UBAP2L (ubiquitin associated protein 2 like) - Rat Genome Database

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Gene: UBAP2L (ubiquitin associated protein 2 like) Homo sapiens
Analyze
Symbol: UBAP2L
Name: ubiquitin associated protein 2 like
RGD ID: 1354268
HGNC Page HGNC:29877
Description: Enables RNA binding activity. Involved in binding activity of sperm to zona pellucida; positive regulation of stress granule assembly; and stress granule assembly. Acts upstream of or within hematopoietic stem cell homeostasis. Part of PcG protein complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ42300; KIAA0144; NEDLBF; NICE-4; NICE4; RNA polymerase II degradation factor UBAP2L; ubiquitin associated protein 2-like; ubiquitin-associated protein 2-like
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381154,220,172 - 154,271,510 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1154,220,179 - 154,271,510 (+)EnsemblGRCh38hg38GRCh38
GRCh371154,192,648 - 154,243,986 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361152,460,067 - 152,509,953 (+)NCBINCBI36Build 36hg18NCBI36
Build 341151,010,630 - 151,056,401NCBI
Celera1127,264,371 - 127,315,051 (+)NCBICelera
Cytogenetic Map1q21.3NCBI
HuRef1125,556,311 - 125,607,005 (+)NCBIHuRef
CHM1_11155,588,964 - 155,639,662 (+)NCBICHM1_1
T2T-CHM13v2.01153,357,369 - 153,408,720 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8590280   PMID:11230159   PMID:12421765   PMID:12477932   PMID:14667819   PMID:15144186   PMID:15302935   PMID:15489334   PMID:15592455   PMID:16009940   PMID:16055720   PMID:16094384  
PMID:16710414   PMID:16713569   PMID:16964243   PMID:17081983   PMID:17148452   PMID:18838386   PMID:19322201   PMID:19738201   PMID:19945174   PMID:20200978   PMID:20237496   PMID:21145461  
PMID:21182205   PMID:21653829   PMID:21873635   PMID:22586326   PMID:22623428   PMID:22658674   PMID:22681889   PMID:22939629   PMID:23349634   PMID:23602568   PMID:23824909   PMID:24104479  
PMID:24457600   PMID:24711643   PMID:24981860   PMID:25069639   PMID:25185265   PMID:25192599   PMID:25281560   PMID:25631074   PMID:25852190   PMID:25900982   PMID:25921289   PMID:26170170  
PMID:26217791   PMID:26310274   PMID:26344197   PMID:26381755   PMID:26496610   PMID:26514267   PMID:26673895   PMID:26760575   PMID:26777405   PMID:26831064   PMID:26949739   PMID:26972000  
PMID:27025967   PMID:27114546   PMID:27505670   PMID:27565346   PMID:27634302   PMID:27647897   PMID:28065597   PMID:28302793   PMID:28334716   PMID:28515276   PMID:28611215   PMID:28754713  
PMID:28846114   PMID:28981479   PMID:29117863   PMID:29128334   PMID:29196913   PMID:29346117   PMID:29395067   PMID:29507755   PMID:29845934   PMID:29961565   PMID:30209976   PMID:30291221  
PMID:30463901   PMID:30472188   PMID:30629181   PMID:30833792   PMID:30948266   PMID:30995489   PMID:31048545   PMID:31091453   PMID:31114027   PMID:31332168   PMID:31586073   PMID:31617661  
PMID:31723608   PMID:31732153   PMID:31882469   PMID:31956030   PMID:32041737   PMID:32129710   PMID:32203420   PMID:32296183   PMID:32302570   PMID:32353859   PMID:32513696   PMID:32529326  
PMID:32687490   PMID:32707033   PMID:32786267   PMID:32788342   PMID:32807991   PMID:32814769   PMID:32869873   PMID:32905556   PMID:33005030   PMID:33022573   PMID:33060197   PMID:33106477  
PMID:33306668   PMID:33397691   PMID:33545068   PMID:33644029   PMID:33729478   PMID:33916271   PMID:34011540   PMID:34079125   PMID:34171383   PMID:34244482   PMID:34244565   PMID:34265304  
PMID:34308648   PMID:34373451   PMID:34650049   PMID:34709727   PMID:34728620   PMID:34795231   PMID:34799561   PMID:34823423   PMID:35013218   PMID:35102251   PMID:35140242   PMID:35241646  
PMID:35256949   PMID:35271311   PMID:35337019   PMID:35338135   PMID:35439318   PMID:35446349   PMID:35546148   PMID:35633597   PMID:35652658   PMID:35819319   PMID:35831314   PMID:35944360  
PMID:35987950   PMID:36057605   PMID:36114006   PMID:36180527   PMID:36199071   PMID:36215168   PMID:36217030   PMID:36232890   PMID:36244648   PMID:36261009   PMID:36373674   PMID:36538041  
PMID:36634849   PMID:36912080   PMID:36964488   PMID:37039032   PMID:37151849   PMID:37536630   PMID:37704626   PMID:37774976   PMID:38113892   PMID:38280479  


Genomics

Comparative Map Data
UBAP2L
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381154,220,172 - 154,271,510 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1154,220,179 - 154,271,510 (+)EnsemblGRCh38hg38GRCh38
GRCh371154,192,648 - 154,243,986 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361152,460,067 - 152,509,953 (+)NCBINCBI36Build 36hg18NCBI36
Build 341151,010,630 - 151,056,401NCBI
Celera1127,264,371 - 127,315,051 (+)NCBICelera
Cytogenetic Map1q21.3NCBI
HuRef1125,556,311 - 125,607,005 (+)NCBIHuRef
CHM1_11155,588,964 - 155,639,662 (+)NCBICHM1_1
T2T-CHM13v2.01153,357,369 - 153,408,720 (+)NCBIT2T-CHM13v2.0
Ubap2l
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39389,906,896 - 89,959,867 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl389,907,447 - 89,959,935 (-)EnsemblGRCm39 Ensembl
GRCm38389,999,589 - 90,052,609 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl390,000,140 - 90,052,628 (-)EnsemblGRCm38mm10GRCm38
MGSCv37389,803,511 - 89,856,437 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36390,086,067 - 90,138,392 (-)NCBIMGSCv36mm8
Celera390,036,129 - 90,089,047 (-)NCBICelera
Cytogenetic Map3F1NCBI
cM Map339.19NCBI
Ubap2l
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82177,736,378 - 177,791,746 (-)NCBIGRCr8
mRatBN7.22175,438,703 - 175,494,085 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2175,438,703 - 175,493,998 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx2182,585,047 - 182,640,443 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.02180,607,425 - 180,662,830 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.02175,208,128 - 175,263,431 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.02189,334,341 - 189,400,334 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2189,334,341 - 189,400,323 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02208,766,347 - 208,832,798 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42182,236,653 - 182,274,323 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.12182,188,831 - 182,224,512 (-)NCBI
Celera2169,378,164 - 169,433,055 (-)NCBICelera
Cytogenetic Map2q34NCBI
Ubap2l
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955545768,058 - 815,632 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955545767,265 - 815,632 (+)NCBIChiLan1.0ChiLan1.0
UBAP2L
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2195,562,493 - 95,613,638 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1195,297,724 - 95,349,197 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01129,575,115 - 129,626,565 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11133,189,194 - 133,240,090 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1133,189,194 - 133,240,090 (+)Ensemblpanpan1.1panPan2
UBAP2L
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1742,973,598 - 43,015,007 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl742,974,092 - 43,010,848 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha742,463,992 - 42,505,420 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0742,843,514 - 42,885,522 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1742,622,858 - 42,664,296 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0742,676,123 - 42,717,542 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0742,960,214 - 43,001,682 (-)NCBIUU_Cfam_GSD_1.0
Ubap2l
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505824,883,283 - 24,929,500 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365803,914,468 - 3,959,789 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365803,913,460 - 3,960,026 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
UBAP2L
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl495,471,126 - 95,520,425 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1495,471,122 - 95,519,800 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24104,388,405 - 104,436,880 (-)NCBISscrofa10.2Sscrofa10.2susScr3
UBAP2L
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1209,546,201 - 9,591,728 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl209,545,581 - 9,591,659 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660388,904,155 - 8,961,258 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ubap2l
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248853,043,328 - 3,089,664 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248853,043,328 - 3,089,657 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in UBAP2L
46 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_014847.4(UBAP2L):c.590+1G>A single nucleotide variant Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies [RCV003325328] Chr1:154236612 [GRCh38]
Chr1:154209088 [GRCh37]
Chr1:1q21.3		 pathogenic
NM_014847.3(UBAP2L):c.2421A>C (p.Pro807=) single nucleotide variant Malignant melanoma [RCV000064180] Chr1:154257413 [GRCh38]
Chr1:154229889 [GRCh37]
Chr1:152496513 [NCBI36]
Chr1:1q21.3		 not provided
NM_006118.3(HAX1):c.500A>G (p.His167Arg) single nucleotide variant Malignant melanoma [RCV000064181] Chr1:154273957 [GRCh38]
Chr1:154246433 [GRCh37]
Chr1:152513057 [NCBI36]
Chr1:1q21.3		 not provided
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2		 pathogenic
NM_014847.4(UBAP2L):c.1582G>A (p.Val528Ile) single nucleotide variant Inborn genetic diseases [RCV003267992] Chr1:154251571 [GRCh38]
Chr1:154224047 [GRCh37]
Chr1:1q21.3		 uncertain significance
Single allele inversion Pediatric metastatic thyroid tumour [RCV000585807] Chr1:154130985..156843877 [GRCh37]
Chr1:1q21.3-23.1		 likely pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NM_014847.4(UBAP2L):c.31C>T (p.Arg11Trp) single nucleotide variant not provided [RCV003313397] Chr1:154225154 [GRCh38]
Chr1:154197630 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q21.3-23.1(chr1:153751465-156660462)x3 copy number gain not provided [RCV000585385] Chr1:153751465..156660462 [GRCh37]
Chr1:1q21.3-23.1		 likely pathogenic
GRCh37/hg19 1q21.3(chr1:150853044-154647786)x3 copy number gain not provided [RCV000684655] Chr1:150853044..154647786 [GRCh37]
Chr1:1q21.3		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
NM_014847.4(UBAP2L):c.2064T>C (p.Thr688=) single nucleotide variant not provided [RCV000901932] Chr1:154255306 [GRCh38]
Chr1:154227782 [GRCh37]
Chr1:1q21.3		 likely benign
NM_014847.4(UBAP2L):c.1491+10C>A single nucleotide variant not provided [RCV000900172] Chr1:154251328 [GRCh38]
Chr1:154223804 [GRCh37]
Chr1:1q21.3		 benign
NM_014847.4(UBAP2L):c.2703G>A (p.Ala901=) single nucleotide variant not provided [RCV000900173] Chr1:154261016 [GRCh38]
Chr1:154233492 [GRCh37]
Chr1:1q21.3		 likely benign
GRCh37/hg19 1q21.3(chr1:153701504-154218584) copy number loss Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome [RCV000767778] Chr1:153701504..154218584 [GRCh37]
Chr1:1q21.3		 pathogenic
GRCh37/hg19 1q21.3(chr1:154213874-154331789)x3 copy number gain not provided [RCV000847973] Chr1:154213874..154331789 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2926_2927del (p.Thr976fs) microsatellite not provided [RCV001059572] Chr1:154266522..154266523 [GRCh38]
Chr1:154238998..154238999 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2475G>A (p.Met825Ile) single nucleotide variant Inborn genetic diseases [RCV003270884] Chr1:154259009 [GRCh38]
Chr1:154231485 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2314G>C (p.Val772Leu) single nucleotide variant Inborn genetic diseases [RCV003249741] Chr1:154257219 [GRCh38]
Chr1:154229695 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2850G>A (p.Ser950=) single nucleotide variant not provided [RCV000946499] Chr1:154261645 [GRCh38]
Chr1:154234121 [GRCh37]
Chr1:1q21.3		 benign
GRCh37/hg19 1q21.3(chr1:153659094-154307972)x3 copy number gain not provided [RCV001005142] Chr1:153659094..154307972 [GRCh37]
Chr1:1q21.3		 uncertain significance
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
NM_014847.4(UBAP2L):c.2724C>A (p.Tyr908Ter) single nucleotide variant Global developmental delay [RCV001527608]|Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies [RCV003325313] Chr1:154261037 [GRCh38]
Chr1:154233513 [GRCh37]
Chr1:1q21.3		 pathogenic|uncertain significance
NC_000001.10:g.(?_154141761)_(156851434_?)dup duplication Charcot-Marie-Tooth disease type 2 [RCV001990060] Chr1:154141761..156851434 [GRCh37]
Chr1:1q21.3-23.1		 uncertain significance
NC_000001.10:g.(?_149895434)_(156851434_?)dup duplication Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency [RCV001958273]|Congenital neutropenia-myelofibrosis-nephromegaly syndrome [RCV001958271]|Kostmann syndrome [RCV003120769]|MHC class II deficiency [RCV001992607] Chr1:149895434..156851434 [GRCh37]
Chr1:1q21.2-23.1		 uncertain significance
NC_000001.10:g.(?_153963273)_(154580482_?)del deletion Kostmann syndrome [RCV003116530] Chr1:153963273..154580482 [GRCh37]
Chr1:1q21.3		 pathogenic
NM_014847.4(UBAP2L):c.88C>T (p.Gln30Ter) single nucleotide variant Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies [RCV003325326] Chr1:154225211 [GRCh38]
Chr1:154197687 [GRCh37]
Chr1:1q21.3		 pathogenic
NM_014847.4(UBAP2L):c.3168+3A>G single nucleotide variant Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies [RCV003325321]|not provided [RCV003129467] Chr1:154268957 [GRCh38]
Chr1:154241433 [GRCh37]
Chr1:1q21.3		 pathogenic
NM_014847.4(UBAP2L):c.403G>C (p.Gly135Arg) single nucleotide variant Inborn genetic diseases [RCV003277868] Chr1:154234714 [GRCh38]
Chr1:154207190 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.1846C>T (p.Gln616Ter) single nucleotide variant not provided [RCV003129273] Chr1:154254081 [GRCh38]
Chr1:154226557 [GRCh37]
Chr1:1q21.3		 pathogenic
NM_014847.4(UBAP2L):c.2870C>T (p.Pro957Leu) single nucleotide variant Inborn genetic diseases [RCV002772917] Chr1:154261665 [GRCh38]
Chr1:154234141 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.655G>A (p.Gly219Ser) single nucleotide variant Inborn genetic diseases [RCV002906045] Chr1:154237088 [GRCh38]
Chr1:154209564 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2682G>C (p.Gln894His) single nucleotide variant Inborn genetic diseases [RCV002738139] Chr1:154260995 [GRCh38]
Chr1:154233471 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.350A>G (p.Asn117Ser) single nucleotide variant Inborn genetic diseases [RCV002660993] Chr1:154234661 [GRCh38]
Chr1:154207137 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.1925C>T (p.Ala642Val) single nucleotide variant Inborn genetic diseases [RCV002984742] Chr1:154255167 [GRCh38]
Chr1:154227643 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2335T>C (p.Ser779Pro) single nucleotide variant Inborn genetic diseases [RCV002674275] Chr1:154257240 [GRCh38]
Chr1:154229716 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.29C>G (p.Ala10Gly) single nucleotide variant Inborn genetic diseases [RCV002669648] Chr1:154225152 [GRCh38]
Chr1:154197628 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.394C>T (p.Arg132Trp) single nucleotide variant Inborn genetic diseases [RCV002812894] Chr1:154234705 [GRCh38]
Chr1:154207181 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.1007A>G (p.His336Arg) single nucleotide variant Inborn genetic diseases [RCV003200410] Chr1:154246368 [GRCh38]
Chr1:154218844 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.1699C>G (p.Gln567Glu) single nucleotide variant Inborn genetic diseases [RCV003218619] Chr1:154253934 [GRCh38]
Chr1:154226410 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.1991C>G (p.Ser664Cys) single nucleotide variant Inborn genetic diseases [RCV003193526] Chr1:154255233 [GRCh38]
Chr1:154227709 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2117C>T (p.Ser706Leu) single nucleotide variant not provided [RCV003229225] Chr1:154255715 [GRCh38]
Chr1:154228191 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2929G>C (p.Gly977Arg) single nucleotide variant Inborn genetic diseases [RCV003210076] Chr1:154266527 [GRCh38]
Chr1:154239003 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2432A>G (p.His811Arg) single nucleotide variant not provided [RCV003223785] Chr1:154257424 [GRCh38]
Chr1:154229900 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.562G>T (p.Gly188Ter) single nucleotide variant Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies [RCV003325327] Chr1:154236583 [GRCh38]
Chr1:154209059 [GRCh37]
Chr1:1q21.3		 pathogenic
GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3 copy number gain Chromosome 1q21.1 duplication syndrome [RCV003329522] Chr1:142535935..157648813 [GRCh37]
Chr1:1q12-23.1		 pathogenic
NM_014847.4(UBAP2L):c.934C>A (p.Gln312Lys) single nucleotide variant Inborn genetic diseases [RCV003386080] Chr1:154246295 [GRCh38]
Chr1:154218771 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.3214C>T (p.Pro1072Ser) single nucleotide variant Inborn genetic diseases [RCV003372438]|Neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies [RCV003492875] Chr1:154270245 [GRCh38]
Chr1:154242721 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.610T>A (p.Tyr204Asn) single nucleotide variant not provided [RCV003332787] Chr1:154237043 [GRCh38]
Chr1:154209519 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.1330A>G (p.Thr444Ala) single nucleotide variant Inborn genetic diseases [RCV003374127] Chr1:154251157 [GRCh38]
Chr1:154223633 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3 copy number gain not specified [RCV003986717] Chr1:144368497..158992086 [GRCh37]
Chr1:1q21.1-23.1		 pathogenic
GRCh37/hg19 1q21.3(chr1:154089394-154912611)x3 copy number gain not specified [RCV003986629] Chr1:154089394..154912611 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3 copy number gain not specified [RCV003987261] Chr1:146577511..157155587 [GRCh37]
Chr1:1q21.1-23.1		 pathogenic
NM_014847.4(UBAP2L):c.2264G>T (p.Ser755Ile) single nucleotide variant Inborn genetic diseases [RCV003357581] Chr1:154257169 [GRCh38]
Chr1:154229645 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_014847.4(UBAP2L):c.2000C>T (p.Thr667Met) single nucleotide variant Inborn genetic diseases [RCV003304154] Chr1:154255242 [GRCh38]
Chr1:154227718 [GRCh37]
Chr1:1q21.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3982
Count of miRNA genes:1133
Interacting mature miRNAs:1474
Transcripts:ENST00000271877, ENST00000343815, ENST00000361546, ENST00000368504, ENST00000412596, ENST00000428595, ENST00000428931, ENST00000433615, ENST00000437652, ENST00000441890, ENST00000456325, ENST00000465855, ENST00000466173, ENST00000475373, ENST00000484696, ENST00000484819, ENST00000489076, ENST00000493867, ENST00000495676
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
D1S3020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,243,764 - 154,243,916UniSTSGRCh37
Build 361152,510,388 - 152,510,540RGDNCBI36
Celera1127,315,486 - 127,315,638RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,607,440 - 125,607,592UniSTS
GeneMap99-GB4 RH Map1554.37UniSTS
Whitehead-YAC Contig Map1 UniSTS
NCBI RH Map11357.8UniSTS
Cda13d03  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,243,785 - 154,243,916UniSTSGRCh37
Build 361152,510,409 - 152,510,540RGDNCBI36
Celera1127,315,507 - 127,315,638RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,607,461 - 125,607,592UniSTS
GeneMap99-GB4 RH Map1555.98UniSTS
NCBI RH Map11228.1UniSTS
D1S2274  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,194,852 - 154,194,958UniSTSGRCh37
GRCh371154,194,757 - 154,194,958UniSTSGRCh37
Build 361152,461,381 - 152,461,582RGDNCBI36
Celera1127,266,473 - 127,266,674RGD
Celera1127,266,568 - 127,266,674UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q21.2UniSTS
HuRef1125,558,509 - 125,558,615UniSTS
HuRef1125,558,414 - 125,558,615UniSTS
SHGC-104553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,201,630 - 154,201,905UniSTSGRCh37
Build 361152,468,254 - 152,468,529RGDNCBI36
Celera1127,273,345 - 127,273,620RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,565,286 - 125,565,561UniSTS
TNG Radiation Hybrid Map169250.0UniSTS
SHGC-143399  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,236,583 - 154,236,888UniSTSGRCh37
Build 361152,503,207 - 152,503,512RGDNCBI36
Celera1127,308,296 - 127,308,601RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,600,247 - 125,600,552UniSTS
TNG Radiation Hybrid Map169269.0UniSTS
RH36191  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,242,990 - 154,243,089UniSTSGRCh37
Build 361152,509,614 - 152,509,713RGDNCBI36
Celera1127,314,712 - 127,314,811RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,606,664 - 125,606,763UniSTS
GeneMap99-GB4 RH Map1555.98UniSTS
NCBI RH Map11222.2UniSTS
SHGC-33740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,243,544 - 154,243,670UniSTSGRCh37
GRCh37X31,686,866 - 31,687,681UniSTSGRCh37
Build 361152,510,168 - 152,510,294RGDNCBI36
CeleraX35,814,364 - 35,815,179UniSTS
Celera1127,315,266 - 127,315,392RGD
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
HuRefX29,425,970 - 29,426,785UniSTS
HuRef1125,607,220 - 125,607,346UniSTS
GeneMap99-GB4 RH Map1541.2UniSTS
Whitehead-RH Map1678.9UniSTS
NCBI RH Map11119.5UniSTS
RH18226  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,243,431 - 154,243,554UniSTSGRCh37
Build 361152,510,055 - 152,510,178RGDNCBI36
Celera1127,315,153 - 127,315,276RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,607,107 - 125,607,230UniSTS
GeneMap99-GB4 RH Map1552.61UniSTS
NCBI RH Map11074.6UniSTS
RH44951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371154,235,746 - 154,235,861UniSTSGRCh37
Build 361152,502,370 - 152,502,485RGDNCBI36
Celera1127,307,459 - 127,307,574RGD
Cytogenetic Map1q21.3UniSTS
HuRef1125,599,410 - 125,599,525UniSTS
GeneMap99-GB4 RH Map1554.37UniSTS
NCBI RH Map11357.8UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2437 2699 1663 563 1788 404 4357 2078 3374 403 1460 1612 175 1 1204 2788 6 2
Low 2 292 63 61 163 61 119 360 16 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001127320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001287815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001287816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330730 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375623 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001375631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245667 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005245673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002972 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024451291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435852 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435856 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435859 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435866 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435874 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435875 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435887 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047435905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339891 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339895 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339896 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339897 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339898 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339907 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339909 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339914 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054339915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AJ243668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ243669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ243670 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK124294 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302662 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL590431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR933686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D63478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC369803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC404293 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000271877   ⟹   ENSP00000271877
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,849 - 154,271,509 (+)Ensembl
RefSeq Acc Id: ENST00000343815   ⟹   ENSP00000345308
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,179 - 154,263,505 (+)Ensembl
RefSeq Acc Id: ENST00000361546   ⟹   ENSP00000355343
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,225,082 - 154,270,853 (+)Ensembl
RefSeq Acc Id: ENST00000368504   ⟹   ENSP00000357490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,822 - 154,235,261 (+)Ensembl
RefSeq Acc Id: ENST00000412596   ⟹   ENSP00000389052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,943 - 154,243,302 (+)Ensembl
RefSeq Acc Id: ENST00000428595   ⟹   ENSP00000398609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,257,071 - 154,270,564 (+)Ensembl
RefSeq Acc Id: ENST00000428931   ⟹   ENSP00000389445
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,955 - 154,270,847 (+)Ensembl
RefSeq Acc Id: ENST00000433615   ⟹   ENSP00000407672
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,255,252 - 154,271,510 (+)Ensembl
RefSeq Acc Id: ENST00000437652   ⟹   ENSP00000389717
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,950 - 154,270,728 (+)Ensembl
RefSeq Acc Id: ENST00000441890   ⟹   ENSP00000399920
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,885 - 154,235,294 (+)Ensembl
RefSeq Acc Id: ENST00000456325   ⟹   ENSP00000415310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,221,328 - 154,237,136 (+)Ensembl
RefSeq Acc Id: ENST00000465855
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,257,345 - 154,261,699 (+)Ensembl
RefSeq Acc Id: ENST00000466173
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,242,930 - 154,251,100 (+)Ensembl
RefSeq Acc Id: ENST00000475373
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,259,736 - 154,263,322 (+)Ensembl
RefSeq Acc Id: ENST00000484696
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,258,631 - 154,261,020 (+)Ensembl
RefSeq Acc Id: ENST00000484819
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,266,452 - 154,269,695 (+)Ensembl
RefSeq Acc Id: ENST00000489076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,255,247 - 154,257,846 (+)Ensembl
RefSeq Acc Id: ENST00000493867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,261,628 - 154,271,173 (+)Ensembl
RefSeq Acc Id: ENST00000495676
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,254,647 - 154,259,983 (+)Ensembl
RefSeq Acc Id: ENST00000613315   ⟹   ENSP00000478447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,849 - 154,263,505 (+)Ensembl
RefSeq Acc Id: ENST00000707139   ⟹   ENSP00000516761
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,220,957 - 154,263,485 (+)Ensembl
RefSeq Acc Id: NM_001127320   ⟹   NP_001120792
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,172 - 154,263,504 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Celera1127,264,371 - 127,315,051 (+)RGD
HuRef1125,556,304 - 125,607,662 (+)NCBI
CHM1_11155,588,957 - 155,632,289 (+)NCBI
T2T-CHM13v2.01153,357,369 - 153,400,701 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001287815   ⟹   NP_001274744
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,263,505 (+)NCBI
HuRef1125,556,304 - 125,607,662 (+)NCBI
CHM1_11155,589,634 - 155,632,289 (+)NCBI
T2T-CHM13v2.01153,358,046 - 153,400,702 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001287816   ⟹   NP_001274745
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
HuRef1125,556,304 - 125,607,662 (+)NCBI
CHM1_11155,589,634 - 155,640,319 (+)NCBI
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001330730   ⟹   NP_001317659
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375612   ⟹   NP_001362541
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375614   ⟹   NP_001362543
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375615   ⟹   NP_001362544
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375616   ⟹   NP_001362545
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375617   ⟹   NP_001362546
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375618   ⟹   NP_001362547
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375619   ⟹   NP_001362548
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,501 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375620   ⟹   NP_001362549
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375621   ⟹   NP_001362550
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375622   ⟹   NP_001362551
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,270,847 (+)NCBI
T2T-CHM13v2.01153,358,501 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375623   ⟹   NP_001362552
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375624   ⟹   NP_001362553
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375625   ⟹   NP_001362554
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375626   ⟹   NP_001362555
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375627   ⟹   NP_001362556
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375628   ⟹   NP_001362557
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375629   ⟹   NP_001362558
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,263,504 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,400,701 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375630   ⟹   NP_001362559
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,263,504 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,400,701 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001375631   ⟹   NP_001362560
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,263,504 (+)NCBI
T2T-CHM13v2.01153,358,501 - 153,400,701 (+)NCBI
Sequence:
RefSeq Acc Id: NM_014847   ⟹   NP_055662
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Build 361152,460,067 - 152,509,953 (+)NCBI Archive
Celera1127,264,371 - 127,315,051 (+)RGD
HuRef1125,556,304 - 125,607,662 (+)NCBI
CHM1_11155,589,634 - 155,639,662 (+)NCBI
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245667   ⟹   XP_005245724
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,270,847 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245668   ⟹   XP_005245725
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245669   ⟹   XP_005245726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245672   ⟹   XP_005245729
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005245673   ⟹   XP_005245730
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,263,504 (+)NCBI
GRCh371154,192,427 - 154,243,986 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011510215   ⟹   XP_011508517
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,270,847 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017002972   ⟹   XP_016858461
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017002982   ⟹   XP_016858471
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047435820   ⟹   XP_047291776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435824   ⟹   XP_047291780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435827   ⟹   XP_047291783
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,172 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435828   ⟹   XP_047291784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435834   ⟹   XP_047291790
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435844   ⟹   XP_047291800
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435852   ⟹   XP_047291808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,270,847 (+)NCBI
RefSeq Acc Id: XM_047435856   ⟹   XP_047291812
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435859   ⟹   XP_047291815
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435866   ⟹   XP_047291822
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,849 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435868   ⟹   XP_047291824
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435869   ⟹   XP_047291825
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,172 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435874   ⟹   XP_047291830
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435875   ⟹   XP_047291831
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,172 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435876   ⟹   XP_047291832
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435877   ⟹   XP_047291833
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435887   ⟹   XP_047291843
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435896   ⟹   XP_047291852
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,271,510 (+)NCBI
RefSeq Acc Id: XM_047435898   ⟹   XP_047291854
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,955 - 154,263,504 (+)NCBI
RefSeq Acc Id: XM_047435905   ⟹   XP_047291861
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,221,304 - 154,263,504 (+)NCBI
RefSeq Acc Id: XM_054339888   ⟹   XP_054195863
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339889   ⟹   XP_054195864
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339890   ⟹   XP_054195865
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339891   ⟹   XP_054195866
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339892   ⟹   XP_054195867
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,357,369 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339893   ⟹   XP_054195868
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339894   ⟹   XP_054195869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339895   ⟹   XP_054195870
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339896   ⟹   XP_054195871
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339897   ⟹   XP_054195872
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,057 (+)NCBI
RefSeq Acc Id: XM_054339898   ⟹   XP_054195873
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339899   ⟹   XP_054195874
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339900   ⟹   XP_054195875
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339901   ⟹   XP_054195876
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339902   ⟹   XP_054195877
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339903   ⟹   XP_054195878
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339904   ⟹   XP_054195879
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,357,369 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339905   ⟹   XP_054195880
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339906   ⟹   XP_054195881
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339907   ⟹   XP_054195882
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,357,369 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339908   ⟹   XP_054195883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339909   ⟹   XP_054195884
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339910   ⟹   XP_054195885
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339911   ⟹   XP_054195886
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339912   ⟹   XP_054195887
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,408,720 (+)NCBI
RefSeq Acc Id: XM_054339913   ⟹   XP_054195888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,152 - 153,400,701 (+)NCBI
RefSeq Acc Id: XM_054339914   ⟹   XP_054195889
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,501 - 153,400,701 (+)NCBI
RefSeq Acc Id: XM_054339915   ⟹   XP_054195890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,358,046 - 153,400,701 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001120792 (Get FASTA)   NCBI Sequence Viewer  
  NP_001274744 (Get FASTA)   NCBI Sequence Viewer  
  NP_001274745 (Get FASTA)   NCBI Sequence Viewer  
  NP_001317659 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362541 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362543 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362544 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362545 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362546 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362547 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362548 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362549 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362550 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362551 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362552 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362553 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362554 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362555 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362556 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362557 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362558 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362559 (Get FASTA)   NCBI Sequence Viewer  
  NP_001362560 (Get FASTA)   NCBI Sequence Viewer  
  NP_055662 (Get FASTA)   NCBI Sequence Viewer  
  XP_005245724 (Get FASTA)   NCBI Sequence Viewer  
  XP_005245725 (Get FASTA)   NCBI Sequence Viewer  
  XP_005245726 (Get FASTA)   NCBI Sequence Viewer  
  XP_005245729 (Get FASTA)   NCBI Sequence Viewer  
  XP_005245730 (Get FASTA)   NCBI Sequence Viewer  
  XP_011508517 (Get FASTA)   NCBI Sequence Viewer  
  XP_016858461 (Get FASTA)   NCBI Sequence Viewer  
  XP_016858471 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291776 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291780 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291783 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291784 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291790 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291800 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291808 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291812 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291815 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291822 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291824 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291825 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291830 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291831 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291832 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291833 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291843 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291852 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291854 (Get FASTA)   NCBI Sequence Viewer  
  XP_047291861 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195863 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195864 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195865 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195866 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195867 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195868 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195869 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195870 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195871 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195872 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195873 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195874 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195875 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195876 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195877 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195878 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195879 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195880 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195881 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195882 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195883 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195884 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195885 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195886 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195887 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195888 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195889 (Get FASTA)   NCBI Sequence Viewer  
  XP_054195890 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH03170 (Get FASTA)   NCBI Sequence Viewer  
  BAA09765 (Get FASTA)   NCBI Sequence Viewer  
  BAG63897 (Get FASTA)   NCBI Sequence Viewer  
  BAG64108 (Get FASTA)   NCBI Sequence Viewer  
  BAG64560 (Get FASTA)   NCBI Sequence Viewer  
  CAB65099 (Get FASTA)   NCBI Sequence Viewer  
  CAB65100 (Get FASTA)   NCBI Sequence Viewer  
  CAB65101 (Get FASTA)   NCBI Sequence Viewer  
  EAW53213 (Get FASTA)   NCBI Sequence Viewer  
  EAW53214 (Get FASTA)   NCBI Sequence Viewer  
  EAW53215 (Get FASTA)   NCBI Sequence Viewer  
  EAW53216 (Get FASTA)   NCBI Sequence Viewer  
  EAW53217 (Get FASTA)   NCBI Sequence Viewer  
  EAW53218 (Get FASTA)   NCBI Sequence Viewer  
  EAW53219 (Get FASTA)   NCBI Sequence Viewer  
  EAW53220 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000271877
  ENSP00000271877.8
  ENSP00000345308
  ENSP00000345308.6
  ENSP00000355343.2
  ENSP00000357490.2
  ENSP00000389052.1
  ENSP00000389445
  ENSP00000389445.1
  ENSP00000389717
  ENSP00000389717.2
  ENSP00000398609.1
  ENSP00000399920.1
  ENSP00000407672.1
  ENSP00000415310.1
  ENSP00000478447
  ENSP00000478447.1
  ENSP00000516761
  ENSP00000516761.1
GenBank Protein Q14157 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001120792   ⟸   NM_001127320
- Peptide Label: isoform b
- UniProtKB: B4DZJ6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_055662   ⟸   NM_014847
- Peptide Label: isoform a
- UniProtKB: Q9UGL4 (UniProtKB/Swiss-Prot),   Q9UGL3 (UniProtKB/Swiss-Prot),   Q9UGL2 (UniProtKB/Swiss-Prot),   Q9BTU3 (UniProtKB/Swiss-Prot),   Q5VU76 (UniProtKB/Swiss-Prot),   Q5VU75 (UniProtKB/Swiss-Prot),   B4E0U8 (UniProtKB/Swiss-Prot),   Q9UGL5 (UniProtKB/Swiss-Prot),   Q14157 (UniProtKB/Swiss-Prot),   Q5VU79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245725   ⟸   XM_005245668
- Peptide Label: isoform X5
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245726   ⟸   XM_005245669
- Peptide Label: isoform X6
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245724   ⟸   XM_005245667
- Peptide Label: isoform X3
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245730   ⟸   XM_005245673
- Peptide Label: isoform X13
- UniProtKB: A0AA34QVE6 (UniProtKB/TrEMBL),   B4DZJ6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005245729   ⟸   XM_005245672
- Peptide Label: isoform X12
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001274745   ⟸   NM_001287816
- Peptide Label: isoform d
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001274744   ⟸   NM_001287815
- Peptide Label: isoform c
- UniProtKB: B4DZJ6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011508517   ⟸   XM_011510215
- Peptide Label: isoform X1
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858461   ⟸   XM_017002972
- Peptide Label: isoform X1
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858471   ⟸   XM_017002982
- Peptide Label: isoform X8
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001317659   ⟸   NM_001330730
- Peptide Label: isoform e
- UniProtKB: F8W726 (UniProtKB/TrEMBL),   B4DYY5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001362554   ⟸   NM_001375625
- Peptide Label: isoform e
- UniProtKB: F8W726 (UniProtKB/TrEMBL),   B4DYY5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362552   ⟸   NM_001375623
- Peptide Label: isoform k
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362556   ⟸   NM_001375627
- Peptide Label: isoform m
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362553   ⟸   NM_001375624
- Peptide Label: isoform l
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362557   ⟸   NM_001375628
- Peptide Label: isoform n
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362555   ⟸   NM_001375626
- Peptide Label: isoform m
- UniProtKB: B4DYY5 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362547   ⟸   NM_001375618
- Peptide Label: isoform a
- UniProtKB: Q9UGL4 (UniProtKB/Swiss-Prot),   Q9UGL3 (UniProtKB/Swiss-Prot),   Q9UGL2 (UniProtKB/Swiss-Prot),   Q9BTU3 (UniProtKB/Swiss-Prot),   Q5VU76 (UniProtKB/Swiss-Prot),   Q5VU75 (UniProtKB/Swiss-Prot),   Q14157 (UniProtKB/Swiss-Prot),   B4E0U8 (UniProtKB/Swiss-Prot),   Q9UGL5 (UniProtKB/Swiss-Prot),   Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362545   ⟸   NM_001375616
- Peptide Label: isoform h
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362550   ⟸   NM_001375621
- Peptide Label: isoform j
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362541   ⟸   NM_001375612
- Peptide Label: isoform f
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362546   ⟸   NM_001375617
- Peptide Label: isoform i
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362543   ⟸   NM_001375614
- Peptide Label: isoform g
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362544   ⟸   NM_001375615
- Peptide Label: isoform h
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362549   ⟸   NM_001375620
- Peptide Label: isoform j
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362559   ⟸   NM_001375630
- Peptide Label: isoform b
- UniProtKB: B4DZJ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362558   ⟸   NM_001375629
- Peptide Label: isoform b
- UniProtKB: B4DZJ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362548   ⟸   NM_001375619
- Peptide Label: isoform a
- UniProtKB: Q9UGL4 (UniProtKB/Swiss-Prot),   Q9UGL3 (UniProtKB/Swiss-Prot),   Q9UGL2 (UniProtKB/Swiss-Prot),   Q9BTU3 (UniProtKB/Swiss-Prot),   Q5VU76 (UniProtKB/Swiss-Prot),   Q5VU75 (UniProtKB/Swiss-Prot),   Q14157 (UniProtKB/Swiss-Prot),   B4E0U8 (UniProtKB/Swiss-Prot),   Q9UGL5 (UniProtKB/Swiss-Prot),   Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362551   ⟸   NM_001375622
- Peptide Label: isoform j
- UniProtKB: Q5VU79 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001362560   ⟸   NM_001375631
- Peptide Label: isoform b
- UniProtKB: B4DZJ6 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000389717   ⟸   ENST00000437652
RefSeq Acc Id: ENSP00000389052   ⟸   ENST00000412596
RefSeq Acc Id: ENSP00000389445   ⟸   ENST00000428931
RefSeq Acc Id: ENSP00000398609   ⟸   ENST00000428595
RefSeq Acc Id: ENSP00000355343   ⟸   ENST00000361546
RefSeq Acc Id: ENSP00000399920   ⟸   ENST00000441890
RefSeq Acc Id: ENSP00000478447   ⟸   ENST00000613315
RefSeq Acc Id: ENSP00000415310   ⟸   ENST00000456325
RefSeq Acc Id: ENSP00000271877   ⟸   ENST00000271877
RefSeq Acc Id: ENSP00000357490   ⟸   ENST00000368504
RefSeq Acc Id: ENSP00000407672   ⟸   ENST00000433615
RefSeq Acc Id: ENSP00000345308   ⟸   ENST00000343815
RefSeq Acc Id: XP_047291825   ⟸   XM_047435869
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047291831   ⟸   XM_047435875
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047291783   ⟸   XM_047435827
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047291822   ⟸   XM_047435866
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047291812   ⟸   XM_047435856
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047291815   ⟸   XM_047435859
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047291832   ⟸   XM_047435876
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047291784   ⟸   XM_047435828
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047291800   ⟸   XM_047435844
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047291854   ⟸   XM_047435898
- Peptide Label: isoform X13
- UniProtKB: A0AA34QVE6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047291833   ⟸   XM_047435877
- Peptide Label: isoform X10
- UniProtKB: F8W726 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047291824   ⟸   XM_047435868
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047291843   ⟸   XM_047435887
- Peptide Label: isoform X11
RefSeq Acc Id: XP_047291830   ⟸   XM_047435874
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047291852   ⟸   XM_047435896
- Peptide Label: isoform X12
RefSeq Acc Id: XP_047291790   ⟸   XM_047435834
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047291776   ⟸   XM_047435820
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047291808   ⟸   XM_047435852
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047291780   ⟸   XM_047435824
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047291861   ⟸   XM_047435905
- Peptide Label: isoform X13
- UniProtKB: A0AA34QVE6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054195879   ⟸   XM_054339904
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054195882   ⟸   XM_054339907
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054195867   ⟸   XM_054339892
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054195874   ⟸   XM_054339899
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054195876   ⟸   XM_054339901
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054195877   ⟸   XM_054339902
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054195880   ⟸   XM_054339905
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054195886   ⟸   XM_054339911
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054195869   ⟸   XM_054339894
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054195864   ⟸   XM_054339889
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054195890   ⟸   XM_054339915
- Peptide Label: isoform X13
- UniProtKB: A0AA34QVE6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054195873   ⟸   XM_054339898
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054195875   ⟸   XM_054339900
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054195883   ⟸   XM_054339908
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054195868   ⟸   XM_054339893
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054195863   ⟸   XM_054339888
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054195871   ⟸   XM_054339896
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054195888   ⟸   XM_054339913
- Peptide Label: isoform X13
- UniProtKB: A0AA34QVE6 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054195884   ⟸   XM_054339909
- Peptide Label: isoform X10
- UniProtKB: F8W726 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054195878   ⟸   XM_054339903
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054195885   ⟸   XM_054339910
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054195881   ⟸   XM_054339906
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054195887   ⟸   XM_054339912
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054195870   ⟸   XM_054339895
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054195865   ⟸   XM_054339890
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054195872   ⟸   XM_054339897
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054195866   ⟸   XM_054339891
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054195889   ⟸   XM_054339914
- Peptide Label: isoform X13
- UniProtKB: A0AA34QVE6 (UniProtKB/TrEMBL)
RefSeq Acc Id: ENSP00000516761   ⟸   ENST00000707139
Protein Domains
UBA

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q14157-F1-model_v2 AlphaFold Q14157 1-1087 view protein structure

Promoters
RGD ID:6785281
Promoter ID:HG_KWN:5268
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000343815,   ENST00000368505
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,458,371 - 152,458,877 (+)MPROMDB
RGD ID:6787107
Promoter ID:HG_KWN:5269
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000368504,   NM_001098616,   NM_014847,   NM_015449,   NM_138740,   OTTHUMT00000087675,   OTTHUMT00000087676,   OTTHUMT00000087678,   OTTHUMT00000087679,   UC001FEJ.2,   UC001FEK.2,   UC001FEL.2,   UC001FEN.1,   UC001FEO.1,   UC009WOS.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,459,496 - 152,460,747 (+)MPROMDB
RGD ID:6787103
Promoter ID:HG_KWN:5270
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000271877,   OTTHUMT00000087673
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,463,576 - 152,464,377 (+)MPROMDB
RGD ID:6787108
Promoter ID:HG_KWN:5271
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   Lymphoblastoid
Transcripts:OTTHUMT00000087689
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,480,879 - 152,481,379 (+)MPROMDB
RGD ID:6787104
Promoter ID:HG_KWN:5272
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000087680,   OTTHUMT00000087681,   UC001FEQ.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,493,301 - 152,493,801 (+)MPROMDB
RGD ID:6787106
Promoter ID:HG_KWN:5276
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   K562,   Lymphoblastoid
Transcripts:OTTHUMT00000087686
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,500,076 - 152,501,077 (+)MPROMDB
RGD ID:6787109
Promoter ID:HG_KWN:5277
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:OTTHUMT00000087688
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,505,126 - 152,505,712 (+)MPROMDB
RGD ID:6857320
Promoter ID:EPDNEW_H1825
Type:initiation region
Name:UBAP2L_5
Description:ubiquitin associated protein 2 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1827  EPDNEW_H1829  EPDNEW_H1830  EPDNEW_H1831  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,195 - 154,220,255EPDNEW
RGD ID:6857324
Promoter ID:EPDNEW_H1827
Type:initiation region
Name:UBAP2L_1
Description:ubiquitin associated protein 2 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1825  EPDNEW_H1829  EPDNEW_H1830  EPDNEW_H1831  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,220,958 - 154,221,018EPDNEW
RGD ID:6857328
Promoter ID:EPDNEW_H1829
Type:initiation region
Name:UBAP2L_4
Description:ubiquitin associated protein 2 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1825  EPDNEW_H1827  EPDNEW_H1830  EPDNEW_H1831  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,225,074 - 154,225,134EPDNEW
RGD ID:6857330
Promoter ID:EPDNEW_H1830
Type:initiation region
Name:UBAP2L_3
Description:ubiquitin associated protein 2 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1825  EPDNEW_H1827  EPDNEW_H1829  EPDNEW_H1831  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,255,294 - 154,255,354EPDNEW
RGD ID:6857332
Promoter ID:EPDNEW_H1831
Type:initiation region
Name:UBAP2L_2
Description:ubiquitin associated protein 2 like
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1825  EPDNEW_H1827  EPDNEW_H1829  EPDNEW_H1830  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,257,085 - 154,257,145EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:29877 AgrOrtholog
COSMIC UBAP2L COSMIC
Ensembl Genes ENSG00000143569 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000271877 ENTREZGENE
  ENST00000271877.11 UniProtKB/TrEMBL
  ENST00000343815 ENTREZGENE
  ENST00000343815.10 UniProtKB/Swiss-Prot
  ENST00000361546.6 UniProtKB/Swiss-Prot
  ENST00000368504.6 UniProtKB/TrEMBL
  ENST00000412596.5 UniProtKB/TrEMBL
  ENST00000428595.1 UniProtKB/TrEMBL
  ENST00000428931 ENTREZGENE
  ENST00000428931.6 UniProtKB/Swiss-Prot
  ENST00000433615.5 UniProtKB/TrEMBL
  ENST00000437652 ENTREZGENE
  ENST00000437652.6 UniProtKB/TrEMBL
  ENST00000441890.5 UniProtKB/TrEMBL
  ENST00000456325.5 UniProtKB/TrEMBL
  ENST00000613315 ENTREZGENE
  ENST00000613315.4 UniProtKB/Swiss-Prot
  ENST00000707139 ENTREZGENE
  ENST00000707139.1 UniProtKB/TrEMBL
Gene3D-CATH DNA helicase RuvA subunit, C-terminal domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000143569 GTEx
HGNC ID HGNC:29877 ENTREZGENE
Human Proteome Map UBAP2L Human Proteome Map
InterPro UBA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UBA-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UBAP2/Lig UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:9898 UniProtKB/Swiss-Prot
NCBI Gene 9898 ENTREZGENE
OMIM 616472 OMIM
PANTHER UBIQUITIN ASSOCIATED PROTEIN 2-LIKE/LINGERER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UBIQUITIN-ASSOCIATED PROTEIN 2-LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DUF3697 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134883839 PharmGKB
PROSITE UBA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART UBA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF46934 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0AA34QVE6 ENTREZGENE, UniProtKB/TrEMBL
  B4DYY5 ENTREZGENE, UniProtKB/TrEMBL
  B4DZJ6 ENTREZGENE, UniProtKB/TrEMBL
  B4E0U8 ENTREZGENE
  F8W726 ENTREZGENE, UniProtKB/TrEMBL
  H0Y5H6_HUMAN UniProtKB/TrEMBL
  H7C2T8_HUMAN UniProtKB/TrEMBL
  Q14157 ENTREZGENE
  Q5VU75 ENTREZGENE
  Q5VU76 ENTREZGENE
  Q5VU77_HUMAN UniProtKB/TrEMBL
  Q5VU78_HUMAN UniProtKB/TrEMBL
  Q5VU79 ENTREZGENE, UniProtKB/TrEMBL
  Q5VU80_HUMAN UniProtKB/TrEMBL
  Q5VU81_HUMAN UniProtKB/TrEMBL
  Q9BTU3 ENTREZGENE
  Q9UGL2 ENTREZGENE
  Q9UGL3 ENTREZGENE
  Q9UGL4 ENTREZGENE
  Q9UGL5 ENTREZGENE
  UBP2L_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B4E0U8 UniProtKB/Swiss-Prot
  Q5VU75 UniProtKB/Swiss-Prot
  Q5VU76 UniProtKB/Swiss-Prot
  Q9BTU3 UniProtKB/Swiss-Prot
  Q9UGL2 UniProtKB/Swiss-Prot
  Q9UGL3 UniProtKB/Swiss-Prot
  Q9UGL4 UniProtKB/Swiss-Prot
  Q9UGL5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-17 UBAP2L  ubiquitin associated protein 2 like    ubiquitin associated protein 2-like  Symbol and/or name change 5135510 APPROVED