Q9H898 (ZMAT4_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 29, 2013.
Version 92.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Zinc finger matrin-type protein 4 | ||
| Gene names |
| ||
| Organism | Homo sapiens (Human) [Reference proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 229 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subcellular location | Nucleus Potential. |
| Sequence similarities | Contains 4 matrin-type zinc fingers. |
Ontologies
| Keywords | |
|---|---|
| Cellular component | Nucleus |
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Repeat Zinc-finger |
| Ligand | DNA-binding Metal-binding Zinc |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| Cellular_component | nucleus Inferred from electronic annotation. Source: UniProtKB-SubCell |
| Molecular_function | DNA binding Inferred from electronic annotation. Source: UniProtKB-KW zinc ion bindingInferred from electronic annotation. Source: InterPro |
| Complete GO annotation... | |
Alternative products
| This entry describes 2 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q9H898-1) This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q9H898-2) The sequence of this isoform differs from the canonical sequence as follows: 117-192: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 229 | 229 | Zinc finger matrin-type protein 4 | PRO_0000298916 | |||||
Regions | |||||||||
| Zinc finger | 14 – 44 | 31 | Matrin-type 1 | ||||||
| Zinc finger | 72 – 106 | 35 | Matrin-type 2 | ||||||
| Zinc finger | 145 – 175 | 31 | Matrin-type 3 | ||||||
| Zinc finger | 198 – 228 | 31 | Matrin-type 4 | ||||||
Natural variations | |||||||||
| Alternative sequence | 117 – 192 | 76 | Missing in isoform 2. | VSP_027476 | |||||
| Natural variant | 201 | 1 | T → A. Ref.2 Corresponds to variant rs17851751 [ dbSNP | Ensembl ]. | VAR_034736 | |||||
Sequences
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References
| [1] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1). Tissue: Thyroid. |
| [2] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), VARIANT ALA-201. Tissue: Brain. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK023904 mRNA. Translation: BAB14719.1. BC019598 mRNA. Translation: AAH19598.1. |
| IPI | IPI00002880. IPI00177490. |
| RefSeq | NP_001129203.1. NM_001135731.1. NP_078921.1. NM_024645.2. |
| UniGene | Hs.591850. |
3D structure databases | |
| ProteinModelPortal | Q9H898. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q9H898. 4 interactions. |
PTM databases | |
| PhosphoSite | Q9H898. |
Polymorphism databases | |
| DMDM | 74733790. |
Proteomic databases | |
| PaxDb | Q9H898. |
| PRIDE | Q9H898. |
Protocols and materials databases | |
| DNASU | 79698. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000297737; ENSP00000297737; ENSG00000165061. ENST00000315769; ENSP00000319785; ENSG00000165061. |
| GeneID | 79698. |
| KEGG | hsa:79698. |
| UCSC | uc003xnr.3. human. uc003xns.3. human. |
Organism-specific databases | |
| CTD | 79698. |
| GeneCards | GC08M040388. |
| HGNC | HGNC:25844. ZMAT4. |
| neXtProt | NX_Q9H898. |
| PharmGKB | PA142670525. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG68898. |
| HOGENOM | HOG000008682. |
| HOVERGEN | HBG061007. |
| InParanoid | Q9H898. |
| OMA | DSDRYCQ. |
| OrthoDB | EOG4KWJTM. |
Gene expression databases | |
| ArrayExpress | Q9H898. |
| Bgee | Q9H898. |
| CleanEx | HS_ZMAT4. |
| Genevestigator | Q9H898. |
Family and domain databases | |
| InterPro | IPR007087. Znf_C2H2. IPR015880. Znf_C2H2-like. IPR022755. Znf_C2H2_jaz. IPR003604. Znf_U1. [Graphical view] |
| Pfam | PF12171. zf-C2H2_jaz. 1 hit. [Graphical view] |
| SMART | SM00355. ZnF_C2H2. 4 hits. SM00451. ZnF_U1. 4 hits. [Graphical view] |
| PROSITE | PS50171. ZF_MATRIN. False negative. [Graphical view] |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 79698. |
| NextBio | 68996. |
Entry information
| Entry name | ZMAT4_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q9H898 Secondary accession number(s): Q8WUT8 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 8 Human chromosome 8: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| SIMILARITY comments Index of protein domains and families |

Clusters with
