ZCCHC7 - zinc finger CCHC-type containing 7 Gene

Homo sapiens

Also known as AIR1; HSPC086

Gene ID: 84186 | Gene type: protein coding

About ZCCHC7

This gene has 9 transcripts (splice variants), 203 orthologues and 3 paralogues. Ubiquitous expression in lymph node (RPKM 3.6), testis (RPKM 2.2) and 25 other tissues.

Summary

Enables RNA binding activity. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Apr 2022]

ZCCHC7 Products(4)

mRNA	Protein	Name
NM_001289119.2	NP_001276048.1	zinc finger CCHC domain-containing protein 7
NM_001289120.2	NP_001276049.1	zinc finger CCHC domain-containing protein 7
NM_001289121.2	NP_001276050.1	zinc finger CCHC domain-containing protein 7
NM_032226.3	NP_115602.2	zinc finger CCHC domain-containing protein 7

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	25416956	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ZCCHC7 Protein Structure

zf-CCHC

0
100
200
300
400
500
543 a.a.

Protein Preferred Names

Protein Names

zinc finger CCHC domain-containing protein 7

TRAMP-like complex RNA-binding factor ZCCHC7

Related Diseases

Diseases

Alias

Trichohepatoenteric Syndrome 1

Trichohepatoenteric Syndrome	Syndromic Diarrhea
Tricho-Hepato-Enteric Syndrome	Sd/The
Syndromic Diarrhea/Tricho-Hepato-Enteric Syndrome	THES1
Phenotypic Diarrhea	Thes
Phenotypic Diarrhea Of Infancy	Diarrhea, Syndromic
Diarrhea, Fatal Infantile, With Trichorrhexis Nodosa	Intractable Diarrhea With Phenotypic Anomalies
Syndromatic Diarrhea	Fatal Infantile Diarrhea With Trichorrhexis Nodosa

Pontocerebellar Hypoplasia, Type 1e

Pontocerebellar Hypoplasia Type 1	PCH1E
Norman Disease	Pch1
Pontocerebellar Hypoplasia With Anterior Horn Cell Disease	Pontocerebellar Hypoplasia With Infantile Spinal Muscular Atrophy
Pontocerebellar Hypoplasia Type 1e	Pontocerebellar Hypoplasia 1e
Doid:0112322	Doid:0112330

Pontocerebellar Hypoplasia

Pch	Congenital Pontocerebellar Hypoplasia
Opch	Hypoplasia, Pontocerebellar
Pontoneocerebellar Hypoplasia	Nonsyndromic Pontocerebellar Hypoplasia

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS16006	ZCCHC7 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	ZCCHC7	RGD	RGD:1310467
Canis familiaris	ZCCHC7	VGNC	VGNC:53504
Bos taurus	ZCCHC7	VGNC	VGNC:37122
Macaca mulatta	ZCCHC7	VGNC	VGNC:82088
Felis catus	ZCCHC7	VGNC	VGNC:103010
Mus musculus	ZCCHC7	MGD	MGI:2442912

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