Mutagenetix > Incidental Mutation

Incidental Mutation 'R7799:Ppp2r5b'

600456

Institutional Source

Beutler Lab

Gene Symbol

Ppp2r5b

Ensembl Gene

ENSMUSG00000024777

Gene Name

protein phosphatase 2, regulatory subunit B', beta

Synonyms

B'beta

MMRRC Submission

045854-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.382) question?

Stock #

R7799 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

6277795-6285902 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 6282628 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Leucine at position 174 (R174L)

Ref Sequence

ENSEMBL: ENSMUSP00000025695 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025695] [ENSMUST00000025698] [ENSMUST00000113526]

AlphaFold

Q6PD28

Predicted Effect

probably benign
Transcript: ENSMUST00000025695
AA Change: R174L

PolyPhen 2 Score 0.430 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000025695
Gene: ENSMUSG00000024777
AA Change: R174L

Domain	Start	End	E-Value	Type
low complexity region	6	25	N/A	INTRINSIC
low complexity region	32	48	N/A	INTRINSIC
Pfam:B56	62	467	5.2e-187	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000025698

SMART Domains

Protein: ENSMUSP00000025698
Gene: ENSMUSG00000024784

Domain	Start	End	E-Value	Type
low complexity region	8	15	N/A	INTRINSIC
Pfam:DAN	17	126	5.1e-8	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000113526

SMART Domains

Protein: ENSMUSP00000109154
Gene: ENSMUSG00000024784

Domain	Start	End	E-Value	Type
low complexity region	8	15	N/A	INTRINSIC
Pfam:DAN	16	123	1.9e-7	PFAM

Coding Region Coverage

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

Validation Efficiency

98% (50/51)

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 2A regulatory subunit B family. Protein phosphatase 2A 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 beta isoform of the regulatory subunit B56 subfamily. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	T	C	3: 137,775,362 (GRCm39)	V1517A	probably benign	Het
Adam17	C	A	12: 21,390,493 (GRCm39)	G410C	probably damaging	Het
Adcy3	A	G	12: 4,254,762 (GRCm39)	D698G	probably damaging	Het
Afap1	T	A	5: 36,131,742 (GRCm39)	N356K	possibly damaging	Het
Afm	A	G	5: 90,671,713 (GRCm39)	N132D	probably benign	Het
Bsdc1	T	A	4: 129,359,141 (GRCm39)		probably null	Het
Ccdc121rt2	T	G	5: 112,597,698 (GRCm39)	Y82D	not run	Het
Ccdc47	T	C	11: 106,101,143 (GRCm39)	E173G	possibly damaging	Het
Cit	T	G	5: 116,001,027 (GRCm39)	F142C	probably benign	Het
Cnga3	A	G	1: 37,300,852 (GRCm39)	D524G	probably damaging	Het
Cpne8	T	A	15: 90,424,450 (GRCm39)	D313V	probably damaging	Het
Ell3	TCTCCTC	TCTC	2: 121,269,937 (GRCm39)		probably benign	Het
Flrt1	C	A	19: 7,073,229 (GRCm39)	L439F	possibly damaging	Het
Gkn1	A	T	6: 87,325,163 (GRCm39)	I82N	probably damaging	Het
Gm14410	C	A	2: 176,885,613 (GRCm39)	C217F	probably damaging	Het
Gm14412	G	T	2: 177,007,590 (GRCm39)	H102N	probably benign	Het
Gm3159	A	T	14: 4,397,585 (GRCm38)		probably benign	Het
Golm2	T	C	2: 121,764,022 (GRCm39)	V434A	probably benign	Het
Helz2	A	G	2: 180,879,782 (GRCm39)	M612T	probably benign	Het
Iars1	T	A	13: 49,876,494 (GRCm39)	I853N	probably damaging	Het
Kcna4	A	C	2: 107,126,237 (GRCm39)	I324L	possibly damaging	Het
Kcnh1	T	C	1: 192,117,183 (GRCm39)	S690P	probably damaging	Het
Kpna3	T	C	14: 61,622,182 (GRCm39)	Y194C	probably damaging	Het
Lrrc56	T	C	7: 140,789,515 (GRCm39)	S511P	probably damaging	Het
Ltbp1	A	G	17: 75,559,351 (GRCm39)	Y280C	probably damaging	Het
Macf1	A	G	4: 123,420,906 (GRCm39)	I116T	probably benign	Het
Mmp16	A	T	4: 18,112,112 (GRCm39)	N496I	probably damaging	Het
Mon2	T	C	10: 122,878,236 (GRCm39)	D229G	probably benign	Het
Or2b2	T	A	13: 21,887,369 (GRCm39)	L66Q	probably damaging	Het
Or2j6	A	T	7: 139,980,377 (GRCm39)	M194K	probably damaging	Het
Or52s1	A	G	7: 102,861,186 (GRCm39)	I40V	probably benign	Het
Or5p61	T	A	7: 107,758,637 (GRCm39)	I148F	probably benign	Het
Or5w14	G	T	2: 87,541,428 (GRCm39)	T274K	possibly damaging	Het
Pkp1	A	G	1: 135,817,695 (GRCm39)	F147L	possibly damaging	Het
Ppp1r3e	T	C	14: 55,114,672 (GRCm39)	Q30R	probably damaging	Het
Pramel58	A	G	5: 94,831,287 (GRCm39)	D98G	possibly damaging	Het
Qrfprl	G	T	6: 65,433,121 (GRCm39)	A314S	possibly damaging	Het
Rbm15	C	T	3: 107,239,459 (GRCm39)	R313H	probably damaging	Het
Rgs18	A	G	1: 144,629,603 (GRCm39)	F219L	probably damaging	Het
Ryr1	T	C	7: 28,702,985 (GRCm39)		probably null	Het
Sirpd	T	A	3: 15,361,723 (GRCm39)		probably null	Het
Sirt4	T	G	5: 115,617,805 (GRCm39)	I284L	probably benign	Het
Slc25a11	A	G	11: 70,536,005 (GRCm39)	V243A	probably benign	Het
Syde1	A	G	10: 78,425,741 (GRCm39)	I142T	probably benign	Het
Synj2	A	G	17: 6,088,098 (GRCm39)	E1383G	probably benign	Het
Syt4	A	T	18: 31,573,245 (GRCm39)	C423*	probably null	Het
Tfr2	T	A	5: 137,569,986 (GRCm39)	Y131N	possibly damaging	Het
Tgm1	C	T	14: 55,949,932 (GRCm39)	R92Q	unknown	Het
Thoc1	A	T	18: 9,984,441 (GRCm39)	D309V	probably damaging	Het
Vmn2r24	C	T	6: 123,757,422 (GRCm39)	H97Y	probably benign	Het
Wbp1	A	T	6: 83,097,176 (GRCm39)	Y89*	probably null	Het
Wnk1	A	G	6: 119,926,137 (GRCm39)	L1358P	probably benign	Het
Zfp14	T	C	7: 29,738,368 (GRCm39)	T206A	possibly damaging	Het
Zfp748	T	C	13: 67,689,608 (GRCm39)	T551A	probably benign	Het
Zfp9	A	T	6: 118,441,843 (GRCm39)	V273E	probably damaging	Het

Other mutations in Ppp2r5b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00598:Ppp2r5b	APN	19	6,280,998 (GRCm39)	missense	probably damaging	1.00
IGL02714:Ppp2r5b	APN	19	6,284,737 (GRCm39)	missense	probably damaging	0.99
IGL02937:Ppp2r5b	APN	19	6,281,016 (GRCm39)	missense	probably damaging	1.00
PIT4696001:Ppp2r5b	UTSW	19	6,284,713 (GRCm39)	missense	probably benign	0.12
R0114:Ppp2r5b	UTSW	19	6,278,461 (GRCm39)	missense	probably benign
R0333:Ppp2r5b	UTSW	19	6,279,077 (GRCm39)	unclassified	probably benign
R0627:Ppp2r5b	UTSW	19	6,282,664 (GRCm39)	unclassified	probably benign
R1477:Ppp2r5b	UTSW	19	6,280,257 (GRCm39)	missense	probably benign	0.01
R1628:Ppp2r5b	UTSW	19	6,280,935 (GRCm39)	critical splice donor site	probably null
R4066:Ppp2r5b	UTSW	19	6,279,360 (GRCm39)	missense	probably damaging	1.00
R4834:Ppp2r5b	UTSW	19	6,280,540 (GRCm39)	missense	possibly damaging	0.81
R5854:Ppp2r5b	UTSW	19	6,280,974 (GRCm39)	missense	probably damaging	1.00
R5895:Ppp2r5b	UTSW	19	6,284,764 (GRCm39)	missense	probably damaging	1.00
R6102:Ppp2r5b	UTSW	19	6,284,768 (GRCm39)	missense	probably benign	0.00
R6285:Ppp2r5b	UTSW	19	6,280,566 (GRCm39)	missense	probably benign	0.08
R7087:Ppp2r5b	UTSW	19	6,282,580 (GRCm39)	missense	possibly damaging	0.46
R7391:Ppp2r5b	UTSW	19	6,278,544 (GRCm39)	missense	probably benign	0.00
R7576:Ppp2r5b	UTSW	19	6,278,514 (GRCm39)	missense	possibly damaging	0.76

Predicted Primers

PCR Primer
(F):5'- TCGCTGTCAAATAGCTCCAG -3'
(R):5'- CCACATCTGCAGGTGTGAAG -3'

Sequencing Primer
(F):5'- TCCAGGAGCTGCAGGAC -3'
(R):5'- ATCTGCAGGTGTGAAGGGCTG -3'

Posted On

2019-11-26