |
13 |
41,263,430 (GRCm39) |
start codon destroyed |
probably null |
0.28 |
R2059:Gcm2
|
UTSW |
13 |
41,263,430 (GRCm39) |
start codon destroyed |
probably null |
0.28 |
R2351:Gcm2
|
UTSW |
13 |
41,257,094 (GRCm39) |
missense |
probably benign |
0.02 |
R4653:Gcm2
|
UTSW |
13 |
41,256,317 (GRCm39) |
missense |
probably benign |
0.21 |
R4782:Gcm2
|
UTSW |
13 |
41,256,970 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4799:Gcm2
|
UTSW |
13 |
41,256,970 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5135:Gcm2
|
UTSW |
13 |
41,256,435 (GRCm39) |
missense |
probably benign |
|
R5162:Gcm2
|
UTSW |
13 |
41,257,131 (GRCm39) |
missense |
probably benign |
0.01 |
R5665:Gcm2
|
UTSW |
13 |
41,263,387 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5756:Gcm2
|
UTSW |
13 |
41,263,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R5771:Gcm2
|
UTSW |
13 |
41,256,991 (GRCm39) |
missense |
probably benign |
0.40 |
R5928:Gcm2
|
UTSW |
13 |
41,256,874 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Gcm2
|
UTSW |
13 |
41,256,603 (GRCm39) |
missense |
probably damaging |
0.99 |
R6394:Gcm2
|
UTSW |
13 |
41,263,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Gcm2
|
UTSW |
13 |
41,259,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Gcm2
|
UTSW |
13 |
41,259,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Gcm2
|
UTSW |
13 |
41,256,840 (GRCm39) |
missense |
probably damaging |
0.98 |
R7413:Gcm2
|
UTSW |
13 |
41,259,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Gcm2
|
UTSW |
13 |
41,256,751 (GRCm39) |
missense |
probably benign |
0.02 |
R8293:Gcm2
|
UTSW |
13 |
41,256,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R8738:Gcm2
|
UTSW |
13 |
41,258,096 (GRCm39) |
missense |
probably benign |
0.41 |
R9087:Gcm2
|
UTSW |
13 |
41,263,406 (GRCm39) |
missense |
|
|
R9316:Gcm2
|
UTSW |
13 |
41,259,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Gcm2
|
UTSW |
13 |
41,258,924 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Gcm2
|
UTSW |
13 |
41,256,268 (GRCm39) |
missense |
probably damaging |
1.00 |
|