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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)
Chlorocebus sabaeus (green monkey) : FAM199X (family with sequence similarity 199, X-linked)
Heterocephalus glaber (naked mole-rat) : 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
GRCh38 EnsemblX104,166,453 - 104,195,902 (+)Ensembl
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

Expression

RNA-SEQ Expression

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

RGD Object Information
RGD ID: 1348985
Created: 2005-03-08
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.