Mutagenetix > Incidental Mutation

Incidental Mutation 'R9397:Epc2'

710874

Institutional Source

Beutler Lab

Gene Symbol

Epc2

Ensembl Gene

ENSMUSG00000069495

Gene Name

enhancer of polycomb homolog 2

Synonyms

D2Ertd694e

MMRRC Submission

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9397 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

49341498-49441954 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 49378822 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Glutamic Acid at position 92 (G92E)

Ref Sequence

ENSEMBL: ENSMUSP00000089758 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092123]

AlphaFold

Q8C0I4

Predicted Effect

probably damaging
Transcript: ENSMUST00000092123
AA Change: G92E

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

SMART Domains

Protein: ENSMUSP00000089758
Gene: ENSMUSG00000069495
AA Change: G92E

Domain	Start	End	E-Value	Type
Pfam:EPL1	7	149	6.5e-18	PFAM
low complexity region	334	342	N/A	INTRINSIC
low complexity region	445	466	N/A	INTRINSIC
low complexity region	485	499	N/A	INTRINSIC
low complexity region	553	564	N/A	INTRINSIC
Pfam:E_Pc_C	578	808	2.1e-70	PFAM

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

Allele List at MGI

All alleles(45) : Targeted(3) Gene trapped(42)

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930555G01Rik	T	G	14: 5,051,639 (GRCm38)	V66G	possibly damaging	Het
A630001G21Rik	G	T	1: 85,653,002 (GRCm39)	Y55*	probably null	Het
Abca8a	G	A	11: 109,921,173 (GRCm39)	T1474I	probably damaging	Het
Acaca	T	G	11: 84,259,551 (GRCm39)	I1962S	probably damaging	Het
Acap1	A	T	11: 69,775,672 (GRCm39)	S455T	probably damaging	Het
Acbd7	G	A	2: 3,337,259 (GRCm39)		probably null	Het
Adamts9	A	G	6: 92,878,444 (GRCm39)	L541P	probably damaging	Het
Ankrd49	T	C	9: 14,692,711 (GRCm39)	N151S	probably benign	Het
Apcdd1	C	T	18: 63,055,731 (GRCm39)		probably benign	Het
Arhgap27	T	C	11: 103,231,115 (GRCm39)	D58G	probably damaging	Het
Btbd18	G	T	2: 84,497,810 (GRCm39)	A483S	probably damaging	Het
C2	A	G	17: 35,094,965 (GRCm39)	S257P	probably damaging	Het
Catsper3	T	A	13: 55,946,725 (GRCm39)	Y141N	probably damaging	Het
Cfap54	G	A	10: 92,833,147 (GRCm39)	L1160F	probably damaging	Het
Chst13	G	A	6: 90,286,506 (GRCm39)	P152L	probably damaging	Het
Cyp4f14	C	T	17: 33,130,516 (GRCm39)	G141D	probably damaging	Het
Duox1	C	T	2: 122,150,783 (GRCm39)	T286I	possibly damaging	Het
Fmnl3	C	T	15: 99,225,938 (GRCm39)		probably null	Het
Glyatl3	G	A	17: 41,223,565 (GRCm39)	R59*	probably null	Het
Gm3633	T	A	14: 42,460,400 (GRCm39)	Q181L		Het
Guca1b	C	T	17: 47,696,560 (GRCm39)	T49M	probably benign	Het
Hdac9	T	A	12: 34,353,275 (GRCm39)	H645L	probably damaging	Het
Hhip	T	C	8: 80,719,112 (GRCm39)	R472G	probably benign	Het
Ifi203	A	G	1: 173,765,547 (GRCm39)	V9A	probably damaging	Het
Igkv9-123	A	T	6: 67,931,443 (GRCm39)	V41D	probably damaging	Het
Il5ra	T	A	6: 106,721,258 (GRCm39)	T14S	probably benign	Het
Ints2	A	G	11: 86,135,311 (GRCm39)	S368P	probably benign	Het
Kat6b	T	A	14: 21,675,244 (GRCm39)	S470T	possibly damaging	Het
Kmt2d	A	G	15: 98,747,994 (GRCm39)	V3110A	unknown	Het
Lama2	T	C	10: 26,981,117 (GRCm39)	N1846D	probably benign	Het
Lrp1b	T	A	2: 40,640,922 (GRCm39)	E3507D		Het
Ly6g6c	A	G	17: 35,288,317 (GRCm39)	N63S	probably benign	Het
Naprt	C	T	15: 75,763,859 (GRCm39)	V354I	probably null	Het
Nars1	A	G	18: 64,642,327 (GRCm39)	S172P	probably benign	Het
Odr4	C	T	1: 150,238,616 (GRCm39)	A434T	probably damaging	Het
Or6c5b	A	G	10: 129,245,909 (GRCm39)	R225G	possibly damaging	Het
Or7e177	T	C	9: 20,211,748 (GRCm39)	I85T	possibly damaging	Het
Pcdhb6	A	G	18: 37,469,353 (GRCm39)	D758G	probably benign	Het
Pkp4	G	A	2: 59,148,856 (GRCm39)	W536*	probably null	Het
Polr3b	C	T	10: 84,467,653 (GRCm39)	L78F	possibly damaging	Het
Rasa4	T	A	5: 136,129,836 (GRCm39)	V272E	possibly damaging	Het
Syne2	A	G	12: 76,040,849 (GRCm39)	T3836A	possibly damaging	Het
Tbpl2	C	T	2: 23,966,070 (GRCm39)	V308I	possibly damaging	Het
Tcea1	T	A	1: 4,962,141 (GRCm39)	I176K	probably damaging	Het
Try5	A	T	6: 41,289,314 (GRCm39)	F87L	probably benign	Het
Ttc8	G	T	12: 98,942,692 (GRCm39)	G411*	probably null	Het
Vmn2r115	G	A	17: 23,564,152 (GRCm39)	W108*	probably null	Het
Zdhhc13	C	T	7: 48,476,628 (GRCm39)	T581I	probably benign	Het
Zfp777	G	T	6: 48,021,190 (GRCm39)	T144K	probably benign	Het

Other mutations in Epc2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01921:Epc2	APN	2	49,422,209 (GRCm39)	missense	probably damaging	1.00
IGL02479:Epc2	APN	2	49,422,147 (GRCm39)	missense	probably benign	0.00
IGL03342:Epc2	APN	2	49,426,658 (GRCm39)	missense	probably benign	0.02
IGL02984:Epc2	UTSW	2	49,418,866 (GRCm39)	missense	probably damaging	1.00
R0014:Epc2	UTSW	2	49,412,537 (GRCm39)	nonsense	probably null
R0014:Epc2	UTSW	2	49,412,537 (GRCm39)	nonsense	probably null
R0360:Epc2	UTSW	2	49,427,145 (GRCm39)	missense	possibly damaging	0.81
R0364:Epc2	UTSW	2	49,427,145 (GRCm39)	missense	possibly damaging	0.81
R0401:Epc2	UTSW	2	49,418,986 (GRCm39)	missense	probably damaging	0.99
R1269:Epc2	UTSW	2	49,412,588 (GRCm39)	missense	probably benign	0.38
R1495:Epc2	UTSW	2	49,426,675 (GRCm39)	missense	probably damaging	1.00
R1573:Epc2	UTSW	2	49,439,984 (GRCm39)	missense	possibly damaging	0.81
R1619:Epc2	UTSW	2	49,439,990 (GRCm39)	missense	probably damaging	0.99
R1721:Epc2	UTSW	2	49,422,117 (GRCm39)	missense	probably damaging	1.00
R1847:Epc2	UTSW	2	49,422,101 (GRCm39)	missense	probably damaging	1.00
R1867:Epc2	UTSW	2	49,422,117 (GRCm39)	missense	probably damaging	1.00
R2113:Epc2	UTSW	2	49,422,235 (GRCm39)	missense	probably benign
R2120:Epc2	UTSW	2	49,437,621 (GRCm39)	splice site	probably benign
R3840:Epc2	UTSW	2	49,378,750 (GRCm39)	missense	probably damaging	1.00
R3841:Epc2	UTSW	2	49,378,750 (GRCm39)	missense	probably damaging	1.00
R4366:Epc2	UTSW	2	49,437,566 (GRCm39)	missense	possibly damaging	0.84
R4864:Epc2	UTSW	2	49,427,177 (GRCm39)	missense	probably benign
R5335:Epc2	UTSW	2	49,403,242 (GRCm39)	missense	probably benign	0.39
R5639:Epc2	UTSW	2	49,341,903 (GRCm39)	missense	possibly damaging	0.78
R5695:Epc2	UTSW	2	49,437,619 (GRCm39)	critical splice donor site	probably null
R6259:Epc2	UTSW	2	49,378,866 (GRCm39)	splice site	probably null
R6420:Epc2	UTSW	2	49,341,912 (GRCm39)	missense	probably damaging	0.98
R6667:Epc2	UTSW	2	49,412,681 (GRCm39)	missense	probably damaging	0.99
R6788:Epc2	UTSW	2	49,422,099 (GRCm39)	missense	probably benign	0.32
R7061:Epc2	UTSW	2	49,425,334 (GRCm39)	missense	probably damaging	1.00
R7672:Epc2	UTSW	2	49,435,831 (GRCm39)	missense	possibly damaging	0.56
R8377:Epc2	UTSW	2	49,412,527 (GRCm39)	missense	probably damaging	0.99
RF009:Epc2	UTSW	2	49,422,249 (GRCm39)	critical splice donor site	probably null
Z1176:Epc2	UTSW	2	49,425,312 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGCGAAGGAGAACTATTCCAAATCG -3'
(R):5'- CAAAGTGATCTCCAAGCTCAAATG -3'

Sequencing Primer
(F):5'- ACGTTTAAATAGAATTATGCACGGAG -3'
(R):5'- TGATCTCCAAGCTCAAATGAAAATAC -3'

Posted On

2022-04-18