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Gene: CT47B1 (cancer/testis antigen family 47 member B1) Homo sapiens
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Symbol: CT47B1
Name: cancer/testis antigen family 47 member B1
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: cancer/testis antigen 47.13; cancer/testis antigen 47B; cancer/testis antigen family 147, member B1; cancer/testis antigen family 47, member B1; cancer/testis CT47 family, member 13; CT47.13; CT47A13
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX120,872,603 - 120,875,929 (-)Ensembl
GRCh38X120,872,552 - 120,875,925 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X120,006,451 - 120,009,779 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X119,891,778 - 119,893,807 (-)NCBINCBI36hg18NCBI36
Cytogenetic MapXq24NCBI
HuRefX109,471,626 - 109,498,844 (-)NCBIHuRef
CHM1_1X119,918,025 - 119,921,367 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on CT47B1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 2306151
Created: 2009-03-20
Species: Homo sapiens
Last Modified: 2019-12-25
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.