Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03267:Zfp367'

415130

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Zfp367

Ensembl Gene

ENSMUSG00000044934

Gene Name

zinc finger protein 367

Synonyms

8030486J21Rik, ZFF29a, ZFF29b

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03267

Quality Score

Status

Chromosome

Chromosomal Location

64280836-64301013 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 64292097 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000113331 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000059817] [ENSMUST00000117241]

AlphaFold

Q0VDT2

Predicted Effect

probably benign
Transcript: ENSMUST00000059817

SMART Domains

Protein: ENSMUSP00000050854
Gene: ENSMUSG00000044934

Domain	Start	End	E-Value	Type
low complexity region	5	14	N/A	INTRINSIC
low complexity region	37	59	N/A	INTRINSIC
low complexity region	77	94	N/A	INTRINSIC
low complexity region	105	113	N/A	INTRINSIC
ZnF_C2H2	157	179	3.44e-4	SMART
ZnF_C2H2	185	209	2.4e-3	SMART
coiled coil region	299	332	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000117241

SMART Domains

Protein: ENSMUSP00000113331
Gene: ENSMUSG00000044934

Domain	Start	End	E-Value	Type
low complexity region	5	14	N/A	INTRINSIC
low complexity region	37	59	N/A	INTRINSIC
low complexity region	77	94	N/A	INTRINSIC
low complexity region	105	113	N/A	INTRINSIC
ZnF_C2H2	157	179	3.44e-4	SMART
ZnF_C2H2	185	209	2.4e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134136

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152644

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acad10	C	T	5: 121,775,412 (GRCm39)	R430Q	probably benign	Het
Arfgef3	T	A	10: 18,467,630 (GRCm39)	I1857F	probably damaging	Het
Baat	T	A	4: 49,490,050 (GRCm39)	M345L	probably benign	Het
Babam1	T	G	8: 71,855,708 (GRCm39)		probably null	Het
Bbs7	A	G	3: 36,627,654 (GRCm39)	F711S	probably damaging	Het
Btrc	A	G	19: 45,507,262 (GRCm39)	E458G	probably damaging	Het
Car6	T	C	4: 150,280,503 (GRCm39)		probably benign	Het
Celsr3	T	C	9: 108,713,724 (GRCm39)		probably benign	Het
Csn2	A	G	5: 87,845,930 (GRCm39)	V3A	possibly damaging	Het
Ddc	T	C	11: 11,826,303 (GRCm39)	Y86C	probably damaging	Het
Dennd1b	A	T	1: 138,990,599 (GRCm39)	R188*	probably null	Het
Dnah1	C	A	14: 31,008,545 (GRCm39)	A2046S	probably benign	Het
Duxf4	T	C	10: 58,071,609 (GRCm39)	T202A	probably damaging	Het
Eif2b4	A	T	5: 31,350,003 (GRCm39)	S20T	possibly damaging	Het
Etl4	T	A	2: 20,789,993 (GRCm39)	C916*	probably null	Het
Fam78a	T	C	2: 31,959,679 (GRCm39)	I144V	probably benign	Het
Fcho1	A	G	8: 72,164,943 (GRCm39)		probably benign	Het
Il9r	T	A	11: 32,141,778 (GRCm39)	H320L	possibly damaging	Het
Kntc1	C	T	5: 123,896,543 (GRCm39)	T135M	probably damaging	Het
Lca5l	T	A	16: 95,960,983 (GRCm39)	Q498L	probably benign	Het
Map4k3	T	C	17: 80,971,457 (GRCm39)	H70R	probably damaging	Het
Mrps26	A	G	2: 130,406,856 (GRCm39)		probably null	Het
Or1j20	G	T	2: 36,760,513 (GRCm39)	A312S	probably benign	Het
Or4k5	A	G	14: 50,386,304 (GRCm39)	V9A	probably damaging	Het
Or8j3b	A	T	2: 86,204,978 (GRCm39)	Y259*	probably null	Het
Pik3cg	C	A	12: 32,255,307 (GRCm39)	G227C	possibly damaging	Het
Ptprn2	C	T	12: 116,839,964 (GRCm39)	Q496*	probably null	Het
Rif1	T	G	2: 51,967,000 (GRCm39)	N96K	possibly damaging	Het
Rreb1	A	C	13: 38,116,169 (GRCm39)	D1176A	probably benign	Het
Slc22a30	A	G	19: 8,315,322 (GRCm39)	I436T	probably benign	Het
Slc51a	G	A	16: 32,297,568 (GRCm39)	R110C	probably damaging	Het
Spata31e5	G	A	1: 28,816,202 (GRCm39)	T610I	probably damaging	Het
Stab1	A	G	14: 30,864,686 (GRCm39)	C1950R	probably damaging	Het
Tns2	T	C	15: 102,013,813 (GRCm39)		probably null	Het
Ttf2	G	A	3: 100,852,120 (GRCm39)	R1009*	probably null	Het
Wfdc16	A	G	2: 164,480,462 (GRCm39)	V11A	possibly damaging	Het
Zfp420	G	A	7: 29,574,908 (GRCm39)	R376H	probably damaging	Het

Other mutations in Zfp367

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01147:Zfp367	APN	13	64,283,253 (GRCm39)	missense	probably damaging	1.00
IGL03151:Zfp367	APN	13	64,293,445 (GRCm39)	missense	probably damaging	1.00
fisher	UTSW	13	64,293,457 (GRCm39)	missense	probably damaging	1.00
Otter	UTSW	13	64,292,069 (GRCm39)	nonsense	probably null
R4608:Zfp367	UTSW	13	64,283,238 (GRCm39)	missense	probably damaging	1.00
R6180:Zfp367	UTSW	13	64,283,204 (GRCm39)	missense	probably damaging	1.00
R6531:Zfp367	UTSW	13	64,292,064 (GRCm39)	missense	probably damaging	1.00
R7727:Zfp367	UTSW	13	64,293,457 (GRCm39)	missense	probably damaging	1.00
R8247:Zfp367	UTSW	13	64,300,482 (GRCm39)	missense	probably benign
R8754:Zfp367	UTSW	13	64,292,069 (GRCm39)	nonsense	probably null
R9557:Zfp367	UTSW	13	64,300,586 (GRCm39)	missense	probably damaging	1.00

Posted On

2016-08-02