UCSC Human Gene Sorter
 
genome assembly search
sort by display output 
#
Name
VisiGene
BLASTP
E-Value
Genome Position
Description
1TRARG1n/a
    
    
     
5e-58chr17 1,290,320trafficking regulator of GLUT4 (SLC2A4) 1 (from RefSeq NM_172367.3)
2ADIPOQ-AS1n/a
    
    
     
n/achr3 186,854,004ADIPOQ antisense RNA 1 (from RefSeq NR_046662.2)
3CIDEAn/a
n/a
n/a
n/a
n/achr18 12,265,978cell death inducing DFFA like effector a, transcript variant 2 (from RefSeq NM_001318383.2)
4LEPn/a
    
    
     
n/achr7 128,249,453leptin (from RefSeq NM_000230.3)
5CD300LGn/a
n/a
n/a
n/a
n/achr17 43,855,407CD300 molecule like family member g, transcript variant 1 (from RefSeq NM_145273.4)
6SLC19A3n/a
n/a
n/a
n/a
n/achr2 227,700,895solute carrier family 19 member 3, transcript variant 1 (from RefSeq NM_025243.4)
7THRSPn/a
    
    
     
n/achr11 78,066,106thyroid hormone responsive (from RefSeq NM_003251.4)
8ENSG00000267653n/a
    
    
     
n/achr17 69,489,447ENSG00000267653 (from geneSymbol)
9TNMDn/a
    
    
     
n/achrX 100,592,410tenomodulin (from RefSeq NM_022144.3)
10AQP7P1n/a
n/a
n/a
n/a
n/achr9 63,325,079aquaporin 7 pseudogene 1 (from HGNC AQP7P1)
11ENSG00000229436n/a
    
    
     
n/achr7 80,662,458ENSG00000229436 (from geneSymbol)
12LINC00993n/a
    
    
     
n/achr10 37,281,959long intergenic non-protein coding RNA 993 (from HGNC LINC00993)
13ENSG00000290801n/a
n/a
n/a
n/a
n/achr10 37,328,052long intergenic non-protein coding RNA 993 (from RefSeq NR_104061.1)
14LVRNn/a
n/a
n/a
n/a
n/achr5 115,995,040laeverin (from RefSeq NM_173800.5)
15AQP7P2n/a
    
    
     
n/achr9 64,629,573aquaporin 7 pseudogene 2 (from HGNC AQP7P2)
16MYMXn/a
    
    
     
n/achr6 44,217,580myomixer, myoblast fusion factor, transcript variant 2 (from RefSeq NM_001347931.2)
17ENSG00000279204n/a
n/a
n/a
n/a
n/achr5 159,107,498ENSG00000279204 (from geneSymbol)
18SLC66A1LPn/a
n/a
n/a
n/a
n/achr3 157,573,983SLC66A1LP (from geneSymbol)
19SLC66A1LPn/a
n/a
n/a
n/a
n/achr3 157,610,569SLC66A1LP (from geneSymbol)
20ENSG00000182021n/a
n/a
n/a
n/a
n/achr9 63,122,991ENSG00000182021 (from geneSymbol)
21ENSG00000234918n/a
    
    
     
n/achr10 37,241,468ENSG00000234918 (from geneSymbol)
22LINC01140n/a
n/a
n/a
n/a
n/achr1 87,149,135long intergenic non-protein coding RNA 1140 (from HGNC LINC01140)
23TPT1P4n/a
    
    
     
n/achr6 144,200,706tumor protein, translationally-controlled 1 pseudogene 4 (from HGNC TPT1P4)
24ENSG00000253123n/a
n/a
n/a
n/a
n/achr8 37,329,298ENSG00000253123 (from geneSymbol)
25OR7E13Pn/a
n/a
n/a
n/a
n/achr11 86,832,994olfactory receptor family 7 subfamily E member 13 pseudogene (from HGNC OR7E13P)
26ENSG00000228522n/a
    
    
     
n/achr9 63,334,540ENSG00000228522 (from geneSymbol)
27FGF13-AS1n/a
n/a
n/a
n/a
n/achrX 138,713,772FGF13 antisense RNA 1 (from HGNC FGF13-AS1)
28HCAR1n/a
n/a
n/a
n/a
n/achr12 122,728,460hydroxycarboxylic acid receptor 1 (from RefSeq NM_032554.4)
29ENSG00000248576n/a
    
    
     
n/achr12 54,165,867uncharacterized LOC102724030 (from RefSeq NR_187804.1)
30TNNn/a
n/a
n/a
n/a
n/achr1 175,107,954tenascin N (from RefSeq NM_022093.2)
31AOC4Pn/a
n/a
n/a
n/a
n/achr17 42,870,824amine oxidase, copper containing 4, pseudogene (from HGNC AOC4P)
32AOC4Pn/a
n/a
n/a
n/a
n/achr17 42,871,498amine oxidase, copper containing 4, pseudogene (from HGNC AOC4P)
33IL6n/a
n/a
n/a
n/a
n/achr7 22,729,599interleukin 6, transcript variant 1 (from RefSeq NM_000600.5)
34IMMP1LP1n/a
    
    
     
n/achr11 63,632,476inner mitochondrial membrane peptidase subunit 1 pseudogene 1 (from HGNC IMMP1LP1)
35CSPG4P13n/a
n/a
n/a
n/a
n/achr15 77,899,679chondroitin sulfate proteoglycan 4 pseudogene 13 (from HGNC CSPG4P13)
36ENSG00000290664n/a
n/a
n/a
n/a
n/achr15 77,903,011ENSG00000290664 (from geneSymbol)
37ACKR2n/a
n/a
n/a
n/a
n/achr3 42,838,365atypical chemokine receptor 2 (from RefSeq NM_001296.5)
38ZNF662n/a
n/a
n/a
n/a
n/achr3 42,912,738zinc finger protein 662, transcript variant 1 (from RefSeq NM_207404.4)
39ENSG00000273328n/a
n/a
n/a
n/a
n/achr3 42,854,904ENSG00000273328 (from geneSymbol)
40ENSG00000290317n/a
n/a
n/a
n/a
n/achr3 42,876,137ENSG00000290317 (from geneSymbol)
41FAM124Bn/a
    
    
     
n/achr2 224,390,402family with sequence similarity 124 member B, transcript variant 1 (from RefSeq NM_001122779.2)
42CYP4Z1n/a
    
    
     
n/achr1 47,092,774cytochrome P450 family 4 subfamily Z member 1 (from RefSeq NM_178134.3)
43TRAV39n/a
    
    
     
n/achr14 22,304,303V region of the variable domain of T cell receptor (TR) alpha  chain that participates in the antigen recognition (PubMed:24600447).  Alpha-beta T cell receptors are antigen specific receptors which are  essential to the immune response and are present on the cell surface of  T lymphocytes. Recognize peptide-major histocompatibility (MH) (pMH)  complexes that are displayed by antigen presenting cells (APC), a  prerequisite for efficient T cell adaptive immunity against pathogens  (PubMed:25493333). Binding of alpha-beta TR to pMH complex initiates  TR-CD3 clustering on the cell surface and intracellular activation of  LCK that phosphorylates the ITAM motifs of CD3G, CD3D, CD3E and CD247  enabling the recruitment of ZAP70. In turn ZAP70 phosphorylates LAT,  which recruits numerous signaling molecules to form the LAT  signalosome. The LAT signalosome propagates signal branching to three  major signaling pathways, the calcium, the mitogen-activated protein  kinase (MAPK) kinase and the nuclear factor NF-kappa-B (NF-kB)  pathways, leading to the mobilization of transcription factors that are  critical for gene expression and essential for T cell growth and  differentiation (PubMed:23524462). The T cell repertoire is generated  in the thymus, by V-(D)-J rearrangement. This repertoire is then shaped  by intrathymic selection events to generate a peripheral T cell pool of  self-MH restricted, non-autoaggressive T cells. Post-thymic interaction  of alpha-beta TR with the pMH complexes shapes TR structural and  functional avidity (PubMed:15040585). (from UniProt A0A0B4J263)
44OR2S1Pn/a
    
    
     
n/achr9 36,013,658olfactory receptor family 2 subfamily S member 1 pseudogene (from HGNC OR2S1P)
45ENSG00000290538n/a
    
    
     
n/achr9 35,988,409ENSG00000290538 (from geneSymbol)
46ENSG00000253105n/a
n/a
n/a
n/a
n/achr8 96,379,119uncharacterized LOC102724804, transcript variant 1 (from RefSeq NR_125828.1)
47ENSG00000225028n/a
    
    
     
n/achr1 47,819,151ENSG00000225028 (from geneSymbol)
48VWFP1n/a
    
    
     
n/achr22 16,697,290von Willebrand factor pseudogene 1 (from HGNC VWFP1)
49ENSG00000273244n/a
    
    
     
n/achr22 16,685,332ENSG00000273244 (from geneSymbol)
50ENSG00000254933n/a
    
    
     
n/achr11 76,192,898ENSG00000254933 (from geneSymbol)