Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00927:Zscan30'

29414

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Zscan30

Ensembl Gene

ENSMUSG00000024274

Gene Name

zinc finger and SCAN domain containing 30

Synonyms

C230097I24Rik, Zfp397os

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.117) question?

Stock #

IGL00927

Quality Score

Status

Chromosome

Chromosomal Location

24097875-24104844 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 24104834 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: ENSMUST00000115829

SMART Domains

Protein: ENSMUSP00000111495
Gene: ENSMUSG00000024274

Domain	Start	End	E-Value	Type
SCAN	44	149	7.42e-54	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224144

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310033P09Rik	A	G	11: 59,099,674 (GRCm39)	T92A	probably damaging	Het
Ankhd1	A	G	18: 36,765,125 (GRCm39)	S1007G	probably benign	Het
Cabp4	A	T	19: 4,189,406 (GRCm39)	S50R	possibly damaging	Het
Camp	A	T	9: 109,678,336 (GRCm39)	L56Q	probably damaging	Het
Cblb	A	G	16: 51,986,461 (GRCm39)	N568S	probably benign	Het
Ccr6	C	A	17: 8,474,825 (GRCm39)	T10K	probably benign	Het
Chit1	T	C	1: 134,072,992 (GRCm39)	F106S	probably damaging	Het
Cyb561d1	A	G	3: 108,106,943 (GRCm39)	L34P	probably damaging	Het
Dcun1d1	A	T	3: 35,975,114 (GRCm39)		probably benign	Het
Deup1	A	G	9: 15,521,967 (GRCm39)		probably benign	Het
Erich1	A	G	8: 14,083,518 (GRCm39)	F184S	probably damaging	Het
Fmnl3	A	G	15: 99,235,509 (GRCm39)		probably null	Het
Grk2	T	C	19: 4,337,982 (GRCm39)	N508S	probably benign	Het
Herc4	A	G	10: 63,109,316 (GRCm39)	I184V	probably benign	Het
Hnrnpm	C	A	17: 33,868,876 (GRCm39)	R517L	probably damaging	Het
Ift56	T	C	6: 38,359,155 (GRCm39)		probably benign	Het
Kif3b	G	A	2: 153,158,381 (GRCm39)	A61T	possibly damaging	Het
Kmt2d	G	A	15: 98,742,890 (GRCm39)		probably benign	Het
Lrrc7	C	A	3: 157,866,727 (GRCm39)	V1005L	possibly damaging	Het
Lrrtm1	A	T	6: 77,221,046 (GRCm39)	M168L	probably benign	Het
Ndc1	C	T	4: 107,241,977 (GRCm39)		probably benign	Het
Nphs1	A	G	7: 30,160,164 (GRCm39)		probably benign	Het
Or52w1	A	T	7: 105,018,454 (GRCm39)	Y298F	probably damaging	Het
Pbld2	T	C	10: 62,907,734 (GRCm39)	V200A	probably benign	Het
Pcdhb21	A	G	18: 37,647,606 (GRCm39)	Y245C	probably damaging	Het
Pcm1	A	G	8: 41,740,918 (GRCm39)	T1055A	probably damaging	Het
Plcl2	C	T	17: 50,913,948 (GRCm39)	S319L	probably benign	Het
Plekha8	C	A	6: 54,606,822 (GRCm39)	Y372*	probably null	Het
Ralb	T	A	1: 119,399,506 (GRCm39)	N184I	probably benign	Het
Robo3	C	T	9: 37,339,050 (GRCm39)		probably null	Het
Slc41a1	T	A	1: 131,766,914 (GRCm39)	L144H	probably damaging	Het
Smg1	C	T	7: 117,739,855 (GRCm39)	G3364D	probably damaging	Het
Spmap2	A	G	10: 79,412,433 (GRCm39)	S329P	probably damaging	Het
Vmn1r123	T	A	7: 20,896,216 (GRCm39)	V36D	possibly damaging	Het
Zbtb7c	T	C	18: 76,278,921 (GRCm39)	S460P	possibly damaging	Het

Other mutations in Zscan30

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02427:Zscan30	APN	18	24,104,533 (GRCm39)	exon	noncoding transcript
R0349:Zscan30	UTSW	18	24,104,455 (GRCm39)	exon	noncoding transcript
R1857:Zscan30	UTSW	18	24,104,524 (GRCm39)	exon	noncoding transcript
R1858:Zscan30	UTSW	18	24,104,524 (GRCm39)	exon	noncoding transcript
R1859:Zscan30	UTSW	18	24,104,524 (GRCm39)	exon	noncoding transcript
R2114:Zscan30	UTSW	18	24,104,173 (GRCm39)	exon	noncoding transcript
R5423:Zscan30	UTSW	18	24,104,773 (GRCm39)	exon	noncoding transcript
R8229:Zscan30	UTSW	18	24,104,737 (GRCm39)	missense	noncoding transcript

Posted On

2013-04-17