Homo sapiens (human): 10456
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Entry
10456 CDS
T01001
Symbol
HAX1, HCLSBP1, HS1BP1, SCN3
Name
(RefSeq) HCLS1 associated protein X-1
KO
K16220
HCLS1-associated protein X-1
Organism
hsa
Homo sapiens (human)
Disease
H00100
Neutropenic disorders
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03019 Messenger RNA biogenesis [BR:
hsa03019
]
10456 (HAX1)
Messenger RNA biogenesis [BR:
hsa03019
]
Eukaryotic type
mRNA surveillance and transport factors
Factors involved in mRNA localization
Trans-acting binding proteins
10456 (HAX1)
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GFIT
Other DBs
NCBI-GeneID:
10456
NCBI-ProteinID:
NP_006109
OMIM:
605998
HGNC:
16915
Ensembl:
ENSG00000143575
UniProt:
O00165
A0A0S2Z591
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Position
1:154272629..154275875
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AA seq
279 aa
AA seq
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MSLFDLFRGFFGFPGPRSHRDPFFGGMTRDEDDDEEEEEEGGSWGRGNPRFHSPQHPPEE
FGFGFSFSPGGGIRFHDNFGFDDLVRDFNSIFSDMGAWTLPSHPPELPGPESETPGERLR
EGQTLRDSMLKYPDSHQPRIFGGVLESDARSESPQPAPDWGSQRPFHRFDDVWPMDPHPR
TREDNDLDSQVSQEGLGPVLQPQPKSYFKSISVTKITKPDGIVEERRTVVDSEGRTETTV
TRHEADSSPRGDPESPRPPALDDAFSILDLFLGRWFRSR
NT seq
840 nt
NT seq
+upstream
nt +downstream
nt
atgagcctctttgatctcttccggggctttttcggctttcctggacctcggagccacaga
gatcccttttttggagggatgactcgagatgaagatgatgatgaggaagaagaagaagaa
gggggctcatggggccgtgggaacccaaggttccatagtcctcagcacccccctgaggaa
tttggcttcggcttcagcttcagcccaggaggagggatacgtttccacgataacttcggc
tttgatgacctagtacgagatttcaatagcatcttcagcgatatgggggcctggaccttg
ccttcccatcctcctgaacttccaggtcctgagtcagagacacctggtgagagactacgg
gagggacagacacttcgggactcaatgcttaagtatccagatagtcaccagcccaggatc
tttgggggggtcttggagagtgatgcaagaagtgaatccccccaaccagcaccagactgg
ggctcccagaggccatttcataggtttgatgatgtatggcctatggacccccatcctaga
accagagaggacaatgatcttgattcccaggtttcccaggagggtcttggcccggttcta
cagccccagcccaaatcctatttcaagagcatctctgtgaccaagatcactaaaccagat
gggatagtggaggagcgccggactgtggtggacagtgagggccggacagagactacagta
acccgacacgaagcagatagcagtcctaggggtgatccagaatcaccaagacctccagcc
ctggatgatgccttttccatcctggacttattcctgggacgttggttccggtcccggtag
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