Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02600:Tmem229b-ps'

300053

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Tmem229b-ps

Ensembl Gene

ENSMUSG00000056219

Gene Name

transmembrane protein 229B, pseudogene

Synonyms

Gm5423

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.209) question?

Stock #

IGL02600

Quality Score

Status

Chromosome

Chromosomal Location

53351060-53351565 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 53351052 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: ENSMUST00000168554

SMART Domains

Protein: ENSMUSP00000132002
Gene: ENSMUSG00000056219

Domain	Start	End	E-Value	Type
Pfam:ABC_trans_CmpB	12	148	8.5e-14	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 28 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca5	T	G	11: 110,200,264 (GRCm39)	I483L	probably benign	Het
Bmpr1b	A	C	3: 141,546,488 (GRCm39)	M466R	probably damaging	Het
Casp8ap2	G	A	4: 32,630,246 (GRCm39)	D42N	probably null	Het
Crebbp	T	A	16: 3,972,882 (GRCm39)	T271S	probably benign	Het
Ddx27	A	G	2: 166,868,124 (GRCm39)	H319R	probably damaging	Het
Dync2i2	T	A	2: 29,923,314 (GRCm39)	D263V	possibly damaging	Het
Gckr	A	G	5: 31,462,374 (GRCm39)	M236V	probably benign	Het
Gm28044	A	C	13: 67,469,025 (GRCm39)		probably benign	Het
Gmnc	T	A	16: 26,781,641 (GRCm39)		probably benign	Het
Gpx3	C	A	11: 54,800,433 (GRCm39)	D210E	possibly damaging	Het
Lpin2	A	G	17: 71,545,693 (GRCm39)	N513S	probably damaging	Het
Myh3	C	T	11: 66,974,227 (GRCm39)	R170C	probably damaging	Het
Nrxn3	G	T	12: 89,478,682 (GRCm39)		probably benign	Het
Nynrin	A	G	14: 56,101,449 (GRCm39)	I373V	probably benign	Het
Or13a21	T	C	7: 139,998,862 (GRCm39)	T275A	probably benign	Het
Or6b6	A	G	7: 106,570,756 (GRCm39)	I265T	possibly damaging	Het
Padi3	A	G	4: 140,525,467 (GRCm39)	V172A	probably benign	Het
Pdzd2	C	A	15: 12,411,105 (GRCm39)	G554W	probably damaging	Het
Plekhg6	G	A	6: 125,347,563 (GRCm39)	R464*	probably null	Het
Rnf123	G	A	9: 107,945,501 (GRCm39)	R390*	probably null	Het
Serinc1	A	G	10: 57,399,127 (GRCm39)	S259P	probably benign	Het
Slfn4	T	A	11: 83,077,832 (GRCm39)	S207T	possibly damaging	Het
Stab2	C	T	10: 86,790,123 (GRCm39)	G548R	probably damaging	Het
Ttn	G	A	2: 76,570,509 (GRCm39)	P26795S	probably damaging	Het
Vmn2r96	A	G	17: 18,817,829 (GRCm39)	M661V	probably benign	Het
Ybey	G	A	10: 76,300,165 (GRCm39)		probably benign	Het
Zbtb17	A	G	4: 141,194,196 (GRCm39)	D715G	possibly damaging	Het
Zgrf1	T	C	3: 127,394,623 (GRCm39)		probably benign	Het

Other mutations in Tmem229b-ps

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02309:Tmem229b-ps	APN	10	53,351,466 (GRCm39)	exon	noncoding transcript
IGL02503:Tmem229b-ps	APN	10	53,351,250 (GRCm39)	exon	noncoding transcript
R1515:Tmem229b-ps	UTSW	10	53,351,542 (GRCm39)	exon	noncoding transcript
R1595:Tmem229b-ps	UTSW	10	53,351,385 (GRCm39)	exon	noncoding transcript
R2010:Tmem229b-ps	UTSW	10	53,351,295 (GRCm39)	exon	noncoding transcript
R2116:Tmem229b-ps	UTSW	10	53,351,552 (GRCm39)	exon	noncoding transcript
R3498:Tmem229b-ps	UTSW	10	53,351,223 (GRCm39)	exon	noncoding transcript
R3499:Tmem229b-ps	UTSW	10	53,351,223 (GRCm39)	exon	noncoding transcript
R4281:Tmem229b-ps	UTSW	10	53,351,474 (GRCm39)	exon	noncoding transcript
R5405:Tmem229b-ps	UTSW	10	53,351,325 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16