Mutagenetix > Incidental Mutation

Incidental Mutation 'R6818:Gm10985'

540713

Institutional Source

Beutler Lab

Gene Symbol

Gm10985

Ensembl Gene

ENSMUSG00000078742

Gene Name

predicted gene 10985

Synonyms

MMRRC Submission

Accession Numbers

Essential gene?

Not available question?

Stock #

R6818 (G1)

Quality Score

139.008

Status

Not validated

Chromosome

Chromosomal Location

53845086-53845278 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 53845253 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Serine at position 19 (Y19S)

Ref Sequence

ENSEMBL: ENSMUSP00000103649 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000108014]

AlphaFold

F6T1P1

Predicted Effect

probably damaging
Transcript: ENSMUST00000108014
AA Change: Y19S

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000158028

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

97% (59/61)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb5	T	A	12: 118,901,354		probably null	Het
Acot4	A	C	12: 84,042,009	E210D	probably damaging	Het
Adamts9	A	C	6: 92,905,191	S476A	probably damaging	Het
Ak1	T	A	2: 32,630,373	M61K	probably damaging	Het
Ambp	G	T	4: 63,154,006	S17*	probably null	Het
Anxa6	T	A	11: 54,979,500	M662L	probably benign	Het
Atp11b	T	C	3: 35,814,180	I467T	possibly damaging	Het
B3gat1	G	T	9: 26,751,702		probably benign	Het
Bccip	T	G	7: 133,717,759	I193S	probably damaging	Het
Ccdc170	A	G	10: 4,541,782	E401G	probably damaging	Het
Cldn16	A	G	16: 26,477,507	T78A	probably damaging	Het
Cldn24	G	T	8: 47,822,722	A194S	probably benign	Het
Cltc	A	G	11: 86,704,228	V1348A	possibly damaging	Het
Clvs1	T	C	4: 9,282,014		probably null	Het
Csmd1	C	T	8: 16,185,327	D1161N	probably damaging	Het
Cuzd1	A	G	7: 131,316,665	V181A	probably damaging	Het
Dhx30	A	G	9: 110,088,031	I435T	probably damaging	Het
Dip2b	T	C	15: 100,193,954	V858A	probably benign	Het
Dnmt3b	C	T	2: 153,686,284	T822M	probably damaging	Het
Dock10	A	T	1: 80,615,365	F97I	possibly damaging	Het
Dock8	T	C	19: 25,169,501		probably null	Het
Dvl2	T	C	11: 70,009,273	L631P	probably damaging	Het
Faf2	T	A	13: 54,641,606		probably null	Het
Fat2	T	A	11: 55,309,341	H969L	probably benign	Het
Fsip2	T	A	2: 82,985,200	V3759E	probably benign	Het
Gm10037	A	G	13: 67,833,867	Q66R	possibly damaging	Het
Gm973	T	C	1: 59,630,169	L793P	probably damaging	Het
Gm996	C	CTCTA	2: 25,579,721		probably null	Het
H2-M1	A	G	17: 36,670,435	I236T	probably damaging	Het
Hif1a	A	T	12: 73,945,563	R765*	probably null	Het
Htt	A	G	5: 34,782,767	K77E	probably damaging	Het
Ift172	G	T	5: 31,265,960	Q826K	probably benign	Het
Inafm1	C	T	7: 16,273,161	A44T	probably damaging	Het
Kctd4	A	G	14: 75,963,308	T240A	probably damaging	Het
Klk1	A	T	7: 44,229,459	I124F	probably damaging	Het
Kremen1	T	C	11: 5,195,051	T442A	probably benign	Het
Mei4	T	A	9: 82,025,521	D202E	probably benign	Het
Mest	T	A	6: 30,746,287	D284E	probably damaging	Het
Nsfl1c	T	A	2: 151,503,020	Y95*	probably null	Het
Olfr121	T	A	17: 37,752,424	V190D	possibly damaging	Het
Olfr1282	T	G	2: 111,335,314	I255L	probably benign	Het
Olfr1349	T	C	7: 6,514,551	M293V	probably damaging	Het
Olfr316	T	A	11: 58,757,957	C97*	probably null	Het
Pgm2	T	A	4: 99,963,566	I220N	probably damaging	Het
Pirt	T	A	11: 66,925,893	V10E	possibly damaging	Het
Prl7d1	C	A	13: 27,714,471	M19I	probably benign	Het
Samhd1	T	C	2: 157,107,497	N490D	probably benign	Het
Scn2a	C	A	2: 65,688,669	S413*	probably null	Het
Serpinb6e	A	T	13: 33,832,354		probably null	Het
Slitrk5	A	G	14: 111,680,294	D450G	probably benign	Het
Tchh	A	G	3: 93,443,411	T53A	probably damaging	Het
Tmem44	A	T	16: 30,543,221		probably null	Het
Tpm3-rs7	A	G	14: 113,315,016	E114G	possibly damaging	Het
Treml2	A	G	17: 48,302,897	Y119C	probably damaging	Het
Ubxn1	T	A	19: 8,873,881		probably null	Het
Vmn2r84	A	T	10: 130,386,278	M691K	probably benign	Het
Vmn2r97	A	T	17: 18,947,931	I816F	possibly damaging	Het
Was	GCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTC	GCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTCCTC	X: 8,086,211		probably benign	Het
Wfdc2	T	C	2: 164,563,150		probably null	Het
Zscan4-ps3	T	C	7: 11,613,059	S341P	probably damaging	Het

Other mutations in Gm10985

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02805:Gm10985	APN	3	53845093	critical splice donor site	probably null
R0027:Gm10985	UTSW	3	53845256	frame shift	probably null
R0184:Gm10985	UTSW	3	53845258	missense	probably damaging	0.99
R1027:Gm10985	UTSW	3	53845253	missense	probably damaging	0.99
R1216:Gm10985	UTSW	3	53845253	missense	probably damaging	0.99
R2126:Gm10985	UTSW	3	53845249	frame shift	probably null
R3757:Gm10985	UTSW	3	53845224	frame shift	probably null
R3870:Gm10985	UTSW	3	53845205	frame shift	probably null
R5567:Gm10985	UTSW	3	53845262	missense	probably damaging	0.99
R5585:Gm10985	UTSW	3	53845253	missense	probably damaging	0.99
R6782:Gm10985	UTSW	3	53845205	frame shift	probably null
R8398:Gm10985	UTSW	3	53845253	missense	probably damaging	0.99

Predicted Primers

Posted On

2018-11-16