Mutagenetix > Incidental Mutation

Incidental Mutation 'R0599:Eapp'

55246

Institutional Source

Beutler Lab

Gene Symbol

Eapp

Ensembl Gene

ENSMUSG00000054302

Gene Name

E2F-associated phosphoprotein

Synonyms

1810011O16Rik, EAPP

MMRRC Submission

038788-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.902) question?

Stock #

R0599 (G1)

Quality Score

179

Status

Validated

Chromosome

Chromosomal Location

54717125-54742682 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 54732747 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Methionine at position 117 (K117M)

Ref Sequence

ENSEMBL: ENSMUSP00000124232 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000067272] [ENSMUST00000110713] [ENSMUST00000160085] [ENSMUST00000161592] [ENSMUST00000162106] [ENSMUST00000163433]

AlphaFold

Q5BU09

Predicted Effect

probably benign
Transcript: ENSMUST00000067272

SMART Domains

Protein: ENSMUSP00000069381
Gene: ENSMUSG00000054302

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000110713
AA Change: K121M

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000106341
Gene: ENSMUSG00000054302
AA Change: K121M

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC
low complexity region	52	68	N/A	INTRINSIC
low complexity region	80	97	N/A	INTRINSIC
low complexity region	116	125	N/A	INTRINSIC
Pfam:Eapp_C	153	241	1.1e-33	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000160085

SMART Domains

Protein: ENSMUSP00000124699
Gene: ENSMUSG00000054302

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC
low complexity region	52	68	N/A	INTRINSIC
low complexity region	80	97	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000161592
AA Change: K121M

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000123698
Gene: ENSMUSG00000054302
AA Change: K121M

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC
low complexity region	52	68	N/A	INTRINSIC
low complexity region	80	97	N/A	INTRINSIC
low complexity region	116	125	N/A	INTRINSIC
Pfam:Eapp_C	136	279	5e-54	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000162106
AA Change: K117M

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

SMART Domains

Protein: ENSMUSP00000124232
Gene: ENSMUSG00000054302
AA Change: K117M

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC
low complexity region	52	68	N/A	INTRINSIC
low complexity region	112	121	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000163433
AA Change: K121M

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000130251
Gene: ENSMUSG00000054302
AA Change: K121M

Domain	Start	End	E-Value	Type
low complexity region	23	34	N/A	INTRINSIC
low complexity region	52	68	N/A	INTRINSIC
low complexity region	80	97	N/A	INTRINSIC
low complexity region	116	125	N/A	INTRINSIC
Pfam:Eapp_C	136	279	5.8e-52	PFAM

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.4%
3x: 98.9%
10x: 97.5%
20x: 95.0%

Validation Efficiency

98% (80/82)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a phosphoprotein that interacts with several members of the E2F family of proteins. The protein localizes to the nucleus, and is present throughout the cell cycle except during mitosis. It functions to modulate E2F-regulated transcription and stimulate proliferation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	A	G	6: 128,529,208 (GRCm39)	L978P	probably damaging	Het
Abcb1a	C	T	5: 8,748,539 (GRCm39)	T290M	probably benign	Het
Abcd3	A	T	3: 121,558,742 (GRCm39)	F585I	probably damaging	Het
Abtb3	G	A	10: 85,494,200 (GRCm39)	G1106D	probably damaging	Het
Acan	A	G	7: 78,761,038 (GRCm39)		probably benign	Het
Anxa6	T	C	11: 54,870,292 (GRCm39)	D667G	possibly damaging	Het
Ap3m2	G	T	8: 23,283,128 (GRCm39)	A208D	possibly damaging	Het
Arhgap17	A	T	7: 122,903,013 (GRCm39)		probably benign	Het
Bptf	A	G	11: 106,959,208 (GRCm39)	V1838A	probably damaging	Het
Brip1	T	A	11: 86,043,563 (GRCm39)	M334L	probably benign	Het
Btbd10	C	T	7: 112,934,516 (GRCm39)		probably benign	Het
Cdh20	C	A	1: 109,980,696 (GRCm39)	T208K	probably damaging	Het
Cnga4	A	G	7: 105,055,025 (GRCm39)	Y100C	probably damaging	Het
Dnah10	G	A	5: 124,878,017 (GRCm39)	V2644M	probably damaging	Het
Dnah9	T	C	11: 65,856,515 (GRCm39)	D2882G	probably damaging	Het
Eml3	T	C	19: 8,916,427 (GRCm39)	V673A	probably benign	Het
Ephb4	G	A	5: 137,368,117 (GRCm39)	C754Y	probably damaging	Het
Eps8l1	A	G	7: 4,480,956 (GRCm39)	D33G	possibly damaging	Het
Farsa	A	G	8: 85,594,212 (GRCm39)	K321E	probably damaging	Het
Fry	G	A	5: 150,360,624 (GRCm39)	R2090Q	probably damaging	Het
Gm10283	A	G	8: 60,954,258 (GRCm39)		probably benign	Het
Grm4	A	G	17: 27,650,464 (GRCm39)	I844T	probably benign	Het
Gtf2h3	A	G	5: 124,726,691 (GRCm39)	D124G	probably benign	Het
Gulo	A	T	14: 66,227,890 (GRCm39)	D347E	probably damaging	Het
Hmcn1	A	G	1: 150,485,552 (GRCm39)	F4350S	possibly damaging	Het
Hspg2	A	G	4: 137,239,712 (GRCm39)	D473G	probably damaging	Het
Il17ra	T	A	6: 120,458,466 (GRCm39)	I539N	probably damaging	Het
Insrr	A	G	3: 87,720,440 (GRCm39)	E1026G	probably damaging	Het
Itga2	A	T	13: 114,993,186 (GRCm39)		probably benign	Het
Kdm1b	A	T	13: 47,212,286 (GRCm39)	D190V	possibly damaging	Het
Lima1	A	T	15: 99,700,040 (GRCm39)	N146K	probably damaging	Het
Mnt	G	T	11: 74,733,122 (GRCm39)	V85L	probably benign	Het
Mon2	T	A	10: 122,861,970 (GRCm39)		probably benign	Het
Mtf1	T	C	4: 124,713,994 (GRCm39)		probably benign	Het
Mylk4	T	C	13: 32,896,737 (GRCm39)		probably null	Het
Myo18b	A	C	5: 113,013,616 (GRCm39)	L780R	probably damaging	Het
Myo1e	A	G	9: 70,283,942 (GRCm39)		probably benign	Het
Obscn	A	G	11: 58,964,522 (GRCm39)	S705P	probably damaging	Het
Ocrl	A	T	X: 47,024,963 (GRCm39)		probably benign	Het
Or1e34	A	T	11: 73,778,730 (GRCm39)	M156K	probably benign	Het
Or4c35	T	C	2: 89,808,545 (GRCm39)	F141S	probably benign	Het
Or51k1	A	T	7: 103,661,395 (GRCm39)	C171*	probably null	Het
Or52ab4	A	G	7: 102,987,393 (GRCm39)	N44S	probably damaging	Het
Otof	T	A	5: 30,528,049 (GRCm39)	K1931N	probably damaging	Het
Plcxd3	A	G	15: 4,546,349 (GRCm39)	S118G	probably damaging	Het
Plcz1	T	A	6: 139,974,268 (GRCm39)	Q58L	probably benign	Het
Proser1	C	A	3: 53,386,485 (GRCm39)	P789Q	probably benign	Het
Rassf4	T	C	6: 116,622,897 (GRCm39)	E38G	probably damaging	Het
Ros1	A	T	10: 51,999,396 (GRCm39)	Y1164N	probably damaging	Het
Rpgrip1l	A	G	8: 92,031,628 (GRCm39)	I83T	probably damaging	Het
Scn9a	T	G	2: 66,357,143 (GRCm39)	K1053Q	probably damaging	Het
Sgsm1	G	T	5: 113,392,894 (GRCm39)	Q1087K	probably damaging	Het
Slc16a10	T	C	10: 40,017,914 (GRCm39)	D40G	probably benign	Het
Slc27a6	A	G	18: 58,689,885 (GRCm39)	D117G	probably damaging	Het
Slc2a9	T	A	5: 38,637,487 (GRCm39)		probably benign	Het
Slc4a1	A	G	11: 102,248,741 (GRCm39)		probably benign	Het
Smarca1	T	A	X: 46,912,303 (GRCm39)	Q982L	probably benign	Het
Sp100	T	A	1: 85,608,831 (GRCm39)	I320N	possibly damaging	Het
Stx8	A	T	11: 68,000,188 (GRCm39)	R209S	probably null	Het
Sulf2	T	C	2: 165,925,799 (GRCm39)	T453A	possibly damaging	Het
Syne2	AGAGTGAG	AGAGTGAGTGAG	12: 76,144,734 (GRCm39)		probably null	Het
Tenm2	T	A	11: 35,915,607 (GRCm39)	I1976F	possibly damaging	Het
Tenm3	G	A	8: 48,730,745 (GRCm39)	S1341L	probably damaging	Het
Tmem130	C	T	5: 144,674,619 (GRCm39)	V369M	probably damaging	Het
Tmem200c	A	G	17: 69,147,506 (GRCm39)	K30E	probably damaging	Het
Tmem225	A	G	9: 40,061,043 (GRCm39)	I117V	possibly damaging	Het
Tmt1a3	A	T	15: 100,233,264 (GRCm39)	N152Y	possibly damaging	Het
Top2a	A	G	11: 98,892,243 (GRCm39)	I1073T	probably damaging	Het
Trps1	A	C	15: 50,695,256 (GRCm39)	Y296*	probably null	Het
Tubg1	T	C	11: 101,016,162 (GRCm39)	M377T	probably benign	Het
Tut7	A	G	13: 59,957,301 (GRCm39)	V7A	probably damaging	Het
Vmn1r35	G	A	6: 66,656,497 (GRCm39)	H58Y	probably benign	Het
Vmn1r56	G	A	7: 5,199,429 (GRCm39)	H63Y	probably benign	Het
Vmn1r75	T	C	7: 11,615,189 (GRCm39)		probably null	Het
Vnn3	T	C	10: 23,741,603 (GRCm39)	S303P	possibly damaging	Het
Wdr49	C	T	3: 75,338,383 (GRCm39)		probably null	Het
Wdr49	T	C	3: 75,357,197 (GRCm39)		probably null	Het
Zzef1	T	C	11: 72,804,004 (GRCm39)	L2582P	probably damaging	Het

Other mutations in Eapp

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00916:Eapp	APN	12	54,739,593 (GRCm39)	missense	possibly damaging	0.78
IGL01964:Eapp	APN	12	54,732,720 (GRCm39)	missense	probably damaging	0.99
IGL02591:Eapp	APN	12	54,739,607 (GRCm39)	missense	probably damaging	1.00
IGL03323:Eapp	APN	12	54,720,400 (GRCm39)	missense	probably damaging	1.00
IGL03328:Eapp	APN	12	54,738,878 (GRCm39)	missense	probably benign	0.04
R0939:Eapp	UTSW	12	54,732,734 (GRCm39)	small deletion	probably benign
R1583:Eapp	UTSW	12	54,732,733 (GRCm39)	nonsense	probably null
R1646:Eapp	UTSW	12	54,732,745 (GRCm39)	nonsense	probably null
R1935:Eapp	UTSW	12	54,720,513 (GRCm39)	missense	probably benign	0.01
R1936:Eapp	UTSW	12	54,720,513 (GRCm39)	missense	probably benign	0.01
R5303:Eapp	UTSW	12	54,739,703 (GRCm39)	missense	probably damaging	1.00
R5537:Eapp	UTSW	12	54,738,844 (GRCm39)	missense	probably benign	0.22
R7638:Eapp	UTSW	12	54,720,508 (GRCm39)	missense	probably benign	0.02
R8041:Eapp	UTSW	12	54,739,650 (GRCm39)	missense	probably damaging	1.00
R8911:Eapp	UTSW	12	54,739,440 (GRCm39)	intron	probably benign
R9294:Eapp	UTSW	12	54,737,061 (GRCm39)	missense	unknown
R9733:Eapp	UTSW	12	54,739,741 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACGGACAGACAGACGGATTAAAGACTAT -3'
(R):5'- CAAGTGCCAGGGCTGCTAAAGAA -3'

Sequencing Primer
(F):5'- GACAGACGGATTAAAGACTATTTGAC -3'
(R):5'- ttcctttatatttgactcactgcc -3'

Posted On

2013-07-11