Homo sapiens (human): 63932 Help Entry 63932             CDS       T01001                                  Symbol STEEP1, CXorf56, MRX107, STEEP, XLID107 Name (RefSeq) STING1 ER exit protein 1   KO K24996   STING ER exit protein Organism hsa  Homo sapiens (human) Disease H00480   X-linked intellectual developmental disorder Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    04131 Membrane trafficking [BR:hsa04131]     63932 (STEEP1) Membrane trafficking [BR:hsa04131]  Endoplasmic reticulum (ER) - Golgi transport   Others    Others     63932 (STEEP1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  STEEP1 DUF4410 VIT1 Motif Other DBs NCBI-GeneID:  63932 NCBI-ProteinID:  NP_071384 OMIM:  301012 HGNC:  26239 Ensembl:  ENSG00000018610 UniProt:  Q9H5V9 Structure PDBPDBj LinkDB All DBs Position X:complement(119538149..119565409) Genome browser AA seq 222 aa AA seqDB search MPKVVSRSVVCSDTRDREEYDDGEKPLHVYYCLCGQMVLVLDCQLEKLPMRPRDRSRVID AAKHAHKFCNTEDEETMYLRRPEGIERQYRKKCAKCGLPLFYQSQPKNAPVTFIVDGAVV KFGQGFGKTNIYTQKQEPPKKVMMTKRTKDMGKFSSVTVSTIDEEEEEIEAREVADSYAQ NAKVIEKQLERKGMSKRRLQELAELEAKKAKMKGTLIDNQFK NT seq 669 nt NT seq  +upstreamnt  +downstreamnt atgccgaaagtagtgtctcggtcagtagtctgctctgacactcgggaccgggaggaatat gacgacggcgagaagcccctccatgtttactactgtttgtgcggccagatggtcctagtg ctggactgccagttagagaaattgcccatgaggccccgggaccggtcccgtgtgattgat gctgccaaacatgcccataagttttgtaacacagaagatgaggagactatgtatctgcgg agacctgaaggcattgaacgacagtacaggaagaaatgtgcaaagtgtggactgccgctc ttctaccaatcccagccaaagaatgctcctgttaccttcattgtggatggagcagtagtc aagtttggccagggctttgggaaaacgaacatatatactcagaaacaagagcctcctaag aaggtgatgatgaccaaacggaccaaagacatgggcaagttcagttctgtcaccgtgtct accattgatgaagaggaagaggagattgaggctagggaagttgctgactcatatgcacag aatgccaaagtgattgaaaaacagctggagcgcaaaggcatgagcaagaggcgactgcaa gagctggctgaattggaagccaagaaagcgaaaatgaaggggaccttgattgacaaccag ttcaaataa

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