Homo sapiens (human): 135886
Help
Entry
135886 CDS
T01001
Symbol
TMEM270, WBSCR28
Name
(RefSeq) transmembrane protein 270
Organism
hsa
Homo sapiens (human)
Disease
H01439
Williams-Beuren syndrome
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
WBS28
Motif
Other DBs
NCBI-GeneID:
135886
NCBI-ProteinID:
NP_872310
OMIM:
612547
HGNC:
23018
Ensembl:
ENSG00000175877
UniProt:
Q6UE05
LinkDB
All DBs
Position
7:73860848..73865890
Genome browser
AA seq
265 aa
AA seq
DB search
MEALPPVRSSLLGILLQVTRLSVLLVQNRDHLYNFLLLKINLFNHWVSGLAQEARGSCNW
QAHLPLGAAACPLGQALWAGLALIQVPVWLVLQGPRLMWAGMWGSTKGLGLALLSAWEQL
GLSVAIWTDLFLSCLHGLMLVALLLVVVTWRVCQKSHCFRLGRQLSKALQVNCVVRKLLV
QLRRLYWWVETMTALTSWHLAYLITWTTCLASHLLQAAFEHTTQLAEAQEVEPQEVSGSS
LLPSLSASSDSESGTVLPEQETPRE
NT seq
798 nt
NT seq
+upstream
nt +downstream
nt
atggaggcccttcctccagtcagatccagccttttggggatcctgttgcaggttacgagg
ctctcagtgctgttggttcagaaccgagatcacctctataatttcctgctcctcaagatc
aacctcttcaaccactgggtgtcagggctggcccaggaggcccgggggtcctgtaactgg
caggcccacctacccctgggagctgcagcctgccccctgggccaggctctctgggctggg
ctggctctgatacaggtccccgtatggctggtgctacagggacccaggctgatgtgggct
ggcatgtggggcagcaccaagggcctgggcctggccttgctcagtgcctgggagcagctg
ggcctgtctgtggccatctggacagatctgtttttgtcatgtctgcacggcctgatgttg
gtggccttgctcttggtggtagtgacctggagggtgtgtcagaagtcccactgcttccga
ctgggcaggcagctcagtaaggccttgcaagtgaactgcgtggtaaggaagctcctggta
cagctgagacgtctgtattggtgggtggagactatgactgccctcacctcctggcacctg
gcctatctcatcacctggaccacctgcctggcctcccacctgctgcaggctgcctttgag
cacacgacccagctggccgaggcccaggaggttgaaccccaggaggtctcagggtcttcc
ttgctgccctcactgtctgcgtcctcggactcagagtctggaacagttttgccagagcaa
gaaactcccagagaataa
DBGET
integrated database retrieval system