Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
C |
T |
11: 9,278,138 (GRCm39) |
S3106F |
probably damaging |
Het |
Acss1 |
G |
T |
2: 150,484,809 (GRCm39) |
R145S |
probably damaging |
Het |
Acss3 |
T |
C |
10: 106,920,783 (GRCm39) |
Y109C |
probably damaging |
Het |
Adgre4 |
G |
T |
17: 56,109,189 (GRCm39) |
G399C |
probably damaging |
Het |
Alpk1 |
A |
G |
3: 127,473,232 (GRCm39) |
S924P |
probably damaging |
Het |
Anapc4 |
T |
A |
5: 53,007,884 (GRCm39) |
D382E |
possibly damaging |
Het |
Arfgef2 |
C |
T |
2: 166,709,253 (GRCm39) |
A1110V |
possibly damaging |
Het |
Arhgap20 |
T |
C |
9: 51,760,311 (GRCm39) |
F721L |
probably benign |
Het |
Arhgef39 |
T |
C |
4: 43,497,185 (GRCm39) |
S269G |
probably benign |
Het |
Asap2 |
C |
T |
12: 21,279,249 (GRCm39) |
T377M |
probably damaging |
Het |
Baiap3 |
G |
T |
17: 25,466,010 (GRCm39) |
A558E |
probably benign |
Het |
Birc6 |
A |
C |
17: 75,009,313 (GRCm39) |
T4862P |
probably benign |
Het |
Cc2d2a |
A |
G |
5: 43,867,884 (GRCm39) |
T843A |
probably benign |
Het |
Ccdc187 |
A |
T |
2: 26,171,079 (GRCm39) |
D466E |
probably benign |
Het |
Ccdc88a |
T |
G |
11: 29,435,888 (GRCm39) |
N1270K |
probably benign |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Cntn1 |
T |
G |
15: 92,150,278 (GRCm39) |
Y371D |
probably benign |
Het |
Cpsf1 |
T |
C |
15: 76,481,528 (GRCm39) |
D1141G |
probably damaging |
Het |
Crebbp |
C |
T |
16: 3,925,935 (GRCm39) |
V1193I |
probably benign |
Het |
Csf2ra |
A |
T |
19: 61,213,597 (GRCm39) |
S371T |
probably null |
Het |
Csf2rb2 |
T |
C |
15: 78,172,115 (GRCm39) |
N432D |
probably benign |
Het |
Cul9 |
A |
T |
17: 46,854,177 (GRCm39) |
L175Q |
probably damaging |
Het |
Dlc1 |
T |
A |
8: 37,405,394 (GRCm39) |
R132* |
probably null |
Het |
Dock5 |
C |
A |
14: 68,013,749 (GRCm39) |
L1324F |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,403,300 (GRCm39) |
V36A |
possibly damaging |
Het |
Fap |
A |
G |
2: 62,378,927 (GRCm39) |
V158A |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,410,277 (GRCm39) |
S319T |
possibly damaging |
Het |
Gatd3a |
T |
C |
10: 78,003,323 (GRCm39) |
I110V |
possibly damaging |
Het |
Gphn |
T |
C |
12: 78,656,013 (GRCm39) |
|
probably null |
Het |
Gucy2g |
A |
G |
19: 55,226,406 (GRCm39) |
I170T |
probably benign |
Het |
Hmgxb4 |
T |
A |
8: 75,748,466 (GRCm39) |
W438R |
probably damaging |
Het |
Igkv14-126 |
G |
T |
6: 67,873,329 (GRCm39) |
G19V |
probably damaging |
Het |
Kansl1l |
C |
T |
1: 66,812,101 (GRCm39) |
C506Y |
probably damaging |
Het |
Kif2a |
T |
C |
13: 107,115,543 (GRCm39) |
T321A |
probably damaging |
Het |
Krtap6-5 |
C |
T |
16: 88,844,607 (GRCm39) |
R42H |
unknown |
Het |
Map4 |
T |
A |
9: 109,864,185 (GRCm39) |
M470K |
probably benign |
Het |
Mill1 |
T |
C |
7: 17,996,982 (GRCm39) |
V191A |
probably benign |
Het |
Mki67 |
C |
A |
7: 135,297,364 (GRCm39) |
A2557S |
possibly damaging |
Het |
Mkln1 |
A |
T |
6: 31,473,681 (GRCm39) |
H669L |
probably damaging |
Het |
Mrgprb3 |
A |
T |
7: 48,293,422 (GRCm39) |
V43E |
possibly damaging |
Het |
Mucl2 |
T |
A |
15: 103,927,860 (GRCm39) |
|
probably null |
Het |
Mybbp1a |
T |
A |
11: 72,337,076 (GRCm39) |
I604N |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,841,164 (GRCm39) |
T2210A |
probably benign |
Het |
Nlrp4f |
T |
C |
13: 65,330,749 (GRCm39) |
I881M |
probably benign |
Het |
Obscn |
C |
A |
11: 58,943,442 (GRCm39) |
A4236S |
probably benign |
Het |
Or13a23-ps1 |
A |
T |
7: 140,119,038 (GRCm39) |
M203L |
unknown |
Het |
Or4a67 |
A |
C |
2: 88,598,630 (GRCm39) |
F10V |
possibly damaging |
Het |
Or8d1 |
A |
G |
9: 38,767,254 (GRCm39) |
K299E |
probably damaging |
Het |
Or8d2b |
G |
A |
9: 38,789,150 (GRCm39) |
R226H |
probably benign |
Het |
Phc3 |
T |
A |
3: 31,015,926 (GRCm39) |
Q83L |
possibly damaging |
Het |
Pira2 |
T |
C |
7: 3,845,070 (GRCm39) |
Y396C |
probably damaging |
Het |
Prss3 |
T |
A |
6: 41,353,872 (GRCm39) |
I24F |
probably damaging |
Het |
Ros1 |
G |
T |
10: 51,999,333 (GRCm39) |
R1206S |
probably benign |
Het |
Smg9 |
A |
T |
7: 24,120,055 (GRCm39) |
Q386L |
probably benign |
Het |
Sncb |
T |
A |
13: 54,907,772 (GRCm39) |
|
probably null |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,222 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
T |
A |
9: 41,957,848 (GRCm39) |
I599F |
probably damaging |
Het |
Sox6 |
C |
A |
7: 115,076,218 (GRCm39) |
E807* |
probably null |
Het |
Ssu2 |
G |
A |
6: 112,360,898 (GRCm39) |
A53V |
probably benign |
Het |
Tas2r123 |
T |
C |
6: 132,824,333 (GRCm39) |
C77R |
probably benign |
Het |
Tcta |
T |
C |
9: 108,181,333 (GRCm39) |
R117G |
unknown |
Het |
Tiam1 |
G |
A |
16: 89,609,894 (GRCm39) |
A1038V |
probably damaging |
Het |
Tram2 |
A |
T |
1: 21,074,273 (GRCm39) |
|
probably benign |
Het |
Tsku |
C |
A |
7: 98,001,704 (GRCm39) |
R209L |
probably damaging |
Het |
Twnk |
T |
C |
19: 45,000,149 (GRCm39) |
F622L |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,670 (GRCm39) |
T106I |
probably damaging |
Het |
Usf1 |
C |
T |
1: 171,245,352 (GRCm39) |
R255W |
probably damaging |
Het |
Usp28 |
T |
A |
9: 48,949,124 (GRCm39) |
L906Q |
probably null |
Het |
Vmn2r31 |
T |
A |
7: 7,399,654 (GRCm39) |
Y101F |
probably benign |
Het |
Vmn2r42 |
A |
G |
7: 8,187,331 (GRCm39) |
S814P |
probably damaging |
Het |
Wnt2b |
T |
C |
3: 104,858,475 (GRCm39) |
R265G |
possibly damaging |
Het |
Zfp62 |
T |
G |
11: 49,106,892 (GRCm39) |
S328A |
possibly damaging |
Het |
Zfp974 |
T |
C |
7: 27,610,589 (GRCm39) |
I379V |
probably benign |
Het |
Zmynd15 |
T |
C |
11: 70,355,065 (GRCm39) |
V484A |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,791,499 (GRCm39) |
L2201P |
probably damaging |
Het |
|
Other mutations in Psg21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01571:Psg21
|
APN |
7 |
18,388,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02390:Psg21
|
APN |
7 |
18,386,556 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02548:Psg21
|
APN |
7 |
18,388,961 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03001:Psg21
|
APN |
7 |
18,386,410 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03135:Psg21
|
APN |
7 |
18,388,843 (GRCm39) |
missense |
probably benign |
0.00 |
R0131:Psg21
|
UTSW |
7 |
18,388,793 (GRCm39) |
missense |
probably benign |
0.39 |
R0551:Psg21
|
UTSW |
7 |
18,386,565 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1512:Psg21
|
UTSW |
7 |
18,390,425 (GRCm39) |
missense |
probably benign |
0.00 |
R1874:Psg21
|
UTSW |
7 |
18,384,741 (GRCm39) |
missense |
probably benign |
0.15 |
R1993:Psg21
|
UTSW |
7 |
18,388,695 (GRCm39) |
missense |
probably benign |
0.04 |
R2327:Psg21
|
UTSW |
7 |
18,386,378 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3414:Psg21
|
UTSW |
7 |
18,386,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R4422:Psg21
|
UTSW |
7 |
18,381,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R5138:Psg21
|
UTSW |
7 |
18,390,453 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R5623:Psg21
|
UTSW |
7 |
18,388,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R5686:Psg21
|
UTSW |
7 |
18,386,183 (GRCm39) |
intron |
probably benign |
|
R6166:Psg21
|
UTSW |
7 |
18,390,664 (GRCm39) |
unclassified |
probably benign |
|
R6177:Psg21
|
UTSW |
7 |
18,386,279 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6190:Psg21
|
UTSW |
7 |
18,388,926 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6210:Psg21
|
UTSW |
7 |
18,386,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R6482:Psg21
|
UTSW |
7 |
18,388,664 (GRCm39) |
splice site |
probably null |
|
R6729:Psg21
|
UTSW |
7 |
18,386,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Psg21
|
UTSW |
7 |
18,386,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Psg21
|
UTSW |
7 |
18,388,668 (GRCm39) |
critical splice donor site |
probably null |
|
R7075:Psg21
|
UTSW |
7 |
18,388,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R7081:Psg21
|
UTSW |
7 |
18,388,774 (GRCm39) |
nonsense |
probably null |
|
R7098:Psg21
|
UTSW |
7 |
18,386,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R7582:Psg21
|
UTSW |
7 |
18,381,128 (GRCm39) |
makesense |
probably null |
|
R7588:Psg21
|
UTSW |
7 |
18,381,134 (GRCm39) |
missense |
probably benign |
0.00 |
R7607:Psg21
|
UTSW |
7 |
18,388,708 (GRCm39) |
missense |
probably benign |
0.02 |
R7830:Psg21
|
UTSW |
7 |
18,381,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7964:Psg21
|
UTSW |
7 |
18,381,136 (GRCm39) |
missense |
probably benign |
0.01 |
R8758:Psg21
|
UTSW |
7 |
18,384,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8988:Psg21
|
UTSW |
7 |
18,386,389 (GRCm39) |
missense |
probably benign |
0.00 |
R9119:Psg21
|
UTSW |
7 |
18,381,409 (GRCm39) |
missense |
probably benign |
0.14 |
R9446:Psg21
|
UTSW |
7 |
18,388,865 (GRCm39) |
missense |
probably benign |
0.00 |
|