Incidental Mutation 'FR4340:Pik3c2g'
ID |
511122 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pik3c2g
|
Ensembl Gene |
ENSMUSG00000030228 |
Gene Name |
phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma |
Synonyms |
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.118)
|
Stock # |
FR4340 ()
|
Quality Score |
214.458 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
139591070-139915010 bp(+) (GRCm39) |
Type of Mutation |
frame shift |
DNA Base Change (assembly) |
AG to AGAGGG
at 139612654 bp (GRCm39)
|
Zygosity |
Homozygous |
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 benign
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 |
|
Coding Region Coverage |
- 1x: 99.7%
- 3x: 99.4%
- 10x: 97.8%
- 20x: 94.3%
|
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: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
AACC |
A |
7: 40,642,479 (GRCm39) |
|
probably benign |
Het |
4930578G10Rik |
G |
T |
4: 42,761,098 (GRCm39) |
|
probably benign |
Het |
7530416G11Rik |
T |
A |
15: 85,378,508 (GRCm39) |
E45V |
unknown |
Homo |
A530064D06Rik |
GTAGGAAGCTTAG |
GTAG |
17: 48,470,549 (GRCm39) |
|
probably benign |
Homo |
Arpc1b |
CC |
CCTGGTC |
5: 145,063,602 (GRCm39) |
|
probably null |
Het |
Arrb2 |
C |
T |
11: 70,329,497 (GRCm39) |
T269M |
probably damaging |
Homo |
Bcas3 |
G |
A |
11: 85,400,323 (GRCm39) |
V431I |
probably benign |
Homo |
Blm |
ACCT |
ACCTGCCT |
7: 80,113,515 (GRCm39) |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,658 (GRCm39) |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCGCCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,655 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
TATTATTAT |
TATTATTATTATTATCATTATTAT |
3: 37,104,901 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCGCC |
8: 85,365,352 (GRCm39) |
|
probably benign |
Het |
Cacna1f |
AGG |
AGGCGG |
X: 7,486,306 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
CTCTGTGGCTGTGGCTGTGGCTGTG |
CTCTGTGGCTGTGTCTGTGGCTGTGGCTGTGGCTGTG |
19: 47,129,690 (GRCm39) |
|
probably benign |
Het |
Casz1 |
ACCACAGCCACAGCCACAGCCAC |
ACCACAGCCACAGCCAC |
4: 149,036,759 (GRCm39) |
|
probably benign |
Homo |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Het |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Het |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Homo |
Cd80 |
GAA |
GAAAAA |
16: 38,306,678 (GRCm39) |
|
probably benign |
Homo |
Cimip2b |
CAGAG |
CAG |
4: 43,427,384 (GRCm39) |
|
probably null |
Homo |
Col2a1 |
C |
A |
15: 97,886,862 (GRCm39) |
|
probably null |
Het |
Col6a5 |
A |
T |
9: 105,811,373 (GRCm39) |
N715K |
unknown |
Homo |
Crygc |
A |
T |
1: 65,110,822 (GRCm39) |
F155Y |
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,811,779 (GRCm39) |
|
probably benign |
Het |
Cyp2d11 |
T |
TGGGA |
15: 82,274,223 (GRCm39) |
|
probably null |
Homo |
Dbr1 |
AGG |
AGGAGGCGG |
9: 99,465,754 (GRCm39) |
|
probably benign |
Het |
Dennd10 |
CT |
CTTTT |
19: 60,803,059 (GRCm39) |
|
probably benign |
Homo |
Dennd2b |
CACCACACTGGGGCAGCCCACACTGGGGCAG |
CCCCACACTGGGGCAG |
7: 109,156,128 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Homo |
Dnah8 |
ACACTGCC |
AC |
17: 30,854,437 (GRCm39) |
|
probably benign |
Het |
Dthd1 |
C |
CTTA |
5: 63,000,369 (GRCm39) |
|
probably benign |
Homo |
Frem3 |
CT |
CTTTT |
8: 81,341,870 (GRCm39) |
|
probably benign |
Homo |
Frmpd2 |
G |
T |
14: 33,232,978 (GRCm39) |
L399F |
probably damaging |
Homo |
G530012D18Rik |
CACACAGAGAGAGAGAGAGAGAGAGA |
CA |
1: 85,504,873 (GRCm39) |
|
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,309,413 (GRCm39) |
I175V |
probably benign |
Het |
Gm14393 |
T |
C |
2: 174,903,427 (GRCm39) |
E160G |
possibly damaging |
Het |
Gm16519 |
A |
AGAAC |
17: 71,236,333 (GRCm39) |
|
probably null |
Homo |
Gm4340 |
GCAG |
GCAACAG |
10: 104,031,959 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAGAAG |
CAGAAGAAG |
10: 104,031,960 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAG |
CAGTAG |
10: 104,031,936 (GRCm39) |
|
probably null |
Het |
Gpatch11 |
AGGAAG |
AGGAAGGGGAAG |
17: 79,149,603 (GRCm39) |
|
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Het |
Ifi208 |
ATGGTG |
ATG |
1: 173,505,264 (GRCm39) |
|
probably benign |
Homo |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Homo |
Ipo9 |
TCC |
TCCCCC |
1: 135,314,007 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Isg20l2 |
AAG |
AAGTAG |
3: 87,839,019 (GRCm39) |
|
probably null |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,800 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,788 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,794 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CCTCCT |
CCTCCTTCTCCT |
11: 99,280,100 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CAC |
CACGAC |
11: 99,277,028 (GRCm39) |
|
probably benign |
Het |
Krt10 |
ACCG |
ACCGCCG |
11: 99,277,029 (GRCm39) |
|
probably benign |
Homo |
Las1l |
TCCTC |
TCCTCTACCTC |
X: 94,984,228 (GRCm39) |
|
probably benign |
Het |
Lce1a1 |
C |
T |
3: 92,554,151 (GRCm39) |
G108S |
unknown |
Het |
Lkaaear1 |
CCAGCTCCAG |
CCAGCTCCAGCTGCAGCTCCAG |
2: 181,339,387 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
CTG |
CTGTTG |
3: 129,582,457 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGAAG |
X: 70,162,452 (GRCm39) |
|
probably benign |
Het |
Mapk7 |
TGCTGGCGCTGGTGCTGGCGCTGG |
TGCTGGCGCTGGCGCTGGTGCTGGCGCTGG |
11: 61,381,032 (GRCm39) |
|
probably benign |
Het |
Mast4 |
GCA |
GCAGTGTCA |
13: 102,872,825 (GRCm39) |
|
probably benign |
Homo |
Mast4 |
TTTT |
TTTTATTT |
13: 102,871,365 (GRCm39) |
|
probably null |
Het |
Med12l |
AGC |
AGCCGC |
3: 59,183,406 (GRCm39) |
|
probably benign |
Het |
Mfsd5 |
G |
A |
15: 102,189,596 (GRCm39) |
V323I |
probably benign |
Het |
Nacad |
GTC |
GTCAGGATC |
11: 6,549,761 (GRCm39) |
|
probably benign |
Het |
Naip1 |
A |
C |
13: 100,559,584 (GRCm39) |
M1140R |
probably benign |
Het |
Nbea |
TTTA |
T |
3: 55,916,633 (GRCm39) |
|
probably benign |
Homo |
Nefh |
CTCACCTGGGGACTTGGCCTC |
CTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,040 (GRCm39) |
|
probably benign |
Homo |
Nefh |
ACTTGGCCTCACCTGGGG |
ACTTGGCCTCACCTGGGGCCTTGGCCTCACCTGGGG |
11: 4,891,033 (GRCm39) |
|
probably benign |
Het |
Nefh |
GCCTCACCTGGGGACTTGGCCTC |
GCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,038 (GRCm39) |
|
probably benign |
Homo |
Neu1 |
TCTTCTA |
T |
17: 35,151,534 (GRCm39) |
|
probably benign |
Het |
Nutf2 |
G |
T |
8: 106,603,202 (GRCm39) |
D78Y |
probably damaging |
Het |
Or51q1 |
TCC |
TCCC |
7: 103,629,110 (GRCm39) |
|
probably null |
Het |
Or5e1 |
AT |
ATGATATT |
7: 108,354,161 (GRCm39) |
|
probably benign |
Homo |
Or5p70 |
A |
G |
7: 107,995,100 (GRCm39) |
T258A |
probably benign |
Het |
Or5p70 |
G |
A |
7: 107,995,105 (GRCm39) |
M259I |
probably benign |
Het |
Pdik1l |
ACCAC |
ACCACCCCCAC |
4: 134,006,823 (GRCm39) |
|
probably benign |
Het |
Phaf1 |
G |
A |
8: 105,967,730 (GRCm39) |
G207E |
probably benign |
Homo |
Plekhs1 |
TCCAGAC |
TCCAGACCTCCCCCCAGAC |
19: 56,468,290 (GRCm39) |
|
probably benign |
Homo |
Prag1 |
C |
CAGT |
8: 36,571,040 (GRCm39) |
|
probably benign |
Homo |
Pramel16 |
G |
A |
4: 143,676,312 (GRCm39) |
T264M |
probably damaging |
Het |
Prkn |
G |
A |
17: 12,073,650 (GRCm39) |
V323M |
probably damaging |
Homo |
Raet1d |
A |
G |
10: 22,247,458 (GRCm39) |
Q178R |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,121,083 (GRCm39) |
K70N |
probably damaging |
Homo |
Serpina3i |
CGG |
CGGTGG |
12: 104,231,423 (GRCm39) |
|
probably benign |
Het |
Sfswap |
ACTCAGCCC |
ACTCAGCCCCCTCAGCCC |
5: 129,646,815 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,784 (GRCm39) |
|
probably benign |
Het |
Sp140l1 |
A |
C |
1: 85,087,072 (GRCm39) |
N6K |
probably damaging |
Het |
Speer4a1 |
C |
A |
5: 26,241,746 (GRCm39) |
E127* |
probably null |
Het |
Sry |
GCTGCTGCTGCTG |
GCTGCTGCTGCTGCTG |
Y: 2,662,824 (GRCm39) |
|
probably benign |
Het |
Tbr1 |
A |
C |
2: 61,636,691 (GRCm39) |
|
probably benign |
Het |
Tdpoz2 |
T |
TCC |
3: 93,558,922 (GRCm39) |
|
probably null |
Homo |
Tdpoz4 |
GAA |
GA |
3: 93,704,187 (GRCm39) |
|
probably null |
Het |
Tgoln1 |
AAG |
AAGCCTCAG |
6: 72,593,334 (GRCm39) |
|
probably benign |
Homo |
Tmbim7 |
C |
T |
5: 3,720,064 (GRCm39) |
R100C |
possibly damaging |
Het |
Tob1 |
CA |
CAGAA |
11: 94,105,303 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,280 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,286 (GRCm39) |
|
probably benign |
Het |
Tomm5 |
GCATCTTCC |
GCATCTTCCACATCTTCC |
4: 45,107,973 (GRCm39) |
|
probably benign |
Het |
Triobp |
TCGG |
TCGGCGG |
15: 78,877,590 (GRCm39) |
|
probably benign |
Homo |
Tsbp1 |
GC |
GCAAC |
17: 34,679,051 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
CAG |
CAGTAG |
17: 34,679,034 (GRCm39) |
|
probably null |
Het |
Tsbp1 |
GCA |
GCATCA |
17: 34,679,042 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
AGG |
AGGGGG |
6: 115,537,027 (GRCm39) |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGGGG |
6: 115,537,030 (GRCm39) |
|
probably benign |
Homo |
Ubtf |
TCC |
TCCCCC |
11: 102,197,776 (GRCm39) |
|
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Homo |
Zc3h13 |
CGGGATGTGCG |
CGGGATGTGCGGGATGTGCG |
14: 75,561,032 (GRCm39) |
|
probably benign |
Homo |
Zfp28 |
G |
A |
7: 6,397,862 (GRCm39) |
G766R |
probably damaging |
Het |
Zfp384 |
AAGCCCAGGCCCAGGCCCAGGCCCA |
AAGCCCAGGCCCAAGCCCAGGCCCAGGCCCAGGCCCA |
6: 125,013,426 (GRCm39) |
|
probably benign |
Het |
Zfp428 |
G |
A |
7: 24,214,506 (GRCm39) |
D41N |
probably damaging |
Homo |
Zfp598 |
CCACAGGC |
CC |
17: 24,898,346 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
CCACCA |
CCACCAACACCA |
17: 24,899,757 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCCCC |
2: 174,487,273 (GRCm39) |
|
probably benign |
Het |
Zfp933 |
GCTT |
GCTTTTCTT |
4: 147,910,186 (GRCm39) |
|
probably null |
Homo |
Zfp936 |
G |
A |
7: 42,838,913 (GRCm39) |
G127R |
possibly 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 |
|
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 |
|
|
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'- AATCTGTGGCAGAGTTAGATCTG -3'
(R):5'- GCAGACGTTAAGTTGTTTTAGTGCAC -3'
Sequencing Primer
(F):5'- taccctgagctactacct -3'
(R):5'- AGTCCATACATTTTCCTGCAGAG -3'
|
Posted On |
2018-04-05 |