Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01667:Gm5581'

103344

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 #

IGL01667

Quality Score

Status

Chromosome

Chromosomal Location

131143329-131144284 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 131144735 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: 34 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Akap13	A	G	7: 75,219,767 (GRCm39)	T57A	probably damaging	Het
Akna	G	T	4: 63,297,396 (GRCm39)	T886N	probably benign	Het
Aqp9	A	G	9: 71,045,495 (GRCm39)	V38A	probably benign	Het
Awat2	C	T	X: 99,447,860 (GRCm39)	G124D	probably damaging	Het
Camsap1	A	G	2: 25,835,293 (GRCm39)		probably benign	Het
Catsperg2	T	C	7: 29,409,558 (GRCm39)	Y545C	probably damaging	Het
Cldn23	A	G	8: 36,293,074 (GRCm39)	F138S	possibly damaging	Het
Clec4a3	A	C	6: 122,929,819 (GRCm39)		probably benign	Het
Dlgap3	C	A	4: 127,127,690 (GRCm39)	T786K	probably benign	Het
Dnah2	A	C	11: 69,435,221 (GRCm39)	S50A	probably benign	Het
Dnah2	A	T	11: 69,411,767 (GRCm39)	I285N	probably damaging	Het
Dnah7a	A	G	1: 53,586,451 (GRCm39)	Y1467H	probably damaging	Het
Fgf22	C	T	10: 79,592,588 (GRCm39)	P115L	probably damaging	Het
Fzd2	G	T	11: 102,496,608 (GRCm39)	V351L	possibly damaging	Het
Gapdhs	T	A	7: 30,436,062 (GRCm39)	E174V	possibly damaging	Het
Gjc2	A	C	11: 59,068,344 (GRCm39)	I46S	probably damaging	Het
Krt1c	C	A	15: 101,724,765 (GRCm39)	V282L	possibly damaging	Het
Myh15	G	A	16: 49,015,942 (GRCm39)	V1873M	probably benign	Het
Myo1b	T	C	1: 51,799,536 (GRCm39)	T931A	probably damaging	Het
Myo6	A	T	9: 80,197,175 (GRCm39)	K965N	unknown	Het
Or5a3	T	C	19: 12,400,120 (GRCm39)	V149A	probably benign	Het
Pcnx3	T	C	19: 5,736,658 (GRCm39)	R160G	probably benign	Het
Slc22a16	T	C	10: 40,461,014 (GRCm39)	I272T	probably damaging	Het
Slc35b4	A	G	6: 34,144,610 (GRCm39)	Y82H	possibly damaging	Het
Spdya	T	C	17: 71,863,254 (GRCm39)	M1T	probably null	Het
St6gal1	A	G	16: 23,140,174 (GRCm39)	N115S	probably benign	Het
Tbc1d12	A	T	19: 38,902,744 (GRCm39)		probably benign	Het
Tfrc	A	G	16: 32,443,261 (GRCm39)		probably benign	Het
Trip11	A	C	12: 101,845,121 (GRCm39)	F1539C	probably damaging	Het
Ttn	A	T	2: 76,611,422 (GRCm39)	I15624N	possibly damaging	Het
Vmn1r169	A	T	7: 23,277,225 (GRCm39)	M206L	probably benign	Het
Zfp362	A	G	4: 128,680,902 (GRCm39)	L141P	probably damaging	Het
Zfp692	A	G	11: 58,202,379 (GRCm39)	H378R	probably damaging	Het
Zfp799	T	C	17: 33,040,794 (GRCm39)	Q52R	possibly damaging	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
IGL02260:Gm5581	APN	6	131,144,909 (GRCm39)	unclassified	noncoding transcript
IGL03212:Gm5581	APN	6	131,158,413 (GRCm39)	exon	noncoding transcript
IGL03306:Gm5581	APN	6	131,145,044 (GRCm39)	unclassified	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

2014-01-21