Homo sapiens (human): 147138
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Entry
147138 CDS
T01001
Symbol
TMC8, EV2, EVER2, EVIN2
Name
(RefSeq) transmembrane channel like 8
KO
K21988
transmembrane channel-like protein
Organism
hsa
Homo sapiens (human)
Disease
H00842
Epidermodysplasia verruciformis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
147138 (TMC8)
03037 Cilium and associated proteins [BR:
hsa03037
]
147138 (TMC8)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
147138 (TMC8)
Cilium and associated proteins [BR:
hsa03037
]
Other cilia and associated proteins
Stereociliary proteins
147138 (TMC8)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TMC
DUF4423_like
DUF4658
Motif
Other DBs
NCBI-GeneID:
147138
NCBI-ProteinID:
NP_689681
OMIM:
605829
HGNC:
20474
Ensembl:
ENSG00000167895
UniProt:
Q8IU68
B3KXZ8
LinkDB
All DBs
Position
17:78130771..78142968
Genome browser
AA seq
726 aa
AA seq
DB search
MLLPRSVSSERAPGVPEPEELWEAEMERLRGSGTPVRGLPYAMMDKRLIWQLREPAGVQT
LRWQRWQRRRQTVERRLREAAQRLARGLGLWEGALYEIGGLFGTGIRSYFTFLRFLLLLN
LLSLLLTASFVLLPLVWLRPPDPGPTLNLTLQCPGSRQSPPGVLRFHNQLWHVLTGRAFT
NTYLFYGAYRVGPESSSVYSIRLAYLLSPLACLLLCFCGTLRRMVKGLPQKTLLGQGYQA
PLSAKVFSSWDFCIRVQEAATIKKHEISNEFKVELEEGRRFQLMQQQTRAQTACRLLSYL
RVNVLNGLLVVGAISAIFWATKYSQDNKEESLFLLLQYLPPGVIALVNFLGPLLFTFLVQ
LENYPPNTEVNLTLIWCVVLKLASLGMFSVSLGQTILCIGRDKSSCESYGYNVCDYQCWE
NSVGEELYKLSIFNFLLTVAFAFLVTLPRRLLVDRFSGRFWAWLEREEFLVPKNVLDIVA
GQTVTWMGLFYCPLLPLLNSVFLFLTFYIKKYTLLKNSRASSRPFRASSSTFFFQLVLLL
GLLLAAVPLGYVVSSIHSSWDCGLFTNYSAPWQVVPELVALGLPPIGQRALHYLGSHAFS
FPLLIMLSLVLTVCVSQTQANARAIHRLRKQLVWQVQEKWHLVEDLSRLLPEPGPSDSPG
PKYPASQASRPQSFCPGCPCPGSPGHQAPRPGPSVVDAAGLRSPCPGQHGAPASARRFRF
PSGAEL
NT seq
2181 nt
NT seq
+upstream
nt +downstream
nt
atgctgctgccgcggtcggtgtcatcggagcgggcccctggggtgccggagccggaggag
ctgtgggaggcagagatggagcggctgcgcggctctgggacgcccgtgcgcgggctgccc
tatgccatgatggacaagcgcctcatctggcagctgcgggagcccgcgggggtgcagacc
ttgcgctggcagcggtggcagcgccggcggcagacggtggaaaggcgcctgcgggaggca
gcgcagcggctggcccggggccttgggctctgggagggggcgctctacgagatcgggggc
ctcttcggcacaggaattcggtcctacttcaccttcctccgcttcctgctgctactcaac
ctgctgagcctgctgctcaccgcaagcttcgtgctgctgcccctggtctggctccgcccc
cctgacccaggccccaccctgaacttgaccctccagtgccctggtagccgccagtccccg
cctggcgttttgaggttccacaatcaactttggcatgttttgactggcagggccttcacc
aacacctatctcttctacggtgcgtaccgagtggggccggagagcagctccgtgtacagc
atccgcctggcctacctcctcagcccgctggcctgcctgctcctctgcttctgtgggact
ctgcggcggatggtgaaggggctgccgcagaagactctgctgggtcagggctatcaggcg
cctctcagcgccaaggtcttctcctcatgggacttctgcatccgggtgcaggaagcagcc
accatcaagaagcatgagatcagcaacgagttcaaggtggagctggaggagggccgtcgc
ttccagctgatgcagcagcagacccgggcccagacggcctgccgcctgctctcctacctg
cgggtcaacgtactcaacgggctcctggtggttggggccatcagcgccatcttctgggct
accaagtactcacaggacaacaaggaggagtccctgtttctgctgctccagtacctgccc
cctggggtcatcgccctggtcaacttcctgggtcccctgctgttcacatttctggtccag
ctggagaactaccctcccaacacggaggtcaacctcactctgatctggtgcgtggtgctg
aagctggccagcttggggatgttctccgtctccctgggtcagaccatactgtgcattggc
agagacaagagcagctgtgagtcctacggctacaacgtttgtgactatcagtgctgggag
aactccgtgggggaggagctgtacaagctgagtatcttcaacttcctcctcaccgtggcc
ttcgccttcctggtcaccctgcctcggaggctgctggtggaccggttctcaggccggttc
tgggcctggctggaacgggaggagttcctggtccccaagaatgtgctggacatcgtggcg
gggcagacggtcacctggatgggcctcttctactgccccctgctgcccctgctgaatagc
gtcttcctcttcctcaccttctacatcaagaagtacaccctcctgaagaactccagggca
tcttcgcggcccttccgtgcctccagctccaccttcttcttccagctagtgctcctcctg
ggcctgcttctggctgcagtgcccctgggctatgtggtcagcagcatccactcctcctgg
gactgcggcctcttcaccaactactcagcaccctggcaagtggtcccggagctggtggcc
cttgggctcccgcccattggccagcgtgccctccactacctgggctcccacgccttcagc
ttccccctcctcatcatgctcagccttgtcctgacggtgtgcgtctcccagacccaggcc
aatgccagggccatccacaggctccggaagcagctggtgtggcaggttcaggagaagtgg
cacctggtggaggacctgtcgcgactgctgccggagccaggcccgagcgactctccgggc
cccaagtaccctgcctcccaagcttcgcgcccgcagtccttctgccccggatgcccatgc
cctggctccccgggccaccaggccccgcggccgggcccctccgtcgtggatgccgcggga
ctgcgttccccttgccctggacagcacggtgccccggcctccgcccgcagattccgcttc
cccagcggcgcggagctgtaa
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