Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00793:Stpg1'

27186

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Stpg1

Ensembl Gene

ENSMUSG00000028801

Gene Name

sperm tail PG rich repeat containing 1

Synonyms

4930403G18Rik, 4930555I21Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

IGL00793

Quality Score

Status

Chromosome

Chromosomal Location

135222101-135265114 bp(+) (GRCm39)

Type of Mutation

utr 5 prime

DNA Base Change (assembly)

A to G at 135233718 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000067647 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063707]

AlphaFold

Q9D2F5

Predicted Effect

probably benign
Transcript: ENSMUST00000063707

SMART Domains

Protein: ENSMUSP00000067647
Gene: ENSMUSG00000028801

Domain	Start	End	E-Value	Type
Pfam:SHIPPO-rpt	194	224	1.8e-5	PFAM
Pfam:SHIPPO-rpt	232	261	7.9e-6	PFAM
Pfam:SHIPPO-rpt	273	312	1e-4	PFAM
Pfam:SHIPPO-rpt	313	334	8.8e-4	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123221

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153891

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
1700102P08Rik	A	G	9: 108,274,605 (GRCm39)	D236G	probably damaging	Het
5031410I06Rik	T	C	5: 26,309,153 (GRCm39)	R50G	probably damaging	Het
Adam32	A	T	8: 25,327,846 (GRCm39)		probably benign	Het
Adm	A	G	7: 110,227,788 (GRCm39)	Y52C	probably damaging	Het
Aff4	A	G	11: 53,302,817 (GRCm39)	T1097A	probably damaging	Het
Ccne1	A	C	7: 37,805,726 (GRCm39)	V50G	probably benign	Het
Copb2	A	G	9: 98,467,057 (GRCm39)	T636A	probably benign	Het
Cxadr	C	A	16: 78,131,115 (GRCm39)	Y210*	probably null	Het
Dnajc17	T	C	2: 119,011,441 (GRCm39)	E163G	probably benign	Het
Dnmt3b	T	A	2: 153,514,422 (GRCm39)	M405K	possibly damaging	Het
Enpp7	A	T	11: 118,881,371 (GRCm39)	N172I	probably damaging	Het
G2e3	T	A	12: 51,414,545 (GRCm39)	S340T	probably benign	Het
Kat2b	A	G	17: 53,972,852 (GRCm39)	N722S	probably benign	Het
Kcnh5	C	A	12: 75,161,120 (GRCm39)	V263F	probably damaging	Het
Ldlrad1	A	G	4: 107,075,086 (GRCm39)	D211G	probably damaging	Het
Lrp1	A	G	10: 127,378,074 (GRCm39)	V4082A	possibly damaging	Het
Maco1	A	G	4: 134,555,517 (GRCm39)	S319P	probably damaging	Het
Mycbp2	A	T	14: 103,364,189 (GRCm39)	V4370D	possibly damaging	Het
Npsr1	G	T	9: 24,165,989 (GRCm39)	R125L	probably damaging	Het
Osbpl9	T	C	4: 108,944,628 (GRCm39)	I116V	probably damaging	Het
Parp4	G	T	14: 56,840,334 (GRCm39)	A580S	possibly damaging	Het
Pfkm	T	C	15: 98,023,475 (GRCm39)	V391A	probably benign	Het
Psen1	T	A	12: 83,769,792 (GRCm39)	S170T	probably damaging	Het
Rsbn1l	C	T	5: 21,101,153 (GRCm39)	V796I	probably benign	Het
Slc39a8	A	G	3: 135,590,494 (GRCm39)	I396V	probably benign	Het
Spag16	T	C	1: 70,338,809 (GRCm39)	C436R	probably damaging	Het
Tmem86b	A	G	7: 4,631,756 (GRCm39)		probably benign	Het
Trf	A	G	9: 103,103,342 (GRCm39)		probably benign	Het
Trim61	A	T	8: 65,466,743 (GRCm39)	Y173N	possibly damaging	Het
Wrap73	T	C	4: 154,237,096 (GRCm39)	S228P	probably damaging	Het
Zfc3h1	T	C	10: 115,252,779 (GRCm39)	V1364A	probably benign	Het

Other mutations in Stpg1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00336:Stpg1	APN	4	135,256,856 (GRCm39)	missense	possibly damaging	0.92
IGL02118:Stpg1	APN	4	135,235,375 (GRCm39)	splice site	probably benign
IGL02432:Stpg1	APN	4	135,235,321 (GRCm39)	missense	probably damaging	0.96
R0362:Stpg1	UTSW	4	135,233,777 (GRCm39)	missense	possibly damaging	0.93
R0594:Stpg1	UTSW	4	135,246,742 (GRCm39)	missense	possibly damaging	0.91
R1233:Stpg1	UTSW	4	135,252,740 (GRCm39)	missense	probably benign
R2509:Stpg1	UTSW	4	135,263,960 (GRCm39)	missense	probably benign	0.12
R3743:Stpg1	UTSW	4	135,242,197 (GRCm39)	missense	probably benign	0.12
R4897:Stpg1	UTSW	4	135,246,676 (GRCm39)	missense	possibly damaging	0.93
R4933:Stpg1	UTSW	4	135,233,727 (GRCm39)	missense	probably benign
R5412:Stpg1	UTSW	4	135,252,786 (GRCm39)	missense	possibly damaging	0.83
R7140:Stpg1	UTSW	4	135,261,033 (GRCm39)	missense	probably benign	0.01
R7313:Stpg1	UTSW	4	135,256,827 (GRCm39)	missense	probably damaging	0.97
R8309:Stpg1	UTSW	4	135,256,903 (GRCm39)	missense	probably benign	0.00
R8787:Stpg1	UTSW	4	135,261,108 (GRCm39)	missense	probably benign	0.04
R9274:Stpg1	UTSW	4	135,252,782 (GRCm39)	missense	possibly damaging	0.85

Posted On

2013-04-17