UCSC Human Gene Sorter
 
genome assembly search
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#
Name
VisiGene
BLASTP
E-Value
Genome Position
Description
1GPR55n/a
n/a
n/a
n/a
7e-175chr2 230,916,285G protein-coupled receptor 55 (from RefSeq NM_005683.4)
2LINC00158n/a
n/a
n/a
n/a
n/achr21 25,408,760long intergenic non-protein coding RNA 158 (from RefSeq NR_024027.2)
3IGHV5-78n/a
    
    
     
n/achr14 106,851,270immunoglobulin heavy variable 5-78 (pseudogene) (from HGNC IGHV5-78)
4EXO1n/a
n/a
n/a
n/a
n/achr1 241,869,071exonuclease 1, transcript variant 2 (from RefSeq NM_130398.4)
5LINC00426n/a
n/a
n/a
n/a
n/achr13 30,358,630long intergenic non-protein coding RNA 426 (from HGNC LINC00426)
6CKAP2Ln/a
n/a
n/a
n/a
n/achr2 112,750,479cytoskeleton associated protein 2 like, transcript variant 3 (from RefSeq NR_130712.2)
7CLSPNn/a
n/a
n/a
n/a
n/achr1 35,751,045claspin, transcript variant 1 (from RefSeq NM_022111.4)
8ESCO2n/a
n/a
n/a
n/a
n/achr8 27,789,935establishment of sister chromatid cohesion N-acetyltransferase 2 (from RefSeq NM_001017420.3)
9ENSG00000253690n/a
    
    
     
n/achr8 28,294,659ENSG00000253690 (from geneSymbol)
10SKA1n/a
n/a
n/a
n/a
n/achr18 50,384,607spindle and kinetochore associated complex subunit 1, transcript variant 2 (from RefSeq NM_145060.4)
11SPC25n/a
n/a
n/a
n/a
n/achr2 168,880,660SPC25 component of NDC80 kinetochore complex (from RefSeq NM_020675.4)
12E2F7n/a
n/a
n/a
n/a
n/achr12 77,043,410E2F transcription factor 7 (from RefSeq NM_203394.3)
13CARD11-AS1n/a
    
    
     
n/achr7 2,945,563CARD11 antisense RNA 1 (from RefSeq NR_187443.1)
14SGO1n/a
n/a
n/a
n/a
n/achr3 20,177,845shugoshin 1, transcript variant 1 (from RefSeq NM_001199251.3)
15SKA3n/a
n/a
n/a
n/a
n/achr13 21,165,073spindle and kinetochore associated complex subunit 3, transcript variant 1 (from RefSeq NM_145061.6)
16POLQn/a
n/a
n/a
n/a
n/achr3 121,488,709DNA polymerase theta (from RefSeq NM_199420.4)
17MYL12BP2n/a
n/a
n/a
n/a
n/achr4 184,299,384myosin light chain 12B pseudogene 2 (from HGNC MYL12BP2)
18BEND4n/a
n/a
n/a
n/a
n/achr4 42,131,754BEN domain containing 4, transcript variant 1 (from RefSeq NM_207406.4)
19CENPKn/a
n/a
n/a
n/a
n/achr5 65,540,467centromere protein K, transcript variant 1 (from RefSeq NM_022145.5)
20LINC02397n/a
    
    
     
n/achr12 92,479,271long intergenic non-protein coding RNA 2397 (from HGNC LINC02397)
21CLLU1n/a
n/a
n/a
n/a
n/achr12 92,426,259chronic lymphocytic leukemia up-regulated 1, transcript variant 2 (from RefSeq NR_027932.1)
22ENSG00000266923n/a
n/a
n/a
n/a
n/achr12 92,452,605ENSG00000266923 (from geneSymbol)
23SGO1-AS1n/a
n/a
n/a
n/a
n/achr3 20,532,595SGO1 antisense RNA 1 (from HGNC SGO1-AS1)
24KIF14n/a
n/a
n/a
n/a
n/achr1 200,586,125kinesin family member 14, transcript variant 1 (from RefSeq NM_014875.3)
25KIF4An/a
n/a
n/a
n/a
n/achrX 70,355,495kinesin family member 4A (from RefSeq NM_012310.5)
26CCL3L3n/a
n/a
n/a
n/a
n/achr17_KI270909v1_alt 251,521C-C motif chemokine ligand 3 like 1, transcript variant 2 (from RefSeq NR_111964.2)
27ASPMn/a
n/a
n/a
n/a
n/achr1 197,115,398assembly factor for spindle microtubules, transcript variant 1 (from RefSeq NM_018136.5)
28NEUROG220303
    
    
     
n/achr4 112,514,848neurogenin 2 (from RefSeq NM_024019.4)
29C10orf88Bn/a
n/a
n/a
n/a
n/achr10 122,888,937C10orf88B (from geneSymbol)
30LINC03047n/a
    
    
     
n/achr8 102,533,704LINC03047 (from geneSymbol)
31XRCC2n/a
    
    
     
n/achr7 152,660,458X-ray repair cross complementing 2 (from RefSeq NM_005431.2)
32TNFSF11n/a
n/a
n/a
n/a
n/achr13 42,591,082TNF superfamily member 11, transcript variant 1 (from RefSeq NM_003701.4)
33ZC3H12Dn/a
n/a
n/a
n/a
n/achr6 149,465,904zinc finger CCCH-type containing 12D (from RefSeq NM_207360.3)
34ENSG00000263680n/a
    
    
     
n/achr17 72,427,395ENSG00000263680 (from geneSymbol)
35ENSG00000232335n/a
    
    
     
n/achr1 35,741,482ENSG00000232335 (from geneSymbol)
36DEPDC1Bn/a
n/a
n/a
n/a
n/achr5 60,648,539DEP domain containing 1B, transcript variant 1 (from RefSeq NM_018369.3)
37KIF18Bn/a
n/a
n/a
n/a
n/achr17 44,936,242kinesin family member 18B, transcript variant 1 (from RefSeq NM_001265577.2)
38ENSG00000268088n/a
    
    
     
n/achr19 39,695,091ENSG00000268088 (from geneSymbol)
39GINS4n/a
n/a
n/a
n/a
n/achr8 41,537,145GINS complex subunit 4 (from RefSeq NM_032336.3)
40TMEM156n/a
    
    
     
n/achr4 38,999,576transmembrane protein 156, transcript variant 1 (from RefSeq NM_024943.3)
41MND1n/a
n/a
n/a
n/a
n/achr4 153,379,903meiotic nuclear divisions 1, transcript variant 1 (from RefSeq NM_032117.4)
42TRD-AS1n/a
n/a
n/a
n/a
n/achr14 22,315,090TRD-AS1 (from geneSymbol)
43DEPDC1n/a
n/a
n/a
n/a
n/achr1 68,485,617DEP domain containing 1, transcript variant 1 (from RefSeq NM_001114120.3)
44TRGV3n/a
    
    
     
n/achr7 38,358,837V region of the variable domain of T cell receptor (TR) gamma  chain that participates in the antigen recognition (PubMed:24600447).  Gamma-delta TRs recognize a variety of self and foreign non-peptide  antigens frequently expressed at the epithelial boundaries between the  host and external environment, including endogenous lipids presented by  MH-like protein CD1D and phosphoantigens presented by butyrophilin-like  molecule BTN3A1. Upon antigen recognition induces rapid, innate-like  immune responses involved in pathogen clearance and tissue repair  (PubMed:23348415, PubMed:28920588). Binding of gamma-delta TR complex  to antigen triggers phosphorylation of immunoreceptor tyrosine-based  activation motifs (ITAMs) in the CD3 chains by the LCK and FYN kinases,  allowing the recruitment, phosphorylation, and activation of ZAP70 that  facilitates phosphorylation of the scaffolding proteins LCP2 and LAT.  This lead to the formation of a supramolecular signalosome that  recruits the phospholipase PLCG1, resulting in calcium mobilization and  ERK activation, ultimately leading to T cell expansion and  differentiation into effector cells (PubMed:25674089). Gamma-delta TRs  are produced through somatic rearrangement of a limited repertoire of  variable (V), diversity (D), and joining (J) genes. The potential  diversity of gamma-delta TRs is conferred by the unique ability to  rearrange (D) genes in tandem and to utilize all three reading frames.  The combinatorial diversity is considerably increased by the sequence  exonuclease trimming and random nucleotide (N) region additions which  occur during the V-(D)-J rearrangements (PubMed:24387714). (from UniProt P03979)
45PIMREGn/a
n/a
n/a
n/a
n/achr17 6,447,962PICALM interacting mitotic regulator, transcript variant 1 (from RefSeq NM_019013.3)
46DBF4P1n/a
n/a
n/a
n/a
n/achr10 64,169,904DBF4 zinc finger pseudogene 1 (from HGNC DBF4P1)
47MTFR2n/a
n/a
n/a
n/a
n/achr6 136,240,672mitochondrial fission regulator 2, transcript variant 1 (from RefSeq NM_001099286.3)
48LGALS14n/a
n/a
n/a
n/a
n/achr19 39,706,962galectin 14, transcript variant 1 (from RefSeq NM_020129.3)
49PDE6Gn/a
n/a
n/a
n/a
n/achr17 81,653,500phosphodiesterase 6G, transcript variant 1 (from RefSeq NM_002602.4)
50NOX5n/a
n/a
n/a
n/a
n/achr15 69,038,728NADPH oxidase 5, transcript variant 1 (from RefSeq NM_024505.4)