Mutagenetix > Incidental Mutation

Incidental Mutation 'R4360:Gm7204'

324878

Institutional Source

Beutler Lab

Gene Symbol

Gm7204

Ensembl Gene

ENSMUSG00000048164

Gene Name

predicted pseudogene 7204

Synonyms

MMRRC Submission

041111-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.193) question?

Stock #

R4360 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

48038968-48039564 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 48039196 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000062591

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.6%

Validation Efficiency

100% (50/50)

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930578I07Rik	T	C	14: 67,175,850 (GRCm39)		noncoding transcript	Het
Adgra3	T	C	5: 50,147,552 (GRCm39)	E496G	possibly damaging	Het
Atg14	C	G	14: 47,805,827 (GRCm39)	E13Q	probably benign	Het
BC023105	G	T	18: 60,575,073 (GRCm39)		noncoding transcript	Het
Chd6	A	G	2: 160,791,776 (GRCm39)	V2527A	possibly damaging	Het
Csn1s2a	G	T	5: 87,929,700 (GRCm39)	V100L	possibly damaging	Het
Fah	G	A	7: 84,238,856 (GRCm39)	L330F	probably damaging	Het
Fmo2	T	C	1: 162,709,583 (GRCm39)	N268S	probably damaging	Het
Foxg1	CCAGCAGCAGCAGCAGCAGC	CCAGCAGCAGCAGCAGC	12: 49,431,475 (GRCm39)		probably benign	Het
Frmd4a	A	T	2: 4,606,052 (GRCm39)	H287L	probably damaging	Het
G2e3	T	A	12: 51,410,197 (GRCm39)		probably benign	Het
Gm1758	A	T	16: 14,324,215 (GRCm39)		noncoding transcript	Het
Gm829	T	C	4: 45,718,819 (GRCm39)		noncoding transcript	Het
Hspa14	A	G	2: 3,503,560 (GRCm39)	V116A	possibly damaging	Het
Hspa4	T	C	11: 53,155,919 (GRCm39)	Y662C	probably damaging	Het
Islr	T	A	9: 58,064,887 (GRCm39)	N207Y	probably damaging	Het
Lipc	T	C	9: 70,759,864 (GRCm39)		probably benign	Het
Ncor2	A	G	5: 125,106,036 (GRCm39)	S1546P	probably damaging	Het
Or13a25	T	C	7: 140,247,730 (GRCm39)	F170L	probably damaging	Het
Or56a3	A	C	7: 104,735,460 (GRCm39)	E179A	probably damaging	Het
Or7g18	G	A	9: 18,787,013 (GRCm39)	C127Y	probably damaging	Het
Parp4	A	G	14: 56,866,661 (GRCm39)	D1075G	possibly damaging	Het
Pkp2	A	G	16: 16,086,546 (GRCm39)	I736V	probably benign	Het
Plekha8	T	C	6: 54,599,171 (GRCm39)	I235T	probably benign	Het
Polq	A	G	16: 36,880,701 (GRCm39)	D955G	probably benign	Het
Pramel16	A	G	4: 143,677,433 (GRCm39)	F49L	possibly damaging	Het
Psmd1	A	G	1: 86,061,459 (GRCm39)	K890E	probably damaging	Het
Rufy4	T	C	1: 74,186,822 (GRCm39)	C537R	probably damaging	Het
Scpep1	A	G	11: 88,821,070 (GRCm39)	Y366H	possibly damaging	Het
Slc18a3	A	G	14: 32,185,882 (GRCm39)	V167A	probably benign	Het
Sp8	A	G	12: 118,812,400 (GRCm39)	D85G	possibly damaging	Het
Stard3nl	G	A	13: 19,554,654 (GRCm39)	S144L	probably damaging	Het
Stk4	A	G	2: 163,930,879 (GRCm39)	E160G	possibly damaging	Het
Tbcb	T	C	7: 29,926,460 (GRCm39)	N119S	probably benign	Het
Tnc	G	T	4: 63,935,161 (GRCm39)	R592S	probably benign	Het
Trem3	T	A	17: 48,556,801 (GRCm39)	S91T	probably benign	Het
Trpc6	A	G	9: 8,610,267 (GRCm39)	E245G	probably benign	Het
Usp40	C	T	1: 87,880,083 (GRCm39)	R1036H	probably damaging	Het
Usp47	G	T	7: 111,654,139 (GRCm39)	G112C	probably damaging	Het
Wdr35	T	C	12: 9,024,149 (GRCm39)		probably benign	Het
Zc3h14	A	G	12: 98,746,456 (GRCm39)	K555R	probably benign	Het
Zfp26	T	C	9: 20,349,869 (GRCm39)	S232G	probably benign	Het
Zfp811	T	C	17: 33,017,432 (GRCm39)	T202A	probably benign	Het

Other mutations in Gm7204

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R4760:Gm7204	UTSW	16	48,039,051 (GRCm39)	exon	noncoding transcript

Predicted Primers

PCR Primer
(F):5'- TACAGGTGTTATGCCAGATGG -3'
(R):5'- GCCAACGGGAAGATCGTTTATTG -3'

Sequencing Primer
(F):5'- CAGGTGTTATGCCAGATGGACAATTC -3'
(R):5'- CAACGGGAAGATCGTTTATTGTTATC -3'

Posted On

2015-07-06