Mutagenetix > Incidental Mutation

Incidental Mutation 'R5274:Esyt3'

403830

Institutional Source

Beutler Lab

Gene Symbol

Esyt3

Ensembl Gene

ENSMUSG00000037681

Gene Name

extended synaptotagmin-like protein 3

Synonyms

D9Ertd280e, Fam62c

MMRRC Submission

042837-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5274 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

99192016-99240610 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 99200350 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 615 (T615A)

Ref Sequence

ENSEMBL: ENSMUSP00000038757 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042158] [ENSMUST00000187520]

AlphaFold

Q5DTI8

Predicted Effect

probably benign
Transcript: ENSMUST00000042158
AA Change: T615A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000038757
Gene: ENSMUSG00000037681
AA Change: T615A

Domain	Start	End	E-Value	Type
transmembrane domain	54	76	N/A	INTRINSIC
Pfam:SMP_LBD	118	295	3.7e-63	PFAM
C2	311	411	9.23e-20	SMART
low complexity region	422	432	N/A	INTRINSIC
C2	449	563	6.6e-7	SMART
low complexity region	658	673	N/A	INTRINSIC
low complexity region	729	739	N/A	INTRINSIC
C2	775	880	4.91e-15	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000186626

Predicted Effect

probably benign
Transcript: ENSMUST00000187520

SMART Domains

Protein: ENSMUSP00000140567
Gene: ENSMUSG00000037681

Domain	Start	End	E-Value	Type
C2	2	83	5.9e-12	SMART
low complexity region	94	104	N/A	INTRINSIC
C2	121	198	2.2e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191694

Coding Region Coverage

1x: 99.5%
3x: 98.9%
10x: 98.0%
20x: 96.9%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice are viable and fertile without overt morphological defects. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921539E11Rik	C	T	4: 103,092,856 (GRCm39)	R155H	probably benign	Het
Ace	T	C	11: 105,858,863 (GRCm39)	M19T	probably benign	Het
Agl	A	G	3: 116,566,135 (GRCm39)	L995P	probably damaging	Het
AY761185	T	C	8: 21,433,889 (GRCm39)	N90S	unknown	Het
Brca2	T	C	5: 150,463,154 (GRCm39)	S973P	probably benign	Het
Cacna1e	T	C	1: 154,576,250 (GRCm39)	T66A	probably damaging	Het
Cbarp	T	C	10: 79,967,649 (GRCm39)	S531G	possibly damaging	Het
Cby2	A	G	14: 75,820,666 (GRCm39)	V362A	probably benign	Het
Cd96	G	T	16: 45,890,066 (GRCm39)	T319K	possibly damaging	Het
Ceacam23	T	C	7: 17,649,642 (GRCm39)		probably null	Het
Chil5	A	C	3: 105,936,169 (GRCm39)	F41C	probably damaging	Het
Col24a1	A	C	3: 145,190,433 (GRCm39)	E1239D	probably benign	Het
Dip2b	A	G	15: 100,109,985 (GRCm39)	E1490G	possibly damaging	Het
Dync1li1	T	C	9: 114,544,273 (GRCm39)	V315A	possibly damaging	Het
Dync2h1	T	C	9: 7,116,540 (GRCm39)	S99G	probably benign	Het
Dynlt5	A	T	4: 102,859,768 (GRCm39)	T103S	possibly damaging	Het
E2f8	C	T	7: 48,516,925 (GRCm39)	R818H	probably damaging	Het
Eomes	T	C	9: 118,309,597 (GRCm39)	V250A	probably damaging	Het
Fbxo38	A	T	18: 62,648,140 (GRCm39)	D799E	probably damaging	Het
Fdft1	A	G	14: 63,389,792 (GRCm39)	F288S	probably damaging	Het
Gm14325	G	A	2: 177,474,777 (GRCm39)	H102Y	possibly damaging	Het
Gm4871	C	G	5: 144,967,180 (GRCm39)	E185Q	probably damaging	Het
Gm5901	C	A	7: 105,026,655 (GRCm39)	P141Q	probably damaging	Het
Herc1	T	A	9: 66,306,691 (GRCm39)	I933N	probably benign	Het
Ifih1	T	C	2: 62,442,062 (GRCm39)	Q385R	probably benign	Het
Ighmbp2	T	C	19: 3,315,518 (GRCm39)	E634G	probably damaging	Het
Klk6	C	G	7: 43,478,553 (GRCm39)		probably null	Het
Kmt2d	A	G	15: 98,752,111 (GRCm39)		probably benign	Het
Lig3	T	A	11: 82,688,118 (GRCm39)		probably null	Het
Lrp1b	T	C	2: 41,234,456 (GRCm39)	D310G	probably null	Het
Mroh6	A	G	15: 75,756,849 (GRCm39)	V571A	possibly damaging	Het
Olfm5	A	G	7: 103,809,190 (GRCm39)	S132P	probably damaging	Het
Or52n20	T	C	7: 104,320,733 (GRCm39)	S275P	probably damaging	Het
Or5p64	A	T	7: 107,854,842 (GRCm39)	F168I	probably benign	Het
Pacc1	T	C	1: 191,080,665 (GRCm39)	V295A	probably damaging	Het
Patj	G	C	4: 98,407,218 (GRCm39)	S4T	probably damaging	Het
Pcdhga12	T	A	18: 37,899,475 (GRCm39)	C102*	probably null	Het
Pik3ap1	T	C	19: 41,270,391 (GRCm39)	D766G	possibly damaging	Het
Plch2	A	T	4: 155,083,411 (GRCm39)	L408Q	probably damaging	Het
Pnma2	G	T	14: 67,154,209 (GRCm39)	R211L	probably damaging	Het
Prkg2	T	A	5: 99,117,850 (GRCm39)	H468L	probably damaging	Het
Rad1	T	A	15: 10,488,059 (GRCm39)		probably null	Het
Rims3	A	G	4: 120,748,571 (GRCm39)	D264G	probably damaging	Het
Rnf123	AT	ATT	9: 107,941,202 (GRCm39)		probably null	Het
Rrm2	T	A	12: 24,760,406 (GRCm39)	Y75*	probably null	Het
Sall3	T	C	18: 81,013,052 (GRCm39)	N1128S	probably benign	Het
Slc26a5	T	C	5: 22,018,899 (GRCm39)	T610A	possibly damaging	Het
Snx29	G	T	16: 11,556,268 (GRCm39)	E766D	probably damaging	Het
Sox17	A	G	1: 4,562,111 (GRCm39)	V298A	possibly damaging	Het
Ss18	G	A	18: 14,774,106 (GRCm39)	Q228*	probably null	Het
Tas2r121	A	G	6: 132,677,811 (GRCm39)	S54P	probably damaging	Het
Ttc21b	T	C	2: 66,066,627 (GRCm39)	E342G	possibly damaging	Het
Ubap2l	A	G	3: 89,920,037 (GRCm39)	Y818H	probably damaging	Het
Usp15	C	A	10: 123,004,256 (GRCm39)	R166I	probably damaging	Het
Vmn1r34	T	G	6: 66,614,123 (GRCm39)	H205P	probably damaging	Het
Vmn2r22	A	T	6: 123,627,593 (GRCm39)	M1K	probably null	Het
Vps51	T	G	19: 6,121,063 (GRCm39)	E283D	probably benign	Het
Zdhhc1	T	C	8: 106,210,402 (GRCm39)	N5S	probably benign	Het
Zfp758	T	A	17: 22,594,836 (GRCm39)	C441S	probably benign	Het
Zp2	T	C	7: 119,737,315 (GRCm39)	E291G	possibly damaging	Het

Other mutations in Esyt3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02576:Esyt3	APN	9	99,197,278 (GRCm39)	missense	probably benign	0.07
IGL02596:Esyt3	APN	9	99,210,068 (GRCm39)	missense	probably benign	0.02
IGL02716:Esyt3	APN	9	99,199,277 (GRCm39)	missense	probably damaging	1.00
IGL02836:Esyt3	APN	9	99,202,960 (GRCm39)	splice site	probably benign
IGL03372:Esyt3	APN	9	99,218,109 (GRCm39)	splice site	probably benign
R0008:Esyt3	UTSW	9	99,220,860 (GRCm39)	missense	possibly damaging	0.89
R1217:Esyt3	UTSW	9	99,200,097 (GRCm39)	missense	possibly damaging	0.92
R1395:Esyt3	UTSW	9	99,198,835 (GRCm39)	unclassified	probably benign
R1478:Esyt3	UTSW	9	99,200,119 (GRCm39)	missense	probably benign	0.03
R1710:Esyt3	UTSW	9	99,218,244 (GRCm39)	missense	probably benign
R1792:Esyt3	UTSW	9	99,240,169 (GRCm39)	nonsense	probably null
R1913:Esyt3	UTSW	9	99,202,364 (GRCm39)	missense	probably benign	0.00
R3792:Esyt3	UTSW	9	99,197,334 (GRCm39)	missense	possibly damaging	0.93
R3793:Esyt3	UTSW	9	99,197,334 (GRCm39)	missense	possibly damaging	0.93
R3937:Esyt3	UTSW	9	99,218,245 (GRCm39)	missense	probably benign
R3964:Esyt3	UTSW	9	99,202,375 (GRCm39)	missense	probably damaging	1.00
R3965:Esyt3	UTSW	9	99,202,375 (GRCm39)	missense	probably damaging	1.00
R4061:Esyt3	UTSW	9	99,202,891 (GRCm39)	missense	probably damaging	1.00
R4088:Esyt3	UTSW	9	99,206,290 (GRCm39)	missense	probably benign
R4436:Esyt3	UTSW	9	99,240,078 (GRCm39)	intron	probably benign
R5590:Esyt3	UTSW	9	99,240,466 (GRCm39)	utr 5 prime	probably benign
R5705:Esyt3	UTSW	9	99,200,260 (GRCm39)	missense	probably benign	0.00
R6543:Esyt3	UTSW	9	99,220,825 (GRCm39)	missense	possibly damaging	0.77
R6738:Esyt3	UTSW	9	99,202,346 (GRCm39)	missense	probably damaging	0.98
R7000:Esyt3	UTSW	9	99,204,206 (GRCm39)	missense	probably damaging	0.99
R7019:Esyt3	UTSW	9	99,197,338 (GRCm39)	missense	probably benign	0.11
R7104:Esyt3	UTSW	9	99,220,840 (GRCm39)	missense	probably damaging	1.00
R7130:Esyt3	UTSW	9	99,200,223 (GRCm39)	missense	probably benign
R7141:Esyt3	UTSW	9	99,203,493 (GRCm39)	missense	probably benign	0.12
R7145:Esyt3	UTSW	9	99,201,627 (GRCm39)	missense	probably damaging	1.00
R7447:Esyt3	UTSW	9	99,203,615 (GRCm39)	missense	probably damaging	1.00
R7459:Esyt3	UTSW	9	99,240,117 (GRCm39)	missense	probably benign	0.00
R7767:Esyt3	UTSW	9	99,207,024 (GRCm39)	missense	probably benign	0.00
R8397:Esyt3	UTSW	9	99,209,966 (GRCm39)	missense	probably benign	0.01
R8560:Esyt3	UTSW	9	99,202,375 (GRCm39)	missense	probably damaging	1.00
R8882:Esyt3	UTSW	9	99,202,909 (GRCm39)	missense	probably damaging	0.99
R9320:Esyt3	UTSW	9	99,194,044 (GRCm39)	missense	probably damaging	1.00
R9537:Esyt3	UTSW	9	99,199,292 (GRCm39)	missense	probably damaging	0.98
R9786:Esyt3	UTSW	9	99,194,038 (GRCm39)	missense	possibly damaging	0.64

Predicted Primers

PCR Primer
(F):5'- TTTCCAGGGGACTCACAGAG -3'
(R):5'- TAGGAACTGGGAACTCTTGAGG -3'

Sequencing Primer
(F):5'- GCACTGTCCTTGCCTTTGGG -3'
(R):5'- CTGGGAACTCTTGAGGACAGG -3'

Posted On

2016-07-22