KEGG   Homo sapiens (human): 51259
Entry
51259             CDS       T01001                                 
Symbol
TMEM216, HSPC244, CORS2, MKS2
Name
(RefSeq) transmembrane protein 216
  KO
K19385  transmembrane protein 216
Organism
hsa  Homo sapiens (human)
Disease
H00261  Meckel syndrome
H00530  Joubert syndrome and related disorders
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    51259 (TMEM216)
Cilium and associated proteins [BR:hsa03037]
 Primary cilia and associated proteins
  MKS complex
   51259 (TMEM216)
SSDB
Motif
Pfam: Transmemb_17
Other DBs
NCBI-GeneID: 51259
NCBI-ProteinID: NP_001167461
OMIM: 613277
HGNC: 25018
Ensembl: ENSG00000187049
UniProt: Q9P0N5
LinkDB
Position
11:61392587..61398846
AA seq 145 aa
MLPRGLKMAPRGKRLSSTPLEILFFLNGWYNATYFLLELFIFLYKGVLLPYPTANLVLDV
VMLLLYLGIEVIRLFFGTKGNLCQRKMPLSISVALTFPSAMMASYYLLLQTYVLRLEAIM
NGILLFFCGSELLLEVLTLAAFSRI
NT seq 438 nt   +upstreamnt  +downstreamnt
atgctgccacggggactgaagatggcgccgcgaggtaaacggttgtcctccaccccgctg
gaaatcctgttctttctgaacgggtggtataatgctacctatttcctgctggaacttttc
atatttctgtataaaggtgtcctgctaccatatccaacagctaacctagtactggatgtg
gtgatgctcctcctttatcttggaattgaagtaattcgcctgttttttggtacaaaggga
aacctctgccagcgaaagatgccgctcagtattagcgtggccttgaccttcccatctgcc
atgatggcctcctattacctgctgctgcagacctacgtactccgcctggaagccatcatg
aatggcatcttgctcttcttctgtggctcagagcttttacttgaggtgctcaccttggct
gctttctccaggatttga

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