Mutagenetix > Incidental Mutation

Incidental Mutation 'R1129:Gm9726'

96499

Institutional Source

Beutler Lab

Gene Symbol

Gm9726

Ensembl Gene

ENSMUSG00000094935

Gene Name

predicted gene 9726

Synonyms

MMRRC Submission

039202-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

R1129 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

93894767-93895444 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to A at 93895300 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: ENSMUST00000180321

SMART Domains

Protein: ENSMUSP00000136020
Gene: ENSMUSG00000094935

Domain	Start	End	E-Value	Type
low complexity region	10	19	N/A	INTRINSIC
LysM	41	85	2.58e-7	SMART
low complexity region	100	108	N/A	INTRINSIC
low complexity region	117	132	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183568

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.3%
20x: 89.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adrm1	G	C	2: 179,814,712 (GRCm39)		probably benign	Het
Bub1b	A	T	2: 118,445,487 (GRCm39)	D269V	probably damaging	Het
Ccdc73	A	G	2: 104,822,535 (GRCm39)	N828S	possibly damaging	Het
Cdk12	T	C	11: 98,136,201 (GRCm39)	S1152P	unknown	Het
Cnnm3	T	C	1: 36,552,097 (GRCm39)	L369P	probably damaging	Het
Cxadr	A	G	16: 78,133,321 (GRCm39)	K360R	probably benign	Het
Dlg2	G	A	7: 92,080,382 (GRCm39)		probably null	Het
Dst	T	C	1: 34,238,635 (GRCm39)	V3779A	probably benign	Het
Fbxo16	G	A	14: 65,532,981 (GRCm39)	R161K	probably benign	Het
H1f6	G	T	13: 23,880,307 (GRCm39)	K153N	possibly damaging	Het
Hectd4	A	G	5: 121,448,662 (GRCm39)	T337A	possibly damaging	Het
Ints1	A	G	5: 139,744,226 (GRCm39)	L1510S	probably benign	Het
Kansl2	T	C	15: 98,431,462 (GRCm39)	Y63C	probably damaging	Het
Lats2	T	C	14: 57,937,790 (GRCm39)	E233G	possibly damaging	Het
Naca	T	C	10: 127,876,071 (GRCm39)		probably benign	Het
Pprc1	G	T	19: 46,052,245 (GRCm39)	A591S	probably benign	Het
Sbsn	C	T	7: 30,452,865 (GRCm39)	P627S	probably benign	Het
Sema6b	T	C	17: 56,431,347 (GRCm39)	E772G	probably benign	Het
Tmem33	A	G	5: 67,421,803 (GRCm39)		probably null	Het
Tmtc4	A	G	14: 123,180,565 (GRCm39)		probably null	Het
Ubqlnl	A	T	7: 103,798,857 (GRCm39)	H213Q	probably damaging	Het
Ugt1a10	T	C	1: 87,983,331 (GRCm39)	M43T	probably benign	Het
Vmn2r68	T	C	7: 84,886,712 (GRCm39)		probably null	Het
Zcchc14	A	G	8: 122,335,154 (GRCm39)		probably benign	Het

Other mutations in Gm9726

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0841:Gm9726	UTSW	12	93,895,054 (GRCm39)	unclassified	noncoding transcript
R1145:Gm9726	UTSW	12	93,895,054 (GRCm39)	unclassified	noncoding transcript

Predicted Primers

PCR Primer
(F):5'- TTCTGGGCAGCAGCCTTCTTTGAC -3'
(R):5'- AATGTAACCGGCCTGGCAGACTTC -3'

Sequencing Primer
(F):5'- GAAGATGATCCGATCTCATCCTTAC -3'
(R):5'- ACGACGAATGTAGTCTCTCG -3'

Posted On

2014-01-05