ZNF35 (zinc finger protein 35) - Rat Genome Database

Name: ZNF35
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: ZNF35 (zinc finger protein 35) Homo sapiens

Analyze

Symbol:

ZNF35

Name:

zinc finger protein 35

RGD ID:

1320503

HGNC Page

HGNC:13099

Description:

Enables DNA-binding transcription factor activity and sequence-specific DNA binding activity. Predicted to be involved in cellular response to retinoic acid; regulation of transcription by RNA polymerase II; and spermatogenesis. Located in nucleus and perinuclear region of cytoplasm.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

HF.10; HF10; Zfp105; zinc finger protein 35 (clone HF.10); zinc finger protein HF.10

RGD Orthologs

Alliance Genes

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Zfp105 (zinc finger protein 105)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OrthoDB, OrthoMCL, Panther, Treefam
Rattus norvegicus (Norway rat):	Zfp105 (zinc finger protein 105)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Pan paniscus (bonobo/pygmy chimpanzee):	ZNF35 (zinc finger protein 35)	NCBI	Ortholog
Canis lupus familiaris (dog):	ZNF35 (zinc finger protein 35)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OrthoDB, Panther, Treefam
Sus scrofa (pig):	ZNF35 (zinc finger protein 35)	HGNC	Ensembl, NCBI, OrthoDB
Chlorocebus sabaeus (green monkey):	ZNF35 (zinc finger protein 35)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Zfp105 (zinc finger protein 105)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Zfp105 (zinc finger protein 105)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Saccharomyces cerevisiae (baker's yeast):	ZAP1	Alliance	DIOPT (Hieranoid\|InParanoid\|SonicParanoid)
Drosophila melanogaster (fruit fly):	CG2712	Alliance	DIOPT (Ensembl Compara\|PANTHER)

Related Pseudogenes:

AC022106.2 LOC100419545

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	3	44,646,506 - 44,660,791 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	44,648,732 - 44,660,791 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	44,690,224 - 44,702,283 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	44,665,237 - 44,677,287 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	44,665,258 - 44,677,279	NCBI
Celera	3	44,628,226 - 44,640,276 (+)	NCBI		Celera
Cytogenetic Map	3	p21.31	NCBI
HuRef	3	44,734,364 - 44,746,410 (+)	NCBI		HuRef
CHM1_1	3	44,640,323 - 44,652,371 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	44,662,214 - 44,676,499 (+)	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

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

17alpha-ethynylestradiol (ISO)

17beta-estradiol (EXP)

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

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

2,4-dinitrotoluene (ISO)

2-hydroxypropanoic acid (EXP)

2-palmitoylglycerol (EXP)

3,4-methylenedioxymethamphetamine (ISO)

4-hydroxyphenyl retinamide (ISO)

atrazine (EXP)

bisphenol A (ISO)

cadmium sulfate (ISO)

copper atom (EXP)

copper(0) (EXP)

copper(II) sulfate (EXP)

disulfiram (EXP)

formaldehyde (EXP)

gentamycin (ISO)

methotrexate (EXP)

Monobutylphthalate (ISO)

paracetamol (EXP)

rac-lactic acid (EXP)

silicon dioxide (EXP)

Soman (ISO)

urethane (EXP)

valproic acid (EXP,ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

cellular response to retinoic acid (ISS)

regulation of DNA-templated transcription (TAS)

regulation of transcription by RNA polymerase II (IBA)

spermatogenesis (ISS)

Cellular Component

nucleus (IBA,IDA,IEA)

perinuclear region of cytoplasm (IDA)

Molecular Function

DNA binding (IEA,TAS)

DNA-binding transcription factor activity (IDA)

DNA-binding transcription factor activity, RNA polymerase II-specific (IBA)

metal ion binding (IEA)

protein binding (IPI)

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

sequence-specific DNA binding (IDA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions
4.	RGD HPO Phenotype Annotation Pipeline	RGD automated import pipeline for human HPO-to-gene-to-disease annotations

Additional References at PubMed

PMID:1572646	PMID:2108922	PMID:3380682	PMID:7814019	PMID:8477855	PMID:12477932	PMID:15342556	PMID:15489334	PMID:19274049	PMID:20186958	PMID:20211142	PMID:21244100
PMID:21832049	PMID:21873635	PMID:26496610	PMID:28514442	PMID:29507755	PMID:30021884	PMID:32296183	PMID:33961781	PMID:36724073	PMID:36949045

Genomics

Comparative Map Data

ZNF35
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	3	44,646,506 - 44,660,791 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	3	44,648,732 - 44,660,791 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	3	44,690,224 - 44,702,283 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	3	44,665,237 - 44,677,287 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	3	44,665,258 - 44,677,279	NCBI
Celera	3	44,628,226 - 44,640,276 (+)	NCBI		Celera
Cytogenetic Map	3	p21.31	NCBI
HuRef	3	44,734,364 - 44,746,410 (+)	NCBI		HuRef
CHM1_1	3	44,640,323 - 44,652,371 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	3	44,662,214 - 44,676,499 (+)	NCBI		T2T-CHM13v2.0

Zfp105
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	9	122,752,105 - 122,764,325 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	9	122,752,137 - 122,760,093 (+)	Ensembl		GRCm39 Ensembl
GRCm38	9	122,923,039 - 122,935,260 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	9	122,923,072 - 122,931,028 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	9	122,832,196 - 122,840,146 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	9	122,771,797 - 122,779,721 (+)	NCBI		MGSCv36	mm8
Celera	9	123,376,377 - 123,384,323 (+)	NCBI		Celera
Cytogenetic Map	9	F4	NCBI
cM Map	9	73.23	NCBI

Zfp105
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	8	131,444,692 - 131,456,159 (+)	NCBI		GRCr8
mRatBN7.2	8	122,567,229 - 122,578,696 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	8	122,567,214 - 122,578,692 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	8	128,164,012 - 128,174,873 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	8	126,362,959 - 126,373,820 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	8	124,191,181 - 124,202,180 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	8	131,998,787 - 132,009,987 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	8	131,998,778 - 132,009,981 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	8	131,153,584 - 131,164,784 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	8	127,657,734 - 127,669,201 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	8	127,680,876 - 127,688,929 (+)	NCBI
Celera	8	121,684,379 - 121,695,727 (+)	NCBI		Celera
Cytogenetic Map	8	q32	NCBI

ZNF35
(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	2	44,595,869 - 44,612,501 (+)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	3	44,600,635 - 44,612,724 (+)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	3	44,538,624 - 44,550,795 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	3	45,596,190 - 45,608,182 (+)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	3	45,598,714 - 45,607,343 (+)	Ensembl	panpan1.1		panPan2

ZNF35
(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	21,319 - 43,809 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	25,846 - 41,516 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	75,737 - 99,807 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	25,019 - 49,099 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	32,083 - 48,976 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UNSW_CanFamBas_1.0	20	87,459 - 111,536 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	46,754 - 70,834 (-)	NCBI		UU_Cfam_GSD_1.0

ZNF35
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	13	27,902,558 - 27,914,479 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	13	27,902,503 - 27,920,494 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1

ZNF35
(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	22	6,124,883 - 6,137,710 (+)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	22	6,127,829 - 6,136,515 (+)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666041	161,028,420 - 161,049,570 (-)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Variants

Variants in ZNF35
18 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
NM_006991.3(ZNF197):c.3021C>T (p.Ile1007=)	single nucleotide variant	Malignant melanoma [RCV000060830]	Chr3:44644151 [GRCh38] Chr3:44685643 [GRCh37] Chr3:44660647 [NCBI36] Chr3:3p21.31	not provided
GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	copy number gain	See cases [RCV000240519]	Chr3:37028313..49929220 [GRCh37] Chr3:3p22.2-21.31	likely pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	copy number gain	See cases [RCV000511055]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	copy number gain	See cases [RCV000512358]	Chr3:61892..197851986 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3	copy number gain	not provided [RCV000682249]	Chr3:16923595..45249923 [GRCh37] Chr3:3p24.3-21.31	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3	copy number gain	not provided [RCV000742138]	Chr3:61495..197838262 [GRCh37] Chr3:3p26.3-q29	pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3	copy number gain	not provided [RCV000742133]	Chr3:60174..197948027 [GRCh37] Chr3:3p26.3-q29	pathogenic
NM_003420.4(ZNF35):c.605A>C (p.Lys202Thr)	single nucleotide variant	Inborn genetic diseases [RCV003246529]	Chr3:44658968 [GRCh38] Chr3:44700460 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.1567A>G (p.Thr523Ala)	single nucleotide variant	Inborn genetic diseases [RCV003239550]	Chr3:44659930 [GRCh38] Chr3:44701422 [GRCh37] Chr3:3p21.31	uncertain significance
GRCh37/hg19 3p21.31(chr3:44444902-45413927)x1	copy number loss	not provided [RCV001005429]	Chr3:44444902..45413927 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.121G>A (p.Glu41Lys)	single nucleotide variant	Inborn genetic diseases [RCV002859892]	Chr3:44651188 [GRCh38] Chr3:44692680 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.1300A>C (p.Ile434Leu)	single nucleotide variant	Inborn genetic diseases [RCV002905650]	Chr3:44659663 [GRCh38] Chr3:44701155 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.786T>G (p.Ser262Arg)	single nucleotide variant	Inborn genetic diseases [RCV002974265]	Chr3:44659149 [GRCh38] Chr3:44700641 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.1019G>A (p.Gly340Glu)	single nucleotide variant	Inborn genetic diseases [RCV002981163]	Chr3:44659382 [GRCh38] Chr3:44700874 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.725G>A (p.Arg242Gln)	single nucleotide variant	Inborn genetic diseases [RCV002887092]	Chr3:44659088 [GRCh38] Chr3:44700580 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.565A>G (p.Lys189Glu)	single nucleotide variant	Inborn genetic diseases [RCV002743663]	Chr3:44658928 [GRCh38] Chr3:44700420 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.608A>G (p.Tyr203Cys)	single nucleotide variant	Inborn genetic diseases [RCV002712945]	Chr3:44658971 [GRCh38] Chr3:44700463 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.133G>A (p.Val45Ile)	single nucleotide variant	Inborn genetic diseases [RCV002935079]	Chr3:44651200 [GRCh38] Chr3:44692692 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.578A>C (p.Asn193Thr)	single nucleotide variant	Inborn genetic diseases [RCV002960803]	Chr3:44658941 [GRCh38] Chr3:44700433 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.1407T>G (p.Asn469Lys)	single nucleotide variant	Inborn genetic diseases [RCV003215324]	Chr3:44659770 [GRCh38] Chr3:44701262 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.676G>A (p.Val226Met)	single nucleotide variant	Inborn genetic diseases [RCV003218218]	Chr3:44659039 [GRCh38] Chr3:44700531 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.479A>T (p.Asn160Ile)	single nucleotide variant	Inborn genetic diseases [RCV003185046]	Chr3:44658842 [GRCh38] Chr3:44700334 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.1264G>A (p.Glu422Lys)	single nucleotide variant	Inborn genetic diseases [RCV003181109]	Chr3:44659627 [GRCh38] Chr3:44701119 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.308T>C (p.Leu103Pro)	single nucleotide variant	Inborn genetic diseases [RCV003188240]	Chr3:44652672 [GRCh38] Chr3:44694164 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.1133T>C (p.Ile378Thr)	single nucleotide variant	Inborn genetic diseases [RCV003356888]	Chr3:44659496 [GRCh38] Chr3:44700988 [GRCh37] Chr3:3p21.31	uncertain significance
NM_003420.4(ZNF35):c.456A>C (p.Leu152Phe)	single nucleotide variant	Inborn genetic diseases [RCV003368793]	Chr3:44658819 [GRCh38] Chr3:44700311 [GRCh37] Chr3:3p21.31	uncertain significance
GRCh37/hg19 3p21.31(chr3:44563378-45177006)x3	copy number gain	not provided [RCV003484127]	Chr3:44563378..45177006 [GRCh37] Chr3:3p21.31	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1822
Count of miRNA genes:	713
Interacting mature miRNAs:	798
Transcripts:	ENST00000296092, ENST00000396056, ENST00000399560, ENST00000415571, ENST00000432115, ENST00000453164, ENST00000542250
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

ZNF35_8735

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	44,701,512 - 44,702,380	UniSTS	GRCh37
Build 36	3	44,676,516 - 44,677,384	RGD	NCBI36
Celera	3	44,639,505 - 44,640,373	RGD
HuRef	3	44,745,639 - 44,746,507	UniSTS

D3S1751E

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	44,699,933 - 44,700,047	UniSTS	GRCh37
Build 36	3	44,674,937 - 44,675,051	RGD	NCBI36
Celera	3	44,637,926 - 44,638,040	RGD
HuRef	3	44,744,060 - 44,744,174	UniSTS

STS-L35269

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	44,702,112 - 44,702,312	UniSTS	GRCh37
Build 36	3	44,677,116 - 44,677,316	RGD	NCBI36
Celera	3	44,640,105 - 44,640,305	RGD
Cytogenetic Map	3	p21.32	UniSTS
HuRef	3	44,746,239 - 44,746,439	UniSTS
GeneMap99-GB4 RH Map	3	144.99	UniSTS

SHGC-76875

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	3	44,689,718 - 44,689,864	UniSTS	GRCh37
Build 36	3	44,664,722 - 44,664,868	RGD	NCBI36
Celera	3	44,627,711 - 44,627,857	RGD
Cytogenetic Map	3	p21	UniSTS
Cytogenetic Map	3	p21.32	UniSTS
HuRef	3	44,733,849 - 44,733,995	UniSTS
TNG Radiation Hybrid Map	3	28062.0	UniSTS
GeneMap99-GB4 RH Map	3	143.05	UniSTS

SHGC-76885

Human Assembly	Chr	Position (strand)	Source
Cytogenetic Map	3	p21.32	UniSTS
TNG Radiation Hybrid Map	3	28043.0	UniSTS
GeneMap99-GB4 RH Map	3	143.78	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

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

129

508

258

158

556

207

Low

2310

2797

1660

599

1288

439

4093

2129

3573

367

901

1405

171

1187

2758

Below cutoff

159

150

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_003420	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448866	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448867	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448868	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448869	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047448870	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054331557	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054331558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054331559	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054331560	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054331561	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347763	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347764	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347765	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347766	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054347767	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC092046	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC099669	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC124045	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AH003302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK300581	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK314821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC013597	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC015892	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BP237260	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BT006962	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471055	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068275	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	KT584479	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	X07289	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000296092 ⟹ ENSP00000296092

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	44,648,742 - 44,660,791 (+)	Ensembl

RefSeq Acc Id:

ENST00000396056 ⟹ ENSP00000379368

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	44,648,732 - 44,660,791 (+)	Ensembl

RefSeq Acc Id:

ENST00000399560 ⟹ ENSP00000391573

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	44,648,742 - 44,658,878 (+)	Ensembl

RefSeq Acc Id:

ENST00000415571 ⟹ ENSP00000404354

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	44,648,741 - 44,658,765 (+)	Ensembl

RefSeq Acc Id:

ENST00000432115 ⟹ ENSP00000404336

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	44,648,741 - 44,652,701 (+)	Ensembl

RefSeq Acc Id:

ENST00000453164 ⟹ ENSP00000401311

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	3	44,648,745 - 44,658,895 (+)	Ensembl

RefSeq Acc Id:

NM_003420 ⟹ NP_003411

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,648,732 - 44,660,791 (+)	NCBI
GRCh37	3	44,690,108 - 44,702,283 (+)	NCBI
Build 36	3	44,665,237 - 44,677,287 (+)	NCBI Archive
Celera	3	44,628,226 - 44,640,276 (+)	RGD
HuRef	3	44,734,364 - 44,746,410 (+)	ENTREZGENE
CHM1_1	3	44,640,323 - 44,652,371 (+)	NCBI
T2T-CHM13v2.0	3	44,664,440 - 44,676,499 (+)	NCBI

Sequence:

show sequence

CTGTCCGGTCATTGTTCTCGTGCCGGTAGAAGCTGAAGTACCGGTCAGCCAGCCTCCTGCTGCA
GAGCCAGTGAACTCAGGTCGGGCTTCTCAGCTGCGCACATAGGCAGTACTCATCTTGGCCCTGG
GAAGAAACTCAAGAAGAAGCTTTTGAAACATAAAGCTTGGATGGGGTTTGACCTCTGCAGGGCA
GCGCCCAGCTATAGGAGTTCCCCTGCTGAGCAGAGAAGATGACTGCAGAATTGAGAGAAGCCAT
GGCCCTAGCCCCATGGGGCCCAGTGAAGGTGAAAAAGGAGGAGGAAGAAGAAGAAAACTTCCCA
GGTCAGGCATCCAGCCAACAAGTGCACTCCGAGAACATCAAAGTCTGGGCCCCAGTGCAGGGTC
TTCAGACAGGCCTTGATGGATCAGAAGAGGAAGAAAAGGGTCAGAACATATCCTGGGATATGGC
GGTAGTCCTGAAAGCAACTCAGGAGGCACCTGCTGCTTCAACCCTTGGCAGCTACTCATTACCA
GGGACTCTGGCCAAGAGTGAGATACTGGAGACTCATGGGACCATGAACTTTCTAGGTGCTGAAA
CCAAGAACCTACAGTTACTGGTTCCAAAAACTGAGATATGTGAGGAAGCTGAAAAACCCCTCAT
CATATCAGAAAGAATCCAGAAAGCTGATCCTCAAGGACCTGAGTTAGGAGAAGCTTGTGAAAAG
GGAAACATGTTAAAGAGGCAGAGAATAAAGAGAGAAAAGAAAGATTTCAGACAAGTGATAGTGA
ATGACTGTCACTTACCTGAAAGCTTCAAAGAAGAGGAAAACCAGAAATGTAAGAAATCTGGAGG
AAAATATAGCCTTAATTCTGGCGCTGTTAAAAATCCAAAAACCCAGCTTGGACAAAAGCCTTTT
ACGTGTAGCGTGTGTGGGAAAGGATTTAGTCAGAGTGCAAACCTCGTTGTGCATCAGCGAATCC
ACACTGGAGAGAAACCCTTTGAATGTCATGAGTGTGGGAAGGCCTTCATTCAGAGTGCAAACCT
CGTTGTGCATCAGAGAATCCACACTGGACAGAAACCTTATGTTTGCTCAAAATGTGGGAAAGCC
TTCACTCAGAGTTCAAATCTGACTGTACATCAAAAAATCCACTCCTTAGAAAAAACTTTTAAGT
GCAATGAATGTGAGAAAGCCTTTAGTTACAGCTCACAACTTGCTCGGCACCAGAAAGTCCACAT
TACGGAAAAATGCTATGAATGTAATGAATGTGGGAAAACATTTACTAGGAGCTCAAACCTCATT
GTCCACCAGAGGATCCACACTGGGGAGAAGCCCTTTGCCTGTAACGACTGTGGCAAAGCCTTTA
CCCAGAGTGCAAATCTTATTGTACATCAGCGAAGCCATACTGGTGAGAAGCCATATGAGTGTAA
AGAGTGTGGGAAAGCCTTTAGTTGTTTTTCACACCTTATTGTGCACCAGAGAATTCACACTGCA
GAGAAACCTTACGACTGCAGCGAATGTGGGAAAGCCTTCAGTCAGCTCTCTTGCCTTATTGTCC
ACCAGAGAATTCACAGTGGAGATCTTCCTTACGTGTGTAATGAATGTGGGAAGGCCTTCACATG
TAGCTCATACCTACTTATTCATCAGAGAATTCATAATGGAGAAAAACCTTACACATGTAATGAG
TGTGGGAAGGCCTTCAGACAGAGGTCGAGCCTCACCGTGCACCAGAGAACCCACACTGGGGAGA
AGCCCTATGAATGTGAGAAGTGTGGTGCAGCTTTCATTTCCAACTCACACCTCATGCGACACCA
TAGAACCCATCTTGTTGAATAACAAGTAAGGAAGAGGAAGACCTCCAGCATTGGTCATAACCTT
CTGCCTCCCTAATGAGACACCTCTTTGCTGTTTTCTTCCTCCTCTATAAAAGTGAGGGCTGTGT
CCTTAAAAGTTATAGTTTTCAGGAATGCAGCAGAAGACACAAGAAAAGCATTTCAGAGGCTAAT
TTAAAACAAAAAGTAAGCACCTAAAGGCAAGGACTTTGTTTTAACTGTACCTTAAGCGGTCATG
TTCTCTGAAGTGGAATGTGGCTTTCCTAGGAATGGGTCGTACAAAGCTAAGTGGTAATGATGCT
ATTTGGGGAAAGGTCTTTTTTGCTTAATTTTGTTTTTTAAAACTCTGATGATTGCTTGAGCAAC
AGGCAGGTTATCTGCCTGGTTGAATTCTGGTTGAACCGTGTATTCTAATATTTCTGGTTAAGTG
GTGACTGGGTAAGGAAACCACTTGGGGTAGCAGTTCAACAATTCACTTACGAATGTTTATAAGC
TTTCCATTTCCTAGGTAATTTTTTAAAAGCCAGTCAAAACAAAAACTTTACTGAAAATGGACAG
AAATAGGAAATGGACTTTTTCCTTACTGTCTATACCTCCTGAACCTTGGTATTGTAAAGATCTG
GGGACCTCTGGGTCTGTTCTGACCATTCCCTAGTCTCCATGGCCAAGCACTCAAGGATTGATGG
ACACCACACACCAGCTATATTCATTTGCCAAGATCAACAGCTCCTTCTCCAAACAACTCAAGCC
CCCAATTCCCATCGCATTCCATTTGGGTGAGATGCAACTAACAGCCCCTTCCTGGATGAAGGAG
TCAAAGAATAAAGCTTGCCTAGAGGCATGCCCCA

hide sequence

RefSeq Acc Id:

XM_047448866 ⟹ XP_047304822

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,648,732 - 44,660,791 (+)	NCBI

RefSeq Acc Id:

XM_047448867 ⟹ XP_047304823

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,648,732 - 44,660,791 (+)	NCBI

RefSeq Acc Id:

XM_047448868 ⟹ XP_047304824

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,648,732 - 44,660,791 (+)	NCBI

RefSeq Acc Id:

XM_047448869 ⟹ XP_047304825

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,646,570 - 44,660,791 (+)	NCBI

RefSeq Acc Id:

XM_047448870 ⟹ XP_047304826

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,646,506 - 44,660,791 (+)	NCBI

RefSeq Acc Id:

XM_054347763 ⟹ XP_054203738

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	44,664,440 - 44,676,499 (+)	NCBI

RefSeq Acc Id:

XM_054347764 ⟹ XP_054203739

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	44,664,283 - 44,676,499 (+)	NCBI

RefSeq Acc Id:

XM_054347765 ⟹ XP_054203740

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	44,664,283 - 44,676,499 (+)	NCBI

RefSeq Acc Id:

XM_054347766 ⟹ XP_054203741

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	44,662,278 - 44,676,499 (+)	NCBI

RefSeq Acc Id:

XM_054347767 ⟹ XP_054203742

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	3	44,662,214 - 44,676,499 (+)	NCBI

Protein Sequences


Protein RefSeqs	NP_003411	(Get FASTA)	NCBI Sequence Viewer
	XP_047304822	(Get FASTA)	NCBI Sequence Viewer
	XP_047304823	(Get FASTA)	NCBI Sequence Viewer
	XP_047304824	(Get FASTA)	NCBI Sequence Viewer
	XP_047304825	(Get FASTA)	NCBI Sequence Viewer
	XP_047304826	(Get FASTA)	NCBI Sequence Viewer
	XP_054187532	(Get FASTA)	NCBI Sequence Viewer
	XP_054187533	(Get FASTA)	NCBI Sequence Viewer
	XP_054187534	(Get FASTA)	NCBI Sequence Viewer
	XP_054187535	(Get FASTA)	NCBI Sequence Viewer
	XP_054187536	(Get FASTA)	NCBI Sequence Viewer
	XP_054203738	(Get FASTA)	NCBI Sequence Viewer
	XP_054203739	(Get FASTA)	NCBI Sequence Viewer
	XP_054203740	(Get FASTA)	NCBI Sequence Viewer
	XP_054203741	(Get FASTA)	NCBI Sequence Viewer
	XP_054203742	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA85451	(Get FASTA)	NCBI Sequence Viewer
	AAH13597	(Get FASTA)	NCBI Sequence Viewer
	AAP35608	(Get FASTA)	NCBI Sequence Viewer
	BAG37343	(Get FASTA)	NCBI Sequence Viewer
	BAG62280	(Get FASTA)	NCBI Sequence Viewer
	CAA30268	(Get FASTA)	NCBI Sequence Viewer
	EAW64715	(Get FASTA)	NCBI Sequence Viewer
	EAW64716	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000296092.3
	ENSP00000379368
	ENSP00000379368.2
	ENSP00000391573.1
	ENSP00000401311.1
	ENSP00000404336.2
	ENSP00000404354.2
	ENSP00000485695
	ENSP00000486354.1
	ENSP00000486615
	ENSP00000486794
	ENSP00000487042
	ENSP00000487287
GenBank Protein	P13682	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:

NP_003411 ⟸ NM_003420

- UniProtKB:

Q53Y54 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot)

- Sequence:

show sequence

MTAELREAMALAPWGPVKVKKEEEEEENFPGQASSQQVHSENIKVWAPVQGLQTGLDGSEEEEK
GQNISWDMAVVLKATQEAPAASTLGSYSLPGTLAKSEILETHGTMNFLGAETKNLQLLVPKTEI
CEEAEKPLIISERIQKADPQGPELGEACEKGNMLKRQRIKREKKDFRQVIVNDCHLPESFKEEE
NQKCKKSGGKYSLNSGAVKNPKTQLGQKPFTCSVCGKGFSQSANLVVHQRIHTGEKPFECHECG
KAFIQSANLVVHQRIHTGQKPYVCSKCGKAFTQSSNLTVHQKIHSLEKTFKCNECEKAFSYSSQ
LARHQKVHITEKCYECNECGKTFTRSSNLIVHQRIHTGEKPFACNDCGKAFTQSANLIVHQRSH
TGEKPYECKECGKAFSCFSHLIVHQRIHTAEKPYDCSECGKAFSQLSCLIVHQRIHSGDLPYVC
NECGKAFTCSSYLLIHQRIHNGEKPYTCNECGKAFRQRSSLTVHQRTHTGEKPYECEKCGAAFI
SNSHLMRHHRTHLVE

hide sequence

RefSeq Acc Id:

ENSP00000391573 ⟸ ENST00000399560

RefSeq Acc Id:

ENSP00000401311 ⟸ ENST00000453164

RefSeq Acc Id:

ENSP00000296092 ⟸ ENST00000296092

RefSeq Acc Id:

ENSP00000404354 ⟸ ENST00000415571

RefSeq Acc Id:

ENSP00000404336 ⟸ ENST00000432115

RefSeq Acc Id:

ENSP00000379368 ⟸ ENST00000396056

RefSeq Acc Id:	XP_047304826 ⟸ XM_047448870
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047304825 ⟸ XM_047448869
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047304822 ⟸ XM_047448866
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047304823 ⟸ XM_047448867
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_047304824 ⟸ XM_047448868
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054203742 ⟸ XM_054347767
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054203741 ⟸ XM_054347766
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054203739 ⟸ XM_054347764
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054203740 ⟸ XM_054347765
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

RefSeq Acc Id:	XP_054203738 ⟸ XM_054347763
- Peptide Label:	isoform X1
- UniProtKB:	Q53Y54 (UniProtKB/Swiss-Prot), P13682 (UniProtKB/Swiss-Prot), B2RBU6 (UniProtKB/Swiss-Prot), Q96D01 (UniProtKB/Swiss-Prot)

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-P13682-F1-model_v2	AlphaFold	P13682	1-527	view protein structure

Promoters

RGD ID:

6864130

Promoter ID:

EPDNEW_H5230

Type:

initiation region

Name:

ZNF35_1

Description:

zinc finger protein 35

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	3	44,648,742 - 44,648,802	EPDNEW

RGD ID:

6801974

Promoter ID:

HG_KWN:44679

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

OTTHUMT00000256749, OTTHUMT00000343848, OTTHUMT00000343849, OTTHUMT00000343850, OTTHUMT00000343851, UC003CNR.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	3	44,664,984 - 44,665,484 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:13099	AgrOrtholog
COSMIC	ZNF35	COSMIC
Ensembl Genes	ENSG00000169981	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	ENSG00000281306	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000296092.7	UniProtKB/TrEMBL
	ENST00000396056	ENTREZGENE
	ENST00000396056.7	UniProtKB/Swiss-Prot
	ENST00000399560.2	UniProtKB/TrEMBL
	ENST00000415571.6	UniProtKB/TrEMBL
	ENST00000432115.6	UniProtKB/TrEMBL
	ENST00000453164.1	UniProtKB/TrEMBL
	ENST00000625394.3	UniProtKB/Swiss-Prot
	ENST00000627641	UniProtKB/TrEMBL
	ENST00000629532	UniProtKB/TrEMBL
	ENST00000629627	UniProtKB/TrEMBL
	ENST00000630364	UniProtKB/TrEMBL
	ENST00000631045	UniProtKB/TrEMBL
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000169981	GTEx
	ENSG00000281306	GTEx
HGNC ID	HGNC:13099	ENTREZGENE
Human Proteome Map	ZNF35	Human Proteome Map
InterPro	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:7584	UniProtKB/Swiss-Prot
NCBI Gene	7584	ENTREZGENE
OMIM	194533	OMIM
PANTHER	FI01120P-RELATED	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN	UniProtKB/Swiss-Prot
Pfam	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA37674	PharmGKB
PROSITE	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF57667	UniProtKB/Swiss-Prot
UniProt	B2RBU6	ENTREZGENE
	C9J011_HUMAN	UniProtKB/TrEMBL
	C9JGR2_HUMAN	UniProtKB/TrEMBL
	C9JGS9_HUMAN	UniProtKB/TrEMBL
	P13682	ENTREZGENE
	Q53Y54	ENTREZGENE
	Q96D01	ENTREZGENE
	ZNF35_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	B2RBU6	UniProtKB/Swiss-Prot
	Q53Y54	UniProtKB/Swiss-Prot
	Q96D01	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)

Send us a Message

Imported Disease Annotations - ClinVar