KEGG   Homo sapiens (human): 63932
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)
SSDB
Motif
Pfam: GFA DUF4410 VIT1
Other DBs
NCBI-GeneID: 63932
NCBI-ProteinID: NP_071384
OMIM: 301012
HGNC: 26239
Ensembl: ENSG00000018610
UniProt: Q9H5V9
Structure
Position
X:complement(119538149..119565409)
AA seq 222 aa
MPKVVSRSVVCSDTRDREEYDDGEKPLHVYYCLCGQMVLVLDCQLEKLPMRPRDRSRVID
AAKHAHKFCNTEDEETMYLRRPEGIERQYRKKCAKCGLPLFYQSQPKNAPVTFIVDGAVV
KFGQGFGKTNIYTQKQEPPKKVMMTKRTKDMGKFSSVTVSTIDEEEEEIEAREVADSYAQ
NAKVIEKQLERKGMSKRRLQELAELEAKKAKMKGTLIDNQFK
NT seq 669 nt   +upstreamnt  +downstreamnt
atgccgaaagtagtgtctcggtcagtagtctgctctgacactcgggaccgggaggaatat
gacgacggcgagaagcccctccatgtttactactgtttgtgcggccagatggtcctagtg
ctggactgccagttagagaaattgcccatgaggccccgggaccggtcccgtgtgattgat
gctgccaaacatgcccataagttttgtaacacagaagatgaggagactatgtatctgcgg
agacctgaaggcattgaacgacagtacaggaagaaatgtgcaaagtgtggactgccgctc
ttctaccaatcccagccaaagaatgctcctgttaccttcattgtggatggagcagtagtc
aagtttggccagggctttgggaaaacgaacatatatactcagaaacaagagcctcctaag
aaggtgatgatgaccaaacggaccaaagacatgggcaagttcagttctgtcaccgtgtct
accattgatgaagaggaagaggagattgaggctagggaagttgctgactcatatgcacag
aatgccaaagtgattgaaaaacagctggagcgcaaaggcatgagcaagaggcgactgcaa
gagctggctgaattggaagccaagaaagcgaaaatgaaggggaccttgattgacaaccag
ttcaaataa

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