MNX1
close
Please copy/paste those URLs into your code to get same results in machine-readable formats:
|
Homo sapiens |
|
MNX1 is differentially expressed in 193 experiments: 66 organism parts: pancreas, amygdala, ... (64 more);, 142 disease states: normal, colon carcinoma, ... (140 more);, 46 cell types 388 cell lines 12 compound treatments and 53 other conditions. |
| Synonyms |
HLXB9, SCRA1, HOXHB9, HB9 |
| Orthologs |
mnx1
(Danio rerio)
F1P1C8_CHICK
(Gallus gallus)
Mnx1
(Mus musculus)
F6U2P7_CIOIN
(Ciona intestinalis)
MNX1
(Bos taurus)
exex
(Drosophila melanogaster)
mnx1
(Xenopus laevis)
MNX1
(Canis familiaris)
(Compare orthologs)
|
| Gene Ontology Term |
neuron differentiation, humoral immune response, regulation of transcription, DNA-dependent, transcription, DNA-dependent, cell morphogenesis involved in neuron differentiation, motor axon guidance, sequence-specific DNA binding, anatomical structure morphogenesis, nucleus, post-embryonic development, neuron projection morphogenesis, regulation of transcription from RNA polymerase II promoter, neuron migration, central nervous system neuron differentiation, diaphragm development, dorsal/ventral neural tube patterning, pancreas development, respiratory system development, spinal cord motor neuron cell fate specification, endocrine pancreas development, nerve development, sequence-specific DNA binding transcription factor activity |
| InterPro ID |
IPR001356, IPR020479 |
| Gene Ontology ID |
GO:0003700, GO:0008045, GO:0009653, GO:0009791, GO:0048812, GO:0048667, GO:0006959, GO:0005634, GO:0001764, GO:0006355, GO:0006357, GO:0006351, GO:0043565, GO:0030182, GO:0060539, GO:0060541, GO:0031016, GO:0031018, GO:0021953, GO:0021904, GO:0021675, GO:0021520 |
| InterPro Term |
Homeobox, Homeobox_eu |
| Ensembl Family Description |
MOTOR NEURON AND PANCREAS HOMEOBOX 1 HOMEOBOX HB9 |
| Ensembl Family |
ENSFM00600000921532 |
| Ensembl Protein ID |
ENSP00000401158, ENSP00000252971, ENSP00000416458, ENSP00000445801, ENSP00000438552 |
| HGNC Symbol |
MNX1 |
| Ensembl Gene ID |
ENSG00000130675 |
| RefSeq ID |
NM_005515, NP_005506, NP_001158727, NM_001165255 |
| Gene-Disease Assocation |
CURRARINO SYNDROME |
| UniProt Accession |
P50219, C9JFT4, C9K088, F5H401 |
| Description |
motor neuron and pancreas homeobox 1 [Source:HGNC Symbol;Acc:4979] |
| EMBL-Bank ID |
AC006357, AF107453, AF107452, U07664, U07663 |
| Entrez Gene ID |
3110 |
| UniGene ID |
Hs.37035 |
| Ensembl Transcript ID |
ENST00000543409, ENST00000469500, ENST00000542972, ENST00000252971, ENST00000425745, ENST00000474448, ENST00000428439, ENST00000479817 |
| Design Element |
U07664_at, ENST00000428439, ENST00000469500, 864_at, Hs.37035.0.S2_3p_at, ENST00000542972, ENST00000543409, ENST00000425745, 214614_at, ENST00000474448, ENST00000479817, ENST00000252971 |
| Search EB-eye |
ENSG00000130675
|
Show more
properties
|
|