Mutagenetix > Incidental Mutation

Incidental Mutation 'R2568:Plekhm3'

254597

Institutional Source

Beutler Lab

Gene Symbol

Plekhm3

Ensembl Gene

ENSMUSG00000051344

Gene Name

pleckstrin homology domain containing, family M, member 3

Synonyms

9430067K14Rik, A230102O09Rik, Plekhm1l

MMRRC Submission

040427-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.166) question?

Stock #

R2568 (G1)

Quality Score

106

Status

Not validated

Chromosome

Chromosomal Location

64785983-64956824 bp(-) (GRCm38)

Type of Mutation

small deletion (1 aa in frame mutation)

DNA Base Change (assembly)

CCTGCTGCTGCTGCTGCTGCTGCTGC to CCTGCTGCTGCTGCTGCTGCTGC at 64937781 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000138002 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000097713] [ENSMUST00000123225] [ENSMUST00000139649]

AlphaFold

Q8BM47

Predicted Effect

probably benign
Transcript: ENSMUST00000097713

SMART Domains

Protein: ENSMUSP00000095320
Gene: ENSMUSG00000051344

Domain	Start	End	E-Value	Type
low complexity region	184	195	N/A	INTRINSIC
PH	213	311	4.86e-3	SMART
PH	362	458	7.88e-12	SMART
low complexity region	489	503	N/A	INTRINSIC
DUF4206	529	732	2.73e-114	SMART
C1	670	722	3.9e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000123225

Predicted Effect

probably benign
Transcript: ENSMUST00000139649

SMART Domains

Protein: ENSMUSP00000138002
Gene: ENSMUSG00000051344

Domain	Start	End	E-Value	Type
low complexity region	184	195	N/A	INTRINSIC
PH	213	311	4.86e-3	SMART
PH	362	458	7.88e-12	SMART
low complexity region	489	503	N/A	INTRINSIC
DUF4206	529	732	2.73e-114	SMART
C1	670	722	3.9e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181350

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.0%
20x: 94.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	T	C	15: 8,201,269 (GRCm38)	V1010A	possibly damaging	Het
4930563D23Rik	A	G	16: 92,321,319 (GRCm38)	L27P	probably damaging	Het
A730071L15Rik	A	T	11: 6,200,161 (GRCm38)		probably benign	Het
Abca13	A	T	11: 9,333,310 (GRCm38)	N3244I	probably benign	Het
Adgrf5	A	G	17: 43,437,671 (GRCm38)	T219A	probably damaging	Het
Adgrg5	A	T	8: 94,934,021 (GRCm38)	N92I	probably damaging	Het
Agt	A	C	8: 124,556,955 (GRCm38)	V475G	probably damaging	Het
Akap6	A	G	12: 52,887,278 (GRCm38)	K518E	possibly damaging	Het
Apoh	T	G	11: 108,404,871 (GRCm38)	D133E	probably benign	Het
Axdnd1	T	A	1: 156,392,749 (GRCm38)	M234L	possibly damaging	Het
Cacna1d	A	G	14: 30,082,511 (GRCm38)	I1335T	probably damaging	Het
Cdh15	G	A	8: 122,862,024 (GRCm38)	R279Q	probably damaging	Het
Cfap206	T	A	4: 34,711,566 (GRCm38)	K444*	probably null	Het
Clasp2	A	G	9: 113,878,764 (GRCm38)	I614M	probably benign	Het
Col6a4	A	T	9: 106,063,076 (GRCm38)	D1218E	possibly damaging	Het
Csmd3	CCTTTGCGCTT	CCTT	15: 47,741,236 (GRCm38)		probably null	Het
D130043K22Rik	C	T	13: 24,883,891 (GRCm38)	T870M	probably damaging	Het
Dagla	C	A	19: 10,248,152 (GRCm38)	A883S	probably benign	Het
Dhx30	A	G	9: 110,097,195 (GRCm38)	V87A	probably damaging	Het
Dtx1	C	A	5: 120,710,184 (GRCm38)	V44L	possibly damaging	Het
Ecm2	T	A	13: 49,530,129 (GRCm38)	S528T	possibly damaging	Het
Egfem1	A	T	3: 29,582,931 (GRCm38)	N172I	probably damaging	Het
Fam102b	T	A	3: 108,978,848 (GRCm38)	N356I	probably benign	Het
Fam13a	T	G	6: 58,935,609 (GRCm38)	R686S	probably damaging	Het
Fmo1	T	A	1: 162,836,259 (GRCm38)	I234L	probably benign	Het
Foxj2	C	T	6: 122,828,372 (GRCm38)	R68W	probably damaging	Het
Foxo6	A	T	4: 120,268,764 (GRCm38)	M278K	probably benign	Het
Fsip2	A	G	2: 82,990,431 (GRCm38)	S5503G	probably benign	Het
Gdf5	C	G	2: 155,942,090 (GRCm38)	R100G	probably benign	Het
Il1b	A	T	2: 129,367,322 (GRCm38)	D129E	probably damaging	Het
Klhl29	A	G	12: 5,091,350 (GRCm38)	S545P	probably damaging	Het
Krt83	G	T	15: 101,487,827 (GRCm38)	R296S	possibly damaging	Het
Llgl1	T	G	11: 60,708,812 (GRCm38)	S509R	probably damaging	Het
Lmod1	A	T	1: 135,363,964 (GRCm38)	K186*	probably null	Het
Lrpprc	C	T	17: 84,726,649 (GRCm38)	A973T	probably damaging	Het
Marco	T	C	1: 120,494,785 (GRCm38)	H49R	possibly damaging	Het
Mylk4	T	C	13: 32,722,018 (GRCm38)	N394S	probably null	Het
Myo5a	A	G	9: 75,123,040 (GRCm38)	Y147C	probably damaging	Het
Myo5a	T	C	9: 75,151,897 (GRCm38)	V469A	probably damaging	Het
Myot	A	G	18: 44,337,216 (GRCm38)	T87A	probably benign	Het
Nav2	A	G	7: 49,597,564 (GRCm38)	H2154R	probably damaging	Het
Nek10	A	G	14: 14,999,112 (GRCm38)	E1037G	possibly damaging	Het
Olfr181	A	G	16: 58,925,923 (GRCm38)	V216A	probably benign	Het
Olfr341	T	C	2: 36,479,974 (GRCm38)	D52G	probably damaging	Het
Olfr677	A	G	7: 105,056,671 (GRCm38)	T142A	probably benign	Het
Pitrm1	G	T	13: 6,575,092 (GRCm38)	V869F	probably benign	Het
Prdx1	T	G	4: 116,693,800 (GRCm38)	I156S	probably benign	Het
Rbks	T	A	5: 31,665,752 (GRCm38)	T107S	probably damaging	Het
Ryr3	G	A	2: 112,675,874 (GRCm38)	R3468W	probably damaging	Het
Scn1a	C	T	2: 66,273,469 (GRCm38)	D1805N	probably damaging	Het
Sirpa	T	C	2: 129,615,648 (GRCm38)	V214A	probably benign	Het
Slc35c1	T	C	2: 92,458,880 (GRCm38)	N94D	probably benign	Het
Sorbs2	A	T	8: 45,795,370 (GRCm38)	K553*	probably null	Het
Tectb	C	G	19: 55,180,999 (GRCm38)		probably benign	Het
Thg1l	A	G	11: 45,951,565 (GRCm38)	V142A	probably benign	Het
Tiparp	T	A	3: 65,553,130 (GRCm38)	Y513*	probably null	Het
Tmc6	A	G	11: 117,772,820 (GRCm38)	V522A	probably benign	Het
Trim39	T	A	17: 36,269,164 (GRCm38)		probably benign	Het
Trrap	G	A	5: 144,843,369 (GRCm38)		probably null	Het
Tulp3	C	T	6: 128,327,638 (GRCm38)	V218I	probably benign	Het
Vmn1r38	T	A	6: 66,776,971 (GRCm38)	I54F	probably benign	Het
Vmn2r23	T	A	6: 123,742,188 (GRCm38)	Y833*	probably null	Het
Zfp810	A	T	9: 22,279,238 (GRCm38)	S125T	probably benign	Het

Other mutations in Plekhm3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01603:Plekhm3	APN	1	64,921,832 (GRCm38)	missense	probably damaging	1.00
IGL01732:Plekhm3	APN	1	64,922,248 (GRCm38)	missense	probably benign	0.44
IGL02422:Plekhm3	APN	1	64,921,866 (GRCm38)	nonsense	probably null
IGL02724:Plekhm3	APN	1	64,795,117 (GRCm38)	missense	probably damaging	0.97
IGL03226:Plekhm3	APN	1	64,921,800 (GRCm38)	missense	possibly damaging	0.58
IGL03250:Plekhm3	APN	1	64,938,047 (GRCm38)	missense	possibly damaging	0.65
R0124:Plekhm3	UTSW	1	64,921,751 (GRCm38)	missense	probably damaging	0.99
R1336:Plekhm3	UTSW	1	64,937,781 (GRCm38)	small deletion	probably benign
R1467:Plekhm3	UTSW	1	64,892,882 (GRCm38)	missense	probably damaging	1.00
R1467:Plekhm3	UTSW	1	64,892,882 (GRCm38)	missense	probably damaging	1.00
R1560:Plekhm3	UTSW	1	64,937,817 (GRCm38)	missense	probably benign	0.03
R1901:Plekhm3	UTSW	1	64,937,781 (GRCm38)	small deletion	probably benign
R2328:Plekhm3	UTSW	1	64,937,781 (GRCm38)	small deletion	probably benign
R2432:Plekhm3	UTSW	1	64,937,856 (GRCm38)	missense	probably damaging	1.00
R3023:Plekhm3	UTSW	1	64,937,781 (GRCm38)	small deletion	probably benign
R4496:Plekhm3	UTSW	1	64,861,236 (GRCm38)	missense	probably damaging	1.00
R4529:Plekhm3	UTSW	1	64,937,825 (GRCm38)	missense	probably benign	0.14
R4682:Plekhm3	UTSW	1	64,937,927 (GRCm38)	missense	possibly damaging	0.94
R4969:Plekhm3	UTSW	1	64,937,919 (GRCm38)	missense	probably damaging	1.00
R5347:Plekhm3	UTSW	1	64,819,990 (GRCm38)	missense	probably damaging	1.00
R5553:Plekhm3	UTSW	1	64,921,886 (GRCm38)	missense	possibly damaging	0.89
R5583:Plekhm3	UTSW	1	64,937,986 (GRCm38)	nonsense	probably null
R5953:Plekhm3	UTSW	1	64,937,895 (GRCm38)	missense	probably damaging	0.98
R6319:Plekhm3	UTSW	1	64,921,934 (GRCm38)	missense	probably benign	0.20
R6970:Plekhm3	UTSW	1	64,892,753 (GRCm38)	missense	possibly damaging	0.80
R7014:Plekhm3	UTSW	1	64,883,270 (GRCm38)	missense	probably damaging	1.00
R7408:Plekhm3	UTSW	1	64,937,984 (GRCm38)	missense	probably benign	0.02
R7570:Plekhm3	UTSW	1	64,937,906 (GRCm38)	missense	probably damaging	1.00
R7663:Plekhm3	UTSW	1	64,883,208 (GRCm38)	missense	probably damaging	0.98
R7719:Plekhm3	UTSW	1	64,921,742 (GRCm38)	missense	probably benign	0.33
R7894:Plekhm3	UTSW	1	64,921,715 (GRCm38)	missense	probably benign
R8808:Plekhm3	UTSW	1	64,883,196 (GRCm38)	missense	possibly damaging	0.96
R9069:Plekhm3	UTSW	1	64,921,643 (GRCm38)	missense	probably benign	0.02
R9296:Plekhm3	UTSW	1	64,922,480 (GRCm38)	missense	probably benign	0.11
R9788:Plekhm3	UTSW	1	64,922,263 (GRCm38)	missense	possibly damaging	0.80

Predicted Primers

PCR Primer
(F):5'- TCCATATGTGGGTACTGGAGAGTC -3'
(R):5'- GACAGCCCCAGATAATCTTTCC -3'

Sequencing Primer
(F):5'- TGGGTACTGGAGAGTCAGCAG -3'
(R):5'- CAGATAATCTTTCCTGGATGGCAC -3'

Posted On

2014-12-04