Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03306:Gm5581'

416374

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5581

Ensembl Gene

ENSMUSG00000061969

Gene Name

predicted gene 5581

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.072) question?

Stock #

IGL03306

Quality Score

Status

Chromosome

Chromosomal Location

131143329-131144284 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to A at 131145044 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000072940

SMART Domains

Protein: ENSMUSP00000072710
Gene: ENSMUSG00000061969

Domain	Start	End	E-Value	Type
KRAB	8	68	1.79e-34	SMART
low complexity region	285	302	N/A	INTRINSIC
low complexity region	355	366	N/A	INTRINSIC
PDB:1MEY\|G	422	507	4e-15	PDB
Blast:HNHc	445	504	4e-6	BLAST
ZnF_C2H2	509	531	9.73e-4	SMART
ZnF_C2H2	537	559	1.5e-4	SMART
ZnF_C2H2	565	587	1.98e-4	SMART
ZnF_C2H2	593	615	1.52e-5	SMART
ZnF_C2H2	621	643	9.73e-4	SMART
ZnF_C2H2	649	671	9.36e-6	SMART
ZnF_C2H2	677	699	3.49e-5	SMART
ZnF_C2H2	705	727	9.88e-5	SMART
ZnF_C2H2	733	755	9.88e-5	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000204992

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Agbl1	T	A	7: 76,239,252 (GRCm39)	F584Y	probably damaging	Het
Amer2	C	A	14: 60,616,001 (GRCm39)	D65E	probably damaging	Het
Arhgap28	A	T	17: 68,159,930 (GRCm39)	L623Q	probably damaging	Het
Cep152	T	C	2: 125,447,328 (GRCm39)	T407A	possibly damaging	Het
Cmpk2	A	G	12: 26,521,442 (GRCm39)	D238G	possibly damaging	Het
Fam169a	C	A	13: 97,243,497 (GRCm39)	Q176K	possibly damaging	Het
Fbxo17	T	A	7: 28,434,782 (GRCm39)	I189N	probably damaging	Het
Gpcpd1	C	T	2: 132,375,993 (GRCm39)		probably null	Het
Lhx2	A	G	2: 38,244,628 (GRCm39)	Y123C	probably damaging	Het
Llgl1	C	A	11: 60,602,180 (GRCm39)	T741N	possibly damaging	Het
Macc1	A	G	12: 119,410,603 (GRCm39)	Q457R	probably benign	Het
Mthfd2l	A	G	5: 91,168,067 (GRCm39)	T321A	probably damaging	Het
Myo6	T	C	9: 80,153,837 (GRCm39)	F271S	probably damaging	Het
Ncoa6	A	G	2: 155,247,427 (GRCm39)	V1959A	probably benign	Het
Npsr1	A	G	9: 24,224,535 (GRCm39)	D304G	probably benign	Het
Nup205	T	C	6: 35,185,104 (GRCm39)	V841A	probably damaging	Het
Or10c1	A	G	17: 37,522,568 (GRCm39)	Y59H	probably damaging	Het
Or1j20	A	T	2: 36,760,537 (GRCm39)		probably benign	Het
Osbpl9	A	G	4: 109,029,529 (GRCm39)		probably benign	Het
Pdgfra	A	G	5: 75,353,194 (GRCm39)	N995D	possibly damaging	Het
Ptgs1	A	T	2: 36,127,717 (GRCm39)	H92L	probably damaging	Het
Rasd1	T	A	11: 59,855,181 (GRCm39)	I100F	possibly damaging	Het
Rbm26	T	C	14: 105,388,758 (GRCm39)	T378A	probably damaging	Het
Slc12a3	T	C	8: 95,078,386 (GRCm39)	S805P	possibly damaging	Het
Smarcal1	G	A	1: 72,665,625 (GRCm39)	V708I	probably benign	Het
Strn	A	G	17: 78,974,652 (GRCm39)	S408P	probably damaging	Het
Suclg1	A	G	6: 73,247,975 (GRCm39)	N232S	probably benign	Het
Tmbim1	A	G	1: 74,332,225 (GRCm39)	Y101H	probably damaging	Het
Ube3a	T	A	7: 58,935,895 (GRCm39)	L614Q	probably damaging	Het
Wrn	A	G	8: 33,826,149 (GRCm39)	L171P	probably damaging	Het
Zfp335	T	C	2: 164,737,904 (GRCm39)		probably benign	Het

Other mutations in Gm5581

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00533:Gm5581	APN	6	131,144,604 (GRCm39)	unclassified	noncoding transcript
IGL01372:Gm5581	APN	6	131,145,366 (GRCm39)	exon	noncoding transcript
IGL01630:Gm5581	APN	6	131,145,259 (GRCm39)	exon	noncoding transcript
IGL01667:Gm5581	APN	6	131,144,735 (GRCm39)	unclassified	noncoding transcript
IGL02260:Gm5581	APN	6	131,144,909 (GRCm39)	unclassified	noncoding transcript
IGL03212:Gm5581	APN	6	131,158,413 (GRCm39)	exon	noncoding transcript
R0366:Gm5581	UTSW	6	131,143,410 (GRCm39)	unclassified	noncoding transcript
R1764:Gm5581	UTSW	6	131,158,362 (GRCm39)	exon	noncoding transcript
R1961:Gm5581	UTSW	6	131,145,125 (GRCm39)	unclassified	noncoding transcript
R2129:Gm5581	UTSW	6	131,145,247 (GRCm39)	exon	noncoding transcript
R3177:Gm5581	UTSW	6	131,143,928 (GRCm39)	unclassified	noncoding transcript
R4026:Gm5581	UTSW	6	131,144,031 (GRCm39)	unclassified	noncoding transcript
R4289:Gm5581	UTSW	6	131,144,519 (GRCm39)	unclassified	noncoding transcript
R4943:Gm5581	UTSW	6	131,144,088 (GRCm39)	unclassified	noncoding transcript
R4961:Gm5581	UTSW	6	131,144,190 (GRCm39)	unclassified	noncoding transcript
R5817:Gm5581	UTSW	6	131,144,132 (GRCm39)	unclassified	noncoding transcript
R5944:Gm5581	UTSW	6	131,145,363 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02