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Gene: FAM199X (family with sequence similarity 199, X-linked) Homo sapiens
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Symbol: FAM199X
Name: family with sequence similarity 199, X-linked
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH 17beta-estradiol; 3-isobutyl-1-methyl-7H-xanthine; benzo[a]pyrene diol epoxide I
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: CXorf39; hypothetical protein LOC139231
Orthologs:
Mus musculus (house mouse) : Fam199x (family with sequence similarity 199, X-linked)  MGI  Alliance
Rattus norvegicus (Norway rat) : Fam199x (family with sequence similarity 199, X-linked)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Fam199x (family with sequence similarity 199, X-linked)
Pan paniscus (bonobo/pygmy chimpanzee) : FAM199X (family with sequence similarity 199, X-linked)
Canis lupus familiaris (dog) : FAM199X (family with sequence similarity 199, X-linked)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Fam199x (family with sequence similarity 199, X-linked)
Sus scrofa (pig) : FAM199X (family with sequence similarity 199, X-linked)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X104,166,453 - 104,195,902 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X103,411,156 - 103,440,583 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X103,297,957 - 103,322,783 (+)NCBINCBI36hg18NCBI36
Build 34X103,217,445 - 103,242,270NCBI
CeleraX103,885,924 - 103,910,751 (+)NCBI
Cytogenetic MapXq22.2NCBI
HuRefX93,038,353 - 93,067,980 (+)NCBIHuRef
CHM1_1X103,322,018 - 103,351,458 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM199X
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1348985
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
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.