Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01986:Gm18856'

181914

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm18856

Ensembl Gene

ENSMUSG00000096192

Gene Name

predicted gene, 18856

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01986

Quality Score

Status

Chromosome

Chromosomal Location

14139060-14140445 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

G to A at 14139413 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000152457 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099747] [ENSMUST00000221300] [ENSMUST00000221974] [ENSMUST00000222110] [ENSMUST00000223483]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000099747

SMART Domains

Protein: ENSMUSP00000097336
Gene: ENSMUSG00000039242

Domain	Start	End	E-Value	Type
signal peptide	1	16	N/A	INTRINSIC
Pfam:Galactosyl_T	300	460	2.9e-26	PFAM
low complexity region	481	492	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000178096

SMART Domains

Protein: ENSMUSP00000136490
Gene: ENSMUSG00000096192

Domain	Start	End	E-Value	Type
BTB	34	145	1.76e-25	SMART
low complexity region	168	176	N/A	INTRINSIC
low complexity region	184	200	N/A	INTRINSIC
low complexity region	241	253	N/A	INTRINSIC
ZnF_C2H2	309	328	5.12e1	SMART
ZnF_C2H2	334	356	7.26e-3	SMART
ZnF_C2H2	362	382	1.26e1	SMART
ZnF_C2H2	390	410	2.41e1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221021

Predicted Effect

probably benign
Transcript: ENSMUST00000221300

Predicted Effect

probably benign
Transcript: ENSMUST00000221333

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000221764

Predicted Effect

probably benign
Transcript: ENSMUST00000221974

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223389

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223307

Predicted Effect

probably benign
Transcript: ENSMUST00000222110

Predicted Effect

probably benign
Transcript: ENSMUST00000223483

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000222015

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
6820408C15Rik	A	T	2: 152,282,956 (GRCm39)	I245F	possibly damaging	Het
Abca3	G	A	17: 24,627,088 (GRCm39)	G1263D	probably damaging	Het
Arap2	A	T	5: 62,779,265 (GRCm39)	S1442T	probably damaging	Het
Arl15	C	A	13: 114,058,902 (GRCm39)	S56R	possibly damaging	Het
Ccdc38	A	T	10: 93,415,705 (GRCm39)	N415Y	probably damaging	Het
Ccny	G	A	18: 9,377,817 (GRCm39)	R81C	probably damaging	Het
Cracd	T	A	5: 77,006,457 (GRCm39)	S939R	unknown	Het
Csmd3	T	C	15: 47,522,591 (GRCm39)	T2693A	possibly damaging	Het
Fancm	C	T	12: 65,173,429 (GRCm39)	Q1914*	probably null	Het
Fcsk	T	C	8: 111,609,889 (GRCm39)	T1042A	probably benign	Het
Gramd1a	A	T	7: 30,833,434 (GRCm39)	L610Q	possibly damaging	Het
Hsd17b4	C	A	18: 50,293,193 (GRCm39)		probably benign	Het
Hspa12a	A	G	19: 58,787,834 (GRCm39)	S663P	probably benign	Het
Insr	C	T	8: 3,208,817 (GRCm39)	V1215I	probably damaging	Het
Kdr	A	G	5: 76,113,519 (GRCm39)	V783A	probably benign	Het
Klhl9	T	C	4: 88,640,016 (GRCm39)	D75G	probably damaging	Het
Lmntd1	A	G	6: 145,365,533 (GRCm39)	S53P	probably damaging	Het
Lrrc41	T	A	4: 115,946,519 (GRCm39)	F411L	probably benign	Het
Lyst	G	A	13: 13,950,212 (GRCm39)		probably null	Het
Mmp17	A	G	5: 129,673,692 (GRCm39)	H257R	probably damaging	Het
Nkiras1	G	A	14: 18,280,071 (GRCm38)	R154Q	probably damaging	Het
Or10ag2	A	G	2: 87,248,880 (GRCm39)	I163V	probably benign	Het
Or2b4	A	G	17: 38,116,957 (GRCm39)	K307R	probably damaging	Het
Or4p21	C	T	2: 88,276,839 (GRCm39)	V148I	probably benign	Het
Or8s16	T	C	15: 98,210,660 (GRCm39)	Y257C	probably damaging	Het
Pcsk6	G	A	7: 65,577,625 (GRCm39)	R60H	probably damaging	Het
Polk	T	C	13: 96,620,331 (GRCm39)	D623G	probably benign	Het
Rlf	A	T	4: 121,005,303 (GRCm39)	C1226S	probably damaging	Het
Rpa2	C	T	4: 132,499,191 (GRCm39)	P87S	probably benign	Het
Rpa2	C	T	4: 132,499,192 (GRCm39)	P87L	probably benign	Het
Sema5a	T	C	15: 32,682,506 (GRCm39)		probably benign	Het
Sis	A	T	3: 72,852,545 (GRCm39)	M529K	probably damaging	Het
Sspo	T	C	6: 48,460,237 (GRCm39)	M3375T	probably benign	Het
Syne3	A	T	12: 104,934,259 (GRCm39)	L83Q	probably damaging	Het
Tec	A	T	5: 72,939,348 (GRCm39)	Y222*	probably null	Het
Tfap2d	C	T	1: 19,189,383 (GRCm39)		probably benign	Het
Trak1	G	A	9: 121,302,033 (GRCm39)	A930T	probably benign	Het
Ugt2b34	G	T	5: 87,049,111 (GRCm39)	H305N	probably benign	Het
Vmn2r95	A	G	17: 18,660,473 (GRCm39)	N295S	probably benign	Het

Other mutations in Gm18856

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00500:Gm18856	APN	13	14,140,319 (GRCm39)	intron	probably benign
IGL01865:Gm18856	APN	13	14,139,508 (GRCm39)	intron	probably benign
IGL02552:Gm18856	APN	13	14,139,805 (GRCm39)	intron	probably benign
IGL02664:Gm18856	APN	13	14,139,809 (GRCm39)	intron	probably benign
R1538:Gm18856	UTSW	13	14,139,274 (GRCm39)	intron	probably benign
R1672:Gm18856	UTSW	13	14,140,342 (GRCm39)	intron	probably benign
R2029:Gm18856	UTSW	13	14,139,376 (GRCm39)	intron	probably benign
R3971:Gm18856	UTSW	13	14,139,433 (GRCm39)	intron	probably benign
R4655:Gm18856	UTSW	13	14,140,232 (GRCm39)	intron	probably benign
R4795:Gm18856	UTSW	13	14,139,793 (GRCm39)	intron	probably benign
R6107:Gm18856	UTSW	13	14,140,319 (GRCm39)	intron	probably benign

Posted On

2014-05-07