Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
23569 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Peptidyl arginine deiminase 4 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
PADI4 |
SynonymsGene synonyms aliases
|
PAD, PAD4, PADI5, PDI4, PDI5 |
ChromosomeChromosome number
|
1 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
1p36.13 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene is a member of a gene family which encodes enzymes responsible for the conversion of arginine residues to citrulline residues. This gene may play a role in granulocyte and macrophage development leading to inflammation and immune response. [prov |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
Q9UM07 |
Protein name |
Protein-arginine deiminase type-4 (EC 3.5.3.15) (HL-60 PAD) (Peptidylarginine deiminase IV) (Protein-arginine deiminase type IV) |
Protein function |
Catalyzes the citrullination/deimination of arginine residues of proteins such as histones, thereby playing a key role in histone code and regulation of stem cell maintenance (PubMed:15339660, PubMed:15345777, PubMed:16567635, PubMed:21245532). |
PDB |
1WD8
,
1WD9
,
1WDA
,
2DEW
,
2DEX
,
2DEY
,
2DW5
,
3APM
,
3APN
,
3B1T
,
3B1U
,
4DKT
,
4X8C
,
4X8G
,
5N0M
,
5N0Y
,
5N0Z
,
5N1B
,
8GOD
,
8R8U
,
8R8V
,
8SMK
,
8SML
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF08526 |
PAD_N |
1 → 111 |
Protein-arginine deiminase (PAD) N-terminal domain |
Domain |
PF08527 |
PAD_M |
113 → 273 |
Protein-arginine deiminase (PAD) middle domain |
Domain |
PF03068 |
PAD |
283 → 660 |
Protein-arginine deiminase (PAD) |
Family |
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Sequence |
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Sequence length |
663 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Carcinoma |
Carcinoma, Carcinoma, Spindle-Cell, Undifferentiated carcinoma |
rs121912654, rs555607708, rs786202962, rs1564055259 |
12376462 |
Rheumatoid arthritis |
Rheumatoid Arthritis |
rs3766379, rs3792876, rs2071592, rs3087456, rs587776843, rs1566328963, rs2240340, rs1557787212 |
24390342, 23143596, 21452313, 21505073, 30423114, 24532676 |
Vasculitis |
Vasculitis |
rs376785840, rs587777240, rs200930463, rs587777241, rs77563738, rs202134424, rs148936893, rs587777242, rs775440641, rs770689762, rs45511697, rs139750129, rs756881285, rs747774101, rs1568966771, rs766602945, rs1601419986, rs1489114116, rs754904956, rs755007390, rs368615054 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Anaplastic carcinoma |
Anaplastic carcinoma |
|
12376462 |
Drachtman weinblatt sitarz syndrome |
Congenital neurologic anomalies |
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