ARPP21 (cAMP regulated phosphoprotein 21) - Rat Genome Database

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Gene: ARPP21 (cAMP regulated phosphoprotein 21) Homo sapiens
Analyze
Symbol: ARPP21
Name: cAMP regulated phosphoprotein 21
RGD ID: 1606317
HGNC Page HGNC:16968
Description: Predicted to enable calmodulin binding activity and nucleic acid binding activity. Predicted to act upstream of or within cellular response to heat. Predicted to be active in cytoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ARPP-21; cAMP regulated phosphoprotein 21kDa; cAMP-regulated phosphoprotein 21; cAMP-regulated phosphoprotein 21kDa; cAMP-regulated phosphoprotein, 21kDa; cyclic AMP-regulated phosphoprotein, 21 kD; FLJ32997; R3H domain containing 3; R3HDM3; RCS; TARPP; thymocyte cAMP-regulated phosphoprotein
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
GRCh38335,638,853 - 35,794,486 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl335,638,945 - 35,794,496 (+)EnsemblGRCh38hg38GRCh38
GRCh37335,680,345 - 35,835,978 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36335,658,853 - 35,810,992 (+)NCBINCBI36Build 36hg18NCBI36
Celera335,625,833 - 35,777,956 (+)NCBICelera
Cytogenetic Map3p22.3NCBI
HuRef335,621,751 - 35,777,104 (+)NCBIHuRef
CHM1_1335,630,728 - 35,786,025 (+)NCBICHM1_1
T2T-CHM13v2.0335,639,532 - 35,795,160 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease 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. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8120638   PMID:8889548   PMID:10854908   PMID:10931946   PMID:12477932   PMID:14702039   PMID:15144186   PMID:15489334   PMID:15499021   PMID:16344560   PMID:17207965   PMID:19734545  
PMID:20379614   PMID:21044950   PMID:21116278   PMID:21873635   PMID:23284306   PMID:24127197   PMID:31653410   PMID:33581934   PMID:34047500  


Genomics

Comparative Map Data
ARPP21
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38335,638,853 - 35,794,486 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl335,638,945 - 35,794,496 (+)EnsemblGRCh38hg38GRCh38
GRCh37335,680,345 - 35,835,978 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36335,658,853 - 35,810,992 (+)NCBINCBI36Build 36hg18NCBI36
Celera335,625,833 - 35,777,956 (+)NCBICelera
Cytogenetic Map3p22.3NCBI
HuRef335,621,751 - 35,777,104 (+)NCBIHuRef
CHM1_1335,630,728 - 35,786,025 (+)NCBICHM1_1
T2T-CHM13v2.0335,639,532 - 35,795,160 (+)NCBIT2T-CHM13v2.0
Arpp21
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm399111,894,159 - 112,065,356 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl9111,894,159 - 112,065,006 (-)EnsemblGRCm39 Ensembl
GRCm389112,065,091 - 112,236,288 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl9112,065,091 - 112,235,938 (-)EnsemblGRCm38mm10GRCm38
MGSCv379111,967,595 - 112,137,345 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv369111,910,149 - 112,032,806 (-)NCBIMGSCv36mm8
Celera9111,791,461 - 111,962,061 (-)NCBICelera
Cytogenetic Map9F3NCBI
cM Map962.46NCBI
Arpp21
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr88120,912,964 - 121,077,586 (-)NCBIGRCr8
mRatBN7.28112,034,636 - 112,199,273 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl8112,034,642 - 112,194,297 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx8117,647,674 - 117,766,644 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.08115,846,974 - 115,965,944 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.08113,689,782 - 113,808,767 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.08120,323,895 - 120,492,790 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl8120,323,897 - 120,446,507 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.08119,663,712 - 119,832,028 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.48116,674,803 - 116,794,799 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.18116,809,093 - 116,814,254 (-)NCBI
Celera8111,310,307 - 111,428,734 (-)NCBICelera
Cytogenetic Map8q32NCBI
Arpp21
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554212,682,413 - 2,839,245 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554212,681,759 - 2,838,014 (+)NCBIChiLan1.0ChiLan1.0
ARPP21
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2235,613,453 - 35,770,649 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1335,618,224 - 35,775,416 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0335,558,119 - 35,715,157 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1335,851,537 - 36,008,599 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl335,852,051 - 36,008,061 (+)Ensemblpanpan1.1panPan2
ARPP21
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1235,722,575 - 5,876,923 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl235,722,727 - 5,876,487 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha235,761,651 - 5,917,334 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0236,001,149 - 6,156,692 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl236,001,177 - 6,156,665 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1235,864,018 - 5,977,322 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0235,968,518 - 6,124,163 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0235,956,227 - 6,111,899 (+)NCBIUU_Cfam_GSD_1.0
Arpp21
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118192,336,169 - 192,486,517 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647325,474,728 - 25,625,095 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647325,475,845 - 25,625,095 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ARPP21
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1320,934,846 - 21,088,420 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11320,955,414 - 21,088,424 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21322,754,689 - 22,908,209 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ARPP21
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11580,048,078 - 80,204,843 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1580,089,657 - 80,204,314 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604153,520,682 - 53,678,746 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Arpp21
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462478813,656,352 - 13,767,654 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462478813,613,751 - 13,766,633 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ARPP21
40 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3p22.3-22.2(chr3:32322382-36775606)x1 copy number loss See cases [RCV000051509] Chr3:32322382..36775606 [GRCh38]
Chr3:32363874..36817097 [GRCh37]
Chr3:32338878..36792101 [NCBI36]
Chr3:3p22.3-22.2
pathogenic
GRCh38/hg38 3p22.3-22.2(chr3:33062199-36829440)x1 copy number loss See cases [RCV000051510] Chr3:33062199..36829440 [GRCh38]
Chr3:33103691..36870931 [GRCh37]
Chr3:33078695..36845935 [NCBI36]
Chr3:3p22.3-22.2
pathogenic
GRCh38/hg38 3p26.3-22.2(chr3:52266-37148076)x3 copy number gain See cases [RCV000051097] Chr3:52266..37148076 [GRCh38]
Chr3:93949..37189567 [GRCh37]
Chr3:68949..37164571 [NCBI36]
Chr3:3p26.3-22.2
pathogenic
GRCh38/hg38 3p25.3-22.2(chr3:11463328-38919543)x3 copy number gain See cases [RCV000051720] Chr3:11463328..38919543 [GRCh38]
Chr3:11504802..38961034 [GRCh37]
Chr3:11479802..38936038 [NCBI36]
Chr3:3p25.3-22.2
pathogenic
NM_016300.4(ARPP21):c.928G>A (p.Glu310Lys) single nucleotide variant Malignant melanoma [RCV000066014] Chr3:35715469 [GRCh38]
Chr3:35756961 [GRCh37]
Chr3:35731965 [NCBI36]
Chr3:3p22.3
not provided
NM_016300.4(ARPP21):c.1300C>T (p.Leu434=) single nucleotide variant Malignant melanoma [RCV000066015] Chr3:35729377 [GRCh38]
Chr3:35770869 [GRCh37]
Chr3:35745873 [NCBI36]
Chr3:3p22.3
not provided
NM_016300.4(ARPP21):c.1440C>T (p.Ile480=) single nucleotide variant Malignant melanoma [RCV000060804] Chr3:35729517 [GRCh38]
Chr3:35771009 [GRCh37]
Chr3:35746013 [NCBI36]
Chr3:3p22.3
not provided
NM_001267616.1(ARPP21):c.-213+16777C>T single nucleotide variant Lung cancer [RCV000093553] Chr3:35657175 [GRCh38]
Chr3:35698667 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001267617.1(ARPP21):c.1483-108C>A single nucleotide variant Lung cancer [RCV000093554] Chr3:35738106 [GRCh38]
Chr3:35779598 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1355G>T (p.Gly452Val) single nucleotide variant Malignant tumor of prostate [RCV000149237] Chr3:35729432 [GRCh38]
Chr3:35770924 [GRCh37]
Chr3:3p22.3
uncertain significance
GRCh38/hg38 3p22.3-22.1(chr3:33728406-40662451)x3 copy number gain See cases [RCV000134924] Chr3:33728406..40662451 [GRCh38]
Chr3:33769898..40703942 [GRCh37]
Chr3:33744902..40678946 [NCBI36]
Chr3:3p22.3-22.1
pathogenic
GRCh38/hg38 3p22.3(chr3:35766275-35885027)x3 copy number gain See cases [RCV000141009] Chr3:35766275..35885027 [GRCh38]
Chr3:35807767..35926519 [GRCh37]
Chr3:35782771..35901523 [NCBI36]
Chr3:3p22.3
benign
GRCh38/hg38 3p26.3-22.1(chr3:53308-41381521)x3 copy number gain See cases [RCV000141810] Chr3:53308..41381521 [GRCh38]
Chr3:94991..41423012 [GRCh37]
Chr3:69991..41398016 [NCBI36]
Chr3:3p26.3-22.1
pathogenic
NC_000003.12:g.35785215_35861393dup duplication Preeclampsia [RCV000161271] Chr3:35785215..35861393 [GRCh38]
Chr3:35826707..35902885 [GRCh37]
Chr3:3p22.3
not provided
GRCh37/hg19 3p22.3(chr3:35832877-35925872)x3 copy number gain Premature ovarian failure [RCV000225262] Chr3:35832877..35925872 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p26.3-22.2(chr3:61891-36710181)x3 copy number gain See cases [RCV000448528] Chr3:61891..36710181 [GRCh37]
Chr3:3p26.3-22.2
pathogenic
GRCh37/hg19 3p26.3-22.2(chr3:61891-37459464)x3 copy number gain See cases [RCV000511463] Chr3:61891..37459464 [GRCh37]
Chr3:3p26.3-22.2
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3 copy number gain not provided [RCV000682249] Chr3:16923595..45249923 [GRCh37]
Chr3:3p24.3-21.31
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p22.3(chr3:35799942-35913342)x3 copy number gain not provided [RCV000742354] Chr3:35799942..35913342 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p22.3(chr3:35799942-35925872)x3 copy number gain not provided [RCV000742355] Chr3:35799942..35925872 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p22.3(chr3:35799942-35938795)x3 copy number gain not provided [RCV000742356] Chr3:35799942..35938795 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p22.3(chr3:35812111-35902885)x3 copy number gain not provided [RCV000742357] Chr3:35812111..35902885 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p22.3(chr3:35812111-35938795)x3 copy number gain not provided [RCV000742358] Chr3:35812111..35938795 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p22.3(chr3:35821184-35925872)x3 copy number gain not provided [RCV000742359] Chr3:35821184..35925872 [GRCh37]
Chr3:3p22.3
benign
GRCh37/hg19 3p22.3(chr3:35021867-36017937)x1 copy number loss not provided [RCV001005423] Chr3:35021867..36017937 [GRCh37]
Chr3:3p22.3
uncertain significance
GRCh37/hg19 3p22.3(chr3:35796715-35948815)x3 copy number gain not provided [RCV000849867] Chr3:35796715..35948815 [GRCh37]
Chr3:3p22.3
uncertain significance
GRCh37/hg19 3p22.3(chr3:35803643-35948815)x3 copy number gain not provided [RCV000847139] Chr3:35803643..35948815 [GRCh37]
Chr3:3p22.3
uncertain significance
GRCh37/hg19 3p22.3(chr3:35796715-35948815)x3 copy number gain not provided [RCV000848416] Chr3:35796715..35948815 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.807G>C (p.Met269Ile) single nucleotide variant Inborn genetic diseases [RCV003240475] Chr3:35708980 [GRCh38]
Chr3:35750472 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2325G>T (p.Gln775His) single nucleotide variant Monomelic amyotrophy [RCV003234973] Chr3:35793739 [GRCh38]
Chr3:35835231 [GRCh37]
Chr3:3p22.3
uncertain significance
GRCh37/hg19 3p26.3-22.2(chr3:61891-36710181) copy number gain not specified [RCV002053300] Chr3:61891..36710181 [GRCh37]
Chr3:3p26.3-22.2
pathogenic
GRCh37/hg19 3p22.3(chr3:35471543-35879518)x3 copy number gain not provided [RCV001834453] Chr3:35471543..35879518 [GRCh37]
Chr3:3p22.3
uncertain significance
NC_000003.11:g.(?_16710965)_(41275270_?)del deletion not provided [RCV001958625] Chr3:16710965..41275270 [GRCh37]
Chr3:3p24.3-22.1
pathogenic
NM_001385562.1(ARPP21):c.1298C>T (p.Pro433Leu) single nucleotide variant Inborn genetic diseases [RCV002773923] Chr3:35729375 [GRCh38]
Chr3:35770867 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.280C>A (p.Leu94Ile) single nucleotide variant Inborn genetic diseases [RCV002660534] Chr3:35687757 [GRCh38]
Chr3:35729249 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2517C>A (p.Ser839Arg) single nucleotide variant Inborn genetic diseases [RCV002758873] Chr3:35793931 [GRCh38]
Chr3:35835423 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2264A>G (p.Tyr755Cys) single nucleotide variant Inborn genetic diseases [RCV002737896] Chr3:35792508 [GRCh38]
Chr3:35834000 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2269A>G (p.Thr757Ala) single nucleotide variant Inborn genetic diseases [RCV002869981] Chr3:35792513 [GRCh38]
Chr3:35834005 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1024T>A (p.Ser342Thr) single nucleotide variant Inborn genetic diseases [RCV002924207] Chr3:35721633 [GRCh38]
Chr3:35763125 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1627G>A (p.Gly543Ser) single nucleotide variant Inborn genetic diseases [RCV002788769] Chr3:35737345 [GRCh38]
Chr3:35778837 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.616T>C (p.Phe206Leu) single nucleotide variant Inborn genetic diseases [RCV002826777] Chr3:35690935 [GRCh38]
Chr3:35732427 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1350G>C (p.Glu450Asp) single nucleotide variant Inborn genetic diseases [RCV002931496] Chr3:35729427 [GRCh38]
Chr3:35770919 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.938G>A (p.Arg313Lys) single nucleotide variant Inborn genetic diseases [RCV002764597] Chr3:35717300 [GRCh38]
Chr3:35758792 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.665A>G (p.Asn222Ser) single nucleotide variant Inborn genetic diseases [RCV002985060] Chr3:35690984 [GRCh38]
Chr3:35732476 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.671C>A (p.Thr224Asn) single nucleotide variant Inborn genetic diseases [RCV002792757] Chr3:35690990 [GRCh38]
Chr3:35732482 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2104A>T (p.Ser702Cys) single nucleotide variant Inborn genetic diseases [RCV002675287] Chr3:35743932 [GRCh38]
Chr3:35785424 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2391G>A (p.Met797Ile) single nucleotide variant Inborn genetic diseases [RCV002807874] Chr3:35793805 [GRCh38]
Chr3:35835297 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.918C>G (p.Ser306Arg) single nucleotide variant Inborn genetic diseases [RCV002835881] Chr3:35715459 [GRCh38]
Chr3:35756951 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1327C>G (p.Pro443Ala) single nucleotide variant Inborn genetic diseases [RCV002723544] Chr3:35729404 [GRCh38]
Chr3:35770896 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1505C>T (p.Pro502Leu) single nucleotide variant Inborn genetic diseases [RCV003196824] Chr3:35737223 [GRCh38]
Chr3:35778715 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.535G>A (p.Ala179Thr) single nucleotide variant Inborn genetic diseases [RCV003217386] Chr3:35690130 [GRCh38]
Chr3:35731622 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.2123C>G (p.Ala708Gly) single nucleotide variant Inborn genetic diseases [RCV003354010] Chr3:35743951 [GRCh38]
Chr3:35785443 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.1250G>A (p.Gly417Asp) single nucleotide variant Inborn genetic diseases [RCV003356075] Chr3:35729327 [GRCh38]
Chr3:35770819 [GRCh37]
Chr3:3p22.3
uncertain significance
NM_001385562.1(ARPP21):c.990C>G (p.Leu330=) single nucleotide variant not provided [RCV003433512] Chr3:35717352 [GRCh38]
Chr3:35758844 [GRCh37]
Chr3:3p22.3
likely benign
NM_001385562.1(ARPP21):c.1888G>A (p.Ala630Thr) single nucleotide variant not provided [RCV003437748] Chr3:35739455 [GRCh38]
Chr3:35780947 [GRCh37]
Chr3:3p22.3
likely benign
NM_001385562.1(ARPP21):c.1698T>C (p.Ser566=) single nucleotide variant not provided [RCV003437747] Chr3:35738267 [GRCh38]
Chr3:35779759 [GRCh37]
Chr3:3p22.3
likely benign
NM_001385562.1(ARPP21):c.320G>A (p.Arg107Lys) single nucleotide variant not provided [RCV003433511] Chr3:35687797 [GRCh38]
Chr3:35729289 [GRCh37]
Chr3:3p22.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:10030
Count of miRNA genes:1319
Interacting mature miRNAs:1732
Transcripts:ENST00000187397, ENST00000337271, ENST00000396481, ENST00000396482, ENST00000412048, ENST00000413378, ENST00000414496, ENST00000417925, ENST00000419330, ENST00000421492, ENST00000425289, ENST00000427542, ENST00000427590, ENST00000428373, ENST00000432450, ENST00000432682, ENST00000434383, ENST00000436702, ENST00000438071, ENST00000438577, ENST00000441454, ENST00000444190, ENST00000446068, ENST00000449196, ENST00000450234, ENST00000452563, ENST00000457165, ENST00000458225, ENST00000461826, ENST00000462173, ENST00000463970, ENST00000473138, ENST00000474696, ENST00000476052, ENST00000476327, ENST00000481854, ENST00000494494
Prediction methods:Microtar, 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
SHGC-76823  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,726,832 - 35,727,004UniSTSGRCh37
Build 36335,701,836 - 35,702,008RGDNCBI36
Celera335,668,813 - 35,668,985RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,667,966 - 35,668,138UniSTS
TNG Radiation Hybrid Map322509.0UniSTS
GeneMap99-GB4 RH Map3125.57UniSTS
WI-10468  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,764,401 - 35,764,525UniSTSGRCh37
Build 36335,739,405 - 35,739,529RGDNCBI36
Celera335,706,371 - 35,706,495RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,705,528 - 35,705,652UniSTS
Whitehead-RH Map3133.0UniSTS
SHGC-32030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,684,120 - 35,684,220UniSTSGRCh37
Build 36335,659,124 - 35,659,224RGDNCBI36
Celera335,626,104 - 35,626,204RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,625,208 - 35,625,308UniSTS
TNG Radiation Hybrid Map322561.0UniSTS
GeneMap99-GB4 RH Map3122.75UniSTS
Whitehead-RH Map3126.3UniSTS
GeneMap99-G3 RH Map31345.0UniSTS
RH79954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,798,583 - 35,798,824UniSTSGRCh37
Build 36335,773,587 - 35,773,828RGDNCBI36
Celera335,740,557 - 35,740,798RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,739,713 - 35,739,954UniSTS
GeneMap99-GB4 RH Map3116.88UniSTS
RH102209  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,686,144 - 35,686,288UniSTSGRCh37
Build 36335,661,148 - 35,661,292RGDNCBI36
Celera335,628,128 - 35,628,272RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,627,232 - 35,627,376UniSTS
GeneMap99-GB4 RH Map3124.93UniSTS
G59816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,727,068 - 35,727,257UniSTSGRCh37
Build 36335,702,072 - 35,702,261RGDNCBI36
Celera335,669,049 - 35,669,238RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,668,202 - 35,668,391UniSTS
TNG Radiation Hybrid Map322500.0UniSTS
D3S2765E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,835,308 - 35,835,447UniSTSGRCh37
Build 36335,810,312 - 35,810,451RGDNCBI36
Celera335,777,276 - 35,777,415RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,776,424 - 35,776,563UniSTS
D3S3241  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,681,896 - 35,682,149UniSTSGRCh37
Build 36335,656,900 - 35,657,153RGDNCBI36
Celera335,623,877 - 35,624,130RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,622,981 - 35,623,234UniSTS
RH71422  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,833,295 - 35,833,423UniSTSGRCh37
Build 36335,808,299 - 35,808,427RGDNCBI36
Celera335,775,263 - 35,775,391RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,774,411 - 35,774,539UniSTS
GeneMap99-GB4 RH Map3125.57UniSTS
SHGC-173166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,784,419 - 35,784,706UniSTSGRCh37
Build 36335,759,423 - 35,759,710RGDNCBI36
Celera335,726,389 - 35,726,676RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,725,539 - 35,725,826UniSTS
TNG Radiation Hybrid Map322477.0UniSTS
UniSTS:224247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,835,697 - 35,835,842UniSTSGRCh37
Build 36335,810,701 - 35,810,846RGDNCBI36
Celera335,777,665 - 35,777,810RGD
HuRef335,776,813 - 35,776,958UniSTS
WI-16264  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,827,380 - 35,827,515UniSTSGRCh37
Build 36335,802,384 - 35,802,519RGDNCBI36
Celera335,769,348 - 35,769,483RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,768,496 - 35,768,631UniSTS
GeneMap99-GB4 RH Map3119.63UniSTS
Whitehead-RH Map3132.6UniSTS
SHGC-76804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37335,790,774 - 35,790,923UniSTSGRCh37
Build 36335,765,778 - 35,765,927RGDNCBI36
Celera335,732,746 - 35,732,895RGD
Cytogenetic Map3p22.3UniSTS
HuRef335,731,902 - 35,732,051UniSTS
TNG Radiation Hybrid Map322477.0UniSTS
GeneMap99-GB4 RH Map3117.5UniSTS
Whitehead-RH Map3132.7UniSTS
SHGC-76827  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map3p22.3UniSTS
TNG Radiation Hybrid Map322403.0UniSTS
GeneMap99-GB4 RH Map3127.01UniSTS
Whitehead-RH Map3134.0UniSTS
NCBI RH Map3342.2UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 1 52 58 6 27 1 719 725 1926 1 1 3 5 718
Low 144 438 302 121 82 79 275 180 1094 54 43 55 44 16 234
Below cutoff 2022 2225 1105 401 1090 293 2962 1187 645 201 1058 1117 110 1104 1774 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_050660 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001025068 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001025069 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267616 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385496 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385536 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385558 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385567 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385573 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385576 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385582 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385587 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385589 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385592 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385593 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001385595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_016300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_198399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_169647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170707 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011533299 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011533300 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011533301 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011533302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011533303 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005574 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005580 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005584 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005588 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005590 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005607 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017005612 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024453324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447337 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047447340 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345009 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345010 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054345027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC016943 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC104308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC133143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF112220 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK091377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK093648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL133109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AV718064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AV718166 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC031106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC036399 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC036548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041385 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC051828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC066651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG535216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ423297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU741999 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX488342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA275579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000187397   ⟹   ENSP00000187397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,642,165 - 35,794,496 (+)Ensembl
RefSeq Acc Id: ENST00000396481   ⟹   ENSP00000379741
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,680,937 - 35,684,791 (+)Ensembl
RefSeq Acc Id: ENST00000396482   ⟹   ENSP00000379742
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,624 - 35,685,885 (+)Ensembl
RefSeq Acc Id: ENST00000412048   ⟹   ENSP00000390151
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,621 - 35,685,887 (+)Ensembl
RefSeq Acc Id: ENST00000413378   ⟹   ENSP00000390169
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,745 - 35,687,773 (+)Ensembl
RefSeq Acc Id: ENST00000414496   ⟹   ENSP00000415134
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,642,340 - 35,690,898 (+)Ensembl
RefSeq Acc Id: ENST00000417925   ⟹   ENSP00000412326
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,785 - 35,794,388 (+)Ensembl
RefSeq Acc Id: ENST00000419330   ⟹   ENSP00000413005
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,643,621 - 35,681,880 (+)Ensembl
RefSeq Acc Id: ENST00000421492   ⟹   ENSP00000398598
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,640,255 - 35,681,847 (+)Ensembl
RefSeq Acc Id: ENST00000425289   ⟹   ENSP00000408271
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,690,072 - 35,729,541 (+)Ensembl
RefSeq Acc Id: ENST00000427542   ⟹   ENSP00000401602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,678,819 - 35,684,089 (+)Ensembl
RefSeq Acc Id: ENST00000427590   ⟹   ENSP00000396116
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,690,075 - 35,737,252 (+)Ensembl
RefSeq Acc Id: ENST00000428373   ⟹   ENSP00000412411
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,639,589 - 35,685,887 (+)Ensembl
RefSeq Acc Id: ENST00000432450   ⟹   ENSP00000412341
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,644 - 35,683,858 (+)Ensembl
RefSeq Acc Id: ENST00000432682   ⟹   ENSP00000389754
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,627 - 35,684,395 (+)Ensembl
RefSeq Acc Id: ENST00000434383
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,680,961 - 35,685,887 (+)Ensembl
RefSeq Acc Id: ENST00000436702   ⟹   ENSP00000397720
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,681,352 - 35,684,141 (+)Ensembl
RefSeq Acc Id: ENST00000438071   ⟹   ENSP00000410171
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,681,497 - 35,684,758 (+)Ensembl
RefSeq Acc Id: ENST00000438577   ⟹   ENSP00000409331
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,642,337 - 35,687,760 (+)Ensembl
RefSeq Acc Id: ENST00000441454   ⟹   ENSP00000406964
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,681,000 - 35,685,887 (+)Ensembl
RefSeq Acc Id: ENST00000444190   ⟹   ENSP00000405276
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,640,964 - 35,794,457 (+)Ensembl
RefSeq Acc Id: ENST00000446068   ⟹   ENSP00000399482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,689,314 - 35,721,631 (+)Ensembl
RefSeq Acc Id: ENST00000449196   ⟹   ENSP00000409808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,641,421 - 35,682,880 (+)Ensembl
RefSeq Acc Id: ENST00000450234   ⟹   ENSP00000411644
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,638,945 - 35,687,789 (+)Ensembl
RefSeq Acc Id: ENST00000452563   ⟹   ENSP00000396324
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,642,290 - 35,683,843 (+)Ensembl
RefSeq Acc Id: ENST00000457165   ⟹   ENSP00000412233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,721,636 - 35,794,459 (+)Ensembl
RefSeq Acc Id: ENST00000461826
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,682,430 - 35,684,410 (+)Ensembl
RefSeq Acc Id: ENST00000462173
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,738,232 - 35,785,232 (+)Ensembl
RefSeq Acc Id: ENST00000463970
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,774,792 - 35,793,745 (+)Ensembl
RefSeq Acc Id: ENST00000473138
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,781,452 - 35,793,800 (+)Ensembl
RefSeq Acc Id: ENST00000474696   ⟹   ENSP00000417838
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,679,620 - 35,684,046 (+)Ensembl
RefSeq Acc Id: ENST00000476052
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,792,177 - 35,794,450 (+)Ensembl
RefSeq Acc Id: ENST00000476327
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,690,925 - 35,729,526 (+)Ensembl
RefSeq Acc Id: ENST00000481854
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,714,964 - 35,729,336 (+)Ensembl
RefSeq Acc Id: ENST00000494494
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,706,974 - 35,715,795 (+)Ensembl
RefSeq Acc Id: ENST00000684406   ⟹   ENSP00000506922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl335,639,525 - 35,794,486 (+)Ensembl
RefSeq Acc Id: NM_001025068   ⟹   NP_001020239
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,685,887 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
Build 36335,696,120 - 35,702,383 (+)NCBI Archive
Celera335,625,833 - 35,777,956 (+)RGD
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,671,171 - 35,677,433 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,686,573 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001025069   ⟹   NP_001020240
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,685,887 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
Build 36335,696,120 - 35,702,383 (+)NCBI Archive
Celera335,625,833 - 35,777,956 (+)RGD
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,671,171 - 35,677,433 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,686,573 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001267616   ⟹   NP_001254545
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,685,887 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,630,728 - 35,677,433 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,686,573 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001267617   ⟹   NP_001254546
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,640,995 - 35,794,486 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,632,572 - 35,786,025 (+)NCBI
T2T-CHM13v2.0335,641,673 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001267618   ⟹   NP_001254547
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,685,887 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,671,168 - 35,677,433 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,686,573 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001267619   ⟹   NP_001254548
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,671,334 - 35,786,025 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385484   ⟹   NP_001372413
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,641,533 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,642,214 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385485   ⟹   NP_001372414
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385486   ⟹   NP_001372415
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385487   ⟹   NP_001372416
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385488   ⟹   NP_001372417
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,638,853 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,639,532 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385489   ⟹   NP_001372418
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,638,853 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,639,532 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385490   ⟹   NP_001372419
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,638,853 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,639,532 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385491   ⟹   NP_001372420
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385492   ⟹   NP_001372421
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385495   ⟹   NP_001372424
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385496   ⟹   NP_001372425
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385497   ⟹   NP_001372426
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385517   ⟹   NP_001372446
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385536   ⟹   NP_001372465
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385556   ⟹   NP_001372485
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385558   ⟹   NP_001372487
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385562   ⟹   NP_001372491
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385563   ⟹   NP_001372492
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385564   ⟹   NP_001372493
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385565   ⟹   NP_001372494
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,641,533 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,642,214 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385566   ⟹   NP_001372495
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385567   ⟹   NP_001372496
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385573   ⟹   NP_001372502
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385574   ⟹   NP_001372503
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385576   ⟹   NP_001372505
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385577   ⟹   NP_001372506
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385578   ⟹   NP_001372507
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385580   ⟹   NP_001372509
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,681,495 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,682,181 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385581   ⟹   NP_001372510
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,680,940 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,681,626 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385582   ⟹   NP_001372511
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385584   ⟹   NP_001372513
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,680,940 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,681,626 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385585   ⟹   NP_001372514
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385587   ⟹   NP_001372516
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,680,940 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,681,626 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385588   ⟹   NP_001372517
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,288 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,679,974 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385589   ⟹   NP_001372518
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385590   ⟹   NP_001372519
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385591   ⟹   NP_001372520
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385592   ⟹   NP_001372521
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385593   ⟹   NP_001372522
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385594   ⟹   NP_001372523
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001385595   ⟹   NP_001372524
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_016300   ⟹   NP_057384
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
Build 36335,658,853 - 35,810,992 (+)NCBI Archive
Celera335,625,833 - 35,777,956 (+)RGD
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,633,914 - 35,786,025 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NM_198399   ⟹   NP_938409
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,680,940 - 35,685,887 (+)NCBI
GRCh37335,680,666 - 35,835,988 (+)NCBI
Build 36335,697,433 - 35,702,383 (+)NCBI Archive
Celera335,625,833 - 35,777,956 (+)RGD
HuRef335,621,751 - 35,777,104 (+)NCBI
CHM1_1335,672,483 - 35,677,433 (+)NCBI
T2T-CHM13v2.0335,681,626 - 35,686,573 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169632
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169633
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169635
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169644
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169645
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169646
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_169647
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170705
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170706
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,643,655 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,644,336 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170707
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011533299   ⟹   XP_011531601
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011533300   ⟹   XP_011531602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011533301   ⟹   XP_011531603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011533302   ⟹   XP_011531604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011533303   ⟹   XP_011531605
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005574   ⟹   XP_016861063
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,641,533 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005575   ⟹   XP_016861064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005580   ⟹   XP_016861069
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005584   ⟹   XP_016861073
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005590   ⟹   XP_016861079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005591   ⟹   XP_016861080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005596   ⟹   XP_016861085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017005598   ⟹   XP_016861087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024453320   ⟹   XP_024309088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,643,655 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024453322   ⟹   XP_024309090
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,643,655 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024453323   ⟹   XP_024309091
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,643,655 - 35,794,486 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047447337   ⟹   XP_047303293
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
RefSeq Acc Id: XM_047447338   ⟹   XP_047303294
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,641,533 - 35,794,486 (+)NCBI
RefSeq Acc Id: XM_047447339   ⟹   XP_047303295
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
RefSeq Acc Id: XM_047447340   ⟹   XP_047303296
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,642,333 - 35,794,486 (+)NCBI
RefSeq Acc Id: XM_054345008   ⟹   XP_054200983
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,642,214 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345009   ⟹   XP_054200984
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345010   ⟹   XP_054200985
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345011   ⟹   XP_054200986
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345012   ⟹   XP_054200987
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345013   ⟹   XP_054200988
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,644,336 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345014   ⟹   XP_054200989
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345015   ⟹   XP_054200990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345016   ⟹   XP_054200991
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345017   ⟹   XP_054200992
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,642,214 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345018   ⟹   XP_054200993
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345019   ⟹   XP_054200994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345020   ⟹   XP_054200995
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345021   ⟹   XP_054200996
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,644,336 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345022   ⟹   XP_054200997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,680,310 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345023   ⟹   XP_054200998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345024   ⟹   XP_054200999
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,643,014 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345025   ⟹   XP_054201000
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345026   ⟹   XP_054201001
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,640,203 - 35,795,160 (+)NCBI
RefSeq Acc Id: XM_054345027   ⟹   XP_054201002
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0335,644,336 - 35,795,160 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001020239 (Get FASTA)   NCBI Sequence Viewer  
  NP_001020240 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254545 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254546 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254547 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254548 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372413 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372414 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372415 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372416 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372417 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372418 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372419 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372420 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372421 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372424 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372425 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372426 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372446 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372465 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372485 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372487 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372491 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372492 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372493 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372494 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372495 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372496 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372502 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372503 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372505 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372506 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372507 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372509 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372510 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372511 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372513 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372514 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372516 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372517 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372518 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372519 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372520 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372521 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372522 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372523 (Get FASTA)   NCBI Sequence Viewer  
  NP_001372524 (Get FASTA)   NCBI Sequence Viewer  
  NP_057384 (Get FASTA)   NCBI Sequence Viewer  
  NP_938409 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531601 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531602 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531603 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531604 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531605 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861063 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861064 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861069 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861073 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861079 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861080 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861085 (Get FASTA)   NCBI Sequence Viewer  
  XP_016861087 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309088 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309090 (Get FASTA)   NCBI Sequence Viewer  
  XP_024309091 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303293 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303294 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303295 (Get FASTA)   NCBI Sequence Viewer  
  XP_047303296 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200983 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200984 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200985 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200986 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200987 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200988 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200989 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200990 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200991 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200992 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200993 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200994 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200995 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200996 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200997 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200998 (Get FASTA)   NCBI Sequence Viewer  
  XP_054200999 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201000 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201001 (Get FASTA)   NCBI Sequence Viewer  
  XP_054201002 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF17207 (Get FASTA)   NCBI Sequence Viewer  
  AAH17805 (Get FASTA)   NCBI Sequence Viewer  
  AAH31106 (Get FASTA)   NCBI Sequence Viewer  
  AAH36399 (Get FASTA)   NCBI Sequence Viewer  
  AAH41385 (Get FASTA)   NCBI Sequence Viewer  
  AAH51828 (Get FASTA)   NCBI Sequence Viewer  
  AAH66651 (Get FASTA)   NCBI Sequence Viewer  
  BAF82338 (Get FASTA)   NCBI Sequence Viewer  
  BAF82557 (Get FASTA)   NCBI Sequence Viewer  
  BAG51459 (Get FASTA)   NCBI Sequence Viewer  
  BAG57707 (Get FASTA)   NCBI Sequence Viewer  
  CAB61414 (Get FASTA)   NCBI Sequence Viewer  
  EAW64470 (Get FASTA)   NCBI Sequence Viewer  
  EAW64471 (Get FASTA)   NCBI Sequence Viewer  
  EAW64472 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000187397
  ENSP00000187397.4
  ENSP00000379741
  ENSP00000379741.2
  ENSP00000379742
  ENSP00000379742.2
  ENSP00000389754.1
  ENSP00000390151
  ENSP00000390151.1
  ENSP00000390169.1
  ENSP00000396116.1
  ENSP00000396324.1
  ENSP00000397720.1
  ENSP00000398598.1
  ENSP00000399482.2
  ENSP00000401602.1
  ENSP00000405276
  ENSP00000405276.1
  ENSP00000406964.1
  ENSP00000408271.1
  ENSP00000409331.1
  ENSP00000409808.1
  ENSP00000410171.1
  ENSP00000411644.1
  ENSP00000412233.1
  ENSP00000412326
  ENSP00000412326.1
  ENSP00000412341.1
  ENSP00000412411
  ENSP00000412411.1
  ENSP00000413005.1
  ENSP00000415134.1
  ENSP00000417838
  ENSP00000417838.1
  ENSP00000506922
  ENSP00000506922.1
GenBank Protein Q9UBL0 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_057384   ⟸   NM_016300
- Peptide Label: isoform 1
- UniProtKB: Q86V31 (UniProtKB/Swiss-Prot),   Q6NYC3 (UniProtKB/Swiss-Prot),   Q4G0V4 (UniProtKB/Swiss-Prot),   Q49AS6 (UniProtKB/Swiss-Prot),   Q49AK3 (UniProtKB/Swiss-Prot),   B4DG96 (UniProtKB/Swiss-Prot),   Q9UF93 (UniProtKB/Swiss-Prot),   Q9UBL0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001020239   ⟸   NM_001025068
- Peptide Label: isoform 2
- UniProtKB: A8K1F3 (UniProtKB/TrEMBL),   A0A024R2J2 (UniProtKB/TrEMBL),   A8K0T4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001020240   ⟸   NM_001025069
- Peptide Label: isoform 2
- UniProtKB: A8K1F3 (UniProtKB/TrEMBL),   A0A024R2J2 (UniProtKB/TrEMBL),   A8K0T4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_938409   ⟸   NM_198399
- Peptide Label: isoform 2
- UniProtKB: A8K1F3 (UniProtKB/TrEMBL),   A0A024R2J2 (UniProtKB/TrEMBL),   A8K0T4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001254545   ⟸   NM_001267616
- Peptide Label: isoform 2
- UniProtKB: A8K1F3 (UniProtKB/TrEMBL),   A0A024R2J2 (UniProtKB/TrEMBL),   A8K0T4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001254546   ⟸   NM_001267617
- Peptide Label: isoform 3
- UniProtKB: Q9UBL0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001254547   ⟸   NM_001267618
- Peptide Label: isoform 2
- UniProtKB: A8K0T4 (UniProtKB/TrEMBL),   A8K1F3 (UniProtKB/TrEMBL),   A0A024R2J2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001254548   ⟸   NM_001267619
- Peptide Label: isoform 4
- UniProtKB: Q9UBL0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011531602   ⟸   XM_011533300
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011531605   ⟸   XM_011533303
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011531601   ⟸   XM_011533299
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011531603   ⟸   XM_011533301
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011531604   ⟸   XM_011533302
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016861069   ⟸   XM_017005580
- Peptide Label: isoform X2
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016861087   ⟸   XM_017005598
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_016861073   ⟸   XM_017005584
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016861080   ⟸   XM_017005591
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_016861085   ⟸   XM_017005596
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_016861063   ⟸   XM_017005574
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016861064   ⟸   XM_017005575
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016861079   ⟸   XM_017005590
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_024309088   ⟸   XM_024453320
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024309090   ⟸   XM_024453322
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_024309091   ⟸   XM_024453323
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: ENSP00000409331   ⟸   ENST00000438577
RefSeq Acc Id: ENSP00000410171   ⟸   ENST00000438071
RefSeq Acc Id: ENSP00000411644   ⟸   ENST00000450234
RefSeq Acc Id: ENSP00000408271   ⟸   ENST00000425289
RefSeq Acc Id: ENSP00000390151   ⟸   ENST00000412048
RefSeq Acc Id: ENSP00000401602   ⟸   ENST00000427542
RefSeq Acc Id: ENSP00000396324   ⟸   ENST00000452563
RefSeq Acc Id: ENSP00000396116   ⟸   ENST00000427590
RefSeq Acc Id: ENSP00000390169   ⟸   ENST00000413378
RefSeq Acc Id: ENSP00000415134   ⟸   ENST00000414496
RefSeq Acc Id: ENSP00000412411   ⟸   ENST00000428373
RefSeq Acc Id: ENSP00000406964   ⟸   ENST00000441454
RefSeq Acc Id: ENSP00000412326   ⟸   ENST00000417925
RefSeq Acc Id: ENSP00000412233   ⟸   ENST00000457165
RefSeq Acc Id: ENSP00000405276   ⟸   ENST00000444190
RefSeq Acc Id: ENSP00000413005   ⟸   ENST00000419330
RefSeq Acc Id: ENSP00000389754   ⟸   ENST00000432682
RefSeq Acc Id: ENSP00000412341   ⟸   ENST00000432450
RefSeq Acc Id: ENSP00000399482   ⟸   ENST00000446068
RefSeq Acc Id: ENSP00000409808   ⟸   ENST00000449196
RefSeq Acc Id: ENSP00000398598   ⟸   ENST00000421492
RefSeq Acc Id: ENSP00000379742   ⟸   ENST00000396482
RefSeq Acc Id: ENSP00000379741   ⟸   ENST00000396481
RefSeq Acc Id: ENSP00000417838   ⟸   ENST00000474696
RefSeq Acc Id: ENSP00000397720   ⟸   ENST00000436702
RefSeq Acc Id: ENSP00000187397   ⟸   ENST00000187397
RefSeq Acc Id: NP_001372418   ⟸   NM_001385489
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372419   ⟸   NM_001385490
- Peptide Label: isoform 6
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001372417   ⟸   NM_001385488
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372493   ⟸   NM_001385564
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372426   ⟸   NM_001385497
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372491   ⟸   NM_001385562
- Peptide Label: isoform 6
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001372424   ⟸   NM_001385495
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001372487   ⟸   NM_001385558
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001372465   ⟸   NM_001385536
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001372492   ⟸   NM_001385563
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001372421   ⟸   NM_001385492
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372485   ⟸   NM_001385556
- Peptide Label: isoform 12
RefSeq Acc Id: NP_001372446   ⟸   NM_001385517
- Peptide Label: isoform 15
RefSeq Acc Id: NP_001372420   ⟸   NM_001385491
- Peptide Label: isoform 14
RefSeq Acc Id: NP_001372425   ⟸   NM_001385496
- Peptide Label: isoform 13
RefSeq Acc Id: NP_001372413   ⟸   NM_001385484
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372494   ⟸   NM_001385565
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372496   ⟸   NM_001385567
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001372414   ⟸   NM_001385485
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372502   ⟸   NM_001385573
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001372503   ⟸   NM_001385574
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372495   ⟸   NM_001385566
- Peptide Label: isoform 11
RefSeq Acc Id: NP_001372517   ⟸   NM_001385588
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372514   ⟸   NM_001385585
- Peptide Label: isoform 9
RefSeq Acc Id: NP_001372519   ⟸   NM_001385590
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001372506   ⟸   NM_001385577
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372524   ⟸   NM_001385595
- Peptide Label: isoform 5
RefSeq Acc Id: NP_001372523   ⟸   NM_001385594
- Peptide Label: isoform 6
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001372518   ⟸   NM_001385589
- Peptide Label: isoform 8
RefSeq Acc Id: NP_001372416   ⟸   NM_001385487
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372507   ⟸   NM_001385578
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372522   ⟸   NM_001385593
- Peptide Label: isoform 16
RefSeq Acc Id: NP_001372521   ⟸   NM_001385592
- Peptide Label: isoform 6
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001372520   ⟸   NM_001385591
- Peptide Label: isoform 7
RefSeq Acc Id: NP_001372415   ⟸   NM_001385486
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372511   ⟸   NM_001385582
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001372505   ⟸   NM_001385576
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372516   ⟸   NM_001385587
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001372513   ⟸   NM_001385584
- Peptide Label: isoform 10
RefSeq Acc Id: NP_001372510   ⟸   NM_001385581
- Peptide Label: isoform 3
RefSeq Acc Id: NP_001372509   ⟸   NM_001385580
- Peptide Label: isoform 3
RefSeq Acc Id: ENSP00000506922   ⟸   ENST00000684406
RefSeq Acc Id: XP_047303294   ⟸   XM_047447338
- Peptide Label: isoform X2
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047303293   ⟸   XM_047447337
- Peptide Label: isoform X2
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047303295   ⟸   XM_047447339
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047303296   ⟸   XM_047447340
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054200986   ⟸   XM_054345011
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200994   ⟸   XM_054345019
- Peptide Label: isoform X2
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054201001   ⟸   XM_054345026
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054200984   ⟸   XM_054345009
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200995   ⟸   XM_054345020
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054200998   ⟸   XM_054345023
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054201000   ⟸   XM_054345025
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054200983   ⟸   XM_054345008
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200992   ⟸   XM_054345017
- Peptide Label: isoform X2
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054200985   ⟸   XM_054345010
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200991   ⟸   XM_054345016
- Peptide Label: isoform X2
- UniProtKB: A0A804HI65 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054200993   ⟸   XM_054345018
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054200999   ⟸   XM_054345024
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054200988   ⟸   XM_054345013
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200996   ⟸   XM_054345021
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054201002   ⟸   XM_054345027
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054200990   ⟸   XM_054345015
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200989   ⟸   XM_054345014
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054200997   ⟸   XM_054345022
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054200987   ⟸   XM_054345012
- Peptide Label: isoform X1
Protein Domains
R3H   SUZ

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9UBL0-F1-model_v2 AlphaFold Q9UBL0 1-812 view protein structure

Promoters
RGD ID:6863930
Promoter ID:EPDNEW_H5130
Type:initiation region
Name:ARPP21_1
Description:cAMP regulated phosphoprotein 21
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5131  EPDNEW_H5132  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,639,525 - 35,639,585EPDNEW
RGD ID:6800638
Promoter ID:HG_KWN:44319
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat
Transcripts:OTTHUMT00000341610,   OTTHUMT00000341622
Position:
Human AssemblyChrPosition (strand)Source
Build 36335,655,961 - 35,656,461 (+)MPROMDB
RGD ID:6800646
Promoter ID:HG_KWN:44320
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat
Transcripts:ENST00000337271,   OTTHUMT00000253334,   OTTHUMT00000341627,   OTTHUMT00000341628,   OTTHUMT00000341630,   OTTHUMT00000341632,   UC003CGA.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36335,657,311 - 35,657,811 (+)MPROMDB
RGD ID:6800645
Promoter ID:HG_KWN:44321
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat
Transcripts:OTTHUMT00000341629
Position:
Human AssemblyChrPosition (strand)Source
Build 36335,659,911 - 35,660,411 (+)MPROMDB
RGD ID:6863932
Promoter ID:EPDNEW_H5131
Type:initiation region
Name:ARPP21_2
Description:cAMP regulated phosphoprotein 21
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5130  EPDNEW_H5132  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,679,624 - 35,679,684EPDNEW
RGD ID:6863934
Promoter ID:EPDNEW_H5132
Type:initiation region
Name:ARPP21_3
Description:cAMP regulated phosphoprotein 21
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H5130  EPDNEW_H5131  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38335,680,940 - 35,681,000EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:16968 AgrOrtholog
COSMIC ARPP21 COSMIC
Ensembl Genes ENSG00000172995 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000187397 ENTREZGENE
  ENST00000187397.8 UniProtKB/Swiss-Prot
  ENST00000396481 ENTREZGENE
  ENST00000396481.6 UniProtKB/Swiss-Prot
  ENST00000396482 ENTREZGENE
  ENST00000396482.6 UniProtKB/Swiss-Prot
  ENST00000412048 ENTREZGENE
  ENST00000412048.5 UniProtKB/Swiss-Prot
  ENST00000413378.5 UniProtKB/TrEMBL
  ENST00000414496.5 UniProtKB/TrEMBL
  ENST00000417925 ENTREZGENE
  ENST00000417925.5 UniProtKB/Swiss-Prot
  ENST00000419330.5 UniProtKB/TrEMBL
  ENST00000421492.5 UniProtKB/TrEMBL
  ENST00000425289.5 UniProtKB/TrEMBL
  ENST00000427542.5 UniProtKB/Swiss-Prot
  ENST00000427590.1 UniProtKB/TrEMBL
  ENST00000428373 ENTREZGENE
  ENST00000428373.5 UniProtKB/Swiss-Prot
  ENST00000432450.5 UniProtKB/TrEMBL
  ENST00000432682.5 UniProtKB/Swiss-Prot
  ENST00000436702.5 UniProtKB/Swiss-Prot
  ENST00000438071.1 UniProtKB/Swiss-Prot
  ENST00000438577.5 UniProtKB/TrEMBL
  ENST00000441454.5 UniProtKB/Swiss-Prot
  ENST00000444190 ENTREZGENE
  ENST00000444190.5 UniProtKB/Swiss-Prot
  ENST00000446068.6 UniProtKB/TrEMBL
  ENST00000449196.5 UniProtKB/TrEMBL
  ENST00000450234.5 UniProtKB/TrEMBL
  ENST00000452563.5 UniProtKB/TrEMBL
  ENST00000457165.5 UniProtKB/TrEMBL
  ENST00000474696 ENTREZGENE
  ENST00000474696.5 UniProtKB/Swiss-Prot
  ENST00000684406 ENTREZGENE
  ENST00000684406.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.1370.50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000172995 GTEx
HGNC ID HGNC:16968 ENTREZGENE
Human Proteome Map ARPP21 Human Proteome Map
InterPro R3H_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  R3H_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SUZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:10777 UniProtKB/Swiss-Prot
NCBI Gene 10777 ENTREZGENE
OMIM 605488 OMIM
PANTHER CAMP-REGULATED PHOSPHOPROTEIN 21 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CAMP-REGULATED PHOSPHOPROTEIN 21 RELATED R3H DOMAIN CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam R3H UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SUZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA166048949 PharmGKB
PROSITE R3H UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SUZ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART R3H UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF82708 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R2J2 ENTREZGENE
  A0A804HI65 ENTREZGENE, UniProtKB/TrEMBL
  A8K0T4 ENTREZGENE, UniProtKB/TrEMBL
  A8K1F3 ENTREZGENE, UniProtKB/TrEMBL
  ARP21_HUMAN UniProtKB/Swiss-Prot
  B4DG96 ENTREZGENE
  C9J091_HUMAN UniProtKB/TrEMBL
  C9J2U3_HUMAN UniProtKB/TrEMBL
  C9J5R1_HUMAN UniProtKB/TrEMBL
  C9JD93_HUMAN UniProtKB/TrEMBL
  C9JI74_HUMAN UniProtKB/TrEMBL
  C9JQQ6_HUMAN UniProtKB/TrEMBL
  C9JTF2_HUMAN UniProtKB/TrEMBL
  C9JTX6_HUMAN UniProtKB/TrEMBL
  F8WDL2_HUMAN UniProtKB/TrEMBL
  H7C0P9_HUMAN UniProtKB/TrEMBL
  H7C1B6_HUMAN UniProtKB/TrEMBL
  H7C2X8_HUMAN UniProtKB/TrEMBL
  H7C3J7_HUMAN UniProtKB/TrEMBL
  Q49AK3 ENTREZGENE
  Q49AS6 ENTREZGENE
  Q4G0V4 ENTREZGENE
  Q6NYC3 ENTREZGENE
  Q86V31 ENTREZGENE
  Q9UBL0 ENTREZGENE
  Q9UF93 ENTREZGENE
UniProt Secondary A0A024R2J2 UniProtKB/TrEMBL
  B4DG96 UniProtKB/Swiss-Prot
  Q49AK3 UniProtKB/Swiss-Prot
  Q49AS6 UniProtKB/Swiss-Prot
  Q4G0V4 UniProtKB/Swiss-Prot
  Q6NYC3 UniProtKB/Swiss-Prot
  Q86V31 UniProtKB/Swiss-Prot
  Q9UF93 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-07 ARPP21  cAMP regulated phosphoprotein 21    cAMP regulated phosphoprotein 21kDa  Symbol and/or name change 5135510 APPROVED
2015-12-08 ARPP21  cAMP regulated phosphoprotein 21kDa    cAMP-regulated phosphoprotein 21kDa  Symbol and/or name change 5135510 APPROVED
2015-11-17 ARPP21  cAMP-regulated phosphoprotein 21kDa    cAMP-regulated phosphoprotein, 21kDa  Symbol and/or name change 5135510 APPROVED
2011-07-27 ARPP21  cAMP-regulated phosphoprotein, 21kDa  ARPP-21  cyclic AMP-regulated phosphoprotein, 21 kD  Symbol and/or name change 5135510 APPROVED