Mutagenetix > Incidental Mutation

Incidental Mutation 'R2070:Exoc2'

227076

Institutional Source

Beutler Lab

Gene Symbol

Exoc2

Ensembl Gene

ENSMUSG00000021357

Gene Name

exocyst complex component 2

Synonyms

2410030I24Rik, Sec5l1, Sec5

MMRRC Submission

040075-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.961) question?

Stock #

R2070 (G1)

Quality Score

223

Status

Not validated

Chromosome

Chromosomal Location

30813919-30974093 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 30815370 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Lysine at position 901 (N901K)

Ref Sequence

ENSEMBL: ENSMUSP00000100010 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000021785] [ENSMUST00000102946]

AlphaFold

Q9D4H1

Predicted Effect

probably benign
Transcript: ENSMUST00000021785
AA Change: N901K

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000021785
Gene: ENSMUSG00000021357
AA Change: N901K

Domain	Start	End	E-Value	Type
Pfam:TIG	8	92	3.2e-10	PFAM
Pfam:Sec5	198	377	3.6e-59	PFAM
low complexity region	572	585	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000102946
AA Change: N901K

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000100010
Gene: ENSMUSG00000021357
AA Change: N901K

Domain	Start	End	E-Value	Type
Pfam:TIG	8	92	2.5e-10	PFAM
Pfam:Sec5	198	377	7.5e-59	PFAM
low complexity region	572	585	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.5%

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 component of the exocyst complex, a multi-protein complex essential for the polarized targeting of exocytic vesicles to specific docking sites on the plasma membrane. Though best characterized in yeast, the component proteins and the functions of the exocyst complex have been demonstrated to be highly conserved in higher eukaryotes. At least eight components of the exocyst complex, including this protein, are found to interact with the actin cytoskeletal remodeling and vesicle transport machinery. This interaction has been shown to mediate filopodia formation in fibroblasts. This protein has been shown to interact with the Ral subfamily of GTPases and thereby mediate exocytosis by tethering vesicles to the plasma membrane. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810021J22Rik	A	G	11: 58,876,769 (GRCm38)	K31E	probably damaging	Het
4930548H24Rik	T	C	5: 31,487,383 (GRCm38)	V160A	possibly damaging	Het
9130011E15Rik	G	T	19: 45,891,285 (GRCm38)	P543Q	probably damaging	Het
Abcc10	G	C	17: 46,303,565 (GRCm38)	N1477K	probably benign	Het
Ablim2	G	A	5: 35,798,513 (GRCm38)	C24Y	probably damaging	Het
Ankle1	T	C	8: 71,409,344 (GRCm38)	F497S	probably damaging	Het
Ash1l	C	G	3: 88,966,203 (GRCm38)	P98A	probably damaging	Het
Atad5	A	T	11: 80,098,052 (GRCm38)		probably null	Het
B3gnt4	A	T	5: 123,511,370 (GRCm38)	H266L	probably benign	Het
Bmi1	A	G	2: 18,684,040 (GRCm38)	I207V	probably benign	Het
Bnip3l	A	G	14: 66,989,222 (GRCm38)	M174T	probably damaging	Het
Bora	T	C	14: 99,062,278 (GRCm38)	S229P	probably damaging	Het
Ccdc27	T	A	4: 154,041,813 (GRCm38)	N73I	unknown	Het
Cdc42bpg	T	A	19: 6,320,488 (GRCm38)	C1204S	probably damaging	Het
Cdsn	A	T	17: 35,554,694 (GRCm38)	D40V	probably damaging	Het
Cilp	T	A	9: 65,279,095 (GRCm38)	V824D	probably damaging	Het
Cmtr1	A	G	17: 29,694,783 (GRCm38)		probably null	Het
Cntnap1	A	G	11: 101,182,979 (GRCm38)	Y652C	probably damaging	Het
Col12a1	T	C	9: 79,647,696 (GRCm38)	I2033M	probably benign	Het
Cwh43	T	C	5: 73,421,517 (GRCm38)	L289P	probably damaging	Het
Ddhd1	T	C	14: 45,610,624 (GRCm38)	D529G	probably damaging	Het
Defb28	T	A	2: 152,520,144 (GRCm38)	S75T	probably benign	Het
Dennd2a	A	T	6: 39,465,119 (GRCm38)	V939D	probably damaging	Het
Dlg5	T	C	14: 24,136,635 (GRCm38)	R1866G	probably damaging	Het
Dsc1	C	T	18: 20,088,296 (GRCm38)		probably null	Het
Ecscr	T	G	18: 35,715,437 (GRCm38)	N184T	probably damaging	Het
Eif4ebp1	G	T	8: 27,273,344 (GRCm38)	R55L	probably damaging	Het
Eml1	G	T	12: 108,512,999 (GRCm38)	V344L	probably damaging	Het
Fam161b	T	A	12: 84,356,428 (GRCm38)	I143F	probably benign	Het
Fam180a	A	G	6: 35,325,911 (GRCm38)	S2P	probably benign	Het
Fam57b	T	C	7: 126,819,840 (GRCm38)	L4P	probably benign	Het
Fat3	T	A	9: 15,999,370 (GRCm38)	I1779F	probably benign	Het
Fat4	A	G	3: 39,010,655 (GRCm38)	K4920R	probably benign	Het
Fsip2	T	A	2: 82,976,355 (GRCm38)	V1006E	probably damaging	Het
Glcci1	A	G	6: 8,558,566 (GRCm38)	S30G	probably damaging	Het
Gm13078	T	G	4: 143,726,902 (GRCm38)	Y193*	probably null	Het
Gm5414	A	T	15: 101,628,060 (GRCm38)	S43R	possibly damaging	Het
Hao1	T	C	2: 134,530,615 (GRCm38)	T158A	probably damaging	Het
Hic1	T	C	11: 75,169,059 (GRCm38)	H154R	possibly damaging	Het
Hmgxb3	T	C	18: 61,171,359 (GRCm38)	Y53C	probably damaging	Het
Ipmk	A	T	10: 71,372,749 (GRCm38)	K122*	probably null	Het
Jakmip2	T	C	18: 43,563,330 (GRCm38)	E518G	probably benign	Het
Kmt2e	A	G	5: 23,501,995 (GRCm38)	T1519A	probably benign	Het
Lfng	T	C	5: 140,612,595 (GRCm38)	I224T	possibly damaging	Het
Magel2	G	A	7: 62,379,096 (GRCm38)	V583I	unknown	Het
Map4k5	C	T	12: 69,816,337 (GRCm38)	V629I	probably damaging	Het
Med12l	A	G	3: 59,244,905 (GRCm38)	D1037G	probably damaging	Het
Morc1	C	T	16: 48,592,611 (GRCm38)	T705I	probably benign	Het
Mptx2	A	T	1: 173,274,578 (GRCm38)	Y181*	probably null	Het
Mrpl24	T	C	3: 87,923,067 (GRCm38)		probably null	Het
Myo5a	A	G	9: 75,181,984 (GRCm38)	E1132G	probably benign	Het
Nedd4l	T	G	18: 65,212,820 (GRCm38)	F814L	probably damaging	Het
Nmral1	T	A	16: 4,716,347 (GRCm38)	I77F	probably damaging	Het
Oit3	T	G	10: 59,431,013 (GRCm38)	I224L	probably benign	Het
Oxsm	A	G	14: 16,241,983 (GRCm38)	L262P	probably benign	Het
Pacs2	C	T	12: 113,061,111 (GRCm38)	T407I	probably damaging	Het
Pard6g	T	C	18: 80,117,725 (GRCm38)	I351T	probably benign	Het
Pdcl2	A	T	5: 76,324,991 (GRCm38)		probably null	Het
Pdzph1	T	C	17: 58,974,097 (GRCm38)	R397G	probably benign	Het
Phip	T	A	9: 82,875,299 (GRCm38)	I1607L	probably benign	Het
Plekhd1	C	A	12: 80,692,907 (GRCm38)	S10*	probably null	Het
Prdm1	C	T	10: 44,441,412 (GRCm38)	D505N	possibly damaging	Het
Psmd13	T	C	7: 140,897,648 (GRCm38)	V320A	probably damaging	Het
Rbak	A	G	5: 143,176,584 (GRCm38)	L8P	probably damaging	Het
Rere	C	A	4: 150,614,590 (GRCm38)		probably benign	Het
Rint1	T	C	5: 23,810,929 (GRCm38)	S456P	possibly damaging	Het
Scn3a	T	C	2: 65,520,866 (GRCm38)	Q446R	possibly damaging	Het
Slitrk5	A	G	14: 111,680,189 (GRCm38)	Y415C	probably damaging	Het
Snrnp200	A	G	2: 127,212,403 (GRCm38)	E210G	possibly damaging	Het
Snrnp200	A	G	2: 127,237,883 (GRCm38)	T1891A	probably benign	Het
Sohlh2	A	G	3: 55,207,622 (GRCm38)	I343V	probably benign	Het
Spin1	T	C	13: 51,144,537 (GRCm38)		probably null	Het
St14	T	A	9: 31,091,373 (GRCm38)	I745F	probably damaging	Het
Sv2a	G	A	3: 96,193,875 (GRCm38)	A730T	possibly damaging	Het
Tars2	C	A	3: 95,747,638 (GRCm38)	G113C	probably damaging	Het
Trp53	A	G	11: 69,589,632 (GRCm38)	D278G	probably damaging	Het
Ubxn7	T	A	16: 32,372,469 (GRCm38)	C160S	possibly damaging	Het
Uty	T	C	Y: 1,169,193 (GRCm38)	E414G	probably benign	Het
Wrap73	T	A	4: 154,148,743 (GRCm38)	S125T	possibly damaging	Het
Wwc2	T	C	8: 47,868,321 (GRCm38)	D586G	unknown	Het
Zfp106	T	C	2: 120,523,529 (GRCm38)	H1490R	probably benign	Het
Zswim5	T	C	4: 116,979,912 (GRCm38)	V731A	probably benign	Het
Zyg11b	G	C	4: 108,250,819 (GRCm38)	N463K	possibly damaging	Het

Other mutations in Exoc2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00095:Exoc2	APN	13	30,820,626 (GRCm38)	missense	probably benign	0.17
IGL01839:Exoc2	APN	13	30,906,799 (GRCm38)	missense	probably damaging	1.00
IGL02092:Exoc2	APN	13	30,875,277 (GRCm38)	missense	probably benign	0.09
IGL02245:Exoc2	APN	13	30,906,859 (GRCm38)	missense	probably benign	0.10
IGL02267:Exoc2	APN	13	30,815,321 (GRCm38)	missense	probably benign
IGL02478:Exoc2	APN	13	30,927,420 (GRCm38)	missense	probably benign
IGL02500:Exoc2	APN	13	30,911,196 (GRCm38)	missense	probably damaging	1.00
IGL03081:Exoc2	APN	13	30,900,902 (GRCm38)	missense	probably benign	0.28
IGL03112:Exoc2	APN	13	30,906,587 (GRCm38)	splice site	probably benign
IGL03409:Exoc2	APN	13	30,940,737 (GRCm38)	utr 5 prime	probably benign
R0284:Exoc2	UTSW	13	30,877,625 (GRCm38)	splice site	probably benign
R0452:Exoc2	UTSW	13	30,886,327 (GRCm38)	splice site	probably benign
R0826:Exoc2	UTSW	13	30,856,797 (GRCm38)	critical splice acceptor site	probably null
R1251:Exoc2	UTSW	13	30,886,276 (GRCm38)	missense	probably benign	0.03
R1367:Exoc2	UTSW	13	30,882,273 (GRCm38)	nonsense	probably null
R1501:Exoc2	UTSW	13	30,935,502 (GRCm38)	missense	probably benign	0.01
R1593:Exoc2	UTSW	13	30,856,761 (GRCm38)	missense	possibly damaging	0.64
R1839:Exoc2	UTSW	13	30,906,497 (GRCm38)	splice site	probably benign
R1872:Exoc2	UTSW	13	30,822,661 (GRCm38)	missense	probably benign	0.17
R2064:Exoc2	UTSW	13	30,935,561 (GRCm38)	missense	probably benign	0.00
R2227:Exoc2	UTSW	13	30,864,884 (GRCm38)	missense	probably benign
R2507:Exoc2	UTSW	13	30,882,365 (GRCm38)	missense	possibly damaging	0.55
R3965:Exoc2	UTSW	13	30,877,582 (GRCm38)	missense	probably benign	0.00
R4601:Exoc2	UTSW	13	30,882,268 (GRCm38)	missense	probably benign	0.05
R4914:Exoc2	UTSW	13	30,876,813 (GRCm38)	missense	probably benign	0.21
R5299:Exoc2	UTSW	13	30,871,918 (GRCm38)	splice site	probably null
R5410:Exoc2	UTSW	13	30,864,856 (GRCm38)	missense	probably damaging	0.98
R5461:Exoc2	UTSW	13	30,925,755 (GRCm38)	missense	possibly damaging	0.66
R5956:Exoc2	UTSW	13	30,820,623 (GRCm38)	missense	probably benign	0.03
R6056:Exoc2	UTSW	13	30,900,829 (GRCm38)	missense	probably benign	0.03
R6107:Exoc2	UTSW	13	30,876,797 (GRCm38)	missense	probably benign
R6548:Exoc2	UTSW	13	30,826,064 (GRCm38)	missense	possibly damaging	0.86
R6692:Exoc2	UTSW	13	30,935,507 (GRCm38)	missense	probably benign	0.09
R6969:Exoc2	UTSW	13	30,911,178 (GRCm38)	missense	probably benign
R7386:Exoc2	UTSW	13	30,906,663 (GRCm38)	splice site	probably null
R7461:Exoc2	UTSW	13	30,882,272 (GRCm38)	missense	probably benign	0.32
R7467:Exoc2	UTSW	13	30,925,733 (GRCm38)	missense	probably damaging	0.98
R7473:Exoc2	UTSW	13	30,822,630 (GRCm38)	critical splice donor site	probably null
R7613:Exoc2	UTSW	13	30,882,272 (GRCm38)	missense	probably benign	0.32
R7767:Exoc2	UTSW	13	30,876,769 (GRCm38)	missense	probably benign	0.01
R7793:Exoc2	UTSW	13	30,911,178 (GRCm38)	missense	probably benign	0.00
R7795:Exoc2	UTSW	13	30,876,773 (GRCm38)	nonsense	probably null
R7993:Exoc2	UTSW	13	30,906,730 (GRCm38)	critical splice donor site	probably null
R8085:Exoc2	UTSW	13	30,940,703 (GRCm38)	missense	probably damaging	1.00
R8330:Exoc2	UTSW	13	30,877,573 (GRCm38)	missense	probably benign
R8716:Exoc2	UTSW	13	30,911,244 (GRCm38)	missense	probably damaging	1.00
R8735:Exoc2	UTSW	13	30,906,839 (GRCm38)	missense	probably damaging	1.00
R8922:Exoc2	UTSW	13	30,871,855 (GRCm38)	missense	probably benign	0.05
R9237:Exoc2	UTSW	13	30,864,875 (GRCm38)	missense	probably benign
R9243:Exoc2	UTSW	13	30,925,795 (GRCm38)	missense	probably benign	0.03
R9365:Exoc2	UTSW	13	30,856,714 (GRCm38)	missense	probably benign	0.00
R9731:Exoc2	UTSW	13	30,877,250 (GRCm38)	missense	probably benign	0.06

Predicted Primers

PCR Primer
(F):5'- TTTCTGCACCACCATGCTGG -3'
(R):5'- ATAAGGTGGGCCCTCTTCCATC -3'

Sequencing Primer
(F):5'- CACCACCATGCTGGGGAAAAG -3'
(R):5'- CCATCAGTCGTTAATTAGAAAATGC -3'

Posted On

2014-09-17