KEGG   Homo sapiens (human): 2036
Entry
2036              CDS       T01001                                 
Symbol
EPB41L1, 4.1N, MRD11
Name
(RefSeq) erythrocyte membrane protein band 4.1 like 1
  KO
K23961  band 4.1-like protein 1/2/3
Organism
hsa  Homo sapiens (human)
Disease
H00773  Autosomal dominant intellectual developmental disorder
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]
    2036 (EPB41L1)
Domain-containing proteins not elsewhere classified [BR:hsa04990]
 Other domain-containing proteins
  FERM domain-containing proteins
   2036 (EPB41L1)
SSDB
Motif
Pfam: 4_1_CTD FERM_C FERM_M FERM_N FA SAB
Other DBs
NCBI-GeneID: 2036
NCBI-ProteinID: NP_036288
OMIM: 602879
HGNC: 3378
Ensembl: ENSG00000088367
UniProt: Q9H4G0
Position
20:36091414..36232799
AA seq 881 aa
MTTETGPDSEVKKAQEEAPQQPEAAAAVTTPVTPAGHGHPEANSNEKHPSQQDTRPAEQS
LDMEEKDYSEADGLSERTTPSKAQKSPQKIAKKYKSAICRVTLLDASEYECEVEKHGRGQ
VLFDLVCEHLNLLEKDYFGLTFCDADSQKNWLDPSKEIKKQIRSSPWNFAFTVKFYPPDP
AQLTEDITRYYLCLQLRADIITGRLPCSFVTHALLGSYAVQAELGDYDAEEHVGNYVSEL
RFAPNQTRELEERIMELHKTYRGMTPGEAEIHFLENAKKLSMYGVDLHHAKDSEGIDIML
GVCANGLLIYRDRLRINRFAWPKILKISYKRSNFYIKIRPGEYEQFESTIGFKLPNHRSA
KRLWKVCIEHHTFFRLVSPEPPPKGFLVMGSKFRYSGRTQAQTRQASALIDRPAPFFERS
SSKRYTMSRSLDGAEFSRPASVSENHDAGPDGDKRDEDGESGGQRSEAEEGEVRTPTKIK
ELKPEQETTPRHKQEFLDKPEDVLLKHQASINELKRTLKEPNSKLIHRDRDWERERRLPS
SPASPSPKGTPEKANERAGLREGSEEKVKPPRPRAPESDTGDEDQDQERDTVFLKDNHLA
IERKCSSITVSSTSSLEAEVDFTVIGDYHGSAFEDFSRSLPELDRDKSDSDTEGLLFSRD
LNKGAPSQDDESGGIEDSPDRGACSTPDMPQFEPVKTETMTVSSLAIRKKIEPEAVLQTR
VSAMDNTQQVDGSASVGREFIATTPSITTETISTTMENSLKSGKGAAAMIPGPQTVATEI
RSLSPIIGKDVLTSTYGATAETLSTSTTTHVTKTVKGGFSETRIEKRIIITGDEDVDQDQ
ALALAIKEAKLQHPDMLVTKAVVYRETDPSPEERDKKPQES
NT seq 2646 nt   +upstreamnt  +downstreamnt
atgacaacagagacaggccccgactctgaggtgaagaaagctcaggaggaggccccgcag
cagcccgaggctgctgccgctgtgaccacccctgtgacccctgcaggccacggccaccca
gaggccaactccaatgagaagcatccatcccagcaggacacgcggcctgctgaacagagc
ctagacatggaggagaaggactacagtgaggccgatggcctttcggagaggaccacgccc
agcaaggcccagaaatcgccccagaagattgccaagaaatacaagagtgccatctgccgg
gtcactctgcttgatgcctcggagtatgagtgtgaggtggagaaacatggccggggccag
gtgctgtttgacctggtctgtgaacacctcaacctcctagagaaggactacttcggcctg
accttctgtgatgctgacagccagaagaactggctggacccctccaaggagatcaagaag
cagatccggagtagcccctggaattttgccttcacagtcaagttctacccgcctgatcct
gcccagctgacagaagacatcacaagatactacctgtgcctgcagctgcgggcagacatc
atcacgggccggctgccatgctcctttgtcacgcatgccctactgggctcctacgctgtg
caggctgagctgggtgactatgatgctgaggagcatgtgggcaactatgtcagcgagctc
cgcttcgcccctaaccagacccgggagctggaggagaggatcatggagctgcataagaca
tatagggggatgaccccgggagaagcagaaatccacttcttagagaatgccaagaagctt
tccatgtacggagtagacctgcaccatgccaaggactctgagggcatcgacatcatgtta
ggcgtttgtgccaatggcctgctcatctaccgggaccggctgagaatcaaccgctttgcc
tggcccaagatcctcaagatctcctacaagaggagtaacttctatatcaagatccggcct
ggggagtatgagcaatttgagagcacaattggctttaagctcccaaaccaccggtcagcc
aagagactgtggaaggtctgcatcgagcatcatacattcttccggctggtgtcccctgag
cccccacccaagggcttcctggtgatgggctccaagttccggtacagtgggaggacccag
gcacagactcgccaggccagcgccctcattgaccggcctgcacccttctttgagcgttct
tccagcaaacggtacaccatgtcccgcagccttgatggagcagagttctcccgcccagcc
tcggtcagcgagaaccatgatgcagggcctgacggtgacaagcgggatgaggatggcgag
tctggggggcaacggtcagaggctgaggagggagaggtcaggactccaaccaagatcaag
gagctaaagccggagcaggaaaccacgccgagacacaagcaggagttcttagacaagcca
gaagatgtcttgctgaagcaccaggccagcatcaatgagctcaaaaggaccctgaaggag
cccaacagcaaactcatccaccgggatcgagactgggaacgggagcgcaggctgccctcc
tcccccgcctccccctcccccaagggcacccctgagaaagccaatgagagagcagggctg
agggagggctccgaggagaaagtcaaaccaccacgtccccgggccccagagagtgacaca
ggcgatgaggaccaggaccaggagagggacacggtgttcctgaaggacaaccacctggcc
attgagcgcaagtgctccagcatcacggtcagctctacgtctagcctggaggctgaggtg
gacttcacggtcattggtgactaccatggcagcgccttcgaagacttctcccgcagcctg
cctgagctcgaccgggacaaaagcgactcggacactgagggcctgctgttctcccgggat
ctcaacaagggggcccccagccaggatgatgagtctgggggcattgaggacagcccggat
cgaggggcctgctccaccccggatatgccccagtttgagcccgtgaaaacagaaaccatg
actgtcagcagtctggccattagaaagaagattgagccggaggccgtactgcagaccaga
gtctccgctatggataacacccagcaggttgatgggagtgcctcagtggggagggagttc
atagcaaccactccctccatcaccacggagaccatatcgaccaccatggagaacagtctc
aagtccgggaagggggcagctgccatgatcccaggcccacagacggtggccacggaaatc
cgttctctttctccgatcatcgggaaagatgtcctcaccagcacctacggcgccactgcg
gaaaccctctcaacctccaccaccacccatgtcaccaaaactgtgaaaggagggttttct
gagacaaggatcgagaagcgaatcatcattactggggatgaagatgtcgatcaagaccag
gccctggctttggccatcaaggaggccaaactgcagcatcctgatatgctggtaaccaaa
gctgtcgtatacagagaaacagacccatccccagaggagagggacaagaagccacaggaa
tcctga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (19)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (11)   
   OC (1)   
Protein sequence (69)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (67)   
DNA sequence (95)   
   RefSeq(nuc) (67)   
   GenBank (14)   
   EMBL (14)   
Protein domain (6)   
   Pfam (6)   
All databases (195)   

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