Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02308:Gm10110'

287681

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm10110

Ensembl Gene

ENSMUSG00000062093

Gene Name

predicted gene 10110

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.184) question?

Stock #

IGL02308

Quality Score

Status

Chromosome

Chromosomal Location

90133664-90136883 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 90135031 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081204]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000081204

SMART Domains

Protein: ENSMUSP00000079967
Gene: ENSMUSG00000062093

Domain	Start	End	E-Value	Type
RRM	12	85	1.47e-21	SMART
RRM	100	171	2.91e-25	SMART
RRM	192	264	1.27e-25	SMART
RRM	295	366	1.92e-25	SMART
low complexity region	478	493	N/A	INTRINSIC
low complexity region	503	516	N/A	INTRINSIC
PolyA	534	597	4.49e-41	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000228705

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 34 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933427D14Rik	G	A	11: 72,093,308 (GRCm39)	S8F	probably damaging	Het
Alpk1	T	A	3: 127,522,931 (GRCm39)	Q37L	probably damaging	Het
Cfap43	T	C	19: 47,736,463 (GRCm39)	T1343A	probably benign	Het
Cmbl	C	A	15: 31,585,554 (GRCm39)	P146Q	possibly damaging	Het
Cog2	A	T	8: 125,259,951 (GRCm39)		probably null	Het
Dgkh	C	A	14: 78,825,016 (GRCm39)	V880L	probably benign	Het
Dop1a	T	C	9: 86,402,141 (GRCm39)	S1114P	probably damaging	Het
Eif5b	T	A	1: 38,080,828 (GRCm39)	V723D	probably damaging	Het
Gdf11	A	G	10: 128,721,253 (GRCm39)	Y314H	probably damaging	Het
Gria1	G	A	11: 57,127,750 (GRCm39)	V320I	probably benign	Het
H2-Q10	T	A	17: 35,784,463 (GRCm39)	*326R	probably null	Het
Irx6	T	A	8: 93,403,659 (GRCm39)	L128Q	probably damaging	Het
Kif21b	T	A	1: 136,087,495 (GRCm39)	L937Q	probably damaging	Het
Lama5	A	G	2: 179,832,120 (GRCm39)		probably benign	Het
Mios	A	G	6: 8,231,269 (GRCm39)	I718V	probably benign	Het
Mroh8	A	G	2: 157,096,893 (GRCm39)	V318A	probably damaging	Het
Nags	A	G	11: 102,039,897 (GRCm39)	*528W	probably null	Het
Nom1	T	A	5: 29,642,708 (GRCm39)	V403D	probably damaging	Het
Npffr2	C	A	5: 89,731,310 (GRCm39)	N413K	probably benign	Het
Olr1	C	T	6: 129,476,860 (GRCm39)	R135K	possibly damaging	Het
Or1e34	A	T	11: 73,779,121 (GRCm39)	Y26N	probably benign	Het
Or52e8	T	A	7: 104,624,665 (GRCm39)	I176F	possibly damaging	Het
Pkhd1	A	G	1: 20,140,600 (GRCm39)		probably null	Het
Ptpro	A	G	6: 137,431,698 (GRCm39)	M1158V	probably benign	Het
Sh3d19	A	G	3: 86,001,017 (GRCm39)	K238E	probably damaging	Het
Smarcc2	G	T	10: 128,318,641 (GRCm39)	R641L	probably damaging	Het
Th	T	C	7: 142,451,794 (GRCm39)	E75G	possibly damaging	Het
Tlr1	A	T	5: 65,083,290 (GRCm39)	L429*	probably null	Het
Top6bl	T	C	19: 4,713,583 (GRCm39)	K132E	probably damaging	Het
Ttn	G	A	2: 76,724,705 (GRCm39)	R2107*	probably null	Het
Ubr2	A	T	17: 47,245,119 (GRCm39)	C1636S	probably damaging	Het
Vmn2r100	T	A	17: 19,741,597 (GRCm39)	I103K	possibly damaging	Het
Vmn2r88	A	G	14: 51,655,437 (GRCm39)	M558V	possibly damaging	Het
Zzef1	G	A	11: 72,777,573 (GRCm39)	M1801I	probably benign	Het

Other mutations in Gm10110

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01390:Gm10110	APN	14	90,135,677 (GRCm39)	exon	noncoding transcript
IGL02977:Gm10110	APN	14	90,134,768 (GRCm39)	exon	noncoding transcript
IGL03230:Gm10110	APN	14	90,135,733 (GRCm39)	exon	noncoding transcript
R0966:Gm10110	UTSW	14	90,135,555 (GRCm39)	exon	noncoding transcript
R1466:Gm10110	UTSW	14	90,135,511 (GRCm39)	exon	noncoding transcript
R1466:Gm10110	UTSW	14	90,135,511 (GRCm39)	exon	noncoding transcript
R1640:Gm10110	UTSW	14	90,135,679 (GRCm39)	exon	noncoding transcript
R1762:Gm10110	UTSW	14	90,134,825 (GRCm39)	exon	noncoding transcript
R1839:Gm10110	UTSW	14	90,135,272 (GRCm39)	exon	noncoding transcript
R2679:Gm10110	UTSW	14	90,134,852 (GRCm39)	exon	noncoding transcript
R3907:Gm10110	UTSW	14	90,135,583 (GRCm39)	exon	noncoding transcript
R4512:Gm10110	UTSW	14	90,135,151 (GRCm39)	exon	noncoding transcript
R4513:Gm10110	UTSW	14	90,135,151 (GRCm39)	exon	noncoding transcript
R4590:Gm10110	UTSW	14	90,134,982 (GRCm39)	exon	noncoding transcript
R4877:Gm10110	UTSW	14	90,134,785 (GRCm39)	exon	noncoding transcript
R5771:Gm10110	UTSW	14	90,134,675 (GRCm39)	exon	noncoding transcript
R6333:Gm10110	UTSW	14	90,135,733 (GRCm39)	exon	noncoding transcript
R6341:Gm10110	UTSW	14	90,134,144 (GRCm39)	exon	noncoding transcript
R8235:Gm10110	UTSW	14	90,135,677 (GRCm39)	missense	noncoding transcript
R8236:Gm10110	UTSW	14	90,135,677 (GRCm39)	missense	noncoding transcript
R8237:Gm10110	UTSW	14	90,135,677 (GRCm39)	missense	noncoding transcript
R8281:Gm10110	UTSW	14	90,135,677 (GRCm39)	missense	noncoding transcript
R8282:Gm10110	UTSW	14	90,135,677 (GRCm39)	missense	noncoding transcript
R8283:Gm10110	UTSW	14	90,135,677 (GRCm39)	missense	noncoding transcript

Posted On

2015-04-16