Mutagenetix > Incidental Mutation

Incidental Mutation 'R4649:Prkcq'

350552

Institutional Source

Beutler Lab

Gene Symbol

Prkcq

Ensembl Gene

ENSMUSG00000026778

Gene Name

protein kinase C, theta

Synonyms

A130035A12Rik, PKC-theta, PKC theta, PKC-0, Pkcq, PKCtheta

MMRRC Submission

041910-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4649 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

11176922-11306033 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 11284333 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 501 (V501A)

Ref Sequence

ENSEMBL: ENSMUSP00000100035 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000028118] [ENSMUST00000102970]

AlphaFold

Q02111

Predicted Effect

possibly damaging
Transcript: ENSMUST00000028118
AA Change: V501A

PolyPhen 2 Score 0.573 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000028118
Gene: ENSMUSG00000026778
AA Change: V501A

Domain	Start	End	E-Value	Type
PDB:2ENJ\|A	3	126	6e-83	PDB
C1	160	209	3.27e-15	SMART
C1	232	281	2.22e-17	SMART
S_TKc	380	634	1.17e-97	SMART
S_TK_X	635	698	2.6e-26	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000102970
AA Change: V501A

PolyPhen 2 Score 0.834 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000100035
Gene: ENSMUSG00000026778
AA Change: V501A

Domain	Start	End	E-Value	Type
PDB:2ENJ\|A	3	126	2e-84	PDB
C1	160	209	3.27e-15	SMART
C1	232	281	2.22e-17	SMART
Pfam:Pkinase_Tyr	380	558	2.8e-27	PFAM
Pfam:Pkinase	380	560	2.2e-47	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000195207

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000195628

Meta Mutation Damage Score

0.5012

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.3%
20x: 95.4%

Validation Efficiency

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. The protein encoded by this gene is one of the PKC family members. It is a calcium-independent and phospholipid-dependent protein kinase. This kinase is important for T-cell activation. It is required for the activation of the transcription factors NF-kappaB and AP-1, and may link the T cell receptor (TCR) signaling complex to the activation of the transcription factors. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for targeted null mutations exhibit reduced T cell proliferative responses and interleukin 2 production and a lack of T cell receptor-initiated NF-kappaB activation in mature T lymphocytes. [provided by MGI curators]

Allele List at MGI

All alleles(3) : Targeted, knock-out(2) Targeted, other(1)

Other mutations in this stock

Total: 106 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	G	T	12: 71,211,320 (GRCm39)	E685*	probably null	Het
2700049A03Rik	A	T	12: 71,211,321 (GRCm39)	E685V	possibly damaging	Het
4933409G03Rik	G	A	2: 68,436,559 (GRCm39)	E168K	unknown	Het
Abca4	G	T	3: 121,963,542 (GRCm39)	V841F	probably damaging	Het
Adcy10	G	A	1: 165,331,618 (GRCm39)	E84K	probably damaging	Het
Adgrg6	C	A	10: 14,344,571 (GRCm39)	M127I	probably damaging	Het
Agpat5	A	G	8: 18,929,668 (GRCm39)	I266V	possibly damaging	Het
Agtpbp1	A	T	13: 59,676,213 (GRCm39)	Y186N	possibly damaging	Het
Alx1	A	T	10: 102,845,193 (GRCm39)	N279K	probably damaging	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
Arsi	A	G	18: 61,050,170 (GRCm39)	Y351C	probably damaging	Het
B4galnt3	T	A	6: 120,201,581 (GRCm39)	R155W	probably damaging	Het
BC028528	T	C	3: 95,795,577 (GRCm39)	E75G	probably damaging	Het
Bmp2k	C	T	5: 97,200,970 (GRCm39)	P297S	possibly damaging	Het
Btnl4	A	G	17: 34,691,602 (GRCm39)	S296P	probably benign	Het
Bzw2	A	T	12: 36,173,980 (GRCm39)	V98E	probably null	Het
Cacna1d	C	T	14: 29,817,365 (GRCm39)	M1232I	probably benign	Het
Cast	A	G	13: 74,894,133 (GRCm39)	S171P	probably benign	Het
Catsperb	G	A	12: 101,507,771 (GRCm39)	A513T	probably benign	Het
Cd19	A	G	7: 126,013,664 (GRCm39)	S42P	probably benign	Het
Chml	A	G	1: 175,514,962 (GRCm39)	S138P	probably benign	Het
Clic6	T	G	16: 92,327,827 (GRCm39)		probably null	Het
Col12a1	A	T	9: 79,547,076 (GRCm39)	V2252E	probably damaging	Het
Cplx2	G	A	13: 54,527,361 (GRCm39)	E82K	probably benign	Het
Csmd2	G	A	4: 128,439,866 (GRCm39)	V3107M	probably benign	Het
Cspg4	T	A	9: 56,794,149 (GRCm39)	V628D	possibly damaging	Het
Dcaf13	G	A	15: 39,001,637 (GRCm39)	R315Q	possibly damaging	Het
Deaf1	A	G	7: 140,877,486 (GRCm39)	V547A	possibly damaging	Het
Dmxl1	C	T	18: 50,011,698 (GRCm39)	T1285I	probably damaging	Het
Dnah3	C	A	7: 119,646,921 (GRCm39)	W1036L	probably damaging	Het
Dnai3	A	G	3: 145,753,922 (GRCm39)	S713P	probably damaging	Het
Dpy19l1	A	C	9: 24,393,350 (GRCm39)	S140A	possibly damaging	Het
Dsg2	T	A	18: 20,735,302 (GRCm39)	D1093E	possibly damaging	Het
Edaradd	T	A	13: 12,523,304 (GRCm39)	H12L	probably damaging	Het
Enam	T	C	5: 88,640,827 (GRCm39)	M163T	probably benign	Het
Fbxo22	T	A	9: 55,128,333 (GRCm39)	V218E	probably damaging	Het
Fbxo34	A	T	14: 47,767,085 (GRCm39)	K148N	probably damaging	Het
Foxi3	A	G	6: 70,933,960 (GRCm39)	D149G	probably damaging	Het
Gbp8	C	T	5: 105,189,807 (GRCm39)	G75D	probably damaging	Het
Gm10784	C	T	13: 50,099,251 (GRCm39)		noncoding transcript	Het
Gm7247	G	A	14: 51,807,051 (GRCm39)		probably null	Het
Grik3	T	A	4: 125,544,278 (GRCm39)	V333E	probably damaging	Het
Gsap	A	T	5: 21,431,309 (GRCm39)	D211V	probably damaging	Het
H2-T15	T	C	17: 36,368,768 (GRCm39)	Y104C	possibly damaging	Het
Ino80	T	C	2: 119,261,489 (GRCm39)	N725S	probably damaging	Het
Itgad	A	G	7: 127,788,703 (GRCm39)	I443V	probably benign	Het
Itsn1	T	A	16: 91,638,476 (GRCm39)	I52N	probably damaging	Het
Kmt2b	TCTCCTCCTCCTCCTCCTCCTCCTCC	TCTCCTCCTCCTCCTCCTCCTCC	7: 30,285,783 (GRCm39)		probably benign	Het
Lamc1	T	G	1: 153,104,523 (GRCm39)	S59R	probably damaging	Het
Lrrk1	T	C	7: 65,922,801 (GRCm39)	I1366V	probably benign	Het
Lyn	C	A	4: 3,738,850 (GRCm39)	Q41K	probably benign	Het
Mapk13	C	T	17: 28,997,461 (GRCm39)	R360*	probably null	Het
Mapk8ip3	T	A	17: 25,123,726 (GRCm39)	I599F	probably damaging	Het
Me1	T	C	9: 86,561,905 (GRCm39)	K60R	probably benign	Het
Mga	T	A	2: 119,771,974 (GRCm39)	D1532E	possibly damaging	Het
Miga1	G	A	3: 151,984,642 (GRCm39)	S427L	probably benign	Het
Mknk2	A	T	10: 80,505,173 (GRCm39)	V186E	probably damaging	Het
Myo1a	C	A	10: 127,546,086 (GRCm39)	N236K	probably benign	Het
Myt1	A	G	2: 181,439,207 (GRCm39)	D243G	probably benign	Het
Ncf4	T	C	15: 78,140,189 (GRCm39)	V196A	possibly damaging	Het
Nlrp5	G	T	7: 23,117,603 (GRCm39)	L442F	probably damaging	Het
Olfm4	G	A	14: 80,258,747 (GRCm39)	D332N	probably benign	Het
Or4a81	C	A	2: 89,619,637 (GRCm39)	V20F	probably benign	Het
Or4b1d	T	A	2: 89,969,432 (GRCm39)	D17V	probably damaging	Het
Osbpl11	T	A	16: 33,016,452 (GRCm39)	M69K	probably benign	Het
Oxnad1	T	A	14: 31,824,366 (GRCm39)	*312K	probably null	Het
Plekhg1	A	G	10: 3,906,985 (GRCm39)	Q634R	probably benign	Het
Plekhh2	T	C	17: 84,882,691 (GRCm39)	Y733H	probably damaging	Het
Ppp1r21	A	G	17: 88,856,941 (GRCm39)	H132R	probably benign	Het
Prpf38b	G	A	3: 108,811,408 (GRCm39)		probably benign	Het
Prpf4b	A	T	13: 35,083,954 (GRCm39)	M908L	probably benign	Het
Prps2	T	C	X: 166,135,288 (GRCm39)	D183G	probably damaging	Het
Pudp	T	C	18: 50,701,259 (GRCm39)	D158G	probably damaging	Het
R3hdm1	T	C	1: 128,112,181 (GRCm39)	S422P	probably damaging	Het
Ranbp3	T	A	17: 57,003,640 (GRCm39)		probably null	Het
Ranbp6	A	G	19: 29,787,721 (GRCm39)	V877A	probably benign	Het
Rgsl1	A	T	1: 153,693,328 (GRCm39)	S618T	probably benign	Het
Rhox2a	A	T	X: 36,509,015 (GRCm39)	I61L	probably benign	Het
Rhox2a	G	C	X: 36,508,962 (GRCm39)	R43P	probably benign	Het
Rnf207	A	C	4: 152,396,612 (GRCm39)	D466E	probably benign	Het
Rnf7	A	G	9: 96,353,883 (GRCm39)	I80T	probably benign	Het
Ros1	T	A	10: 52,005,764 (GRCm39)	I878F	possibly damaging	Het
Rsbn1	T	A	3: 103,861,096 (GRCm39)		probably null	Het
Sbk1	T	C	7: 125,890,301 (GRCm39)	S105P	probably damaging	Het
Sdk1	T	C	5: 141,992,380 (GRCm39)	Y790H	probably damaging	Het
Sec62	T	A	3: 30,864,683 (GRCm39)	N182K	unknown	Het
Slc15a1	T	C	14: 121,715,504 (GRCm39)	Y345C	probably damaging	Het
Slc27a1	G	A	8: 72,023,408 (GRCm39)	A15T	probably benign	Het
Slc35d1	A	G	4: 103,070,426 (GRCm39)	F110L	probably damaging	Het
Slc39a5	T	A	10: 128,233,136 (GRCm39)	S333C	probably benign	Het
Tarbp1	A	G	8: 127,173,934 (GRCm39)	S927P	probably damaging	Het
Tns1	A	G	1: 73,992,930 (GRCm39)	S583P	probably damaging	Het
Trim38	A	T	13: 23,966,952 (GRCm39)	D133V	probably damaging	Het
Trim40	T	C	17: 37,193,531 (GRCm39)		probably null	Het
Trim42	C	A	9: 97,244,998 (GRCm39)	V601L	probably benign	Het
Trpc7	G	A	13: 57,035,367 (GRCm39)	R189C	probably damaging	Het
Ttc29	A	T	8: 79,060,208 (GRCm39)	Y376F	probably benign	Het
Vmn2r63	A	G	7: 42,553,114 (GRCm39)	I714T	possibly damaging	Het
Vmn2r68	C	A	7: 84,870,743 (GRCm39)	A847S	probably benign	Het
Zbp1	G	A	2: 173,049,608 (GRCm39)	P385S	possibly damaging	Het
Zfat	A	G	15: 68,056,325 (GRCm39)	Y237H	probably damaging	Het
Zfp236	A	T	18: 82,615,784 (GRCm39)	W1840R	probably damaging	Het
Zfp426	G	T	9: 20,381,923 (GRCm39)	Q341K	possibly damaging	Het
Zfp462	T	A	4: 55,009,349 (GRCm39)	N438K	probably benign	Het
Zfp952	T	A	17: 33,221,899 (GRCm39)	V88E	probably damaging	Het
Znfx1	G	T	2: 166,898,276 (GRCm39)	A216D	probably benign	Het

Other mutations in Prkcq

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01654:Prkcq	APN	2	11,288,654 (GRCm39)	missense	probably damaging	1.00
IGL01656:Prkcq	APN	2	11,231,766 (GRCm39)	missense	probably damaging	1.00
IGL01732:Prkcq	APN	2	11,265,644 (GRCm39)	splice site	probably benign
IGL02136:Prkcq	APN	2	11,265,479 (GRCm39)	missense	probably benign	0.00
IGL02161:Prkcq	APN	2	11,281,887 (GRCm39)	missense	probably benign
IGL02178:Prkcq	APN	2	11,281,851 (GRCm39)	missense	possibly damaging	0.93
IGL03107:Prkcq	APN	2	11,265,597 (GRCm39)	missense	probably damaging	1.00
IGL03149:Prkcq	APN	2	11,237,356 (GRCm39)	missense	probably benign	0.11
banks	UTSW	2	11,304,221 (GRCm39)	missense	probably damaging	1.00
celina	UTSW	2	11,288,660 (GRCm39)	missense	possibly damaging	0.82
celina2	UTSW	2	11,231,797 (GRCm39)	critical splice donor site	probably null
Megabytes	UTSW	2	11,295,262 (GRCm39)	nonsense	probably null
Monmouth	UTSW	2	11,284,335 (GRCm39)	missense	probably damaging	1.00
3-1:Prkcq	UTSW	2	11,304,905 (GRCm39)	missense	probably damaging	1.00
K3955:Prkcq	UTSW	2	11,251,604 (GRCm39)	splice site	probably benign
R0049:Prkcq	UTSW	2	11,288,643 (GRCm39)	missense	probably benign	0.04
R0049:Prkcq	UTSW	2	11,288,643 (GRCm39)	missense	probably benign	0.04
R0183:Prkcq	UTSW	2	11,257,973 (GRCm39)	missense	probably damaging	1.00
R0366:Prkcq	UTSW	2	11,251,649 (GRCm39)	splice site	probably benign
R0388:Prkcq	UTSW	2	11,259,045 (GRCm39)	missense	probably benign
R1385:Prkcq	UTSW	2	11,261,097 (GRCm39)	missense	probably damaging	1.00
R1687:Prkcq	UTSW	2	11,295,344 (GRCm39)	missense	probably damaging	1.00
R1693:Prkcq	UTSW	2	11,259,010 (GRCm39)	missense	probably damaging	0.99
R1760:Prkcq	UTSW	2	11,304,881 (GRCm39)	missense	probably damaging	1.00
R1764:Prkcq	UTSW	2	11,237,442 (GRCm39)	missense	probably damaging	1.00
R1968:Prkcq	UTSW	2	11,250,208 (GRCm39)	missense	probably damaging	1.00
R2020:Prkcq	UTSW	2	11,284,332 (GRCm39)	missense	probably benign
R2108:Prkcq	UTSW	2	11,237,380 (GRCm39)	missense	probably damaging	1.00
R2762:Prkcq	UTSW	2	11,237,451 (GRCm39)	missense	possibly damaging	0.75
R3402:Prkcq	UTSW	2	11,288,660 (GRCm39)	missense	possibly damaging	0.82
R3429:Prkcq	UTSW	2	11,251,781 (GRCm39)	missense	probably damaging	1.00
R3545:Prkcq	UTSW	2	11,288,627 (GRCm39)	missense	probably benign	0.11
R3547:Prkcq	UTSW	2	11,288,627 (GRCm39)	missense	probably benign	0.11
R3893:Prkcq	UTSW	2	11,231,782 (GRCm39)	missense	probably damaging	1.00
R4086:Prkcq	UTSW	2	11,288,679 (GRCm39)	missense	probably damaging	0.97
R4423:Prkcq	UTSW	2	11,260,980 (GRCm39)	missense	possibly damaging	0.66
R4541:Prkcq	UTSW	2	11,288,623 (GRCm39)	missense	possibly damaging	0.84
R4652:Prkcq	UTSW	2	11,284,333 (GRCm39)	missense	possibly damaging	0.83
R4820:Prkcq	UTSW	2	11,231,797 (GRCm39)	critical splice donor site	probably null
R5197:Prkcq	UTSW	2	11,304,227 (GRCm39)	missense	probably damaging	1.00
R6008:Prkcq	UTSW	2	11,261,097 (GRCm39)	missense	probably damaging	1.00
R7030:Prkcq	UTSW	2	11,231,661 (GRCm39)	splice site	probably null
R7231:Prkcq	UTSW	2	11,295,262 (GRCm39)	nonsense	probably null
R7461:Prkcq	UTSW	2	11,304,221 (GRCm39)	missense	probably damaging	1.00
R7613:Prkcq	UTSW	2	11,304,221 (GRCm39)	missense	probably damaging	1.00
R8441:Prkcq	UTSW	2	11,253,037 (GRCm39)	missense	probably benign	0.11
R8491:Prkcq	UTSW	2	11,284,335 (GRCm39)	missense	probably damaging	1.00
R8724:Prkcq	UTSW	2	11,304,784 (GRCm39)	missense	probably benign	0.17
R9031:Prkcq	UTSW	2	11,251,819 (GRCm39)	missense	probably damaging	0.99
R9164:Prkcq	UTSW	2	11,231,716 (GRCm39)	missense	probably damaging	0.96
R9621:Prkcq	UTSW	2	11,261,014 (GRCm39)	missense	probably benign	0.00
R9661:Prkcq	UTSW	2	11,250,141 (GRCm39)	nonsense	probably null
Z1177:Prkcq	UTSW	2	11,304,192 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GGGGTTTACTCTGCTGTCCC -3'
(R):5'- GACCCAGAAGCACGAGGTAC -3'

Sequencing Primer
(F):5'- CTGTCCTCATGCTGTGTCTTGG -3'
(R):5'- TAATGTTGTCAGAGATGAATAGTGGC -3'

Posted On

2015-10-08