QuickView for KERA;jsessionid=7D29A8820CE63C1EE5AFBA827D143A08 (gene)

Gene Symbol:

KERA Homo sapiens

Full name:

keratocan

Synonyms:

CNA2, KTN, SLRR2B, keratocan, keratan sulfate proteoglycan keratocan

Genomic Location:

Chr 12: 89968399-89976262

Description:

The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).

The protein encoded by this gene is a keratan sulfate proteoglycan that is involved in corneal transparency. Defects in this gene are a cause of autosomal recessive cornea plana 2 (CNA2).

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Bos taurus ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

TGGAAA_NFAT_Q4_01 ,  TAL1ALPHAE47_01 ,  TGGNNNNNNKCCAR_UNKNOWN ,  NKX3A_01 ,  CTTTGA_LEF1_Q2 ,  TAL1BETAE47_01 ,  RP58_01 ,  SOX5_01 ,  TTGTTT_FOXO4_01 ,  YY1_02 ,  TAL1BETAITF2_01 ,  SRY_02

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Cytogenetic Map:

12q21.33

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