JAG1
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Homo sapiens |
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JAG1 is differentially expressed in 386 experiments: 180 organism parts: bone marrow, prostate, ... (178 more);, 261 disease states: normal, control, ... (259 more);, 121 cell types 495 cell lines 54 compound treatments and 78 other conditions. |
| Synonyms |
CD339, JAGL1, AWS, HJ1, AGS, AHD |
| Orthologs |
Jag1
(Mus musculus)
ENSCING00000004617
(Ciona intestinalis)
jag1b
(Danio rerio)
Jag1
(Rattus norvegicus)
JAG1
(Bos taurus)
jag1a
(Danio rerio)
Q90819_CHICK
(Gallus gallus)
Ser
(Drosophila melanogaster)
jag1
(Xenopus laevis)
JAG1
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
angiogenesis, plasma membrane, protein binding, morphogenesis of an epithelial sheet, regulation of cell proliferation, cell fate determination, membrane, positive regulation of Notch signaling pathway, structural molecule activity, growth factor activity, extracellular region, cell communication, Notch receptor processing, hemopoiesis, multicellular organismal development, integral to plasma membrane, regulation of cell migration, Notch binding, nervous system development, Notch signaling pathway, apical part of cell, integral to membrane, negative regulation of cell differentiation, calcium ion binding, organ morphogenesis, inner ear development, positive regulation of myeloid cell differentiation, keratinocyte differentiation, myoblast differentiation, negative regulation of neuron differentiation, response to muramyl dipeptide, endothelial cell differentiation, negative regulation of fat cell differentiation, auditory receptor cell differentiation, distal tubule development, neuronal stem cell maintenance, loop of Henle development, negative regulation of stem cell differentiation |
| Gene Ontology ID |
GO:0002011, GO:0009887, GO:0016020, GO:0016021, GO:0008083, GO:0007154, GO:0007275, GO:0007220, GO:0007219, GO:0007399, GO:0005509, GO:0005515, GO:0005576, GO:0005886, GO:0005887, GO:0005112, GO:0005198, GO:0045747, GO:0042127, GO:0001709, GO:0045596, GO:0001525, GO:0045177, GO:0030097, GO:0030334, GO:0048839, GO:0042491, GO:0032495, GO:0045665, GO:0045639, GO:0045599, GO:0045445, GO:0045446, GO:0030216, GO:0072070, GO:0072017, GO:2000737, GO:0097150 |
| Ensembl Family Description |
JAGGED PRECURSOR |
| InterPro ID |
IPR011651, IPR001007, IPR000742, IPR006209, IPR006210, IPR001774, IPR001881, IPR006552, IPR013111 |
| InterPro Term |
Notch_ligand_N, VWF_C, EGF_extracell, EGF, DSL, VWC_out, EGF_3, EGF-like, EGF-like_Ca-bd |
| Ensembl Family |
ENSFM00570000851117 |
| Ensembl Protein ID |
ENSP00000254958, ENSP00000389519 |
| UniGene ID |
Hs.713934, Hs.728907 |
| EMBL-Bank ID |
AF028593, FJ439571, FJ439570, AL035456, U77720, AF003837, U61276, AK302554, FJ013354, U73936, BC126207, BC126205 |
| Gene-Disease Assocation |
TETRALOGY OF FALLOT, JAGGED 1; JAG1, ALAGILLE SYNDROME 1; ALGS1 |
| UniProt Accession |
B7U6M8, B7U6M9, B5M914, B4DYR1, P78504 |
| Description |
jagged 1 [Source:HGNC Symbol;Acc:6188] |
| HGNC Symbol |
JAG1 |
| RefSeq ID |
NP_000205, NM_000214 |
| Ensembl Gene ID |
ENSG00000101384 |
| Entrez Gene ID |
182 |
| Ensembl Transcript ID |
ENST00000488480, ENST00000254958, ENST00000423891 |
| Design Element |
ENST00000423891, 74827_s_at, ENST00000488480, 209098_s_at, g1438936_3p_a_at, 35414_s_at, 209099_x_at, 209097_3p_s_at, Hs.91143.0.A1_3p_at, 209097_s_at, 216268_s_at, Hs.91143.0.A1_3p_a_at, g1695273_3p_a_at, U61276_s_at, U73936_at, ENST00000254958, 33178_at |
| Search EB-eye |
ENSG00000101384
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