WHSC1L1
close
Please copy/paste those URLs into your code to get same results in machine-readable formats:
|
Homo sapiens |
|
WHSC1L1 is differentially expressed in 272 experiments: 137 organism parts: skin, blood, ... (135 more);, 194 disease states: normal, breast carcinoma, ... (192 more);, 88 cell types 407 cell lines 34 compound treatments and 79 other conditions. |
| Synonyms |
FLJ20353, NSD3 |
| Orthologs |
Whsc1l1
(Mus musculus)
E1C6X8_CHICK
(Gallus gallus)
Whsc1l1
(Rattus norvegicus)
WHSC1L1
(Bos taurus)
whsc1l1
(Danio rerio)
WHSC1L1
(Xenopus laevis)
WHSC1L1
(Canis familiaris)
(Compare orthologs)
|
| Gene Ontology ID |
GO:0008168, GO:0008270, GO:0016049, GO:0016571, GO:0016568, GO:0016740, GO:0005515, GO:0005694, GO:0005634, GO:0046872, GO:0006355, GO:0018024, GO:0030154, GO:0034968 |
| Gene Ontology Term |
protein binding, regulation of transcription, DNA-dependent, histone methylation, metal ion binding, cell differentiation, cell growth, methyltransferase activity, nucleus, transferase activity, chromosome, chromatin modification, histone-lysine N-methyltransferase activity, zinc ion binding, histone lysine methylation |
| InterPro ID |
IPR001214, IPR019787, IPR000313, IPR001965, IPR006560, IPR003616 |
| InterPro Term |
Znf_PHD-finger, AWS, Znf_PHD, Post-SET_dom, PWWP, SET_dom |
| Ensembl Family Description |
HISTONE LYSINE N METHYLTRANSFERASE EC_2.1.1.43 NUCLEAR SET DOMAIN CONTAINING WOLF HIRSCHHORN SYNDROME CANDIDATE 1 |
| Ensembl Family |
ENSFM00250000000687 |
| EMBL-Bank ID |
AF332468, AF332469, BC107734, AF255649, BC143510, BC012059, AC087623, AC087362, AK127594, AK022560, AK000360, BC101717, CH471080, BC113469, BC115006, AJ295991, AJ295992, AJ295990, BC062631 |
| UniProt Accession |
B7ZL11, C9JY66, Q9BZ95, E9PQ95, E9PKA2 |
| Entrez Gene ID |
54904 |
| Description |
Wolf-Hirschhorn syndrome candidate 1-like 1 [Source:HGNC Symbol;Acc:12767] |
| RefSeq ID |
NP_075447, NP_060248, NM_023034, NM_017778 |
| Ensembl Protein ID |
ENSP00000387883, ENSP00000313983, ENSP00000313410, ENSP00000393284, ENSP00000431598, ENSP00000435422, ENSP00000435073, ENSP00000432544, ENSP00000434730 |
| UniGene ID |
Hs.608111, Hs.722308 |
| HGNC Symbol |
WHSC1L1 |
| Ensembl Gene ID |
ENSG00000147548 |
| Ensembl Transcript ID |
ENST00000528828, ENST00000528627, ENST00000316985, ENST00000526050, ENST00000528304, ENST00000534155, ENST00000534539, ENST00000525081, ENST00000527502, ENST00000529223, ENST00000433384, ENST00000317025, ENST00000446459 |
| Gene-Disease Assocation |
LEUKEMIA, ACUTE MYELOID; AML |
| Design Element |
ENST00000446459, 224076_s_at, 42709_at, 90289_at, ENST00000529223, ENST00000317025, 221248_s_at, ENST00000527502, ENST00000528304, ENST00000525081, ENST00000433384, g13699810_3p_s_at, 218173_s_at, Hs.27721.0.A1_3p_s_at, ENST00000526050, Hs.120750.0.A1_3p_at, 222544_s_at, 45738_at, ENST00000316985, 238496_at, 72889_r_at, g13699812_3p_a_at, ENST00000534155, ENST00000528627, ENST00000528828, g12005822_3p_a_at, ENST00000534539 |
| Search EB-eye |
ENSG00000147548
|
 Show more
properties
|
|
