Mutagenetix > Incidental Mutation

Incidental Mutation 'R1495:Gm5141'

168802

Institutional Source

Beutler Lab

Gene Symbol

Gm5141

Ensembl Gene

ENSMUSG00000091183

Gene Name

predicted gene 5141

Synonyms

MMRRC Submission

039546-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R1495 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

62772200-62785808 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 62774270 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Serine at position 362 (C362S)

Ref Sequence

ENSEMBL: ENSMUSP00000144368 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000167516] [ENSMUST00000201047]

AlphaFold

A0A0J9YUW3

Predicted Effect

probably damaging
Transcript: ENSMUST00000167516
AA Change: C361S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000126604
Gene: ENSMUSG00000091183
AA Change: C361S

Domain	Start	End	E-Value	Type
KRAB	3	65	2.32e-19	SMART
ZnF_C2H2	132	154	1.51e0	SMART
ZnF_C2H2	160	182	6.52e-5	SMART
ZnF_C2H2	188	210	5.42e-2	SMART
ZnF_C2H2	216	238	1.84e-4	SMART
ZnF_C2H2	244	266	1.3e-4	SMART
ZnF_C2H2	272	294	1.22e-4	SMART
ZnF_C2H2	300	322	1.82e-3	SMART
ZnF_C2H2	328	350	2.79e-4	SMART
ZnF_C2H2	356	378	3.89e-3	SMART
ZnF_C2H2	384	406	4.94e-5	SMART
ZnF_C2H2	412	434	5.67e-5	SMART
ZnF_C2H2	440	462	7.49e-5	SMART
ZnF_C2H2	468	490	5.21e-4	SMART
ZnF_C2H2	496	518	4.87e-4	SMART
ZnF_C2H2	524	546	1.22e-4	SMART
ZnF_C2H2	552	574	1.18e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000179519

Predicted Effect

probably damaging
Transcript: ENSMUST00000201047
AA Change: C362S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000144368
Gene: ENSMUSG00000091183
AA Change: C362S

Domain	Start	End	E-Value	Type
KRAB	4	66	9.8e-22	SMART
ZnF_C2H2	133	155	6.5e-3	SMART
ZnF_C2H2	161	183	2.7e-7	SMART
ZnF_C2H2	189	211	2.4e-4	SMART
ZnF_C2H2	217	239	8.1e-7	SMART
ZnF_C2H2	245	267	5.6e-7	SMART
ZnF_C2H2	273	295	5.1e-7	SMART
ZnF_C2H2	301	323	7.9e-6	SMART
ZnF_C2H2	329	351	1.2e-6	SMART
ZnF_C2H2	357	379	1.7e-5	SMART
ZnF_C2H2	385	407	2.1e-7	SMART
ZnF_C2H2	413	435	2.4e-7	SMART
ZnF_C2H2	441	463	3.2e-7	SMART
ZnF_C2H2	469	491	2.2e-6	SMART
ZnF_C2H2	497	519	2.2e-6	SMART
ZnF_C2H2	525	547	5.4e-7	SMART
ZnF_C2H2	553	575	4.9e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000202582

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.5%
20x: 93.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4833420G17Rik	A	G	13: 119,477,820	N488S	probably benign	Het
A430105I19Rik	T	G	2: 118,760,532	K173N	probably damaging	Het
Acot10	G	A	15: 20,665,507	R383C	probably damaging	Het
Acsm2	A	G	7: 119,578,126	D263G	probably damaging	Het
Adcy2	G	T	13: 68,796,535	Q243K	probably benign	Het
Aggf1	G	A	13: 95,356,413	R563*	probably null	Het
Agt	A	G	8: 124,559,455	F296S	probably damaging	Het
Akap14	T	C	X: 37,163,965	D39G	possibly damaging	Het
Akt3	T	C	1: 177,103,042	M117V	probably benign	Het
Ankar	T	C	1: 72,643,291	T1154A	probably benign	Het
Arvcf	T	A	16: 18,389,386	L70Q	probably damaging	Het
Ccdc171	A	T	4: 83,681,095	K724*	probably null	Het
Ccdc91	A	G	6: 147,534,172	T85A	possibly damaging	Het
Cdh3	C	T	8: 106,538,997	T224I	probably damaging	Het
Clstn3	T	C	6: 124,449,917	I482V	probably benign	Het
Cnot9	A	G	1: 74,523,600	E176G	probably damaging	Het
Cntnap4	T	G	8: 112,881,763	L1272V	possibly damaging	Het
Cyb5a	T	A	18: 84,851,480	M1K	probably null	Het
Cyp2c23	A	G	19: 44,005,508	I473T	probably benign	Het
Dbil5	T	A	11: 76,218,450	M60K	probably benign	Het
Dgkg	A	T	16: 22,500,379	L644Q	probably damaging	Het
Disp3	T	C	4: 148,249,825	I1004V	probably benign	Het
Egf	T	A	3: 129,713,006	I599F	probably damaging	Het
Epc2	A	G	2: 49,536,663	T145A	probably damaging	Het
Extl1	TGCGTTGCACCGATACCGGG	TG	4: 134,357,677		probably benign	Het
Extl3	A	T	14: 65,075,867	V622E	probably benign	Het
Fam227a	C	T	15: 79,626,245	V403I	probably benign	Het
Fat2	T	A	11: 55,262,673	D3571V	probably benign	Het
Fcho2	A	G	13: 98,749,850		probably null	Het
Fras1	A	G	5: 96,528,586	N64S	possibly damaging	Het
Gabbr1	A	G	17: 37,055,940	N352S	possibly damaging	Het
Gabra1	T	C	11: 42,154,944	N113S	probably damaging	Het
Glg1	T	C	8: 111,197,675	Y227C	probably damaging	Het
Gm14851	T	A	8: 21,095,201	Q75L	probably benign	Het
Gprc6a	T	A	10: 51,628,437	T104S	probably benign	Het
Jph1	A	C	1: 17,091,652	V262G	probably benign	Het
Kank1	C	G	19: 25,410,349	T434R	probably damaging	Het
Kmt2e	A	G	5: 23,499,327	S1173G	possibly damaging	Het
Krt75	G	A	15: 101,573,873		probably benign	Het
Lyzl1	G	T	18: 4,181,192	W77L	probably null	Het
Nipbl	T	G	15: 8,351,280	N676T	probably benign	Het
Obscn	C	T	11: 59,080,160	S2300N	probably damaging	Het
Olfr459	T	G	6: 41,771,903	Y132S	probably damaging	Het
Osbpl1a	T	A	18: 12,758,839	M350L	probably benign	Het
Pecam1	T	C	11: 106,688,856	D460G	probably damaging	Het
Pik3c2a	T	A	7: 116,388,065	K540N	probably benign	Het
Prdm12	T	A	2: 31,640,193	I32N	probably damaging	Het
Prkd1	T	C	12: 50,366,352	S679G	probably damaging	Het
Psen2	C	T	1: 180,228,854	A393T	probably damaging	Het
Ptprh	T	A	7: 4,580,889	T235S	probably benign	Het
Ranbp3	C	T	17: 56,705,527	P182L	probably benign	Het
Serpinb7	A	T	1: 107,451,660	K266*	probably null	Het
Sesn3	T	C	9: 14,308,521	S69P	probably damaging	Het
Slc12a6	T	C	2: 112,354,190	M818T	probably damaging	Het
Slc25a53	C	A	X: 137,015,335	C4F	unknown	Het
Snx1	T	A	9: 66,096,597	L255F	probably benign	Het
Sptbn2	T	G	19: 4,718,976	S46A	possibly damaging	Het
Taf4	A	G	2: 179,933,027	F595S	probably damaging	Het
Tec	A	T	5: 72,786,755	V103E	probably damaging	Het
Tmco5b	T	C	2: 113,290,791	S147P	possibly damaging	Het
Uchl5	C	T	1: 143,799,937	T93I	possibly damaging	Het
Usp14	A	T	18: 10,004,994	S225T	probably benign	Het
Usp45	C	A	4: 21,797,385	Q238K	possibly damaging	Het
Vmn1r6	T	A	6: 57,003,073	M218K	possibly damaging	Het
Zfp84	T	A	7: 29,777,303	Y473*	probably null	Het
Zyg11b	G	A	4: 108,266,213	P186S	probably damaging	Het

Other mutations in Gm5141

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0220:Gm5141	UTSW	13	62774457	missense	probably damaging	1.00
R0427:Gm5141	UTSW	13	62774711	missense	probably damaging	1.00
R0534:Gm5141	UTSW	13	62774594	missense	probably damaging	1.00
R0652:Gm5141	UTSW	13	62774132	missense	probably damaging	1.00
R2079:Gm5141	UTSW	13	62774610	missense	probably benign	0.06
R4780:Gm5141	UTSW	13	62774950	missense	unknown
R5588:Gm5141	UTSW	13	62773770	missense	probably benign	0.06
R6292:Gm5141	UTSW	13	62774438	missense	probably damaging	1.00
R6455:Gm5141	UTSW	13	62774783	missense	probably damaging	1.00
R6605:Gm5141	UTSW	13	62774387	missense	probably damaging	1.00
R7091:Gm5141	UTSW	13	62773964	missense	possibly damaging	0.80
R7199:Gm5141	UTSW	13	62777063	missense	possibly damaging	0.92
R8933:Gm5141	UTSW	13	62777040	nonsense	probably null

Predicted Primers

Posted On

2014-04-13