Mutagenetix > Incidental Mutation

Incidental Mutation 'R6240:Tnpo1'

505193

Institutional Source

Beutler Lab

Gene Symbol

Tnpo1

Ensembl Gene

ENSMUSG00000009470

Gene Name

transportin 1

Synonyms

D13Ertd688e, Kpnb2

MMRRC Submission

044364-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.969) question?

Stock #

R6240 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

98975527-99062892 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 99000337 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Methionine at position 335 (I335M)

Ref Sequence

ENSEMBL: ENSMUSP00000136917 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109399] [ENSMUST00000109401] [ENSMUST00000179301]

AlphaFold

Q8BFY9

Predicted Effect

probably damaging
Transcript: ENSMUST00000109399
AA Change: I335M

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000105026
Gene: ENSMUSG00000009470
AA Change: I335M

Domain	Start	End	E-Value	Type
IBN_N	33	101	1.53e-6	SMART
low complexity region	350	368	N/A	INTRINSIC
low complexity region	393	410	N/A	INTRINSIC
Pfam:HEAT_EZ	411	465	4.7e-12	PFAM
Pfam:HEAT	439	469	6.8e-5	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000109401
AA Change: I343M

PolyPhen 2 Score 0.971 (Sensitivity: 0.77; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000105028
Gene: ENSMUSG00000009470
AA Change: I343M

Domain	Start	End	E-Value	Type
IBN_N	41	109	1.53e-6	SMART
low complexity region	358	376	N/A	INTRINSIC
low complexity region	401	418	N/A	INTRINSIC
Pfam:HEAT_EZ	419	473	6.6e-15	PFAM
Pfam:HEAT	447	477	1.3e-5	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000179301
AA Change: I335M

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000136917
Gene: ENSMUSG00000009470
AA Change: I335M

Domain	Start	End	E-Value	Type
IBN_N	33	101	1.53e-6	SMART
low complexity region	350	368	N/A	INTRINSIC
low complexity region	393	410	N/A	INTRINSIC
Pfam:HEAT_EZ	411	465	4.2e-12	PFAM
Pfam:HEAT	439	469	6.1e-5	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224022

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224099

Meta Mutation Damage Score

0.1431

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.5%

Validation Efficiency

98% (62/63)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the beta subunit of the karyopherin receptor complex which interacts with nuclear localization signals to target nuclear proteins to the nucleus. The karyopherin receptor complex is a heterodimer of an alpha subunit which recognizes the nuclear localization signal and a beta subunit which docks the complex at nucleoporins. Alternate splicing of this gene results in two transcript variants encoding different proteins. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930578I06Rik	C	A	14: 64,223,701 (GRCm39)	R25L	probably damaging	Het
Adamts1	G	A	16: 85,599,045 (GRCm39)	S185L	probably benign	Het
Adamts12	A	T	15: 11,286,044 (GRCm39)	D751V	probably benign	Het
Adgrg3	A	G	8: 95,766,544 (GRCm39)	D405G	probably benign	Het
Ahi1	A	G	10: 20,852,980 (GRCm39)	D516G	probably damaging	Het
Ahnak	A	T	19: 8,990,947 (GRCm39)	D4077V	probably damaging	Het
Arhgef18	G	A	8: 3,489,658 (GRCm39)	R330Q	probably damaging	Het
Arid1a	A	G	4: 133,407,997 (GRCm39)	V2170A	unknown	Het
Asxl3	C	T	18: 22,598,565 (GRCm39)	L227F	probably damaging	Het
B3glct	A	G	5: 149,650,253 (GRCm39)	I119V	probably benign	Het
Brd10	A	T	19: 29,694,640 (GRCm39)	S1618T	probably benign	Het
Cad	T	A	5: 31,230,322 (GRCm39)	M1512K	probably benign	Het
Cdc25a	A	G	9: 109,713,226 (GRCm39)	T172A	probably damaging	Het
Cdh18	A	G	15: 23,227,022 (GRCm39)	D161G	possibly damaging	Het
Clmp	A	G	9: 40,693,707 (GRCm39)	N308S	probably damaging	Het
Dlg5	A	T	14: 24,199,596 (GRCm39)		probably null	Het
Dscam	G	A	16: 96,420,702 (GRCm39)	T1728M	probably damaging	Het
E4f1	A	G	17: 24,663,556 (GRCm39)	S524P	possibly damaging	Het
Epha5	G	C	5: 84,265,438 (GRCm39)	A452G	probably benign	Het
Fzd3	T	C	14: 65,447,304 (GRCm39)	T542A	probably damaging	Het
Glyctk	A	T	9: 106,033,461 (GRCm39)		probably null	Het
Gm10382	G	A	5: 125,466,660 (GRCm39)		probably benign	Het
Hnmt	T	A	2: 23,904,281 (GRCm39)	M127L	probably benign	Het
Hoxc10	T	A	15: 102,879,265 (GRCm39)	W262R	probably damaging	Het
Icam5	T	A	9: 20,944,454 (GRCm39)	W52R	possibly damaging	Het
Jazf1	A	T	6: 52,754,537 (GRCm39)	C180S	probably damaging	Het
Kcnk2	A	G	1: 188,975,179 (GRCm39)	W286R	probably damaging	Het
Kcnmb2	C	T	3: 32,236,045 (GRCm39)	S98F	probably damaging	Het
Mob3a	C	G	10: 80,525,698 (GRCm39)	E204D	possibly damaging	Het
Morc3	C	G	16: 93,659,572 (GRCm39)	H459D	probably damaging	Het
Mroh2b	A	T	15: 4,964,126 (GRCm39)	N876I	probably benign	Het
Myo16	A	T	8: 10,420,930 (GRCm39)	T257S	probably damaging	Het
Nat1	A	T	8: 67,944,354 (GRCm39)	R243S	possibly damaging	Het
Nudt9	T	C	5: 104,194,955 (GRCm39)	V17A	probably benign	Het
Or13p8	A	G	4: 118,583,668 (GRCm39)	S75G	probably benign	Het
Or4c111	A	G	2: 88,843,970 (GRCm39)	I146T	probably benign	Het
Or4c11c	A	G	2: 88,661,707 (GRCm39)	D82G	probably benign	Het
Or4m1	A	G	14: 50,558,043 (GRCm39)	V83A	probably benign	Het
Or6c70	C	A	10: 129,710,546 (GRCm39)	V27L	probably benign	Het
Pcdh7	T	C	5: 57,878,704 (GRCm39)	L753P	probably damaging	Het
Pcf11	T	A	7: 92,295,710 (GRCm39)	E1446D	probably damaging	Het
Pepd	A	G	7: 34,721,176 (GRCm39)	I267V	probably benign	Het
Plk2	T	A	13: 110,536,008 (GRCm39)	Y571N	probably damaging	Het
Plk2	T	A	13: 110,536,568 (GRCm39)	V620E	probably damaging	Het
Prag1	T	C	8: 36,570,506 (GRCm39)	L363P	probably benign	Het
Psmd3	A	G	11: 98,584,479 (GRCm39)	T387A	probably damaging	Het
Ptgs1	G	A	2: 36,127,297 (GRCm39)	C61Y	probably damaging	Het
Rab18	T	C	18: 6,784,635 (GRCm39)	Y109H	probably benign	Het
Robo2	G	A	16: 73,779,027 (GRCm39)	P358L	probably damaging	Het
Smarcc2	C	T	10: 128,323,893 (GRCm39)		probably benign	Het
Spata31e4	G	A	13: 50,855,453 (GRCm39)	D364N	probably damaging	Het
Srgap1	A	G	10: 121,883,061 (GRCm39)	I13T	probably benign	Het
Tcf12	T	A	9: 71,851,298 (GRCm39)	K110*	probably null	Het
Tdrd1	T	C	19: 56,829,767 (GRCm39)	S214P	probably benign	Het
Tdrd3	T	A	14: 87,743,322 (GRCm39)	N417K	probably damaging	Het
Tmem255b	A	G	8: 13,504,216 (GRCm39)	Y136C	probably damaging	Het
Tmem63c	A	T	12: 87,123,179 (GRCm39)	I448F	possibly damaging	Het
Vmn1r1	T	C	1: 181,985,186 (GRCm39)	T160A	probably damaging	Het
Vmn1r203	A	G	13: 22,708,899 (GRCm39)	N227D	possibly damaging	Het
Vmn2r6	T	A	3: 64,464,226 (GRCm39)	S203C	probably damaging	Het
Zfp628	A	G	7: 4,922,848 (GRCm39)	T357A	possibly damaging	Het
Zfp872	A	G	9: 22,111,180 (GRCm39)	K220E	probably damaging	Het

Other mutations in Tnpo1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00765:Tnpo1	APN	13	98,986,612 (GRCm39)	splice site	probably benign
IGL02572:Tnpo1	APN	13	98,985,667 (GRCm39)	missense	probably damaging	1.00
IGL03040:Tnpo1	APN	13	98,996,463 (GRCm39)	missense	probably damaging	0.99
IGL03237:Tnpo1	APN	13	99,000,348 (GRCm39)	missense	probably damaging	0.98
IGL03379:Tnpo1	APN	13	99,000,348 (GRCm39)	missense	probably damaging	0.98
IGL03393:Tnpo1	APN	13	99,024,981 (GRCm39)	missense	probably damaging	0.99
IGL03405:Tnpo1	APN	13	99,000,348 (GRCm39)	missense	probably damaging	0.98
IGL03407:Tnpo1	APN	13	99,000,348 (GRCm39)	missense	probably damaging	0.98
Domineight	UTSW	13	99,003,637 (GRCm39)	frame shift	probably null
invert	UTSW	13	98,991,954 (GRCm39)	missense	probably damaging	1.00
R0308:Tnpo1	UTSW	13	98,983,011 (GRCm39)	missense	probably damaging	0.97
R0465:Tnpo1	UTSW	13	99,021,142 (GRCm39)	missense	probably damaging	0.97
R0492:Tnpo1	UTSW	13	98,991,954 (GRCm39)	missense	probably damaging	1.00
R0707:Tnpo1	UTSW	13	98,991,954 (GRCm39)	missense	probably damaging	1.00
R0732:Tnpo1	UTSW	13	99,000,320 (GRCm39)	missense	probably damaging	0.99
R1314:Tnpo1	UTSW	13	98,997,230 (GRCm39)	missense	probably damaging	0.99
R1449:Tnpo1	UTSW	13	99,015,220 (GRCm39)	missense	probably damaging	0.99
R1468:Tnpo1	UTSW	13	98,986,665 (GRCm39)	missense	probably benign	0.25
R1468:Tnpo1	UTSW	13	98,986,665 (GRCm39)	missense	probably benign	0.25
R1488:Tnpo1	UTSW	13	98,993,415 (GRCm39)	missense	probably damaging	0.98
R1961:Tnpo1	UTSW	13	98,989,440 (GRCm39)	missense	probably damaging	1.00
R3123:Tnpo1	UTSW	13	99,003,637 (GRCm39)	frame shift	probably null
R3124:Tnpo1	UTSW	13	99,003,637 (GRCm39)	frame shift	probably null
R4151:Tnpo1	UTSW	13	98,989,407 (GRCm39)	missense	probably damaging	1.00
R4272:Tnpo1	UTSW	13	99,003,637 (GRCm39)	frame shift	probably null
R4274:Tnpo1	UTSW	13	99,003,637 (GRCm39)	frame shift	probably null
R5154:Tnpo1	UTSW	13	99,006,813 (GRCm39)	missense	possibly damaging	0.84
R5763:Tnpo1	UTSW	13	98,996,445 (GRCm39)	missense	possibly damaging	0.54
R5765:Tnpo1	UTSW	13	98,996,349 (GRCm39)	missense	probably benign	0.08
R5827:Tnpo1	UTSW	13	98,993,416 (GRCm39)	missense	probably damaging	1.00
R6279:Tnpo1	UTSW	13	99,027,216 (GRCm39)	missense	possibly damaging	0.90
R6294:Tnpo1	UTSW	13	99,027,282 (GRCm39)	missense	probably benign	0.03
R7055:Tnpo1	UTSW	13	98,991,987 (GRCm39)	missense	possibly damaging	0.85
R7509:Tnpo1	UTSW	13	99,006,751 (GRCm39)	missense	probably benign	0.00
R7707:Tnpo1	UTSW	13	99,027,295 (GRCm39)	missense	probably benign	0.00
R8314:Tnpo1	UTSW	13	99,021,133 (GRCm39)	missense	possibly damaging	0.87
R8730:Tnpo1	UTSW	13	98,989,916 (GRCm39)	missense	probably benign	0.00
R9488:Tnpo1	UTSW	13	98,990,003 (GRCm39)	missense	probably damaging	1.00
R9511:Tnpo1	UTSW	13	99,003,621 (GRCm39)	missense	possibly damaging	0.94
Z1088:Tnpo1	UTSW	13	98,997,178 (GRCm39)	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- AATTAAAAGCTGGTCAGGCAC -3'
(R):5'- TCAGCATGTGTCATAGACTCC -3'

Sequencing Primer
(F):5'- CAGCCAAGCAGTGAAGCCTC -3'
(R):5'- AAGGGGACTAGGTCTCATCC -3'

Posted On

2018-02-28