Homo sapiens (human): 2038
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Entry
2038 CDS
T01001
Symbol
EPB42, PA, SPH5
Name
(RefSeq) protein 4.2 isoform 2
KO
K25094
erythrocyte membrane protein band 4.2
Organism
hsa
Homo sapiens (human)
Disease
H00230
Hereditary spherocytosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
2038 (EPB42)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Actin filaments / Microfilaments
Actin-binding proteins
Others
2038 (EPB42)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Transglut_C
Transglut_N
Transglut_core
A2M
LysM2_NFP
Motif
Other DBs
NCBI-GeneID:
2038
NCBI-ProteinID:
NP_001107606
OMIM:
177070
HGNC:
3381
Ensembl:
ENSP00000396616.2
UniProt:
P16452
Structure
PDB
PDBj
LinkDB
All DBs
Position
15:complement(43197227..43225737)
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AA seq
691 aa
AA seq
DB search
MGQALGIKSCDFQAARNNEEHHTKALSSRRLFVRRGQPFTIILYFRAPVRAFLPALKKVA
LTAQTGEQPSKINRTQATFPISSLGDRKWWSAVVEERDAQSWTISVTTPADAVIGHYSLL
LQVSGRKQLLLGQFTLLFNPWNREDAVFLKNEAQRMEYLLNQNGLIYLGTADCIQAESWD
FGQFEGDVIDLSLRLLSKDKQVEKWSQPVHVARVLGALLHFLKEQRVLPTPQTQATQEGA
LLNKRRGSVPILRQWLTGRGRPVYDGQAWVLAAVACTVLRCLGIPARVVTTFASAQGTGG
RLLIDEYYNEEGLQNGEGQRGRIWIFQTSTECWMTRPALPQGYDGWQILHPSAPNGGGVL
GSCDLVPVRAVKEGTLGLTPAVSDLFAAINASCVVWKCCEDGTLELTDSNTKYVGNNIST
KGVGSDRCEDITQNYKYPEGSLQEKEVLERVEKEKMEREKDNGIRPPSLETASPLYLLLK
APSSLPLRGDAQISVTLVNHSEQEKAVQLAIGVQAVHYNGVLAAKLWRKKLHLTLSANLE
KIITIGLFFSNFERNPPENTFLRLTAMATHSESNLSCFAQEDIAICRPHLAIKMPEKAEQ
YQPLTASVSLQNSLDAPMEDCVISILGRGLIHRERSYRFRSVWPENTMCAKFQFTPTHVG
LQRLTVEVDCNMFQNLTNYKSVTVVAPELSA
NT seq
2076 nt
NT seq
+upstream
nt +downstream
nt
atgggacaggccctgggtatcaagagctgtgactttcaggcagcaagaaacaatgaggag
caccacaccaaggccctcagctcccggcgcctctttgtgaggagggggcagcccttcacc
atcatcctgtacttccgcgctccagtccgtgcatttctgcctgccctgaagaaggtggcc
ctcactgcacaaactggagagcagccttccaagatcaacaggacccaagccacattccca
atttccagtctgggggaccgaaagtggtggagtgcagtggtggaggagagagatgcccag
tcctggaccatctctgtgaccacacctgcggacgctgtcattggccactactcgcttctg
ctgcaggtctcaggcaggaagcaactcctcttgggtcagttcacactgctttttaacccc
tggaatagagaggatgctgtgttcctgaagaatgaggctcagcgcatggagtacttgttg
aaccagaatggtctcatctacctgggtacagctgactgcatccaggcagagtcctgggac
tttggccagttcgagggggatgtcattgacctcagcctgcgcttgctgagcaaggacaag
caggtagagaagtggagccagccggtgcacgtggcccgtgtgttgggtgccttgctgcat
tttctcaaggagcagagggtcctgcccaccccgcagacccaggccacccaggaaggggcc
ttgctgaacaagcgccggggcagcgtgcccatcctgcggcagtggctcaccggccgaggc
cgacctgtgtatgatggccaggcctgggtgttggctgctgttgcttgcacagtgctgcga
tgcctgggaatccctgcccgcgtggtgaccacgtttgcctcagcacagggcaccggtggg
cgtcttctcatagatgaatactataatgaggagggacttcagaacggagaaggccagaga
ggcagaatctggatcttccagacttccacagagtgctggatgacgcggcctgccttgccc
cagggttatgatggatggcagattctgcacccaagtgctcctaatggaggtggagtcctg
gggtcctgtgatctggtgccggtcagagcagtcaaggaggggacgctggggctgacccca
gcagtgtcagacctttttgctgccataaatgcctcatgtgtggtctggaagtgctgtgag
gatgggacactggagttgactgactccaacacaaagtatgttggcaacaacatcagcacc
aagggtgtgggcagtgaccgctgcgaggacatcactcagaactacaagtatcctgaaggg
tctcttcaggaaaaagaggtgctggagagagtcgagaaagagaaaatggaacgtgagaaa
gacaacggcatccgtcctcccagtctcgagactgccagtcctctgtacctgctcttgaaa
gcacccagctccctacccctgagaggggatgcccagatctcagtgacgctggttaatcac
agtgagcaggagaaggcagtgcagctggcaattggggtccaggctgtacactacaacggt
gtccttgctgccaagctctggaggaagaagctgcacctcacgctcagtgccaacctggaa
aagataataaccatcggcctgttcttctccaattttgagcgaaacccacccgagaacacc
ttccttagactcaccgccatggcaacacactctgaatccaaccttagctgctttgctcag
gaagacattgccatttgtagaccacaccttgccatcaagatgccagagaaagcagagcag
tatcaacccctcacagcctcagtcagcctccagaactccctagatgcccccatggaggac
tgtgtgatctccatcctgggaagggggctcattcacagagagaggagctacagattccgt
tcagtgtggcctgaaaacaccatgtgtgccaagttccagttcacgccaacacatgtgggg
ctccagagactcactgtggaagtggactgcaacatgttccagaacctaaccaactataaa
agcgtcaccgtggtagcccctgaactatcagcttaa
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