Mutagenetix > Incidental Mutation

Incidental Mutation 'R4620:Xpo4'

345266

Institutional Source

Beutler Lab

Gene Symbol

Xpo4

Ensembl Gene

ENSMUSG00000021952

Gene Name

exportin 4

Synonyms

B430309A01Rik

MMRRC Submission

042008-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.722) question?

Stock #

R4620 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

57814978-57902887 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 57867782 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Glutamine at position 155 (L155Q)

Ref Sequence

ENSEMBL: ENSMUSP00000133280 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000089482] [ENSMUST00000174152] [ENSMUST00000174545]

AlphaFold

Q9ESJ0

Predicted Effect

probably damaging
Transcript: ENSMUST00000089482
AA Change: L155Q

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

SMART Domains

Protein: ENSMUSP00000086909
Gene: ENSMUSG00000021952
AA Change: L155Q

Domain	Start	End	E-Value	Type
Blast:IBN_N	37	103	8e-19	BLAST
low complexity region	165	174	N/A	INTRINSIC
low complexity region	459	468	N/A	INTRINSIC
low complexity region	506	517	N/A	INTRINSIC
low complexity region	911	922	N/A	INTRINSIC
Pfam:CRM1_C	954	1144	6.3e-8	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000174152

Predicted Effect

probably damaging
Transcript: ENSMUST00000174545
AA Change: L155Q

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

SMART Domains

Protein: ENSMUSP00000133280
Gene: ENSMUSG00000021952
AA Change: L155Q

Domain	Start	End	E-Value	Type
Blast:IBN_N	37	103	8e-19	BLAST
low complexity region	165	174	N/A	INTRINSIC
low complexity region	459	468	N/A	INTRINSIC
low complexity region	506	517	N/A	INTRINSIC
low complexity region	911	922	N/A	INTRINSIC
Pfam:CRM1_C	952	1143	5.2e-9	PFAM

Meta Mutation Damage Score

0.5530

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

99% (80/81)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] XPO4 belongs to a large family of karyopherins (see MIM 602738) that mediate the transport of proteins and other cargo between the nuclear and cytoplasmic compartments (Lipowsky et al., 2000 [PubMed 10944119]).[supplied by OMIM, Mar 2009]
PHENOTYPE: Mice homozygous for a gene trapped allele appear phenotypically normal. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310057M21Rik	A	T	7: 130,945,335 (GRCm39)	Y433*	probably null	Het
Apba2	C	T	7: 64,364,215 (GRCm39)	R331C	probably damaging	Het
Apod	T	C	16: 31,116,211 (GRCm39)	D173G	probably benign	Het
B3gnt5	A	T	16: 19,588,632 (GRCm39)	M284L	probably benign	Het
Birc6	A	C	17: 74,947,145 (GRCm39)	T2955P	probably benign	Het
Blvra	T	C	2: 126,938,885 (GRCm39)	I287T	probably damaging	Het
Capn5	T	C	7: 97,778,578 (GRCm39)	Y347C	probably damaging	Het
Cdcp2	A	G	4: 106,963,927 (GRCm39)	E259G	probably damaging	Het
Cdh2	A	G	18: 16,781,665 (GRCm39)	V85A	probably benign	Het
Cdk5rap2	A	G	4: 70,184,943 (GRCm39)	I1169T	probably benign	Het
Cenpj	A	G	14: 56,772,911 (GRCm39)	V1043A	probably damaging	Het
Cfap54	T	A	10: 92,805,619 (GRCm39)	H1497L	probably benign	Het
Chat	A	G	14: 32,175,775 (GRCm39)	M95T	probably damaging	Het
Csmd1	T	C	8: 16,052,694 (GRCm39)		probably null	Het
Csmd3	T	C	15: 47,449,149 (GRCm39)	E3615G	probably benign	Het
Cyp2c68	A	T	19: 39,701,006 (GRCm39)		probably null	Het
Dll1	C	T	17: 15,590,828 (GRCm39)	A332T	probably benign	Het
Dmrta1	A	T	4: 89,577,021 (GRCm39)	Q159L	probably benign	Het
Dnai3	A	T	3: 145,748,564 (GRCm39)	L850Q	probably damaging	Het
Eci3	A	T	13: 35,132,741 (GRCm39)	M212K	probably damaging	Het
Eml4	T	C	17: 83,768,962 (GRCm39)	F557L	probably benign	Het
Fat3	A	T	9: 15,908,190 (GRCm39)	V2604D	probably damaging	Het
Frem3	T	C	8: 81,395,586 (GRCm39)	V1871A	possibly damaging	Het
Gart	T	C	16: 91,422,321 (GRCm39)	N732S	probably damaging	Het
Gas2l2	T	C	11: 83,313,924 (GRCm39)	I463V	probably benign	Het
H2-M3	C	A	17: 37,583,310 (GRCm39)	T257K	probably damaging	Het
Hdgf	A	G	3: 87,821,883 (GRCm39)	N166S	possibly damaging	Het
Hoxb3	A	T	11: 96,236,599 (GRCm39)	N226Y	probably damaging	Het
Itgav	T	C	2: 83,586,246 (GRCm39)	Y169H	probably benign	Het
Kalrn	T	G	16: 33,849,075 (GRCm39)	I426L	probably damaging	Het
Kcnh3	G	A	15: 99,131,982 (GRCm39)	V646M	probably damaging	Het
Kif6	T	C	17: 50,208,324 (GRCm39)	V735A	probably benign	Het
Krt1c	T	A	15: 101,726,026 (GRCm39)	I171F	probably damaging	Het
Megf8	G	A	7: 25,054,523 (GRCm39)	A1880T	possibly damaging	Het
Miox	A	T	15: 89,220,324 (GRCm39)	Y172F	probably benign	Het
Myo18a	G	A	11: 77,708,773 (GRCm39)	R48H	possibly damaging	Het
Ndufb7	T	C	8: 84,293,487 (GRCm39)	S14P	probably damaging	Het
Npepps	A	T	11: 97,129,070 (GRCm39)	H371Q	probably damaging	Het
Or10d5j	C	T	9: 39,868,205 (GRCm39)	V9M	probably damaging	Het
Or52e15	T	A	7: 104,645,830 (GRCm39)	I94F	probably damaging	Het
Or52e19	C	T	7: 102,959,165 (GRCm39)	T79I	probably benign	Het
Or8b12c	A	G	9: 37,716,115 (GRCm39)	T303A	probably benign	Het
Orc5	A	T	5: 22,734,174 (GRCm39)	D203E	probably damaging	Het
Pappa	A	G	4: 65,245,265 (GRCm39)	T1518A	probably benign	Het
Pde6a	A	G	18: 61,395,563 (GRCm39)	D602G	probably damaging	Het
Pnliprp2	G	A	19: 58,750,718 (GRCm39)	V136I	possibly damaging	Het
Postn	A	C	3: 54,284,414 (GRCm39)	D627A	probably damaging	Het
Prpf39	T	C	12: 65,089,337 (GRCm39)	V25A	probably benign	Het
Pxdc1	A	G	13: 34,836,297 (GRCm39)	I41T	probably damaging	Het
Rab11fip1	T	A	8: 27,644,243 (GRCm39)	E514V	probably damaging	Het
Rag1	A	T	2: 101,474,025 (GRCm39)	H372Q	probably damaging	Het
Ranbp1	A	G	16: 18,057,968 (GRCm39)		probably benign	Het
Rexo5	A	G	7: 119,426,526 (GRCm39)	I317V	probably benign	Het
Rragc	A	G	4: 123,818,622 (GRCm39)	Q279R	probably damaging	Het
Sbf1	A	G	15: 89,191,129 (GRCm39)	S187P	probably damaging	Het
Senp3	T	A	11: 69,567,944 (GRCm39)	Y432F	probably benign	Het
Slfn5	G	A	11: 82,852,478 (GRCm39)	C868Y	probably damaging	Het
Sorcs2	C	T	5: 36,194,838 (GRCm39)	A722T	probably benign	Het
Sptb	A	T	12: 76,630,581 (GRCm39)	C2244*	probably null	Het
Srbd1	A	T	17: 86,416,693 (GRCm39)	F488L	probably benign	Het
Sucnr1	A	G	3: 59,994,190 (GRCm39)	I239M	possibly damaging	Het
Themis2	A	G	4: 132,513,333 (GRCm39)	W298R	probably damaging	Het
Tmem168	T	G	6: 13,594,952 (GRCm39)	N37T	probably benign	Het
Tmem62	A	G	2: 120,826,845 (GRCm39)		probably benign	Het
Tmprss15	T	C	16: 78,818,358 (GRCm39)	D524G	probably damaging	Het
Trav5-4	G	T	14: 53,941,853 (GRCm39)	M75I	probably benign	Het
Trio	T	A	15: 27,871,257 (GRCm39)	H620L	probably damaging	Het
Ubap2	C	T	4: 41,233,698 (GRCm39)	G64E	probably damaging	Het
Usp32	C	A	11: 84,949,953 (GRCm39)		probably null	Het
Wdfy3	A	T	5: 102,054,011 (GRCm39)	F1603Y	probably damaging	Het
Zbtb21	T	C	16: 97,751,092 (GRCm39)	T1092A	possibly damaging	Het
Zfp780b	A	T	7: 27,662,178 (GRCm39)	Y792*	probably null	Het

Other mutations in Xpo4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01944:Xpo4	APN	14	57,841,855 (GRCm39)	missense	probably benign
IGL02537:Xpo4	APN	14	57,831,290 (GRCm39)	missense	probably benign
IGL02554:Xpo4	APN	14	57,827,545 (GRCm39)	missense	probably benign	0.00
IGL02826:Xpo4	APN	14	57,866,877 (GRCm39)	missense	possibly damaging	0.50
IGL03071:Xpo4	APN	14	57,855,685 (GRCm39)	missense	possibly damaging	0.66
PIT4131001:Xpo4	UTSW	14	57,822,068 (GRCm39)	missense	probably null	0.98
R0245:Xpo4	UTSW	14	57,867,697 (GRCm39)	missense	probably damaging	1.00
R0546:Xpo4	UTSW	14	57,850,731 (GRCm39)	missense	probably benign	0.07
R0606:Xpo4	UTSW	14	57,875,665 (GRCm39)	unclassified	probably benign
R0761:Xpo4	UTSW	14	57,850,840 (GRCm39)	missense	probably damaging	0.99
R1775:Xpo4	UTSW	14	57,841,129 (GRCm39)	missense	probably benign
R1853:Xpo4	UTSW	14	57,823,364 (GRCm39)	missense	possibly damaging	0.72
R1923:Xpo4	UTSW	14	57,828,328 (GRCm39)	missense	probably damaging	0.98
R2007:Xpo4	UTSW	14	57,824,101 (GRCm39)	missense	probably null	0.19
R2035:Xpo4	UTSW	14	57,823,383 (GRCm39)	missense	possibly damaging	0.57
R2174:Xpo4	UTSW	14	57,827,547 (GRCm39)	missense	probably damaging	1.00
R2421:Xpo4	UTSW	14	57,866,960 (GRCm39)	missense	probably benign	0.00
R2937:Xpo4	UTSW	14	57,841,897 (GRCm39)	missense	probably benign	0.03
R2938:Xpo4	UTSW	14	57,841,897 (GRCm39)	missense	probably benign	0.03
R4066:Xpo4	UTSW	14	57,825,511 (GRCm39)	missense	probably benign	0.07
R4086:Xpo4	UTSW	14	57,880,490 (GRCm39)	intron	probably benign
R4373:Xpo4	UTSW	14	57,828,479 (GRCm39)	nonsense	probably null
R4703:Xpo4	UTSW	14	57,827,565 (GRCm39)	missense	probably benign	0.01
R4755:Xpo4	UTSW	14	57,855,638 (GRCm39)	missense	probably benign	0.01
R4831:Xpo4	UTSW	14	57,827,559 (GRCm39)	missense	probably damaging	1.00
R4905:Xpo4	UTSW	14	57,875,746 (GRCm39)	missense	possibly damaging	0.70
R4943:Xpo4	UTSW	14	57,875,697 (GRCm39)	missense	possibly damaging	0.68
R5074:Xpo4	UTSW	14	57,822,098 (GRCm39)	missense	probably benign	0.02
R5279:Xpo4	UTSW	14	57,850,866 (GRCm39)	missense	probably benign	0.37
R5375:Xpo4	UTSW	14	57,875,764 (GRCm39)	missense	probably damaging	0.99
R5690:Xpo4	UTSW	14	57,828,446 (GRCm39)	missense	probably benign	0.03
R5936:Xpo4	UTSW	14	57,880,956 (GRCm39)	missense	probably benign
R6393:Xpo4	UTSW	14	57,875,770 (GRCm39)	missense	probably damaging	1.00
R6824:Xpo4	UTSW	14	57,850,860 (GRCm39)	missense	probably damaging	1.00
R6893:Xpo4	UTSW	14	57,819,767 (GRCm39)	missense	probably benign
R6923:Xpo4	UTSW	14	57,841,168 (GRCm39)	missense	probably benign	0.19
R7028:Xpo4	UTSW	14	57,834,508 (GRCm39)	missense	probably benign	0.22
R7442:Xpo4	UTSW	14	57,867,680 (GRCm39)	missense	probably benign	0.00
R7469:Xpo4	UTSW	14	57,835,436 (GRCm39)	missense	probably benign
R7490:Xpo4	UTSW	14	57,840,078 (GRCm39)	frame shift	probably null
R7622:Xpo4	UTSW	14	57,834,468 (GRCm39)	missense	possibly damaging	0.94
R7667:Xpo4	UTSW	14	57,827,416 (GRCm39)	missense	probably damaging	0.97
R7789:Xpo4	UTSW	14	57,850,806 (GRCm39)	missense	probably benign	0.00
R7895:Xpo4	UTSW	14	57,840,048 (GRCm39)	missense	probably benign	0.03
R8000:Xpo4	UTSW	14	57,827,403 (GRCm39)	missense	probably damaging	1.00
R8372:Xpo4	UTSW	14	57,835,341 (GRCm39)	critical splice donor site	probably null
R8395:Xpo4	UTSW	14	57,885,924 (GRCm39)	missense	probably benign	0.01
R8420:Xpo4	UTSW	14	57,841,913 (GRCm39)	missense	probably damaging	0.99
R8836:Xpo4	UTSW	14	57,902,367 (GRCm39)	missense	probably benign	0.03
R8841:Xpo4	UTSW	14	57,835,413 (GRCm39)	missense	probably damaging	0.97
R8989:Xpo4	UTSW	14	57,828,475 (GRCm39)	missense	probably benign	0.00
R9229:Xpo4	UTSW	14	57,851,156 (GRCm39)	missense	probably benign
R9374:Xpo4	UTSW	14	57,828,512 (GRCm39)	missense	possibly damaging	0.94
R9551:Xpo4	UTSW	14	57,828,512 (GRCm39)	missense	possibly damaging	0.94
R9628:Xpo4	UTSW	14	57,842,630 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCAGGCATAAGCTACCACTC -3'
(R):5'- ATGTCAGCATTTTCCACACTACTTG -3'

Sequencing Primer
(F):5'- CAAATGCTCTCATCATTGGGAAC -3'
(R):5'- TACTTGAAAAGGAGAGCCAGTCTTC -3'

Posted On

2015-09-25