Mutagenetix > Incidental Mutation

Incidental Mutation 'R6299:Exoc3l4'

508990

Institutional Source

Beutler Lab

Gene Symbol

Exoc3l4

Ensembl Gene

ENSMUSG00000021280

Gene Name

exocyst complex component 3-like 4

Synonyms

1600013K19Rik, 1200009I06Rik

MMRRC Submission

044465-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.099) question?

Stock #

R6299 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

111383864-111398114 bp(+) (GRCm39)

Type of Mutation

start codon destroyed

DNA Base Change (assembly)

A to T at 111388513 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 1 (M1L)

Ref Sequence

ENSEMBL: ENSMUSP00000152337 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072646] [ENSMUST00000220537] [ENSMUST00000220852] [ENSMUST00000221144] [ENSMUST00000222897] [ENSMUST00000223431] [ENSMUST00000223050] [ENSMUST00000222437]

AlphaFold

no structure available at present

Predicted Effect

possibly damaging
Transcript: ENSMUST00000072646
AA Change: M1L

PolyPhen 2 Score 0.588 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000072438
Gene: ENSMUSG00000021280
AA Change: M1L

Domain	Start	End	E-Value	Type
low complexity region	75	89	N/A	INTRINSIC
Pfam:Sec6	181	708	7.1e-111	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181085

Predicted Effect

unknown
Transcript: ENSMUST00000220537
AA Change: M1L

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000220636

Predicted Effect

probably benign
Transcript: ENSMUST00000220852
AA Change: M1L

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)

Predicted Effect

probably benign
Transcript: ENSMUST00000221144
AA Change: M1L

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222126

Predicted Effect

possibly damaging
Transcript: ENSMUST00000222897
AA Change: M1L

PolyPhen 2 Score 0.588 (Sensitivity: 0.87; Specificity: 0.91)

Predicted Effect

probably benign
Transcript: ENSMUST00000223431
AA Change: M1L

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000223050
AA Change: M1L

PolyPhen 2 Score 0.588 (Sensitivity: 0.87; Specificity: 0.91)

Predicted Effect

probably benign
Transcript: ENSMUST00000222437
AA Change: M1L

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.2%

Validation Efficiency

100% (61/61)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Bms1	G	A	6: 118,395,476 (GRCm39)	R24W	probably damaging	Het
C130050O18Rik	A	T	5: 139,400,126 (GRCm39)	S60C	probably damaging	Het
Cabcoco1	A	G	10: 68,272,720 (GRCm39)	Y222H	probably damaging	Het
Cc2d1b	T	C	4: 108,485,335 (GRCm39)	V559A	probably benign	Het
Cgrrf1	T	A	14: 47,077,647 (GRCm39)	N46K	probably damaging	Het
Clca3a1	T	C	3: 144,464,275 (GRCm39)	D114G	probably damaging	Het
Clcnkb	T	A	4: 141,138,034 (GRCm39)	L279F	probably damaging	Het
Cr2	T	C	1: 194,850,954 (GRCm39)	T151A	probably damaging	Het
Creb3l3	C	T	10: 80,924,447 (GRCm39)	E236K	probably damaging	Het
Dcstamp	T	A	15: 39,618,599 (GRCm39)	V336D	probably damaging	Het
Dop1a	T	G	9: 86,386,265 (GRCm39)	F379V	probably damaging	Het
Esf1	T	C	2: 139,965,554 (GRCm39)	K714R	possibly damaging	Het
Extl3	T	C	14: 65,314,121 (GRCm39)	R354G	probably benign	Het
Fastkd3	T	C	13: 68,735,855 (GRCm39)	L535P	probably damaging	Het
Gab2	A	G	7: 96,731,066 (GRCm39)	T12A	probably benign	Het
Gm10549	C	A	18: 33,597,358 (GRCm39)		probably benign	Het
Golga4	T	A	9: 118,386,438 (GRCm39)	S1187T	probably benign	Het
Haus3	A	G	5: 34,325,140 (GRCm39)	V173A	probably benign	Het
Herc2	T	A	7: 55,784,803 (GRCm39)	Y1416N	possibly damaging	Het
Hspg2	A	G	4: 137,272,016 (GRCm39)	Y2566C	probably damaging	Het
Inpp5f	A	T	7: 128,237,884 (GRCm39)	T34S	possibly damaging	Het
Iqck	G	A	7: 118,475,485 (GRCm39)	G70S	unknown	Het
Jade1	T	C	3: 41,568,160 (GRCm39)	F743L	probably damaging	Het
Kif5a	T	C	10: 127,069,690 (GRCm39)	K845R	probably damaging	Het
Klhl30	A	G	1: 91,285,636 (GRCm39)		probably null	Het
Map2k1	T	C	9: 64,121,772 (GRCm39)	D67G	possibly damaging	Het
Mcm9	A	C	10: 53,413,777 (GRCm39)	C434W	probably damaging	Het
Muc4	T	G	16: 32,570,853 (GRCm39)	S638A	possibly damaging	Het
Nectin3	A	G	16: 46,284,345 (GRCm39)	V113A	probably damaging	Het
Nfya	T	C	17: 48,699,938 (GRCm39)		probably benign	Het
Nup155	G	T	15: 8,157,922 (GRCm39)	A460S	possibly damaging	Het
Nup210	T	C	6: 91,051,270 (GRCm39)	E371G	possibly damaging	Het
Olfm3	T	C	3: 114,914,632 (GRCm39)	S228P	probably damaging	Het
Or52n20	C	A	7: 104,320,075 (GRCm39)	D55E	probably benign	Het
Or8b51	A	T	9: 38,569,073 (GRCm39)	I205N	possibly damaging	Het
Plin1	A	C	7: 79,371,224 (GRCm39)	V500G	probably benign	Het
Ppfia1	A	C	7: 144,064,049 (GRCm39)	M513R	probably benign	Het
Ppp1cb	T	A	5: 32,640,798 (GRCm39)	C27*	probably null	Het
Prss22	T	A	17: 24,215,408 (GRCm39)	I123F	probably damaging	Het
Rbm24	G	T	13: 46,572,549 (GRCm39)	V15L	probably damaging	Het
Reln	T	C	5: 22,491,942 (GRCm39)	T97A	possibly damaging	Het
Sipa1l2	T	C	8: 126,180,203 (GRCm39)	T1065A	possibly damaging	Het
Sipa1l3	A	C	7: 29,065,974 (GRCm39)		probably null	Het
Snrnp200	T	A	2: 127,064,081 (GRCm39)	Y689*	probably null	Het
Srcap	T	C	7: 127,129,626 (GRCm39)		probably benign	Het
Sv2a	T	C	3: 96,095,565 (GRCm39)		probably null	Het
Tcf12	A	T	9: 71,766,211 (GRCm39)	V474D	probably damaging	Het
Tpcn2	A	T	7: 144,815,980 (GRCm39)	S403T	probably damaging	Het
Trim65	C	A	11: 116,017,377 (GRCm39)	A362S	probably benign	Het
Trmt1	T	A	8: 85,423,919 (GRCm39)	C36*	probably null	Het
Trpm8	T	A	1: 88,282,201 (GRCm39)	L699Q	probably damaging	Het
Ube2m	A	C	7: 12,769,797 (GRCm39)	I116R	probably damaging	Het
Ulk1	T	C	5: 110,938,963 (GRCm39)	K492E	possibly damaging	Het
Usp40	T	A	1: 87,925,649 (GRCm39)	K193N	probably damaging	Het
Vmn1r3	A	G	4: 3,185,098 (GRCm39)	S70P	possibly damaging	Het
Vmn2r2	T	A	3: 64,024,074 (GRCm39)	K836*	probably null	Het
Vmn2r75	T	A	7: 85,814,482 (GRCm39)	H337L	probably benign	Het
Wars1	G	A	12: 108,827,309 (GRCm39)	T437M	probably benign	Het
Zdhhc5	T	C	2: 84,520,825 (GRCm39)	T451A	probably benign	Het
Zfp788	T	G	7: 41,297,965 (GRCm39)	H180Q	possibly damaging	Het
Zkscan7	A	G	9: 122,717,782 (GRCm39)	E59G	probably damaging	Het

Other mutations in Exoc3l4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01663:Exoc3l4	APN	12	111,395,845 (GRCm39)	splice site	probably benign
IGL02048:Exoc3l4	APN	12	111,394,917 (GRCm39)	missense	probably benign	0.00
IGL03049:Exoc3l4	APN	12	111,389,835 (GRCm39)	missense	probably damaging	0.96
IGL03069:Exoc3l4	APN	12	111,390,457 (GRCm39)	missense	probably damaging	1.00
IGL03123:Exoc3l4	APN	12	111,388,547 (GRCm39)	missense	probably damaging	1.00
R0631:Exoc3l4	UTSW	12	111,394,400 (GRCm39)	missense	probably benign	0.34
R1377:Exoc3l4	UTSW	12	111,395,104 (GRCm39)	missense	probably damaging	1.00
R2223:Exoc3l4	UTSW	12	111,392,586 (GRCm39)	missense	possibly damaging	0.73
R2402:Exoc3l4	UTSW	12	111,388,690 (GRCm39)	missense	possibly damaging	0.94
R2884:Exoc3l4	UTSW	12	111,394,956 (GRCm39)	missense	possibly damaging	0.93
R3770:Exoc3l4	UTSW	12	111,391,989 (GRCm39)	missense	probably benign
R4843:Exoc3l4	UTSW	12	111,394,487 (GRCm39)	intron	probably benign
R4903:Exoc3l4	UTSW	12	111,395,155 (GRCm39)	missense	probably benign	0.00
R4964:Exoc3l4	UTSW	12	111,395,155 (GRCm39)	missense	probably benign	0.00
R4966:Exoc3l4	UTSW	12	111,395,155 (GRCm39)	missense	probably benign	0.00
R5082:Exoc3l4	UTSW	12	111,394,424 (GRCm39)	missense	probably benign	0.04
R5152:Exoc3l4	UTSW	12	111,397,327 (GRCm39)	utr 3 prime	probably benign
R5210:Exoc3l4	UTSW	12	111,395,275 (GRCm39)	intron	probably benign
R5667:Exoc3l4	UTSW	12	111,389,851 (GRCm39)	missense	probably damaging	1.00
R5671:Exoc3l4	UTSW	12	111,389,851 (GRCm39)	missense	probably damaging	1.00
R5712:Exoc3l4	UTSW	12	111,390,476 (GRCm39)	nonsense	probably null
R5873:Exoc3l4	UTSW	12	111,389,850 (GRCm39)	missense	probably damaging	1.00
R5947:Exoc3l4	UTSW	12	111,388,835 (GRCm39)	missense	possibly damaging	0.94
R6332:Exoc3l4	UTSW	12	111,394,402 (GRCm39)	missense	possibly damaging	0.79
R6489:Exoc3l4	UTSW	12	111,395,131 (GRCm39)	missense	probably damaging	1.00
R7225:Exoc3l4	UTSW	12	111,390,058 (GRCm39)	missense	probably benign	0.10
R7643:Exoc3l4	UTSW	12	111,388,369 (GRCm39)	intron	probably benign
R7731:Exoc3l4	UTSW	12	111,397,182 (GRCm39)	missense	possibly damaging	0.94
R7791:Exoc3l4	UTSW	12	111,389,974 (GRCm39)	missense	probably damaging	1.00
R8723:Exoc3l4	UTSW	12	111,397,092 (GRCm39)	splice site	probably benign
R8942:Exoc3l4	UTSW	12	111,392,003 (GRCm39)	missense	probably benign	0.17
R8942:Exoc3l4	UTSW	12	111,392,002 (GRCm39)	missense	possibly damaging	0.53
R9145:Exoc3l4	UTSW	12	111,388,586 (GRCm39)	missense	probably benign
R9334:Exoc3l4	UTSW	12	111,397,117 (GRCm39)	missense	probably damaging	0.99
Z1088:Exoc3l4	UTSW	12	111,395,921 (GRCm39)	missense	probably benign	0.29
Z1176:Exoc3l4	UTSW	12	111,390,154 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2018-04-02