RUNX2
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Homo sapiens |
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RUNX2 is differentially expressed in 306 experiments: 157 organism parts: skeletal muscle, bone marrow, ... (155 more);, 200 disease states: normal, control, ... (198 more);, 111 cell types 402 cell lines 39 compound treatments and 78 other conditions. |
| Synonyms |
CCD, AML3, PEBP2A1, PEBP2aA1, CBFA1, CCD1 |
| Orthologs |
ENSCING00000002253
(Ciona intestinalis)
RUNX2
(Bos taurus)
RUNX2
(Gallus gallus)
runx2a
(Danio rerio)
Runx2
(Mus musculus)
runx2b
(Danio rerio)
Runx2
(Rattus norvegicus)
RunxB
(Drosophila melanogaster)
RunxA
(Drosophila melanogaster)
run
(Drosophila melanogaster)
lz
(Drosophila melanogaster)
Runx2
(Mus musculus)
runx2
(Xenopus laevis)
RUNX2
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0003677, GO:0003700, GO:0005524, GO:0005515, GO:0005634, GO:0006355, GO:0006351, GO:0045892, GO:0045893, GO:0001503, GO:0001649 |
| InterPro ID |
IPR000040, IPR013524, IPR016554, IPR013711 |
| Gene Ontology Term |
DNA binding, negative regulation of transcription, DNA-dependent, protein binding, regulation of transcription, DNA-dependent, transcription, DNA-dependent, ATP binding, nucleus, positive regulation of transcription, DNA-dependent, osteoblast differentiation, ossification, sequence-specific DNA binding transcription factor activity |
| InterPro Term |
AML1_Runt, AML1/Runt_N, RunxI, TF_Runt-rel_RUNX |
| Ensembl Family |
ENSFM00250000000641 |
| Ensembl Family Description |
RUNT RELATED TRANSCRIPTION FACTOR ACUTE MYELOID LEUKEMIA CORE BINDING FACTOR SUBUNIT ALPHA CBF ALPHA ONCOGENE AML POLYOMAVIRUS ENHANCER BINDING 2 ALPHA SUBUNIT PEA2 ALPHA PEBP2 ALPHA SL3 3 ENHANCER FACTOR 1 ALPHA SUBUNIT SL3/AKV CORE BINDING FACTOR ALPHA |
| RefSeq ID |
NP_001019801, NM_001015051, NM_001024630, NM_004348, NP_001015051, NP_004339 |
| EMBL-Bank ID |
AL161907, L40992, AF001449, AF001447, AF001448, AF001446, AF001445, AF001444, AF001443, AF001450, AL096865, BC108919, BC108920, AF053949, AF053952, AL358135, AL513219 |
| UniGene ID |
Hs.599884, Hs.717834, Hs.608062, Hs.659574, Hs.535845 |
| Description |
runt-related transcription factor 2 [Source:HGNC Symbol;Acc:10472] |
| HGNC Symbol |
RUNX2 |
| Ensembl Gene ID |
ENSG00000124813 |
| UniProt Accession |
Q13950, Q5T802, Q5T801, Q32MY8, F6RGB9, F8W8U5 |
| Ensembl Protein ID |
ENSP00000360493, ENSP00000360491, ENSP00000360486, ENSP00000352514, ENSP00000319087, ENSP00000420707, ENSP00000446290 |
| Entrez Gene ID |
860 |
| Ensembl Transcript ID |
ENST00000541979, ENST00000465038, ENST00000473041, ENST00000352853, ENST00000478660, ENST00000483377, ENST00000483243, ENST00000359524, ENST00000371432, ENST00000371436, ENST00000371438 |
| Gene-Disease Assocation |
CLEIDOCRANIAL DYSPLASIA; CCD |
| Design Element |
ENST00000478660, ENST00000541979, ENST00000371438, ENST00000371436, 236859_at, Hs.50115.0.S1_3p_at, ENST00000483377, L40992_at, ENST00000371432, 232231_at, 216994_s_at, ENST00000352853, 236858_s_at, ENST00000359524, g10863884_3p_a_at, 221282_x_at, ENST00000465038, 34502_g_at, 73682_at, 53261_at, 39187_at, ENST00000483243, 34501_at, Hs.122116.0.A1_3p_at, ENST00000473041 |
| Search EB-eye |
ENSG00000124813
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