Mutagenetix > Incidental Mutation

Incidental Mutation 'R7385:Eif4enif1'

573045

Institutional Source

Beutler Lab

Gene Symbol

Eif4enif1

Ensembl Gene

ENSMUSG00000020454

Gene Name

eukaryotic translation initiation factor 4E nuclear import factor 1

Synonyms

D11Ertd166e, 2610509L04Rik, Clast4, A930019J01Rik

MMRRC Submission

045467-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.494) question?

Stock #

R7385 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

3152392-3194588 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 3170269 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 107 (D107E)

Ref Sequence

ENSEMBL: ENSMUSP00000105676 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020734] [ENSMUST00000110048] [ENSMUST00000110049] [ENSMUST00000120721] [ENSMUST00000125637] [ENSMUST00000179770]

AlphaFold

Q9EST3

Predicted Effect

probably damaging
Transcript: ENSMUST00000020734
AA Change: D107E

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

SMART Domains

Protein: ENSMUSP00000020734
Gene: ENSMUSG00000020454
AA Change: D107E

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	29	688	1.2e-189	PFAM
low complexity region	835	851	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000110048
AA Change: D107E

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

SMART Domains

Protein: ENSMUSP00000105675
Gene: ENSMUSG00000020454
AA Change: D107E

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	29	688	1.2e-189	PFAM
low complexity region	835	851	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000110049
AA Change: D107E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000105676
Gene: ENSMUSG00000020454
AA Change: D107E

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	29	712	2.7e-184	PFAM
low complexity region	859	875	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000120721

SMART Domains

Protein: ENSMUSP00000112550
Gene: ENSMUSG00000020454

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	29	99	3.6e-29	PFAM
Pfam:EIF4E-T	98	327	5.1e-41	PFAM
Pfam:EIF4E-T	282	537	7.7e-30	PFAM
low complexity region	684	700	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000125637
AA Change: D107E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000118527
Gene: ENSMUSG00000020454
AA Change: D107E

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	29	194	1.5e-73	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000159304

SMART Domains

Protein: ENSMUSP00000125536
Gene: ENSMUSG00000020457

Domain	Start	End	E-Value	Type
Pfam:TGS	13	58	5.7e-14	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000179770
AA Change: D107E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000136768
Gene: ENSMUSG00000020454
AA Change: D107E

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	29	710	4.3e-160	PFAM
low complexity region	859	875	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (75/75)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a nucleocytoplasmic shuttle protein for the translation initiation factor eIF4E. This shuttle protein interacts with the importin alpha-beta complex to mediate nuclear import of eIF4E. It is predominantly cytoplasmic; its own nuclear import is regulated by a nuclear localization signal and nuclear export signals. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]

Allele List at MGI

Other mutations in this stock

Total: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahctf1	T	C	1: 179,580,946 (GRCm39)	E1752G	possibly damaging	Het
Aqp3	T	C	4: 41,095,178 (GRCm39)	T68A	probably damaging	Het
Arhgap40	A	G	2: 158,385,147 (GRCm39)	K463R	probably damaging	Het
Asb10	A	T	5: 24,738,736 (GRCm39)	C440*	probably null	Het
Bach1	A	G	16: 87,526,385 (GRCm39)	T616A	probably damaging	Het
Braf	T	A	6: 39,642,042 (GRCm39)		probably null	Het
Cacna1s	A	T	1: 136,020,371 (GRCm39)	N803Y	probably damaging	Het
Cald1	A	G	6: 34,663,000 (GRCm39)	E21G	probably damaging	Het
Caskin1	G	T	17: 24,722,898 (GRCm39)	G589C	probably damaging	Het
Cdc37l1	T	C	19: 28,968,071 (GRCm39)		probably null	Het
Cntnap5b	G	A	1: 100,306,815 (GRCm39)	G844D	probably damaging	Het
Col5a1	T	C	2: 27,914,762 (GRCm39)	L1615P	unknown	Het
Cpt1a	C	A	19: 3,430,155 (GRCm39)	P672T	probably damaging	Het
Defb22	A	G	2: 152,328,117 (GRCm39)	Y23H	probably damaging	Het
Depdc1b	G	C	13: 108,500,166 (GRCm39)	K226N	probably damaging	Het
Derl2	A	G	11: 70,909,764 (GRCm39)		probably benign	Het
Dnaja2	T	C	8: 86,265,982 (GRCm39)	T368A	probably benign	Het
Dsg3	C	A	18: 20,673,254 (GRCm39)	T975K	possibly damaging	Het
Fut11	A	G	14: 20,746,325 (GRCm39)	D389G	probably damaging	Het
Gopc	C	T	10: 52,225,328 (GRCm39)	G299E	probably damaging	Het
Gprin1	T	C	13: 54,886,423 (GRCm39)	D617G	probably benign	Het
Grin2d	A	G	7: 45,506,960 (GRCm39)	V505A	probably damaging	Het
Heatr6	T	C	11: 83,650,161 (GRCm39)	Y206H	probably damaging	Het
Hhex	C	A	19: 37,425,713 (GRCm39)	N147K	probably damaging	Het
Igkv4-80	G	A	6: 68,993,699 (GRCm39)	S64F	probably damaging	Het
Jakmip3	A	G	7: 138,625,068 (GRCm39)	K360R	possibly damaging	Het
Kat5	AG	A	19: 5,658,297 (GRCm39)		probably null	Het
Kat5	T	A	19: 5,658,302 (GRCm39)	N191I	probably benign	Het
Kifc5b	A	G	17: 27,144,597 (GRCm39)	D572G	probably damaging	Het
Lrp5	C	A	19: 3,662,197 (GRCm39)		probably null	Het
Lrtm1	A	G	14: 28,749,673 (GRCm39)	M345V	probably benign	Het
Mbd5	T	C	2: 49,162,461 (GRCm39)	V981A	probably benign	Het
Mier3	G	A	13: 111,841,783 (GRCm39)	G115S	possibly damaging	Het
Mrgprd	A	G	7: 144,875,261 (GRCm39)	N44S	probably damaging	Het
Mrps10	C	A	17: 47,689,146 (GRCm39)	P181Q	probably damaging	Het
Myot	T	A	18: 44,470,075 (GRCm39)	C17*	probably null	Het
Myt1	A	G	2: 181,409,498 (GRCm39)		probably null	Het
Ncoa6	C	A	2: 155,249,721 (GRCm39)	L1194F	probably damaging	Het
Or4d11	T	C	19: 12,013,363 (GRCm39)	T248A	probably benign	Het
Or4d6	T	C	19: 12,086,061 (GRCm39)	N57S	probably damaging	Het
Or4e5	T	C	14: 52,727,638 (GRCm39)	Y261C	probably damaging	Het
Or7a39	C	A	10: 78,715,288 (GRCm39)	T94K	probably damaging	Het
Or7e165	T	A	9: 19,694,507 (GRCm39)	I26N	possibly damaging	Het
Osbpl6	G	A	2: 76,379,794 (GRCm39)	G128E	probably damaging	Het
P3h3	A	T	6: 124,832,233 (GRCm39)	Y218N	probably damaging	Het
Paxip1	A	G	5: 27,986,418 (GRCm39)		probably null	Het
Pdia5	T	C	16: 35,250,284 (GRCm39)	Y225C	probably damaging	Het
Pik3c2g	T	G	6: 139,801,079 (GRCm39)	M526R		Het
Prox1	A	G	1: 189,894,323 (GRCm39)	F41L	probably benign	Het
Psd3	A	T	8: 68,453,408 (GRCm39)	F284I	probably damaging	Het
Rev3l	T	A	10: 39,699,678 (GRCm39)	C1392S	probably benign	Het
Rfxank	A	T	8: 70,587,285 (GRCm39)	V212E	probably damaging	Het
Ros1	T	C	10: 52,031,222 (GRCm39)	D482G	probably benign	Het
Sat2	A	T	11: 69,513,763 (GRCm39)	I94F	probably damaging	Het
Scarf2	T	C	16: 17,621,702 (GRCm39)	L384P	probably damaging	Het
Sec14l2	C	A	11: 4,066,750 (GRCm39)	E21*	probably null	Het
Slitrk5	T	A	14: 111,918,131 (GRCm39)	V585E	probably benign	Het
Spata31h1	T	A	10: 82,123,571 (GRCm39)	E3146D	probably benign	Het
Spata31h1	T	C	10: 82,123,729 (GRCm39)	S3094G	probably benign	Het
Tas2r130	T	A	6: 131,607,226 (GRCm39)	M190L	probably benign	Het
Ticrr	G	A	7: 79,341,597 (GRCm39)	S1061N	possibly damaging	Het
Tlr9	C	A	9: 106,102,463 (GRCm39)	H585N	probably damaging	Het
Tmem219	A	T	7: 126,495,947 (GRCm39)	I142N	probably damaging	Het
Tnni2	A	G	7: 141,996,915 (GRCm39)	N8S	probably benign	Het
Tnpo2	G	A	8: 85,776,748 (GRCm39)	R485H	probably damaging	Het
Ttc8	A	G	12: 98,908,547 (GRCm39)	E72G	possibly damaging	Het
Upf1	A	G	8: 70,793,268 (GRCm39)	Y297H	probably damaging	Het
Vmn1r4	A	G	6: 56,933,721 (GRCm39)	K75R	probably damaging	Het
Vmn2r78	G	A	7: 86,571,633 (GRCm39)	G481D	probably benign	Het
Vmn2r96	A	G	17: 18,803,302 (GRCm39)	Y404C	probably damaging	Het
Vps50	T	A	6: 3,602,708 (GRCm39)	S942T	probably benign	Het
Xkr7	C	A	2: 152,895,983 (GRCm39)	S279*	probably null	Het
Zan	G	A	5: 137,432,416 (GRCm39)	Q2294*	probably null	Het
Zan	T	C	5: 137,448,753 (GRCm39)	Y1700C	unknown	Het

Other mutations in Eif4enif1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01139:Eif4enif1	APN	11	3,171,143 (GRCm39)	missense	probably damaging	0.96
IGL02237:Eif4enif1	APN	11	3,177,876 (GRCm39)	nonsense	probably null
IGL02372:Eif4enif1	APN	11	3,179,986 (GRCm39)	missense	probably benign	0.09
PIT4283001:Eif4enif1	UTSW	11	3,184,464 (GRCm39)	missense	probably damaging	1.00
R0079:Eif4enif1	UTSW	11	3,192,676 (GRCm39)	nonsense	probably null
R1177:Eif4enif1	UTSW	11	3,179,902 (GRCm39)	missense	probably damaging	1.00
R1220:Eif4enif1	UTSW	11	3,189,493 (GRCm39)	splice site	probably benign
R1511:Eif4enif1	UTSW	11	3,186,278 (GRCm39)	missense	probably benign	0.00
R1675:Eif4enif1	UTSW	11	3,165,686 (GRCm39)	missense	probably benign	0.02
R1908:Eif4enif1	UTSW	11	3,177,455 (GRCm39)	missense	probably damaging	1.00
R1940:Eif4enif1	UTSW	11	3,193,279 (GRCm39)	missense	probably damaging	1.00
R2173:Eif4enif1	UTSW	11	3,192,367 (GRCm39)	splice site	probably null
R2215:Eif4enif1	UTSW	11	3,177,476 (GRCm39)	missense	probably damaging	1.00
R2517:Eif4enif1	UTSW	11	3,171,168 (GRCm39)	missense	probably damaging	1.00
R2869:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R2869:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R2870:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R2870:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R2871:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R2871:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R2873:Eif4enif1	UTSW	11	3,192,586 (GRCm39)	missense	probably damaging	1.00
R3147:Eif4enif1	UTSW	11	3,194,003 (GRCm39)	splice site	probably null
R4195:Eif4enif1	UTSW	11	3,193,186 (GRCm39)	missense	possibly damaging	0.89
R4196:Eif4enif1	UTSW	11	3,193,186 (GRCm39)	missense	possibly damaging	0.89
R4708:Eif4enif1	UTSW	11	3,170,323 (GRCm39)	missense	probably damaging	1.00
R4755:Eif4enif1	UTSW	11	3,194,016 (GRCm39)	missense	probably damaging	1.00
R5310:Eif4enif1	UTSW	11	3,192,687 (GRCm39)	missense	probably damaging	1.00
R5546:Eif4enif1	UTSW	11	3,193,989 (GRCm39)	missense	probably damaging	0.99
R5816:Eif4enif1	UTSW	11	3,192,401 (GRCm39)	missense	probably benign	0.13
R6018:Eif4enif1	UTSW	11	3,192,481 (GRCm39)	missense	probably damaging	0.97
R6036:Eif4enif1	UTSW	11	3,189,420 (GRCm39)	missense	probably damaging	1.00
R6036:Eif4enif1	UTSW	11	3,189,420 (GRCm39)	missense	probably damaging	1.00
R6267:Eif4enif1	UTSW	11	3,177,793 (GRCm39)	missense	probably damaging	1.00
R6514:Eif4enif1	UTSW	11	3,190,996 (GRCm39)	missense	probably null	0.01
R6638:Eif4enif1	UTSW	11	3,192,463 (GRCm39)	missense	probably damaging	0.96
R7040:Eif4enif1	UTSW	11	3,184,040 (GRCm39)	missense	probably benign	0.33
R7232:Eif4enif1	UTSW	11	3,165,678 (GRCm39)	missense	possibly damaging	0.75
R7478:Eif4enif1	UTSW	11	3,177,709 (GRCm39)	nonsense	probably null
R7749:Eif4enif1	UTSW	11	3,192,608 (GRCm39)	missense	probably damaging	0.99
R8381:Eif4enif1	UTSW	11	3,177,470 (GRCm39)	missense	probably damaging	1.00
R9029:Eif4enif1	UTSW	11	3,174,716 (GRCm39)	missense	probably damaging	1.00
R9622:Eif4enif1	UTSW	11	3,165,714 (GRCm39)	missense	probably benign	0.26
R9646:Eif4enif1	UTSW	11	3,170,280 (GRCm39)	missense	probably damaging	1.00
R9694:Eif4enif1	UTSW	11	3,170,384 (GRCm39)	missense	probably damaging	0.98
R9747:Eif4enif1	UTSW	11	3,163,267 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GTTTAGGTTGCACATCTAGATGC -3'
(R):5'- CCCGGGCAGAAATTATCCTTC -3'

Sequencing Primer
(F):5'- GCGCTATCTCATTGGTAAAGGCAC -3'
(R):5'- GGGCAGAAATTATCCTTCCACTG -3'

Posted On

2019-09-13