Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00960:Zfa-ps'

28385

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Zfa-ps

Ensembl Gene

ENSMUSG00000049576

Gene Name

zinc finger protein, autosomal, pseudogene

Synonyms

Zfa

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.218) question?

Stock #

IGL00960

Quality Score

Status

Chromosome

Chromosomal Location

52418416-52421835 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 52420043 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: ENSMUST00000180526

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000180673

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 29 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc10	C	A	17: 46,634,671 (GRCm39)	R444L	probably damaging	Het
Baiap2	T	A	11: 119,890,118 (GRCm39)	S460T	possibly damaging	Het
Cckar	A	G	5: 53,858,634 (GRCm39)	Y158H	probably damaging	Het
Cdk4	A	G	10: 126,900,166 (GRCm39)	Y21C	probably damaging	Het
Entpd1	C	T	19: 40,699,714 (GRCm39)	P42S	probably benign	Het
Epha8	A	T	4: 136,679,150 (GRCm39)		probably null	Het
Fastkd1	A	T	2: 69,524,997 (GRCm39)		probably benign	Het
Fmnl2	A	G	2: 53,013,494 (GRCm39)	D951G	probably damaging	Het
Hnrnpm	C	A	17: 33,868,876 (GRCm39)	R517L	probably damaging	Het
Kcnj5	T	A	9: 32,233,719 (GRCm39)	T199S	probably damaging	Het
Med13	T	C	11: 86,181,866 (GRCm39)		probably benign	Het
Mycbp2	G	T	14: 103,466,820 (GRCm39)	H1314Q	possibly damaging	Het
Ncapd2	A	T	6: 125,150,811 (GRCm39)	S795T	probably benign	Het
Nf1	T	C	11: 79,335,947 (GRCm39)	S1042P	probably damaging	Het
Nlgn1	C	A	3: 25,966,861 (GRCm39)	L197F	probably damaging	Het
Nsun7	A	G	5: 66,446,846 (GRCm39)	Y428C	probably benign	Het
Or10d5j	A	G	9: 39,867,455 (GRCm39)	Y259H	probably damaging	Het
Parp14	T	C	16: 35,661,589 (GRCm39)	D1453G	probably benign	Het
Pcdhb8	A	T	18: 37,489,026 (GRCm39)	I235F	probably benign	Het
Pclo	T	C	5: 14,725,234 (GRCm39)	V1364A	unknown	Het
Polq	T	C	16: 36,880,874 (GRCm39)	S734P	probably damaging	Het
Sco1	T	C	11: 66,954,864 (GRCm39)	*290Q	probably null	Het
Slc22a3	A	T	17: 12,644,497 (GRCm39)	I496N	probably damaging	Het
Slc5a8	T	G	10: 88,757,627 (GRCm39)	I539S	probably benign	Het
Tecta	A	G	9: 42,270,376 (GRCm39)	F1311L	possibly damaging	Het
Tex261	A	T	6: 83,752,650 (GRCm39)	I19N	possibly damaging	Het
Tfr2	T	C	5: 137,569,954 (GRCm39)	V120A	probably benign	Het
Vmn2r71	A	T	7: 85,273,582 (GRCm39)	S799C	probably damaging	Het
Zar1	G	A	5: 72,734,628 (GRCm39)	T197I	probably damaging	Het

Other mutations in Zfa-ps

Allele	Source	Chr	Coord	Type	Predicted Effect
R0057:Zfa-ps	UTSW	10	52,421,202 (GRCm39)	exon	noncoding transcript
R0057:Zfa-ps	UTSW	10	52,421,202 (GRCm39)	exon	noncoding transcript
R1159:Zfa-ps	UTSW	10	52,419,654 (GRCm39)	exon	noncoding transcript
R2145:Zfa-ps	UTSW	10	52,419,373 (GRCm39)	exon	noncoding transcript
R2290:Zfa-ps	UTSW	10	52,421,112 (GRCm39)	exon	noncoding transcript
R2509:Zfa-ps	UTSW	10	52,420,339 (GRCm39)	exon	noncoding transcript
R3738:Zfa-ps	UTSW	10	52,420,636 (GRCm39)	exon	noncoding transcript
R4035:Zfa-ps	UTSW	10	52,420,636 (GRCm39)	exon	noncoding transcript
R4290:Zfa-ps	UTSW	10	52,419,807 (GRCm39)	exon	noncoding transcript
R4545:Zfa-ps	UTSW	10	52,421,032 (GRCm39)	exon	noncoding transcript
R4862:Zfa-ps	UTSW	10	52,419,192 (GRCm39)	exon	noncoding transcript
R5135:Zfa-ps	UTSW	10	52,419,118 (GRCm39)	exon	noncoding transcript
R5270:Zfa-ps	UTSW	10	52,419,552 (GRCm39)	exon	noncoding transcript

Posted On

2013-04-17