Homo sapiens (human): 643226
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Entry
643226 CDS
T01001
Symbol
GRXCR2, DFNB101
Name
(RefSeq) glutaredoxin and cysteine rich domain containing 2
KO
K24294
glutaredoxin domain-contaning cysteine-rich protein 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
03037 Cilium and associated proteins [BR:
hsa03037
]
643226 (GRXCR2)
Cilium and associated proteins [BR:
hsa03037
]
Other cilia and associated proteins
Stereociliary proteins
643226 (GRXCR2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
GRXCR1_C
DnaJ_CXXCXGXG
Motif
Other DBs
NCBI-GeneID:
643226
NCBI-ProteinID:
NP_001073985
OMIM:
615762
HGNC:
33862
Ensembl:
ENSG00000204928
UniProt:
A6NFK2
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All DBs
Position
5:complement(145857670..145931673)
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AA seq
248 aa
AA seq
DB search
MEDPEKKLNQKSDGKPRKVRFKISSSYSGRVLKQVFEDGQELESPKEEYPHSFLQESLET
MDGVYGSGEVPRPQMCSPKLTAQRISVFREGNAYTLAGGQPRFNDYKANDHKPLPIIDFG
KIIIYTNNLKIIRTPMDKRDFVRKILQKEEEAEEESLMNKEESYGGRDQHDRPLVEAEST
LPQNRYTQEGDIPEDSCFHCRGSGSATCSLCHGSKFSMLANRFKESYRALRCPACNENGL
QPCQICNQ
NT seq
747 nt
NT seq
+upstream
nt +downstream
nt
atggaggaccctgagaaaaagctgaatcagaagagtgatggcaaaccccggaaagtacga
tttaaaatctcctcctcctacagcggtcgagtattgaagcaggtctttgaggatgggcag
gaattagagtcaccaaaggaggaataccctcacagttttctgcaagagtctcttgaaaca
atggatggtgtttatgggtctggggaagtccccaggccccagatgtgctcccctaagctg
actgctcagaggatcagtgtgtttagagagggtaatgcctacaccttggcaggcggccag
cctcggttcaacgattacaaggcgaatgaccataagcccctacctattatagattttgga
aagataatcatctacactaataacctgaaaatcattcgaaccccaatggacaagagagat
tttgtgaggaaaattctccagaaggaagaggaggctgaggaagagtctctgatgaacaaa
gaagaaagctatggaggcagggaccagcacgatagacctttggtggaggcagaaagcaca
ttaccccaaaaccggtatacacaggaaggggatattcccgaggacagctgttttcactgc
cgagggtcgggcagtgccacctgctctctgtgccacggcagcaagttctcgatgctggcc
aacagatttaaggagtcctatcgggccctgaggtgccctgcctgcaatgagaatggccta
cagccttgccagatttgcaatcaatag
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