Mutagenetix > Incidental Mutation

Incidental Mutation 'R5224:Plpp1'

402517

Institutional Source

Beutler Lab

Gene Symbol

Plpp1

Ensembl Gene

ENSMUSG00000021759

Gene Name

phospholipid phosphatase 1

Synonyms

Hpic53, LPP-1, mPAP, Ppap2a, LPP1, Lipid phosphate phosphatase 1

MMRRC Submission

042797-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5224 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

112937326-113004428 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 112988046 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 56 (Y56*)

Ref Sequence

ENSEMBL: ENSMUSP00000064423 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000016144] [ENSMUST00000070951]

AlphaFold

Q61469

Predicted Effect

probably benign
Transcript: ENSMUST00000016144

SMART Domains

Protein: ENSMUSP00000016144
Gene: ENSMUSG00000021759

Domain	Start	End	E-Value	Type
Blast:acidPPc	5	61	1e-14	BLAST
acidPPc	103	244	4.28e-45	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000070951
AA Change: Y56*

SMART Domains

Protein: ENSMUSP00000064423
Gene: ENSMUSG00000021759
AA Change: Y56*

Domain	Start	End	E-Value	Type
Blast:acidPPc	5	72	5e-38	BLAST
acidPPc	102	243	4.28e-45	SMART

Meta Mutation Damage Score

0.9344

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 95.2%

Validation Efficiency

98% (58/59)

MGI Phenotype

PHENOTYPE: Mice homozygous for a hypomorphic allele are viable and fertile with elevated plasma levels of lysophosphatidic acid. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abtb3	CGTGACCTTTCTGGT	CGT	10: 85,481,386 (GRCm39)		probably benign	Het
Ahi1	A	G	10: 20,862,921 (GRCm39)	S699G	probably damaging	Het
Atp10d	C	T	5: 72,426,669 (GRCm39)	A959V	probably benign	Het
Axl	T	C	7: 25,486,369 (GRCm39)	M112V	probably benign	Het
Brd10	A	T	19: 29,696,450 (GRCm39)	S1014R	possibly damaging	Het
Camk1g	A	T	1: 193,037,342 (GRCm39)	D119E	probably damaging	Het
Capn8	A	C	1: 182,424,554 (GRCm39)	N117T	probably damaging	Het
Cct3	G	A	3: 88,204,532 (GRCm39)		probably benign	Het
Csmd3	T	C	15: 47,752,080 (GRCm39)	T1293A	possibly damaging	Het
Depdc1b	A	G	13: 108,521,354 (GRCm39)	D387G	probably damaging	Het
Dtx3l	A	G	16: 35,759,163 (GRCm39)	Y29H	possibly damaging	Het
Erp44	A	T	4: 48,279,435 (GRCm39)	N2K	probably benign	Het
Fmn1	A	G	2: 113,195,470 (GRCm39)	E390G	unknown	Het
Ganab	T	A	19: 8,887,955 (GRCm39)	D396E	probably benign	Het
Gatd3a	A	G	10: 77,999,367 (GRCm39)	V148A	probably damaging	Het
Gcc2	T	A	10: 58,121,982 (GRCm39)	S1140T	probably damaging	Het
Gm7008	T	C	12: 40,273,342 (GRCm39)		probably benign	Het
Gphn	T	A	12: 78,637,361 (GRCm39)	F354I	probably damaging	Het
H2-T7	G	A	17: 36,454,231 (GRCm39)		noncoding transcript	Het
Hnrnpul1	G	A	7: 25,444,600 (GRCm39)	T236M	probably damaging	Het
Itpr2	T	A	6: 146,068,149 (GRCm39)	M2410L	probably benign	Het
Jaml	T	A	9: 45,015,564 (GRCm39)	M356K	probably damaging	Het
Kbtbd12	T	A	6: 88,594,681 (GRCm39)		probably benign	Het
Ldlrad3	G	T	2: 101,943,954 (GRCm39)	N39K	probably damaging	Het
Lrp1b	G	A	2: 41,000,852 (GRCm39)	T2238I	possibly damaging	Het
Lypd8	T	A	11: 58,277,634 (GRCm39)	C139S	possibly damaging	Het
Masp1	G	T	16: 23,313,445 (GRCm39)	H163Q	probably damaging	Het
Mpo	T	C	11: 87,687,283 (GRCm39)		probably benign	Het
Muc19	A	T	15: 91,825,910 (GRCm39)		noncoding transcript	Het
Muc5ac	T	A	7: 141,347,708 (GRCm39)	S438T	probably benign	Het
Nav2	T	C	7: 49,201,473 (GRCm39)	V160A	probably benign	Het
Nlrc5	G	T	8: 95,220,944 (GRCm39)	A1128S	probably benign	Het
Nlrp5	T	A	7: 23,117,401 (GRCm39)	L375Q	probably damaging	Het
Nlrp9a	A	G	7: 26,256,717 (GRCm39)	T112A	probably benign	Het
Nppa	T	C	4: 148,085,773 (GRCm39)	S127P	probably damaging	Het
Or8k24	A	G	2: 86,216,193 (GRCm39)	S190P	possibly damaging	Het
Osbpl1a	T	C	18: 13,066,753 (GRCm39)	N2S	probably benign	Het
Otoa	A	G	7: 120,739,016 (GRCm39)	T742A	probably damaging	Het
Pcdh10	A	G	3: 45,347,249 (GRCm39)	R1015G	probably damaging	Het
Pdzrn3	C	T	6: 101,130,272 (GRCm39)	D515N	probably damaging	Het
Ppp1r12a	A	G	10: 108,096,886 (GRCm39)	T236A	probably benign	Het
Rhag	T	C	17: 41,139,395 (GRCm39)	L110P	probably damaging	Het
Scn11a	T	A	9: 119,583,858 (GRCm39)	N1586Y	probably damaging	Het
Sgms2	T	A	3: 131,135,766 (GRCm39)	K36I	probably damaging	Het
Slc22a2	A	G	17: 12,805,719 (GRCm39)	N157D	probably damaging	Het
Stx19	T	G	16: 62,642,937 (GRCm39)	M251R	probably benign	Het
Suco	A	G	1: 161,662,274 (GRCm39)	I719T	probably benign	Het
Tnr	A	G	1: 159,750,885 (GRCm39)	D1282G	probably damaging	Het
Tram1	T	C	1: 13,648,349 (GRCm39)	R154G	probably benign	Het
Ubtfl1	G	T	9: 18,321,326 (GRCm39)	V285L	probably benign	Het
Ugt2b38	A	G	5: 87,571,601 (GRCm39)	S144P	probably benign	Het
Washc2	T	G	6: 116,185,965 (GRCm39)	*58G	probably null	Het
Zfp354a	T	A	11: 50,960,876 (GRCm39)	S362R	probably damaging	Het

Other mutations in Plpp1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00780:Plpp1	APN	13	112,988,040 (GRCm39)	missense	probably damaging	1.00
IGL02139:Plpp1	APN	13	112,993,433 (GRCm39)	missense	probably benign	0.09
IGL02269:Plpp1	APN	13	112,993,526 (GRCm39)	missense	probably damaging	1.00
PIT4260001:Plpp1	UTSW	13	112,993,419 (GRCm39)	missense	probably damaging	1.00
R0550:Plpp1	UTSW	13	112,971,519 (GRCm39)	missense	probably benign	0.02
R1301:Plpp1	UTSW	13	112,971,477 (GRCm39)	missense	probably damaging	1.00
R1473:Plpp1	UTSW	13	112,996,198 (GRCm39)	missense	probably damaging	1.00
R5306:Plpp1	UTSW	13	112,988,089 (GRCm39)	critical splice donor site	probably null
R6108:Plpp1	UTSW	13	113,003,399 (GRCm39)	missense	possibly damaging	0.93
R6111:Plpp1	UTSW	13	113,003,451 (GRCm39)	missense	probably damaging	1.00
R6500:Plpp1	UTSW	13	113,003,454 (GRCm39)	missense	probably damaging	1.00
R7520:Plpp1	UTSW	13	112,937,781 (GRCm39)	missense	possibly damaging	0.89
R7716:Plpp1	UTSW	13	112,996,186 (GRCm39)	missense	probably damaging	1.00
R7716:Plpp1	UTSW	13	112,993,323 (GRCm39)	missense	probably benign	0.27
R8080:Plpp1	UTSW	13	113,004,002 (GRCm39)	missense	probably benign	0.19
R8209:Plpp1	UTSW	13	113,003,465 (GRCm39)	missense	probably benign	0.44
R8226:Plpp1	UTSW	13	113,003,465 (GRCm39)	missense	probably benign	0.44
R8514:Plpp1	UTSW	13	112,971,462 (GRCm39)	missense	probably damaging	1.00
R8924:Plpp1	UTSW	13	112,943,057 (GRCm39)	intron	probably benign
R8948:Plpp1	UTSW	13	112,993,511 (GRCm39)	missense	probably damaging	0.98
R9130:Plpp1	UTSW	13	112,988,038 (GRCm39)	missense

Predicted Primers

PCR Primer
(F):5'- GACGTTCAAAGCAATCGCATC -3'
(R):5'- GCCTTTCAGAATCTCAGGCTC -3'

Sequencing Primer
(F):5'- AATCGCATCTCTAAAGTCTTTTCGGG -3'
(R):5'- GAATCTCAGGCTCTATGAAATACAC -3'

Posted On

2016-07-22