Homo sapiens (human): 9338
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
BEX
Motif
Other DBs
NCBI-GeneID:
9338
NCBI-ProteinID:
NP_001006640
OMIM:
300237
HGNC:
11616
Ensembl:
ENSG00000172465
UniProt:
Q15170
LinkDB
All DBs
Position
X:103628716..103630953
Genome browser
AA seq
159 aa
AA seq
DB search
MDKPRKENEEEPQSAPKTDEERPPVEHSPEKQSPEEQSSEEQSSEEEFFPEELLPELLPE
MLLSEERPPQEGLSRKDLFEGRPPMEQPPCGVGKHKLEEGSFKERLARSRPQFRGDIHGR
NLSNEEMIQAADELEEMKRVRNKLMIMHWKAKRSRPYPI
NT seq
480 nt
NT seq
+upstream
nt +downstream
nt
atggacaaaccacgcaaagaaaatgaagaagagccgcagagcgcgcccaagaccgatgag
gagaggcctccggtggagcactctcccgaaaagcagtcccccgaggagcagtcttcggag
gagcagtcctcggaggaggagttctttcctgaggagctcttgcctgagctcctgcctgag
atgctcctctcggaggagcgccctccgcaggagggtctttccaggaaggacctgtttgag
gggcgccctcccatggagcagcctccttgtggagtaggaaaacataagcttgaagaagga
agctttaaagaaaggttggctcgttctcgcccgcaatttagaggggacatacatggcaga
aatttaagcaatgaggagatgatacaggcagcagatgagctagaagagatgaaaagagta
agaaacaaactgatgataatgcactggaaggcaaaacggagccgtccttatcctatttaa
DBGET
integrated database retrieval system
