Mutagenetix > Incidental Mutation

Incidental Mutation 'R1773:Scg2'

196770

Institutional Source

Beutler Lab

Gene Symbol

Scg2

Ensembl Gene

ENSMUSG00000050711

Gene Name

secretogranin II

Synonyms

SgII, Chgc

MMRRC Submission

039804-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1773 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

79434669-79440120 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 79435635 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 417 (N417S)

Ref Sequence

ENSEMBL: ENSMUSP00000139740 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049972] [ENSMUST00000185234]

AlphaFold

Q03517

Predicted Effect

probably benign
Transcript: ENSMUST00000049972
AA Change: N457S

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000062556
Gene: ENSMUSG00000050711
AA Change: N457S

Domain	Start	End	E-Value	Type
Pfam:Granin	27	614	7.2e-235	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000185234
AA Change: N417S

PolyPhen 2 Score 0.037 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000139740
Gene: ENSMUSG00000050711
AA Change: N417S

Domain	Start	End	E-Value	Type
Pfam:Granin	27	319	1.4e-123	PFAM
Pfam:Granin	316	574	7.1e-91	PFAM

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.4%
20x: 92.9%

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 member of the chromogranin/secretogranin family of neuroendocrine secretory proteins. Studies in rodents suggest that the full-length protein, secretogranin II, is involved in the packaging or sorting of peptide hormones and neuropeptides into secretory vesicles. The full-length protein is cleaved to produce the active peptide secretoneurin, which exerts chemotaxic effects on specific cell types, and EM66, whose function is unknown. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 96 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310022A10Rik	A	G	7: 27,580,595 (GRCm38)	K334E	probably damaging	Het
Abca12	A	G	1: 71,288,596 (GRCm38)	Y1442H	probably damaging	Het
Acot12	A	G	13: 91,757,557 (GRCm38)	T79A	probably benign	Het
Adipoq	A	C	16: 23,155,238 (GRCm38)	Q26P	unknown	Het
Akap13	T	A	7: 75,683,451 (GRCm38)	N1582K	possibly damaging	Het
Alg9	A	G	9: 50,779,096 (GRCm38)	T133A	probably benign	Het
Anks3	T	C	16: 4,947,294 (GRCm38)	T418A	probably benign	Het
Ano3	A	C	2: 110,761,455 (GRCm38)	L37R	probably damaging	Het
Ano9	A	G	7: 141,108,378 (GRCm38)	F178L	possibly damaging	Het
Arhgef12	A	G	9: 43,005,542 (GRCm38)		probably null	Het
Arl16	T	A	11: 120,465,763 (GRCm38)	I137F	possibly damaging	Het
Brpf1	T	A	6: 113,319,931 (GRCm38)	S959T	possibly damaging	Het
C530008M17Rik	G	T	5: 76,867,205 (GRCm38)	A42S	possibly damaging	Het
Ccdc27	C	T	4: 154,041,765 (GRCm38)	R89Q	unknown	Het
Cd109	A	C	9: 78,703,724 (GRCm38)	Q1207H	probably benign	Het
Cd14	A	T	18: 36,725,304 (GRCm38)	V366D	possibly damaging	Het
Cep290	G	A	10: 100,510,573 (GRCm38)	V538I	probably benign	Het
Cep57	G	A	9: 13,816,068 (GRCm38)	A202V	probably damaging	Het
Chl1	T	C	6: 103,647,331 (GRCm38)		probably null	Het
Cmah	T	G	13: 24,417,299 (GRCm38)	F29L	probably benign	Het
Crybg1	A	G	10: 43,992,548 (GRCm38)	V1378A	possibly damaging	Het
Cryzl2	A	G	1: 157,470,722 (GRCm38)	K227R	probably benign	Het
D130043K22Rik	T	G	13: 24,882,602 (GRCm38)	V794G	possibly damaging	Het
Ddx4	T	A	13: 112,599,902 (GRCm38)	T645S	probably benign	Het
Dhcr7	C	T	7: 143,847,458 (GRCm38)	R453C	possibly damaging	Het
Dhx8	T	C	11: 101,752,363 (GRCm38)	Y754H	possibly damaging	Het
Dip2b	T	A	15: 100,193,961 (GRCm38)	D860E	probably benign	Het
Dnah7a	T	C	1: 53,432,887 (GRCm38)		probably null	Het
Dst	A	G	1: 34,291,899 (GRCm38)	D6937G	probably damaging	Het
Dusp1	A	G	17: 26,507,107 (GRCm38)	I204T	probably damaging	Het
Dync2h1	T	A	9: 7,128,256 (GRCm38)	Q1859L	probably damaging	Het
E4f1	C	A	17: 24,446,584 (GRCm38)	G328V	probably damaging	Het
Eml5	T	C	12: 98,798,839 (GRCm38)	Y1617C	probably damaging	Het
Espn	G	T	4: 152,128,229 (GRCm38)	P622Q	probably damaging	Het
Fam184b	G	A	5: 45,584,334 (GRCm38)	P185L	possibly damaging	Het
Fam71f1	T	C	6: 29,334,153 (GRCm38)	S335P	possibly damaging	Het
Fn1	T	A	1: 71,637,383 (GRCm38)	D563V	probably damaging	Het
Gad2	A	G	2: 22,690,207 (GRCm38)	Y540C	probably benign	Het
Gdf11	T	C	10: 128,891,294 (GRCm38)	D131G	probably damaging	Het
Gm19965	T	A	1: 116,821,259 (GRCm38)	Y223*	probably null	Het
H2-M10.6	A	G	17: 36,812,184 (GRCm38)	K3R	probably benign	Het
Hid1	A	G	11: 115,348,510 (GRCm38)	Y776H	probably damaging	Het
Hivep3	A	T	4: 120,098,837 (GRCm38)	K1450I	probably damaging	Het
Icam5	T	C	9: 21,033,525 (GRCm38)	L128P	possibly damaging	Het
Idnk	T	C	13: 58,157,712 (GRCm38)	V9A	probably damaging	Het
Il4ra	A	T	7: 125,567,182 (GRCm38)	T33S	possibly damaging	Het
Ino80	A	G	2: 119,418,409 (GRCm38)	V990A	probably benign	Het
Krtap4-9	T	C	11: 99,785,570 (GRCm38)		probably benign	Het
Lrrk2	A	G	15: 91,779,981 (GRCm38)	I1974V	possibly damaging	Het
Mcm3ap	C	T	10: 76,471,160 (GRCm38)	A369V	probably benign	Het
Nek6	A	G	2: 38,582,419 (GRCm38)	M252V	probably benign	Het
Nfasc	T	A	1: 132,610,839 (GRCm38)	I443F	probably damaging	Het
Nme8	T	G	13: 19,697,036 (GRCm38)	M1L	probably damaging	Het
Npnt	T	A	3: 132,904,693 (GRCm38)	Q423L	possibly damaging	Het
Nup133	A	T	8: 123,930,983 (GRCm38)	C404*	probably null	Het
Olfr1232	A	G	2: 89,325,742 (GRCm38)	V146A	probably benign	Het
Olfr1307	A	G	2: 111,944,859 (GRCm38)	V199A	possibly damaging	Het
Olfr1535	T	C	13: 21,555,812 (GRCm38)	D70G	probably damaging	Het
Olfr262	T	C	19: 12,241,659 (GRCm38)	M1V	probably null	Het
Olfr684	T	C	7: 105,156,983 (GRCm38)	E233G	probably benign	Het
Olfr806	A	G	10: 129,738,443 (GRCm38)	L158S	probably damaging	Het
Otog	T	A	7: 46,288,159 (GRCm38)	I1764N	probably benign	Het
Oxa1l	A	G	14: 54,363,452 (GRCm38)	I127M	probably benign	Het
P4hb	C	A	11: 120,572,726 (GRCm38)	V28F	probably damaging	Het
Pbld2	C	T	10: 63,054,371 (GRCm38)	A186V	probably benign	Het
Pdzph1	G	T	17: 58,974,813 (GRCm38)	T158K	probably damaging	Het
Pgm1	T	A	5: 64,107,851 (GRCm38)		probably null	Het
Phip	A	T	9: 82,876,189 (GRCm38)	S1484T	probably benign	Het
Pikfyve	T	C	1: 65,246,370 (GRCm38)	S923P	probably benign	Het
Pikfyve	T	C	1: 65,192,271 (GRCm38)	L100P	probably damaging	Het
Pla2g4e	A	G	2: 120,244,721 (GRCm38)	S63P	probably benign	Het
Plekhh2	A	G	17: 84,599,265 (GRCm38)	E1176G	probably damaging	Het
Prlr	T	A	15: 10,325,318 (GRCm38)	Y192*	probably null	Het
Pten	T	A	19: 32,798,072 (GRCm38)	C71S	probably damaging	Het
Rbbp8nl	A	G	2: 180,281,194 (GRCm38)	L202P	probably benign	Het
Ripor2	T	A	13: 24,701,254 (GRCm38)	S491T	probably benign	Het
Robo1	A	T	16: 73,004,511 (GRCm38)	I1008F	probably benign	Het
Scn8a	A	G	15: 101,039,615 (GRCm38)	I1581V	probably damaging	Het
Slc22a8	T	A	19: 8,594,229 (GRCm38)	I108N	probably damaging	Het
Slc9a8	A	T	2: 167,471,465 (GRCm38)	T416S	possibly damaging	Het
Spata32	T	A	11: 103,208,818 (GRCm38)	E287V	probably damaging	Het
Spata5	T	C	3: 37,439,185 (GRCm38)	F515L	probably damaging	Het
Tgfbrap1	C	T	1: 43,075,352 (GRCm38)	G196D	probably damaging	Het
Tgm5	G	T	2: 121,077,650 (GRCm38)	T15K	possibly damaging	Het
Tmc1	C	T	19: 20,826,501 (GRCm38)		probably null	Het
Tmem177	T	C	1: 119,910,576 (GRCm38)	I124M	possibly damaging	Het
Trim30a	A	G	7: 104,435,901 (GRCm38)	F34S	probably damaging	Het
Tsn	T	C	1: 118,305,239 (GRCm38)	T112A	probably benign	Het
Tspyl5	T	G	15: 33,686,776 (GRCm38)	N341T	probably benign	Het
Vmn2r108	C	T	17: 20,469,073 (GRCm38)	C540Y	probably damaging	Het
Vrtn	C	T	12: 84,650,224 (GRCm38)	R583W	probably damaging	Het
Wnt1	T	C	15: 98,791,757 (GRCm38)	S142P	probably damaging	Het
Wrn	A	T	8: 33,343,561 (GRCm38)	I108N	probably damaging	Het
Zfhx2	A	C	14: 55,072,891 (GRCm38)	C733G	possibly damaging	Het
Zfp219	T	C	14: 52,007,106 (GRCm38)	T539A	probably damaging	Het
Zswim8	T	A	14: 20,711,530 (GRCm38)	M177K	probably damaging	Het

Other mutations in Scg2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01347:Scg2	APN	1	79,436,821 (GRCm38)	missense	probably benign	0.16
IGL02083:Scg2	APN	1	79,436,224 (GRCm38)	missense	probably benign	0.00
IGL02316:Scg2	APN	1	79,435,681 (GRCm38)	missense	probably damaging	1.00
IGL02338:Scg2	APN	1	79,436,493 (GRCm38)	missense	possibly damaging	0.93
R0281:Scg2	UTSW	1	79,435,512 (GRCm38)	missense	possibly damaging	0.95
R0384:Scg2	UTSW	1	79,435,549 (GRCm38)	missense	probably benign	0.42
R0501:Scg2	UTSW	1	79,435,603 (GRCm38)	missense	probably damaging	1.00
R0909:Scg2	UTSW	1	79,435,782 (GRCm38)	missense	possibly damaging	0.74
R2254:Scg2	UTSW	1	79,436,500 (GRCm38)	missense	probably damaging	1.00
R4074:Scg2	UTSW	1	79,436,857 (GRCm38)	missense	probably damaging	0.97
R4076:Scg2	UTSW	1	79,436,857 (GRCm38)	missense	probably damaging	0.97
R4097:Scg2	UTSW	1	79,435,821 (GRCm38)	missense	probably damaging	0.99
R4560:Scg2	UTSW	1	79,435,181 (GRCm38)	missense	probably damaging	1.00
R4621:Scg2	UTSW	1	79,436,664 (GRCm38)	missense	probably benign	0.08
R4876:Scg2	UTSW	1	79,435,919 (GRCm38)	missense	probably damaging	1.00
R4944:Scg2	UTSW	1	79,436,476 (GRCm38)	nonsense	probably null
R5829:Scg2	UTSW	1	79,436,920 (GRCm38)	missense	probably damaging	1.00
R6158:Scg2	UTSW	1	79,435,400 (GRCm38)	missense	probably damaging	1.00
R6248:Scg2	UTSW	1	79,436,306 (GRCm38)	missense	probably benign	0.29
R6365:Scg2	UTSW	1	79,435,300 (GRCm38)	missense	probably benign
R6459:Scg2	UTSW	1	79,436,290 (GRCm38)	missense	probably damaging	1.00
R6676:Scg2	UTSW	1	79,435,782 (GRCm38)	missense	possibly damaging	0.74
R6693:Scg2	UTSW	1	79,436,020 (GRCm38)	missense	probably benign	0.01
R7259:Scg2	UTSW	1	79,436,985 (GRCm38)	missense	probably benign
R7393:Scg2	UTSW	1	79,435,231 (GRCm38)	missense	probably damaging	1.00
R7578:Scg2	UTSW	1	79,436,895 (GRCm38)	missense	probably damaging	0.99
R7608:Scg2	UTSW	1	79,436,181 (GRCm38)	missense	probably benign	0.00
R8166:Scg2	UTSW	1	79,435,583 (GRCm38)	missense	possibly damaging	0.56
R8247:Scg2	UTSW	1	79,436,519 (GRCm38)	missense	possibly damaging	0.92
R8296:Scg2	UTSW	1	79,435,505 (GRCm38)	missense	probably benign	0.13
R8308:Scg2	UTSW	1	79,436,859 (GRCm38)	missense	probably benign	0.18
R8789:Scg2	UTSW	1	79,435,783 (GRCm38)	missense	probably benign	0.05
R9252:Scg2	UTSW	1	79,436,352 (GRCm38)	missense	probably damaging	0.98
R9286:Scg2	UTSW	1	79,435,936 (GRCm38)	missense	probably damaging	1.00
R9489:Scg2	UTSW	1	79,435,219 (GRCm38)	missense	probably damaging	1.00
R9605:Scg2	UTSW	1	79,435,219 (GRCm38)	missense	probably damaging	1.00
Z1176:Scg2	UTSW	1	79,436,789 (GRCm38)	missense	probably benign	0.17

Predicted Primers

PCR Primer
(F):5'- ATGTTCCTTGATGGCCTGCTCG -3'
(R):5'- TAGATGACATCCCAGAGGCTGACC -3'

Sequencing Primer
(F):5'- GCTCAGGGTACTTAACTAGCATC -3'
(R):5'- TCCCAGAGGCTGACCTAGAC -3'

Posted On

2014-05-23