Homo sapiens (human): 54440
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Entry
54440 CDS
T01001
Symbol
SASH3, 753P9, CXorf9, HACS2, IMD102, SH3D6C, SLY
Name
(RefSeq) SAM and SH3 domain containing 3
KO
K23706
SAM and SH3 domain-containing protein 3
Organism
hsa
Homo sapiens (human)
Disease
H01725
Primary immunodeficiency disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04990 Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
54440 (SASH3)
Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
Src homology (SH) domain-containing proteins
Other SH2 and SH3-containing proteins
54440 (SASH3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
SPIDER
SAM_1
SAM_2
SH3_2
SH3_1
SH3_9
Motif
Other DBs
NCBI-GeneID:
54440
NCBI-ProteinID:
NP_061863
OMIM:
300441
HGNC:
15975
Ensembl:
ENSG00000122122
UniProt:
O75995
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All DBs
Position
X:129779949..129795201
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AA seq
380 aa
AA seq
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MLRRKPSNASEKEPTQKKKLSLQRSSSFKDFAKSKPSSPVVSEKEFNLDDNIPEDDSGVP
TPEDAGKSGKKLGKKWRAVISRTMNRKMGKMMVKALSEEMADTLEEGSASPTSPDYSLDS
PGPEKMALAFSEQEEHELPVLSRQASTGSELCSPSPGSGSFGEEPPAPQYTGPFCGRARV
HTDFTPSPYDHDSLKLQKGDVIQIIEKPPVGTWLGLLNGKVGSFKFIYVDVLPEEAVGHA
RPSRRQSKGKRPKPKTLHELLERIGLEEHTSTLLLNGYQTLEDFKELRETHLNELNIMDP
QHRAKLLTAAELLLDYDTGSEEAEEGAESSQEPVAHTVSEPKVDIPRDSGCFEGSESGRD
DAELAGTEEQLQGLSLAGAP
NT seq
1143 nt
NT seq
+upstream
nt +downstream
nt
atgctgcgccgcaagccctccaatgccagtgagaaggagcccactcagaagaaaaagctc
tcccttcagcgctccagcagcttcaaggattttgccaaatccaaacccagctcccccgtg
gtgagcgagaaggagtttaatctggatgataacattccagaagatgactcaggtgtcccc
accccagaagatgctgggaagagtggcaaaaagctggggaagaagtggagggcagtgatt
tcccgaaccatgaacaggaagatgggcaagatgatggtgaaggccctgtcagaagagatg
gcagacactctggaggagggctctgcctccccgacatctccagactacagcctggacagc
cctggccctgagaagatggcgctggccttttctgagcaagaggagcatgaacttccggtg
ctcagccgccaggcatcaacaggcagtgagctctgcagccccagcccaggttctggcagc
ttcggggaggaaccacctgccccccagtacacagggcctttctgtggccgggcacgagtc
cacaccgacttcactcccagcccctatgaccacgactcgctgaaactgcagaaaggagat
gtgatccagatcattgaaaagccacctgtgggcacgtggctgggcctactcaatggcaag
gtgggctctttcaaattcatctatgtggatgtgctgcccgaggaggccgtggggcatgcc
cgccccagccgccgacagagcaagggcaagaggcccaagcctaagaccctgcatgagctg
ctggagcgcatcggcctggaggagcacacatccaccctcctgctcaatggctaccagaca
ctggaagacttcaaagagctgcgagaaacacacctcaatgagctgaacatcatggatcca
cagcaccgggccaagctgctcacggccgccgagctgctgctggactatgacactggcagt
gaggaggctgaagagggcgccgagagcagccaggagccagtggcacacacagtgtcggaa
cccaaggtggacatcccgcgcgactcaggctgctttgagggctcggagagcgggcgcgat
gacgcagagctggcaggcactgaggagcagctgcaaggcctctccctggccggggcacct
tga
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