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Protein Ontology report - histone-lysine N-methyltransferase, H3 lysine-36 specific (human)
PR:Q96L73 -
http://purl.obolibrary.org/obo/PR_Q96L73
Protein Forms
Ontology Information
Show OBO stanza
/
GPI
PRO ID
PR:Q96L73
PRO name
histone-lysine N-methyltransferase, H3 lysine-36 specific (human)
Synonyms
PRO-Short-label
:
EXACT:
hNSD1
Gene-based
:
RELATED:
ARA267 | KMT3B | NSD1
Other
:
EXACT:
androgen receptor coactivator 267 kDa protein (human) | androgen receptor-associated protein of 267 kDa (human) | H3-K36-HMTase (human) | lysine N-methyltransferase 3B (human) | NR-binding SET domain-containing protein (human) | nuclear receptor-binding SET domain-containing protein 1 (human)
Definition
"A histone-lysine N-methyltransferase, H3 lysine-36 specific that is encoded in the genome of human." [PRO:DNx,
UniProtKB:Q96L73
]
PRO Category
organism-gene
Parent
PR:000011441
PR:000029067
Gene Template
HGNC:14234
NSD1 (human)
Taxon
NCBITaxon:9606
Homo sapiens
Terms by PRO Category
Organism-Independent
Organism-Specific
Category
Number of Terms
Category
Number of Terms
Gene
0
Organism-Gene
1
Sequence
0
Organism-Sequence
3
Modification
0
Organism-Modification
2
Term Hierarchy
Visualization
DAG:
OLS:
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Related Cross References
Db identifiers
UniProtKB:Q96L73
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Protein Forms
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Extended View
Category
PRO Form Name
Ann.
Has Annotation?
Comp.
In Complex?
organism-gene
PR:Q96L73
histone-lysine N-methyltransferase, H3 lysine-36 specific (human), hNSD1
organism-sequence
PR:Q96L73-1
histone-lysine N-methyltransferase, H3 lysine-36 specific isoform h1 (human), hNSD1/iso:h1
organism-sequence
PR:Q96L73-2
histone-lysine N-methyltransferase, H3 lysine-36 specific isoform h2 (human), hNSD1/iso:h2
organism-sequence
PR:Q96L73-3
histone-lysine N-methyltransferase, H3 lysine-36 specific isoform h3 (human), hNSD1/iso:h3
organism-modification
PR:000073834
histone-lysine N-methyltransferase, H3 lysine-36 specific hydroxylated 1 (human), hNSD1/Hy:1
organism-modification
PR:000083365
histone-lysine N-methyltransferase, H3 lysine-36 specific methylated 1 (human), hNSD1/Me:1