Mutagenetix > Incidental Mutation

Incidental Mutation 'R8307:Ppp2r2c'

641122

Institutional Source

Beutler Lab

Gene Symbol

Ppp2r2c

Ensembl Gene

ENSMUSG00000029120

Gene Name

protein phosphatase 2, regulatory subunit B, gamma

Synonyms

6330548O06Rik, IMYPNO1, PR52

MMRRC Submission

067717-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.476) question?

Stock #

R8307 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

37025857-37112422 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 37104430 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 270 (D270G)

Ref Sequence

ENSEMBL: ENSMUSP00000031003 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000031003]

AlphaFold

Q8BG02

Predicted Effect

probably damaging
Transcript: ENSMUST00000031003
AA Change: D270G

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000031003
Gene: ENSMUSG00000029120
AA Change: D270G

Domain	Start	End	E-Value	Type
WD40	13	52	1.99e0	SMART
WD40	79	119	2.38e1	SMART
WD40	161	200	1.11e0	SMART
WD40	211	251	5.7e1	SMART
WD40	270	308	4.11e1	SMART
Blast:WD40	312	366	1e-24	BLAST
WD40	402	439	3.07e1	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

100% (56/56)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The product of this gene belongs to the phosphatase 2 regulatory subunit B family. Protein phosphatase 2 is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a gamma isoform of the regulatory subunit B55 subfamily. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2510039O18Rik	C	A	4: 148,025,837 (GRCm39)	T119K	probably benign	Het
Abca13	T	A	11: 9,227,922 (GRCm39)	L655*	probably null	Het
Aifm2	A	G	10: 61,562,171 (GRCm39)	Y69C	probably damaging	Het
Atp2c1	C	T	9: 105,320,030 (GRCm39)	V448I	probably benign	Het
Barx2	A	G	9: 31,770,307 (GRCm39)	S74P	probably damaging	Het
Bod1l	T	C	5: 41,978,498 (GRCm39)	K939E	probably damaging	Het
Cdh12	C	A	15: 21,358,949 (GRCm39)	F124L	probably benign	Het
Cdh12	T	A	15: 21,358,950 (GRCm39)	Y125N	probably damaging	Het
Cdx2	A	G	5: 147,243,477 (GRCm39)	Y106H	possibly damaging	Het
Chmp1a	C	T	8: 123,932,980 (GRCm39)	G158S	probably damaging	Het
Cilp	G	A	9: 65,186,286 (GRCm39)	G794S	probably damaging	Het
Cntnap1	A	T	11: 101,079,702 (GRCm39)	Y1277F	possibly damaging	Het
Csde1	A	G	3: 102,946,389 (GRCm39)		probably benign	Het
Dennd4c	A	C	4: 86,744,109 (GRCm39)	D1317A	probably benign	Het
Dgcr2	C	T	16: 17,676,242 (GRCm39)	G176D	probably benign	Het
Dock2	A	T	11: 34,260,362 (GRCm39)	M993K	possibly damaging	Het
Dpy19l1	G	A	9: 24,414,297 (GRCm39)	P44S	probably benign	Het
Dsg2	C	T	18: 20,708,121 (GRCm39)	P74L	probably benign	Het
Epg5	T	A	18: 78,065,894 (GRCm39)	F2078Y	probably damaging	Het
Fancl	A	G	11: 26,349,642 (GRCm39)		probably benign	Het
Fbn1	C	A	2: 125,347,402 (GRCm39)	R41L	possibly damaging	Het
Gemin5	G	A	11: 58,042,420 (GRCm39)	T467M	probably damaging	Het
Hexb	T	C	13: 97,330,707 (GRCm39)	Q102R	probably benign	Het
Hmcn2	A	G	2: 31,286,127 (GRCm39)	D2093G	probably damaging	Het
Hmmr	G	A	11: 40,612,499 (GRCm39)	S206F	probably damaging	Het
Igkv1-131	A	G	6: 67,743,051 (GRCm39)	Y111H	probably damaging	Het
Il6st	G	T	13: 112,624,281 (GRCm39)	G177V	probably benign	Het
Kank4	G	A	4: 98,666,915 (GRCm39)	Q511*	probably null	Het
Krt90	A	G	15: 101,467,634 (GRCm39)	L248P	probably damaging	Het
Krtap5-2	A	G	7: 141,728,586 (GRCm39)	C187R	unknown	Het
Lonp1	C	A	17: 56,933,573 (GRCm39)	A101S	probably benign	Het
Nckap5l	A	G	15: 99,321,058 (GRCm39)	C1241R	probably damaging	Het
Or1j11	A	G	2: 36,312,333 (GRCm39)	T308A	probably benign	Het
Or4c11c	G	A	2: 88,661,633 (GRCm39)	M57I	possibly damaging	Het
Or6c203	T	C	10: 129,010,101 (GRCm39)	D263G	probably benign	Het
Pcdh15	T	A	10: 74,342,307 (GRCm39)	C1131*	probably null	Het
Pcdhgc3	A	G	18: 37,940,847 (GRCm39)	D416G	probably damaging	Het
Pikfyve	T	C	1: 65,284,894 (GRCm39)	M786T	possibly damaging	Het
Pink1	A	T	4: 138,045,273 (GRCm39)	M297K	probably benign	Het
Pln	T	C	10: 53,219,975 (GRCm39)	Y6H	unknown	Het
Pramel58	T	G	5: 94,831,416 (GRCm39)	L141R	probably damaging	Het
Prcd	A	T	11: 116,550,199 (GRCm39)	T76S	possibly damaging	Het
Pxylp1	A	G	9: 96,721,137 (GRCm39)		probably null	Het
Rab11fip4	A	T	11: 79,581,600 (GRCm39)	N532Y	possibly damaging	Het
Ralgapa1	C	A	12: 55,788,308 (GRCm39)	V592L	probably damaging	Het
Robo2	T	C	16: 73,753,498 (GRCm39)	D793G	probably damaging	Het
Sec14l1	G	A	11: 117,034,242 (GRCm39)		probably null	Het
Srcap	T	A	7: 127,124,541 (GRCm39)	V237E	probably damaging	Het
Srl	A	G	16: 4,315,009 (GRCm39)	I211T	probably benign	Het
Tasor	G	T	14: 27,193,622 (GRCm39)	A941S	probably damaging	Het
Tet3	A	G	6: 83,356,909 (GRCm39)	V883A	probably damaging	Het
Trim46	A	G	3: 89,151,223 (GRCm39)	Y113H	probably benign	Het
Trim58	G	A	11: 58,537,909 (GRCm39)	A267T	probably benign	Het
Tsks	G	A	7: 44,607,086 (GRCm39)	G140S		Het
Vmn2r110	C	A	17: 20,803,319 (GRCm39)	V419L	probably benign	Het
Vmn2r66	A	G	7: 84,656,270 (GRCm39)	F249L	probably benign	Het
Vps8	A	C	16: 21,314,652 (GRCm39)	D584A	probably benign	Het
Zfp605	T	A	5: 110,276,063 (GRCm39)	C394S	probably damaging	Het
Zscan4e	A	G	7: 11,041,059 (GRCm39)	I271T	probably benign	Het

Other mutations in Ppp2r2c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01319:Ppp2r2c	APN	5	37,104,465 (GRCm39)	missense	possibly damaging	0.82
IGL01583:Ppp2r2c	APN	5	37,026,166 (GRCm39)	start codon destroyed	probably null	0.99
IGL01662:Ppp2r2c	APN	5	37,083,744 (GRCm39)	missense	probably damaging	1.00
IGL01674:Ppp2r2c	APN	5	37,097,570 (GRCm39)	missense	possibly damaging	0.63
IGL02027:Ppp2r2c	APN	5	37,109,816 (GRCm39)	missense	probably damaging	0.99
IGL03118:Ppp2r2c	APN	5	37,083,660 (GRCm39)	missense	probably damaging	1.00
R0034:Ppp2r2c	UTSW	5	37,084,883 (GRCm39)	missense	probably benign	0.02
R2036:Ppp2r2c	UTSW	5	37,109,748 (GRCm39)	missense	possibly damaging	0.84
R4877:Ppp2r2c	UTSW	5	37,026,214 (GRCm39)	missense	probably damaging	0.98
R4980:Ppp2r2c	UTSW	5	37,109,732 (GRCm39)	missense	probably benign	0.01
R5838:Ppp2r2c	UTSW	5	37,097,531 (GRCm39)	missense	probably benign	0.14
R6291:Ppp2r2c	UTSW	5	37,097,468 (GRCm39)	missense	possibly damaging	0.95
R6940:Ppp2r2c	UTSW	5	37,084,875 (GRCm39)	missense	probably damaging	0.98
R7405:Ppp2r2c	UTSW	5	37,104,486 (GRCm39)	missense	possibly damaging	0.71
R7695:Ppp2r2c	UTSW	5	37,104,526 (GRCm39)	missense	probably damaging	1.00
R7967:Ppp2r2c	UTSW	5	37,097,450 (GRCm39)	missense	possibly damaging	0.88
R9643:Ppp2r2c	UTSW	5	37,080,383 (GRCm39)	missense	probably damaging	0.99
R9715:Ppp2r2c	UTSW	5	37,097,488 (GRCm39)	missense	possibly damaging	0.92
X0013:Ppp2r2c	UTSW	5	37,083,669 (GRCm39)	missense	probably damaging	1.00
Z1176:Ppp2r2c	UTSW	5	37,088,621 (GRCm39)	missense	probably benign	0.09

Predicted Primers

PCR Primer
(F):5'- GTCCTTAGAGCCCAGGGTTTTG -3'
(R):5'- AGATCTCACACCATGCAGAG -3'

Sequencing Primer
(F):5'- AGAGCCCAGGGTTTTGGTAGG -3'
(R):5'- GCCCTGAGGATGCCAGAATTCTATAC -3'

Posted On

2020-07-28