======= RHAG =======
== Gene Information ==
* **Official Symbol**: RHAG
* **Official Name**: Rh associated glycoprotein
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=6005|6005]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q02094|Q02094]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=RHAG&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20RHAG|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/180297|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.[provided by RefSeq, Mar 2009].
* **UniProt Summary**: Associated with rhesus blood group antigen expression (PubMed:19744193). May be part of an oligomeric complex which is likely to have a transport or channel function in the erythrocyte membrane (PubMed:11062476, PubMed:11861637). Involved in ammonia transport across the erythrocyte membrane (PubMed:21849667, PubMed:22012326). Seems to act in monovalent cation transport (PubMed:18931342, PubMed:21849667). {ECO:0000269|PubMed:11062476, ECO:0000269|PubMed:11861637, ECO:0000269|PubMed:18931342, ECO:0000269|PubMed:19744193, ECO:0000269|PubMed:21849667, ECO:0000269|PubMed:22012326}.
|Ammonium transp|
|carbon dioxide transmembrane transporter activity|
|carbon dioxide transmembrane transport|
|leak channel activity|
|carbon dioxide transport|
|ammonium transmembrane transporter activity|
|multicellular organismal iron ion homeostasis|
|one-carbon compound transport|
|ammonium transmembrane transport|
|gas transport|
|ankyrin binding|
|erythrocyte development|
|bicarbonate transport|
|ammonium transport|
|myeloid cell development|
|drug transmembrane transport|
|iron ion homeostasis|
|erythrocyte differentiation|
|erythrocyte homeostasis|
|myeloid cell homeostasis|
|transition metal ion homeostasis|
|drug transport|
|homeostasis of number of cells|
|myeloid cell differentiation|
|multicellular organismal homeostasis|
|monovalent inorganic cation transport|
|organic anion transport|
|hemopoiesis|
|anion transport|
|hematopoietic or lymphoid organ development|
|cation transmembrane transport|
|metal ion homeostasis|
|cellular ion homeostasis|
|immune system development|
|cation homeostasis|
|inorganic ion homeostasis|
|cellular chemical homeostasis|
|ion homeostasis|
|cation transport|
|cellular homeostasis|
|ion transmembrane transport|
|response to drug|
|chemical homeostasis|
|transmembrane transport|
|ion transport|
|integral component of plasma membrane|
|homeostatic process|
|cell development|
|nitrogen compound transport|
|membrane|
\\
=== CRISPR Data ===
No hits were found.
No correlation found to any other genes in chemogenomics.
Global Fraction of Cell Lines Where Essential: 0/739
^Tissue^Fraction Of Cell Lines Where Essential^
|1290807.0|0/1|
|909776.0|0/1|
|bile duct|0/28|
|blood|0/28|
|bone|0/26|
|breast|0/33|
|central nervous system|0/56|
|cervix|0/4|
|colorectal|0/17|
|esophagus|0/13|
|fibroblast|0/1|
|gastric|0/16|
|kidney|0/21|
|liver|0/20|
|lung|0/75|
|lymphocyte|0/16|
|ovary|0/26|
|pancreas|0/24|
|peripheral nervous system|0/16|
|plasma cell|0/15|
|prostate|0/1|
|skin|0/24|
|soft tissue|0/9|
|thyroid|0/2|
|upper aerodigestive|0/22|
|urinary tract|0/29|
|uterus|0/5|
== Essentiality in NALM6 ==
* **Essentiality Rank**: 15896
* **Expression level (log2 read counts)**: -7.68
{{:chemogenomics:nalm6 dist.png?nolink |}}