WHSC1
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Homo sapiens |
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WHSC1 is differentially expressed in 371 experiments: 168 organism parts: bone marrow, testis, ... (166 more);, 264 disease states: normal, prostate carcinoma, ... (262 more);, 136 cell types 521 cell lines 58 compound treatments and 85 other conditions. |
| Synonyms |
NSD2, MMSET |
| Orthologs |
E1C765_CHICK
(Gallus gallus)
WHSC1
(Bos taurus)
Whsc1
(Rattus norvegicus)
Whsc1
(Mus musculus)
whsc1
(Danio rerio)
whsc1
(Xenopus laevis)
WHSC1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0008168, GO:0003682, GO:0003677, GO:0008270, GO:0016568, GO:0009653, GO:0031965, GO:0016740, GO:0005515, GO:0005730, GO:0005737, GO:0005694, GO:0005634, GO:0000122, GO:0046872, GO:0006355, GO:0018024, GO:0060348, GO:0003149, GO:0003289, GO:0003290, GO:0034968, GO:0018022 |
| Gene Ontology Term |
DNA binding, protein binding, regulation of transcription, DNA-dependent, cytoplasm, metal ion binding, methyltransferase activity, anatomical structure morphogenesis, nucleus, chromatin binding, transferase activity, chromosome, chromatin modification, negative regulation of transcription from RNA polymerase II promoter, nucleolus, histone-lysine N-methyltransferase activity, nuclear membrane, zinc ion binding, membranous septum morphogenesis, atrial septum primum morphogenesis, bone development, histone lysine methylation, atrial septum secundum morphogenesis, peptidyl-lysine methylation |
| InterPro ID |
IPR001214, IPR019787, IPR000910, IPR000313, IPR001965, IPR001841, IPR006560, IPR003616 |
| InterPro Term |
Znf_PHD-finger, AWS, Znf_RING, Znf_PHD, Post-SET_dom, HMG_HMG1/HMG2, 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 |
AY694128, BC020545, AJ007042, BC094825, AF330040, AF071594, AF071593, AB029013, AC105448, BC141815, AF178211, AF178210, AF178213, AF178212, AF178215, AF178214, AF178216, AF178217, AF178218, AF178219, AF178198, AF178199, AF178205, AF178204, AF178207, AF178206, AF178209, AF178208, AF178200, AF178201, AF178202, AF178203, BC152412, CH471131, BC052254, AL132868, AK289697, BC070176, AF083387, AF083386, AF083389, AF083388, AF083390, AF083391 |
| Ensembl Protein ID |
ENSP00000425094, ENSP00000427434, ENSP00000427516, ENSP00000372344, ENSP00000372347, ENSP00000372348, ENSP00000372351, ENSP00000422878, ENSP00000416725, ENSP00000424482, ENSP00000381311, ENSP00000329167, ENSP00000421681, ENSP00000425761, ENSP00000399251, ENSP00000308780, ENSP00000421551, ENSP00000423972 |
| Ensembl Gene ID |
ENSG00000109685 |
| RefSeq ID |
NM_001042424, NP_015627, NM_007331, NP_579890, NP_579889, NP_579878, NP_579877, NM_133335, NM_133330, NM_133334, NM_133331, NP_001035889 |
| UniProt Accession |
D6R9V2, O96028, D6RIS1, D6RFE7, Q05CW4, A2A2T2 |
| Description |
Wolf-Hirschhorn syndrome candidate 1 [Source:HGNC Symbol;Acc:12766] |
| HGNC Symbol |
WHSC1 |
| UniGene ID |
Hs.113876, Hs.704199 |
| Entrez Gene ID |
7468 |
| Ensembl Transcript ID |
ENST00000503207, ENST00000503128, ENST00000507820, ENST00000436793, ENST00000513726, ENST00000482415, ENST00000505643, ENST00000508803, ENST00000508355, ENST00000508299, ENST00000514045, ENST00000514329, ENST00000382895, ENST00000382892, ENST00000382891, ENST00000382888, ENST00000512700, ENST00000420906, ENST00000509115, ENST00000511904, ENST00000515695, ENST00000515806, ENST00000507094, ENST00000353275, ENST00000398261, ENST00000502425, ENST00000312087 |
| Gene-Disease Assocation |
WOLF-HIRSCHHORN SYNDROME; WHS |
| Design Element |
209052_s_at, 88837_at, 60844_at, ENST00000420906, 87565_at, ENST00000507094, ENST00000513726, ENST00000353275, Hs.110457.0.S3_3p_a_at, ENST00000502425, ENST00000515695, 58244_at, 65059_at, 209054_s_at, ENST00000512700, ENST00000382892, ENST00000382891, 43329_at, 222777_s_at, 74492_at, ENST00000382895, ENST00000503207, ENST00000511904, ENST00000508299, ENST00000382888, ENST00000508355, Hs.110457.3.S2_3p_a_at, ENST00000508803, 222778_s_at, ENST00000436793, ENST00000505643, g3249714_3p_at, ENST00000312087, ENST00000398261, 38988_at, ENST00000482415, 89995_at, Hs.110457.0.S1_3p_a_at, ENST00000514329, 209053_s_at, 223472_at, ENST00000509115, g4378016_3p_a_at, ENST00000507820, Hs.110457.3.S1_3p_a_at, ENST00000515806, ENST00000514045, ENST00000503128 |
| Search EB-eye |
ENSG00000109685
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