Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01951:Gm5862'

279192

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5862

Ensembl Gene

ENSMUSG00000067700

Gene Name

predicted gene 5862

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.196) question?

Stock #

IGL01951

Quality Score

Status

Chromosome

Chromosomal Location

26223419-26227889 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 26227769 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Glycine at position 41 (W41G)

Ref Sequence

ENSEMBL: ENSMUSP00000072133 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072286]

AlphaFold

K7N5V5

Predicted Effect

probably benign
Transcript: ENSMUST00000072286
AA Change: W41G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000072133
Gene: ENSMUSG00000067700
AA Change: W41G

Domain	Start	End	E-Value	Type
Pfam:Takusan	50	134	1.6e-25	PFAM
low complexity region	154	168	N/A	INTRINSIC
low complexity region	235	259	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921539E11Rik	A	G	4: 103,092,865 (GRCm39)	I152T	probably damaging	Het
A2m	C	T	6: 121,644,149 (GRCm39)	T949I	possibly damaging	Het
Begain	T	A	12: 108,999,571 (GRCm39)	Y605F	probably benign	Het
Cavin2	A	G	1: 51,328,570 (GRCm39)	E9G	possibly damaging	Het
Cdh16	A	G	8: 105,344,323 (GRCm39)	V72A	probably damaging	Het
Dgkd	T	C	1: 87,844,638 (GRCm39)	L268P	probably damaging	Het
Eps8	T	A	6: 137,514,669 (GRCm39)	Y28F	possibly damaging	Het
Erap1	T	C	13: 74,823,414 (GRCm39)	I816T	probably damaging	Het
Fli1	A	T	9: 32,372,660 (GRCm39)	F126Y	probably damaging	Het
Gm10717	C	T	9: 3,025,616 (GRCm39)	S67L	probably benign	Het
Gm10718	A	T	9: 3,025,118 (GRCm39)	Y194F	probably benign	Het
Gm21957	A	T	7: 124,819,004 (GRCm39)		noncoding transcript	Het
Hectd1	T	A	12: 51,841,280 (GRCm39)	R618*	probably null	Het
Homez	T	C	14: 55,095,633 (GRCm39)	E25G	probably damaging	Het
Ifngr1	C	A	10: 19,485,202 (GRCm39)	N400K	possibly damaging	Het
Lin7a	G	A	10: 107,247,886 (GRCm39)	V186I	possibly damaging	Het
Lpcat2	G	T	8: 93,644,675 (GRCm39)	S448I	probably damaging	Het
Lrp10	C	A	14: 54,706,119 (GRCm39)	Y436*	probably null	Het
Myef2l	G	A	3: 10,154,118 (GRCm39)	V296M	probably damaging	Het
Myo1f	A	G	17: 33,816,991 (GRCm39)	H707R	possibly damaging	Het
Neurl4	A	G	11: 69,800,449 (GRCm39)	N1147D	probably damaging	Het
Or4b1b	G	T	2: 90,112,351 (GRCm39)	D189E	probably damaging	Het
Or6b3	T	C	1: 92,438,853 (GRCm39)	D299G	probably null	Het
Pak6	T	C	2: 118,523,741 (GRCm39)	S299P	probably benign	Het
Panx2	A	G	15: 88,952,970 (GRCm39)	D487G	probably damaging	Het
Sbspon	T	C	1: 15,929,158 (GRCm39)	N211S	probably benign	Het
Sgsm1	T	A	5: 113,434,633 (GRCm39)		probably benign	Het
Slc38a4	T	C	15: 96,917,644 (GRCm39)	Y27C	probably benign	Het
Sorbs1	A	G	19: 40,306,460 (GRCm39)		probably benign	Het
Sp140l2	A	G	1: 85,231,907 (GRCm39)		probably benign	Het
Ssh1	A	T	5: 114,104,308 (GRCm39)	Y35N	possibly damaging	Het
Stx2	A	T	5: 129,069,329 (GRCm39)	F127L	probably damaging	Het
Synm	A	T	7: 67,388,885 (GRCm39)	I325N	probably damaging	Het
Szt2	A	G	4: 118,233,690 (GRCm39)		probably benign	Het
Tbc1d23	A	G	16: 57,007,048 (GRCm39)		probably benign	Het
Tmem50a	T	C	4: 134,625,739 (GRCm39)		probably benign	Het
Tpx2	T	G	2: 152,726,096 (GRCm39)	L354V	probably benign	Het
Trafd1	G	A	5: 121,512,094 (GRCm39)	R399C	possibly damaging	Het
Trem3	C	T	17: 48,556,903 (GRCm39)	R125W	probably damaging	Het
Ubp1	T	A	9: 113,780,686 (GRCm39)	Y92*	probably null	Het
Wnk1	T	A	6: 119,940,446 (GRCm39)	T62S	probably damaging	Het
Zbtb6	T	C	2: 37,319,343 (GRCm39)	E195G	probably benign	Het
Zc3h15	A	G	2: 83,491,829 (GRCm39)	D306G	probably damaging	Het

Other mutations in Gm5862

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01606:Gm5862	APN	5	26,224,514 (GRCm39)	missense	probably benign
IGL01863:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01868:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01873:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01881:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01902:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01905:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01909:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01917:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01924:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL01927:Gm5862	APN	5	26,227,769 (GRCm39)	missense	probably benign
IGL03374:Gm5862	APN	5	26,224,510 (GRCm39)	missense	probably damaging	0.98
R2475:Gm5862	UTSW	5	26,224,490 (GRCm39)	missense	probably damaging	1.00
R3828:Gm5862	UTSW	5	26,224,345 (GRCm39)	missense	probably benign	0.27
R4591:Gm5862	UTSW	5	26,224,486 (GRCm39)	missense	possibly damaging	0.95
R6916:Gm5862	UTSW	5	26,224,346 (GRCm39)	missense	probably benign
R8291:Gm5862	UTSW	5	26,224,444 (GRCm39)	missense	probably benign	0.32
R8927:Gm5862	UTSW	5	26,226,678 (GRCm39)	missense	probably damaging	0.98
R8928:Gm5862	UTSW	5	26,226,678 (GRCm39)	missense	probably damaging	0.98
R9074:Gm5862	UTSW	5	26,226,624 (GRCm39)	missense	probably damaging	0.98
Z1176:Gm5862	UTSW	5	26,223,485 (GRCm39)	frame shift	probably null

Posted On

2015-04-16