Incidental Mutation 'R0919:Prkce'
| ID |
82798 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Prkce
|
| Ensembl Gene |
ENSMUSG00000045038 |
| Gene Name |
protein kinase C, epsilon |
| Synonyms |
PKCepsilon, PCK epsilon, Pkce, PKC[e], 5830406C15Rik |
| MMRRC Submission |
039069-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0919 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
17 |
| Chromosomal Location |
86475213-86965347 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 86937588 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Isoleucine
at position 674
(V674I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000094874
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000097274]
[ENSMUST00000097275]
|
| AlphaFold |
P16054 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000097274
AA Change: V674I
PolyPhen 2
Score 0.060 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000094873
Gene: ENSMUSG00000045038
AA Change: V674I
| Domain | Start | End | E-Value | Type |
|---|
|
C2
|
7 |
114 |
5.78e-12 |
SMART |
|
C1
|
170 |
220 |
4.48e-13 |
SMART |
|
C1
|
243 |
292 |
8.29e-17 |
SMART |
|
S_TKc
|
408 |
668 |
1.3e-104 |
SMART |
|
S_TK_X
|
669 |
732 |
2.56e-25 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000097275
AA Change: V674I
PolyPhen 2
Score 0.060 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000094874
Gene: ENSMUSG00000045038
AA Change: V674I
| Domain | Start | End | E-Value | Type |
|---|
|
C2
|
7 |
114 |
5.78e-12 |
SMART |
|
C1
|
170 |
220 |
4.48e-13 |
SMART |
|
C1
|
243 |
292 |
8.29e-17 |
SMART |
|
S_TKc
|
408 |
668 |
1.3e-104 |
SMART |
|
S_TK_X
|
669 |
732 |
2.56e-25 |
SMART |
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.8%
- 10x: 97.5%
- 20x: 95.6%
|
| Validation Efficiency |
96% (43/45) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This kinase has been shown to be involved in many different cellular functions, such as neuron channel activation, apoptosis, cardioprotection from ischemia, heat shock response, as well as insulin exocytosis. Knockout studies in mice suggest that this kinase is important for lipopolysaccharide (LPS)-mediated signaling in activated macrophages and may also play a role in controlling anxiety-like behavior. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit reduced ethanol self-administration and are more sensitive to the acute behavioral effects of ethanol and other drugs that activate GABA(A) receptors. Mutants show reduced anxiety and stress hormones. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alpk2 |
C |
A |
18: 65,440,544 (GRCm39) |
C283F |
probably benign |
Het |
| Anapc1 |
T |
C |
2: 128,459,651 (GRCm39) |
R1803G |
probably benign |
Het |
| Anapc4 |
T |
C |
5: 53,012,979 (GRCm39) |
V423A |
probably benign |
Het |
| Arfgef3 |
A |
G |
10: 18,465,483 (GRCm39) |
I2120T |
possibly damaging |
Het |
| Btaf1 |
T |
A |
19: 36,968,143 (GRCm39) |
H1109Q |
probably benign |
Het |
| Cfap418 |
A |
G |
4: 10,882,462 (GRCm39) |
T124A |
probably benign |
Het |
| Cfap70 |
G |
A |
14: 20,454,232 (GRCm39) |
P851S |
probably benign |
Het |
| Clcf1 |
T |
A |
19: 4,272,252 (GRCm39) |
L103Q |
probably damaging |
Het |
| Col11a2 |
T |
A |
17: 34,278,124 (GRCm39) |
V1032E |
possibly damaging |
Het |
| Cyp2c38 |
T |
G |
19: 39,393,113 (GRCm39) |
D318A |
probably benign |
Het |
| Dbpht2 |
A |
G |
12: 74,345,774 (GRCm39) |
|
noncoding transcript |
Het |
| Dhx34 |
A |
C |
7: 15,935,883 (GRCm39) |
V893G |
probably damaging |
Het |
| Fsip2 |
T |
A |
2: 82,815,828 (GRCm39) |
C3854S |
possibly damaging |
Het |
| Htr1a |
T |
C |
13: 105,581,344 (GRCm39) |
Y195H |
probably damaging |
Het |
| Insr |
A |
G |
8: 3,208,769 (GRCm39) |
S1231P |
probably damaging |
Het |
| Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
| Kpna4 |
A |
T |
3: 68,993,161 (GRCm39) |
|
probably benign |
Het |
| Or52d13 |
A |
G |
7: 103,110,019 (GRCm39) |
I132T |
probably damaging |
Het |
| Or52e8 |
A |
T |
7: 104,624,519 (GRCm39) |
Y228* |
probably null |
Het |
| Or5m3 |
A |
G |
2: 85,838,984 (GRCm39) |
Y288C |
possibly damaging |
Het |
| Osbpl7 |
G |
A |
11: 96,946,927 (GRCm39) |
R239H |
possibly damaging |
Het |
| Prkrip1 |
T |
C |
5: 136,226,685 (GRCm39) |
M52V |
possibly damaging |
Het |
| Sash1 |
A |
G |
10: 8,605,843 (GRCm39) |
M849T |
probably benign |
Het |
| Scaf8 |
T |
C |
17: 3,247,395 (GRCm39) |
L906S |
probably damaging |
Het |
| Sfmbt2 |
T |
C |
2: 10,582,382 (GRCm39) |
L676P |
probably benign |
Het |
| Sgsm1 |
C |
T |
5: 113,406,708 (GRCm39) |
V923I |
probably damaging |
Het |
| Slc38a3 |
A |
T |
9: 107,533,158 (GRCm39) |
L305Q |
probably damaging |
Het |
| Slc44a5 |
A |
G |
3: 153,949,223 (GRCm39) |
Y232C |
probably damaging |
Het |
| Spag17 |
A |
T |
3: 99,979,259 (GRCm39) |
|
probably benign |
Het |
| Synm |
T |
C |
7: 67,385,095 (GRCm39) |
I414V |
probably damaging |
Het |
| Tbc1d12 |
C |
T |
19: 38,902,493 (GRCm39) |
H551Y |
possibly damaging |
Het |
| Timm21 |
G |
C |
18: 84,967,387 (GRCm39) |
L130V |
probably damaging |
Het |
| Trpc7 |
C |
T |
13: 56,970,462 (GRCm39) |
|
probably benign |
Het |
| Trpm7 |
G |
A |
2: 126,673,158 (GRCm39) |
R532C |
probably damaging |
Het |
| Ttn |
T |
A |
2: 76,777,086 (GRCm39) |
K1485* |
probably null |
Het |
| Txn2 |
T |
C |
15: 77,811,949 (GRCm39) |
D69G |
probably damaging |
Het |
| U2af2 |
C |
T |
7: 5,072,433 (GRCm39) |
|
probably benign |
Het |
| Ubn1 |
T |
C |
16: 4,882,255 (GRCm39) |
Y239H |
probably damaging |
Het |
| Ubtf |
A |
G |
11: 102,200,603 (GRCm39) |
|
probably benign |
Het |
| Usp49 |
T |
A |
17: 47,983,376 (GRCm39) |
V127D |
probably benign |
Het |
| Washc2 |
C |
T |
6: 116,185,225 (GRCm39) |
R20W |
probably damaging |
Het |
| Zscan10 |
T |
C |
17: 23,828,981 (GRCm39) |
S476P |
probably damaging |
Het |
|
| Other mutations in Prkce |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01308:Prkce
|
APN |
17 |
86,932,890 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01401:Prkce
|
APN |
17 |
86,476,268 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01508:Prkce
|
APN |
17 |
86,937,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02500:Prkce
|
APN |
17 |
86,476,342 (GRCm39) |
missense |
probably benign |
0.16 |
|
IGL02957:Prkce
|
APN |
17 |
86,803,454 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
IGL03114:Prkce
|
APN |
17 |
86,961,983 (GRCm39) |
missense |
probably damaging |
0.97 |
|
Pinnacles
|
UTSW |
17 |
86,784,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0063:Prkce
|
UTSW |
17 |
86,789,539 (GRCm39) |
splice site |
probably benign |
|
|
R0063:Prkce
|
UTSW |
17 |
86,789,539 (GRCm39) |
splice site |
probably benign |
|
|
R0403:Prkce
|
UTSW |
17 |
86,476,081 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0900:Prkce
|
UTSW |
17 |
86,932,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1413:Prkce
|
UTSW |
17 |
86,803,446 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1430:Prkce
|
UTSW |
17 |
86,866,565 (GRCm39) |
splice site |
probably benign |
|
|
R1843:Prkce
|
UTSW |
17 |
86,782,974 (GRCm39) |
nonsense |
probably null |
|
|
R2129:Prkce
|
UTSW |
17 |
86,803,463 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2341:Prkce
|
UTSW |
17 |
86,781,870 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2511:Prkce
|
UTSW |
17 |
86,932,754 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2679:Prkce
|
UTSW |
17 |
86,483,654 (GRCm39) |
intron |
probably benign |
|
|
R3724:Prkce
|
UTSW |
17 |
86,476,051 (GRCm39) |
nonsense |
probably null |
|
|
R3853:Prkce
|
UTSW |
17 |
86,476,277 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4364:Prkce
|
UTSW |
17 |
86,784,279 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4467:Prkce
|
UTSW |
17 |
86,927,339 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R4523:Prkce
|
UTSW |
17 |
86,798,178 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R4838:Prkce
|
UTSW |
17 |
86,937,511 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5140:Prkce
|
UTSW |
17 |
86,789,570 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5579:Prkce
|
UTSW |
17 |
86,927,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6026:Prkce
|
UTSW |
17 |
86,800,658 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6048:Prkce
|
UTSW |
17 |
86,800,775 (GRCm39) |
missense |
probably benign |
|
|
R6212:Prkce
|
UTSW |
17 |
86,866,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6484:Prkce
|
UTSW |
17 |
86,798,237 (GRCm39) |
missense |
probably benign |
|
|
R6788:Prkce
|
UTSW |
17 |
86,937,489 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6915:Prkce
|
UTSW |
17 |
86,800,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7349:Prkce
|
UTSW |
17 |
86,800,783 (GRCm39) |
missense |
probably benign |
|
|
R7447:Prkce
|
UTSW |
17 |
86,866,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7566:Prkce
|
UTSW |
17 |
86,800,757 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7577:Prkce
|
UTSW |
17 |
86,800,721 (GRCm39) |
nonsense |
probably null |
|
|
R7638:Prkce
|
UTSW |
17 |
86,476,028 (GRCm39) |
missense |
probably benign |
0.26 |
|
R8237:Prkce
|
UTSW |
17 |
86,866,646 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8711:Prkce
|
UTSW |
17 |
86,795,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8869:Prkce
|
UTSW |
17 |
86,476,370 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9342:Prkce
|
UTSW |
17 |
86,781,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
RF010:Prkce
|
UTSW |
17 |
86,795,627 (GRCm39) |
missense |
probably damaging |
0.97 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCCTTGCTGTGAATAAGTGACTGCC -3'
(R):5'- AATGTCTAGGGTCTCAGACGCCTC -3'
Sequencing Primer
(F):5'- acgagcctgtctgtgcc -3'
(R):5'- TCAGACGCCTCTGGGAGAC -3'
|
| Posted On |
2013-11-08 |
Incidental Mutation