APOL2 (apolipoprotein L2) - Rat Genome Database

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Gene: APOL2 (apolipoprotein L2) Homo sapiens
Analyze
Symbol: APOL2
Name: apolipoprotein L2
RGD ID: 1320008
HGNC Page HGNC:619
Description: Predicted to enable lipid binding activity. Predicted to be involved in lipid transport and lipoprotein metabolic process. Located in membrane. Implicated in schizophrenia.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: APOL-II; APOL3; apolipoprotein L, 2; apolipoprotein L-II
RGD Orthologs
Rat
Bonobo
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382236,226,209 - 36,239,954 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2236,226,209 - 36,239,954 (-)EnsemblGRCh38hg38GRCh38
GRCh372236,622,255 - 36,636,000 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362234,952,201 - 34,965,946 (-)NCBINCBI36Build 36hg18NCBI36
Build 342234,946,754 - 34,960,500NCBI
Celera2220,424,825 - 20,438,568 (-)NCBICelera
Cytogenetic Map22q12.3NCBI
HuRef2219,590,366 - 19,604,109 (-)NCBIHuRef
CHM1_12236,581,376 - 36,595,119 (-)NCBICHM1_1
T2T-CHM13v2.02236,686,335 - 36,700,070 (-)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. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7566098   PMID:10591208   PMID:11290834   PMID:11374903   PMID:11944986   PMID:12477932   PMID:14702039   PMID:15107424   PMID:15489334   PMID:15949655   PMID:18632255   PMID:19946888  
PMID:20602615   PMID:20665705   PMID:21873635   PMID:24623722   PMID:24901046   PMID:26186194   PMID:26496610   PMID:26638075   PMID:26760575   PMID:27432908   PMID:28514442   PMID:28712289  
PMID:29117863   PMID:30021884   PMID:30442662   PMID:31466081   PMID:31536960   PMID:32296183   PMID:32393512   PMID:32687490   PMID:32788342   PMID:32877691   PMID:33729478   PMID:33961781  
PMID:34079125   PMID:34316015   PMID:34948065   PMID:35696571   PMID:36517590   PMID:36724073   PMID:36949045   PMID:37120454   PMID:37314216   PMID:37433992   PMID:38569033   PMID:39147351  


Genomics

Comparative Map Data
APOL2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382236,226,209 - 36,239,954 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2236,226,209 - 36,239,954 (-)EnsemblGRCh38hg38GRCh38
GRCh372236,622,255 - 36,636,000 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362234,952,201 - 34,965,946 (-)NCBINCBI36Build 36hg18NCBI36
Build 342234,946,754 - 34,960,500NCBI
Celera2220,424,825 - 20,438,568 (-)NCBICelera
Cytogenetic Map22q12.3NCBI
HuRef2219,590,366 - 19,604,109 (-)NCBIHuRef
CHM1_12236,581,376 - 36,595,119 (-)NCBICHM1_1
T2T-CHM13v2.02236,686,335 - 36,700,070 (-)NCBIT2T-CHM13v2.0
Apol2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87111,211,944 - 111,219,209 (-)NCBIGRCr8
mRatBN7.27109,331,367 - 109,338,632 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl7109,331,392 - 109,338,558 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.07118,727,658 - 118,735,453 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7118,979,608 - 118,983,984 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl7118,728,617 - 118,732,738 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.07118,725,207 - 118,732,485 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47115,668,899 - 115,673,029 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.17115,703,128 - 115,711,697 (-)NCBI
Celera7105,672,006 - 105,679,878 (-)NCBICelera
Cytogenetic Map7q34NCBI
LOC100982122
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22346,111,536 - 46,125,016 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12248,803,106 - 48,816,584 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02217,172,486 - 17,186,260 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12235,011,137 - 35,024,913 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2235,011,137 - 35,024,913 (-)Ensemblpanpan1.1panPan2
LOC100156062
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1511,543,551 - 11,567,675 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.259,313,095 - 9,331,836 (+)NCBISscrofa10.2Sscrofa10.2susScr3
APOL2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11918,945,972 - 18,956,039 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666045106,942,769 - 106,954,000 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in APOL2
34 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 22q12.3-13.1(chr22:35333993-38900177)x1 copy number loss See cases [RCV000051364] Chr22:35333993..38900177 [GRCh38]
Chr22:35729986..39296182 [GRCh37]
Chr22:34059986..37626128 [NCBI36]
Chr22:22q12.3-13.1		 pathogenic
GRCh38/hg38 22q12.3-13.1(chr22:36068124-38002382)x3 copy number gain See cases [RCV000051683] Chr22:36068124..38002382 [GRCh38]
Chr22:36464172..38398389 [GRCh37]
Chr22:34794118..36728335 [NCBI36]
Chr22:22q12.3-13.1		 pathogenic
GRCh38/hg38 22q12.3-13.33(chr22:33768441-50739977)x3 copy number gain See cases [RCV000051682] Chr22:33768441..50739977 [GRCh38]
Chr22:34164428..51178405 [GRCh37]
Chr22:32494428..49525271 [NCBI36]
Chr22:22q12.3-13.33		 pathogenic
GRCh38/hg38 22q12.3(chr22:35753347-36593973)x3 copy number gain See cases [RCV000052854] Chr22:35753347..36593973 [GRCh38]
Chr22:36149394..36990020 [GRCh37]
Chr22:34479340..35319966 [NCBI36]
Chr22:22q12.3		 uncertain significance
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 copy number gain See cases [RCV000133646] Chr22:16916608..50739836 [GRCh38]
Chr22:17397498..51178264 [GRCh37]
Chr22:15777498..49525130 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 copy number gain See cases [RCV000134730] Chr22:16916743..50739785 [GRCh38]
Chr22:17397633..51178213 [GRCh37]
Chr22:15777633..49525079 [NCBI36]
Chr22:22q11.1-13.33		 pathogenic
GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3 copy number gain See cases [RCV000138172] Chr22:23279231..36247369 [GRCh38]
Chr22:23621418..36643415 [GRCh37]
Chr22:21951418..34973361 [NCBI36]
Chr22:22q11.23-12.3		 pathogenic
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3 copy number gain See cases [RCV000137926] Chr22:20907226..37187347 [GRCh38]
Chr22:21261514..37583387 [GRCh37]
Chr22:19591514..35913333 [NCBI36]
Chr22:22q11.21-12.3		 pathogenic
GRCh38/hg38 22q12.3(chr22:36218250-36311777)x3 copy number gain See cases [RCV000141655] Chr22:36218250..36311777 [GRCh38]
Chr22:36614296..36707822 [GRCh37]
Chr22:34944242..35037768 [NCBI36]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q12.3-13.1(chr22:35680095-38098981)x1 copy number loss See cases [RCV000207444] Chr22:35680095..38098981 [GRCh37]
Chr22:22q12.3-13.1		 pathogenic
GRCh37/hg19 22q12.3(chr22:36623928-36677639)x3 copy number gain See cases [RCV000239870] Chr22:36623928..36677639 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 copy number gain See cases [RCV000240091] Chr22:16054691..51237518 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3 copy number gain See cases [RCV000240469] Chr22:35728929..51220961 [GRCh37]
Chr22:22q12.3-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 copy number gain See cases [RCV000446956] Chr22:16054691..51220902 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3(chr22:36614412-36716248)x3 copy number gain See cases [RCV000448104] Chr22:36614412..36716248 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 copy number gain See cases [RCV000448847] Chr22:16054691..51237463 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3(chr22:36623928-36677580)x3 copy number gain See cases [RCV000447827] Chr22:36623928..36677580 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) copy number gain See cases [RCV000510873] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_030882.4(APOL2):c.842G>T (p.Gly281Val) single nucleotide variant not specified [RCV004332783] Chr22:36227576 [GRCh38]
Chr22:36623622 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.835A>C (p.Thr279Pro) single nucleotide variant not specified [RCV004312039] Chr22:36227583 [GRCh38]
Chr22:36623629 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.517A>G (p.Asn173Asp) single nucleotide variant not specified [RCV004308763] Chr22:36227901 [GRCh38]
Chr22:36623947 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 copy number gain See cases [RCV000512333] Chr22:16888900..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3-13.1(chr22:35674826-39466442)x3 copy number gain See cases [RCV000512385] Chr22:35674826..39466442 [GRCh37]
Chr22:22q12.3-13.1		 likely pathogenic
GRCh37/hg19 22q12.3(chr22:36614412-36716248)x3 copy number gain not provided [RCV000684454] Chr22:36614412..36716248 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 copy number gain not provided [RCV000846344] Chr22:16888899..51197838 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 copy number gain not provided [RCV000741689] Chr22:16054667..51243435 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3(chr22:36611863-36714089)x3 copy number gain not provided [RCV000741937] Chr22:36611863..36714089 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q12.3(chr22:36614056-36710183)x3 copy number gain not provided [RCV000741938] Chr22:36614056..36710183 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q12.3(chr22:36616135-36712903)x3 copy number gain not provided [RCV000741939] Chr22:36616135..36712903 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q12.3(chr22:36616135-36713869)x3 copy number gain not provided [RCV000741940] Chr22:36616135..36713869 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 copy number gain not provided [RCV000741691] Chr22:16114244..51195728 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3(chr22:36616135-36714652)x3 copy number gain not provided [RCV000741941] Chr22:36616135..36714652 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 copy number gain not provided [RCV000741692] Chr22:16114244..51211392 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
NM_030882.4(APOL2):c.233G>A (p.Arg78Lys) single nucleotide variant not provided [RCV000963050] Chr22:36228185 [GRCh38]
Chr22:36624231 [GRCh37]
Chr22:22q12.3		 benign
GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3 copy number gain not provided [RCV001007181] Chr22:30654764..51197838 [GRCh37]
Chr22:22q12.2-13.33		 pathogenic
GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3 copy number gain See cases [RCV001263056] Chr22:16197005..51224252 [GRCh37]
Chr22:22q11.1-13.33		 pathogenic
GRCh37/hg19 22q12.3(chr22:36296883-36631953)x3 copy number gain not provided [RCV001832996] Chr22:36296883..36631953 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q12.3(chr22:36614412-36716248) copy number gain not specified [RCV002052754] Chr22:36614412..36716248 [GRCh37]
Chr22:22q12.3		 uncertain significance
NC_000022.10:g.(?_35776672)_(42486826_?)dup duplication Adenylosuccinate lyase deficiency [RCV003119093] Chr22:35776672..42486826 [GRCh37]
Chr22:22q12.3-13.2		 uncertain significance
NM_030882.4(APOL2):c.136A>G (p.Arg46Gly) single nucleotide variant not specified [RCV004204938] Chr22:36231341 [GRCh38]
Chr22:36627387 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.536C>T (p.Ala179Val) single nucleotide variant not specified [RCV004100444] Chr22:36227882 [GRCh38]
Chr22:36623928 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.59T>G (p.Val20Gly) single nucleotide variant not specified [RCV004087392] Chr22:36231418 [GRCh38]
Chr22:36627464 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.391A>T (p.Thr131Ser) single nucleotide variant not specified [RCV004194934] Chr22:36228027 [GRCh38]
Chr22:36624073 [GRCh37]
Chr22:22q12.3		 likely benign
NM_030882.4(APOL2):c.673C>T (p.Arg225Cys) single nucleotide variant not specified [RCV004197807] Chr22:36227745 [GRCh38]
Chr22:36623791 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.206A>T (p.Asn69Ile) single nucleotide variant not specified [RCV004141887] Chr22:36228212 [GRCh38]
Chr22:36624258 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.836C>T (p.Thr279Ile) single nucleotide variant not specified [RCV004187570] Chr22:36227582 [GRCh38]
Chr22:36623628 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.607A>T (p.Thr203Ser) single nucleotide variant not specified [RCV004082780] Chr22:36227811 [GRCh38]
Chr22:36623857 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.538C>G (p.Gln180Glu) single nucleotide variant not specified [RCV004167875] Chr22:36227880 [GRCh38]
Chr22:36623926 [GRCh37]
Chr22:22q12.3		 likely benign
NM_030882.4(APOL2):c.341C>T (p.Thr114Ile) single nucleotide variant not specified [RCV004214931] Chr22:36228077 [GRCh38]
Chr22:36624123 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.622A>C (p.Thr208Pro) single nucleotide variant not specified [RCV004077025] Chr22:36227796 [GRCh38]
Chr22:36623842 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.650C>T (p.Thr217Ile) single nucleotide variant not specified [RCV004111585] Chr22:36227768 [GRCh38]
Chr22:36623814 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.67G>A (p.Glu23Lys) single nucleotide variant not specified [RCV004079470] Chr22:36231410 [GRCh38]
Chr22:36627456 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.760G>A (p.Gly254Ser) single nucleotide variant not specified [RCV004194743] Chr22:36227658 [GRCh38]
Chr22:36623704 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.259C>T (p.Arg87Trp) single nucleotide variant not specified [RCV004188734] Chr22:36228159 [GRCh38]
Chr22:36624205 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.298C>T (p.Arg100Cys) single nucleotide variant not specified [RCV004260996] Chr22:36228120 [GRCh38]
Chr22:36624166 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.281A>G (p.Asp94Gly) single nucleotide variant not specified [RCV004253191] Chr22:36228137 [GRCh38]
Chr22:36624183 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.269G>C (p.Arg90Thr) single nucleotide variant not specified [RCV004250235] Chr22:36228149 [GRCh38]
Chr22:36624195 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.158G>A (p.Arg53His) single nucleotide variant not specified [RCV004328267] Chr22:36228260 [GRCh38]
Chr22:36624306 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.490A>T (p.Ile164Phe) single nucleotide variant not specified [RCV004302097] Chr22:36227928 [GRCh38]
Chr22:36623974 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.298C>G (p.Arg100Gly) single nucleotide variant not specified [RCV004343550] Chr22:36228120 [GRCh38]
Chr22:36624166 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.712G>A (p.Ala238Thr) single nucleotide variant not specified [RCV004354328] Chr22:36227706 [GRCh38]
Chr22:36623752 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.256C>T (p.Pro86Ser) single nucleotide variant not specified [RCV004350388] Chr22:36228162 [GRCh38]
Chr22:36624208 [GRCh37]
Chr22:22q12.3		 uncertain significance
GRCh37/hg19 22q12.3(chr22:36340692-36640557)x3 copy number gain not provided [RCV003485245] Chr22:36340692..36640557 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.222C>G (p.Asp74Glu) single nucleotide variant not specified [RCV004417854] Chr22:36228196 [GRCh38]
Chr22:36624242 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.988A>C (p.Met330Leu) single nucleotide variant not specified [RCV004419929] Chr22:36227430 [GRCh38]
Chr22:36623476 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.157C>T (p.Arg53Cys) single nucleotide variant not specified [RCV004417853] Chr22:36228261 [GRCh38]
Chr22:36624307 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.467G>A (p.Gly156Glu) single nucleotide variant not specified [RCV004417856] Chr22:36227951 [GRCh38]
Chr22:36623997 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.623C>T (p.Thr208Ile) single nucleotide variant not specified [RCV004419927] Chr22:36227795 [GRCh38]
Chr22:36623841 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.455G>T (p.Gly152Val) single nucleotide variant not specified [RCV004417855] Chr22:36227963 [GRCh38]
Chr22:36624009 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.746T>C (p.Ile249Thr) single nucleotide variant not specified [RCV004664573] Chr22:36227672 [GRCh38]
Chr22:36623718 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.94G>A (p.Asp32Asn) single nucleotide variant not specified [RCV004653822] Chr22:36231383 [GRCh38]
Chr22:36627429 [GRCh37]
Chr22:22q12.3		 uncertain significance
NM_030882.4(APOL2):c.299G>A (p.Arg100His) single nucleotide variant not specified [RCV004653811] Chr22:36228119 [GRCh38]
Chr22:36624165 [GRCh37]
Chr22:22q12.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3763
Count of miRNA genes:932
Interacting mature miRNAs:1152
Transcripts:ENST00000249066, ENST00000358502, ENST00000451256, ENST00000454728, ENST00000473549, ENST00000476579, ENST00000484830, ENST00000489186, ENST00000529194
Prediction methods:Microtar, Miranda, Rnahybrid
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1581529BP71_HBlood pressure QTL 71 (human)20.001Blood pressurepulse pressure221109496637094966Human
2289428BW313_HBody weight QTL 313 (human)2.090.0015Body weightBMI221134428437344284Human
406980538GWAS629514_Haging, epigenetic status QTL GWAS629514 (human)5e-08aging, epigenetic status223623779036237791Human
406994446GWAS643422_Hlevel of apolipoprotein L2 in blood serum QTL GWAS643422 (human)8e-58level of apolipoprotein L2 in blood serum223622678236226783Human
406979694GWAS628670_Haging, epigenetic status QTL GWAS628670 (human)0.0000004aging, epigenetic status223623564536235646Human

Markers in Region
D22S1173  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,636,625 - 36,636,886UniSTSGRCh37
Build 362234,966,571 - 34,966,832RGDNCBI36
Celera2220,439,193 - 20,439,454RGD
Cytogenetic Map22q12UniSTS
HuRef2219,604,734 - 19,604,999UniSTS
Marshfield Genetic Map2237.82RGD
Marshfield Genetic Map2237.82UniSTS
Genethon Genetic Map2232.6UniSTS
deCODE Assembly Map2242.01UniSTS
Stanford-G3 RH Map221009.0UniSTS
GeneMap99-G3 RH Map221009.0UniSTS
RH80142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,663,369 - 36,663,546UniSTSGRCh37
GRCh372236,622,280 - 36,622,457UniSTSGRCh37
Build 362234,952,226 - 34,952,403RGDNCBI36
Celera2220,465,937 - 20,466,114UniSTS
Celera2220,424,850 - 20,425,027RGD
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map22q12UniSTS
HuRef2219,590,391 - 19,590,568UniSTS
HuRef2219,631,446 - 19,631,623UniSTS
GeneMap99-GB4 RH Map22117.88UniSTS
D22S592  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,663,624 - 36,663,823UniSTSGRCh37
GRCh372236,622,003 - 36,622,202UniSTSGRCh37
Build 362234,951,949 - 34,952,148RGDNCBI36
Celera2220,424,573 - 20,424,772RGD
Celera2220,466,192 - 20,466,391UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map22q12UniSTS
HuRef2219,631,701 - 19,631,900UniSTS
HuRef2219,590,114 - 19,590,313UniSTS
APOL2_299.2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,622,173 - 36,623,032UniSTSGRCh37
GRCh372236,662,482 - 36,663,653UniSTSGRCh37
Build 362234,952,119 - 34,952,978RGDNCBI36
Celera2220,465,050 - 20,466,221UniSTS
Celera2220,424,743 - 20,425,602RGD
HuRef2219,590,284 - 19,591,144UniSTS
HuRef2219,630,597 - 19,631,730UniSTS
APOL3_301  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,622,255 - 36,623,028UniSTSGRCh37
GRCh372236,536,377 - 36,537,145UniSTSGRCh37
Build 362234,866,323 - 34,867,091RGDNCBI36
Celera2220,424,825 - 20,425,598UniSTS
Celera2220,338,949 - 20,339,717RGD
HuRef2219,590,366 - 19,591,140UniSTS
HuRef2219,504,525 - 19,505,293UniSTS
AL021679  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,627,881 - 36,628,012UniSTSGRCh37
Build 362234,957,827 - 34,957,958RGDNCBI36
Celera2220,430,446 - 20,430,577RGD
Cytogenetic Map22q12UniSTS
HuRef2219,595,988 - 19,596,119UniSTS
D22S541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,649,842 - 36,649,962UniSTSGRCh37
GRCh372236,634,756 - 36,634,876UniSTSGRCh37
Build 362234,964,702 - 34,964,822RGDNCBI36
Celera2220,437,324 - 20,437,444RGD
Celera2220,452,410 - 20,452,530UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map22q12UniSTS
HuRef2219,617,956 - 19,618,076UniSTS
HuRef2219,602,865 - 19,602,985UniSTS
D22S924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372236,631,766 - 36,631,962UniSTSGRCh37
Build 362234,961,712 - 34,961,908RGDNCBI36
Celera2220,434,332 - 20,434,530RGD
Cytogenetic Map22q12UniSTS
HuRef2219,599,873 - 19,600,071UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2252 4974 1726 2351 6 624 1950 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_023229 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_030882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_145637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530074 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530076 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011530078 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017028724 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047441284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047441285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054325434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB208990 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF305225 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF305429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF324223 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF324224 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH010392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056938 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK303978 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL031426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068256 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY306110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z82215 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Z95114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000249066   ⟹   ENSP00000249066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,226,210 - 36,239,954 (-)Ensembl
Ensembl Acc Id: ENST00000358502   ⟹   ENSP00000351292
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,226,209 - 36,239,527 (-)Ensembl
Ensembl Acc Id: ENST00000451256   ⟹   ENSP00000403153
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,227,342 - 36,239,527 (-)Ensembl
Ensembl Acc Id: ENST00000454728   ⟹   ENSP00000400486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,228,195 - 36,239,561 (-)Ensembl
Ensembl Acc Id: ENST00000473549
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,236,933 - 36,239,673 (-)Ensembl
Ensembl Acc Id: ENST00000476579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,236,885 - 36,239,239 (-)Ensembl
Ensembl Acc Id: ENST00000484830
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,236,964 - 36,239,570 (-)Ensembl
Ensembl Acc Id: ENST00000489186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,236,927 - 36,239,582 (-)Ensembl
Ensembl Acc Id: ENST00000529194   ⟹   ENSP00000431231
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2236,228,032 - 36,239,227 (-)Ensembl
RefSeq Acc Id: NM_030882   ⟹   NP_112092
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,226,209 - 36,239,527 (-)NCBI
GRCh372236,622,255 - 36,636,000 (-)RGD
Build 362234,952,201 - 34,965,635 (-)NCBI Archive
Celera2220,424,825 - 20,438,568 (-)RGD
HuRef2219,590,366 - 19,604,109 (-)RGD
CHM1_12236,581,376 - 36,594,808 (-)NCBI
T2T-CHM13v2.02236,686,335 - 36,699,643 (-)NCBI
Sequence:
RefSeq Acc Id: NM_145637   ⟹   NP_663612
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,226,209 - 36,239,954 (-)NCBI
GRCh372236,622,255 - 36,636,000 (-)RGD
Build 362234,952,201 - 34,965,946 (-)NCBI Archive
Celera2220,424,825 - 20,438,568 (-)RGD
HuRef2219,590,366 - 19,604,109 (-)RGD
CHM1_12236,581,376 - 36,595,119 (-)NCBI
T2T-CHM13v2.02236,686,335 - 36,700,070 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011530077   ⟹   XP_011528379
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,226,209 - 36,239,527 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047441284   ⟹   XP_047297240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,226,209 - 36,236,848 (-)NCBI
RefSeq Acc Id: XM_047441285   ⟹   XP_047297241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,226,209 - 36,239,954 (-)NCBI
RefSeq Acc Id: XM_054325432   ⟹   XP_054181407
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02236,686,335 - 36,696,964 (-)NCBI
RefSeq Acc Id: XM_054325433   ⟹   XP_054181408
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02236,686,335 - 36,700,070 (-)NCBI
RefSeq Acc Id: XM_054325434   ⟹   XP_054181409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02236,686,335 - 36,699,550 (-)NCBI
RefSeq Acc Id: NP_663612   ⟸   NM_145637
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_112092   ⟸   NM_030882
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011528379   ⟸   XM_011530077
- Peptide Label: isoform X1
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000403153   ⟸   ENST00000451256
Ensembl Acc Id: ENSP00000400486   ⟸   ENST00000454728
Ensembl Acc Id: ENSP00000249066   ⟸   ENST00000249066
Ensembl Acc Id: ENSP00000431231   ⟸   ENST00000529194
Ensembl Acc Id: ENSP00000351292   ⟸   ENST00000358502
RefSeq Acc Id: XP_047297241   ⟸   XM_047441285
- Peptide Label: isoform X1
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047297240   ⟸   XM_047441284
- Peptide Label: isoform X1
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054181408   ⟸   XM_054325433
- Peptide Label: isoform X1
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054181409   ⟸   XM_054325434
- Peptide Label: isoform X1
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054181407   ⟸   XM_054325432
- Peptide Label: isoform X1
- UniProtKB: Q9UGT1 (UniProtKB/Swiss-Prot),   Q9BT28 (UniProtKB/Swiss-Prot),   Q9BQE5 (UniProtKB/Swiss-Prot),   Q969T6 (UniProtKB/Swiss-Prot),   Q5TH96 (UniProtKB/Swiss-Prot),   Q59GW9 (UniProtKB/Swiss-Prot),   O95915 (UniProtKB/Swiss-Prot),   B0QYK7 (UniProtKB/Swiss-Prot),   Q9UH10 (UniProtKB/Swiss-Prot)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BQE5-F1-model_v2 AlphaFold Q9BQE5 1-337 view protein structure

Promoters
RGD ID:6800472
Promoter ID:HG_KWN:42591
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_030882,   NM_145637,   OTTHUMT00000319281,   OTTHUMT00000319282,   OTTHUMT00000319283,   OTTHUMT00000319284,   OTTHUMT00000319285,   UC003APB.1
Position:
Human AssemblyChrPosition (strand)Source
Build 362234,964,076 - 34,965,797 (-)MPROMDB
RGD ID:13603890
Promoter ID:EPDNEW_H28128
Type:initiation region
Name:APOL2_1
Description:apolipoprotein L2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28129  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,239,527 - 36,239,587EPDNEW
RGD ID:13603888
Promoter ID:EPDNEW_H28129
Type:initiation region
Name:APOL2_2
Description:apolipoprotein L2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H28128  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh382236,239,978 - 36,240,038EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:619 AgrOrtholog
COSMIC APOL2 COSMIC
Ensembl Genes ENSG00000128335 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000249066 ENTREZGENE
  ENST00000249066.10 UniProtKB/Swiss-Prot
  ENST00000358502 ENTREZGENE
  ENST00000358502.10 UniProtKB/Swiss-Prot
  ENST00000451256.6 UniProtKB/TrEMBL
  ENST00000454728.5 UniProtKB/TrEMBL
  ENST00000529194.5 UniProtKB/TrEMBL
GTEx ENSG00000128335 GTEx
HGNC ID HGNC:619 ENTREZGENE
Human Proteome Map APOL2 Human Proteome Map
InterPro ApoL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:23780 UniProtKB/Swiss-Prot
NCBI Gene 23780 ENTREZGENE
OMIM 607252 OMIM
PANTHER APOLIPOPROTEIN L2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR14096 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam ApoL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA24905 PharmGKB
UniProt APOL2_HUMAN UniProtKB/Swiss-Prot
  B0QYK7 ENTREZGENE
  B0QYK8_HUMAN UniProtKB/TrEMBL
  E9PM95_HUMAN UniProtKB/TrEMBL
  J3KQL8_HUMAN UniProtKB/TrEMBL
  O95915 ENTREZGENE
  Q59GW9 ENTREZGENE
  Q5TH96 ENTREZGENE
  Q969T6 ENTREZGENE
  Q9BQE5 ENTREZGENE
  Q9BT28 ENTREZGENE
  Q9UGT1 ENTREZGENE
  Q9UH10 ENTREZGENE
UniProt Secondary B0QYK7 UniProtKB/Swiss-Prot
  O95915 UniProtKB/Swiss-Prot
  Q59GW9 UniProtKB/Swiss-Prot
  Q5TH96 UniProtKB/Swiss-Prot
  Q969T6 UniProtKB/Swiss-Prot
  Q9BT28 UniProtKB/Swiss-Prot
  Q9UGT1 UniProtKB/Swiss-Prot
  Q9UH10 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-22 APOL2  apolipoprotein L2  APOL2  apolipoprotein L, 2  Symbol and/or name change 5135510 APPROVED