1. Gene
  2. ZNHIT1 - zinc finger HIT-type containing 1 Gene

ZNHIT1 - zinc finger HIT-type containing 1 Gene

Homo sapiens

Also known as CG1I; ZNFN4A1

Gene ID: 10467 | Gene type: protein coding

About ZNHIT1

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:101,218,165-101,224,190 (from NCBI)

This gene has 4 transcripts (splice variants) and 179 orthologues. Ubiquitous expression in liver (RPKM 23.5), kidney (RPKM 21.2) and 25 other tissues.

Summary

Predicted to enable histone deacetylase binding activity and nucleosome binding activity. Predicted to be involved in histone exchange. Predicted to act upstream of or within several processes, including negative regulation of G0 to G1 transition; negative regulation of transcription by RNA polymerase II; and regulation of histone deacetylation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ZNHIT1 Products(1)

mRNA Protein Name
NM_006349.3 NP_006340.1 zinc finger HIT domain-containing protein 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables histone binding IPI
IPI: Inferred from physical interaction
20473270 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
15647280 GOA
Biological Process GO Annotation Evidence Reference Source
involved in muscle cell differentiation IMP
IMP: Inferred from mutant phenotype
20473270 GOA
involved in positive regulation of DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator IDA
IDA: Inferred from direct assay
17700068 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nucleus IDA
IDA: Inferred from direct assay
17892483 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

ZNHIT1 Protein Structure

zf-HIT

zf-HIT: HIT zinc finger (113 - 141)

  • 0
  • 100
  • 154 a.a.
Protein Preferred Names Protein Names

zinc finger HIT domain-containing protein 1

H_DJ0747G18.14

ZNHIT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
ZNHIT1 O43257 KRTAP10-7 Homo sapiens P60409 25416956
Intra
ZNHIT1 O43257 KRTAP10-7 Homo sapiens P60409 25416956
Intra
ZNHIT1 O43257 KRTAP10-7 Homo sapiens P60409 25416956
Intra
ZNHIT1 O43257 KRTAP12-2 Homo sapiens P59991 32296183
Intra
ZNHIT1 O43257 KRTAP12-2 Homo sapiens P59991 32296183
Intra
ZNHIT1 O43257 KRTAP12-2 Homo sapiens P59991 32296183
Intra
ZNHIT1 O43257 H2AZ1 Homo sapiens P0C0S5 20473270
Intra
ZNHIT1 O43257 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ZNHIT1 O43257 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ZNHIT1 O43257 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ZNHIT1 O43257 MYO5B Homo sapiens Q9ULV0-2 32296183
Intra
ZNHIT1 O43257 APBB2 Homo sapiens Q92870-2 32814053
Intra
ZNHIT1 O43257 APBB2 Homo sapiens Q92870-2 32814053
Intra
ZNHIT1 O43257 APBB2 Homo sapiens Q92870-2 32814053
Intra
ZNHIT1 O43257 KANK2 Homo sapiens Q63ZY3 32296183
Intra
ZNHIT1 O43257 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
ZNHIT1 O43257 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
ZNHIT1 O43257 TP53BP1 Homo sapiens Q12888 17380123
Intra
ZNHIT1 O43257 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
ZNHIT1 O43257 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
ZNHIT1 O43257 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
ZNHIT1 O43257 EEF1D Homo sapiens P29692-2 32814053
Intra
ZNHIT1 O43257 EEF1D Homo sapiens P29692-2 32814053
Intra
ZNHIT1 O43257 EEF1D Homo sapiens P29692-2 32814053
Intra
ZNHIT1 O43257 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
ZNHIT1 O43257 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
ZNHIT1 O43257 DNM1L Homo sapiens O00429-3 32814053
Intra
ZNHIT1 O43257 DNM1L Homo sapiens O00429-3 32814053
Intra
ZNHIT1 O43257 DNM1L Homo sapiens O00429-3 32814053
Intra
ZNHIT1 O43257 MAPK9 Homo sapiens P45984 32296183
Intra
ZNHIT1 O43257 MDFI Homo sapiens Q99750 32296183
Intra
ZNHIT1 O43257 MDFI Homo sapiens Q99750 32296183
Intra
ZNHIT1 O43257 MDFI Homo sapiens Q99750 32296183
Intra
ZNHIT1 O43257 MAPK14 Homo sapiens Q16539 17380123
Intra
ZNHIT1 O43257 COL8A1 Homo sapiens P27658 32296183
Intra
ZNHIT1 O43257 FHL5 Homo sapiens Q5TD97 32296183
Intra
ZNHIT1 O43257 FHL5 Homo sapiens Q5TD97 32296183
Intra
ZNHIT1 O43257 FHL5 Homo sapiens Q5TD97 32296183
Intra
ZNHIT1 O43257 BCL6 Homo sapiens P41182 32296183
Intra
ZNHIT1 O43257 ACTR6 Homo sapiens Q9GZN1 16230350
Intra
ZNHIT1 O43257 ACTR6 Homo sapiens Q9GZN1 33961781
Intra
ZNHIT1 O43257 ACTR6 Homo sapiens Q9GZN1 15647280
Intra
ZNHIT1 O43257 ACTR6 Homo sapiens Q9GZN1 20473270
Intra
ZNHIT1 O43257 OTX2 Homo sapiens P32243-2 32296183
Intra
ZNHIT1 O43257 OTX2 Homo sapiens P32243-2 32296183
Intra
ZNHIT1 O43257 OTX2 Homo sapiens P32243-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ZNHIT1 Proteins

Cat. No. Product Name Accession Purity
HY-P71028 ZNHIT1 Protein, Human (His) O43257 (M1-V154) ≥95%

Related Diseases

Diseases Alias
Floating-Harbor Syndrome

FLHS

Fhs

Pelletier-Leisti Syndrome

Short Stature With Delayed Bone Age, Expressive Language Delay, A Triangular Face With A Prominent Nose And Deep-Set Eyes

Leisti-Hollander-Rimoin Syndrome

Hemophagocytic Lymphohistiocytosis, Familial, 1

Familial Hemophagocytic Lymphohistiocytosis

Fhl

Familial Erythrophagocytic Lymphohistiocytosis

Hemophagocytic Syndrome

FHL1

Hplh1

Hlh1

Fel

Familial Hemophagocytic Lymphohistiocytosis 1

Primary Hemophagocytic Lymphohistiocytosis

Familial Hlh

Hlh

Familial Hemophagocytic Lymphocytosis

Hemophagocytic Lymphohistiocytosis, Familial

Reticulosis, Familial Histiocytic

Hemophagocytic Reticulosis, Familial

Erythrophagocytic Lymphohistiocytosis, Familial

Familial Histiocytic Reticulosis

Familial Hemophagocytic Histiocytosis

Familial Hemophagocytic Reticulosis

Fhlh

Hplh

Primary Hemophagocytic Hymphohistiocytosis

Genetic Hemophagocytic Lymphohistiocytosis

Hemophagocytic Lymphohistiocytosis

Familial Hemophagocytic Lymphohistiocytosis Type 1

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

Orthologs Information

Species Symbol Source ID
Canis familiaris ZNHIT1 VGNC VGNC:48835
Felis catus ZNHIT1 VGNC VGNC:67366
Macaca mulatta ZNHIT1 VGNC VGNC:79332
Bos taurus ZNHIT1 VGNC VGNC:37358
Mus musculus ZNHIT1 MGD MGI:1917353
Rattus norvegicus ZNHIT1 RGD RGD:2322870
Others ZNHIT1 NCBI