KEGG   Homo sapiens (human): 9338
Entry
9338              CDS       T01001                                 
Symbol
TCEAL1, HIJRS, NEDGFAX, SIIR, WEX9, p21, pp21
Name
(RefSeq) transcription elongation factor A like 1
  KO
K26769  transcription elongation factor A protein-like 1
Organism
hsa  Homo sapiens (human)
Disease
H02535  Neurodevelopmental disorder with dysmorphic facies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03021 Transcription machinery [BR:hsa03021]
    9338 (TCEAL1)
Transcription machinery [BR:hsa03021]
 Eukaryotic type
  RNA polymerase II system
   Other transcription-related factors
    Others
     9338 (TCEAL1)
SSDB
Motif
Pfam: BEX
Other DBs
NCBI-GeneID: 9338
NCBI-ProteinID: NP_001006640
OMIM: 300237
HGNC: 11616
Ensembl: ENSG00000172465
UniProt: Q15170
Position
X:103628716..103630953
AA seq 159 aa
MDKPRKENEEEPQSAPKTDEERPPVEHSPEKQSPEEQSSEEQSSEEEFFPEELLPELLPE
MLLSEERPPQEGLSRKDLFEGRPPMEQPPCGVGKHKLEEGSFKERLARSRPQFRGDIHGR
NLSNEEMIQAADELEEMKRVRNKLMIMHWKAKRSRPYPI
NT seq 480 nt   +upstreamnt  +downstreamnt
atggacaaaccacgcaaagaaaatgaagaagagccgcagagcgcgcccaagaccgatgag
gagaggcctccggtggagcactctcccgaaaagcagtcccccgaggagcagtcttcggag
gagcagtcctcggaggaggagttctttcctgaggagctcttgcctgagctcctgcctgag
atgctcctctcggaggagcgccctccgcaggagggtctttccaggaaggacctgtttgag
gggcgccctcccatggagcagcctccttgtggagtaggaaaacataagcttgaagaagga
agctttaaagaaaggttggctcgttctcgcccgcaatttagaggggacatacatggcaga
aatttaagcaatgaggagatgatacaggcagcagatgagctagaagagatgaaaagagta
agaaacaaactgatgataatgcactggaaggcaaaacggagccgtccttatcctatttaa

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