Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03182:Gm826'

412292

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm826

Ensembl Gene

ENSMUSG00000074623

Gene Name

predicted gene 826

Synonyms

Gm46773, LOC329554

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.092) question?

Stock #

IGL03182

Quality Score

Status

Chromosome

Chromosomal Location

160153313-160176082 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 160169035 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Serine at position 91 (R91S)

Ref Sequence

ENSEMBL: ENSMUSP00000096729 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099127]

AlphaFold

Q3UQ74

Predicted Effect

unknown
Transcript: ENSMUST00000099127
AA Change: R91S

SMART Domains

Protein: ENSMUSP00000096729
Gene: ENSMUSG00000074623
AA Change: R91S

Domain	Start	End	E-Value	Type
low complexity region	72	89	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138905

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 42 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Agbl3	A	T	6: 34,780,435 (GRCm39)	K469N	probably damaging	Het
Aldh2	A	G	5: 121,718,787 (GRCm39)		probably benign	Het
Ankfy1	T	C	11: 72,619,580 (GRCm39)		probably benign	Het
Ankhd1	C	T	18: 36,711,827 (GRCm39)	T209I	probably benign	Het
Aox3	G	A	1: 58,205,046 (GRCm39)	V754I	probably benign	Het
Arfgef3	C	T	10: 18,476,292 (GRCm39)	R1509H	probably damaging	Het
Ccdc157	A	G	11: 4,101,832 (GRCm39)	S30P	probably damaging	Het
Cept1	T	A	3: 106,411,866 (GRCm39)	E369D	probably damaging	Het
Clcnka	T	C	4: 141,121,798 (GRCm39)	Y236C	probably damaging	Het
Ddx42	A	T	11: 106,138,353 (GRCm39)	L717F	probably benign	Het
Dnah11	A	T	12: 117,994,026 (GRCm39)	I2340N	probably damaging	Het
Dsel	T	C	1: 111,787,868 (GRCm39)	E889G	probably damaging	Het
Fasn	T	C	11: 120,703,552 (GRCm39)	Y1560C	probably damaging	Het
Fermt2	A	T	14: 45,699,225 (GRCm39)	M623K	possibly damaging	Het
Gm21970	T	A	16: 91,190,726 (GRCm39)	S110T	possibly damaging	Het
Lrrn3	A	G	12: 41,504,020 (GRCm39)	L99S	probably damaging	Het
Megf8	T	A	7: 25,046,773 (GRCm39)	M1552K	possibly damaging	Het
Mgll	G	T	6: 88,800,173 (GRCm39)	V191F	probably damaging	Het
Nkapd1	T	C	9: 50,523,698 (GRCm39)	N50S	possibly damaging	Het
Nol8	C	A	13: 49,817,557 (GRCm39)	H778N	probably damaging	Het
Or1e26	T	A	11: 73,480,268 (GRCm39)	T99S	probably benign	Het
Or5b116	A	C	19: 13,422,807 (GRCm39)	T144P	possibly damaging	Het
Or8g30	A	T	9: 39,230,277 (GRCm39)	M211K	probably benign	Het
Or8k40	A	T	2: 86,584,366 (GRCm39)	S239T	probably damaging	Het
Pfkfb3	A	T	2: 11,506,474 (GRCm39)	I13N	probably damaging	Het
Pim1	T	A	17: 29,710,740 (GRCm39)	D114E	possibly damaging	Het
Pkd1	T	C	17: 24,792,792 (GRCm39)	L1493P	probably damaging	Het
Plb1	A	T	5: 32,502,259 (GRCm39)		probably benign	Het
Plch1	A	T	3: 63,610,015 (GRCm39)	Y872*	probably null	Het
Rictor	A	G	15: 6,819,079 (GRCm39)	D1434G	probably benign	Het
Rptor	G	A	11: 119,615,971 (GRCm39)	G162R	probably damaging	Het
Serping1	T	C	2: 84,596,162 (GRCm39)	D424G	probably damaging	Het
Slit2	A	G	5: 48,377,395 (GRCm39)	I475V	possibly damaging	Het
Snx31	G	T	15: 36,525,833 (GRCm39)	Q289K	probably benign	Het
Tbc1d13	G	A	2: 30,037,379 (GRCm39)	A254T	probably damaging	Het
Tek	T	C	4: 94,740,002 (GRCm39)	I750T	probably damaging	Het
Tet2	A	T	3: 133,177,159 (GRCm39)	L1296*	probably null	Het
Tmem145	T	A	7: 25,014,304 (GRCm39)	F459I	probably damaging	Het
Uba5	A	T	9: 103,931,328 (GRCm39)	V247D	possibly damaging	Het
Vmn1r83	T	C	7: 12,055,617 (GRCm39)	M147V	probably benign	Het
Vwde	T	C	6: 13,187,138 (GRCm39)	D783G	probably damaging	Het
Zfp609	A	G	9: 65,608,287 (GRCm39)	S1198P	probably benign	Het

Other mutations in Gm826

Allele	Source	Chr	Coord	Type	Predicted Effect
R2365:Gm826	UTSW	2	160,169,130 (GRCm39)	missense	unknown
R3762:Gm826	UTSW	2	160,155,423 (GRCm39)	intron	probably benign
R3769:Gm826	UTSW	2	160,169,165 (GRCm39)	missense	unknown
R4564:Gm826	UTSW	2	160,153,913 (GRCm39)	utr 3 prime	probably benign
R6125:Gm826	UTSW	2	160,169,034 (GRCm39)	missense	unknown
R6442:Gm826	UTSW	2	160,169,328 (GRCm39)	start gained	probably benign
R7048:Gm826	UTSW	2	160,169,026 (GRCm39)	nonsense	probably null
R7074:Gm826	UTSW	2	160,153,810 (GRCm39)	missense	unknown
R7491:Gm826	UTSW	2	160,153,942 (GRCm39)	missense	unknown
R7883:Gm826	UTSW	2	160,169,213 (GRCm39)	missense	unknown

Posted On

2016-08-02