Mutagenetix > Incidental Mutations

Incidental Mutation 'IGL01291:Gm5155'

72931

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5155

Ensembl Gene

ENSMUSG00000078793

Gene Name

predicted gene 5155

Synonyms

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL01291

Quality Score

Status

Chromosome

Chromosomal Location

17871768-17919024 bp(+) (GRCm38)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 17905116 bp

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000072381

SMART Domains

Protein: ENSMUSP00000072218
Gene: ENSMUSG00000078793

Domain	Start	End	E-Value	Type
IG	40	141	2.27e-2	SMART
IG_like	160	261	2.73e1	SMART
IG_like	277	378	6.69e0	SMART
IG_like	397	498	4.07e1	SMART
IG_like	514	615	6.52e0	SMART
IG_like	634	735	1.05e1	SMART
IG	753	853	1.28e-1	SMART
IGc2	869	933	3.82e-9	SMART

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acacb	T	A	5: 114,225,870	F1464Y	probably benign	Het
Adgrg6	G	A	10: 14,410,530	A1114V	possibly damaging	Het
Agl	A	G	3: 116,772,789	I975T	possibly damaging	Het
Arhgef11	T	C	3: 87,733,174	W1213R	probably benign	Het
Ccar1	T	A	10: 62,756,649	E708V	probably damaging	Het
Cilp	T	C	9: 65,278,983	S787P	possibly damaging	Het
Col5a1	T	A	2: 27,971,444		probably benign	Het
Col6a3	G	A	1: 90,802,292	T1157I	probably damaging	Het
Dock3	T	C	9: 106,958,400		probably benign	Het
Dusp19	A	G	2: 80,624,274	T113A	probably benign	Het
Dync1h1	A	C	12: 110,649,104	Y2957S	probably benign	Het
Fcho1	A	T	8: 71,712,547	L422Q	probably benign	Het
Gca	T	A	2: 62,690,443	Y210*	probably null	Het
Gpnmb	T	C	6: 49,055,681	V513A	probably benign	Het
Irx4	A	G	13: 73,267,667	T192A	probably damaging	Het
Isca1	T	C	13: 59,758,971	T54A	probably benign	Het
L3mbtl1	T	C	2: 162,970,180	V715A	probably benign	Het
Lama1	G	A	17: 67,738,870	D257N	probably damaging	Het
Lgr5	T	C	10: 115,478,534	H166R	probably damaging	Het
M6pr	A	G	6: 122,312,259	R9G	probably benign	Het
Olfr1076	G	A	2: 86,509,169	A237T	possibly damaging	Het
Pank4	T	C	4: 154,974,646	M412T	probably damaging	Het
Psd	A	G	19: 46,314,747	V100A	possibly damaging	Het
Rab11fip3	T	C	17: 26,016,113	T28A	probably damaging	Het
Rnpepl1	A	T	1: 92,919,746	D685V	probably benign	Het
Rrad	T	C	8: 104,630,651	E88G	probably benign	Het
Sdk2	T	A	11: 113,843,080	M846L	probably benign	Het
Sparcl1	A	T	5: 104,094,715	V36E	possibly damaging	Het
Srrm4	C	T	5: 116,467,569	E210K	unknown	Het
Stk25	A	T	1: 93,623,423		probably null	Het
Tacr3	A	T	3: 134,930,049	Y338F	probably damaging	Het
Tap2	A	T	17: 34,209,210	Q286L	probably benign	Het
Tbce	A	T	13: 14,009,740		probably benign	Het
Tubgcp5	C	A	7: 55,808,529	A396E	possibly damaging	Het
Ube2o	T	C	11: 116,540,134	D980G	probably damaging	Het
Vmn1r86	T	C	7: 13,102,506	M98V	probably benign	Het
Vmn2r58	T	A	7: 41,864,511	H236L	probably benign	Het
Zfp521	T	C	18: 13,817,246	H1217R	probably damaging	Het
Zfyve1	A	T	12: 83,555,005	F110I	probably benign	Het

Other mutations in Gm5155

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00480:Gm5155	APN	7	17910697	missense	probably benign	0.32
IGL01085:Gm5155	APN	7	17915691	missense	possibly damaging	0.71
IGL01135:Gm5155	APN	7	17902471	exon	noncoding transcript
IGL02252:Gm5155	APN	7	17910532	missense	possibly damaging	0.93
IGL03243:Gm5155	APN	7	17918649	exon	noncoding transcript
R0113:Gm5155	UTSW	7	17908948	exon	noncoding transcript
R0833:Gm5155	UTSW	7	17904981	missense	possibly damaging	0.95
R0836:Gm5155	UTSW	7	17904981	missense	possibly damaging	0.95
R1462:Gm5155	UTSW	7	17915591	exon	noncoding transcript
R1473:Gm5155	UTSW	7	17905091	exon	noncoding transcript
R1817:Gm5155	UTSW	7	17873330	exon	noncoding transcript
R1905:Gm5155	UTSW	7	17873552	exon	noncoding transcript
R2362:Gm5155	UTSW	7	17902473	exon	noncoding transcript
R3721:Gm5155	UTSW	7	17902738	missense	probably benign	0.41
R4305:Gm5155	UTSW	7	17905193	missense	probably benign	0.19
R4567:Gm5155	UTSW	7	17908966	missense	probably damaging	0.97
R4587:Gm5155	UTSW	7	17886224	missense	possibly damaging	0.47
R4691:Gm5155	UTSW	7	17908966	missense	possibly damaging	0.93
R4989:Gm5155	UTSW	7	17905218	splice site	probably null
R5023:Gm5155	UTSW	7	17902706	missense	probably damaging	1.00
R5024:Gm5155	UTSW	7	17910682	missense	probably benign	0.06
R5274:Gm5155	UTSW	7	17915717	splice site	probably null
R5279:Gm5155	UTSW	7	17873289	splice site	noncoding transcript
R5304:Gm5155	UTSW	7	17902692	missense	probably benign	0.06
R5312:Gm5155	UTSW	7	17909142	missense	probably damaging	1.00
R5899:Gm5155	UTSW	7	17917444	missense	possibly damaging	0.92

Posted On

2013-10-07