Incidental Mutation 'V7581:Pik3cd'
ID |
152550 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pik3cd
|
Ensembl Gene |
ENSMUSG00000039936 |
Gene Name |
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta |
Synonyms |
2410099E07Rik, p110delta, 2610208K16Rik |
Accession Numbers |
|
Is this an essential gene? |
Probably essential
(E-score: 0.958)
|
Stock # |
V7581 ()
of strain
stinger
|
Quality Score |
218 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
149649168-149702571 bp(-) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 149657319 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Arginine
at position 390
(L390R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000136045
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038859]
[ENSMUST00000105688]
[ENSMUST00000105689]
[ENSMUST00000105690]
[ENSMUST00000118704]
[ENSMUST00000122059]
[ENSMUST00000127273]
[ENSMUST00000131224]
[ENSMUST00000134534]
[ENSMUST00000146612]
[ENSMUST00000177654]
|
AlphaFold |
O35904 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000038859
AA Change: L390R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000036434 Gene: ENSMUSG00000039936 AA Change: L390R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
412 |
1.87e-28 |
SMART |
PI3Ka
|
496 |
685 |
8.56e-87 |
SMART |
PI3Kc
|
776 |
1042 |
5.65e-128 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105688
AA Change: L390R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000101313 Gene: ENSMUSG00000039936 AA Change: L390R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
412 |
1.87e-28 |
SMART |
PI3Ka
|
496 |
685 |
8.56e-87 |
SMART |
PI3Kc
|
775 |
1041 |
5.65e-128 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105689
AA Change: L390R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000101314 Gene: ENSMUSG00000039936 AA Change: L390R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
412 |
1.87e-28 |
SMART |
PI3Ka
|
496 |
684 |
1.35e-84 |
SMART |
PI3Kc
|
774 |
1040 |
5.65e-128 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000105690
AA Change: L390R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000101315 Gene: ENSMUSG00000039936 AA Change: L390R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
412 |
1.87e-28 |
SMART |
PI3Ka
|
496 |
688 |
1.22e-82 |
SMART |
PI3Kc
|
778 |
1044 |
5.65e-128 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000118704
AA Change: L390R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000112863 Gene: ENSMUSG00000039936 AA Change: L390R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
412 |
1.87e-28 |
SMART |
PI3Ka
|
496 |
687 |
1.8e-80 |
SMART |
PI3Kc
|
777 |
1043 |
5.65e-128 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000122059
AA Change: L386R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000113844 Gene: ENSMUSG00000039936 AA Change: L386R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
408 |
6.47e-23 |
SMART |
PI3Ka
|
492 |
681 |
8.56e-87 |
SMART |
PI3Kc
|
771 |
1037 |
5.65e-128 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000127273
|
SMART Domains |
Protein: ENSMUSP00000119858 Gene: ENSMUSG00000039936
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
Blast:PI3K_rbd
|
126 |
171 |
1e-15 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000131224
|
SMART Domains |
Protein: ENSMUSP00000115542 Gene: ENSMUSG00000039936
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000134534
|
SMART Domains |
Protein: ENSMUSP00000118988 Gene: ENSMUSG00000039936
Domain | Start | End | E-Value | Type |
Pfam:PI3K_p85B
|
31 |
62 |
1.9e-10 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146612
|
SMART Domains |
Protein: ENSMUSP00000121843 Gene: ENSMUSG00000039936
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000177654
AA Change: L390R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000136045 Gene: ENSMUSG00000039936 AA Change: L390R
Domain | Start | End | E-Value | Type |
PI3K_p85B
|
31 |
108 |
2.24e-26 |
SMART |
PI3K_rbd
|
174 |
281 |
1.3e-13 |
SMART |
PI3K_C2
|
309 |
412 |
1.87e-28 |
SMART |
PI3Ka
|
496 |
688 |
1.22e-82 |
SMART |
PI3Kc
|
778 |
1044 |
5.65e-128 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000185093
|
Meta Mutation Damage Score |
0.9432  |
Coding Region Coverage |
- 1x: 99.0%
- 3x: 98.2%
- 10x: 95.7%
- 20x: 90.5%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Phosphoinositide 3-kinases (PI3Ks) phosphorylate inositol lipids and are involved in the immune response. The protein encoded by this gene is a class I PI3K found primarily in leukocytes. Like other class I PI3Ks (p110-alpha p110-beta, and p110-gamma), the encoded protein binds p85 adapter proteins and GTP-bound RAS. However, unlike the other class I PI3Ks, this protein phosphorylates itself, not p85 protein.[provided by RefSeq, Jul 2010] PHENOTYPE: Homozygotes for targeted null mutations exhibit impaired B and T cell antigen receptor signaling, reduced or ablated immune responses and decreased immunoglobulin levels. Mutants also develop inflammatory bowel disease. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
A |
T |
4: 122,701,257 |
H102L |
possibly damaging |
Het |
Abcb10 |
GGCCATCG |
GG |
8: 123,969,761 |
|
probably benign |
Het |
Atp6v1h |
A |
G |
1: 5,124,443 |
T282A |
possibly damaging |
Het |
Clasp1 |
G |
A |
1: 118,581,348 |
R1027Q |
probably damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,201,011 |
T870A |
probably benign |
Het |
Dnah12 |
T |
A |
14: 26,773,093 |
N1369K |
possibly damaging |
Het |
Dnajc22 |
T |
A |
15: 99,101,482 |
Y183N |
probably damaging |
Het |
Dpyd |
C |
T |
3: 118,897,126 |
Q295* |
probably null |
Het |
Erv3 |
T |
C |
2: 131,855,926 |
H171R |
possibly damaging |
Het |
Fam221b |
T |
C |
4: 43,665,865 |
T249A |
probably benign |
Het |
Fcgr1 |
T |
C |
3: 96,284,276 |
*405W |
probably null |
Het |
Glrx3 |
A |
G |
7: 137,459,153 |
H172R |
probably benign |
Het |
Gm10770 |
T |
A |
2: 150,179,484 |
K38* |
probably null |
Het |
Gm4787 |
G |
A |
12: 81,377,567 |
Q606* |
probably null |
Het |
Hira |
G |
A |
16: 18,894,821 |
A29T |
probably damaging |
Het |
Hnrnpab |
A |
T |
11: 51,602,624 |
N252K |
probably benign |
Het |
Izumo4 |
A |
T |
10: 80,703,891 |
T155S |
probably benign |
Het |
Kcnb2 |
A |
G |
1: 15,710,091 |
I396V |
probably benign |
Het |
Klc1 |
A |
T |
12: 111,774,572 |
I161F |
probably benign |
Het |
Lpar5 |
C |
A |
6: 125,081,727 |
A137E |
possibly damaging |
Het |
Lrp4 |
C |
T |
2: 91,488,518 |
S900L |
possibly damaging |
Het |
Muc6 |
T |
G |
7: 141,647,613 |
E808A |
probably benign |
Het |
Olfr1406 |
G |
T |
1: 173,183,964 |
L157I |
probably benign |
Het |
Olfr480 |
G |
T |
7: 108,066,678 |
T40K |
probably benign |
Het |
Otop3 |
T |
A |
11: 115,344,838 |
L432Q |
probably damaging |
Het |
Papln |
C |
T |
12: 83,778,834 |
R608C |
possibly damaging |
Het |
Pelp1 |
T |
A |
11: 70,398,150 |
T257S |
probably damaging |
Het |
Ppwd1 |
A |
G |
13: 104,220,237 |
Y257H |
probably damaging |
Het |
Prkcb |
G |
T |
7: 122,528,476 |
W274C |
probably damaging |
Het |
Rbbp8nl |
T |
A |
2: 180,278,208 |
T558S |
probably benign |
Het |
Recql4 |
T |
C |
15: 76,706,169 |
D705G |
possibly damaging |
Het |
Slc30a4 |
T |
A |
2: 122,689,538 |
M136L |
probably benign |
Het |
Slc5a6 |
C |
T |
5: 31,042,613 |
|
probably null |
Het |
Spaca1 |
T |
C |
4: 34,039,311 |
E192G |
probably damaging |
Het |
Spata31 |
C |
A |
13: 64,921,648 |
P537T |
probably benign |
Het |
Tmc3 |
T |
C |
7: 83,622,505 |
V955A |
probably benign |
Het |
Tnrc6c |
G |
A |
11: 117,723,326 |
R770H |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,806,111 |
N56K |
probably damaging |
Het |
Tprkb |
A |
G |
6: 85,928,782 |
K150E |
probably damaging |
Het |
Trps1 |
T |
C |
15: 50,831,577 |
K150E |
probably damaging |
Het |
Tspyl3 |
A |
G |
2: 153,225,060 |
V86A |
probably benign |
Het |
Vmn2r68 |
C |
T |
7: 85,221,880 |
V732I |
probably benign |
Het |
Wdr60 |
A |
C |
12: 116,211,840 |
S906A |
possibly damaging |
Het |
Zfp292 |
C |
T |
4: 34,806,783 |
C2087Y |
possibly damaging |
Het |
Zfp933 |
G |
A |
4: 147,826,470 |
A223V |
probably damaging |
Het |
Zmynd8 |
G |
A |
2: 165,812,394 |
R724* |
probably null |
Het |
|
Other mutations in Pik3cd |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01308:Pik3cd
|
APN |
4 |
149657460 |
missense |
probably damaging |
1.00 |
IGL01536:Pik3cd
|
APN |
4 |
149652666 |
missense |
probably damaging |
1.00 |
IGL01636:Pik3cd
|
APN |
4 |
149654315 |
missense |
possibly damaging |
0.82 |
IGL02794:Pik3cd
|
APN |
4 |
149654571 |
missense |
probably benign |
|
grand_tetons
|
UTSW |
4 |
149652699 |
missense |
probably damaging |
1.00 |
Helena
|
UTSW |
4 |
149651820 |
missense |
probably damaging |
1.00 |
stinger
|
UTSW |
4 |
149657319 |
missense |
probably damaging |
1.00 |
F5770:Pik3cd
|
UTSW |
4 |
149657319 |
missense |
probably damaging |
1.00 |
R0003:Pik3cd
|
UTSW |
4 |
149656379 |
critical splice donor site |
probably null |
|
R0309:Pik3cd
|
UTSW |
4 |
149663220 |
missense |
probably damaging |
1.00 |
R1246:Pik3cd
|
UTSW |
4 |
149659800 |
missense |
probably damaging |
1.00 |
R1259:Pik3cd
|
UTSW |
4 |
149650648 |
nonsense |
probably null |
|
R1533:Pik3cd
|
UTSW |
4 |
149655196 |
missense |
probably damaging |
1.00 |
R1756:Pik3cd
|
UTSW |
4 |
149658750 |
missense |
probably benign |
0.02 |
R1796:Pik3cd
|
UTSW |
4 |
149654119 |
missense |
possibly damaging |
0.83 |
R1887:Pik3cd
|
UTSW |
4 |
149652634 |
missense |
probably damaging |
1.00 |
R1988:Pik3cd
|
UTSW |
4 |
149663203 |
missense |
probably damaging |
1.00 |
R2089:Pik3cd
|
UTSW |
4 |
149652699 |
missense |
probably damaging |
1.00 |
R2091:Pik3cd
|
UTSW |
4 |
149652699 |
missense |
probably damaging |
1.00 |
R4997:Pik3cd
|
UTSW |
4 |
149658984 |
missense |
probably damaging |
1.00 |
R5391:Pik3cd
|
UTSW |
4 |
149659131 |
missense |
probably damaging |
0.98 |
R5603:Pik3cd
|
UTSW |
4 |
149658855 |
missense |
probably benign |
|
R6282:Pik3cd
|
UTSW |
4 |
149659743 |
missense |
probably benign |
0.00 |
R6453:Pik3cd
|
UTSW |
4 |
149652302 |
missense |
probably damaging |
1.00 |
R7286:Pik3cd
|
UTSW |
4 |
149659714 |
missense |
probably benign |
0.08 |
R7423:Pik3cd
|
UTSW |
4 |
149651763 |
critical splice donor site |
probably null |
|
R7508:Pik3cd
|
UTSW |
4 |
149654583 |
missense |
possibly damaging |
0.78 |
R7665:Pik3cd
|
UTSW |
4 |
149654050 |
missense |
possibly damaging |
0.70 |
R7897:Pik3cd
|
UTSW |
4 |
149657269 |
missense |
probably benign |
0.06 |
R8039:Pik3cd
|
UTSW |
4 |
149659866 |
missense |
possibly damaging |
0.91 |
R8476:Pik3cd
|
UTSW |
4 |
149651820 |
missense |
probably damaging |
1.00 |
R9015:Pik3cd
|
UTSW |
4 |
149655598 |
missense |
probably benign |
0.06 |
R9252:Pik3cd
|
UTSW |
4 |
149655630 |
missense |
possibly damaging |
0.88 |
V7580:Pik3cd
|
UTSW |
4 |
149657319 |
missense |
probably damaging |
1.00 |
V7582:Pik3cd
|
UTSW |
4 |
149657319 |
missense |
probably damaging |
1.00 |
V7583:Pik3cd
|
UTSW |
4 |
149657319 |
missense |
probably damaging |
1.00 |
X0023:Pik3cd
|
UTSW |
4 |
149660034 |
missense |
probably benign |
0.04 |
Z1176:Pik3cd
|
UTSW |
4 |
149654847 |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- GGAGCTGCCTACAAAAGCCTACTG -3'
(R):5'- TGCCTTGGGCTATCAATGCACTG -3'
Sequencing Primer
(F):5'- TCACAGGCTATCCCTAGAGTGAG -3'
(R):5'- cacacacacacacacacac -3'
|
Posted On |
2014-01-29 |