Mutagenetix > Incidental Mutation

Incidental Mutation 'R4471:Nemf'

329453

Institutional Source

Beutler Lab

Gene Symbol

Nemf

Ensembl Gene

ENSMUSG00000020982

Gene Name

nuclear export mediator factor

Synonyms

Sdccag1, 1500011I12Rik, 4933405E14Rik

MMRRC Submission

041728-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4471 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

69358315-69403975 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 69361216 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Tyrosine at position 956 (H956Y)

Ref Sequence

ENSEMBL: ENSMUSP00000021368 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021362] [ENSMUST00000021368]

AlphaFold

Q8CCP0

Predicted Effect

probably benign
Transcript: ENSMUST00000021362

SMART Domains

Protein: ENSMUSP00000021362
Gene: ENSMUSG00000020978

Domain	Start	End	E-Value	Type
internal_repeat_1	7	117	3.66e-6	PROSPERO
internal_repeat_2	66	163	6.25e-5	PROSPERO
Pfam:Kelch_1	217	258	1.4e-6	PFAM
Pfam:Kelch_2	217	262	1.2e-7	PFAM
Pfam:Kelch_4	217	266	8.4e-8	PFAM
Pfam:Kelch_3	227	276	5.1e-9	PFAM
Pfam:Kelch_5	265	305	1.4e-6	PFAM
Pfam:Kelch_4	267	310	2e-9	PFAM
Pfam:Kelch_3	278	326	1.4e-7	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000021368
AA Change: H956Y

PolyPhen 2 Score 0.043 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000021368
Gene: ENSMUSG00000020982
AA Change: H956Y

Domain	Start	End	E-Value	Type
Pfam:FbpA	6	523	5.5e-42	PFAM
Pfam:DUF814	530	630	9e-27	PFAM
low complexity region	697	708	N/A	INTRINSIC
low complexity region	861	879	N/A	INTRINSIC
low complexity region	894	918	N/A	INTRINSIC
Pfam:DUF3441	956	1055	9.8e-33	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221112

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221193

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221278

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221794

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.4%

Validation Efficiency

99% (69/70)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a component of the ribosome quality control complex. The encoded protein facilitates the recognition and ubiquitination of stalled 60S subunits by the ubiquitin ligase listerin. A similar protein in fly functions as a tumor suppressor. [provided by RefSeq, Jul 2016]

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alpk1	A	G	3: 127,473,175 (GRCm39)	S943P	probably damaging	Het
Ankdd1a	T	C	9: 65,410,791 (GRCm39)	D398G	probably damaging	Het
Ankrd13b	T	A	11: 77,367,040 (GRCm39)	K49M	probably damaging	Het
Asah1	A	G	8: 41,796,761 (GRCm39)		probably null	Het
Cdc34b	A	G	11: 94,633,064 (GRCm39)	E88G	probably benign	Het
Cdh2	T	C	18: 16,907,533 (GRCm39)		probably null	Het
Ceacam1	T	A	7: 25,174,025 (GRCm39)	N210I	possibly damaging	Het
Celf3	A	G	3: 94,395,585 (GRCm39)		probably null	Het
Cfap20dc	A	G	14: 8,536,571 (GRCm38)	L212P	probably damaging	Het
Cmya5	A	T	13: 93,228,833 (GRCm39)	M2085K	probably benign	Het
Cpne6	G	A	14: 55,754,089 (GRCm39)	V469M	probably damaging	Het
Cyp2j12	A	G	4: 96,021,306 (GRCm39)	V100A	probably benign	Het
Dnajb4	A	T	3: 151,890,799 (GRCm39)	H333Q	probably benign	Het
Eif3f	T	C	7: 108,540,153 (GRCm39)	V316A	possibly damaging	Het
Eml1	T	C	12: 108,472,894 (GRCm39)		probably benign	Het
Ern1	C	A	11: 106,310,868 (GRCm39)	V302L	possibly damaging	Het
Fam110b	A	T	4: 5,799,092 (GRCm39)	H170L	probably benign	Het
Fn3krp	T	G	11: 121,317,499 (GRCm39)	D146E	probably benign	Het
Git1	A	G	11: 77,390,650 (GRCm39)	T129A	probably benign	Het
Glrp1	T	A	1: 88,431,196 (GRCm39)	Q58L	unknown	Het
Gpatch2	A	G	1: 186,965,337 (GRCm39)	E281G	probably damaging	Het
Hipk2	T	A	6: 38,713,857 (GRCm39)		probably benign	Het
Hydin	A	G	8: 111,313,764 (GRCm39)	N4214S	probably damaging	Het
Icam5	T	A	9: 20,946,802 (GRCm39)	C443*	probably null	Het
Impdh1	G	A	6: 29,204,631 (GRCm39)	Q307*	probably null	Het
Ivns1abp	C	T	1: 151,236,990 (GRCm39)	T447M	probably benign	Het
Lman1	A	T	18: 66,124,797 (GRCm39)		probably benign	Het
Mdn1	A	G	4: 32,668,860 (GRCm39)	E306G	probably benign	Het
Msc	G	C	1: 14,825,902 (GRCm39)	P24R	probably damaging	Het
Mtif2	T	C	11: 29,490,053 (GRCm39)		probably benign	Het
Mvp	C	T	7: 126,601,130 (GRCm39)	M1I	probably null	Het
Myh7	A	T	14: 55,229,311 (GRCm39)	Y162*	probably null	Het
Nktr	T	C	9: 121,577,962 (GRCm39)		probably benign	Het
Nrxn3	T	C	12: 90,171,515 (GRCm39)	S276P	probably damaging	Het
Or8d1	T	C	9: 38,766,927 (GRCm39)	S190P	probably damaging	Het
Patj	A	G	4: 98,423,816 (GRCm39)	K621E	probably damaging	Het
Prss2	A	G	6: 41,499,780 (GRCm39)	I24V	probably damaging	Het
R3hcc1l	T	C	19: 42,571,259 (GRCm39)		probably benign	Het
Rest	T	C	5: 77,429,027 (GRCm39)	V482A	probably benign	Het
Rexo1	A	T	10: 80,378,492 (GRCm39)	S476T	probably damaging	Het
Rin2	C	T	2: 145,702,366 (GRCm39)	T354I	probably benign	Het
Slc16a3	T	C	11: 120,846,774 (GRCm39)		probably benign	Het
Slc5a4b	G	A	10: 75,894,725 (GRCm39)	Q594*	probably null	Het
Slk	T	G	19: 47,603,862 (GRCm39)	V202G	probably damaging	Het
Smarca2	T	A	19: 26,597,277 (GRCm39)	V53D	possibly damaging	Het
Snrnp200	T	A	2: 127,080,673 (GRCm39)	V2036E	probably benign	Het
Sox5	A	G	6: 143,790,491 (GRCm39)	M523T	possibly damaging	Het
Syt17	A	G	7: 118,036,040 (GRCm39)		probably null	Het
Taf2	T	C	15: 54,922,276 (GRCm39)	D337G	possibly damaging	Het
Tcstv2a	G	T	13: 120,725,579 (GRCm39)	R81L	probably benign	Het
Tecrl	A	G	5: 83,461,134 (GRCm39)	Y108H	probably benign	Het
Tln1	A	T	4: 43,551,018 (GRCm39)	F409L	probably benign	Het
Tmem59l	A	G	8: 70,939,951 (GRCm39)	L6S	unknown	Het
Ttc23	G	A	7: 67,319,904 (GRCm39)	R187Q	probably benign	Het
Ttl	T	C	2: 128,923,977 (GRCm39)	V230A	probably benign	Het
Ube2u	G	A	4: 100,338,843 (GRCm39)	W36*	probably null	Het
Ube4a	A	T	9: 44,857,830 (GRCm39)		probably benign	Het
Ulk1	C	T	5: 110,937,223 (GRCm39)	R691Q	probably benign	Het
Unc45a	A	G	7: 79,982,728 (GRCm39)	I399T	possibly damaging	Het
Utp25	C	T	1: 192,812,445 (GRCm39)	R5Q	possibly damaging	Het
Wdr59	A	C	8: 112,193,419 (GRCm39)		probably null	Het
Zfp24	A	G	18: 24,151,172 (GRCm39)		probably benign	Het
Zfp777	A	T	6: 48,019,041 (GRCm39)	W342R	probably damaging	Het
Zfp979	A	T	4: 147,697,913 (GRCm39)	C265*	probably null	Het
Zzef1	T	A	11: 72,804,157 (GRCm39)	L2633Q	probably damaging	Het

Other mutations in Nemf

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01508:Nemf	APN	12	69,391,760 (GRCm39)	splice site	probably benign
IGL02499:Nemf	APN	12	69,368,903 (GRCm39)	missense	probably damaging	1.00
IGL03352:Nemf	APN	12	69,378,679 (GRCm39)	missense	probably damaging	1.00
kaempfer	UTSW	12	69,399,110 (GRCm39)	missense	probably benign	0.01
R0335:Nemf	UTSW	12	69,400,577 (GRCm39)	missense	probably benign	0.16
R0538:Nemf	UTSW	12	69,403,088 (GRCm39)	missense	probably damaging	1.00
R0581:Nemf	UTSW	12	69,369,045 (GRCm39)	missense	probably benign
R0909:Nemf	UTSW	12	69,388,384 (GRCm39)	missense	probably damaging	1.00
R1792:Nemf	UTSW	12	69,359,343 (GRCm39)	missense	probably damaging	1.00
R1899:Nemf	UTSW	12	69,393,152 (GRCm39)	missense	probably null
R2080:Nemf	UTSW	12	69,400,560 (GRCm39)	splice site	probably benign
R3704:Nemf	UTSW	12	69,377,904 (GRCm39)	missense	probably damaging	1.00
R3842:Nemf	UTSW	12	69,378,723 (GRCm39)	missense	probably damaging	0.98
R4666:Nemf	UTSW	12	69,359,054 (GRCm39)	missense	probably damaging	1.00
R4720:Nemf	UTSW	12	69,371,062 (GRCm39)	missense	probably benign	0.05
R5198:Nemf	UTSW	12	69,402,821 (GRCm39)	missense	probably damaging	1.00
R5474:Nemf	UTSW	12	69,363,109 (GRCm39)	missense	probably benign	0.03
R6893:Nemf	UTSW	12	69,399,110 (GRCm39)	missense	probably benign	0.01
R7008:Nemf	UTSW	12	69,400,567 (GRCm39)	critical splice donor site	probably null
R7008:Nemf	UTSW	12	69,388,395 (GRCm39)	missense	possibly damaging	0.91
R7098:Nemf	UTSW	12	69,359,241 (GRCm39)	missense	probably damaging	1.00
R7154:Nemf	UTSW	12	69,363,515 (GRCm39)	critical splice donor site	probably null
R7452:Nemf	UTSW	12	69,384,733 (GRCm39)	splice site	probably null
R8130:Nemf	UTSW	12	69,402,826 (GRCm39)	missense	possibly damaging	0.91
R8340:Nemf	UTSW	12	69,400,659 (GRCm39)	missense	possibly damaging	0.94
R8914:Nemf	UTSW	12	69,363,089 (GRCm39)	nonsense	probably null
R9089:Nemf	UTSW	12	69,400,628 (GRCm39)	missense	probably damaging	1.00
R9150:Nemf	UTSW	12	69,387,820 (GRCm39)	missense	probably benign	0.00
R9228:Nemf	UTSW	12	69,388,093 (GRCm39)	missense	probably damaging	1.00
R9644:Nemf	UTSW	12	69,359,436 (GRCm39)	missense	possibly damaging	0.64

Predicted Primers

PCR Primer
(F):5'- TTGAGACTTGCAGAGTTACATACAG -3'
(R):5'- CCCTAAGTAAAAGGTTTTGTCACTG -3'

Sequencing Primer
(F):5'- GCAGAGTTACATACAGCACATATG -3'
(R):5'- GGTTTTGTCACTGGTTAAAAACAC -3'

Posted On

2015-07-21