Homo sapiens (human): 51259
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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)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Transmemb_17
Motif
Other DBs
NCBI-GeneID:
51259
NCBI-ProteinID:
NP_001167461
OMIM:
613277
HGNC:
25018
Ensembl:
ENSG00000187049
UniProt:
Q9P0N5
LinkDB
All DBs
Position
11:61392587..61398846
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AA seq
145 aa
AA seq
DB search
MLPRGLKMAPRGKRLSSTPLEILFFLNGWYNATYFLLELFIFLYKGVLLPYPTANLVLDV
VMLLLYLGIEVIRLFFGTKGNLCQRKMPLSISVALTFPSAMMASYYLLLQTYVLRLEAIM
NGILLFFCGSELLLEVLTLAAFSRI
NT seq
438 nt
NT seq
+upstream
nt +downstream
nt
atgctgccacggggactgaagatggcgccgcgaggtaaacggttgtcctccaccccgctg
gaaatcctgttctttctgaacgggtggtataatgctacctatttcctgctggaacttttc
atatttctgtataaaggtgtcctgctaccatatccaacagctaacctagtactggatgtg
gtgatgctcctcctttatcttggaattgaagtaattcgcctgttttttggtacaaaggga
aacctctgccagcgaaagatgccgctcagtattagcgtggccttgaccttcccatctgcc
atgatggcctcctattacctgctgctgcagacctacgtactccgcctggaagccatcatg
aatggcatcttgctcttcttctgtggctcagagcttttacttgaggtgctcaccttggct
gctttctccaggatttga
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integrated database retrieval system