Mutagenetix > Incidental Mutation

Incidental Mutation 'R1764:Prkcq'

193250

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

039796-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1764 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

11176922-11306033 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 11237442 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Methionine at position 74 (V74M)

Ref Sequence

ENSEMBL: ENSMUSP00000100035 (fasta)

Gene Model

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

AlphaFold

Q02111

Predicted Effect

probably damaging
Transcript: ENSMUST00000028118
AA Change: V74M

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000028118
Gene: ENSMUSG00000026778
AA Change: V74M

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

probably damaging
Transcript: ENSMUST00000102970
AA Change: V74M

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000100035
Gene: ENSMUSG00000026778
AA Change: V74M

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: ENSMUST00000114853

SMART Domains

Protein: ENSMUSP00000110503
Gene: ENSMUSG00000026778

Domain	Start	End	E-Value	Type
PDB:2ENJ\|A	3	126	9e-86	PDB
Blast:C2	6	101	2e-44	BLAST
C1	160	209	3.27e-15	SMART
C1	232	281	2.22e-17	SMART
Pfam:Pkinase	380	465	1.7e-8	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000192244

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000195207

Meta Mutation Damage Score

0.1854

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.1%
20x: 92.2%

Validation Efficiency

94% (94/100)

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: 95 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930522L14Rik	A	G	5: 109,884,655 (GRCm39)	V401A	probably benign	Het
Abca7	G	T	10: 79,844,784 (GRCm39)	W1502L	probably damaging	Het
Adcy7	A	G	8: 89,035,468 (GRCm39)	E124G	probably benign	Het
Aif1l	G	A	2: 31,855,118 (GRCm39)	E66K	probably benign	Het
Aldh8a1	A	T	10: 21,271,392 (GRCm39)	M373L	probably benign	Het
Alg6	T	C	4: 99,629,815 (GRCm39)	Y131H	probably benign	Het
Arhgef6	T	C	X: 56,383,922 (GRCm39)	M5V	probably benign	Het
Arrdc4	A	T	7: 68,391,622 (GRCm39)	I215K	probably damaging	Het
Asb4	A	G	6: 5,390,798 (GRCm39)		probably null	Het
Astn1	T	C	1: 158,331,821 (GRCm39)	I305T	probably benign	Het
Atp5f1b	T	A	10: 127,919,949 (GRCm39)		probably benign	Het
Atp8a1	C	A	5: 67,788,910 (GRCm39)	M1044I	probably benign	Het
Atp9b	C	T	18: 80,952,806 (GRCm39)		probably null	Het
Brd10	T	A	19: 29,696,560 (GRCm39)	T978S	possibly damaging	Het
Btaf1	A	G	19: 36,928,518 (GRCm39)	H113R	probably benign	Het
C87436	G	T	6: 86,430,594 (GRCm39)	C338F	possibly damaging	Het
Casz1	T	C	4: 149,027,357 (GRCm39)		probably benign	Het
Cbr3	T	A	16: 93,487,370 (GRCm39)	H184Q	probably damaging	Het
Cct8l1	T	C	5: 25,722,097 (GRCm39)	S271P	possibly damaging	Het
Cdc34	A	G	10: 79,521,174 (GRCm39)	K77R	probably benign	Het
Cdc34	G	T	10: 79,521,172 (GRCm39)		probably null	Het
Cdh20	A	G	1: 104,862,070 (GRCm39)		probably benign	Het
Celsr3	A	G	9: 108,706,157 (GRCm39)	E880G	probably damaging	Het
Cers1	T	G	8: 70,774,141 (GRCm39)		probably null	Het
Cntn5	T	C	9: 9,673,988 (GRCm39)	I705V	probably benign	Het
Dennd4c	T	A	4: 86,721,247 (GRCm39)	D636E	probably damaging	Het
Dnah11	T	C	12: 118,154,560 (GRCm39)	E240G	probably benign	Het
Dnah2	T	C	11: 69,314,369 (GRCm39)	Y4100C	probably damaging	Het
Dpysl3	T	C	18: 43,496,583 (GRCm39)	E151G	probably damaging	Het
Efcab9	T	G	11: 32,474,457 (GRCm39)	T9P	possibly damaging	Het
Eif4g2	A	T	7: 110,673,694 (GRCm39)	F725Y	probably damaging	Het
Epha6	T	A	16: 59,596,091 (GRCm39)	I867F	probably null	Het
Erbin	T	C	13: 103,979,959 (GRCm39)		probably benign	Het
Evi5l	A	G	8: 4,253,560 (GRCm39)	E468G	probably damaging	Het
Filip1l	C	T	16: 57,390,401 (GRCm39)	R330W	probably damaging	Het
Fmo3	C	T	1: 162,786,142 (GRCm39)	V283M	possibly damaging	Het
Gabarapl1	A	T	6: 129,510,481 (GRCm39)	K24N	possibly damaging	Het
Gigyf1	C	T	5: 137,520,770 (GRCm39)		probably benign	Het
Gm5581	T	A	6: 131,158,362 (GRCm39)		noncoding transcript	Het
Gon4l	G	T	3: 88,799,906 (GRCm39)	K850N	probably damaging	Het
Igf2bp3	C	T	6: 49,085,980 (GRCm39)	R233H	probably damaging	Het
Iqcf4	G	A	9: 106,445,893 (GRCm39)	R85C	probably benign	Het
Kalrn	C	T	16: 34,033,243 (GRCm39)	R473Q	probably damaging	Het
Lmod2	T	A	6: 24,603,376 (GRCm39)	V117E	probably damaging	Het
Mapk11	A	G	15: 89,028,594 (GRCm39)		probably null	Het
Mcm3	G	A	1: 20,876,103 (GRCm39)	R664C	probably damaging	Het
Mex3d	A	G	10: 80,222,770 (GRCm39)	M162T	probably benign	Het
Mrgprb3	A	G	7: 48,292,771 (GRCm39)	I260T	probably benign	Het
Ncor2	G	T	5: 125,105,679 (GRCm39)	A1637D	possibly damaging	Het
Nedd4	T	A	9: 72,638,189 (GRCm39)	D441E	probably damaging	Het
Nek5	A	T	8: 22,599,928 (GRCm39)	C194S	probably damaging	Het
Nos1ap	T	C	1: 170,146,447 (GRCm39)	D369G	possibly damaging	Het
Ntrk1	G	T	3: 87,687,391 (GRCm39)	T681K	probably damaging	Het
Or13a24	T	C	7: 140,154,383 (GRCm39)	W106R	probably damaging	Het
Or4f14	A	G	2: 111,742,526 (GRCm39)	F250L	possibly damaging	Het
Otogl	C	T	10: 107,735,322 (GRCm39)	W154*	probably null	Het
Pcdh20	T	C	14: 88,706,620 (GRCm39)	T227A	possibly damaging	Het
Pcdhb17	T	C	18: 37,620,324 (GRCm39)	S705P	probably damaging	Het
Piezo2	T	C	18: 63,257,713 (GRCm39)	H335R	possibly damaging	Het
Pkn2	T	C	3: 142,499,615 (GRCm39)	Q954R	probably damaging	Het
Pramel23	C	A	4: 143,424,840 (GRCm39)	C201F	probably benign	Het
Prkrip1	A	T	5: 136,218,489 (GRCm39)		probably null	Het
Pttg1ip2	A	T	5: 5,528,943 (GRCm39)	I24N	possibly damaging	Het
Rb1cc1	A	G	1: 6,284,904 (GRCm39)		probably benign	Het
Rbm5	A	T	9: 107,644,763 (GRCm39)	Y11*	probably null	Het
Rsf1	CG	CGACGGCGGTG	7: 97,229,115 (GRCm39)		probably benign	Het
Ryr3	C	A	2: 112,690,805 (GRCm39)	V1082L	probably damaging	Het
Scart2	A	G	7: 139,877,178 (GRCm39)	E831G	probably benign	Het
Sel1l3	C	A	5: 53,327,789 (GRCm39)	E497*	probably null	Het
Serpina6	A	T	12: 103,620,182 (GRCm39)	I189N	probably damaging	Het
Serpinb11	A	T	1: 107,304,532 (GRCm39)	T166S	probably benign	Het
Skint7	T	C	4: 111,839,270 (GRCm39)	L188S	probably benign	Het
Slc25a45	C	T	19: 5,934,958 (GRCm39)	A269V	probably damaging	Het
Sltm	A	G	9: 70,469,082 (GRCm39)	T114A	probably benign	Het
Sned1	G	A	1: 93,209,376 (GRCm39)	V830M	possibly damaging	Het
Spen	C	A	4: 141,200,261 (GRCm39)	V2766L	probably damaging	Het
Srgap2	T	A	1: 131,247,275 (GRCm39)	I445F	possibly damaging	Het
Stox2	A	T	8: 47,647,051 (GRCm39)	Y200*	probably null	Het
Strada	C	A	11: 106,055,010 (GRCm39)	R384L	probably damaging	Het
Tctn2	G	A	5: 124,757,094 (GRCm39)		noncoding transcript	Het
Tgfbr3l	G	T	8: 4,299,282 (GRCm39)	R461L	probably benign	Het
Tmem65	A	G	15: 58,661,998 (GRCm39)		probably benign	Het
Tpst1	G	T	5: 130,143,343 (GRCm39)	V294F	possibly damaging	Het
Trim23	A	G	13: 104,335,126 (GRCm39)	Y384C	probably damaging	Het
Ube3b	C	G	5: 114,542,678 (GRCm39)	L512V	possibly damaging	Het
Ubxn4	T	A	1: 128,183,916 (GRCm39)	V92E	probably damaging	Het
Vmn2r57	A	T	7: 41,050,067 (GRCm39)	C561S	probably damaging	Het
Vwa8	A	G	14: 79,145,635 (GRCm39)	D104G	probably damaging	Het
Wdr25	T	A	12: 108,992,364 (GRCm39)	L73*	probably null	Het
Wnt9a	G	A	11: 59,221,728 (GRCm39)	A209T	probably benign	Het
Zcchc17	A	C	4: 130,223,388 (GRCm39)	C133G	probably damaging	Het
Zdhhc18	T	A	4: 133,335,987 (GRCm39)	M375L	probably benign	Het
Zfhx3	T	C	8: 109,678,276 (GRCm39)	F3109L	probably benign	Het
Zfp202	T	A	9: 40,121,762 (GRCm39)	D286E	probably benign	Het
Zzef1	T	C	11: 72,784,158 (GRCm39)	L2021P	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
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
R4649:Prkcq	UTSW	2	11,284,333 (GRCm39)	missense	possibly damaging	0.83
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'- GGACCTGTCTCATCTGCCCTAGATTG -3'
(R):5'- AGGGAGTCTGCTTACTCATGTCCTC -3'

Sequencing Primer
(F):5'- GCGAGCCCACTATTAAATGGAATTG -3'
(R):5'- agcacacacctgtaaaccc -3'

Posted On

2014-05-23