Homo sapiens (human): 26022
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Entry
26022 CDS
T01001
Symbol
TMEM98, TADA1
Name
(RefSeq) transmembrane protein 98
KO
K25292
transmembrane protein 98
Organism
hsa
Homo sapiens (human)
Disease
H02172
Nanophthalmos
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
26022 (TMEM98)
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GFIT
Motif
Pfam:
GCIP_C
FAM163
Motif
Other DBs
NCBI-GeneID:
26022
NCBI-ProteinID:
NP_001028676
OMIM:
615949
HGNC:
24529
Ensembl:
ENSG00000006042
UniProt:
Q9Y2Y6
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Position
17:32928153..32944315
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AA seq
226 aa
AA seq
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METVVIVAIGVLATIFLASFAALVLVCRQRYCRPRDLLQRYDSKPIVDLIGAMETQSEPS
ELELDDVVITNPHIEAILENEDWIEDASGLMSHCIAILKICHTLTEKLVAMTMGSGAKMK
TSASVSDIIVVAKRISPRVDDVVKSMYPPLDPKLLDARTTALLLSVSHLVLVTRNACHLT
GGLDWIDQSLSAAEEHLEVLREAALASEPDKGLPGPEGFLQEQSAI
NT seq
681 nt
NT seq
+upstream
nt +downstream
nt
atggagactgtggtgattgttgccataggtgtgctggccaccatctttctggcttcgttt
gcagccttggtgctggtttgcaggcagcgctactgccggccgcgagacctgctgcagcgc
tatgattctaagcccattgtggacctcattggtgccatggagacccagtctgagccctct
gagttagaactggacgatgtcgttatcaccaacccccacattgaggccattctggagaat
gaagactggatcgaagatgcctcgggtctcatgtcccactgcattgccatcttgaagatt
tgtcacactctgacagagaagcttgttgccatgacaatgggctctggggccaagatgaag
acttcagccagtgtcagcgacatcattgtggtggccaagcggatcagccccagggtggat
gatgttgtgaagtcgatgtaccctccgttggaccccaaactcctggacgcacggacgact
gccctgctcctgtctgtcagtcacctggtgctggtgacaaggaatgcctgccatctgacg
ggaggcctggactggattgaccagtctctgtcggctgctgaggagcatttggaagtcctt
cgagaagcagccctagcttctgagccagataaaggcctcccaggccctgaaggcttcctg
caggagcagtctgcaatttag
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