Incidental Mutation 'R7923:Pik3c2g'
ID |
648529 |
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 |
045970-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.118)
|
Stock # |
R7923 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
139591070-139915010 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 139610791 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000141141
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000032353]
[ENSMUST00000185968]
[ENSMUST00000187618]
[ENSMUST00000190962]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably null
Transcript: ENSMUST00000032353
|
SMART Domains |
Protein: ENSMUSP00000032353 Gene: ENSMUSG00000030228
Domain | Start | End | E-Value | Type |
SCOP:d1e8xa3
|
223 |
344 |
4e-33 |
SMART |
Blast:PI3K_rbd
|
272 |
345 |
7e-44 |
BLAST |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000185968
|
SMART Domains |
Protein: ENSMUSP00000140368 Gene: ENSMUSG00000030228
Domain | Start | End | E-Value | Type |
SCOP:d1e8xa3
|
223 |
371 |
2e-42 |
SMART |
Blast:PI3K_rbd
|
272 |
371 |
2e-64 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186585
|
Predicted Effect |
probably null
Transcript: ENSMUST00000187618
|
SMART Domains |
Protein: ENSMUSP00000141025 Gene: ENSMUSG00000030228
Domain | Start | End | E-Value | Type |
SCOP:d1e8xa3
|
223 |
344 |
4e-33 |
SMART |
Blast:PI3K_rbd
|
272 |
345 |
7e-44 |
BLAST |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000190962
|
SMART Domains |
Protein: ENSMUSP00000141141 Gene: ENSMUSG00000030228
Domain | Start | End | E-Value | Type |
SCOP:d1e8xa3
|
223 |
344 |
4e-33 |
SMART |
Blast:PI3K_rbd
|
272 |
345 |
7e-44 |
BLAST |
|
Meta Mutation Damage Score |
0.9492 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.3%
- 20x: 97.4%
|
Validation Efficiency |
|
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: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
C |
T |
8: 73,198,755 (GRCm39) |
T54M |
probably damaging |
Het |
Aacs |
T |
A |
5: 125,588,948 (GRCm39) |
S409T |
probably damaging |
Het |
Atf6 |
T |
C |
1: 170,622,275 (GRCm39) |
M449V |
probably benign |
Het |
B4galt1 |
C |
T |
4: 40,809,373 (GRCm39) |
G332S |
probably benign |
Het |
Bcl11a |
G |
T |
11: 24,113,680 (GRCm39) |
R341M |
probably damaging |
Het |
Brf2 |
G |
A |
8: 27,614,218 (GRCm39) |
Q323* |
probably null |
Het |
Bscl2 |
T |
C |
19: 8,824,883 (GRCm39) |
V322A |
probably benign |
Het |
Btnl9 |
T |
C |
11: 49,071,565 (GRCm39) |
Y86C |
probably damaging |
Het |
C4b |
T |
A |
17: 34,961,354 (GRCm39) |
I202F |
probably damaging |
Het |
Cbfb |
T |
A |
8: 105,921,225 (GRCm39) |
|
probably null |
Het |
Cc2d2b |
T |
A |
19: 40,795,293 (GRCm39) |
Y963N |
possibly damaging |
Het |
Cep135 |
A |
T |
5: 76,757,539 (GRCm39) |
D391V |
possibly damaging |
Het |
Cfap97d2 |
A |
C |
8: 13,788,456 (GRCm39) |
H140P |
unknown |
Het |
Col12a1 |
A |
G |
9: 79,585,775 (GRCm39) |
V1228A |
probably benign |
Het |
Cr2 |
T |
A |
1: 194,850,995 (GRCm39) |
Y157F |
probably benign |
Het |
Creg2 |
C |
T |
1: 39,690,071 (GRCm39) |
G13E |
probably benign |
Het |
Cul5 |
G |
T |
9: 53,535,466 (GRCm39) |
A595E |
probably benign |
Het |
Cyp4f16 |
A |
G |
17: 32,765,721 (GRCm39) |
E368G |
possibly damaging |
Het |
Dhrs7l |
G |
T |
12: 72,666,132 (GRCm39) |
Q180K |
probably benign |
Het |
Eln |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
5: 134,739,935 (GRCm39) |
|
probably benign |
Het |
Eps15 |
G |
A |
4: 109,173,069 (GRCm39) |
D177N |
possibly damaging |
Het |
Erbb4 |
C |
T |
1: 68,298,368 (GRCm39) |
R684H |
probably damaging |
Het |
Ermp1 |
C |
T |
19: 29,606,058 (GRCm39) |
V419I |
probably benign |
Het |
Foxi3 |
T |
C |
6: 70,937,700 (GRCm39) |
S311P |
probably benign |
Het |
Fras1 |
C |
T |
5: 96,887,177 (GRCm39) |
A2653V |
probably damaging |
Het |
Gbp3 |
A |
T |
3: 142,273,373 (GRCm39) |
N307Y |
probably damaging |
Het |
Ggcx |
G |
A |
6: 72,404,900 (GRCm39) |
R436Q |
probably damaging |
Het |
Gimap3 |
A |
T |
6: 48,742,561 (GRCm39) |
V123D |
probably benign |
Het |
Gm14326 |
A |
T |
2: 177,587,680 (GRCm39) |
Y439N |
probably damaging |
Het |
Gm5591 |
A |
G |
7: 38,221,338 (GRCm39) |
S244P |
probably benign |
Het |
Gm9507 |
A |
T |
10: 77,647,371 (GRCm39) |
C103S |
unknown |
Het |
Guf1 |
G |
A |
5: 69,718,502 (GRCm39) |
V214I |
probably benign |
Het |
Ido2 |
T |
C |
8: 25,066,209 (GRCm39) |
Y19C |
probably damaging |
Het |
Idua |
T |
C |
5: 108,828,449 (GRCm39) |
S268P |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,839,849 (GRCm39) |
Y719H |
probably damaging |
Het |
Itgb4 |
A |
T |
11: 115,873,525 (GRCm39) |
|
probably null |
Het |
Itprid2 |
G |
T |
2: 79,492,959 (GRCm39) |
E1169* |
probably null |
Het |
Kctd19 |
T |
A |
8: 106,111,690 (GRCm39) |
T868S |
probably damaging |
Het |
Lonrf2 |
A |
T |
1: 38,839,843 (GRCm39) |
H417Q |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,268,732 (GRCm39) |
T4184A |
possibly damaging |
Het |
Mapk15 |
T |
C |
15: 75,868,295 (GRCm39) |
F219S |
probably damaging |
Het |
Myh7b |
A |
T |
2: 155,467,886 (GRCm39) |
Y808F |
probably benign |
Het |
Myo19 |
T |
G |
11: 84,776,536 (GRCm39) |
F64C |
possibly damaging |
Het |
Mysm1 |
A |
T |
4: 94,850,002 (GRCm39) |
V434D |
probably damaging |
Het |
Naf1 |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
8: 67,313,200 (GRCm39) |
|
probably benign |
Het |
Nbeal2 |
A |
T |
9: 110,460,514 (GRCm39) |
Y1780* |
probably null |
Het |
Ndc80 |
A |
T |
17: 71,803,296 (GRCm39) |
M615K |
probably benign |
Het |
Nfkbib |
C |
A |
7: 28,465,688 (GRCm39) |
V54F |
probably damaging |
Het |
Npy5r |
A |
G |
8: 67,134,404 (GRCm39) |
F130L |
probably damaging |
Het |
Nt5c3 |
T |
C |
6: 56,860,027 (GRCm39) |
E304G |
probably benign |
Het |
Odaph |
A |
G |
5: 92,142,558 (GRCm39) |
D40G |
possibly damaging |
Het |
Or2ag13 |
T |
A |
7: 106,313,649 (GRCm39) |
K80* |
probably null |
Het |
Or2y1d |
C |
T |
11: 49,321,432 (GRCm39) |
T43I |
probably benign |
Het |
Or5b3 |
T |
C |
19: 13,388,182 (GRCm39) |
M83T |
probably benign |
Het |
Or8d6 |
A |
T |
9: 39,854,263 (GRCm39) |
K236* |
probably null |
Het |
Palm3 |
T |
A |
8: 84,756,090 (GRCm39) |
I534K |
probably benign |
Het |
Pde10a |
A |
G |
17: 9,147,964 (GRCm39) |
N89S |
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,223,183 (GRCm39) |
K870E |
|
Het |
Pnpla6 |
T |
A |
8: 3,581,737 (GRCm39) |
Y662* |
probably null |
Het |
Proser3 |
A |
T |
7: 30,249,086 (GRCm39) |
F2Y |
possibly damaging |
Het |
Psma5 |
A |
G |
3: 108,172,445 (GRCm39) |
I54V |
probably benign |
Het |
Qrich2 |
C |
A |
11: 116,348,163 (GRCm39) |
G887V |
probably damaging |
Het |
Rdx |
A |
G |
9: 51,977,201 (GRCm39) |
D150G |
possibly damaging |
Het |
Reln |
C |
T |
5: 22,339,690 (GRCm39) |
V221I |
probably benign |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Samd14 |
A |
G |
11: 94,914,284 (GRCm39) |
|
probably null |
Het |
Scimp |
A |
T |
11: 70,682,341 (GRCm39) |
I125N |
possibly damaging |
Het |
Sec23a |
A |
G |
12: 59,039,033 (GRCm39) |
F289L |
probably damaging |
Het |
Sipa1l3 |
G |
A |
7: 29,038,571 (GRCm39) |
Q1408* |
probably null |
Het |
Skor2 |
T |
C |
18: 76,946,416 (GRCm39) |
L46P |
unknown |
Het |
Slc12a1 |
A |
T |
2: 125,056,012 (GRCm39) |
I848F |
possibly damaging |
Het |
Slc47a1 |
A |
G |
11: 61,254,229 (GRCm39) |
L211P |
probably damaging |
Het |
Slc7a10 |
T |
C |
7: 34,894,554 (GRCm39) |
V71A |
probably damaging |
Het |
Smco1 |
C |
A |
16: 32,092,865 (GRCm39) |
Q179K |
possibly damaging |
Het |
Smg1 |
A |
G |
7: 117,742,545 (GRCm39) |
L3223P |
possibly damaging |
Het |
Smpdl3a |
T |
C |
10: 57,677,141 (GRCm39) |
S80P |
probably damaging |
Het |
Spire2 |
A |
G |
8: 124,059,726 (GRCm39) |
R75G |
probably benign |
Het |
Sptbn2 |
T |
A |
19: 4,796,827 (GRCm39) |
H1808Q |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,228,151 (GRCm39) |
E720G |
possibly damaging |
Het |
Supv3l1 |
T |
C |
10: 62,280,860 (GRCm39) |
D177G |
probably damaging |
Het |
Syne1 |
C |
T |
10: 5,214,738 (GRCm39) |
E3215K |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,231,037 (GRCm39) |
V2548A |
unknown |
Het |
Thap1 |
CAGCATCTGCTCGGAGCA |
CAGCA |
8: 26,650,884 (GRCm39) |
|
probably null |
Het |
Washc2 |
A |
G |
6: 116,203,385 (GRCm39) |
E384G |
possibly damaging |
Het |
Zfp712 |
T |
A |
13: 67,190,249 (GRCm39) |
N93Y |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
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 |
R7213:Pik3c2g
|
UTSW |
6 |
139,805,990 (GRCm39) |
missense |
|
|
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 |
|
|
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'- TCGCTGGATATTTCATGAGCTC -3'
(R):5'- TTCCCGGCGAGGTTTCTATAC -3'
Sequencing Primer
(F):5'- GGATATTTCATGAGCTCTTTCTCAC -3'
(R):5'- GCGTTCAAATATCCAAGCCTGTGG -3'
|
Posted On |
2020-09-15 |