ZNF358 (zinc finger protein 358) - Rat Genome Database

Name: ZNF358
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: ZNF358 (zinc finger protein 358) Homo sapiens

Analyze

Symbol:

ZNF358

Name:

zinc finger protein 358

RGD ID:

1321306

HGNC Page

HGNC:16838

Description:

Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in several processes, including embryonic forelimb morphogenesis; neural tube development; and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be part of PcG protein complex and transcription regulator complex.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

FLJ10390; ZFEND

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	7,513,880 - 7,521,025 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	7,515,292 - 7,521,025 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	7,580,989 - 7,585,911 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	7,487,004 - 7,491,911 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	7,487,074 - 7,491,911	NCBI
Celera	19	7,453,515 - 7,458,434 (+)	NCBI		Celera
Cytogenetic Map	19	p13.2	NCBI
HuRef	19	7,255,266 - 7,257,086 (+)	NCBI		HuRef
CHM1_1	19	7,584,011 - 7,585,831 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	7,514,603 - 7,521,761 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

hereditary spastic paraplegia 39 (IAGP)

mucolipidosis type IV (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17beta-estradiol (EXP)

2,2',4,4'-Tetrabromodiphenyl ether (ISO)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

2-palmitoylglycerol (EXP)

3-isobutyl-1-methyl-7H-xanthine (EXP)

acrylamide (ISO)

aflatoxin B1 (ISO)

antirheumatic drug (EXP)

benzo[a]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (EXP)

cadmium atom (EXP)

chlorpyrifos (ISO)

dexamethasone (EXP)

diethylstilbestrol (ISO)

elemental selenium (EXP)

endosulfan (ISO)

ethanol (ISO)

FR900359 (EXP)

indometacin (EXP)

mancozeb (EXP)

paracetamol (ISO)

selenium atom (EXP)

sodium arsenite (EXP)

thioacetamide (ISO)

trichloroethene (ISO)

triptonide (ISO)

valproic acid (EXP)

vitamin E (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

embryonic forelimb morphogenesis (ISS)

neural tube development (ISS)

regulation of transcription by RNA polymerase II (IBA)

stem cell population maintenance (ISS)

Cellular Component

nucleus (IEA)

Molecular Function

DNA binding (IEA)

DNA-binding transcription factor activity (IBA)

metal ion binding (IEA)

RNA polymerase II cis-regulatory region sequence-specific DNA binding (IBA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:11013137	PMID:12036583	PMID:12477932	PMID:14702039	PMID:15489334	PMID:21873635	PMID:24104479	PMID:26186194	PMID:28514442	PMID:33961781	PMID:35013218

Genomics

Comparative Map Data

ZNF358
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	7,513,880 - 7,521,025 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	7,515,292 - 7,521,025 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	7,580,989 - 7,585,911 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	7,487,004 - 7,491,911 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	7,487,074 - 7,491,911	NCBI
Celera	19	7,453,515 - 7,458,434 (+)	NCBI		Celera
Cytogenetic Map	19	p13.2	NCBI
HuRef	19	7,255,266 - 7,257,086 (+)	NCBI		HuRef
CHM1_1	19	7,584,011 - 7,585,831 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	19	7,514,603 - 7,521,761 (+)	NCBI		T2T-CHM13v2.0

Zfp358
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	8	3,543,138 - 3,547,208 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	8	3,543,138 - 3,547,208 (+)	Ensembl		GRCm39 Ensembl
GRCm38	8	3,493,138 - 3,497,208 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	8	3,493,138 - 3,497,208 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	8	3,493,138 - 3,497,208 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	8	3,493,171 - 3,497,208 (+)	NCBI		MGSCv36	mm8
Celera	8	3,719,112 - 3,723,182 (+)	NCBI		Celera
Cytogenetic Map	8	A1.1	NCBI
cM Map	8	1.92	NCBI

Zfp358
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	12	6,350,266 - 6,354,359 (+)	NCBI		GRCr8
mRatBN7.2	12	1,552,367 - 1,556,460 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	12	1,552,366 - 1,556,460 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	12	2,216,693 - 2,220,785 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	12	2,840,263 - 2,844,355 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	12	1,612,277 - 1,616,370 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	12	2,046,472 - 2,050,565 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	12	2,046,472 - 2,050,565 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	12	4,209,518 - 4,213,613 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	12	2,658,623 - 2,662,716 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	12	2,658,625 - 2,662,716 (-)	NCBI
Celera	12	3,408,729 - 3,412,822 (+)	NCBI		Celera
Cytogenetic Map	12	p12	NCBI

Znf358
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0	NW_004955563	1,714,393 - 1,716,499 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZNF358
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	20	12,186,904 - 12,192,614 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	11,305,440 - 11,310,704 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	6,806,690 - 6,811,914 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	7,664,219 - 7,670,123 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	7,668,319 - 7,670,046 (+)	Ensembl	panpan1.1		panPan2

ZNF358
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	20	52,311,253 - 52,316,235 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	52,297,507 - 52,317,158 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	52,115,460 - 52,120,363 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	52,840,528 - 52,845,434 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	52,810,257 - 52,845,852 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	20	52,044,340 - 52,049,239 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	20	52,488,002 - 52,492,899 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	52,718,895 - 52,723,796 (+)	NCBI		UU_Cfam_GSD_1.0

Znf358
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405118	213,236,010 - 213,245,945 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936588	4,597,045 - 4,598,700 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936588	4,592,060 - 4,598,775 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZNF358
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	71,615,551 - 71,619,865 (-)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	71,615,475 - 71,619,683 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	72,153,917 - 72,158,957 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZNF358
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	6	7,011,795 - 7,017,516 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	7,015,733 - 7,017,439 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666081	851,029 - 856,800 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Znf358
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624828	629,530 - 632,986 (+)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624828	629,686 - 632,799 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZNF358
30 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19p13.3-13.2(chr19:265917-8564134)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]\|See cases [RCV000052876]	Chr19:265917..8564134 [GRCh38] Chr19:265917..8629018 [GRCh37] Chr19:216917..8535018 [NCBI36] Chr19:19p13.3-13.2	pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3	copy number gain	See cases [RCV000052879]	Chr19:1972245..9648879 [GRCh38] Chr19:1972244..9759555 [GRCh37] Chr19:1923244..9620555 [NCBI36] Chr19:19p13.3-13.2	pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:4039158-9176125)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052881]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052881]\|See cases [RCV000052881]	Chr19:4039158..9176125 [GRCh38] Chr19:4039156..9286801 [GRCh37] Chr19:3990156..9147801 [NCBI36] Chr19:19p13.3-13.2	pathogenic
GRCh38/hg38 19p13.2(chr19:7194917-7827432)x3	copy number gain	See cases [RCV000054108]	Chr19:7194917..7827432 [GRCh38] Chr19:7194928..7892318 [GRCh37] Chr19:7145928..7798318 [NCBI36] Chr19:19p13.2	uncertain significance
GRCh37/hg19 19p13.2(chr19:7528817-7589886)x3	copy number gain	not provided [RCV000752549]	Chr19:7528817..7589886 [GRCh37] Chr19:19p13.2	benign
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
NM_018083.5(ZNF358):c.49C>A (p.Pro17Thr)	single nucleotide variant	not specified [RCV004294344]	Chr19:7519291 [GRCh38] Chr19:7584177 [GRCh37] Chr19:19p13.2	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-13.2(chr19:3120160-9732820)x3	copy number gain	not provided [RCV000684096]	Chr19:3120160..9732820 [GRCh37] Chr19:19p13.3-13.2	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.2(chr19:7508522-7624054)x3	copy number gain	not provided [RCV000752546]	Chr19:7508522..7624054 [GRCh37] Chr19:19p13.2	benign
GRCh37/hg19 19p13.2(chr19:7527216-7611117)x3	copy number gain	not provided [RCV000752547]	Chr19:7527216..7611117 [GRCh37] Chr19:19p13.2	benign
GRCh37/hg19 19p13.2(chr19:7527216-7618660)x3	copy number gain	not provided [RCV000752548]	Chr19:7527216..7618660 [GRCh37] Chr19:19p13.2	benign
NM_018083.5(ZNF358):c.1643T>C (p.Leu548Pro)	single nucleotide variant	not specified [RCV004318643]	Chr19:7520885 [GRCh38] Chr19:7585771 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.111C>T (p.Asp37=)	single nucleotide variant	not provided [RCV000955547]	Chr19:7519353 [GRCh38] Chr19:7584239 [GRCh37] Chr19:19p13.2	benign
NM_018083.5(ZNF358):c.201C>G (p.Val67=)	single nucleotide variant	not provided [RCV000963963]	Chr19:7519443 [GRCh38] Chr19:7584329 [GRCh37] Chr19:19p13.2	benign
NC_000019.9:g.(?_6361586)_(8212364_?)del	deletion	Mucolipidosis type IV [RCV003109715]	Chr19:6361586..8212364 [GRCh37] Chr19:19p13.3-13.2	pathogenic
NC_000019.9:g.(?_7527018)_(7624057_?)dup	duplication	Hereditary spastic paraplegia 39 [RCV003105488]\|not provided [RCV003105489]	Chr19:7527018..7624057 [GRCh37] Chr19:19p13.2	uncertain significance\|no classifications from unflagged records
NM_018083.5(ZNF358):c.1200A>G (p.Ala400=)	single nucleotide variant	not provided [RCV002263136]	Chr19:7520442 [GRCh38] Chr19:7585328 [GRCh37] Chr19:19p13.2	likely benign
NM_018083.5(ZNF358):c.253C>T (p.Pro85Ser)	single nucleotide variant	not specified [RCV004240446]	Chr19:7519495 [GRCh38] Chr19:7584381 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1557C>A (p.Asp519Glu)	single nucleotide variant	not specified [RCV004136974]	Chr19:7520799 [GRCh38] Chr19:7585685 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.377G>A (p.Gly126Asp)	single nucleotide variant	not specified [RCV004096862]	Chr19:7519619 [GRCh38] Chr19:7584505 [GRCh37] Chr19:19p13.2	likely benign
NM_018083.5(ZNF358):c.1681G>A (p.Gly561Arg)	single nucleotide variant	not specified [RCV004139489]	Chr19:7520923 [GRCh38] Chr19:7585809 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.856A>G (p.Thr286Ala)	single nucleotide variant	not specified [RCV004132052]	Chr19:7520098 [GRCh38] Chr19:7584984 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1153G>A (p.Gly385Ser)	single nucleotide variant	not specified [RCV004151679]	Chr19:7520395 [GRCh38] Chr19:7585281 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1355T>A (p.Leu452His)	single nucleotide variant	not specified [RCV004244394]	Chr19:7520597 [GRCh38] Chr19:7585483 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.811G>T (p.Gly271Cys)	single nucleotide variant	not specified [RCV004201232]	Chr19:7520053 [GRCh38] Chr19:7584939 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.8G>A (p.Arg3His)	single nucleotide variant	not specified [RCV004102880]	Chr19:7519250 [GRCh38] Chr19:7584136 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1114G>A (p.Glu372Lys)	single nucleotide variant	not specified [RCV004128271]	Chr19:7520356 [GRCh38] Chr19:7585242 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.361G>T (p.Asp121Tyr)	single nucleotide variant	not specified [RCV004099258]	Chr19:7519603 [GRCh38] Chr19:7584489 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.226G>A (p.Glu76Lys)	single nucleotide variant	not specified [RCV004193667]	Chr19:7519468 [GRCh38] Chr19:7584354 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.404C>T (p.Ala135Val)	single nucleotide variant	not specified [RCV004193137]	Chr19:7519646 [GRCh38] Chr19:7584532 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.967C>A (p.His323Asn)	single nucleotide variant	not specified [RCV004174096]	Chr19:7520209 [GRCh38] Chr19:7585095 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1318C>T (p.Pro440Ser)	single nucleotide variant	not specified [RCV004166407]	Chr19:7520560 [GRCh38] Chr19:7585446 [GRCh37] Chr19:19p13.2	likely benign
NM_018083.5(ZNF358):c.1186G>C (p.Val396Leu)	single nucleotide variant	not specified [RCV004218416]	Chr19:7520428 [GRCh38] Chr19:7585314 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1222G>C (p.Ala408Pro)	single nucleotide variant	not specified [RCV004230679]	Chr19:7520464 [GRCh38] Chr19:7585350 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.260C>T (p.Pro87Leu)	single nucleotide variant	not specified [RCV004328035]	Chr19:7519502 [GRCh38] Chr19:7584388 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.107T>C (p.Leu36Pro)	single nucleotide variant	not specified [RCV004326178]	Chr19:7519349 [GRCh38] Chr19:7584235 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1177C>T (p.His393Tyr)	single nucleotide variant	not specified [RCV004358816]	Chr19:7520419 [GRCh38] Chr19:7585305 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.570C>G (p.His190Gln)	single nucleotide variant	not specified [RCV004354822]	Chr19:7519812 [GRCh38] Chr19:7584698 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.19G>C (p.Val7Leu)	single nucleotide variant	not specified [RCV004340343]	Chr19:7519261 [GRCh38] Chr19:7584147 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.345C>T (p.Pro115=)	single nucleotide variant	not provided [RCV003429161]	Chr19:7519587 [GRCh38] Chr19:7584473 [GRCh37] Chr19:19p13.2	likely benign
NM_018083.5(ZNF358):c.1215_1241del (p.Ala408_Ala416del)	deletion	not provided [RCV003421782]	Chr19:7520452..7520478 [GRCh38] Chr19:7585338..7585364 [GRCh37] Chr19:19p13.2	likely benign
NM_018083.5(ZNF358):c.1209T>A (p.Ala403=)	single nucleotide variant	not provided [RCV003421781]	Chr19:7520451 [GRCh38] Chr19:7585337 [GRCh37] Chr19:19p13.2	likely benign
NM_018083.5(ZNF358):c.1228G>A (p.Ala410Thr)	single nucleotide variant	not specified [RCV004486707]	Chr19:7520470 [GRCh38] Chr19:7585356 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.52G>A (p.Val18Ile)	single nucleotide variant	not specified [RCV004486715]	Chr19:7519294 [GRCh38] Chr19:7584180 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1456C>A (p.Pro486Thr)	single nucleotide variant	not specified [RCV004486709]	Chr19:7520698 [GRCh38] Chr19:7585584 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.188A>T (p.Asp63Val)	single nucleotide variant	not specified [RCV004486712]	Chr19:7519430 [GRCh38] Chr19:7584316 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.47G>A (p.Arg16Lys)	single nucleotide variant	not specified [RCV004486713]	Chr19:7519289 [GRCh38] Chr19:7584175 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.482G>T (p.Arg161Leu)	single nucleotide variant	not specified [RCV004486714]	Chr19:7519724 [GRCh38] Chr19:7584610 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.538C>A (p.Arg180Ser)	single nucleotide variant	not specified [RCV004486716]	Chr19:7519780 [GRCh38] Chr19:7584666 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1537G>A (p.Asp513Asn)	single nucleotide variant	not specified [RCV004486711]	Chr19:7520779 [GRCh38] Chr19:7585665 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.713C>T (p.Pro238Leu)	single nucleotide variant	not specified [RCV004486717]	Chr19:7519955 [GRCh38] Chr19:7584841 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1478C>A (p.Ser493Tyr)	single nucleotide variant	not specified [RCV004486710]	Chr19:7520720 [GRCh38] Chr19:7585606 [GRCh37] Chr19:19p13.2	uncertain significance
NM_018083.5(ZNF358):c.1378C>T (p.Arg460Cys)	single nucleotide variant	not specified [RCV004486708]	Chr19:7520620 [GRCh38] Chr19:7585506 [GRCh37] Chr19:19p13.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1198
Count of miRNA genes:	575
Interacting mature miRNAs:	642
Transcripts:	ENST00000394341, ENST00000596712, ENST00000597229
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region

RH68764

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	7,585,753 - 7,585,875	UniSTS	GRCh37
Build 36	19	7,491,753 - 7,491,875	RGD	NCBI36
Celera	19	7,458,276 - 7,458,398	RGD
Cytogenetic Map	19	p13.2	UniSTS
HuRef	19	7,256,928 - 7,257,050	UniSTS
GeneMap99-GB4 RH Map	19	40.39	UniSTS

RH93812

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	7,585,582 - 7,585,721	UniSTS	GRCh37
Build 36	19	7,491,582 - 7,491,721	RGD	NCBI36
Celera	19	7,458,105 - 7,458,244	RGD
Cytogenetic Map	19	p13.2	UniSTS
HuRef	19	7,256,757 - 7,256,896	UniSTS
GeneMap99-GB4 RH Map	19	41.03	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

adipose tissue

appendage

entire extraembryonic component

High

Medium

2408

2409

1710

614

917

455

4353

2180

3708

416

1434

1594

169

1204

2788

Low

573

967

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_018083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005272460	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_011527695	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047438181	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319835	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319836	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054319837	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC008878	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK001252	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC003585	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC014002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BI601846	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	C15772	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471139	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000596712 ⟹ ENSP00000472777

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	7,515,292 - 7,519,751 (+)	Ensembl

RefSeq Acc Id:

ENST00000597229 ⟹ ENSP00000472305

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	7,516,103 - 7,521,025 (+)	Ensembl

RefSeq Acc Id:

NM_018083 ⟹ NP_060553

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	7,516,103 - 7,521,025 (+)	NCBI
GRCh37	19	7,580,169 - 7,585,911 (+)	NCBI
Build 36	19	7,487,004 - 7,491,911 (+)	NCBI Archive
Celera	19	7,453,515 - 7,458,434 (+)	RGD
HuRef	19	7,255,266 - 7,257,086 (+)	ENTREZGENE
CHM1_1	19	7,584,011 - 7,585,831 (+)	NCBI
T2T-CHM13v2.0	19	7,516,829 - 7,521,761 (+)	NCBI

Sequence:

show sequence

CCCTCTCGCTCCCCGGGAGCGCCTGGCGGGGCCGCTGGGCCGAGGGGGCCGCCGGCGGGGCTGG
CGGGCGGGGGGCTTCCTGCGGGCCCGGGGGGAGCCGGCGGCCGGCGCGGGCGCGGCGGGCCGGG
CAGGGGCGAGGGGCGCCGGGTCTTGCCCCAGAAGCTGCGGGCACATCCACGCCTGAAATGCGGC
GCTCAGTCCTGGTCAGGAACCCAGGCCACAAAGGCCTGAGACCCGTTTATGAAGAGCTCGACTC
TGACTCCGAGGACCTAGACCCCAATCCTGAAGATCTGGACCCGGTTTCTGAAGACCCAGAGCCT
GATCCTGAAGACCTCAACACTGTCCCGGAAGACGTGGACCCCAGCTATGAAGATCTGGAGCCCG
TCTCGGAGGATCTGGACCCCGACGCCGAAGCTCCGGGCTCGGAACCCCAAGATCCCGACCCCAT
GTCTTCGAGTTTCGACCTCGATCCAGATGTGATTGGCCCCGTACCCCTGATTCTCGATCCTAAC
AGCGACACCCTCAGCCCCGGCGATCCAAAAGTGGACCCCATCTCCTCTGGCCTCACTGCCACCC
CCCAGGTCTTGGCCACCAGCCCCGCGGTGCTCCCCGCCCCCGCCAGCCCGCCCCGGCCCTTCTC
CTGCCCGGATTGCGGGCGAGCCTTCCGCCGCAGCTCCGGGCTGAGCCAGCATCGCCGCACGCAC
AGCGGCGAGAAGCCGTACCGCTGCCCCGACTGCGGGAAGTCCTTCAGCCACGGTGCCACCCTGG
CTCAGCACCGTGGCATCCACACTGGGGCGCGGCCGTACCAGTGCGCGGCCTGCGGCAAGGCCTT
CGGCTGGCGCTCCACGCTGCTGAAACATCGCAGCAGCCACAGCGGGGAGAAGCCGCACCACTGC
CCGGTGTGTGGCAAGGCCTTCGGGCACGGCTCGCTCCTGGCACAGCACCTGCGCACGCACGGCG
GCCCGCGGCCCCACAAGTGCCCGGTGTGCGCCAAGGGCTTCGGCCAGGGCTCTGCGCTGCTCAA
ACACCTGCGCACGCACACGGGCGAGCGGCCCTACCCGTGTCCGCAGTGCGGCAAGGCCTTCGGG
CAGAGCTCGGCGCTGCTGCAGCACCAGCGCACACACACGGCCGAGCGCCCCTACCGCTGCCCCC
ACTGCGGCAAAGCCTTCGGGCAGAGCTCCAACTTGCAACACCACCTGCGCATCCACACGGGCGA
GCGGCCCTACGCCTGCCCGCACTGCTCCAAGGCCTTCGGCCAGAGCTCAGCGCTGCTCCAGCAC
CTGCACGTGCATTCGGGCGAGCGTCCCTATCGCTGTCAGCTCTGCGGGAAGGCCTTCGGCCAGG
CCTCCAGCCTCACCAAGCACAAACGGGTGCATGAGGGTGCAGCCGCTGCTGCAGCTGCCGCGGC
CGCTGCAGCTGCAGCAGCGGCCGCCGGCCTGGGCCTCGGGCCTGGCCTAAGCCCTGCATCCATG
ATGAGGCCGGGGCAGGTCTCCCTCCTGGGTCCTGATGCTGTTTCTGTGCTCGGCTCTGGCTTGG
GCCTCAGCCCTGGCACCAGCTCTGGCCGCAACCCTGACCCTGGCTCTGGGCCGGGCACTCTGCC
GGATCCCAGCTCCAAACCCCTCCCCGGCTCCAGATCCACCCCCAGCCCTACTCCTGTGGAATCT
TCTGACCCAAAGGCTGGGCACGACGCTGGTCCCGACCTTGTGCCCAGCCCAGACCTTGATCCTG
TGCCCAGCCCAGACCCTGATCCTGTGCCCAGCCCTGATCCCAACCCTGTGTCCTGCCCTGACCC
CTGTTCTCCCACTCGTGGCACTGTCAGCCCAGCCCTCCCTACCGGCGAGAGTCCAGAGTGGGTA
CAGGAGCAAGGGGCACTGCTGGGGCCTGATGGCTGAAGGAGACGCCGGCATCCTCGGGGGCCTG
GGGAAGTTGTGTGTTGTGCAGTCAGTAAAATCCTCCCACTGCCTCCGG

hide sequence

RefSeq Acc Id:

XM_005272460 ⟹ XP_005272517

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	7,515,252 - 7,521,025 (+)	NCBI
GRCh37	19	7,580,169 - 7,585,911 (+)	NCBI

Sequence:

show sequence

TCTGTGTCTCCAAGGAAAGTTTGCCCCGAGCCCTTCCCGGCCCGGCGTAGGGTTCTCCGGAAAC
CATCACTCACATCTAGCACTTGGAGGCCTCCAGGGACAGCGGTGACCCACCATCTGGGTCTTGC
CCCAGAAGCTGCGGGCACATCCACGCCTGAAATGCGGCGCTCAGTCCTGGTCAGGAACCCAGGC
CACAAAGGCCTGAGACCCGTTTATGAAGAGCTCGACTCTGACTCCGAGGACCTAGACCCCAATC
CTGAAGATCTGGACCCGGTTTCTGAAGACCCAGAGCCTGATCCTGAAGACCTCAACACTGTCCC
GGAAGACGTGGACCCCAGCTATGAAGATCTGGAGCCCGTCTCGGAGGATCTGGACCCCGACGCC
GAAGCTCCGGGCTCGGAACCCCAAGATCCCGACCCCATGTCTTCGAGTTTCGACCTCGATCCAG
ATGTGATTGGCCCCGTACCCCTGATTCTCGATCCTAACAGCGACACCCTCAGCCCCGGCGATCC
AAAAGTGGACCCCATCTCCTCTGGCCTCACTGCCACCCCCCAGGTCTTGGCCACCAGCCCCGCG
GTGCTCCCCGCCCCCGCCAGCCCGCCCCGGCCCTTCTCCTGCCCGGATTGCGGGCGAGCCTTCC
GCCGCAGCTCCGGGCTGAGCCAGCATCGCCGCACGCACAGCGGCGAGAAGCCGTACCGCTGCCC
CGACTGCGGGAAGTCCTTCAGCCACGGTGCCACCCTGGCTCAGCACCGTGGCATCCACACTGGG
GCGCGGCCGTACCAGTGCGCGGCCTGCGGCAAGGCCTTCGGCTGGCGCTCCACGCTGCTGAAAC
ATCGCAGCAGCCACAGCGGGGAGAAGCCGCACCACTGCCCGGTGTGTGGCAAGGCCTTCGGGCA
CGGCTCGCTCCTGGCACAGCACCTGCGCACGCACGGCGGCCCGCGGCCCCACAAGTGCCCGGTG
TGCGCCAAGGGCTTCGGCCAGGGCTCTGCGCTGCTCAAACACCTGCGCACGCACACGGGCGAGC
GGCCCTACCCGTGTCCGCAGTGCGGCAAGGCCTTCGGGCAGAGCTCGGCGCTGCTGCAGCACCA
GCGCACACACACGGCCGAGCGCCCCTACCGCTGCCCCCACTGCGGCAAAGCCTTCGGGCAGAGC
TCCAACTTGCAACACCACCTGCGCATCCACACGGGCGAGCGGCCCTACGCCTGCCCGCACTGCT
CCAAGGCCTTCGGCCAGAGCTCAGCGCTGCTCCAGCACCTGCACGTGCATTCGGGCGAGCGTCC
CTATCGCTGTCAGCTCTGCGGGAAGGCCTTCGGCCAGGCCTCCAGCCTCACCAAGCACAAACGG
GTGCATGAGGGTGCAGCCGCTGCTGCAGCTGCCGCGGCCGCTGCAGCTGCAGCAGCGGCCGCCG
GCCTGGGCCTCGGGCCTGGCCTAAGCCCTGCATCCATGATGAGGCCGGGGCAGGTCTCCCTCCT
GGGTCCTGATGCTGTTTCTGTGCTCGGCTCTGGCTTGGGCCTCAGCCCTGGCACCAGCTCTGGC
CGCAACCCTGACCCTGGCTCTGGGCCGGGCACTCTGCCGGATCCCAGCTCCAAACCCCTCCCCG
GCTCCAGATCCACCCCCAGCCCTACTCCTGTGGAATCTTCTGACCCAAAGGCTGGGCACGACGC
TGGTCCCGACCTTGTGCCCAGCCCAGACCTTGATCCTGTGCCCAGCCCAGACCCTGATCCTGTG
CCCAGCCCTGATCCCAACCCTGTGTCCTGCCCTGACCCCTGTTCTCCCACTCGTGGCACTGTCA
GCCCAGCCCTCCCTACCGGCGAGAGTCCAGAGTGGGTACAGGAGCAAGGGGCACTGCTGGGGCC
TGATGGCTGAAGGAGACGCCGGCATCCTCGGGGGCCTGGGGAAGTTGTGTGTTGTGCAGTCAGT
AAAATCCTCCCACTGCCTCCGG

hide sequence

RefSeq Acc Id:

XM_011527695 ⟹ XP_011525997

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	7,518,683 - 7,521,025 (+)	NCBI

Sequence:

show sequence

AGTTCCAGTCTGCAGTGAGCTATGTCTTGCCCCAGAAGCTGCGGGCACATCCACGCCTGAAATG
CGGCGCTCAGTCCTGGTCAGGAACCCAGGCCACAAAGGCCTGAGACCCGTTTATGAAGAGCTCG
ACTCTGACTCCGAGGACCTAGACCCCAATCCTGAAGATCTGGACCCGGTTTCTGAAGACCCAGA
GCCTGATCCTGAAGACCTCAACACTGTCCCGGAAGACGTGGACCCCAGCTATGAAGATCTGGAG
CCCGTCTCGGAGGATCTGGACCCCGACGCCGAAGCTCCGGGCTCGGAACCCCAAGATCCCGACC
CCATGTCTTCGAGTTTCGACCTCGATCCAGATGTGATTGGCCCCGTACCCCTGATTCTCGATCC
TAACAGCGACACCCTCAGCCCCGGCGATCCAAAAGTGGACCCCATCTCCTCTGGCCTCACTGCC
ACCCCCCAGGTCTTGGCCACCAGCCCCGCGGTGCTCCCCGCCCCCGCCAGCCCGCCCCGGCCCT
TCTCCTGCCCGGATTGCGGGCGAGCCTTCCGCCGCAGCTCCGGGCTGAGCCAGCATCGCCGCAC
GCACAGCGGCGAGAAGCCGTACCGCTGCCCCGACTGCGGGAAGTCCTTCAGCCACGGTGCCACC
CTGGCTCAGCACCGTGGCATCCACACTGGGGCGCGGCCGTACCAGTGCGCGGCCTGCGGCAAGG
CCTTCGGCTGGCGCTCCACGCTGCTGAAACATCGCAGCAGCCACAGCGGGGAGAAGCCGCACCA
CTGCCCGGTGTGTGGCAAGGCCTTCGGGCACGGCTCGCTCCTGGCACAGCACCTGCGCACGCAC
GGCGGCCCGCGGCCCCACAAGTGCCCGGTGTGCGCCAAGGGCTTCGGCCAGGGCTCTGCGCTGC
TCAAACACCTGCGCACGCACACGGGCGAGCGGCCCTACCCGTGTCCGCAGTGCGGCAAGGCCTT
CGGGCAGAGCTCGGCGCTGCTGCAGCACCAGCGCACACACACGGCCGAGCGCCCCTACCGCTGC
CCCCACTGCGGCAAAGCCTTCGGGCAGAGCTCCAACTTGCAACACCACCTGCGCATCCACACGG
GCGAGCGGCCCTACGCCTGCCCGCACTGCTCCAAGGCCTTCGGCCAGAGCTCAGCGCTGCTCCA
GCACCTGCACGTGCATTCGGGCGAGCGTCCCTATCGCTGTCAGCTCTGCGGGAAGGCCTTCGGC
CAGGCCTCCAGCCTCACCAAGCACAAACGGGTGCATGAGGGTGCAGCCGCTGCTGCAGCTGCCG
CGGCCGCTGCAGCTGCAGCAGCGGCCGCCGGCCTGGGCCTCGGGCCTGGCCTAAGCCCTGCATC
CATGATGAGGCCGGGGCAGGTCTCCCTCCTGGGTCCTGATGCTGTTTCTGTGCTCGGCTCTGGC
TTGGGCCTCAGCCCTGGCACCAGCTCTGGCCGCAACCCTGACCCTGGCTCTGGGCCGGGCACTC
TGCCGGATCCCAGCTCCAAACCCCTCCCCGGCTCCAGATCCACCCCCAGCCCTACTCCTGTGGA
ATCTTCTGACCCAAAGGCTGGGCACGACGCTGGTCCCGACCTTGTGCCCAGCCCAGACCTTGAT
CCTGTGCCCAGCCCAGACCCTGATCCTGTGCCCAGCCCTGATCCCAACCCTGTGTCCTGCCCTG
ACCCCTGTTCTCCCACTCGTGGCACTGTCAGCCCAGCCCTCCCTACCGGCGAGAGTCCAGAGTG
GGTACAGGAGCAAGGGGCACTGCTGGGGCCTGATGGCTGAAGGAGACGCCGGCATCCTCGGGGG
CCTGGGGAAGTTGTGTGTTGTGCAGTCAGTAAAATCCTCCCACTGCCTCCGG

hide sequence

RefSeq Acc Id:

XM_047438181 ⟹ XP_047294137

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	7,513,880 - 7,521,025 (+)	NCBI

RefSeq Acc Id:

XM_054319835 ⟹ XP_054175810

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	7,514,603 - 7,521,761 (+)	NCBI

RefSeq Acc Id:

XM_054319836 ⟹ XP_054175811

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	7,516,014 - 7,521,761 (+)	NCBI

RefSeq Acc Id:

XM_054319837 ⟹ XP_054175812

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	19	7,519,419 - 7,521,761 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_060553	(Get FASTA)	NCBI Sequence Viewer
	XP_005272517	(Get FASTA)	NCBI Sequence Viewer
	XP_011525997	(Get FASTA)	NCBI Sequence Viewer
	XP_047294137	(Get FASTA)	NCBI Sequence Viewer
	XP_054175810	(Get FASTA)	NCBI Sequence Viewer
	XP_054175811	(Get FASTA)	NCBI Sequence Viewer
	XP_054175812	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAH03585	(Get FASTA)	NCBI Sequence Viewer
	AAH14002	(Get FASTA)	NCBI Sequence Viewer
	BAA91582	(Get FASTA)	NCBI Sequence Viewer
	EAW69035	(Get FASTA)	NCBI Sequence Viewer
	EAW69036	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000472305
	ENSP00000472305.1
	ENSP00000472777.1
GenBank Protein	Q9NW07	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_060553 ⟸ NM_018083

- UniProtKB:

Q9BTM7 (UniProtKB/Swiss-Prot), Q9NW07 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MRRSVLVRNPGHKGLRPVYEELDSDSEDLDPNPEDLDPVSEDPEPDPEDLNTVPEDVDPSYEDL
EPVSEDLDPDAEAPGSEPQDPDPMSSSFDLDPDVIGPVPLILDPNSDTLSPGDPKVDPISSGLT
ATPQVLATSPAVLPAPASPPRPFSCPDCGRAFRRSSGLSQHRRTHSGEKPYRCPDCGKSFSHGA
TLAQHRGIHTGARPYQCAACGKAFGWRSTLLKHRSSHSGEKPHHCPVCGKAFGHGSLLAQHLRT
HGGPRPHKCPVCAKGFGQGSALLKHLRTHTGERPYPCPQCGKAFGQSSALLQHQRTHTAERPYR
CPHCGKAFGQSSNLQHHLRIHTGERPYACPHCSKAFGQSSALLQHLHVHSGERPYRCQLCGKAF
GQASSLTKHKRVHEGAAAAAAAAAAAAAAAAAGLGLGPGLSPASMMRPGQVSLLGPDAVSVLGS
GLGLSPGTSSGRNPDPGSGPGTLPDPSSKPLPGSRSTPSPTPVESSDPKAGHDAGPDLVPSPDL
DPVPSPDPDPVPSPDPNPVSCPDPCSPTRGTVSPALPTGESPEWVQEQGALLGPDG

hide sequence

RefSeq Acc Id:	XP_005272517 ⟸ XM_005272460
- Peptide Label:	isoform X2
- UniProtKB:	Q9BTM7 (UniProtKB/Swiss-Prot), Q9NW07 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRRSVLVRNPGHKGLRPVYEELDSDSEDLDPNPEDLDPVSEDPEPDPEDLNTVPEDVDPSYEDL EPVSEDLDPDAEAPGSEPQDPDPMSSSFDLDPDVIGPVPLILDPNSDTLSPGDPKVDPISSGLT ATPQVLATSPAVLPAPASPPRPFSCPDCGRAFRRSSGLSQHRRTHSGEKPYRCPDCGKSFSHGA TLAQHRGIHTGARPYQCAACGKAFGWRSTLLKHRSSHSGEKPHHCPVCGKAFGHGSLLAQHLRT HGGPRPHKCPVCAKGFGQGSALLKHLRTHTGERPYPCPQCGKAFGQSSALLQHQRTHTAERPYR CPHCGKAFGQSSNLQHHLRIHTGERPYACPHCSKAFGQSSALLQHLHVHSGERPYRCQLCGKAF GQASSLTKHKRVHEGAAAAAAAAAAAAAAAAAGLGLGPGLSPASMMRPGQVSLLGPDAVSVLGS GLGLSPGTSSGRNPDPGSGPGTLPDPSSKPLPGSRSTPSPTPVESSDPKAGHDAGPDLVPSPDL DPVPSPDPDPVPSPDPNPVSCPDPCSPTRGTVSPALPTGESPEWVQEQGALLGPDG hide sequence

RefSeq Acc Id:	XP_011525997 ⟸ XM_011527695
- Peptide Label:	isoform X2
- UniProtKB:	Q9BTM7 (UniProtKB/Swiss-Prot), Q9NW07 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MRRSVLVRNPGHKGLRPVYEELDSDSEDLDPNPEDLDPVSEDPEPDPEDLNTVPEDVDPSYEDL EPVSEDLDPDAEAPGSEPQDPDPMSSSFDLDPDVIGPVPLILDPNSDTLSPGDPKVDPISSGLT ATPQVLATSPAVLPAPASPPRPFSCPDCGRAFRRSSGLSQHRRTHSGEKPYRCPDCGKSFSHGA TLAQHRGIHTGARPYQCAACGKAFGWRSTLLKHRSSHSGEKPHHCPVCGKAFGHGSLLAQHLRT HGGPRPHKCPVCAKGFGQGSALLKHLRTHTGERPYPCPQCGKAFGQSSALLQHQRTHTAERPYR CPHCGKAFGQSSNLQHHLRIHTGERPYACPHCSKAFGQSSALLQHLHVHSGERPYRCQLCGKAF GQASSLTKHKRVHEGAAAAAAAAAAAAAAAAAGLGLGPGLSPASMMRPGQVSLLGPDAVSVLGS GLGLSPGTSSGRNPDPGSGPGTLPDPSSKPLPGSRSTPSPTPVESSDPKAGHDAGPDLVPSPDL DPVPSPDPDPVPSPDPNPVSCPDPCSPTRGTVSPALPTGESPEWVQEQGALLGPDG hide sequence

RefSeq Acc Id:

ENSP00000472777 ⟸ ENST00000596712

RefSeq Acc Id:

ENSP00000472305 ⟸ ENST00000597229

RefSeq Acc Id:	XP_047294137 ⟸ XM_047438181
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054175810 ⟸ XM_054319835
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054175811 ⟸ XM_054319836
- Peptide Label:	isoform X2
- UniProtKB:	Q9BTM7 (UniProtKB/Swiss-Prot), Q9NW07 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054175812 ⟸ XM_054319837
- Peptide Label:	isoform X2
- UniProtKB:	Q9BTM7 (UniProtKB/Swiss-Prot), Q9NW07 (UniProtKB/Swiss-Prot)

Protein Domains

C2H2-type

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9NW07-F1-model_v2	AlphaFold	Q9NW07	1-568	view protein structure

Promoters

RGD ID:

6796311

Promoter ID:

HG_KWN:28709

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

ENST00000361576

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	19	7,486,639 - 7,487,139 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:16838	AgrOrtholog
COSMIC	ZNF358	COSMIC
Ensembl Genes	ENSG00000198816	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000596712.1	UniProtKB/TrEMBL
	ENST00000597229	ENTREZGENE
	ENST00000597229.2	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000198816	GTEx
HGNC ID	HGNC:16838	ENTREZGENE
Human Proteome Map	ZNF358	Human Proteome Map
InterPro	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:140467	UniProtKB/Swiss-Prot
NCBI Gene	140467	ENTREZGENE
OMIM	619496	OMIM
PANTHER	GENE 12845-RELATED	UniProtKB/Swiss-Prot
	TRANSCRIPTIONAL REPRESSOR PROTEIN YY	UniProtKB/Swiss-Prot
Pfam	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA38189	PharmGKB
PROSITE	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF57667	UniProtKB/Swiss-Prot
UniProt	M0R2S5_HUMAN	UniProtKB/TrEMBL
	Q9BTM7	ENTREZGENE
	Q9NW07	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	Q9BTM7	UniProtKB/Swiss-Prot

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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Imported Disease Annotations - ClinVar