UCSC Human Gene Sorter
 
genome assembly search
sort by display output
#
Name
VisiGene
BLASTP
E-Value
Genome Position
Description                                       
1EPB41L4A-DTn/a
n/a
n/a
n/a
n/achr5 112,420,280EPB41L4A divergent transcript (from RefSeq NR_027706.1)
2RPS21P1n/a
    
    
     
n/achr1 235,433,108ribosomal protein S21 pseudogene 1 (from HGNC RPS21P1)
3ENSG00000265413n/a
    
    
     
n/achr18 8,404,004ENSG00000265413 (from geneSymbol)
4ENSG00000266171n/a
    
    
     
n/achr18 736,602ENSG00000266171 (from geneSymbol)
5MIPEPP3n/a
    
    
     
n/achr13 21,302,316mitochondrial intermediate peptidase pseudogene 3 (from HGNC MIPEPP3)
6ENSG00000270184n/a
    
    
     
n/achr16 85,785,999ENSG00000270184 (from geneSymbol)
7FBXW4P1n/a
n/a
n/a
n/a
n/achr22 23,263,886F-box and WD repeat domain containing 4 pseudogene 1 (from RefSeq NR_033408.1)
8ENSG00000247934n/a
n/a
n/a
n/a
n/achr12 28,176,832ENSG00000247934 (from geneSymbol)
9ENSG00000272275n/a
    
    
     
n/achr2 10,768,966ENSG00000272275 (from geneSymbol)
10ENSG00000266865n/a
n/a
n/a
n/a
n/achr17 31,020,350ENSG00000266865 (from geneSymbol)
11WDPCPn/a
n/a
n/a
n/a
n/achr2 63,354,018WD repeat containing planar cell polarity effector, transcript variant 7 (from RefSeq NR_148705.2)
12KMT5AP2n/a
n/a
n/a
n/a
n/achr2 91,748,463KMT5AP2 (from geneSymbol)
13CKS1BP2n/a
n/a
n/a
n/a
n/achr10 29,698,054CDC28 protein kinase regulatory subunit 1B pseudogene 2 (from HGNC CKS1BP2)
14CALCRL-AS1n/a
n/a
n/a
n/a
n/achr2 187,279,781CALCRL and TFPI antisense RNA 1, transcript variant 2 (from RefSeq NR_187179.1)
15RNU1-103Pn/a
    
    
     
n/achr16 85,781,837RNA, U1 small nuclear 103, pseudogene (from HGNC RNU1-103P)
16ZNF396n/a
n/a
n/a
n/a
n/achr18 35,372,015zinc finger protein 396, transcript variant 2 (from RefSeq NM_001322290.2)
17HMGB1P31n/a
    
    
     
n/achr2 54,051,547high mobility group box 1 pseudogene 31 (from HGNC HMGB1P31)
18MYLK4n/a
n/a
n/a
n/a
n/achr6 2,707,279myosin light chain kinase family member 4, transcript variant 1 (from RefSeq NM_001012418.5)
19ZNF460n/a
n/a
n/a
n/a
n/achr19 57,287,277zinc finger protein 460, transcript variant 1 (from RefSeq NM_006635.4)
20RPL22P24n/a
    
    
     
n/achr1 185,171,522ribosomal protein L22 pseudogene 24 (from HGNC RPL22P24)
21C10orf143n/a
n/a
n/a
n/a
n/achr10 130,087,363chromosome 10 open reading frame 143, transcript variant 2 (from RefSeq NR_149170.2)
22BDH2P1n/a
n/a
n/a
n/a
n/achr6 99,175,1113-hydroxybutyrate dehydrogenase 2, pseudogene 1 (from HGNC BDH2P1)
23APLFn/a
n/a
n/a
n/a
n/achr2 68,523,873aprataxin and PNKP like factor (from RefSeq NM_173545.3)
24FKBP9P1n/a
n/a
n/a
n/a
n/achr7 55,697,952FK506 binding protein 9 pseudogene 1 (from HGNC FKBP9P1)
25ENSG00000231731n/a
n/a
n/a
n/a
n/achr2 127,484,829ENSG00000231731 (from geneSymbol)
26ENSG00000269843n/a
    
    
     
n/achr19 40,834,215ENSG00000269843 (from geneSymbol)
27ZNF763n/a
n/a
n/a
n/a
n/achr19 11,972,828zinc finger protein 763, transcript variant 4 (from RefSeq NM_001367174.2)
28ENSG00000268886n/a
    
    
     
n/achr19 52,580,722ENSG00000268886 (from geneSymbol)
29TSEN34n/a
n/a
n/a
n/a
n/achr19 54,192,920tRNA splicing endonuclease subunit 34, transcript variant 2 (from RefSeq NM_001077446.4)
30TOMM20P4n/a
    
    
     
n/achrX 73,223,341TOMM20 pseudogene 4 (from HGNC TOMM20P4)
31HTR7P1n/a
n/a
n/a
n/a
n/achr12 13,002,1665-hydroxytryptamine receptor 7 pseudogene 1 (from HGNC HTR7P1)
32ENSG00000255621n/a
    
    
     
n/achr12 13,020,565ENSG00000255621 (from geneSymbol)
33HTR7P1n/a
n/a
n/a
n/a
n/achr12 13,002,6255-hydroxytryptamine receptor 7 pseudogene 1 (from RefSeq NR_002774.3)
34ENSG00000202343n/a
    
    
     
n/achr6 149,594,692ENSG00000202343 (from geneSymbol)
35MPHOSPH10P2n/a
    
    
     
n/achr15 32,497,174MPHOSPH10P2 (from geneSymbol)
36CCDC122n/a
n/a
n/a
n/a
n/achr13 43,858,046coiled-coil domain containing 122, transcript variant 1 (from RefSeq NM_144974.5)
37HMGB3P24n/a
    
    
     
n/achr9 36,304,211high mobility group box 3 pseudogene 24 (from HGNC HMGB3P24)
38ZNF322n/a
n/a
n/a
n/a
n/achr6 26,647,064zinc finger protein 322, transcript variant 2 (from RefSeq NM_024639.5)
39ENSG00000224331n/a
    
    
     
n/achr2 164,687,441ENSG00000224331 (from geneSymbol)
40ENSG00000219755n/a
    
    
     
n/achr6 99,576,084ENSG00000219755 (from geneSymbol)
41ENSG00000265194n/a
    
    
     
n/achr9 21,860,418ENSG00000265194 (from geneSymbol)
42ENSG00000272914n/a
    
    
     
n/achr10 30,832,607ENSG00000272914 (from geneSymbol)
43ENSG00000241269n/a
    
    
     
n/achr7 5,420,297ENSG00000241269 (from geneSymbol)
44DGCR11n/a
    
    
     
n/achr22 19,047,268DiGeorge syndrome critical region gene 11 (from RefSeq NR_024157.1)
45RPL31P17n/a
    
    
     
n/achr2 222,726,645ribosomal protein L31 pseudogene 17 (from HGNC RPL31P17)
46TCEA1P4n/a
    
    
     
n/achr9 32,979,981transcription elongation factor A1 pseudogene 4 (from HGNC TCEA1P4)
47ENSG00000268442n/a
    
    
     
n/achr19 24,162,897hepatitis A virus cellular receptor 1 pseudogene 1 (from RefSeq NR_003603.1)
48C4orf36n/a
n/a
n/a
n/a
n/achr4 86,884,313chromosome 4 open reading frame 36, transcript variant 1 (from RefSeq NM_144645.4)
49ENSG00000284968n/a
n/a
n/a
n/a
n/achr4 86,930,416ENSG00000284968 (from geneSymbol)
50C4orf36n/a
n/a
n/a
n/a
n/achr4 86,910,602chromosome 4 open reading frame 36, transcript variant 20 (from RefSeq NR_183022.1)