Mutagenetix > Incidental Mutation

Incidental Mutation 'R5359:Gm1968'

424254

Institutional Source

Beutler Lab

Gene Symbol

Gm1968

Ensembl Gene

ENSMUSG00000075286

Gene Name

predicted gene 1968

Synonyms

MMRRC Submission

042938-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.128) question?

Stock #

R5359 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

29776745-29797942 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 29777617 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000100016]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000100016

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000231469

Coding Region Coverage

1x: 99.4%
3x: 98.8%
10x: 97.6%
20x: 96.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ap5b1	T	A	19: 5,619,126 (GRCm39)	I182N	possibly damaging	Het
Arap2	A	T	5: 62,840,762 (GRCm39)	C701*	probably null	Het
Bcr	T	A	10: 75,001,917 (GRCm39)	F940L	probably damaging	Het
Cav2	A	T	6: 17,287,064 (GRCm39)		probably benign	Het
Cdk2	T	C	10: 128,539,857 (GRCm39)		probably benign	Het
Clic4	G	A	4: 134,944,446 (GRCm39)	A243V	probably benign	Het
Dap3	A	T	3: 88,838,296 (GRCm39)	V99D	probably damaging	Het
Dennd5a	T	C	7: 109,497,169 (GRCm39)	E1110G	probably damaging	Het
Dhx30	T	C	9: 109,922,203 (GRCm39)	N160D	probably damaging	Het
Dnai7	T	G	6: 145,142,618 (GRCm39)	T120P	probably damaging	Het
Dock9	A	G	14: 121,890,472 (GRCm39)	M268T	possibly damaging	Het
Dspp	T	A	5: 104,323,752 (GRCm39)	D298E	probably damaging	Het
Elane	A	G	10: 79,722,870 (GRCm39)	E92G	probably damaging	Het
Erp44	A	T	4: 48,211,704 (GRCm39)	D197E	probably benign	Het
Fkbpl	G	A	17: 34,864,303 (GRCm39)	A24T	probably benign	Het
Gbf1	T	C	19: 46,272,164 (GRCm39)		probably null	Het
Hydin	T	A	8: 111,265,004 (GRCm39)	V2729E	probably benign	Het
Insyn2b	G	A	11: 34,352,788 (GRCm39)	E277K	probably damaging	Het
Iqgap1	T	C	7: 80,416,707 (GRCm39)	T106A	probably benign	Het
Kcnj6	G	C	16: 94,633,312 (GRCm39)	Y248*	probably null	Het
Mllt3	A	G	4: 87,759,164 (GRCm39)	S295P	probably benign	Het
Or2w1b	A	C	13: 21,300,437 (GRCm39)	T192P	probably damaging	Het
Pex11b	G	A	3: 96,551,229 (GRCm39)	C224Y	probably damaging	Het
Pik3c2g	A	G	6: 139,599,121 (GRCm39)	Y79C	probably damaging	Het
Plcz1	T	C	6: 139,974,178 (GRCm39)	Y88C	probably damaging	Het
Pole	A	G	5: 110,480,354 (GRCm39)	N99S	probably benign	Het
Pyroxd1	T	G	6: 142,307,717 (GRCm39)	Y496D	probably damaging	Het
Rasef	A	G	4: 73,689,565 (GRCm39)	L68P	probably damaging	Het
Rgs13	T	A	1: 144,015,322 (GRCm39)	M132L	probably damaging	Het
RP24-187P11.4	T	G	9: 109,349,944 (GRCm39)		noncoding transcript	Het
Rsph4a	A	G	10: 33,784,232 (GRCm39)	T285A	probably benign	Het
Ryr3	A	T	2: 112,606,186 (GRCm39)		probably null	Het
Slc30a1	T	A	1: 191,641,865 (GRCm39)	*504R	probably null	Het
Spcs1	T	C	14: 30,722,074 (GRCm39)	R156G	probably damaging	Het
Supv3l1	A	G	10: 62,268,178 (GRCm39)	F556L	probably damaging	Het
Thumpd2	C	T	17: 81,334,206 (GRCm39)	V461M	probably benign	Het
Timm50	A	G	7: 28,007,592 (GRCm39)	L158P	probably damaging	Het
Tnrc6c	T	C	11: 117,649,731 (GRCm39)		silent	Het
Ttn	G	A	2: 76,726,147 (GRCm39)	Q1807*	probably null	Het
Zdhhc14	A	G	17: 5,543,821 (GRCm39)	I34V	probably benign	Het
Zgrf1	T	A	3: 127,394,814 (GRCm39)	M506K	possibly damaging	Het

Other mutations in Gm1968

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01293:Gm1968	APN	16	29,777,632 (GRCm39)	exon	noncoding transcript
IGL01300:Gm1968	APN	16	29,781,038 (GRCm39)	exon	noncoding transcript
R1539:Gm1968	UTSW	16	29,777,659 (GRCm39)	exon	noncoding transcript
R5339:Gm1968	UTSW	16	29,781,077 (GRCm39)	exon	noncoding transcript
R5610:Gm1968	UTSW	16	29,777,557 (GRCm39)	exon	noncoding transcript
R8227:Gm1968	UTSW	16	29,777,380 (GRCm39)	missense	noncoding transcript

Predicted Primers

PCR Primer
(F):5'- CCATGGAGGTCAGAGGCATG -3'
(R):5'- TGAGCTCCGATTTGGGTCC -3'

Sequencing Primer
(F):5'- ACAGGTTCAGAGGTTCAGTCC -3'
(R):5'- TCCGATTTGGGTCCCACTGG -3'

Posted On

2016-08-04