Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: FAM197Y9 (family with sequence similarity 197 Y-linked member 9) Homo sapiens
Analyze
Symbol: FAM197Y9
Name: family with sequence similarity 197 Y-linked member 9
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 197, Y-linked, member 9
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblY6,256,267 - 6,265,595 (-)EnsemblGRCh38hg38GRCh38
GRCh38Y6,258,333 - 6,263,935 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37Y6,130,045 - 6,132,240 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36Y6,190,045 - 6,192,364 (-)NCBINCBI36hg18NCBI36
Cytogenetic MapYp11.2NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM197Y9
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 2797679
Created: 2010-07-04
Species: Homo sapiens
Last Modified: 2020-03-10
Status: ACTIVE



NHLBI Logo

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