Homo sapiens (human): 100127206
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Entry
100127206 CDS
T01001
Symbol
MINAR2, DFNB120, KIAA1024L
Name
(RefSeq) membrane integral NOTCH2 associated receptor 2
KO
K24830
major intrinsically disordered Notch2-binding receptor 2
Organism
hsa
Homo sapiens (human)
Disease
H00605
Deafness, autosomal recessive
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
]
100127206 (MINAR2)
Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
Other domain-containing proteins
Others
100127206 (MINAR2)
BRITE hierarchy
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MINAR1_C
Motif
Other DBs
NCBI-GeneID:
100127206
NCBI-ProteinID:
NP_001244237
OMIM:
620215
HGNC:
33914
Ensembl:
ENSG00000186367
UniProt:
P59773
LinkDB
All DBs
Position
5:129748094..129766732
Genome browser
AA seq
190 aa
AA seq
DB search
MDLSVLPNNNHPDKFLQLDVKSLTRSSALLQASLVRFPGGNYPAAQHWQNLVYSQREKKN
IAAQRIRGSSADSLVTADSPPPSMSSVMKNNPLYGDLSLEEAMEERKKNPSWTIEEYDKH
SLHTNLSGHLKENPNDLRFWLGDMYTPGFDTLLKKEEKQEKHSKFCRMGLILLVVISILV
TIVTIITFFT
NT seq
573 nt
NT seq
+upstream
nt +downstream
nt
atggatctctctgttttgccaaataacaaccatcctgacaaattcctgcagcttgacgta
aagtctttaacgaggagctcagccctccttcaggccagcctggtgaggtttccgggtgga
aattatcctgctgcacaacactggcaaaaccttgtctactcacagagggaaaagaagaat
attgctgctcaacgaattaggggatccagtgcagacagccttgtcactgctgatagcccc
ccaccatccatgtcatcagttatgaagaataacccactctatggtgacctaagtttggag
gaagctatggaagaaagaaaaaagaacccctcatggaccattgaggaatatgacaaacat
tccctgcacacaaacctctctggacatctgaaggaaaatcctaatgacctgcggttttgg
ttgggagacatgtacactccaggttttgacactttattgaaaaaggaagagaaacaagag
aagcattcaaaattctgtcgtatgggtctgattttacttgtcgttatctccatcttggtt
accatagtgactatcattacttttttcacctga
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integrated database retrieval system
