QuickView for RBM10;jsessionid=025EF5FECEE11645C1A2480A8FD1E277 (gene)

Gene Symbol:

RBM10 Homo sapiens

Full name:

RNA binding motif protein 10

Synonyms:

DXS8237E, GPATC9, GPATCH9, S1-1, TARPS, ZRANB5, RNA-binding protein 10, RNA-binding protein S1-1, g patch domain-containing protein 9

Genomic Location:

Chr X: 46889575-46931156

Description:

This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript va...

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This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

GATTGGY_NFY_Q6_01 ,  NFY_C ,  GCCATNTTG_YY1_Q6 ,  GGGCGGR_SP1_Q6 ,  CCCNNGGGAR_OLF1_01 ,  TGACAGNY_MEIS1_01 ,  ZF5_B ,  TGACATY_UNKNOWN

miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-326

Cytogenetic Map:

Xp11.3

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