FOXP1
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Homo sapiens |
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FOXP1 is differentially expressed in 233 experiments: 116 organism parts: liver, mammary gland, ... (114 more);, 118 disease states: normal, breast carcinoma, ... (116 more);, 103 cell types 379 cell lines 43 compound treatments and 63 other conditions. |
| Synonyms |
HSPC215, QRF1, hFKH1B, 12CC4 |
| Orthologs |
FOXP1_BOVIN
(Bos taurus)
Foxp1
(Mus musculus)
FOXP1
(Gallus gallus)
Q4H3H6_CIOIN
(Ciona intestinalis)
Foxp1
(Rattus norvegicus)
FKH2
(Saccharomyces cerevisiae)
FKH1
(Saccharomyces cerevisiae)
foxp1
(Xenopus laevis)
FOXP1
(Canis familiaris)
FoxP
(Drosophila melanogaster)
(Compare orthologs)
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| Gene Ontology ID |
GO:0008134, GO:0003682, GO:0003677, GO:0003690, GO:0008270, GO:0008301, GO:0003700, GO:0003705, GO:0008045, GO:0009790, GO:0007389, GO:0007507, GO:0007519, GO:0051090, GO:0042803, GO:0005622, GO:0005515, GO:0005737, GO:0005634, GO:0005667, GO:0055007, GO:0000122, GO:0046872, GO:0006355, GO:0006351, GO:0046982, GO:0045944, GO:0043565, GO:0045892, GO:0045893, GO:0045214, GO:0060501, GO:0060043, GO:0048745, GO:0002639, GO:0002329, GO:0002053, GO:0050679, GO:0001701, GO:0030324, GO:0033152, GO:0021517, GO:0072358, GO:2000727 |
| Ensembl Family Description |
FORKHEAD BOX |
| Gene Ontology Term |
pattern specification process, embryo development, DNA binding, negative regulation of transcription, DNA-dependent, protein binding, cardiac muscle cell differentiation, regulation of transcription, DNA-dependent, cytoplasm, double-stranded DNA binding, intracellular, transcription, DNA-dependent, metal ion binding, DNA bending activity, motor axon guidance, transcription factor binding, sequence-specific DNA binding, positive regulation of transcription from RNA polymerase II promoter, sarcomere organization, nucleus, heart development, protein heterodimerization activity, transcription factor complex, chromatin binding, protein homodimerization activity, negative regulation of transcription from RNA polymerase II promoter, skeletal muscle tissue development, positive regulation of transcription, DNA-dependent, zinc ion binding, positive regulation of mesenchymal cell proliferation, regulation of cardiac muscle cell proliferation, positive regulation of epithelial cell proliferation involved in lung morphogenesis, in utero embryonic development, immunoglobulin V(D)J recombination, ventral spinal cord development, positive regulation of immunoglobulin production, positive regulation of epithelial cell proliferation, smooth muscle tissue development, lung development, pre-B cell differentiation, sequence-specific DNA binding transcription factor activity, regulation of sequence-specific DNA binding transcription factor activity, cardiovascular system development, positive regulation of cardiac muscle cell differentiation, sequence-specific distal enhancer binding RNA polymerase II transcription factor activity |
| InterPro ID |
IPR001766 |
| InterPro Term |
TF_fork_head |
| Ensembl Family |
ENSFM00250000000673 |
| RefSeq ID |
NM_001012505, NP_116071, NP_001012523, NM_032682, NP_001231739, NP_001231737, NP_001231743, NP_001231744, NP_001231745, NP_001231742, NP_001231741, NM_001244810, NM_001244816, NM_001244812, NM_001244813, NM_001244814, NM_001244815, NM_001244808 |
| Ensembl Protein ID |
ENSP00000418102, ENSP00000418225, ENSP00000418784, ENSP00000418883, ENSP00000333560, ENSP00000418524, ENSP00000344830, ENSP00000351025, ENSP00000318721, ENSP00000318902, ENSP00000419393, ENSP00000319243, ENSP00000420736, ENSP00000417941, ENSP00000417857 |
| Entrez Gene ID |
27086 |
| EMBL-Bank ID |
AC138058, AF250920, AF146697, AF146698, AF146696, DQ845346, AK074569, BC080521, BC071893, AK297649, AF275309, CH471055, AK092383, AK027264, BC131720, AB052767, AC103586, AC097632, AC097634, BT006643, AF151049, AC104645, AC104442, BC005055, BC054815 |
| UniGene ID |
Hs.604002, Hs.712967, Hs.712809, Hs.431498, Hs.601368, Hs.59368 |
| UniProt Accession |
Q9H334, Q8IXF4, C9J0F0, Q548T7, C9IYY1, C9J5T4, Q8N2P0, Q8NAN6, B4DMV4, A3KMG1, Q9BSG9, F5GYL1, E7ETP1, E9PFD3 |
| Description |
forkhead box P1 [Source:HGNC Symbol;Acc:3823] |
| HGNC Symbol |
FOXP1 |
| Ensembl Gene ID |
ENSG00000114861 |
| Ensembl Transcript ID |
ENST00000491238, ENST00000485326, ENST00000493089, ENST00000493010, ENST00000327590, ENST00000460805, ENST00000475937, ENST00000471386, ENST00000358280, ENST00000339693, ENST00000497553, ENST00000497355, ENST00000318779, ENST00000318796, ENST00000318789, ENST00000468577, ENST00000484350, ENST00000472382, ENST00000470112, ENST00000498215, ENST00000498154 |
| Gene-Disease Assocation |
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES |
| Design Element |
Hs.108327.1.A1_3p_at, ENST00000498154, Hs.59368.0.A1_3p_at, ENST00000493010, 223937_at, ENST00000471386, ENST00000470112, gnf1h00883_s_at, ENST00000484350, ENST00000318789, 223936_s_at, ENST00000491238, gnf1h00882_at, gnf1h09448_s_at, ENST00000460805, ENST00000358280, ENST00000485326, 53603_at, ENST00000468577, Hs.108327.1.A2_3p_at, ENST00000475937, ENST00000339693, 223287_s_at, ENST00000472382, 224837_at, ENST00000318796, ENST00000318779, 229844_at, ENST00000497553, g13477186_3p_at, ENST00000327590, 74636_at, ENST00000497355, ENST00000498215, 224838_at, g12043713_3p_a_at, 54990_at, ENST00000493089, 223936_3p_s_at, g13477186_3p_a_at |
| Search EB-eye |
ENSG00000114861
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