Homo sapiens (human): 54084
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Entry
54084 CDS
T01001
Symbol
TSPEAR, C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR
Name
(RefSeq) thrombospondin type laminin G domain and EAR repeats
KO
K24437
thrombospondin-type laminin G domain and EAR repeat-containing protein
Organism
hsa
Homo sapiens (human)
Disease
H00605
Deafness, autosomal recessive
H00625
Tooth agenesis
H02456
Ectodermal dysplasia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
54084 (TSPEAR)
04990 Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
54084 (TSPEAR)
Cilium and associated proteins [BR:
hsa03037
]
Other cilia and associated proteins
Stereociliary proteins
54084 (TSPEAR)
Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
Thrombospondin domain-containing proteins
Other thrombospondin domain-containing proteins
54084 (TSPEAR)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EPTP
Motif
Other DBs
NCBI-GeneID:
54084
NCBI-ProteinID:
NP_659428
OMIM:
612920
HGNC:
1268
Ensembl:
ENSG00000175894
UniProt:
Q8WU66
LinkDB
All DBs
Position
21:complement(44497893..44711572)
Genome browser
AA seq
669 aa
AA seq
DB search
MSALLSLCFVLPLAAPGHGTQGWEPCTDLRPLDILAEVVPSDGATSGIRIVQVHGARGLQ
LSVAAPRTMSFPASRIFSQCDLFPEEFSIVVTLRVPNLPPKRNEYLLTVVAEESDLLLLG
LRLSPAQLHFLFLREDTAGAWQTRVSFRSPALVDGRWHTLVLAVSAGVFSLTTDCGLPVD
IMADVPFPATLSVKGARFFVGSRRRAKGLFMGLVRQLVLLPGSDATPRLCPSRNAPLAVL
SIPRVLQALTGKPEDNEVLKYPYETNIRVTLGPQPPCTEVEDAQFWFDASRKGLYLCVGN
EWVSVLAAKERLDYVEEHQNLSTNSETLGIEVFRIPQVGLFVATANRKATSAVYKWTEEK
FVSYQNIPTHQAQAWRHFTIGKKIFLAVANFEPDEKGQEFSVIYKWSHRKLKFTPYQSIA
THSARDWEAFEVDGEHFLAVANHREGDNHNIDSVIYKWNPATRLFEANQTIATSGAYDWE
FFSVGPYSFLVVANTFNGTSTKVHSHLYIRLLGSFQLFQSFPTFGAADWEVFQIGERIFL
AVANSHSYDVEMQVQNDSYVINSVIYELNVTAQAFVKFQDILTCSALDWEFFSVGEDYFL
VVANSFDGRTFSVNSIIYRWQGYEGFVAVHSLPTVGCRDWEAFSTTAGAYLIYSSAKEPL
SRVLRLRTR
NT seq
2010 nt
NT seq
+upstream
nt +downstream
nt
atgtctgccctgctgagtctgtgttttgtgctgcccctggcggcccccggccacggcacg
cagggttgggagccctgcacagacctgcgccccctggacatcctggcggaagtggtccct
tctgatggcgccacaagcgggatcaggatagttcaggttcacggtgcacggggactccag
ctctcagtagccgccccccgcaccatgagcttcccagcatccaggattttctcccagtgt
gacctcttccctgaagaattttccatcgtcgtaactttgagagttcccaatcttccaccc
aagaggaacgagtacctgctgacggtggtggcagaggagagcgacctgctgctgctcggc
ctgcggttgtcacctgcccagctgcacttcctgttccttcgcgaggacacggccggcgcc
tggcagacccgagtgtccttccgcagcccggccctggtggatggccgctggcacacactg
gtcctggctgtgtccgcaggcgtcttctccctcaccacggactgcggcctcccggtggac
ataatggccgatgtgcccttcccagccaccctgtcagtgaaaggagctcgattcttcgtc
ggcagccggaggagagccaaaggcctgttcatgggactggtgaggcaactggtcctgctg
ccgggctcagacgccaccccaaggctgtgtcccagcaggaacgccccgctggcggtgctg
tccatcccacgggtcctgcaggctctcacggggaagccagaagataacgaggtgctaaaa
tatccctatgaaaccaacattcgagtgacgctgggaccccagccaccgtgtaccgaggtg
gaagacgcccagttctggtttgatgccagccggaagggcctgtatctgtgtgttggcaac
gagtgggtctccgtgttagcagccaaagaaagactggactacgtggaggagcatcagaac
ttgtccaccaactcagagaccctgggcattgaggtgttccgcatccctcaggtggggctc
tttgtggccacagccaatcgcaaagccacatccgccgtctacaagtggaccgaagagaag
ttcgtctcatatcagaacatccccacgcaccaagcacaggcctggaggcatttcaccatc
gggaaaaagatcttcctggcagtggctaattttgaaccagatgagaagggtcaggagttc
tctgtcatttacaaatggagccacagaaagctgaagtttaccccatatcagagcattgcc
acacacagcgcccgagactgggaggccttcgaggtggatggggagcacttcctggcggtg
gccaaccaccgggaaggcgacaaccacaacatcgacagtgtcatctacaagtggaacccg
gcaacccggctcttcgaggccaaccagaccatcgccacctccggcgcctacgactgggag
ttcttcagtgtggggccctactcgttcctggtggtggccaacaccttcaacggcacctcc
accaaggtgcactcgcacctctacatccgactcctgggctccttccagctcttccagtcc
ttcccgacgttcggtgctgcagactgggaggtcttccagatcggggagaggatcttcctc
gctgtggcaaacagtcacagctacgatgtggagatgcaagtccagaatgattcctatgtc
atcaactccgtcatctacgagctgaacgtgaccgcgcaggcctttgtcaagttccaggac
attctcacctgcagtgctctggactgggagtttttctcggtgggagaagattatttcctg
gtggtggccaactccttcgatgggcgtaccttctcggtgaacagtattatttacaggtgg
cagggctacgagggcttcgtggcggtgcacagcctccccaccgtcggctgcagggactgg
gaggccttcagcaccacggctggtgcctacctcatctactccagcgccaaggagcccctc
tccagggtcctgcggctgaggacacgctga
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