Mutagenetix > Incidental Mutation

Incidental Mutation 'R3819:Plcl1'

274797

Institutional Source

Beutler Lab

Gene Symbol

Plcl1

Ensembl Gene

ENSMUSG00000038349

Gene Name

phospholipase C-like 1

Synonyms

C230017K02Rik, PRIP-1, PLC-L

MMRRC Submission

040773-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.897) question?

Stock #

R3819 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

55445080-55793444 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 55735758 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 366 (D366E)

Ref Sequence

ENSEMBL: ENSMUSP00000037854 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042986]

AlphaFold

Q3USB7

Predicted Effect

probably benign
Transcript: ENSMUST00000042986
AA Change: D366E

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

SMART Domains

Protein: ENSMUSP00000037854
Gene: ENSMUSG00000038349
AA Change: D366E

Domain	Start	End	E-Value	Type
low complexity region	21	41	N/A	INTRINSIC
low complexity region	49	60	N/A	INTRINSIC
PH	115	226	6.98e-4	SMART
low complexity region	301	310	N/A	INTRINSIC
Pfam:EF-hand_like	316	398	5.9e-27	PFAM
PLCXc	399	543	2.13e-82	SMART
low complexity region	550	564	N/A	INTRINSIC
PLCYc	586	702	2.15e-69	SMART
C2	723	829	1.02e-21	SMART
low complexity region	1080	1092	N/A	INTRINSIC

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.7%
20x: 96.1%

Validation Efficiency

100% (38/38)

MGI Phenotype

PHENOTYPE: Homozygous null mutants display impaired motor coordination and decreased sensitivity to the sedative diazepam. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 38 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aak1	T	C	6: 86,936,024 (GRCm39)		probably benign	Het
Atp1b1	C	T	1: 164,270,874 (GRCm39)	R35H	probably benign	Het
Barx1	T	C	13: 48,818,960 (GRCm39)	I200T	possibly damaging	Het
Coil	T	C	11: 88,872,619 (GRCm39)	F380L	probably benign	Het
Csmd1	C	T	8: 16,052,522 (GRCm39)	A2201T	probably damaging	Het
Dab2ip	T	C	2: 35,603,222 (GRCm39)	C417R	probably damaging	Het
Dhx57	A	G	17: 80,572,503 (GRCm39)		probably null	Het
Gabrg3	G	A	7: 57,031,412 (GRCm39)	Q43*	probably null	Het
Gbp7	C	A	3: 142,249,826 (GRCm39)	H432Q	possibly damaging	Het
Gjb2	A	G	14: 57,337,530 (GRCm39)	V226A	probably benign	Het
Gsdme	A	C	6: 50,196,391 (GRCm39)	S340A	probably benign	Het
Hivep2	T	C	10: 14,019,685 (GRCm39)	V2152A	possibly damaging	Het
Hjurp	G	C	1: 88,204,937 (GRCm39)		probably benign	Het
Kcnd3	C	T	3: 105,566,082 (GRCm39)	A421V	probably damaging	Het
Krt34	T	C	11: 99,930,844 (GRCm39)	E186G	probably damaging	Het
Ly9	G	T	1: 171,416,653 (GRCm39)	T537N	possibly damaging	Het
Msantd4	A	G	9: 4,385,237 (GRCm39)	K321E	probably damaging	Het
Or5ac22	A	G	16: 59,135,434 (GRCm39)	F112S	probably damaging	Het
Or5p59	A	G	7: 107,702,705 (GRCm39)	Y63C	possibly damaging	Het
Or8b12c	C	T	9: 37,715,465 (GRCm39)	S86L	probably benign	Het
Or8b40	A	T	9: 38,027,922 (GRCm39)	T277S	possibly damaging	Het
Or8b55	A	G	9: 38,727,722 (GRCm39)	K308E	possibly damaging	Het
Paxbp1	A	C	16: 90,819,640 (GRCm39)		probably benign	Het
Pramel22	T	A	4: 143,382,365 (GRCm39)	E110D	probably benign	Het
Prdm5	T	C	6: 65,913,041 (GRCm39)	F391L	possibly damaging	Het
Rasef	C	G	4: 73,677,942 (GRCm39)	D95H	probably damaging	Het
Rufy4	T	C	1: 74,186,822 (GRCm39)	C537R	probably damaging	Het
Skint3	A	T	4: 112,113,085 (GRCm39)	I232F	possibly damaging	Het
Slc43a3	T	C	2: 84,774,896 (GRCm39)	I158T	probably damaging	Het
Smad1	G	A	8: 80,070,359 (GRCm39)	A393V	probably benign	Het
Sorl1	A	G	9: 41,975,345 (GRCm39)	L487P	possibly damaging	Het
Sspo	A	T	6: 48,458,037 (GRCm39)	E3269V	possibly damaging	Het
Stat3	C	T	11: 100,789,459 (GRCm39)	S377N	probably damaging	Het
Tbpl2	A	G	2: 23,966,024 (GRCm39)	V321A	probably damaging	Het
Tnfrsf11a	C	T	1: 105,737,085 (GRCm39)	T64I	probably damaging	Het
Ttn	T	C	2: 76,729,047 (GRCm39)		probably benign	Het
Wdr37	A	G	13: 8,903,632 (GRCm39)		probably benign	Het
Xdh	A	T	17: 74,213,720 (GRCm39)	I811K	probably benign	Het

Other mutations in Plcl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00233:Plcl1	APN	1	55,445,695 (GRCm39)	missense	probably benign
IGL00491:Plcl1	APN	1	55,752,657 (GRCm39)	critical splice donor site	probably null
IGL00753:Plcl1	APN	1	55,735,897 (GRCm39)	missense	probably damaging	1.00
IGL01415:Plcl1	APN	1	55,735,555 (GRCm39)	missense	possibly damaging	0.92
IGL03024:Plcl1	APN	1	55,734,946 (GRCm39)	missense	probably damaging	1.00
K3955:Plcl1	UTSW	1	55,737,098 (GRCm39)	missense	possibly damaging	0.78
PIT4791001:Plcl1	UTSW	1	55,741,090 (GRCm39)	missense	probably benign	0.03
R0066:Plcl1	UTSW	1	55,752,634 (GRCm39)	missense	probably damaging	0.99
R0066:Plcl1	UTSW	1	55,752,634 (GRCm39)	missense	probably damaging	0.99
R0083:Plcl1	UTSW	1	55,737,098 (GRCm39)	missense	possibly damaging	0.78
R0086:Plcl1	UTSW	1	55,754,742 (GRCm39)	missense	probably damaging	1.00
R0092:Plcl1	UTSW	1	55,735,924 (GRCm39)	missense	probably damaging	0.98
R0108:Plcl1	UTSW	1	55,737,098 (GRCm39)	missense	possibly damaging	0.78
R1716:Plcl1	UTSW	1	55,734,997 (GRCm39)	missense	probably damaging	0.99
R2061:Plcl1	UTSW	1	55,790,504 (GRCm39)	missense	probably benign	0.01
R2128:Plcl1	UTSW	1	55,736,997 (GRCm39)	missense	probably damaging	1.00
R2869:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R2869:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R2870:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R2870:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R2872:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R2872:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R2873:Plcl1	UTSW	1	55,736,309 (GRCm39)	missense	probably benign	0.09
R3974:Plcl1	UTSW	1	55,737,374 (GRCm39)	missense	probably benign	0.30
R3975:Plcl1	UTSW	1	55,737,374 (GRCm39)	missense	probably benign	0.30
R4214:Plcl1	UTSW	1	55,790,494 (GRCm39)	nonsense	probably null
R4400:Plcl1	UTSW	1	55,754,736 (GRCm39)	missense	probably damaging	1.00
R4452:Plcl1	UTSW	1	55,736,045 (GRCm39)	missense	probably benign	0.00
R4615:Plcl1	UTSW	1	55,737,293 (GRCm39)	missense	probably benign	0.00
R5060:Plcl1	UTSW	1	55,735,671 (GRCm39)	missense	possibly damaging	0.84
R5422:Plcl1	UTSW	1	55,736,543 (GRCm39)	missense	probably benign	0.00
R5568:Plcl1	UTSW	1	55,735,309 (GRCm39)	missense	possibly damaging	0.82
R5781:Plcl1	UTSW	1	55,735,148 (GRCm39)	missense	possibly damaging	0.92
R5809:Plcl1	UTSW	1	55,735,160 (GRCm39)	missense	probably damaging	1.00
R6009:Plcl1	UTSW	1	55,735,405 (GRCm39)	missense	probably damaging	1.00
R6339:Plcl1	UTSW	1	55,735,474 (GRCm39)	missense	probably damaging	1.00
R6431:Plcl1	UTSW	1	55,736,411 (GRCm39)	missense	probably benign	0.03
R6534:Plcl1	UTSW	1	55,735,907 (GRCm39)	missense	probably damaging	1.00
R6565:Plcl1	UTSW	1	55,737,117 (GRCm39)	nonsense	probably null
R6678:Plcl1	UTSW	1	55,734,935 (GRCm39)	missense	probably benign	0.13
R6773:Plcl1	UTSW	1	55,790,461 (GRCm39)	missense	probably benign	0.03
R6925:Plcl1	UTSW	1	55,445,757 (GRCm39)	nonsense	probably null
R7168:Plcl1	UTSW	1	55,736,622 (GRCm39)	missense	probably damaging	1.00
R7256:Plcl1	UTSW	1	55,737,377 (GRCm39)	missense	probably benign	0.45
R7522:Plcl1	UTSW	1	55,735,523 (GRCm39)	missense	probably benign	0.31
R7527:Plcl1	UTSW	1	55,736,273 (GRCm39)	missense	probably damaging	1.00
R7536:Plcl1	UTSW	1	55,752,640 (GRCm39)	nonsense	probably null
R7585:Plcl1	UTSW	1	55,445,608 (GRCm39)	missense	probably benign	0.00
R7591:Plcl1	UTSW	1	55,736,608 (GRCm39)	missense	probably benign	0.01
R7689:Plcl1	UTSW	1	55,736,627 (GRCm39)	missense	probably damaging	1.00
R7960:Plcl1	UTSW	1	55,736,443 (GRCm39)	missense	possibly damaging	0.48
R8029:Plcl1	UTSW	1	55,735,237 (GRCm39)	missense	probably benign	0.26
R8241:Plcl1	UTSW	1	55,734,976 (GRCm39)	missense	probably benign	0.01
R8323:Plcl1	UTSW	1	55,736,895 (GRCm39)	missense	possibly damaging	0.58
R9000:Plcl1	UTSW	1	55,736,990 (GRCm39)	missense	probably damaging	1.00
R9331:Plcl1	UTSW	1	55,736,030 (GRCm39)	missense	possibly damaging	0.95
R9358:Plcl1	UTSW	1	55,735,810 (GRCm39)	missense	probably damaging	1.00
R9432:Plcl1	UTSW	1	55,445,587 (GRCm39)	missense	probably benign
R9452:Plcl1	UTSW	1	55,734,992 (GRCm39)	missense	probably damaging	1.00
R9652:Plcl1	UTSW	1	55,735,450 (GRCm39)	missense	probably benign	0.00
R9802:Plcl1	UTSW	1	55,735,241 (GRCm39)	missense	probably damaging	0.98
Z1176:Plcl1	UTSW	1	55,790,443 (GRCm39)	nonsense	probably null
Z1176:Plcl1	UTSW	1	55,735,199 (GRCm39)	missense	probably benign	0.20
Z1177:Plcl1	UTSW	1	55,736,043 (GRCm39)	missense	possibly damaging	0.72

Predicted Primers

PCR Primer
(F):5'- AACTACCCGGGTGACAGAAG -3'
(R):5'- TATCTGCTGGTCCCCTGAACTG -3'

Sequencing Primer
(F):5'- AGAGGAATTTTGTGAAGCATTTTGC -3'
(R):5'- GGTCCCCTGAACTGATCTTC -3'

Posted On

2015-04-02