Mutagenetix > Incidental Mutation

Incidental Mutation 'R1657:Snap47'

186478

Institutional Source

Beutler Lab

Gene Symbol

Snap47

Ensembl Gene

ENSMUSG00000009894

Gene Name

synaptosomal-associated protein, 47

Synonyms

SNAP-47, 1110031B06Rik

MMRRC Submission

039693-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1657 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

59407134-59451186 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 59428770 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 181 (S181T)

Ref Sequence

ENSEMBL: ENSMUSP00000010038 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000010038] [ENSMUST00000120940] [ENSMUST00000136436] [ENSMUST00000156146]

AlphaFold

Q8R570

Predicted Effect

probably benign
Transcript: ENSMUST00000010038
AA Change: S181T

PolyPhen 2 Score 0.079 (Sensitivity: 0.93; Specificity: 0.85)

SMART Domains

Protein: ENSMUSP00000010038
Gene: ENSMUSG00000009894
AA Change: S181T

Domain	Start	End	E-Value	Type
coiled coil region	125	173	N/A	INTRINSIC
SCOP:d1fpza_	181	234	3e-3	SMART
low complexity region	335	349	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000120940
AA Change: S181T

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000113555
Gene: ENSMUSG00000009894
AA Change: S181T

Domain	Start	End	E-Value	Type
coiled coil region	125	173	N/A	INTRINSIC
SCOP:d1fpza_	181	234	3e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000136436
AA Change: S181T

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000115762
Gene: ENSMUSG00000009894
AA Change: S181T

Domain	Start	End	E-Value	Type
coiled coil region	125	173	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000156146
AA Change: S181T

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)

SMART Domains

Protein: ENSMUSP00000121880
Gene: ENSMUSG00000009894
AA Change: S181T

Domain	Start	End	E-Value	Type
coiled coil region	125	173	N/A	INTRINSIC

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.5%
20x: 93.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610009B22Rik	T	C	11: 51,685,678 (GRCm38)	Q131R	probably benign	Het
3632451O06Rik	G	C	14: 49,773,560 (GRCm38)	T230S	probably damaging	Het
Acaca	T	G	11: 84,264,084 (GRCm38)	D988E	probably benign	Het
Als2	A	G	1: 59,180,601 (GRCm38)	V1185A	probably damaging	Het
Amdhd2	A	G	17: 24,156,055 (GRCm38)	V391A	probably damaging	Het
Caprin1	A	T	2: 103,769,506 (GRCm38)	V608E	probably damaging	Het
Celsr3	T	A	9: 108,842,952 (GRCm38)	C2512*	probably null	Het
Cfl1	A	T	19: 5,493,555 (GRCm38)	R187W	probably damaging	Het
Cgnl1	C	T	9: 71,725,944 (GRCm38)	V42I	probably damaging	Het
Chd2	A	G	7: 73,480,430 (GRCm38)	Y826H	probably damaging	Het
Col9a2	C	A	4: 121,040,974 (GRCm38)	P28T	unknown	Het
Cyp3a44	G	A	5: 145,779,743 (GRCm38)	P346S	probably damaging	Het
Dact2	A	G	17: 14,197,990 (GRCm38)	V151A	probably benign	Het
Dhx29	T	C	13: 112,952,843 (GRCm38)	I716T	probably damaging	Het
Esam	T	C	9: 37,537,621 (GRCm38)	S342P	probably damaging	Het
Fam189a2	C	A	19: 23,975,635 (GRCm38)	C437F	probably damaging	Het
Fer1l4	A	G	2: 156,035,598 (GRCm38)	V1053A	possibly damaging	Het
Grk3	A	G	5: 112,966,982 (GRCm38)	F124S	probably damaging	Het
H2-DMa	G	A	17: 34,137,399 (GRCm38)		probably null	Het
Hsd3b5	T	A	3: 98,619,720 (GRCm38)	I137F	possibly damaging	Het
Itgav	A	T	2: 83,801,779 (GRCm38)	I902F	probably benign	Het
Itsn1	G	T	16: 91,909,223 (GRCm38)	C179F	probably damaging	Het
Kcnh8	G	A	17: 52,839,125 (GRCm38)	R347H	probably damaging	Het
Kif9	T	C	9: 110,489,966 (GRCm38)	M166T	possibly damaging	Het
Kmt5c	C	T	7: 4,746,454 (GRCm38)	Q324*	probably null	Het
Lcn9	G	A	2: 25,824,710 (GRCm38)	E154K	probably benign	Het
Mfge8	A	T	7: 79,141,773 (GRCm38)	L227Q	probably benign	Het
Mroh2b	A	T	15: 4,931,043 (GRCm38)	R753*	probably null	Het
Mtif2	G	A	11: 29,540,721 (GRCm38)	R475Q	probably benign	Het
Nln	C	T	13: 104,036,947 (GRCm38)	V584I	possibly damaging	Het
Nr2e3	T	C	9: 59,948,767 (GRCm38)	E129G	probably benign	Het
Ocstamp	T	C	2: 165,397,516 (GRCm38)	D250G	probably damaging	Het
Olfr1065	A	C	2: 86,445,218 (GRCm38)	L255V	probably damaging	Het
Olfr403	A	T	11: 74,195,896 (GRCm38)	H131L	probably damaging	Het
Olfr503	T	C	7: 108,545,377 (GRCm38)	I284T	possibly damaging	Het
Pld1	A	T	3: 28,071,187 (GRCm38)	I417L	probably benign	Het
Polr1a	A	T	6: 71,941,535 (GRCm38)	K692N	probably damaging	Het
Qsox2	A	T	2: 26,220,747 (GRCm38)	Y152*	probably null	Het
Rpap1	T	C	2: 119,783,778 (GRCm38)	D46G	possibly damaging	Het
Rpe65	A	G	3: 159,614,448 (GRCm38)	T246A	probably damaging	Het
Scn5a	T	C	9: 119,562,380 (GRCm38)	D82G	probably damaging	Het
Sema3d	A	G	5: 12,584,974 (GRCm38)	E669G	possibly damaging	Het
Serpinb6c	T	C	13: 33,880,226 (GRCm38)	N282S	probably benign	Het
Snx9	A	C	17: 5,918,436 (GRCm38)	T336P	possibly damaging	Het
Sphkap	G	A	1: 83,277,515 (GRCm38)	R838*	probably null	Het
Terb1	A	T	8: 104,488,491 (GRCm38)	D284E	possibly damaging	Het
Tmem266	C	T	9: 55,418,008 (GRCm38)	A153V	probably damaging	Het
Ttn	T	C	2: 76,742,804 (GRCm38)	E25915G	possibly damaging	Het
Tubal3	A	G	13: 3,933,011 (GRCm38)	T264A	possibly damaging	Het
Vldlr	G	A	19: 27,245,670 (GRCm38)	R747Q	probably benign	Het
Zc3h8	G	T	2: 128,929,957 (GRCm38)		probably benign	Het
Zfp184	C	T	13: 21,959,273 (GRCm38)	T383M	probably damaging	Het
Zfp455	T	C	13: 67,198,639 (GRCm38)	F38S	possibly damaging	Het
Zfp746	A	G	6: 48,082,174 (GRCm38)	V167A	possibly damaging	Het
Zfp985	T	A	4: 147,584,110 (GRCm38)	N478K	probably benign	Het

Other mutations in Snap47

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01777:Snap47	APN	11	59,421,651 (GRCm38)	critical splice acceptor site	probably null
IGL02113:Snap47	APN	11	59,428,436 (GRCm38)	missense	probably damaging	0.99
IGL03290:Snap47	APN	11	59,428,598 (GRCm38)	missense	probably damaging	1.00
R0126:Snap47	UTSW	11	59,437,987 (GRCm38)	missense	probably damaging	0.99
R0582:Snap47	UTSW	11	59,428,433 (GRCm38)	nonsense	probably null
R0633:Snap47	UTSW	11	59,428,613 (GRCm38)	missense	probably benign	0.25
R0883:Snap47	UTSW	11	59,438,500 (GRCm38)	utr 5 prime	probably benign
R1855:Snap47	UTSW	11	59,428,333 (GRCm38)	unclassified	probably benign
R2761:Snap47	UTSW	11	59,438,059 (GRCm38)	missense	probably benign	0.01
R4079:Snap47	UTSW	11	59,428,551 (GRCm38)	missense	probably benign	0.38
R4805:Snap47	UTSW	11	59,428,517 (GRCm38)	missense	possibly damaging	0.91
R4960:Snap47	UTSW	11	59,428,543 (GRCm38)	missense	probably damaging	1.00
R5212:Snap47	UTSW	11	59,428,352 (GRCm38)	missense	probably damaging	0.99
R5793:Snap47	UTSW	11	59,438,192 (GRCm38)	missense	probably damaging	1.00
R7243:Snap47	UTSW	11	59,428,722 (GRCm38)	missense	probably benign	0.04
R7603:Snap47	UTSW	11	59,428,547 (GRCm38)	missense	probably damaging	1.00
R7870:Snap47	UTSW	11	59,438,078 (GRCm38)	missense	probably benign	0.11
R8001:Snap47	UTSW	11	59,438,354 (GRCm38)	missense	probably benign	0.20
R9156:Snap47	UTSW	11	59,428,464 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGTGAGCTTTCCCAGCTTGGAATG -3'
(R):5'- AGCAGTCTGCTGAGAACAGCAAC -3'

Sequencing Primer
(F):5'- GGAATGAGACTCTGCTCTCTCAG -3'
(R):5'- tcgggaggcagaggcag -3'

Posted On

2014-05-09