Mutagenetix > Incidental Mutation

Incidental Mutation 'R1915:Lcp1'

214806

Institutional Source

Beutler Lab

Gene Symbol

Lcp1

Ensembl Gene

ENSMUSG00000021998

Gene Name

lymphocyte cytosolic protein 1

Synonyms

L-fimbrin, L-plastin, D14Ertd310e, Pls2

MMRRC Submission

039933-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R1915 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

75368545-75468282 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 75436737 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 28 (Y28N)

Ref Sequence

ENSEMBL: ENSMUSP00000118721 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000122840] [ENSMUST00000124499] [ENSMUST00000125833] [ENSMUST00000131802] [ENSMUST00000134114] [ENSMUST00000143539] [ENSMUST00000145303]

AlphaFold

Q61233

Predicted Effect

possibly damaging
Transcript: ENSMUST00000122840
AA Change: Y28N

PolyPhen 2 Score 0.792 (Sensitivity: 0.85; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000117984
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	81	7.7e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000124499
AA Change: Y28N

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000121201
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	81	7.7e-3	SMART
CH	122	234	1.15e-24	SMART
CH	266	373	1.51e-19	SMART
CH	396	501	1.87e-24	SMART
CH	517	622	8.55e-19	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000125833
AA Change: Y28N

PolyPhen 2 Score 0.378 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000116033
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	81	7.7e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130510

Predicted Effect

probably benign
Transcript: ENSMUST00000131802
AA Change: Y28N

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000117137
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	81	7.7e-3	SMART
CH	122	234	1.15e-24	SMART
CH	266	373	1.51e-19	SMART
CH	396	501	1.87e-24	SMART
CH	517	622	8.55e-19	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000134114
AA Change: Y28N

PolyPhen 2 Score 0.378 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000121376
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	81	7.7e-3	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000143539
AA Change: Y28N

PolyPhen 2 Score 0.807 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000118721
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	76	4.45e1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000145303
AA Change: Y28N

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000116271
Gene: ENSMUSG00000021998
AA Change: Y28N

Domain	Start	End	E-Value	Type
EFh	13	41	6.91e-5	SMART
EFh	53	81	7.7e-3	SMART
CH	122	234	1.15e-24	SMART
CH	266	373	1.51e-19	SMART
CH	396	501	1.87e-24	SMART
CH	517	622	8.55e-19	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149883

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161819

Meta Mutation Damage Score

0.2707

Coding Region Coverage

1x: 97.5%
3x: 97.0%
10x: 95.6%
20x: 93.4%

Validation Efficiency

100% (85/85)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. Plastin 1 (otherwise known as Fimbrin) is a third distinct plastin isoform which is specifically expressed at high levels in the small intestine. The L isoform is expressed only in hemopoietic cell lineages, while the T isoform has been found in all other normal cells of solid tissues that have replicative potential (fibroblasts, endothelial cells, epithelial cells, melanocytes, etc.). However, L-plastin has been found in many types of malignant human cells of non-hemopoietic origin suggesting that its expression is induced accompanying tumorigenesis in solid tissues. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased susceptibility to S. aureus infection, defective neutrophil killing of S. aureus, and impaired adhesion-dependent respiratory bursts in neutrophils. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca6	T	C	11: 110,103,036 (GRCm39)	R852G	probably benign	Het
Adam2	C	A	14: 66,275,006 (GRCm39)	V576F	possibly damaging	Het
Afmid	T	C	11: 117,726,625 (GRCm39)	F250L	possibly damaging	Het
Apc2	A	T	10: 80,151,701 (GRCm39)	I2252L	probably benign	Het
Bcar1	A	G	8: 112,442,030 (GRCm39)	V270A	probably damaging	Het
Btnl7-ps	T	A	17: 34,760,619 (GRCm39)		noncoding transcript	Het
Cdkn2aip	T	C	8: 48,164,961 (GRCm39)	T251A	probably benign	Het
Cdx1	A	G	18: 61,152,970 (GRCm39)	V212A	probably benign	Het
Cep95	C	T	11: 106,705,464 (GRCm39)	T483I	probably damaging	Het
Cfap100	T	C	6: 90,389,329 (GRCm39)		probably benign	Het
Cfap54	A	G	10: 92,720,564 (GRCm39)	V2630A	unknown	Het
Chia1	T	A	3: 106,035,875 (GRCm39)	N238K	probably benign	Het
Cldn23	T	A	8: 36,293,099 (GRCm39)	I130F	possibly damaging	Het
Cntrl	T	C	2: 35,052,873 (GRCm39)	M1126T	probably benign	Het
Col28a1	A	G	6: 8,176,333 (GRCm39)	F8S	probably benign	Het
Cpeb3	C	T	19: 37,031,665 (GRCm39)	R579Q	probably damaging	Het
Creld2	G	A	15: 88,704,834 (GRCm39)	W103*	probably null	Het
Dbh	A	G	2: 27,058,234 (GRCm39)	D134G	probably damaging	Het
Dcbld1	G	T	10: 52,193,131 (GRCm39)	C292F	probably damaging	Het
Dlgap5	T	C	14: 47,645,230 (GRCm39)	K304E	probably benign	Het
Dnajc2	A	G	5: 21,986,317 (GRCm39)		probably null	Het
Eps8l2	G	A	7: 140,941,765 (GRCm39)	V650M	probably damaging	Het
Erlin1	T	C	19: 44,047,504 (GRCm39)	Y139C	probably damaging	Het
Exoc3	A	G	13: 74,321,413 (GRCm39)		probably null	Het
F5	C	A	1: 164,010,486 (GRCm39)	R406S	probably damaging	Het
Fahd1	A	T	17: 25,068,622 (GRCm39)	W152R	possibly damaging	Het
Farp2	T	A	1: 93,456,424 (GRCm39)	S36T	probably benign	Het
Foxs1	A	G	2: 152,774,760 (GRCm39)	C98R	probably damaging	Het
Gal3st4	T	A	5: 138,263,672 (GRCm39)	K442N	probably benign	Het
Gm10644	G	A	8: 84,660,479 (GRCm39)		probably benign	Het
Gm8674	A	T	13: 50,054,889 (GRCm39)		noncoding transcript	Het
Gpr88	G	T	3: 116,046,073 (GRCm39)	S79R	possibly damaging	Het
Heatr9	T	G	11: 83,409,035 (GRCm39)	I171L	possibly damaging	Het
Hectd4	A	G	5: 121,460,357 (GRCm39)	T2209A	probably benign	Het
Hsh2d	A	G	8: 72,947,365 (GRCm39)	T21A	probably damaging	Het
Irf4	A	T	13: 30,945,445 (GRCm39)	Q397L	probably benign	Het
Itgae	T	A	11: 73,009,469 (GRCm39)		probably benign	Het
Jrkl	A	T	9: 13,245,609 (GRCm39)	D17E	possibly damaging	Het
Kcna4	T	C	2: 107,127,123 (GRCm39)	V619A	probably benign	Het
Kcnh6	T	A	11: 105,908,270 (GRCm39)	Y295*	probably null	Het
Kif1b	G	A	4: 149,351,673 (GRCm39)	T263I	probably damaging	Het
Large2	G	T	2: 92,196,170 (GRCm39)		probably benign	Het
Man1c1	G	C	4: 134,430,749 (GRCm39)	P11R	probably damaging	Het
Mccc2	T	C	13: 100,085,038 (GRCm39)		probably null	Het
Mlh3	T	C	12: 85,308,442 (GRCm39)	Y1115C	probably benign	Het
Mlst8	C	T	17: 24,696,264 (GRCm39)	W155*	probably null	Het
Myh10	T	C	11: 68,681,034 (GRCm39)	L1025P	probably damaging	Het
Myof	T	A	19: 37,966,141 (GRCm39)	N393I	probably damaging	Het
Nalcn	C	T	14: 123,540,181 (GRCm39)	V1140I	probably benign	Het
Ncald	C	T	15: 37,397,324 (GRCm39)	A119T	probably benign	Het
Nipbl	T	C	15: 8,373,114 (GRCm39)	E1044G	possibly damaging	Het
Nup58	T	C	14: 60,475,980 (GRCm39)	K279R	probably benign	Het
Oas1a	A	T	5: 121,043,876 (GRCm39)	N85K	possibly damaging	Het
Or11g1	C	T	14: 50,651,798 (GRCm39)	P266S	probably damaging	Het
Or8b12i	T	C	9: 20,082,324 (GRCm39)	Y181C	probably benign	Het
Or8k30	A	G	2: 86,339,343 (GRCm39)	D180G	probably damaging	Het
Pou2f2	C	T	7: 24,799,581 (GRCm39)	A92T	possibly damaging	Het
Ppp1r16a	T	C	15: 76,577,268 (GRCm39)	L212P	probably damaging	Het
Pram1	A	T	17: 33,860,131 (GRCm39)	I233F	probably benign	Het
Ptbp3	A	T	4: 59,517,635 (GRCm39)	L84Q	probably damaging	Het
Ptgr2	A	T	12: 84,349,096 (GRCm39)	Q145L	probably benign	Het
Ptpn23	A	T	9: 110,215,575 (GRCm39)	D1396E	probably damaging	Het
Pudp	T	C	18: 50,701,278 (GRCm39)	N152D	probably benign	Het
Rbm20	T	A	19: 53,852,518 (GRCm39)	L1166Q	probably damaging	Het
Rictor	T	G	15: 6,789,053 (GRCm39)	I223R	probably damaging	Het
Ripor1	A	T	8: 106,343,518 (GRCm39)	E270D	probably damaging	Het
Rorc	T	C	3: 94,298,480 (GRCm39)	C322R	probably damaging	Het
Rpgrip1l	T	C	8: 91,959,552 (GRCm39)	D1116G	probably benign	Het
Rsf1	GCG	GCGACGGCGACG	7: 97,229,114 (GRCm39)		probably benign	Het
Sptan1	C	G	2: 29,901,048 (GRCm39)	Q1425E	probably benign	Het
Srd5a3	G	A	5: 76,295,552 (GRCm39)	V81I	probably benign	Het
Stk36	T	A	1: 74,673,346 (GRCm39)	S1080T	probably benign	Het
Sugp2	T	A	8: 70,706,310 (GRCm39)	I790K	probably damaging	Het
Syde2	T	G	3: 145,720,071 (GRCm39)	Y764*	probably null	Het
Tmem130	A	G	5: 144,674,666 (GRCm39)	F353S	probably damaging	Het
Tmem131	T	A	1: 36,835,347 (GRCm39)	K1591N	probably damaging	Het
Urb2	C	A	8: 124,756,537 (GRCm39)	T748K	possibly damaging	Het
Uri1	A	T	7: 37,661,103 (GRCm39)	I480K	probably damaging	Het
Zcchc3	A	C	2: 152,255,601 (GRCm39)	V366G	probably benign	Het
Zfp292	G	A	4: 34,805,100 (GRCm39)	S2648F	possibly damaging	Het
Zfp54	T	C	17: 21,654,414 (GRCm39)	Y303H	probably benign	Het
Zfp729b	A	G	13: 67,741,339 (GRCm39)	F319L	probably damaging	Het
Zfp934	G	A	13: 62,665,769 (GRCm39)	H291Y	probably damaging	Het

Other mutations in Lcp1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01103:Lcp1	APN	14	75,464,533 (GRCm39)	critical splice donor site	probably null
IGL01768:Lcp1	APN	14	75,461,573 (GRCm39)	missense	probably benign	0.40
IGL01801:Lcp1	APN	14	75,436,815 (GRCm39)	missense	probably benign	0.10
IGL01940:Lcp1	APN	14	75,453,805 (GRCm39)	missense	probably benign	0.17
IGL02135:Lcp1	APN	14	75,437,926 (GRCm39)	missense	probably benign	0.00
IGL02185:Lcp1	APN	14	75,466,740 (GRCm39)	missense	possibly damaging	0.73
IGL02478:Lcp1	APN	14	75,461,536 (GRCm39)	missense	probably benign	0.04
IGL02604:Lcp1	APN	14	75,461,566 (GRCm39)	missense	probably benign	0.11
R0244:Lcp1	UTSW	14	75,464,441 (GRCm39)	missense	possibly damaging	0.92
R0295:Lcp1	UTSW	14	75,436,860 (GRCm39)	missense	probably null	0.59
R0313:Lcp1	UTSW	14	75,436,873 (GRCm39)	missense	probably damaging	1.00
R0415:Lcp1	UTSW	14	75,464,446 (GRCm39)	missense	possibly damaging	0.88
R0751:Lcp1	UTSW	14	75,436,827 (GRCm39)	missense	probably benign	0.00
R0811:Lcp1	UTSW	14	75,451,928 (GRCm39)	missense	probably benign	0.00
R0812:Lcp1	UTSW	14	75,451,928 (GRCm39)	missense	probably benign	0.00
R1200:Lcp1	UTSW	14	75,466,742 (GRCm39)	missense	possibly damaging	0.73
R1713:Lcp1	UTSW	14	75,436,884 (GRCm39)	critical splice donor site	probably null
R1969:Lcp1	UTSW	14	75,437,946 (GRCm39)	missense	probably damaging	1.00
R1970:Lcp1	UTSW	14	75,437,946 (GRCm39)	missense	probably damaging	1.00
R1971:Lcp1	UTSW	14	75,437,946 (GRCm39)	missense	probably damaging	1.00
R2045:Lcp1	UTSW	14	75,437,841 (GRCm39)	missense	probably benign	0.01
R2064:Lcp1	UTSW	14	75,435,515 (GRCm39)	critical splice acceptor site	probably null
R3949:Lcp1	UTSW	14	75,443,569 (GRCm39)	missense	possibly damaging	0.68
R4062:Lcp1	UTSW	14	75,452,620 (GRCm39)	missense	probably damaging	1.00
R4521:Lcp1	UTSW	14	75,452,608 (GRCm39)	missense	possibly damaging	0.94
R4811:Lcp1	UTSW	14	75,437,848 (GRCm39)	missense	probably damaging	0.99
R4854:Lcp1	UTSW	14	75,437,929 (GRCm39)	missense	probably damaging	1.00
R4974:Lcp1	UTSW	14	75,445,911 (GRCm39)	nonsense	probably null
R5539:Lcp1	UTSW	14	75,466,738 (GRCm39)	missense	probably benign	0.08
R5561:Lcp1	UTSW	14	75,449,948 (GRCm39)	missense	probably benign	0.01
R5724:Lcp1	UTSW	14	75,464,422 (GRCm39)	missense	probably benign	0.18
R5989:Lcp1	UTSW	14	75,436,827 (GRCm39)	missense	probably benign	0.00
R6731:Lcp1	UTSW	14	75,443,629 (GRCm39)	missense	probably damaging	1.00
R7346:Lcp1	UTSW	14	75,447,946 (GRCm39)	missense	possibly damaging	0.49
R7670:Lcp1	UTSW	14	75,437,871 (GRCm39)	missense	probably benign	0.12
R7698:Lcp1	UTSW	14	75,443,651 (GRCm39)	nonsense	probably null
R9780:Lcp1	UTSW	14	75,440,178 (GRCm39)	missense	probably damaging	1.00
S24628:Lcp1	UTSW	14	75,464,446 (GRCm39)	missense	possibly damaging	0.88
X0027:Lcp1	UTSW	14	75,464,526 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCCAAGAGCAATAGGCCTCC -3'
(R):5'- ATCGCCTCTCTGGATGTTTG -3'

Sequencing Primer
(F):5'- CCTCCTGGCAGGTTTCTG -3'
(R):5'- CAAGTTTCAAGTGCATGGCC -3'

Posted On

2014-07-14