Mutagenetix > Incidental Mutation

Incidental Mutation 'R5352:Ppp1r36'

423857

Institutional Source

Beutler Lab

Gene Symbol

Ppp1r36

Ensembl Gene

ENSMUSG00000052221

Gene Name

protein phosphatase 1, regulatory subunit 36

Synonyms

MMRRC Submission

042931-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.074) question?

Stock #

R5352 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

76417538-76439492 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 76428083 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 85 (V85A)

Ref Sequence

ENSEMBL: ENSMUSP00000152006 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063977] [ENSMUST00000220187]

AlphaFold

D3Z0R2

Predicted Effect

possibly damaging
Transcript: ENSMUST00000063977
AA Change: V114A

PolyPhen 2 Score 0.511 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000069849
Gene: ENSMUSG00000052221
AA Change: V114A

Domain	Start	End	E-Value	Type
Pfam:PPPI_inhib	52	402	5.7e-109	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218732

Predicted Effect

probably damaging
Transcript: ENSMUST00000220187
AA Change: V85A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

Meta Mutation Damage Score

0.1073

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.9%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630010A05Rik	T	G	16: 14,618,701	L206*	probably null	Het
Adgrv1	T	C	13: 81,494,657	Y3218C	probably damaging	Het
Agtpbp1	G	A	13: 59,473,746	T41M	probably damaging	Het
Akap6	A	T	12: 52,796,097	E76V	probably damaging	Het
Ank2	C	A	3: 127,498,991		probably benign	Het
Atp6ap1l	A	C	13: 90,883,756	L269R	probably damaging	Het
Blk	A	G	14: 63,375,971	S363P	probably damaging	Het
Btnl9	T	C	11: 49,178,840	N204S	probably benign	Het
Cc2d2a	G	T	5: 43,706,213	W672C	probably damaging	Het
Ccnf	A	G	17: 24,243,273		probably null	Het
Cdc45	C	T	16: 18,795,897	R205H	probably damaging	Het
Chst1	A	G	2: 92,613,365	T61A	possibly damaging	Het
Col6a4	G	A	9: 106,061,544	T1325I	probably damaging	Het
Col7a1	A	C	9: 108,961,411	T976P	unknown	Het
Corin	C	T	5: 72,305,033	S811N	probably benign	Het
Dnal1	T	C	12: 84,136,548	V27A	possibly damaging	Het
Dupd1	G	A	14: 21,677,023	R186W	probably benign	Het
F830045P16Rik	T	A	2: 129,472,901	H152L	probably damaging	Het
Flnc	A	G	6: 29,449,318	S1405G	possibly damaging	Het
Foxj1	T	C	11: 116,334,079	N154S	possibly damaging	Het
Gm12183	T	C	11: 48,752,162		noncoding transcript	Het
Gm27047	G	A	6: 130,631,019		noncoding transcript	Het
Grm5	A	G	7: 88,074,850	I783V	probably damaging	Het
Hk1	A	T	10: 62,304,770	S113T	probably damaging	Het
Iqca	A	T	1: 90,130,196	N260K	probably benign	Het
Iws1	A	T	18: 32,083,404	K399M	probably damaging	Het
Kdm4d	A	G	9: 14,464,358	I68T	probably damaging	Het
Man2a1	T	C	17: 64,731,246	I75T	probably damaging	Het
Med13	T	A	11: 86,301,468	I824L	possibly damaging	Het
Meioc	A	T	11: 102,675,313	E585V	probably benign	Het
Mrgpre	A	C	7: 143,781,094	F224C	probably damaging	Het
Muc5b	T	A	7: 141,864,558	F3747Y	possibly damaging	Het
Nlrp4e	T	C	7: 23,353,173	V839A	probably benign	Het
Nup210	A	T	6: 91,069,316	V545E	probably damaging	Het
Ola1	T	C	2: 73,099,330	T310A	probably damaging	Het
Pdxdc1	T	C	16: 13,840,311	N516S	probably benign	Het
Phlpp1	A	G	1: 106,172,725	D241G	probably benign	Het
Rasa3	A	C	8: 13,631,778	L57R	possibly damaging	Het
Rp1	T	C	1: 4,347,098	S1264G	probably benign	Het
Rprd1b	A	G	2: 158,058,736	E247G	probably damaging	Het
Sag	G	T	1: 87,812,993	V46L	probably benign	Het
Sat2	A	T	11: 69,622,315	I17F	probably damaging	Het
Slc39a6	A	T	18: 24,601,036	Y199N	probably benign	Het
Slc9a3r2	C	T	17: 24,642,255	R66H	probably damaging	Het
Snx2	A	G	18: 53,197,925		probably null	Het
Thbs4	T	C	13: 92,763,590	D466G	probably damaging	Het
Tmem208	A	G	8: 105,328,431	D91G	probably damaging	Het
Tmf1	A	G	6: 97,176,809	L101P	probably damaging	Het
Tnni1	A	G	1: 135,805,592	T51A	probably benign	Het
Tor3a	T	G	1: 156,674,193	E38A	probably damaging	Het
Trim31	T	A	17: 36,899,918	D147E	possibly damaging	Het
Uhrf1bp1	G	A	17: 27,887,515	S1005N	probably benign	Het
Vmn1r48	G	T	6: 90,036,147	A232E	probably benign	Het
Vmn1r89	T	G	7: 13,219,357	F7V	probably benign	Het
Zfp160	A	G	17: 21,026,852	T555A	probably benign	Het
Zfp981	C	A	4: 146,537,005	T129K	probably benign	Het
Zfpm2	T	A	15: 40,870,542	F106I	probably benign	Het

Other mutations in Ppp1r36

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01585:Ppp1r36	APN	12	76439117	critical splice acceptor site	probably null
IGL01744:Ppp1r36	APN	12	76439232	missense	possibly damaging	0.83
IGL03295:Ppp1r36	APN	12	76438418	missense	probably damaging	0.97
R0099:Ppp1r36	UTSW	12	76436282	splice site	probably null
R0332:Ppp1r36	UTSW	12	76427903	missense	probably benign	0.32
R0463:Ppp1r36	UTSW	12	76418967	missense	probably damaging	0.98
R0491:Ppp1r36	UTSW	12	76439291	missense	probably benign	0.01
R1664:Ppp1r36	UTSW	12	76436254	missense	possibly damaging	0.84
R2011:Ppp1r36	UTSW	12	76418926	critical splice acceptor site	probably null
R3918:Ppp1r36	UTSW	12	76417657	missense	probably benign	0.00
R5464:Ppp1r36	UTSW	12	76428078	critical splice acceptor site	probably null
R5490:Ppp1r36	UTSW	12	76437986	missense	probably damaging	0.98
R5490:Ppp1r36	UTSW	12	76437987	missense	possibly damaging	0.85
R5523:Ppp1r36	UTSW	12	76438118	missense	possibly damaging	0.71
R5844:Ppp1r36	UTSW	12	76426792	missense	possibly damaging	0.71
R5849:Ppp1r36	UTSW	12	76439157	missense	probably damaging	0.99
R5866:Ppp1r36	UTSW	12	76426805	missense	possibly damaging	0.71
R5996:Ppp1r36	UTSW	12	76439162	missense	possibly damaging	0.71
R6443:Ppp1r36	UTSW	12	76417639	missense	probably benign
R6612:Ppp1r36	UTSW	12	76437604	missense	possibly damaging	0.52
R6756:Ppp1r36	UTSW	12	76427922	missense	probably benign	0.28
R7896:Ppp1r36	UTSW	12	76428149	splice site	probably null
R7938:Ppp1r36	UTSW	12	76438406	missense	probably damaging	0.99
R8377:Ppp1r36	UTSW	12	76438441	missense	possibly damaging	0.86
R8468:Ppp1r36	UTSW	12	76436205	missense	probably damaging	0.98
R8784:Ppp1r36	UTSW	12	76439193	missense	probably benign	0.00
R9567:Ppp1r36	UTSW	12	76439126	missense	probably benign	0.06
R9720:Ppp1r36	UTSW	12	76438524	missense	possibly damaging	0.87
X0025:Ppp1r36	UTSW	12	76426810	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- GGTTGACAGATAAAAGGTTTGCCTC -3'
(R):5'- CTCAGGTAGCTCTCCCAGATTC -3'

Sequencing Primer
(F):5'- AAGGTTTGCCTCAAGGGATG -3'
(R):5'- CAGATTCTAGTCTAGACTTGCGCAG -3'

Posted On

2016-08-04