Mutagenetix > Incidental Mutation

Incidental Mutation 'R4654:Ipo11'

351570

Institutional Source

Beutler Lab

Gene Symbol

Ipo11

Ensembl Gene

ENSMUSG00000042590

Gene Name

importin 11

Synonyms

Ranbp11, 1700081H05Rik, 2510001A17Rik, E330021B14Rik

MMRRC Submission

041914-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R4654 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

106930947-107073466 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to G at 106970692 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080856] [ENSMUST00000186033]

AlphaFold

Q8K2V6

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000057427

SMART Domains

Protein: ENSMUSP00000053644
Gene: ENSMUSG00000078933

Domain	Start	End	E-Value	Type
transmembrane domain	99	116	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000080856

SMART Domains

Protein: ENSMUSP00000079667
Gene: ENSMUSG00000042590

Domain	Start	End	E-Value	Type
IBN_N	28	100	7.71e-12	SMART
low complexity region	375	382	N/A	INTRINSIC
low complexity region	563	570	N/A	INTRINSIC
low complexity region	845	856	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000186033

SMART Domains

Protein: ENSMUSP00000140046
Gene: ENSMUSG00000042590

Domain	Start	End	E-Value	Type
IBN_N	28	100	7.71e-12	SMART
low complexity region	375	382	N/A	INTRINSIC
low complexity region	563	570	N/A	INTRINSIC
low complexity region	854	865	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190794

Predicted Effect

probably benign
Transcript: ENSMUST00000190801

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191256

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191312

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 95.2%

Validation Efficiency

97% (98/101)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Importins, including IPO11, are a members of the karyopherin/importin-beta family of transport receptors (see KPNB1; 602738) that mediate nucleocytoplasmic transport of protein and RNA cargoes (Plafker and Macara, 2000 [PubMed 11032817]).[supplied by OMIM, Sep 2008]

Allele List at MGI

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam3	A	T	8: 25,193,819 (GRCm39)	C398S	probably damaging	Het
Adamts10	A	G	17: 33,756,304 (GRCm39)	K316E	possibly damaging	Het
Ap1m1	T	C	8: 73,006,717 (GRCm39)	F238L	possibly damaging	Het
Aph1a	T	A	3: 95,803,088 (GRCm39)	D180E	probably benign	Het
Atp9b	A	G	18: 80,935,093 (GRCm39)	F201L	probably benign	Het
Btbd9	A	C	17: 30,704,561 (GRCm39)		probably benign	Het
C2cd5	T	C	6: 142,975,910 (GRCm39)	T768A	probably benign	Het
Casq1	C	T	1: 172,037,965 (GRCm39)		probably benign	Het
Cimap2	C	A	4: 106,467,612 (GRCm39)	M341I	probably benign	Het
Cltc	A	T	11: 86,617,196 (GRCm39)	M351K	probably benign	Het
Cnp	A	G	11: 100,469,877 (GRCm39)	E271G	possibly damaging	Het
Col22a1	T	C	15: 71,845,544 (GRCm39)	D406G	possibly damaging	Het
Cylc2	T	C	4: 51,228,279 (GRCm39)	S117P	probably benign	Het
Cyp2b13	T	C	7: 25,761,072 (GRCm39)	L43P	probably damaging	Het
Cyp3a16	A	G	5: 145,373,267 (GRCm39)	V500A	probably benign	Het
Dclk2	T	C	3: 86,743,683 (GRCm39)	D262G	probably damaging	Het
Dcun1d3	A	C	7: 119,458,742 (GRCm39)	Y98D	probably damaging	Het
Ddx39b	A	G	17: 35,472,464 (GRCm39)	*429W	probably null	Het
Dennd5b	T	C	6: 148,908,335 (GRCm39)	N986S	probably damaging	Het
Dipk1a	T	C	5: 108,057,982 (GRCm39)		probably null	Het
Dusp9	G	A	X: 72,684,378 (GRCm39)	R182Q	probably benign	Het
Ecpas	A	T	4: 58,834,523 (GRCm39)	I785N	possibly damaging	Het
Edil3	A	G	13: 89,437,589 (GRCm39)	K397E	probably damaging	Het
Ehd1	T	C	19: 6,326,994 (GRCm39)		probably benign	Het
Fam13a	A	T	6: 58,964,152 (GRCm39)	H93Q	probably benign	Het
Farp1	T	C	14: 121,513,716 (GRCm39)	I837T	possibly damaging	Het
Fbxl5	T	A	5: 43,922,771 (GRCm39)	I216F	probably damaging	Het
Gadl1	G	A	9: 115,770,408 (GRCm39)	E74K	probably damaging	Het
Gnpnat1	A	G	14: 45,618,436 (GRCm39)	V122A	probably damaging	Het
Hdac10	C	T	15: 89,011,036 (GRCm39)		probably benign	Het
Heatr5b	T	C	17: 79,128,130 (GRCm39)	S502G	possibly damaging	Het
Hr	C	A	14: 70,801,013 (GRCm39)	A695E	probably damaging	Het
Ift80	A	T	3: 68,825,870 (GRCm39)	I490N	possibly damaging	Het
Iqch	T	G	9: 63,432,195 (GRCm39)	Y400S	probably damaging	Het
Jag2	C	T	12: 112,877,266 (GRCm39)	D702N	probably benign	Het
Kiss1r	T	A	10: 79,757,624 (GRCm39)	L326Q	probably damaging	Het
Lrrc42	A	T	4: 107,104,746 (GRCm39)	I73N	probably damaging	Het
Lrrc55	C	T	2: 85,026,880 (GRCm39)	G48D	possibly damaging	Het
Lrrk2	T	C	15: 91,649,884 (GRCm39)	S1674P	probably damaging	Het
Mctp2	A	G	7: 71,739,942 (GRCm39)	L816P	probably damaging	Het
Mipol1	A	T	12: 57,352,918 (GRCm39)	T86S	probably benign	Het
Mkrn3	C	T	7: 62,069,452 (GRCm39)	R113H	probably damaging	Het
Mmp1b	A	G	9: 7,370,849 (GRCm39)	V302A	probably benign	Het
Msc	A	T	1: 14,826,053 (GRCm39)		probably null	Het
Msmo1	C	A	8: 65,180,888 (GRCm39)	V9L	probably benign	Het
Nbeal2	G	A	9: 110,461,072 (GRCm39)	R1630C	probably damaging	Het
Nlgn1	C	T	3: 26,187,850 (GRCm39)	V12I	possibly damaging	Het
Npas3	T	C	12: 54,108,915 (GRCm39)		probably null	Het
Nr2e3	A	G	9: 59,856,355 (GRCm39)		probably benign	Het
Oca2	C	T	7: 55,978,560 (GRCm39)	A576V	probably benign	Het
Or5b21	T	A	19: 12,839,596 (GRCm39)	C152*	probably null	Het
Or6d12	T	C	6: 116,493,409 (GRCm39)	Y224H	probably damaging	Het
Or6z7	T	C	7: 6,484,045 (GRCm39)	T37A	probably benign	Het
Parp6	A	G	9: 59,548,383 (GRCm39)		probably null	Het
Pate13	T	A	9: 35,820,287 (GRCm39)	C4S	probably damaging	Het
Phlpp1	A	T	1: 106,267,231 (GRCm39)	M715L	probably benign	Het
Pi4k2a	G	A	19: 42,101,544 (GRCm39)		probably null	Het
Pik3ap1	A	G	19: 41,316,348 (GRCm39)	S305P	probably damaging	Het
Plcg2	G	A	8: 118,231,054 (GRCm39)	M45I	probably benign	Het
Ppm1m	A	T	9: 106,073,601 (GRCm39)	L317H	probably damaging	Het
Ppp1r21	T	G	17: 88,866,227 (GRCm39)	M341R	probably benign	Het
Prdx3	A	G	19: 60,853,674 (GRCm39)	V217A	possibly damaging	Het
Ptk2b	A	G	14: 66,400,496 (GRCm39)	V773A	possibly damaging	Het
Raly	T	C	2: 154,699,376 (GRCm39)	V60A	probably damaging	Het
Reps1	A	G	10: 17,990,148 (GRCm39)	D420G	probably damaging	Het
Rev1	A	T	1: 38,118,337 (GRCm39)		probably benign	Het
Rgs2	T	G	1: 143,878,650 (GRCm39)		probably benign	Het
Rlf	G	T	4: 121,007,798 (GRCm39)	T394K	probably benign	Het
Rptn	A	T	3: 93,304,792 (GRCm39)	R708S	possibly damaging	Het
Sec23b	T	A	2: 144,414,494 (GRCm39)	M402K	probably benign	Het
Skic2	A	G	17: 35,068,922 (GRCm39)	C26R	probably damaging	Het
Slx9	T	C	10: 77,325,860 (GRCm39)	M170V	possibly damaging	Het
Smpd4	A	G	16: 17,459,992 (GRCm39)		probably benign	Het
Synj2	A	G	17: 6,063,813 (GRCm39)	E434G	probably damaging	Het
Tatdn2	T	A	6: 113,684,326 (GRCm39)	F64I	probably benign	Het
Tex21	A	C	12: 76,263,860 (GRCm39)	H177Q	probably benign	Het
Tln1	T	A	4: 43,535,954 (GRCm39)	Q2077L	probably null	Het
Tnrc6c	T	C	11: 117,611,797 (GRCm39)	V145A	probably benign	Het
Ttn	C	T	2: 76,616,936 (GRCm39)		probably benign	Het
Uggt2	A	G	14: 119,269,670 (GRCm39)	F954S	possibly damaging	Het
Ugt2a1	A	G	5: 87,634,083 (GRCm39)	S175P	probably damaging	Het
Vcl	A	G	14: 21,035,820 (GRCm39)		probably null	Het
Vegfa	A	T	17: 46,336,176 (GRCm39)		probably benign	Het
Vmn2r68	G	A	7: 84,882,769 (GRCm39)	Q328*	probably null	Het
Vmn2r7	A	G	3: 64,626,864 (GRCm39)	Y142H	probably benign	Het
Wdr17	C	T	8: 55,134,434 (GRCm39)	G349R	probably damaging	Het
Ybx3	G	T	6: 131,347,290 (GRCm39)	R282S	probably damaging	Het
Zfp566	T	C	7: 29,777,194 (GRCm39)	H329R	probably damaging	Het
Zfp786	T	C	6: 47,797,868 (GRCm39)	I357V	probably benign	Het
Zfr2	C	A	10: 81,087,083 (GRCm39)		probably null	Het

Other mutations in Ipo11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00693:Ipo11	APN	13	107,033,768 (GRCm39)	missense	probably damaging	1.00
IGL00900:Ipo11	APN	13	106,983,952 (GRCm39)	missense	possibly damaging	0.81
IGL00971:Ipo11	APN	13	106,993,277 (GRCm39)	missense	probably damaging	1.00
IGL01023:Ipo11	APN	13	107,033,767 (GRCm39)	missense	probably benign	0.44
IGL01331:Ipo11	APN	13	106,932,254 (GRCm39)	missense	possibly damaging	0.92
IGL01608:Ipo11	APN	13	106,971,002 (GRCm39)	intron	probably benign
IGL02021:Ipo11	APN	13	106,993,745 (GRCm39)	missense	probably damaging	1.00
IGL02620:Ipo11	APN	13	107,012,789 (GRCm39)	critical splice acceptor site	probably null
IGL02651:Ipo11	APN	13	107,012,114 (GRCm39)	missense	probably damaging	1.00
IGL02699:Ipo11	APN	13	107,025,905 (GRCm39)	missense	possibly damaging	0.94
IGL02928:Ipo11	APN	13	107,025,863 (GRCm39)	splice site	probably benign
R0017:Ipo11	UTSW	13	107,023,238 (GRCm39)	missense	probably benign	0.00
R0017:Ipo11	UTSW	13	107,023,238 (GRCm39)	missense	probably benign	0.00
R0032:Ipo11	UTSW	13	106,970,971 (GRCm39)	intron	probably benign
R0164:Ipo11	UTSW	13	107,046,702 (GRCm39)	splice site	probably benign
R0333:Ipo11	UTSW	13	107,007,271 (GRCm39)	missense	probably benign	0.00
R0499:Ipo11	UTSW	13	107,061,595 (GRCm39)	missense	probably benign	0.00
R0555:Ipo11	UTSW	13	107,028,969 (GRCm39)	missense	probably damaging	1.00
R0718:Ipo11	UTSW	13	107,056,119 (GRCm39)	missense	possibly damaging	0.91
R0899:Ipo11	UTSW	13	107,037,324 (GRCm39)	nonsense	probably null
R1590:Ipo11	UTSW	13	107,023,225 (GRCm39)	missense	probably damaging	1.00
R1700:Ipo11	UTSW	13	106,932,170 (GRCm39)	missense	probably benign
R1851:Ipo11	UTSW	13	106,948,765 (GRCm39)	missense	possibly damaging	0.73
R1852:Ipo11	UTSW	13	106,948,765 (GRCm39)	missense	possibly damaging	0.73
R1853:Ipo11	UTSW	13	106,997,395 (GRCm39)	missense	probably benign	0.19
R2012:Ipo11	UTSW	13	107,056,130 (GRCm39)	missense	probably benign	0.01
R2168:Ipo11	UTSW	13	107,016,118 (GRCm39)	splice site	probably null
R2183:Ipo11	UTSW	13	107,061,595 (GRCm39)	missense	probably benign	0.00
R4254:Ipo11	UTSW	13	107,029,017 (GRCm39)	missense	probably benign	0.00
R4607:Ipo11	UTSW	13	107,037,319 (GRCm39)	missense	probably damaging	0.98
R4610:Ipo11	UTSW	13	107,016,245 (GRCm39)	missense	probably benign	0.06
R4792:Ipo11	UTSW	13	106,970,668 (GRCm39)	intron	probably benign
R4990:Ipo11	UTSW	13	106,997,395 (GRCm39)	missense	probably benign	0.19
R5309:Ipo11	UTSW	13	106,970,481 (GRCm39)	intron	probably benign
R5580:Ipo11	UTSW	13	107,037,255 (GRCm39)	missense	probably benign
R5822:Ipo11	UTSW	13	106,984,926 (GRCm39)	unclassified	probably benign
R6459:Ipo11	UTSW	13	107,002,277 (GRCm39)	splice site	probably null
R6597:Ipo11	UTSW	13	107,002,371 (GRCm39)	critical splice donor site	probably null
R6803:Ipo11	UTSW	13	106,993,766 (GRCm39)	missense	probably benign
R6882:Ipo11	UTSW	13	107,037,190 (GRCm39)	splice site	probably null
R7071:Ipo11	UTSW	13	107,061,604 (GRCm39)	missense	probably damaging	1.00
R7202:Ipo11	UTSW	13	107,012,078 (GRCm39)	missense	probably damaging	1.00
R7214:Ipo11	UTSW	13	107,032,365 (GRCm39)	missense	probably null
R7221:Ipo11	UTSW	13	107,029,065 (GRCm39)	missense	probably damaging	1.00
R7392:Ipo11	UTSW	13	107,028,199 (GRCm39)	nonsense	probably null
R7871:Ipo11	UTSW	13	107,028,976 (GRCm39)	missense	probably benign	0.01
R8189:Ipo11	UTSW	13	107,061,604 (GRCm39)	missense	probably damaging	1.00
R8426:Ipo11	UTSW	13	106,978,678 (GRCm39)	missense	possibly damaging	0.92
R8951:Ipo11	UTSW	13	106,978,690 (GRCm39)	missense	possibly damaging	0.80
R8981:Ipo11	UTSW	13	107,061,633 (GRCm39)	missense	probably benign	0.18
R9272:Ipo11	UTSW	13	107,046,713 (GRCm39)	missense	probably benign	0.00
R9765:Ipo11	UTSW	13	107,061,556 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATGTTCAAAGAGAATGACTTGTGCC -3'
(R):5'- AGACACAGCTCACTTCTGTTAC -3'

Sequencing Primer
(F):5'- GAGAATGACTTGTGCCCCATTTTCAG -3'
(R):5'- AAAACACTGCTCTACCAATTGATG -3'

Posted On

2015-10-08