Mutagenetix > Incidental Mutations

Incidental Mutation 'R8110:Gm8882'

630803

Institutional Source

Beutler Lab

Gene Symbol

Gm8882

Ensembl Gene

ENSMUSG00000030143

Gene Name

predicted gene 8882

Synonyms

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R8110 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

132361041-132364134 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 132361568 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Aspartic acid at position 229 (G229D)

Ref Sequence

ENSEMBL: ENSMUSP00000079660 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080849]

AlphaFold

E9Q7E4

Predicted Effect

unknown
Transcript: ENSMUST00000080849
AA Change: G229D

SMART Domains

Protein: ENSMUSP00000079660
Gene: ENSMUSG00000030143
AA Change: G229D

Domain	Start	End	E-Value	Type
Pfam:Pro-rich	1	118	2.2e-32	PFAM
Pfam:Pro-rich	155	228	6.3e-14	PFAM
Pfam:Pro-rich	211	277	5.8e-10	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.6%
20x: 93.1%

Validation Efficiency

99% (73/74)

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610010F05Rik	G	T	11: 23,576,764	T696N	probably benign	Het
Ankrd45	T	C	1: 161,151,319		probably null	Het
Appl1	C	A	14: 26,927,794	G592*	probably null	Het
Arfgef2	T	A	2: 166,878,544	M1501K	probably benign	Het
Calcrl	C	T	2: 84,339,339	A333T	probably damaging	Het
Cd200r3	T	A	16: 44,951,472	I33N	probably benign	Het
Ceacam15	A	G	7: 16,673,409	L61P	probably benign	Het
Cfap69	T	A	5: 5,582,515	H827L	possibly damaging	Het
Csmd3	T	A	15: 47,644,270	E2780V	probably damaging	Het
Cyp2u1	G	A	3: 131,293,654	T426I	probably damaging	Het
Eefsec	A	C	6: 88,376,330	I119S	probably damaging	Het
Fem1b	T	C	9: 62,796,268	N570S	probably damaging	Het
Fmo9	A	G	1: 166,663,526	M461T	probably benign	Het
Fryl	A	G	5: 73,133,277	Y95H	probably benign	Het
Fsip2	T	C	2: 82,958,673	I346T	probably benign	Het
Fto	T	C	8: 91,485,190	F381S	probably damaging	Het
Gabbr1	G	C	17: 37,048,583	S150T	probably benign	Het
Galnt9	G	T	5: 110,615,473	W448L	probably damaging	Het
Gcnt2	G	T	13: 40,917,722		probably benign	Het
Gm10800	CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA	CAAGAAAACTGAAAATCA	2: 98,667,016		probably null	Het
Gm17727	T	C	9: 35,778,033	*84W	probably null	Het
Gmcl1	G	T	6: 86,721,426	A163E	probably damaging	Het
Hectd4	A	G	5: 121,332,949	Y2633C	possibly damaging	Het
Hsd11b2	A	G	8: 105,522,634	I214V	probably damaging	Het
Hspa12a	T	A	19: 58,821,013	E217V	possibly damaging	Het
Itih2	A	G	2: 10,097,137	F845L	probably damaging	Het
Kcnn3	T	A	3: 89,661,233	L606H	probably damaging	Het
Krt6b	G	A	15: 101,680,142	R28C	probably damaging	Het
Lama2	T	A	10: 26,990,870	D2876V	probably damaging	Het
Lmbrd2	T	C	15: 9,175,192	S397P	probably damaging	Het
Lmf2	C	T	15: 89,352,358		probably null	Het
Lrp2	A	G	2: 69,506,453	I1325T	probably benign	Het
Ltbp2	A	T	12: 84,803,902	C879*	probably null	Het
Map3k1	A	G	13: 111,755,313	V1136A	probably damaging	Het
Mettl3	G	T	14: 52,300,252	H84N	probably benign	Het
Mia2	A	G	12: 59,109,087		probably null	Het
Mlip	G	T	9: 77,239,579	T92K	probably damaging	Het
Nalcn	T	A	14: 123,464,701	Y466F	probably benign	Het
Nav2	T	A	7: 49,551,950	L235*	probably null	Het
Nbn	T	C	4: 15,981,588	V560A	probably benign	Het
Ncln	A	T	10: 81,493,153	Y144N	possibly damaging	Het
Nfe2l2	A	C	2: 75,679,421	D18E	probably benign	Het
Olfr102	A	G	17: 37,313,713	F224L	probably benign	Het
Olfr1131	T	C	2: 87,628,607	I48T	possibly damaging	Het
Olfr356	T	C	2: 36,937,709	C197R	possibly damaging	Het
Olfr432	G	A	1: 174,050,525	A51T	probably benign	Het
Otop3	A	T	11: 115,339,395	M33L	probably benign	Het
Pdzd2	G	A	15: 12,373,506	S2181L	probably benign	Het
Phf14	T	C	6: 11,953,423	I387T	possibly damaging	Het
Prdm9	T	A	17: 15,554,698	N318Y	probably damaging	Het
Proca1	A	G	11: 78,204,911	D123G	probably damaging	Het
Prune2	G	A	19: 17,120,719	G1196S	probably benign	Het
Psd3	T	A	8: 68,121,056	S158C	probably damaging	Het
Rps18	A	G	17: 33,955,136	V15A	probably benign	Het
Sharpin	C	A	15: 76,347,765	R271L	possibly damaging	Het
Smad5	C	A	13: 56,723,888	Q99K	probably damaging	Het
Sox5	T	C	6: 144,116,474	M151V	possibly damaging	Het
Sphkap	A	T	1: 83,278,771	F419Y	possibly damaging	Het
Tbx20	T	A	9: 24,725,525	Y422F	probably damaging	Het
Tcirg1	A	C	19: 3,899,099	F397V	probably damaging	Het
Tex36	G	A	7: 133,595,283	S35F	possibly damaging	Het
Tsen54	G	T	11: 115,814,934	A26S	unknown	Het
Usp50	T	A	2: 126,780,330		probably null	Het
Vmn2r5	A	T	3: 64,491,288	F757I	probably benign	Het
Zbbx	T	C	3: 75,155,442	T3A	possibly damaging	Het
Zfp28	T	A	7: 6,389,829	M168K	probably benign	Het
Zfp568	G	T	7: 30,023,126	G499W	probably damaging	Het
Zfp7	C	G	15: 76,890,931	P391R	possibly damaging	Het

Other mutations in Gm8882

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02797:Gm8882	APN	6	132363045	critical splice acceptor site	probably null
IGL02961:Gm8882	APN	6	132361408	missense	unknown
R0334:Gm8882	UTSW	6	132364058	missense	unknown
R1167:Gm8882	UTSW	6	132361590	missense	unknown
R1635:Gm8882	UTSW	6	132363006	critical splice donor site	probably null
R3956:Gm8882	UTSW	6	132361851	missense	unknown
R4734:Gm8882	UTSW	6	132361928	missense	unknown
R5275:Gm8882	UTSW	6	132361877	missense	unknown
R5295:Gm8882	UTSW	6	132361877	missense	unknown
R5506:Gm8882	UTSW	6	132361856	missense	unknown
R5580:Gm8882	UTSW	6	132361469	missense	unknown
R5975:Gm8882	UTSW	6	132362073	missense	unknown
R6503:Gm8882	UTSW	6	132361692	nonsense	probably null
R8714:Gm8882	UTSW	6	132364088	missense	unknown
R8931:Gm8882	UTSW	6	132361934	missense
R9054:Gm8882	UTSW	6	132361893	missense	unknown

Predicted Primers

PCR Primer
(F):5'- TCTCTGGTAAGGAAACAGATGG -3'
(R):5'- GCCTGGAAATCAACAAGGTCC -3'

Sequencing Primer
(F):5'- TGGTTATGCAAAAAGTGACCAC -3'
(R):5'- AGAGACCTCCTCAGCCTG -3'

Posted On

2020-06-30