KEGG   Homo sapiens (human): 10943
Entry
10943             CDS       T01001                                 
Symbol
MSL3, MRSXBA, MRXS36, MRXSBA, MSL3L1
Name
(RefSeq) MSL complex subunit 3 isoform a
  KO
K18403  male-specific lethal 3
Organism
hsa  Homo sapiens (human)
Disease
H00658  X-linked syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    10943 (MSL3)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   HAT complexes
    MSL complex
     10943 (MSL3)
SSDB
Motif
Pfam: MRG MSL3_chromo-like Tudor-knot Chromo
Other DBs
NCBI-GeneID: 10943
NCBI-ProteinID: NP_523353
OMIM: 300609
HGNC: 7370
Ensembl: ENSP00000312244.4
UniProt: Q8N5Y2
Structure
Position
X:11758159..11775772
AA seq 521 aa
MSASEGMKFKFHSGEKVLCFEPDPTKARVLYDAKIVDVIVGKDEKGRKIPEYLIHFNGWN
RSWDRWAAEDHVLRDTDENRRLQRKLARKAVARLRSTGRKKKRCRLPGVDSVLKGLPTEE
KDENDENSLSSSSDCSENKDEEISEESDIEEKTEVKEEPELQTRREMEERTITIEIPEVL
KKQLEDDCYYINRRKRLVKLPCQTNIITILESYVKHFAINAAFSANERPRHHHVMPHANM
NVHYIPAEKNVDLCKEMVDGLRITFDYTLPLVLLYPYEQAQYKKVTSSKFFLPIKESATS
TNRSQEELSPSPPLLNPSTPQSTESQPTTGEPATPKRRKAEPEALQSLRRSTRHSANCDR
LSESSASPQPKRRQQDTSASMPKLFLHLEKKTPVHSRSSSPIPLTPSKEGSAVFAGFEGR
RTNEINEVLSWKLVPDNYPPGDQPPPPSYIYGAQHLLRLFVKLPEILGKMSFSEKNLKAL
LKHFDLFLRFLAEYHDDFFPESAYVAACEAHYSTKNPRAIY
NT seq 1566 nt   +upstreamnt  +downstreamnt
atgagcgcgagcgagggcatgaaatttaaattccactcaggggagaaagtgctgtgcttc
gagcctgaccccaccaaggcgcgagtgctgtacgatgccaagattgttgatgttattgtt
gggaaagacgaaaaaggcagaaagatcccagaatatctgatccattttaatggttggaac
agaagctgggatagatgggcagcagaagatcatgtgcttcgtgataccgatgaaaatcgt
agattacagcgtaaattggcaagaaaagctgtagctcgcctgaggagcacaggaagaaag
aagaagcgctgcaggttgcctggtgtggactctgtcttaaaaggcctccccactgaagaa
aaagatgaaaatgatgaaaactcattaagcagttcctctgactgtagtgaaaacaaggat
gaagaaataagtgaagaaagtgatattgaagaaaagactgaagtgaaagaagaaccagag
cttcaaacaagaagggaaatggaagaaagaacaataactatagaaatccctgaagttctg
aagaagcagctggaggatgattgttactacattaacaggaggaaacggttagtgaaactt
ccatgccagaccaacatcataacgattttggaatcctatgtgaagcattttgctatcaat
gcagccttttcagccaatgagaggcctcgtcaccatcacgttatgccacatgccaacatg
aacgtgcattatatcccagcagaaaagaatgttgacctttgtaaggagatggtggatgga
ttaagaataacctttgattacactctcccgttggttttactctatccatatgaacaagct
cagtataaaaaggtgacttcgtctaaattttttcttccaattaaggaaagtgccacaagc
actaacaggagccaggaggaactctctcccagtccgcctttgttgaatccatccacgcca
cagtccacagagagtcagccgaccaccggtgaaccagccacccccaaaaggcgcaaagct
gagccagaagcattgcagtctctgaggcggtccacgcgccacagtgccaactgtgacagg
ctttctgagagcagcgcttcacctcagcccaagcgccggcagcaggacacatccgccagc
atgcccaagctcttcctgcacctggaaaagaagacacctgtgcatagcagatcatcttca
cctattcctctgactcctagcaaggaagggagtgctgtgtttgctggctttgaagggaga
agaactaatgaaataaacgaggtcctctcctggaagcttgtgcctgacaattacccccca
ggtgaccagccgcctccaccctcttacatttatggggcacaacatttgctgcgattgttt
gtgaaacttccagaaatccttggaaagatgtccttttctgagaagaatctgaaggcttta
ttgaagcactttgatctctttttgaggtttttagcagaataccacgatgacttcttccca
gagtcggcttatgtcgctgcctgtgaggcacattacagcaccaagaacccccgggcaatt
tattaa

  All links  
Disease (2)   
   OMIM (2)   
Gene (14)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (7)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (46)   
   RefSeq(nuc) (6)   
   GenBank (20)   
   EMBL (20)   
3D Structure (3)   
   PDB (3)   
Protein domain (4)   
   Pfam (4)   
All databases (76)   

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