Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02477:Plce1'

295019

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Plce1

Ensembl Gene

ENSMUSG00000024998

Gene Name

phospholipase C, epsilon 1

Synonyms

4933403A21Rik, PLCepsilon

Accession Numbers

Is this an essential gene?

Possibly essential (E-score: 0.634) question?

Stock #

IGL02477

Quality Score

Status

Chromosome

Chromosomal Location

38481109-38785030 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

C to T at 38719553 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138360 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000169713] [ENSMUST00000182267] [ENSMUST00000182481]

AlphaFold

Q8K4S1

Predicted Effect

probably benign
Transcript: ENSMUST00000169713

SMART Domains

Protein: ENSMUSP00000130604
Gene: ENSMUSG00000024998

Domain	Start	End	E-Value	Type
low complexity region	471	489	N/A	INTRINSIC
RasGEF	525	828	8.06e-9	SMART
low complexity region	1162	1172	N/A	INTRINSIC
Pfam:EF-hand_like	1305	1369	7.6e-11	PFAM
PLCXc	1373	1521	1.05e-81	SMART
low complexity region	1561	1575	N/A	INTRINSIC
SCOP:d1qasa3	1634	1662	1e-3	SMART
low complexity region	1666	1680	N/A	INTRINSIC
PLCYc	1710	1826	4.28e-46	SMART
C2	1850	1948	3.7e-10	SMART
PDB:2BYE\|A	1986	2094	6e-47	PDB
RA	2115	2218	1.12e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182267

SMART Domains

Protein: ENSMUSP00000138330
Gene: ENSMUSG00000024998

Domain	Start	End	E-Value	Type
low complexity region	471	489	N/A	INTRINSIC
RasGEF	525	828	8.06e-9	SMART
low complexity region	1162	1172	N/A	INTRINSIC
Pfam:EF-hand_like	1305	1369	5.9e-11	PFAM
PLCXc	1373	1521	1.05e-81	SMART
low complexity region	1552	1581	N/A	INTRINSIC
SCOP:d1qasa3	1648	1676	1e-3	SMART
low complexity region	1680	1694	N/A	INTRINSIC
PLCYc	1724	1840	4.28e-46	SMART
C2	1864	1962	3.7e-10	SMART
PDB:2BYE\|A	2000	2108	6e-47	PDB
RA	2129	2232	1.12e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000182481

SMART Domains

Protein: ENSMUSP00000138360
Gene: ENSMUSG00000024998

Domain	Start	End	E-Value	Type
low complexity region	471	489	N/A	INTRINSIC
RasGEF	525	828	8.06e-9	SMART
low complexity region	1162	1172	N/A	INTRINSIC
Pfam:EF-hand_like	1305	1369	8e-11	PFAM
PLCXc	1373	1521	1.05e-81	SMART
low complexity region	1561	1575	N/A	INTRINSIC
SCOP:d1qasa3	1634	1662	1e-3	SMART
low complexity region	1666	1680	N/A	INTRINSIC
PLCYc	1710	1826	4.28e-46	SMART
C2	1850	1948	3.7e-10	SMART
PDB:2BYE\|A	1986	2094	6e-47	PDB
RA	2115	2218	1.12e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000182589

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome; characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]
PHENOTYPE: Homozygous mutation of this gene results in a congenital semilunar valvulogenesis defect which causes regurgitation and stenosis, and decreased incidence of induced skin tumors. Another mutant exhibits decreased cardiac contraction and increased hypertrophy in response to chronic stress. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921539E11Rik	T	A	4: 103,270,746	I61F	probably benign	Het
Abr	T	C	11: 76,461,360	K280E	probably damaging	Het
Acaca	T	C	11: 84,307,168		probably benign	Het
Cep131	C	T	11: 120,070,580	V582I	probably damaging	Het
Colec12	A	G	18: 9,859,858	N613D	unknown	Het
Cyp4f39	A	G	17: 32,489,645	T389A	probably benign	Het
D630003M21Rik	T	C	2: 158,217,488	N164S	probably benign	Het
Eef1akmt2	A	T	7: 132,850,589		probably null	Het
Elp3	T	C	14: 65,563,311	T283A	probably benign	Het
Fads3	C	A	19: 10,056,442	P397Q	probably damaging	Het
Fam171a1	T	C	2: 3,202,575	V198A	possibly damaging	Het
Fam171a2	T	C	11: 102,440,028	I208M	probably benign	Het
Fbxw17	G	A	13: 50,423,817	V119M	possibly damaging	Het
Gtf2ird1	G	A	5: 134,379,978	T140M	probably damaging	Het
Hspa14	C	T	2: 3,496,624	S277N	probably damaging	Het
Hspg2	C	T	4: 137,544,512		probably benign	Het
Ing2	G	T	8: 47,669,268	R82S	possibly damaging	Het
Kat6a	A	G	8: 22,929,300	Y693C	probably damaging	Het
Kcna7	A	G	7: 45,409,623	M445V	probably benign	Het
Lifr	T	G	15: 7,186,923	I793S	probably damaging	Het
Lrrd1	T	A	5: 3,865,770	M789K	probably benign	Het
Myom3	T	A	4: 135,779,368	L484Q	probably benign	Het
Nav2	T	A	7: 49,582,875	M1860K	probably damaging	Het
Nipbl	C	T	15: 8,323,647		probably null	Het
Nsun7	T	A	5: 66,276,649	I214K	probably damaging	Het
Olfr181	T	C	16: 58,925,763	I269M	probably benign	Het
Olfr898	C	T	9: 38,349,125	S8L	probably benign	Het
Osm	T	A	11: 4,239,604	N129K	probably damaging	Het
Plch1	A	G	3: 63,753,293	F302L	probably damaging	Het
Pld2	T	C	11: 70,540,925	V27A	possibly damaging	Het
Prex2	A	G	1: 11,204,154	D1350G	probably benign	Het
Psme4	T	A	11: 30,842,083	V1190D	probably damaging	Het
Sema3g	G	T	14: 31,227,866	R668L	probably damaging	Het
Sprr2f	T	A	3: 92,365,897	M1K	probably null	Het
Sult6b2	G	A	6: 142,801,721	P101S	probably damaging	Het
Trem3	G	A	17: 48,249,836	V112I	probably benign	Het
Ttll9	T	A	2: 153,000,197	F324I	possibly damaging	Het
Ttn	T	A	2: 76,726,760	D29967V	probably damaging	Het
Ubr4	A	G	4: 139,436,205	K2639E	probably damaging	Het
Vwce	T	C	19: 10,664,618		probably null	Het
Zbtb14	T	A	17: 69,387,695	D129E	probably benign	Het
Zmym6	C	T	4: 127,078,502	Q16*	probably null	Het

Other mutations in Plce1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Plce1	APN	19	38745788	missense	probably damaging	0.99
IGL00336:Plce1	APN	19	38651906	missense	probably damaging	1.00
IGL00430:Plce1	APN	19	38725017	missense	probably damaging	1.00
IGL00466:Plce1	APN	19	38721029	missense	probably damaging	0.99
IGL00477:Plce1	APN	19	38525132	missense	probably benign	0.39
IGL00839:Plce1	APN	19	38698562	missense	probably damaging	1.00
IGL01292:Plce1	APN	19	38651785	splice site	probably benign
IGL01665:Plce1	APN	19	38524887	missense	probably benign	0.01
IGL01826:Plce1	APN	19	38739238	splice site	probably benign
IGL01833:Plce1	APN	19	38720981	missense	probably damaging	1.00
IGL02201:Plce1	APN	19	38769446	splice site	probably benign
IGL02276:Plce1	APN	19	38524757	missense	probably benign	0.05
IGL02746:Plce1	APN	19	38698472	missense	probably damaging	1.00
Angel_food	UTSW	19	38727013	splice site	probably benign
Heavenly	UTSW	19	38777989	missense	probably damaging	1.00
R0058:Plce1	UTSW	19	38525184	missense	possibly damaging	0.90
R0058:Plce1	UTSW	19	38525184	missense	possibly damaging	0.90
R0064:Plce1	UTSW	19	38780784	critical splice donor site	probably null
R0116:Plce1	UTSW	19	38721821	missense	probably benign
R0138:Plce1	UTSW	19	38524419	missense	possibly damaging	0.49
R0240:Plce1	UTSW	19	38728886	missense	probably damaging	0.99
R0240:Plce1	UTSW	19	38728886	missense	probably damaging	0.99
R0504:Plce1	UTSW	19	38778021	splice site	probably benign
R0506:Plce1	UTSW	19	38760138	missense	probably benign	0.04
R0578:Plce1	UTSW	19	38777939	missense	probably damaging	1.00
R0645:Plce1	UTSW	19	38777989	missense	probably damaging	1.00
R0730:Plce1	UTSW	19	38716691	missense	probably damaging	0.98
R0920:Plce1	UTSW	19	38736521	missense	probably damaging	1.00
R1223:Plce1	UTSW	19	38702013	missense	probably damaging	1.00
R1223:Plce1	UTSW	19	38767226	missense	probably damaging	1.00
R1484:Plce1	UTSW	19	38705339	nonsense	probably null
R1488:Plce1	UTSW	19	38716803	missense	possibly damaging	0.92
R1598:Plce1	UTSW	19	38720996	missense	probably damaging	1.00
R1624:Plce1	UTSW	19	38724775	missense	probably damaging	1.00
R1732:Plce1	UTSW	19	38716838	missense	possibly damaging	0.56
R1778:Plce1	UTSW	19	38780790	splice site	probably benign
R1797:Plce1	UTSW	19	38758948	critical splice donor site	probably null
R1872:Plce1	UTSW	19	38760077	missense	probably damaging	1.00
R1876:Plce1	UTSW	19	38780623	missense	probably damaging	1.00
R1991:Plce1	UTSW	19	38777924	missense	probably damaging	1.00
R2080:Plce1	UTSW	19	38727013	splice site	probably benign
R2103:Plce1	UTSW	19	38777924	missense	probably damaging	1.00
R2376:Plce1	UTSW	19	38777986	missense	probably benign	0.02
R2471:Plce1	UTSW	19	38779926	missense	probably damaging	1.00
R2511:Plce1	UTSW	19	38760054	missense	probably damaging	1.00
R2842:Plce1	UTSW	19	38524283	missense	probably damaging	1.00
R3037:Plce1	UTSW	19	38777884	missense	probably damaging	0.98
R3104:Plce1	UTSW	19	38620519	missense	probably benign	0.00
R3700:Plce1	UTSW	19	38705337	missense	probably damaging	1.00
R3750:Plce1	UTSW	19	38777899	missense	probably benign
R3753:Plce1	UTSW	19	38651834	missense	probably benign	0.09
R4027:Plce1	UTSW	19	38524265	missense	probably damaging	1.00
R4057:Plce1	UTSW	19	38760119	missense	probably damaging	1.00
R4376:Plce1	UTSW	19	38705447	critical splice donor site	probably null
R4433:Plce1	UTSW	19	38767301	missense	probably damaging	1.00
R4520:Plce1	UTSW	19	38524319	missense	possibly damaging	0.46
R4521:Plce1	UTSW	19	38524319	missense	possibly damaging	0.46
R4522:Plce1	UTSW	19	38524319	missense	possibly damaging	0.46
R4524:Plce1	UTSW	19	38524319	missense	possibly damaging	0.46
R4650:Plce1	UTSW	19	38524644	missense	probably benign	0.30
R4673:Plce1	UTSW	19	38749396	missense	possibly damaging	0.51
R4701:Plce1	UTSW	19	38725007	missense	probably benign	0.33
R4828:Plce1	UTSW	19	38769499	missense	probably damaging	1.00
R5103:Plce1	UTSW	19	38767215	missense	probably damaging	1.00
R5112:Plce1	UTSW	19	38651833	missense	probably benign	0.00
R5236:Plce1	UTSW	19	38770347	missense	probably benign	0.11
R5268:Plce1	UTSW	19	38758835	missense	possibly damaging	0.71
R5288:Plce1	UTSW	19	38760091	missense	probably damaging	1.00
R5384:Plce1	UTSW	19	38760091	missense	probably damaging	1.00
R5386:Plce1	UTSW	19	38760091	missense	probably damaging	1.00
R5448:Plce1	UTSW	19	38779917	missense	probably damaging	1.00
R5452:Plce1	UTSW	19	38620482	missense	probably benign	0.01
R6004:Plce1	UTSW	19	38721871	missense	probably damaging	1.00
R6062:Plce1	UTSW	19	38524751	missense	probably benign
R6147:Plce1	UTSW	19	38702037	missense	probably damaging	1.00
R6247:Plce1	UTSW	19	38745845	missense	probably damaging	1.00
R6278:Plce1	UTSW	19	38725051	splice site	probably null
R6306:Plce1	UTSW	19	38769465	missense	probably damaging	1.00
R6317:Plce1	UTSW	19	38524530	nonsense	probably null
R6437:Plce1	UTSW	19	38525132	missense	probably benign	0.39
R6522:Plce1	UTSW	19	38748521	splice site	probably null
R7034:Plce1	UTSW	19	38739357	missense	probably damaging	1.00
R7036:Plce1	UTSW	19	38739357	missense	probably damaging	1.00
R7037:Plce1	UTSW	19	38702017	missense	probably damaging	1.00
R7069:Plce1	UTSW	19	38758940	missense	probably damaging	1.00
R7180:Plce1	UTSW	19	38779785	missense	probably damaging	1.00
R7189:Plce1	UTSW	19	38760137	missense	probably damaging	0.97
R7227:Plce1	UTSW	19	38726902	missense	probably benign	0.00
R7253:Plce1	UTSW	19	38698508	missense	probably damaging	1.00
R7278:Plce1	UTSW	19	38779896	missense	possibly damaging	0.58
R7287:Plce1	UTSW	19	38701903	missense	probably benign	0.02
R7422:Plce1	UTSW	19	38651885	missense	probably damaging	1.00
R7557:Plce1	UTSW	19	38765404	missense	probably benign	0.30
R7607:Plce1	UTSW	19	38524752	missense	probably benign
R7615:Plce1	UTSW	19	38524665	missense	probably benign	0.18
R7653:Plce1	UTSW	19	38749319	missense	probably benign	0.20
R7685:Plce1	UTSW	19	38748433	missense	probably benign	0.00
R7716:Plce1	UTSW	19	38716851	missense	probably benign
R7744:Plce1	UTSW	19	38620455	missense	possibly damaging	0.93
R7790:Plce1	UTSW	19	38780696	missense	probably damaging	0.97
R7921:Plce1	UTSW	19	38620553	missense	probably benign	0.03
R8070:Plce1	UTSW	19	38701839	missense	probably damaging	0.99
R8087:Plce1	UTSW	19	38736521	missense	probably damaging	1.00
R8116:Plce1	UTSW	19	38524818	missense	probably benign	0.32
R8178:Plce1	UTSW	19	38772979	missense	possibly damaging	0.93
R8321:Plce1	UTSW	19	38651936	missense	probably benign	0.00
R8416:Plce1	UTSW	19	38772997	missense	possibly damaging	0.77
R8544:Plce1	UTSW	19	38524459	missense	probably benign	0.00
R8713:Plce1	UTSW	19	38524901	missense	probably benign	0.01
R8850:Plce1	UTSW	19	38524367	missense	probably benign
R9217:Plce1	UTSW	19	38760107	missense	probably damaging	1.00
R9231:Plce1	UTSW	19	38716596	missense	probably benign	0.13
R9232:Plce1	UTSW	19	38716979	missense	probably benign	0.16
R9332:Plce1	UTSW	19	38737933	missense	probably damaging	1.00
R9473:Plce1	UTSW	19	38777893	missense	possibly damaging	0.93
R9474:Plce1	UTSW	19	38777893	missense	possibly damaging	0.93
R9475:Plce1	UTSW	19	38777893	missense	possibly damaging	0.93
R9476:Plce1	UTSW	19	38777893	missense	possibly damaging	0.93
R9751:Plce1	UTSW	19	38728970	missense	probably damaging	1.00
R9780:Plce1	UTSW	19	38620690	missense	possibly damaging	0.94
R9781:Plce1	UTSW	19	38525210	missense	probably damaging	1.00
RF018:Plce1	UTSW	19	38717207	missense	probably damaging	0.99
X0022:Plce1	UTSW	19	38726999	missense	probably damaging	1.00
X0065:Plce1	UTSW	19	38777914	missense	possibly damaging	0.48
Z1176:Plce1	UTSW	19	38701894	missense	probably damaging	1.00
Z1176:Plce1	UTSW	19	38724980	nonsense	probably null
Z1176:Plce1	UTSW	19	38769460	missense	probably damaging	1.00
Z1177:Plce1	UTSW	19	38651842	missense	probably null	0.48

Posted On

2015-04-16