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Gene: CHCHD4P2 (coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 2) Homo sapiens

Symbol:

CHCHD4P2

Name:

coiled-coil-helix-coiled-coil-helix domain containing 4 pseudogene 2

RGD ID:

7174867

HGNC Page

Description:

Type:

pseudo (Ensembl: processed_pseudogene)

RefSeq Status:

Related Functional Gene:

CHCHD4

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	9	108,097,246 - 108,097,962 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	9	108,097,432 - 108,097,851 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	9	110,859,526 - 110,860,242 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	9	109,899,357 - 109,899,952 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	9	81,358,515 - 81,359,110 (-)	NCBI		Celera
Cytogenetic Map	9	q31.2	NCBI
HuRef	9	80,458,494 - 80,458,910 (-)	NCBI		HuRef
CHM1_1	9	111,006,553 - 111,006,969 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	9	120,265,773 - 120,266,489 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

Model

Predicted Target Of

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.

D9S1091

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	9	110,861,493 - 110,861,695	UniSTS	GRCh37
Build 36	9	109,901,314 - 109,901,516	RGD	NCBI36
Celera	9	81,360,472 - 81,360,674	RGD
Cytogenetic Map	9	q31.2	UniSTS
HuRef	9	80,460,272 - 80,460,474	UniSTS
Whitehead-RH Map	9	404.6	UniSTS
Whitehead-YAC Contig Map	9		UniSTS
NCBI RH Map	9	970.4	UniSTS

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	nervous system	renal system	reproductive system	respiratory system	sensory system
190	414	733	268	1035	162	165	29	210	15	976	929	865	232	111	579	129	14


RefSeq Transcripts	NG_030088	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC068050	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068269	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000431135

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	9	108,097,432 - 108,097,851 (-)	Ensembl

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


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


Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable

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