Homo sapiens (human): 55858
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Entry
55858 CDS
T01001
Symbol
TMEM165, CDG2K, FT27, GDT1, SLC64A1, TMPT27, TPARL
Name
(RefSeq) transmembrane protein 165
KO
K23541
Ca2+/H+ antiporter, TMEM165/GDT1 family
Organism
hsa
Homo sapiens (human)
Disease
H00119
Congenital disorders of glycosylation type II
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
55858 (TMEM165)
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
55858 (TMEM165)
Membrane trafficking [BR:
hsa04131
]
Endosome - Golgi transport
Others
Others
55858 (TMEM165)
Transporters [BR:
hsa02000
]
Other transporters
Electrochemical potential-driven transporters [TC:
2
]
55858 (TMEM165)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
UPF0016
Mntp
Motif
Other DBs
NCBI-GeneID:
55858
NCBI-ProteinID:
NP_060945
OMIM:
614726
HGNC:
30760
Ensembl:
ENSG00000134851
UniProt:
Q9HC07
LinkDB
All DBs
Position
4:55395957..55453397
Genome browser
AA seq
324 aa
AA seq
DB search
MAAAAPGNGRASAPRLLLLFLVPLLWAPAAVRAGPDEDLSHRNKEPPAPAQQLQPQPVAV
QGPEPARVEKIFTPAAPVHTNKEDPATQTNLGFIHAFVAAISVIIVSELGDKTFFIAAIM
AMRYNRLTVLAGAMLALGLMTCLSVLFGYATTVIPRVYTYYVSTVLFAIFGIRMLREGLK
MSPDEGQEELEEVQAELKKKDEEFQRTKLLNGPGDVETGTSITVPQKKWLHFISPIFVQA
LTLTFLAEWGDRSQLTTIVLAAREDPYGVAVGGTVGHCLCTGLAVIGGRMIAQKISVRTV
TIIGGIVFLAFAFSALFISPDSGF
NT seq
975 nt
NT seq
+upstream
nt +downstream
nt
atggcggccgcggctccagggaacggccgcgcatcggcgccccggctgcttctgctcttt
ctggttccgctgctgtgggccccggctgcggtccgggccggcccagatgaagaccttagc
caccggaacaaagaaccgccggcgccggcccagcagctgcagccgcagcctgtggctgtg
cagggccccgagccggcccgggtcgagaaaatatttacaccagcagctccagttcatacc
aataaagaagatcctgctacccaaactaatttgggatttatccatgcatttgtcgctgcc
atatcagttattattgtatctgaattgggtgataagacattttttatagcagccatcatg
gcaatgcgctataaccgcctgaccgtgctggctggtgcaatgcttgccttgggactaatg
acatgcttgtcagttttgtttggctatgccaccacagtcatccccagggtctatacatac
tatgtttcaactgtattatttgccatttttggcattagaatgcttcgggaaggcttaaag
atgagccctgatgagggtcaagaggaactggaagaagttcaagctgaattaaagaagaaa
gatgaagaatttcaacgaaccaaacttttaaatggaccgggagatgttgaaacgggtaca
agcataacagtacctcagaaaaagtggttgcattttatttcacccatttttgttcaagct
cttacattaacattcttagcagaatggggtgatcgctctcaactaactacaattgtattg
gcagctagagaggacccctatggtgtagccgtgggtggaactgtggggcactgcctgtgc
acgggattggcagtaattggaggaagaatgatagcacagaaaatctctgtcagaactgtg
acaatcataggaggcatcgtttttttggcgtttgcattttctgcactatttataagccct
gattctggtttttaa
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