Incidental Mutation 'R7213:Pik3c2g'
ID |
561204 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pik3c2g
|
Ensembl Gene |
ENSMUSG00000030228 |
Gene Name |
phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma |
Synonyms |
|
MMRRC Submission |
045341-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.118)
|
Stock # |
R7213 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
6 |
Chromosomal Location |
139591070-139915010 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 139805990 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 604
(I604F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000107499
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000087657]
[ENSMUST00000111868]
[ENSMUST00000218528]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000087657
AA Change: I236F
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000084939 Gene: ENSMUSG00000030228 AA Change: I236F
Domain | Start | End | E-Value | Type |
PI3Kc
|
125 |
387 |
2.11e-109 |
SMART |
PX
|
411 |
515 |
1.24e-21 |
SMART |
C2
|
550 |
647 |
1.34e-7 |
SMART |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000107499 Gene: ENSMUSG00000030228 AA Change: I604F
Domain | Start | End | E-Value | Type |
SCOP:d1e8xa2
|
1 |
83 |
4e-16 |
SMART |
PI3Ka
|
103 |
288 |
7.6e-29 |
SMART |
PI3Kc
|
375 |
637 |
2.11e-109 |
SMART |
PX
|
661 |
765 |
1.24e-21 |
SMART |
C2
|
800 |
897 |
1.34e-7 |
SMART |
|
Predicted Effect |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
99% (80/81) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the phosphoinositide 3-kinase (PI3K) family. PI3-kinases play roles in signaling pathways involved in cell proliferation, oncogenic transformation, cell survival, cell migration, and intracellular protein trafficking. This protein contains a lipid kinase catalytic domain as well as a C-terminal C2 domain, a characteristic of class II PI3-kinases. C2 domains act as calcium-dependent phospholipid binding motifs that mediate translocation of proteins to membranes, and may also mediate protein-protein interactions. This gene may play a role in several diseases, including type II diabetes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] PHENOTYPE: Mice homozygous for a knock-out allelel exhibit reduced liver glucogen accumulation, hyperlipidemia, adiposity and insulin resistance with age or after consumption of a high-fat diet. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
G |
T |
9: 124,056,530 (GRCm39) |
Y131* |
probably null |
Het |
2310009B15Rik |
A |
T |
1: 138,781,367 (GRCm39) |
V94D |
probably damaging |
Het |
Actr1b |
T |
A |
1: 36,741,221 (GRCm39) |
N120I |
probably damaging |
Het |
Adam17 |
A |
T |
12: 21,386,679 (GRCm39) |
Y452* |
probably null |
Het |
Adam19 |
A |
T |
11: 46,012,298 (GRCm39) |
T265S |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,441,733 (GRCm39) |
T945A |
probably benign |
Het |
Bpifa5 |
G |
A |
2: 154,007,903 (GRCm39) |
V182M |
possibly damaging |
Het |
Celsr3 |
C |
T |
9: 108,726,239 (GRCm39) |
T3156I |
probably damaging |
Het |
Cntrl |
A |
G |
2: 35,025,692 (GRCm39) |
M674V |
possibly damaging |
Het |
Cry2 |
C |
T |
2: 92,244,004 (GRCm39) |
V390I |
probably benign |
Het |
Cspg4b |
T |
A |
13: 113,454,475 (GRCm39) |
F174I |
|
Het |
Cwc25 |
G |
T |
11: 97,644,855 (GRCm39) |
Q168K |
probably benign |
Het |
Dcbld2 |
C |
T |
16: 58,271,126 (GRCm39) |
A301V |
probably benign |
Het |
Dclre1a |
T |
C |
19: 56,518,067 (GRCm39) |
Y1004C |
probably damaging |
Het |
Ddhd1 |
A |
C |
14: 45,895,210 (GRCm39) |
S87A |
probably benign |
Het |
Ear1 |
A |
G |
14: 44,056,611 (GRCm39) |
C86R |
probably damaging |
Het |
Epha5 |
T |
C |
5: 84,381,782 (GRCm39) |
|
probably null |
Het |
Fat2 |
A |
T |
11: 55,171,871 (GRCm39) |
Y2947* |
probably null |
Het |
Fat4 |
G |
A |
3: 39,053,236 (GRCm39) |
V4077M |
possibly damaging |
Het |
Fbxl12 |
A |
T |
9: 20,550,304 (GRCm39) |
V140E |
probably damaging |
Het |
Fbxo16 |
A |
G |
14: 65,536,868 (GRCm39) |
|
probably null |
Het |
Fto |
A |
T |
8: 92,118,135 (GRCm39) |
Q29L |
probably benign |
Het |
Gk5 |
C |
T |
9: 96,027,765 (GRCm39) |
T200M |
probably damaging |
Het |
Gm5916 |
C |
T |
9: 36,039,946 (GRCm39) |
G14E |
possibly damaging |
Het |
Gm9972 |
A |
T |
11: 42,927,235 (GRCm39) |
|
probably benign |
Het |
Gpr139 |
T |
A |
7: 118,744,322 (GRCm39) |
M88L |
probably benign |
Het |
Gpr26 |
T |
C |
7: 131,569,219 (GRCm39) |
L188P |
probably damaging |
Het |
H2ac4 |
G |
T |
13: 23,935,146 (GRCm39) |
A11S |
unknown |
Het |
Hbp1 |
A |
T |
12: 31,987,196 (GRCm39) |
S219T |
probably benign |
Het |
Hr |
A |
T |
14: 70,795,790 (GRCm39) |
E445V |
probably damaging |
Het |
Il12rb1 |
A |
G |
8: 71,269,097 (GRCm39) |
K426E |
probably benign |
Het |
Itgbl1 |
G |
A |
14: 124,210,709 (GRCm39) |
C469Y |
probably damaging |
Het |
Kdm2b |
A |
T |
5: 123,059,532 (GRCm39) |
N523K |
probably damaging |
Het |
Kptn |
A |
G |
7: 15,854,704 (GRCm39) |
N125S |
possibly damaging |
Het |
Krt17 |
T |
C |
11: 100,149,356 (GRCm39) |
N238S |
probably benign |
Het |
Lemd3 |
G |
A |
10: 120,814,145 (GRCm39) |
R363* |
probably null |
Het |
Mmrn1 |
G |
A |
6: 60,921,527 (GRCm39) |
|
probably benign |
Het |
Mtus1 |
T |
C |
8: 41,537,524 (GRCm39) |
D64G |
probably damaging |
Het |
Muc16 |
A |
G |
9: 18,552,712 (GRCm39) |
V4527A |
probably benign |
Het |
Naip2 |
T |
A |
13: 100,323,991 (GRCm39) |
D193V |
probably damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,360,645 (GRCm39) |
H1462R |
probably benign |
Het |
Or2n1b |
T |
C |
17: 38,459,965 (GRCm39) |
V162A |
probably benign |
Het |
Or5ak20 |
A |
T |
2: 85,183,900 (GRCm39) |
Y123* |
probably null |
Het |
Pappa2 |
T |
A |
1: 158,764,456 (GRCm39) |
T352S |
possibly damaging |
Het |
Pcnt |
A |
G |
10: 76,244,738 (GRCm39) |
L1114P |
probably damaging |
Het |
Pde6b |
T |
C |
5: 108,551,956 (GRCm39) |
Y212H |
probably damaging |
Het |
Pld2 |
A |
G |
11: 70,444,198 (GRCm39) |
D498G |
probably benign |
Het |
Prag1 |
A |
T |
8: 36,613,769 (GRCm39) |
Q1107L |
probably damaging |
Het |
Pwp1 |
A |
T |
10: 85,712,173 (GRCm39) |
I110F |
probably benign |
Het |
Rims4 |
C |
T |
2: 163,705,981 (GRCm39) |
V218I |
probably benign |
Het |
Rnf10 |
C |
T |
5: 115,380,532 (GRCm39) |
S754N |
probably damaging |
Het |
Rnf10 |
T |
C |
5: 115,380,533 (GRCm39) |
S754G |
probably damaging |
Het |
Sel1l2 |
A |
T |
2: 140,086,055 (GRCm39) |
V512E |
probably damaging |
Het |
Shank2 |
T |
A |
7: 143,585,146 (GRCm39) |
M49K |
probably benign |
Het |
Sipa1 |
T |
C |
19: 5,710,551 (GRCm39) |
D153G |
probably damaging |
Het |
Slc46a2 |
C |
T |
4: 59,914,279 (GRCm39) |
V215I |
possibly damaging |
Het |
Slco6c1 |
G |
A |
1: 97,055,671 (GRCm39) |
L77F |
probably benign |
Het |
Smarca2 |
T |
C |
19: 26,624,531 (GRCm39) |
L397P |
possibly damaging |
Het |
Spg7 |
C |
T |
8: 123,816,971 (GRCm39) |
A554V |
probably damaging |
Het |
Stab1 |
T |
A |
14: 30,865,630 (GRCm39) |
M1753L |
probably benign |
Het |
Stk11 |
A |
G |
10: 79,952,452 (GRCm39) |
M1V |
probably null |
Het |
Supt6 |
C |
A |
11: 78,122,976 (GRCm39) |
G136C |
probably damaging |
Het |
Svil |
G |
T |
18: 5,094,574 (GRCm39) |
R1418L |
probably damaging |
Het |
Tfg |
A |
G |
16: 56,521,516 (GRCm39) |
S167P |
probably benign |
Het |
Timeless |
T |
C |
10: 128,079,158 (GRCm39) |
V335A |
probably benign |
Het |
Tll2 |
C |
A |
19: 41,108,666 (GRCm39) |
R328L |
probably damaging |
Het |
Tomm7 |
T |
C |
5: 24,049,059 (GRCm39) |
S5G |
possibly damaging |
Het |
Ttc39c |
G |
A |
18: 12,820,138 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,556,105 (GRCm39) |
E30300G |
probably benign |
Het |
Tuba4a |
A |
T |
1: 75,192,341 (GRCm39) |
D452E |
possibly damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,587,927 (GRCm39) |
I233V |
probably benign |
Het |
Tubgcp5 |
T |
A |
7: 55,455,860 (GRCm39) |
V296E |
probably damaging |
Het |
Vmn2r53 |
T |
C |
7: 12,334,983 (GRCm39) |
S226G |
probably benign |
Het |
Xrcc6 |
T |
C |
15: 81,901,027 (GRCm39) |
|
probably benign |
Het |
Zfhx4 |
C |
A |
3: 5,461,704 (GRCm39) |
D1192E |
probably benign |
Het |
Zfp180 |
G |
T |
7: 23,803,938 (GRCm39) |
W119L |
possibly damaging |
Het |
Zfp3 |
A |
G |
11: 70,663,351 (GRCm39) |
I437V |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,976,689 (GRCm39) |
Q986L |
probably benign |
Het |
Zfp937 |
T |
A |
2: 150,081,385 (GRCm39) |
C472S |
probably damaging |
Het |
|
Other mutations in Pik3c2g |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Pik3c2g
|
APN |
6 |
139,841,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01355:Pik3c2g
|
APN |
6 |
139,798,583 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01579:Pik3c2g
|
APN |
6 |
139,700,467 (GRCm39) |
nonsense |
probably null |
|
IGL01580:Pik3c2g
|
APN |
6 |
139,599,514 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01587:Pik3c2g
|
APN |
6 |
139,700,467 (GRCm39) |
nonsense |
probably null |
|
IGL01813:Pik3c2g
|
APN |
6 |
139,599,407 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02218:Pik3c2g
|
APN |
6 |
139,806,081 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02479:Pik3c2g
|
APN |
6 |
139,863,730 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02480:Pik3c2g
|
APN |
6 |
139,798,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02721:Pik3c2g
|
APN |
6 |
139,682,699 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02967:Pik3c2g
|
APN |
6 |
139,913,554 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03221:Pik3c2g
|
APN |
6 |
139,718,133 (GRCm39) |
critical splice acceptor site |
probably null |
|
FR4304:Pik3c2g
|
UTSW |
6 |
139,612,654 (GRCm39) |
frame shift |
probably null |
|
FR4340:Pik3c2g
|
UTSW |
6 |
139,612,654 (GRCm39) |
frame shift |
probably null |
|
FR4976:Pik3c2g
|
UTSW |
6 |
139,612,652 (GRCm39) |
frame shift |
probably null |
|
IGL02837:Pik3c2g
|
UTSW |
6 |
139,603,562 (GRCm39) |
nonsense |
probably null |
|
PIT4531001:Pik3c2g
|
UTSW |
6 |
139,805,096 (GRCm39) |
missense |
|
|
R0002:Pik3c2g
|
UTSW |
6 |
139,714,471 (GRCm39) |
missense |
probably benign |
0.08 |
R0081:Pik3c2g
|
UTSW |
6 |
139,903,519 (GRCm39) |
missense |
probably benign |
0.05 |
R0098:Pik3c2g
|
UTSW |
6 |
139,639,441 (GRCm39) |
missense |
unknown |
|
R0719:Pik3c2g
|
UTSW |
6 |
139,606,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R0740:Pik3c2g
|
UTSW |
6 |
139,610,791 (GRCm39) |
critical splice donor site |
probably null |
|
R0837:Pik3c2g
|
UTSW |
6 |
139,903,425 (GRCm39) |
splice site |
probably benign |
|
R0840:Pik3c2g
|
UTSW |
6 |
139,841,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1306:Pik3c2g
|
UTSW |
6 |
139,718,154 (GRCm39) |
missense |
probably benign |
|
R1501:Pik3c2g
|
UTSW |
6 |
139,789,796 (GRCm39) |
critical splice donor site |
probably null |
|
R1591:Pik3c2g
|
UTSW |
6 |
139,693,904 (GRCm39) |
missense |
probably benign |
0.00 |
R1666:Pik3c2g
|
UTSW |
6 |
139,612,634 (GRCm39) |
intron |
probably benign |
|
R1907:Pik3c2g
|
UTSW |
6 |
139,789,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Pik3c2g
|
UTSW |
6 |
139,846,112 (GRCm39) |
critical splice donor site |
probably null |
|
R1982:Pik3c2g
|
UTSW |
6 |
139,599,546 (GRCm39) |
missense |
probably damaging |
0.97 |
R2171:Pik3c2g
|
UTSW |
6 |
139,801,012 (GRCm39) |
nonsense |
probably null |
|
R2188:Pik3c2g
|
UTSW |
6 |
139,798,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R3777:Pik3c2g
|
UTSW |
6 |
139,599,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R3778:Pik3c2g
|
UTSW |
6 |
139,599,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R3965:Pik3c2g
|
UTSW |
6 |
139,801,018 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4076:Pik3c2g
|
UTSW |
6 |
139,798,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R4078:Pik3c2g
|
UTSW |
6 |
139,612,608 (GRCm39) |
intron |
probably benign |
|
R4108:Pik3c2g
|
UTSW |
6 |
139,676,096 (GRCm39) |
missense |
probably benign |
0.00 |
R4461:Pik3c2g
|
UTSW |
6 |
139,787,407 (GRCm39) |
intron |
probably benign |
|
R4474:Pik3c2g
|
UTSW |
6 |
139,610,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R4509:Pik3c2g
|
UTSW |
6 |
139,665,732 (GRCm39) |
missense |
probably benign |
0.25 |
R4646:Pik3c2g
|
UTSW |
6 |
139,665,744 (GRCm39) |
missense |
probably benign |
0.05 |
R4732:Pik3c2g
|
UTSW |
6 |
139,881,711 (GRCm39) |
missense |
probably benign |
0.28 |
R4733:Pik3c2g
|
UTSW |
6 |
139,881,711 (GRCm39) |
missense |
probably benign |
0.28 |
R4854:Pik3c2g
|
UTSW |
6 |
139,714,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Pik3c2g
|
UTSW |
6 |
139,913,528 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4959:Pik3c2g
|
UTSW |
6 |
139,789,657 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4973:Pik3c2g
|
UTSW |
6 |
139,789,657 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5032:Pik3c2g
|
UTSW |
6 |
139,841,928 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Pik3c2g
|
UTSW |
6 |
139,665,873 (GRCm39) |
missense |
probably null |
0.00 |
R5072:Pik3c2g
|
UTSW |
6 |
139,665,873 (GRCm39) |
missense |
probably null |
0.00 |
R5073:Pik3c2g
|
UTSW |
6 |
139,665,873 (GRCm39) |
missense |
probably null |
0.00 |
R5074:Pik3c2g
|
UTSW |
6 |
139,665,873 (GRCm39) |
missense |
probably null |
0.00 |
R5107:Pik3c2g
|
UTSW |
6 |
139,612,623 (GRCm39) |
intron |
probably benign |
|
R5186:Pik3c2g
|
UTSW |
6 |
139,599,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5253:Pik3c2g
|
UTSW |
6 |
139,841,983 (GRCm39) |
critical splice donor site |
probably null |
|
R5359:Pik3c2g
|
UTSW |
6 |
139,599,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5394:Pik3c2g
|
UTSW |
6 |
139,665,808 (GRCm39) |
missense |
probably benign |
|
R5417:Pik3c2g
|
UTSW |
6 |
139,682,669 (GRCm39) |
missense |
probably benign |
|
R5435:Pik3c2g
|
UTSW |
6 |
139,661,581 (GRCm39) |
splice site |
probably null |
|
R5580:Pik3c2g
|
UTSW |
6 |
139,603,531 (GRCm39) |
missense |
probably damaging |
0.99 |
R5664:Pik3c2g
|
UTSW |
6 |
139,682,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R5908:Pik3c2g
|
UTSW |
6 |
139,714,436 (GRCm39) |
missense |
|
|
R5914:Pik3c2g
|
UTSW |
6 |
139,599,477 (GRCm39) |
missense |
probably benign |
0.00 |
R6046:Pik3c2g
|
UTSW |
6 |
139,842,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Pik3c2g
|
UTSW |
6 |
139,599,137 (GRCm39) |
missense |
probably damaging |
0.96 |
R6298:Pik3c2g
|
UTSW |
6 |
139,603,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R6382:Pik3c2g
|
UTSW |
6 |
139,665,724 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6480:Pik3c2g
|
UTSW |
6 |
139,676,195 (GRCm39) |
missense |
probably benign |
0.27 |
R6917:Pik3c2g
|
UTSW |
6 |
139,841,899 (GRCm39) |
missense |
probably benign |
0.00 |
R6929:Pik3c2g
|
UTSW |
6 |
139,903,502 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7022:Pik3c2g
|
UTSW |
6 |
139,599,061 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7144:Pik3c2g
|
UTSW |
6 |
139,606,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Pik3c2g
|
UTSW |
6 |
139,700,589 (GRCm39) |
missense |
|
|
R7332:Pik3c2g
|
UTSW |
6 |
139,841,981 (GRCm39) |
missense |
|
|
R7357:Pik3c2g
|
UTSW |
6 |
139,610,791 (GRCm39) |
critical splice donor site |
probably null |
|
R7359:Pik3c2g
|
UTSW |
6 |
139,913,620 (GRCm39) |
missense |
unknown |
|
R7385:Pik3c2g
|
UTSW |
6 |
139,801,079 (GRCm39) |
missense |
|
|
R7455:Pik3c2g
|
UTSW |
6 |
139,913,643 (GRCm39) |
missense |
unknown |
|
R7651:Pik3c2g
|
UTSW |
6 |
139,599,070 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7888:Pik3c2g
|
UTSW |
6 |
139,842,470 (GRCm39) |
missense |
|
|
R7923:Pik3c2g
|
UTSW |
6 |
139,610,791 (GRCm39) |
critical splice donor site |
probably null |
|
R7964:Pik3c2g
|
UTSW |
6 |
139,827,786 (GRCm39) |
missense |
|
|
R8005:Pik3c2g
|
UTSW |
6 |
139,599,067 (GRCm39) |
missense |
probably benign |
0.01 |
R8371:Pik3c2g
|
UTSW |
6 |
139,881,782 (GRCm39) |
missense |
unknown |
|
R8724:Pik3c2g
|
UTSW |
6 |
139,913,619 (GRCm39) |
missense |
unknown |
|
R8733:Pik3c2g
|
UTSW |
6 |
139,714,426 (GRCm39) |
nonsense |
probably null |
|
R8809:Pik3c2g
|
UTSW |
6 |
139,714,436 (GRCm39) |
missense |
|
|
R8888:Pik3c2g
|
UTSW |
6 |
139,676,092 (GRCm39) |
nonsense |
probably null |
|
R8931:Pik3c2g
|
UTSW |
6 |
139,821,093 (GRCm39) |
missense |
probably benign |
0.02 |
R9188:Pik3c2g
|
UTSW |
6 |
139,599,401 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9336:Pik3c2g
|
UTSW |
6 |
139,821,161 (GRCm39) |
missense |
|
|
R9383:Pik3c2g
|
UTSW |
6 |
139,827,742 (GRCm39) |
nonsense |
probably null |
|
R9524:Pik3c2g
|
UTSW |
6 |
139,606,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9531:Pik3c2g
|
UTSW |
6 |
139,841,926 (GRCm39) |
missense |
|
|
R9630:Pik3c2g
|
UTSW |
6 |
139,599,237 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9697:Pik3c2g
|
UTSW |
6 |
139,913,517 (GRCm39) |
missense |
unknown |
|
R9708:Pik3c2g
|
UTSW |
6 |
139,606,865 (GRCm39) |
missense |
probably benign |
|
R9717:Pik3c2g
|
UTSW |
6 |
139,841,910 (GRCm39) |
missense |
|
|
RF015:Pik3c2g
|
UTSW |
6 |
139,700,497 (GRCm39) |
missense |
|
|
RF032:Pik3c2g
|
UTSW |
6 |
139,612,656 (GRCm39) |
frame shift |
probably null |
|
X0024:Pik3c2g
|
UTSW |
6 |
139,805,984 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- ACACACATGGATTGATAGGTAGTAG -3'
(R):5'- GGATTTGACACAAGTTATTTGCTAGGC -3'
Sequencing Primer
(F):5'- TAGATAGGTAGATGGATAGTCAG -3'
(R):5'- AGGCTCCTTTTCCATTACATGCTAG -3'
|
Posted On |
2019-06-26 |