Mutagenetix > Incidental Mutation

Incidental Mutation 'R8508:Pnliprp2'

655735

Institutional Source

Beutler Lab

Gene Symbol

Pnliprp2

Ensembl Gene

ENSMUSG00000025091

Gene Name

pancreatic lipase-related protein 2

Synonyms

PLRP2

MMRRC Submission

067844-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.106) question?

Stock #

R8508 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

58759723-58777533 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 58763374 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 184 (S184R)

Ref Sequence

ENSEMBL: ENSMUSP00000026081 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000026081]

AlphaFold

P17892

Predicted Effect

probably damaging
Transcript: ENSMUST00000026081
AA Change: S184R

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

SMART Domains

Protein: ENSMUSP00000026081
Gene: ENSMUSG00000025091
AA Change: S184R

Domain	Start	End	E-Value	Type
signal peptide	1	30	N/A	INTRINSIC
Pfam:Lipase	31	367	4.1e-166	PFAM
LH2	370	482	7.49e-27	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a lipase that hydrolyzes galactolipids, the main components of plant membrane lipids. An allelic polymorphism in this gene results in both coding and non-coding variants; the reference genome represents the non-coding allele. [provided by RefSeq, Aug 2015]
PHENOTYPE: Mice homozygous for disruptions in this gene display deficient lipid absorbtion before weaning which results in growth retardation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438H23Rik	T	G	16: 91,055,612 (GRCm38)	Y212S	probably damaging	Het
Angpt1	T	C	15: 42,512,399 (GRCm38)	N154D	probably damaging	Het
Angpt2	G	A	8: 18,741,119 (GRCm38)	R54*	probably null	Het
Ankrd27	T	A	7: 35,601,626 (GRCm38)	L117*	probably null	Het
Arhgap21	C	T	2: 20,854,180 (GRCm38)	M1234I	probably benign	Het
Arhgef33	A	G	17: 80,367,335 (GRCm38)	E387G	probably damaging	Het
Atp13a4	T	A	16: 29,454,769 (GRCm38)	K444*	probably null	Het
Atp6v1a	G	A	16: 44,101,862 (GRCm38)	R338C	probably damaging	Het
Canx	T	C	11: 50,311,647 (GRCm38)	D44G	possibly damaging	Het
Ccdc141	T	A	2: 77,132,244 (GRCm38)	M119L	probably benign	Het
Ckmt1	A	C	2: 121,362,691 (GRCm38)	Q299P	possibly damaging	Het
Dhx16	T	C	17: 35,885,920 (GRCm38)	S601P	probably damaging	Het
Dna2	A	C	10: 62,950,894 (GRCm38)	R140S	probably damaging	Het
Dock1	A	G	7: 134,782,409 (GRCm38)	T670A	probably benign	Het
Eif1ad10	T	G	12: 88,249,685 (GRCm38)	E139A	unknown	Het
Eogt	A	G	6: 97,143,998 (GRCm38)	S85P	possibly damaging	Het
Fbf1	A	T	11: 116,165,881 (GRCm38)	M1K	probably null	Het
Fbxl12	C	A	9: 20,638,864 (GRCm38)	R165L	possibly damaging	Het
Flnb	G	A	14: 7,950,394 (GRCm38)	V2571I	probably damaging	Het
Gm43518	A	G	5: 123,938,259 (GRCm38)	E123G	unknown	Het
Gpatch2	A	G	1: 187,304,355 (GRCm38)	N374S	probably benign	Het
Hey1	G	C	3: 8,664,776 (GRCm38)	A207G	probably benign	Het
Hoxa11	T	C	6: 52,245,802 (GRCm38)		probably benign	Het
Hydin	G	A	8: 110,582,018 (GRCm38)	V3979I	probably benign	Het
Ighe	C	T	12: 113,271,793 (GRCm38)	W277*	probably null	Het
Kmt2c	G	T	5: 25,314,122 (GRCm38)	T2330K	probably benign	Het
Krt6a	T	A	15: 101,692,735 (GRCm38)	K261M	probably damaging	Het
Lats2	A	C	14: 57,722,705 (GRCm38)	S161A	probably benign	Het
Med13l	T	A	5: 118,754,321 (GRCm38)	D1936E	probably benign	Het
Mipol1	T	C	12: 57,306,088 (GRCm38)	V71A	possibly damaging	Het
Mphosph8	A	T	14: 56,676,546 (GRCm38)	K415*	probably null	Het
Npepps	A	G	11: 97,244,426 (GRCm38)		probably null	Het
Ntn4	A	T	10: 93,741,104 (GRCm38)	N545Y	possibly damaging	Het
Or11g1	A	C	14: 50,413,675 (GRCm38)	M44L	probably benign	Het
Or1n1b	A	G	2: 36,890,354 (GRCm38)	S165P	probably damaging	Het
Or2m12	T	C	16: 19,286,701 (GRCm38)	D14G	probably benign	Het
Or9i2	A	T	19: 13,838,402 (GRCm38)	M257K	possibly damaging	Het
Osbpl2	T	A	2: 180,155,343 (GRCm38)	V358E	possibly damaging	Het
Pdcd11	C	A	19: 47,119,806 (GRCm38)	P1204Q	probably damaging	Het
Ppm1g	G	T	5: 31,204,528 (GRCm38)	R373S	probably damaging	Het
Rnf130	A	G	11: 50,087,437 (GRCm38)	D275G	probably damaging	Het
Rps18-ps5	A	G	13: 28,257,711 (GRCm38)	I26V	probably benign	Het
Setd5	T	C	6: 113,121,087 (GRCm38)	S696P	probably damaging	Het
Sgip1	A	G	4: 102,915,071 (GRCm38)	Q219R	probably benign	Het
Slc1a2	T	C	2: 102,736,085 (GRCm38)		probably null	Het
Slc22a12	T	C	19: 6,542,437 (GRCm38)	T106A	probably benign	Het
Slc22a14	A	G	9: 119,180,585 (GRCm38)	L148P	probably damaging	Het
Slc2a9	A	T	5: 38,382,078 (GRCm38)	F375I	probably damaging	Het
Sorbs3	A	T	14: 70,202,947 (GRCm38)	D117E	probably benign	Het
Spata31d1e	A	G	13: 59,743,598 (GRCm38)	L136P	probably benign	Het
Sphkap	G	A	1: 83,276,500 (GRCm38)	T1176I	probably damaging	Het
Supt16	A	T	14: 52,181,589 (GRCm38)	V193D	probably damaging	Het
Sytl3	A	G	17: 6,728,291 (GRCm38)	T362A	probably damaging	Het
Tctn1	T	A	5: 122,246,611 (GRCm38)	Q410L	probably benign	Het
Trbc2	T	C	6: 41,547,777 (GRCm38)	Y133H		Het
Ttc28	G	A	5: 111,233,341 (GRCm38)	D1240N	probably benign	Het
Vmn2r120	A	G	17: 57,525,843 (GRCm38)	V112A	probably benign	Het
Zfp354b	A	T	11: 50,923,470 (GRCm38)	S209R	probably benign	Het
Zfp362	T	C	4: 128,774,606 (GRCm38)	H391R	probably damaging	Het

Other mutations in Pnliprp2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00786:Pnliprp2	APN	19	58,760,497 (GRCm38)	missense	probably benign
IGL02739:Pnliprp2	APN	19	58,760,509 (GRCm38)	critical splice donor site	probably null
IGL02881:Pnliprp2	APN	19	58,771,446 (GRCm38)	missense	probably benign	0.01
IGL03411:Pnliprp2	APN	19	58,760,415 (GRCm38)	missense	probably benign
R0140:Pnliprp2	UTSW	19	58,766,363 (GRCm38)	missense	probably benign	0.00
R0558:Pnliprp2	UTSW	19	58,774,087 (GRCm38)	missense	probably benign	0.00
R1873:Pnliprp2	UTSW	19	58,763,389 (GRCm38)	missense	probably benign	0.00
R1874:Pnliprp2	UTSW	19	58,763,389 (GRCm38)	missense	probably benign	0.00
R1875:Pnliprp2	UTSW	19	58,763,389 (GRCm38)	missense	probably benign	0.00
R2382:Pnliprp2	UTSW	19	58,768,630 (GRCm38)	missense	probably benign	0.00
R3893:Pnliprp2	UTSW	19	58,766,273 (GRCm38)	missense	probably benign	0.19
R3915:Pnliprp2	UTSW	19	58,760,362 (GRCm38)	missense	probably damaging	1.00
R4620:Pnliprp2	UTSW	19	58,762,286 (GRCm38)	missense	possibly damaging	0.67
R4893:Pnliprp2	UTSW	19	58,771,421 (GRCm38)	missense	probably benign	0.08
R4957:Pnliprp2	UTSW	19	58,775,145 (GRCm38)	missense	possibly damaging	0.72
R4959:Pnliprp2	UTSW	19	58,766,318 (GRCm38)	missense	probably benign	0.16
R4973:Pnliprp2	UTSW	19	58,766,318 (GRCm38)	missense	probably benign	0.16
R5346:Pnliprp2	UTSW	19	58,759,800 (GRCm38)	missense	probably benign
R6049:Pnliprp2	UTSW	19	58,760,452 (GRCm38)	missense	possibly damaging	0.77
R6228:Pnliprp2	UTSW	19	58,763,442 (GRCm38)	critical splice donor site	probably null
R6394:Pnliprp2	UTSW	19	58,761,598 (GRCm38)	missense	probably benign
R6829:Pnliprp2	UTSW	19	58,759,873 (GRCm38)	missense	probably benign
R7235:Pnliprp2	UTSW	19	58,775,227 (GRCm38)	missense	probably benign	0.03
R7534:Pnliprp2	UTSW	19	58,775,142 (GRCm38)	missense	probably benign
R7834:Pnliprp2	UTSW	19	58,774,159 (GRCm38)	missense	probably benign	0.25
R8015:Pnliprp2	UTSW	19	58,766,282 (GRCm38)	missense	probably damaging	0.99
R9000:Pnliprp2	UTSW	19	58,774,123 (GRCm38)	missense	probably benign	0.00
R9560:Pnliprp2	UTSW	19	58,774,091 (GRCm38)	missense	possibly damaging	0.94
X0058:Pnliprp2	UTSW	19	58,774,142 (GRCm38)	missense	possibly damaging	0.59
Z1088:Pnliprp2	UTSW	19	58,762,325 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGAATCTTTTCCCCTGGAGTC -3'
(R):5'- TGACTATGGATTTTCTAGCAGGC -3'

Sequencing Primer
(F):5'- GGAGTCTCCAGCTCCATCC -3'
(R):5'- TCAGGACATCACCTAATATAAGGAG -3'

Posted On

2020-10-20