Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL02372:Eif4enif1'

290977

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Eif4enif1

Ensembl Gene

ENSMUSG00000020454

Gene Name

eukaryotic translation initiation factor 4E nuclear import factor 1

Synonyms

D11Ertd166e, 2610509L04Rik, Clast4, A930019J01Rik

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.476) question?

Stock #

IGL02372

Quality Score

Status

Chromosome

Chromosomal Location

3202392-3244588 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 3229986 bp

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 302 (L302P)

Ref Sequence

ENSEMBL: ENSMUSP00000112550 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020734] [ENSMUST00000110048] [ENSMUST00000110049] [ENSMUST00000120721] [ENSMUST00000135223] [ENSMUST00000179770]

Predicted Effect

probably benign
Transcript: ENSMUST00000020734
AA Change: L465P

PolyPhen 2 Score 0.032 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000020734
Gene: ENSMUSG00000020454
AA Change: L465P

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 benign
Transcript: ENSMUST00000110048
AA Change: L465P

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000105675
Gene: ENSMUSG00000020454
AA Change: L465P

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 benign
Transcript: ENSMUST00000110049
AA Change: L465P

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000105676
Gene: ENSMUSG00000020454
AA Change: L465P

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
AA Change: L302P

PolyPhen 2 Score 0.090 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000112550
Gene: ENSMUSG00000020454
AA Change: L302P

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

noncoding transcript
Transcript: ENSMUST00000127950

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132425

Predicted Effect

probably benign
Transcript: ENSMUST00000135223
AA Change: L64P

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000122912
Gene: ENSMUSG00000020454
AA Change: L64P

Domain	Start	End	E-Value	Type
Pfam:EIF4E-T	1	239	1.5e-16	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143770

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 benign
Transcript: ENSMUST00000179770
AA Change: L465P

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000136768
Gene: ENSMUSG00000020454
AA Change: L465P

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

Validation Efficiency

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: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700001P01Rik	A	T	11: 97,775,699	Y54N	probably damaging	Het
Alyref	A	G	11: 120,594,875		probably benign	Het
Ankrd27	A	G	7: 35,633,036		probably null	Het
Arc	A	G	15: 74,672,105	S90P	probably damaging	Het
Atp6v1e1	T	A	6: 120,801,123	K150N	probably benign	Het
Atrn	T	C	2: 131,002,754		probably benign	Het
Ccnb1	A	G	13: 100,781,316	Y259H	probably damaging	Het
Celsr1	A	G	15: 85,929,907	V1938A	probably benign	Het
Ckmt2	A	G	13: 91,865,224	V37A	probably benign	Het
Dpys	G	T	15: 39,793,271	P467T	probably benign	Het
Ehbp1l1	T	C	19: 5,710,834	T1535A	possibly damaging	Het
Faf1	T	G	4: 109,935,582	F584V	probably benign	Het
Glb1l2	G	A	9: 26,796,476	R72C	probably damaging	Het
Gm9892	T	C	8: 52,196,836		noncoding transcript	Het
Hecw1	G	T	13: 14,264,121	D892E	probably damaging	Het
Hr	A	G	14: 70,558,350	E474G	possibly damaging	Het
Ltbp1	T	G	17: 75,252,406	F297V	probably damaging	Het
Myc	A	G	15: 61,987,858	N127D	probably damaging	Het
Nbn	T	A	4: 15,986,613	N671K	probably benign	Het
Nup210l	C	A	3: 90,201,971	T1607N	possibly damaging	Het
Olfr281	A	T	15: 98,456,828	T173S	probably damaging	Het
Osbpl1a	T	A	18: 12,841,313	K22*	probably null	Het
Phf20l1	T	C	15: 66,641,801	L942P	probably damaging	Het
Plekhg5	C	T	4: 152,102,080	R40W	probably damaging	Het
Pomt2	C	T	12: 87,122,835		probably benign	Het
Rab3gap1	A	G	1: 127,919,561		probably benign	Het
Sbk1	T	C	7: 126,291,058	L81P	probably damaging	Het
Scrib	G	A	15: 76,048,255	P1524S	probably damaging	Het
Smpdl3a	T	A	10: 57,807,515	N240K	probably benign	Het
Smyd4	A	T	11: 75,390,285	K195*	probably null	Het
Tulp3	A	T	6: 128,327,598	M231K	possibly damaging	Het
Zfp87	A	G	13: 67,520,620		probably benign	Het

Other mutations in Eif4enif1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01139:Eif4enif1	APN	11	3221143	missense	probably damaging	0.96
IGL02237:Eif4enif1	APN	11	3227876	nonsense	probably null
PIT4283001:Eif4enif1	UTSW	11	3234464	missense	probably damaging	1.00
R0079:Eif4enif1	UTSW	11	3242676	nonsense	probably null
R1177:Eif4enif1	UTSW	11	3229902	missense	probably damaging	1.00
R1220:Eif4enif1	UTSW	11	3239493	splice site	probably benign
R1511:Eif4enif1	UTSW	11	3236278	missense	probably benign	0.00
R1675:Eif4enif1	UTSW	11	3215686	missense	probably benign	0.02
R1908:Eif4enif1	UTSW	11	3227455	missense	probably damaging	1.00
R1940:Eif4enif1	UTSW	11	3243279	missense	probably damaging	1.00
R2173:Eif4enif1	UTSW	11	3242367	splice site	probably null
R2215:Eif4enif1	UTSW	11	3227476	missense	probably damaging	1.00
R2517:Eif4enif1	UTSW	11	3221168	missense	probably damaging	1.00
R2869:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R2869:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R2870:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R2870:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R2871:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R2871:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R2873:Eif4enif1	UTSW	11	3242586	missense	probably damaging	1.00
R3147:Eif4enif1	UTSW	11	3244003	splice site	probably null
R4195:Eif4enif1	UTSW	11	3243186	missense	possibly damaging	0.89
R4196:Eif4enif1	UTSW	11	3243186	missense	possibly damaging	0.89
R4708:Eif4enif1	UTSW	11	3220323	missense	probably damaging	1.00
R4755:Eif4enif1	UTSW	11	3244016	missense	probably damaging	1.00
R5310:Eif4enif1	UTSW	11	3242687	missense	probably damaging	1.00
R5546:Eif4enif1	UTSW	11	3243989	missense	probably damaging	0.99
R5816:Eif4enif1	UTSW	11	3242401	missense	probably benign	0.13
R6018:Eif4enif1	UTSW	11	3242481	missense	probably damaging	0.97
R6036:Eif4enif1	UTSW	11	3239420	missense	probably damaging	1.00
R6036:Eif4enif1	UTSW	11	3239420	missense	probably damaging	1.00
R6267:Eif4enif1	UTSW	11	3227793	missense	probably damaging	1.00
R6514:Eif4enif1	UTSW	11	3240996	missense	probably null	0.01
R6638:Eif4enif1	UTSW	11	3242463	missense	probably damaging	0.96
R7040:Eif4enif1	UTSW	11	3234040	missense	probably benign	0.33
R7232:Eif4enif1	UTSW	11	3215678	missense	possibly damaging	0.75
R7385:Eif4enif1	UTSW	11	3220269	missense	probably damaging	1.00
R7478:Eif4enif1	UTSW	11	3227709	nonsense	probably null
R7749:Eif4enif1	UTSW	11	3242608	missense	probably damaging	0.99
R8381:Eif4enif1	UTSW	11	3227470	missense	probably damaging	1.00

Posted On

2015-04-16