CYP26B1 (cytochrome P450 family 26 subfamily B member 1) - Rat Genome Database

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Gene: CYP26B1 (cytochrome P450 family 26 subfamily B member 1) Homo sapiens
Analyze
Symbol: CYP26B1
Name: cytochrome P450 family 26 subfamily B member 1
RGD ID: 736189
HGNC Page HGNC:20581
Description: Enables oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen; retinoic acid 4-hydroxylase activity; and retinoic acid binding activity. Involved in bone morphogenesis; retinoic acid catabolic process; and xenobiotic metabolic process. Located in cytoplasm. Biomarker of hepatocellular carcinoma.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CYP26A2; cytochrome P450 26A2; cytochrome P450 26B1; cytochrome P450 CYP26B1 variant 2; cytochrome P450 family 26 subfamily A member 1; cytochrome P450 retinoic acid-inactivating 2; cytochrome P450 retinoid metabolizing protein; cytochrome P450, family 26, subfamily B, polypeptide 1; cytochrome P450, subfamily XXVIB, polypeptide 1; cytochrome P450RAI-2; DKFZp686G0638; MGC129613; P450RAI-2; P450RAI2; retinoic acid-metabolizing cytochrome; RHFCA
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
GRCh38272,129,238 - 72,147,862 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl272,129,238 - 72,147,862 (-)EnsemblGRCh38hg38GRCh38
GRCh37272,356,367 - 72,374,991 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36272,209,875 - 72,228,471 (-)NCBINCBI36Build 36hg18NCBI36
Build 34272,268,021 - 72,286,618NCBI
Celera272,206,377 - 72,224,974 (-)NCBICelera
Cytogenetic Map2p13.2NCBI
HuRef272,092,551 - 72,111,176 (-)NCBIHuRef
CHM1_1272,285,791 - 72,304,416 (-)NCBICHM1_1
T2T-CHM13v2.0272,142,327 - 72,160,951 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dichloroethane  (ISO)
17alpha-ethynylestradiol  (EXP,ISO)
17beta-estradiol  (EXP)
2,2',5,5'-tetrachlorobiphenyl  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,4-D  (ISO)
2-hydroxypropanoic acid  (EXP)
4,4'-sulfonyldiphenol  (EXP,ISO)
4-hydroxyphenyl retinamide  (ISO)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrylamide  (ISO)
aldehydo-D-glucose  (ISO)
all-trans-retinoic acid  (EXP,ISO)
all-trans-retinol  (ISO)
ammonium chloride  (ISO)
arecoline  (EXP)
aristolochic acid A  (EXP)
arotinoid acid  (EXP)
arsane  (EXP,ISO)
arsenic atom  (EXP,ISO)
arsenite(3-)  (EXP)
azoxystrobin  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (ISO)
bisphenol F  (ISO)
bromobenzene  (ISO)
Butylbenzyl phthalate  (ISO)
C60 fullerene  (ISO)
cadmium atom  (ISO)
calcitriol  (EXP)
camptothecin  (EXP)
carbon nanotube  (ISO)
CGP 52608  (EXP)
CHIR 99021  (EXP)
chloroprene  (ISO)
choline  (ISO)
cisplatin  (EXP,ISO)
cocaine  (ISO)
copper(II) sulfate  (EXP)
cortisol  (EXP)
cyhalothrin  (ISO)
cypermethrin  (ISO)
cyproconazole  (ISO)
D-glucose  (ISO)
deguelin  (EXP)
dextran sulfate  (ISO)
dibenz[a,h]anthracene  (ISO)
dibutyl phthalate  (ISO)
diethyl maleate  (ISO)
diethylstilbestrol  (EXP)
diisobutyl phthalate  (ISO)
diisononyl phthalate  (ISO)
dioxygen  (ISO)
diquat  (ISO)
disodium selenite  (ISO)
diuron  (ISO)
doxorubicin  (EXP)
endosulfan  (ISO)
fipronil  (EXP)
fluconazole  (ISO)
fluoxetine  (ISO)
flusilazole  (ISO)
folic acid  (ISO)
fructose  (ISO)
furan  (ISO)
genistein  (ISO)
gentamycin  (ISO)
glucose  (ISO)
hexaconazole  (ISO)
hexadecanoic acid  (EXP)
isoprenaline  (ISO)
isotretinoin  (EXP)
ketoconazole  (EXP)
kojic acid  (EXP)
L-ascorbic acid  (EXP)
L-ascorbic acid 2-phosphate  (EXP)
L-methionine  (ISO)
leflunomide  (ISO)
lipopolysaccharide  (EXP,ISO)
manganese atom  (ISO)
manganese(0)  (ISO)
manganese(II) chloride  (ISO)
methoxychlor  (ISO)
mono(2-ethylhexyl) phthalate  (ISO)
N,N-diethyl-m-toluamide  (EXP)
nitrofen  (ISO)
oleic acid  (EXP)
oxaliplatin  (ISO)
paracetamol  (ISO)
paraquat  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (EXP,ISO)
phenylephrine  (ISO)
picoxystrobin  (EXP)
quercitrin  (EXP)
quinalphos  (ISO)
quinolines  (EXP)
rac-lactic acid  (EXP)
raloxifene  (EXP)
resveratrol  (ISO)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP,ISO)
sodium arsenite  (EXP,ISO)
Soman  (ISO)
sotorasib  (EXP)
streptozocin  (ISO)
sulforaphane  (ISO)
sunitinib  (EXP)
tamoxifen  (EXP,ISO)
titanium dioxide  (ISO)
toluene  (ISO)
topotecan  (ISO)
trametinib  (EXP)
trichloroethene  (ISO)
trichostatin A  (EXP)
trimellitic anhydride  (ISO)
triphenyl phosphate  (ISO)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vinyl carbamate  (ISO)
XAV939  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
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. Physiological insights into all-trans-retinoic acid biosynthesis. Napoli JL Biochim Biophys Acta. 2012 Jan;1821(1):152-67. Epub 2011 May 19.
3. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
4. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
7. RGD HPO Phenotype Annotation Pipeline RGD automated import pipeline for human HPO-to-gene-to-disease annotations
8. Multiple retinol and retinal dehydrogenases catalyze all-trans-retinoic acid biosynthesis in astrocytes. Wang C, etal., J Biol Chem. 2011 Feb 25;286(8):6542-53. Epub 2010 Dec 7.
9. Comprehensive Molecular Analyses of a Macrophage-Related Gene Signature With Regard to Prognosis, Immune Features, and Biomarkers for Immunotherapy in Hepatocellular Carcinoma Based on WGCNA and the LASSO Algorithm. Wang T, etal., Front Immunol. 2022 May 27;13:843408. doi: 10.3389/fimmu.2022.843408. eCollection 2022.
10. Acidic retinoids synergize with vitamin A to enhance retinol uptake and STRA6, LRAT, and CYP26B1 expression in neonatal lung. Wu L and Ross AC, J Lipid Res. 2010 Feb;51(2):378-87. Epub 2009 Aug 20.
Additional References at PubMed
PMID:10545224   PMID:10823918   PMID:11744378   PMID:12101034   PMID:12477932   PMID:14532297   PMID:15128046   PMID:15489334   PMID:15815621   PMID:16574820   PMID:16933217   PMID:19322201  
PMID:19703508   PMID:19884280   PMID:19953087   PMID:20375987   PMID:20606468   PMID:21482329   PMID:21641851   PMID:21873635   PMID:21945024   PMID:22019272   PMID:22020119   PMID:22415012  
PMID:22666329   PMID:22899867   PMID:22965740   PMID:22985482   PMID:23298258   PMID:23303528   PMID:23320086   PMID:23409080   PMID:23554885   PMID:23587162   PMID:23837398   PMID:23977348  
PMID:24726878   PMID:25056061   PMID:25114974   PMID:25168891   PMID:25839051   PMID:26374207   PMID:26937021   PMID:27410456   PMID:27416800   PMID:29379198   PMID:29606097   PMID:29676528  
PMID:31419517   PMID:32513696   PMID:32521127   PMID:32814053   PMID:33961781   PMID:34470463   PMID:36769350   PMID:37042568   PMID:37100236   PMID:37755482  


Genomics

Comparative Map Data
CYP26B1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38272,129,238 - 72,147,862 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl272,129,238 - 72,147,862 (-)EnsemblGRCh38hg38GRCh38
GRCh37272,356,367 - 72,374,991 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36272,209,875 - 72,228,471 (-)NCBINCBI36Build 36hg18NCBI36
Build 34272,268,021 - 72,286,618NCBI
Celera272,206,377 - 72,224,974 (-)NCBICelera
Cytogenetic Map2p13.2NCBI
HuRef272,092,551 - 72,111,176 (-)NCBIHuRef
CHM1_1272,285,791 - 72,304,416 (-)NCBICHM1_1
T2T-CHM13v2.0272,142,327 - 72,160,951 (-)NCBIT2T-CHM13v2.0
Cyp26b1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39684,548,396 - 84,570,890 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl684,548,396 - 84,570,890 (-)EnsemblGRCm39 Ensembl
GRCm38684,571,414 - 84,593,908 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl684,571,414 - 84,593,908 (-)EnsemblGRCm38mm10GRCm38
MGSCv37684,521,408 - 84,543,902 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36684,537,602 - 84,559,404 (-)NCBIMGSCv36mm8
Celera686,552,442 - 86,574,953 (-)NCBICelera
Cytogenetic Map6C3NCBI
cM Map636.45NCBI
Cyp26b1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84118,599,356 - 118,616,176 (-)NCBIGRCr8
mRatBN7.24117,041,808 - 117,058,628 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4117,041,808 - 117,058,628 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4122,523,010 - 122,539,827 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04118,298,178 - 118,314,997 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04116,911,101 - 116,927,919 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04116,261,796 - 116,278,615 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4116,261,796 - 116,278,615 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04180,848,037 - 180,865,444 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44118,734,786 - 118,751,606 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.14118,979,266 - 118,996,087 (-)NCBI
Celera4106,028,365 - 106,045,185 (-)NCBICelera
Cytogenetic Map4q34NCBI
LOC102023166
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542413,336,189 - 13,355,423 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495542413,336,189 - 13,355,368 (+)NCBIChiLan1.0ChiLan1.0
CYP26B1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21254,241,428 - 54,260,740 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A54,244,188 - 54,263,488 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A72,172,658 - 72,191,410 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A73,667,847 - 73,686,433 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A73,670,830 - 73,686,433 (-)Ensemblpanpan1.1panPan2
CYP26B1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11750,633,397 - 50,653,882 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1750,633,413 - 50,653,894 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1750,280,509 - 50,301,422 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01751,501,857 - 51,522,773 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1751,503,195 - 51,522,777 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11750,510,776 - 50,531,647 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01750,576,538 - 50,597,422 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01751,150,622 - 51,171,524 (+)NCBIUU_Cfam_GSD_1.0
LOC101975674
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629212,541,815 - 12,561,209 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649116,010,070 - 16,028,895 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649116,010,394 - 16,028,852 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CYP26B1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl370,572,197 - 70,593,408 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1370,573,551 - 70,593,416 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2373,914,357 - 73,934,214 (+)NCBISscrofa10.2Sscrofa10.2susScr3
CYP26B1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11435,030,011 - 35,057,164 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1435,038,654 - 35,057,176 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604577,009,329 - 77,029,165 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
LOC101714280
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247621,456,440 - 1,472,381 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247621,455,828 - 1,474,201 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CYP26B1
111 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_019885.4(CYP26B1):c.1088G>T (p.Arg363Leu) single nucleotide variant Lethal occipital encephalocele-skeletal dysplasia syndrome [RCV000023400]|not provided [RCV000059690] Chr2:72133081 [GRCh38]
Chr2:72360210 [GRCh37]
Chr2:2p13.2		 pathogenic|not provided
NM_019885.4(CYP26B1):c.436T>C (p.Ser146Pro) single nucleotide variant Lethal occipital encephalocele-skeletal dysplasia syndrome [RCV000023401]|not provided [RCV000059691] Chr2:72135413 [GRCh38]
Chr2:72362542 [GRCh37]
Chr2:2p13.2		 pathogenic|not provided
NM_019885.3(CYP26B1):c.1078G>A (p.Glu360Lys) single nucleotide variant Malignant melanoma [RCV000065666] Chr2:72133091 [GRCh38]
Chr2:72360220 [GRCh37]
Chr2:72213728 [NCBI36]
Chr2:2p13.2		 not provided
NM_019885.4(CYP26B1):c.704G>A (p.Arg235Gln) single nucleotide variant not provided [RCV003061534] Chr2:72135145 [GRCh38]
Chr2:72362274 [GRCh37]
Chr2:72215782 [NCBI36]
Chr2:2p13.2		 uncertain significance|not provided
NM_019885.3(CYP26B1):c.906C>T (p.Ala302=) single nucleotide variant Malignant melanoma [RCV000060604] Chr2:72133263 [GRCh38]
Chr2:72360392 [GRCh37]
Chr2:72213900 [NCBI36]
Chr2:2p13.2		 not provided
NM_019885.3(CYP26B1):c.607C>T (p.Pro203Ser) single nucleotide variant Malignant melanoma [RCV000060605] Chr2:72135242 [GRCh38]
Chr2:72362371 [GRCh37]
Chr2:72215879 [NCBI36]
Chr2:2p13.2		 not provided
NM_019885.4(CYP26B1):c.1259C>G (p.Ala420Gly) single nucleotide variant not provided [RCV000514998] Chr2:72132507 [GRCh38]
Chr2:72359636 [GRCh37]
Chr2:2p13.2		 benign|likely benign
GRCh38/hg38 2p13.3-13.2(chr2:70709155-72346899)x3 copy number gain See cases [RCV000133956] Chr2:70709155..72346899 [GRCh38]
Chr2:70936287..72574028 [GRCh37]
Chr2:70789795..72427536 [NCBI36]
Chr2:2p13.3-13.2		 uncertain significance
GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3 copy number gain See cases [RCV000136053] Chr2:58279519..83586962 [GRCh38]
Chr2:58506654..83814086 [GRCh37]
Chr2:58360158..83667597 [NCBI36]
Chr2:2p16.1-11.2		 pathogenic
GRCh38/hg38 2p16.3-11.2(chr2:47620388-86702722)x3 copy number gain See cases [RCV000137586] Chr2:47620388..86702722 [GRCh38]
Chr2:47847527..86929845 [GRCh37]
Chr2:47701031..86783356 [NCBI36]
Chr2:2p16.3-11.2		 uncertain significance
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3 copy number gain See cases [RCV000141494] Chr2:7495123..87705899 [GRCh38]
Chr2:7635254..88005418 [GRCh37]
Chr2:7552705..87786533 [NCBI36]
Chr2:2p25.1-11.2		 benign
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3 copy number gain See cases [RCV000448688] Chr2:62245236..86978895 [GRCh37]
Chr2:2p15-11.2		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_019885.4(CYP26B1):c.1190G>A (p.Arg397Gln) single nucleotide variant not provided [RCV000498080] Chr2:72132576 [GRCh38]
Chr2:72359705 [GRCh37]
Chr2:2p13.2		 likely pathogenic
NM_019885.4(CYP26B1):c.1088G>A (p.Arg363His) single nucleotide variant not provided [RCV000498598] Chr2:72133081 [GRCh38]
Chr2:72360210 [GRCh37]
Chr2:2p13.2		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_019885.4(CYP26B1):c.1247G>A (p.Arg416His) single nucleotide variant Inborn genetic diseases [RCV003299200] Chr2:72132519 [GRCh38]
Chr2:72359648 [GRCh37]
Chr2:2p13.2		 uncertain significance
Single allele duplication not provided [RCV000677942] Chr2:63671346..85698002 [GRCh37]
Chr2:2p15-11.2		 pathogenic
Single allele deletion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_019885.4(CYP26B1):c.205-327T>G single nucleotide variant not provided [RCV001545275] Chr2:72144540 [GRCh38]
Chr2:72371669 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1005C>T (p.Gly335=) single nucleotide variant not provided [RCV000970949] Chr2:72133164 [GRCh38]
Chr2:72360293 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1017C>T (p.Cys339=) single nucleotide variant CYP26B1-related condition [RCV003910793]|not provided [RCV000903594] Chr2:72133152 [GRCh38]
Chr2:72360281 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.862-5T>G single nucleotide variant not provided [RCV000884475] Chr2:72133312 [GRCh38]
Chr2:72360441 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.64G>C (p.Val22Leu) single nucleotide variant CYP26B1-related condition [RCV003910628]|not provided [RCV000892811] Chr2:72147771 [GRCh38]
Chr2:72374900 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.903G>A (p.Thr301=) single nucleotide variant not provided [RCV000923496] Chr2:72133266 [GRCh38]
Chr2:72360395 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1290T>C (p.His430=) single nucleotide variant not provided [RCV000927759] Chr2:72132476 [GRCh38]
Chr2:72359605 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.909C>T (p.Ser303=) single nucleotide variant not provided [RCV000906451] Chr2:72133260 [GRCh38]
Chr2:72360389 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1417C>T (p.Arg473Cys) single nucleotide variant not provided [RCV000973307] Chr2:72132349 [GRCh38]
Chr2:72359478 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.1138G>A (p.Glu380Lys) single nucleotide variant not provided [RCV000888502] Chr2:72133031 [GRCh38]
Chr2:72360160 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.705+7A>G single nucleotide variant not provided [RCV000964865] Chr2:72135137 [GRCh38]
Chr2:72362266 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.1179G>T (p.Met393Ile) single nucleotide variant Craniosynostosis syndrome [RCV000984629] Chr2:72132587 [GRCh38]
Chr2:72359716 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1098G>A (p.Thr366=) single nucleotide variant not provided [RCV000924306] Chr2:72133071 [GRCh38]
Chr2:72360200 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.74_77dup (p.Val28fs) duplication Craniosynostosis syndrome [RCV000985271] Chr2:72147757..72147758 [GRCh38]
Chr2:72374886..72374887 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.540C>T (p.Asn180=) single nucleotide variant not provided [RCV000916220] Chr2:72135309 [GRCh38]
Chr2:72362438 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.572G>A (p.Arg191His) single nucleotide variant CYP26B1-related condition [RCV003950405]|not provided [RCV000892508] Chr2:72135277 [GRCh38]
Chr2:72362406 [GRCh37]
Chr2:2p13.2		 benign|likely benign|conflicting interpretations of pathogenicity
NC_000002.11:g.(?_71004499)_(74779761_?)del deletion Dystonic disorder [RCV003113211]|Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency [RCV003113210]|not provided [RCV003107716] Chr2:71004499..74779761 [GRCh37]
Chr2:2p13.3-13.1		 pathogenic|no classifications from unflagged records
NM_019885.4(CYP26B1):c.1417C>A (p.Arg473Ser) single nucleotide variant not provided [RCV001567253] Chr2:72132349 [GRCh38]
Chr2:72359478 [GRCh37]
Chr2:2p13.2		 conflicting interpretations of pathogenicity|uncertain significance
NM_019885.4(CYP26B1):c.1147-20C>T single nucleotide variant not provided [RCV001570747] Chr2:72132639 [GRCh38]
Chr2:72359768 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.430-110T>G single nucleotide variant not provided [RCV001553007] Chr2:72135529 [GRCh38]
Chr2:72362658 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1147-119G>A single nucleotide variant not provided [RCV001658971] Chr2:72132738 [GRCh38]
Chr2:72359867 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.861+217dup duplication not provided [RCV001589830] Chr2:72134543..72134544 [GRCh38]
Chr2:72361672..72361673 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.186C>A (p.Thr62=) single nucleotide variant not provided [RCV001657504] Chr2:72147649 [GRCh38]
Chr2:72374778 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.430-187C>T single nucleotide variant not provided [RCV001577525] Chr2:72135606 [GRCh38]
Chr2:72362735 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.429+147C>T single nucleotide variant not provided [RCV001544834] Chr2:72143842 [GRCh38]
Chr2:72370971 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.678C>T (p.Val226=) single nucleotide variant not provided [RCV000980010] Chr2:72135171 [GRCh38]
Chr2:72362300 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.831C>T (p.His277=) single nucleotide variant not provided [RCV000884388] Chr2:72134791 [GRCh38]
Chr2:72361920 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.1110C>T (p.Gly370=) single nucleotide variant not provided [RCV000909428] Chr2:72133059 [GRCh38]
Chr2:72360188 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.51G>A (p.Ala17=) single nucleotide variant not provided [RCV000954880] Chr2:72147784 [GRCh38]
Chr2:72374913 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.504A>G (p.Thr168=) single nucleotide variant not provided [RCV000908238] Chr2:72135345 [GRCh38]
Chr2:72362474 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.1495G>A (p.Glu499Lys) single nucleotide variant CYP26B1-related condition [RCV003943078]|not provided [RCV000955938] Chr2:72132271 [GRCh38]
Chr2:72359400 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.205-144A>C single nucleotide variant not provided [RCV001557030] Chr2:72144357 [GRCh38]
Chr2:72371486 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.687C>T (p.Pro229=) single nucleotide variant not provided [RCV001557770] Chr2:72135162 [GRCh38]
Chr2:72362291 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.862-105G>T single nucleotide variant not provided [RCV001665455] Chr2:72133412 [GRCh38]
Chr2:72360541 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.861+191C>T single nucleotide variant not provided [RCV001587495] Chr2:72134570 [GRCh38]
Chr2:72361699 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.791T>C (p.Leu264Ser) single nucleotide variant not provided [RCV001538165] Chr2:72134831 [GRCh38]
Chr2:72361960 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.205-330G>C single nucleotide variant not provided [RCV001588620] Chr2:72144543 [GRCh38]
Chr2:72371672 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.861+25G>T single nucleotide variant not provided [RCV001709212] Chr2:72134736 [GRCh38]
Chr2:72361865 [GRCh37]
Chr2:2p13.2		 benign
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_019885.4(CYP26B1):c.115G>A (p.Ala39Thr) single nucleotide variant CYP26B1-related condition [RCV003931217]|not provided [RCV001575658] Chr2:72147720 [GRCh38]
Chr2:72374849 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.1333C>T (p.His445Tyr) single nucleotide variant Lethal occipital encephalocele-skeletal dysplasia syndrome [RCV001292624] Chr2:72132433 [GRCh38]
Chr2:72359562 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.205-233C>T single nucleotide variant not provided [RCV001686226] Chr2:72144446 [GRCh38]
Chr2:72371575 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.*44T>C single nucleotide variant not provided [RCV001619580] Chr2:72132183 [GRCh38]
Chr2:72359312 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.1377T>C (p.Ala459=) single nucleotide variant not provided [RCV001675559] Chr2:72132389 [GRCh38]
Chr2:72359518 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.1414C>T (p.Pro472Ser) single nucleotide variant not provided [RCV001727141] Chr2:72132352 [GRCh38]
Chr2:72359481 [GRCh37]
Chr2:2p13.2		 conflicting interpretations of pathogenicity|uncertain significance
NM_019885.4(CYP26B1):c.321G>A (p.Met107Ile) single nucleotide variant not provided [RCV003237695] Chr2:72144097 [GRCh38]
Chr2:72371226 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.344C>T (p.Thr115Ile) single nucleotide variant Inborn genetic diseases [RCV003355533]|Lethal occipital encephalocele-skeletal dysplasia syndrome [RCV003314016]|not provided [RCV001767468] Chr2:72144074 [GRCh38]
Chr2:72371203 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.862-184C>T single nucleotide variant not provided [RCV001733210] Chr2:72133491 [GRCh38]
Chr2:72360620 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1505C>T (p.Pro502Leu) single nucleotide variant Inborn genetic diseases [RCV002543992]|not provided [RCV001768676] Chr2:72132261 [GRCh38]
Chr2:72359390 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1528G>A (p.Ala510Thr) single nucleotide variant Inborn genetic diseases [RCV002552133]|not provided [RCV001877727] Chr2:72132238 [GRCh38]
Chr2:72359367 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.547C>G (p.Gln183Glu) single nucleotide variant not provided [RCV002014520] Chr2:72135302 [GRCh38]
Chr2:72362431 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1208C>T (p.Ala403Val) single nucleotide variant not provided [RCV001917195] Chr2:72132558 [GRCh38]
Chr2:72359687 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1231G>A (p.Val411Met) single nucleotide variant Inborn genetic diseases [RCV002555753]|not provided [RCV001939793] Chr2:72132535 [GRCh38]
Chr2:72359664 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1435G>A (p.Val479Ile) single nucleotide variant not provided [RCV001904262] Chr2:72132331 [GRCh38]
Chr2:72359460 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1147-12A>G single nucleotide variant not provided [RCV002114673] Chr2:72132631 [GRCh38]
Chr2:72359760 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.990C>T (p.Gly330=) single nucleotide variant not provided [RCV002174583] Chr2:72133179 [GRCh38]
Chr2:72360308 [GRCh37]
Chr2:2p13.2		 likely benign
NC_000002.11:g.(?_72359356)_(74779761_?)del deletion MOGS-congenital disorder of glycosylation [RCV003109485]|not provided [RCV003116543] Chr2:72359356..74779761 [GRCh37]
Chr2:2p13.2-13.1		 pathogenic|no classifications from unflagged records
NC_000002.11:g.(?_69240632)_(74779761_?)dup duplication not provided [RCV003122858] Chr2:69240632..74779761 [GRCh37]
Chr2:2p13.3-13.1		 uncertain significance
NM_019885.4(CYP26B1):c.628C>G (p.Leu210Val) single nucleotide variant not provided [RCV002274558] Chr2:72135221 [GRCh38]
Chr2:72362350 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1040C>T (p.Thr347Met) single nucleotide variant not provided [RCV002267412] Chr2:72133129 [GRCh38]
Chr2:72360258 [GRCh37]
Chr2:2p13.2		 uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13		 pathogenic
NM_019885.4(CYP26B1):c.1443C>A (p.His481Gln) single nucleotide variant not provided [RCV003236153] Chr2:72132323 [GRCh38]
Chr2:72359452 [GRCh37]
Chr2:2p13.2		 uncertain significance
GRCh37/hg19 2p13.2(chr2:72286238-72717551)x3 copy number gain not provided [RCV002472472] Chr2:72286238..72717551 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.428A>G (p.Lys143Arg) single nucleotide variant Inborn genetic diseases [RCV002879807] Chr2:72143990 [GRCh38]
Chr2:72371119 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.942G>A (p.Lys314=) single nucleotide variant not provided [RCV002903459] Chr2:72133227 [GRCh38]
Chr2:72360356 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.529G>A (p.Glu177Lys) single nucleotide variant not provided [RCV002994000] Chr2:72135320 [GRCh38]
Chr2:72362449 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.679G>A (p.Asp227Asn) single nucleotide variant Inborn genetic diseases [RCV002907746]|not provided [RCV002907745] Chr2:72135170 [GRCh38]
Chr2:72362299 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1273A>G (p.Lys425Glu) single nucleotide variant Inborn genetic diseases [RCV002799700] Chr2:72132493 [GRCh38]
Chr2:72359622 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1418G>T (p.Arg473Leu) single nucleotide variant Inborn genetic diseases [RCV002736931] Chr2:72132348 [GRCh38]
Chr2:72359477 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1395G>A (p.Glu465=) single nucleotide variant not provided [RCV003021479] Chr2:72132371 [GRCh38]
Chr2:72359500 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.454G>A (p.Glu152Lys) single nucleotide variant CYP26B1-related condition [RCV003963375]|not provided [RCV002885812] Chr2:72135395 [GRCh38]
Chr2:72362524 [GRCh37]
Chr2:2p13.2		 benign|likely benign
NM_019885.4(CYP26B1):c.1039A>G (p.Thr347Ala) single nucleotide variant Inborn genetic diseases [RCV002757735] Chr2:72133130 [GRCh38]
Chr2:72360259 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.420C>T (p.Asn140=) single nucleotide variant not provided [RCV002953062] Chr2:72143998 [GRCh38]
Chr2:72371127 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.541G>A (p.Val181Met) single nucleotide variant not provided [RCV002619050] Chr2:72135308 [GRCh38]
Chr2:72362437 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.910G>A (p.Ala304Thr) single nucleotide variant not provided [RCV003080735] Chr2:72133259 [GRCh38]
Chr2:72360388 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.787T>C (p.Tyr263His) single nucleotide variant Inborn genetic diseases [RCV002869138] Chr2:72134835 [GRCh38]
Chr2:72361964 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.86C>A (p.Ser29Ter) single nucleotide variant Lethal occipital encephalocele-skeletal dysplasia syndrome [RCV002508181] Chr2:72147749 [GRCh38]
Chr2:72374878 [GRCh37]
Chr2:2p13.2		 likely pathogenic
NM_019885.4(CYP26B1):c.598T>C (p.Phe200Leu) single nucleotide variant Inborn genetic diseases [RCV002935545] Chr2:72135251 [GRCh38]
Chr2:72362380 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1509G>T (p.Glu503Asp) single nucleotide variant Inborn genetic diseases [RCV002769761] Chr2:72132257 [GRCh38]
Chr2:72359386 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.528C>T (p.Pro176=) single nucleotide variant not provided [RCV003086030] Chr2:72135321 [GRCh38]
Chr2:72362450 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.539A>G (p.Asn180Ser) single nucleotide variant Inborn genetic diseases [RCV002961663] Chr2:72135310 [GRCh38]
Chr2:72362439 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.967C>T (p.Arg323Trp) single nucleotide variant not provided [RCV003009058] Chr2:72133202 [GRCh38]
Chr2:72360331 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.806T>A (p.Leu269His) single nucleotide variant not provided [RCV002721612] Chr2:72134816 [GRCh38]
Chr2:72361945 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.186C>G (p.Thr62=) single nucleotide variant not provided [RCV002610477] Chr2:72147649 [GRCh38]
Chr2:72374778 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1018G>A (p.Glu340Lys) single nucleotide variant Inborn genetic diseases [RCV002652566] Chr2:72133151 [GRCh38]
Chr2:72360280 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.968G>A (p.Arg323Gln) single nucleotide variant not provided [RCV002610787] Chr2:72133201 [GRCh38]
Chr2:72360330 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1418G>A (p.Arg473His) single nucleotide variant Inborn genetic diseases [RCV003204786] Chr2:72132348 [GRCh38]
Chr2:72359477 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1357G>A (p.Val453Met) single nucleotide variant Inborn genetic diseases [RCV003174711] Chr2:72132409 [GRCh38]
Chr2:72359538 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.557A>G (p.Gln186Arg) single nucleotide variant Inborn genetic diseases [RCV003184641] Chr2:72135292 [GRCh38]
Chr2:72362421 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.71T>C (p.Leu24Pro) single nucleotide variant Inborn genetic diseases [RCV003366458] Chr2:72147764 [GRCh38]
Chr2:72374893 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1005C>G (p.Gly335=) single nucleotide variant not provided [RCV003427017] Chr2:72133164 [GRCh38]
Chr2:72360293 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.555G>A (p.Ala185=) single nucleotide variant not provided [RCV003545834] Chr2:72135294 [GRCh38]
Chr2:72362423 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.460C>G (p.Leu154Val) single nucleotide variant not provided [RCV003825073] Chr2:72135389 [GRCh38]
Chr2:72362518 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1302C>T (p.Phe434=) single nucleotide variant not provided [RCV003738903] Chr2:72132464 [GRCh38]
Chr2:72359593 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1236C>T (p.Phe412=) single nucleotide variant not provided [RCV003545674] Chr2:72132530 [GRCh38]
Chr2:72359659 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.951T>C (p.Thr317=) single nucleotide variant not provided [RCV003699343] Chr2:72133218 [GRCh38]
Chr2:72360347 [GRCh37]
Chr2:2p13.2		 benign
NM_019885.4(CYP26B1):c.1261C>T (p.Arg421Trp) single nucleotide variant not provided [RCV003817404] Chr2:72132505 [GRCh38]
Chr2:72359634 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.213C>A (p.Gly71=) single nucleotide variant not provided [RCV003834800] Chr2:72144205 [GRCh38]
Chr2:72371334 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1134C>G (p.Thr378=) single nucleotide variant not provided [RCV003664873] Chr2:72133035 [GRCh38]
Chr2:72360164 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.285C>A (p.Arg95=) single nucleotide variant not provided [RCV003842061] Chr2:72144133 [GRCh38]
Chr2:72371262 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1447G>A (p.Val483Met) single nucleotide variant not provided [RCV003732166] Chr2:72132319 [GRCh38]
Chr2:72359448 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1030C>T (p.Arg344Cys) single nucleotide variant not provided [RCV003557089] Chr2:72133139 [GRCh38]
Chr2:72360268 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.1137C>T (p.Phe379=) single nucleotide variant not provided [RCV003731539] Chr2:72133032 [GRCh38]
Chr2:72360161 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.866G>A (p.Gly289Glu) single nucleotide variant not provided [RCV003731690] Chr2:72133303 [GRCh38]
Chr2:72360432 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.1413C>G (p.Phe471Leu) single nucleotide variant not provided [RCV003872390] Chr2:72132353 [GRCh38]
Chr2:72359482 [GRCh37]
Chr2:2p13.2		 uncertain significance
GRCh37/hg19 2p13.3-12(chr2:71076472-76368354)x1 copy number loss not specified [RCV003986388] Chr2:71076472..76368354 [GRCh37]
Chr2:2p13.3-12		 likely pathogenic
NM_019885.4(CYP26B1):c.1257G>A (p.Gln419=) single nucleotide variant not provided [RCV003732284] Chr2:72132509 [GRCh38]
Chr2:72359638 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.204+14C>T single nucleotide variant not provided [RCV003823924] Chr2:72147617 [GRCh38]
Chr2:72374746 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.204+7G>A single nucleotide variant CYP26B1-related condition [RCV003963935] Chr2:72147624 [GRCh38]
Chr2:72374753 [GRCh37]
Chr2:2p13.2		 likely benign
NM_019885.4(CYP26B1):c.549G>C (p.Gln183His) single nucleotide variant CYP26B1-related condition [RCV003971942] Chr2:72135300 [GRCh38]
Chr2:72362429 [GRCh37]
Chr2:2p13.2		 uncertain significance
NM_019885.4(CYP26B1):c.719G>A (p.Arg240Gln) single nucleotide variant Inborn genetic diseases [RCV003202197] Chr2:72134903 [GRCh38]
Chr2:72362032 [GRCh37]
Chr2:2p13.2		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4194
Count of miRNA genes:1063
Interacting mature miRNAs:1334
Transcripts:ENST00000001146, ENST00000412253, ENST00000461519, ENST00000474509, ENST00000546307
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
SGC32318  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37272,356,428 - 72,356,552UniSTSGRCh37
Build 36272,209,936 - 72,210,060RGDNCBI36
Celera272,206,438 - 72,206,562RGD
Cytogenetic Map2p13.2UniSTS
HuRef272,092,612 - 72,092,736UniSTS
GeneMap99-GB4 RH Map2222.31UniSTS
Whitehead-RH Map2306.7UniSTS


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 114 512 814 108 55 18 2698 121 1378 70 531 711 97 1150 1429
Low 2155 1602 624 245 536 175 1444 1854 2188 301 851 853 72 54 1302 4
Below cutoff 140 780 273 259 727 261 207 214 146 47 62 43 2 57 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007957 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001277742 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_019885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005264433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011532988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047445120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343034 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054343038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA484668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF252297 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294933 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW873673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC069443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC109205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC308258 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ467289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000001146   ⟹   ENSP00000001146
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl272,129,238 - 72,147,862 (-)Ensembl
RefSeq Acc Id: ENST00000412253   ⟹   ENSP00000401465
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl272,129,393 - 72,143,084 (-)Ensembl
RefSeq Acc Id: ENST00000461519   ⟹   ENSP00000430871
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl272,135,280 - 72,144,415 (-)Ensembl
RefSeq Acc Id: ENST00000474509   ⟹   ENSP00000430888
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl272,134,851 - 72,147,862 (-)Ensembl
RefSeq Acc Id: ENST00000546307   ⟹   ENSP00000443304
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl272,129,238 - 72,147,862 (-)Ensembl
RefSeq Acc Id: NM_001277742   ⟹   NP_001264671
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,129,238 - 72,147,862 (-)NCBI
HuRef272,092,551 - 72,111,176 (-)NCBI
CHM1_1272,285,791 - 72,304,416 (-)NCBI
T2T-CHM13v2.0272,142,327 - 72,160,951 (-)NCBI
Sequence:
RefSeq Acc Id: NM_019885   ⟹   NP_063938
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,129,238 - 72,147,862 (-)NCBI
GRCh37272,356,367 - 72,374,991 (-)NCBI
Build 36272,209,875 - 72,228,471 (-)NCBI Archive
HuRef272,092,551 - 72,111,176 (-)NCBI
CHM1_1272,285,791 - 72,304,416 (-)NCBI
T2T-CHM13v2.0272,142,327 - 72,160,951 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005264433   ⟹   XP_005264490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,129,238 - 72,145,004 (-)NCBI
GRCh37272,356,367 - 72,374,991 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011532988   ⟹   XP_011531290
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,129,238 - 72,136,284 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047445119   ⟹   XP_047301075
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,129,238 - 72,145,004 (-)NCBI
RefSeq Acc Id: XM_047445120   ⟹   XP_047301076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,129,238 - 72,143,178 (-)NCBI
RefSeq Acc Id: XM_054343033   ⟹   XP_054199008
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0272,142,327 - 72,158,108 (-)NCBI
RefSeq Acc Id: XM_054343034   ⟹   XP_054199009
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0272,142,327 - 72,158,105 (-)NCBI
RefSeq Acc Id: XM_054343035   ⟹   XP_054199010
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0272,142,327 - 72,160,341 (-)NCBI
RefSeq Acc Id: XM_054343036   ⟹   XP_054199011
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0272,142,327 - 72,160,582 (-)NCBI
RefSeq Acc Id: XM_054343037   ⟹   XP_054199012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0272,142,327 - 72,149,372 (-)NCBI
RefSeq Acc Id: XM_054343038   ⟹   XP_054199013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0272,142,327 - 72,156,267 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001264671 (Get FASTA)   NCBI Sequence Viewer  
  NP_063938 (Get FASTA)   NCBI Sequence Viewer  
  XP_005264490 (Get FASTA)   NCBI Sequence Viewer  
  XP_011531290 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301075 (Get FASTA)   NCBI Sequence Viewer  
  XP_047301076 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199008 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199009 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199010 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199011 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199012 (Get FASTA)   NCBI Sequence Viewer  
  XP_054199013 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF76003 (Get FASTA)   NCBI Sequence Viewer  
  AAH69443 (Get FASTA)   NCBI Sequence Viewer  
  AAI09206 (Get FASTA)   NCBI Sequence Viewer  
  AAY14690 (Get FASTA)   NCBI Sequence Viewer  
  ACR19332 (Get FASTA)   NCBI Sequence Viewer  
  BAG36224 (Get FASTA)   NCBI Sequence Viewer  
  BAH11892 (Get FASTA)   NCBI Sequence Viewer  
  BAH11930 (Get FASTA)   NCBI Sequence Viewer  
  BAH12154 (Get FASTA)   NCBI Sequence Viewer  
  CAH18425 (Get FASTA)   NCBI Sequence Viewer  
  EAW99761 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000001146
  ENSP00000001146.2
  ENSP00000401465
  ENSP00000401465.1
  ENSP00000430871.1
  ENSP00000430888.1
  ENSP00000443304
  ENSP00000443304.1
GenBank Protein Q9NR63 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_063938   ⟸   NM_019885
- Peptide Label: isoform 1
- UniProtKB: Q53TW1 (UniProtKB/Swiss-Prot),   Q32MC0 (UniProtKB/Swiss-Prot),   E4W5W7 (UniProtKB/Swiss-Prot),   B7Z3B8 (UniProtKB/Swiss-Prot),   B7Z2P4 (UniProtKB/Swiss-Prot),   B7Z2K6 (UniProtKB/Swiss-Prot),   B2R8M7 (UniProtKB/Swiss-Prot),   Q9NP41 (UniProtKB/Swiss-Prot),   Q9NR63 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001264671   ⟸   NM_001277742
- Peptide Label: isoform 2
- UniProtKB: Q9NR63 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005264490   ⟸   XM_005264433
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011531290   ⟸   XM_011532988
- Peptide Label: isoform X3
- UniProtKB: E7ER08 (UniProtKB/TrEMBL),   Q68D05 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000401465   ⟸   ENST00000412253
RefSeq Acc Id: ENSP00000443304   ⟸   ENST00000546307
RefSeq Acc Id: ENSP00000430888   ⟸   ENST00000474509
RefSeq Acc Id: ENSP00000430871   ⟸   ENST00000461519
RefSeq Acc Id: ENSP00000001146   ⟸   ENST00000001146
RefSeq Acc Id: XP_047301075   ⟸   XM_047445119
- Peptide Label: isoform X2
RefSeq Acc Id: XP_047301076   ⟸   XM_047445120
- Peptide Label: isoform X3
- UniProtKB: E7ER08 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054199011   ⟸   XM_054343036
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199010   ⟸   XM_054343035
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199008   ⟸   XM_054343033
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054199009   ⟸   XM_054343034
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054199013   ⟸   XM_054343038
- Peptide Label: isoform X3
- UniProtKB: E7ER08 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054199012   ⟸   XM_054343037
- Peptide Label: isoform X3
- UniProtKB: E7ER08 (UniProtKB/TrEMBL)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NR63-F1-model_v2 AlphaFold Q9NR63 1-512 view protein structure

Promoters
RGD ID:6860650
Promoter ID:EPDNEW_H3490
Type:initiation region
Name:CYP26B1_4
Description:cytochrome P450 family 26 subfamily B member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3491  EPDNEW_H3492  EPDNEW_H3493  EPDNEW_H3494  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,147,825 - 72,147,885EPDNEW
RGD ID:6860652
Promoter ID:EPDNEW_H3491
Type:initiation region
Name:CYP26B1_2
Description:cytochrome P450 family 26 subfamily B member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3490  EPDNEW_H3492  EPDNEW_H3493  EPDNEW_H3494  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,147,965 - 72,148,025EPDNEW
RGD ID:6860654
Promoter ID:EPDNEW_H3492
Type:initiation region
Name:CYP26B1_1
Description:cytochrome P450 family 26 subfamily B member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3490  EPDNEW_H3491  EPDNEW_H3493  EPDNEW_H3494  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,148,346 - 72,148,406EPDNEW
RGD ID:6860656
Promoter ID:EPDNEW_H3493
Type:initiation region
Name:CYP26B1_3
Description:cytochrome P450 family 26 subfamily B member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3490  EPDNEW_H3491  EPDNEW_H3492  EPDNEW_H3494  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,149,117 - 72,149,177EPDNEW
RGD ID:6860658
Promoter ID:EPDNEW_H3494
Type:multiple initiation site
Name:CYP26B1_5
Description:cytochrome P450 family 26 subfamily B member 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3490  EPDNEW_H3491  EPDNEW_H3492  EPDNEW_H3493  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38272,154,538 - 72,154,598EPDNEW
RGD ID:6797036
Promoter ID:HG_KWN:33211
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000327529
Position:
Human AssemblyChrPosition (strand)Source
Build 36272,224,016 - 72,224,617 (-)MPROMDB
RGD ID:6797039
Promoter ID:HG_KWN:33212
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000327531
Position:
Human AssemblyChrPosition (strand)Source
Build 36272,225,316 - 72,225,816 (-)MPROMDB
RGD ID:6797038
Promoter ID:HG_KWN:33213
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:OTTHUMT00000251969,   OTTHUMT00000327530
Position:
Human AssemblyChrPosition (strand)Source
Build 36272,228,966 - 72,229,466 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20581 AgrOrtholog
COSMIC CYP26B1 COSMIC
Ensembl Genes ENSG00000003137 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000001146 ENTREZGENE
  ENST00000001146.7 UniProtKB/Swiss-Prot
  ENST00000412253 ENTREZGENE
  ENST00000412253.1 UniProtKB/TrEMBL
  ENST00000461519.1 UniProtKB/TrEMBL
  ENST00000474509.1 UniProtKB/TrEMBL
  ENST00000546307 ENTREZGENE
  ENST00000546307.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.630.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000003137 GTEx
HGNC ID HGNC:20581 ENTREZGENE
Human Proteome Map CYP26B1 Human Proteome Map
InterPro Cyt_P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_E_grp-IV UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:56603 UniProtKB/Swiss-Prot
NCBI Gene 56603 ENTREZGENE
OMIM 605207 OMIM
PANTHER CYTOCHROME P450 26 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CYTOCHROME P450 26B1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam p450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134879191 PharmGKB
PRINTS EP450IV UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CYTOCHROME_P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48264 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R8M7 ENTREZGENE
  B7Z2K6 ENTREZGENE
  B7Z2P4 ENTREZGENE
  B7Z3B8 ENTREZGENE
  CP26B_HUMAN UniProtKB/Swiss-Prot
  E4W5W7 ENTREZGENE
  E5RHM2_HUMAN UniProtKB/TrEMBL
  E5RHN4_HUMAN UniProtKB/TrEMBL
  E7ER08 ENTREZGENE, UniProtKB/TrEMBL
  Q32MC0 ENTREZGENE
  Q53TW1 ENTREZGENE
  Q68D05 ENTREZGENE, UniProtKB/TrEMBL
  Q9NP41 ENTREZGENE
  Q9NR63 ENTREZGENE
UniProt Secondary B2R8M7 UniProtKB/Swiss-Prot
  B7Z2K6 UniProtKB/Swiss-Prot
  B7Z2P4 UniProtKB/Swiss-Prot
  B7Z3B8 UniProtKB/Swiss-Prot
  E4W5W7 UniProtKB/Swiss-Prot
  Q32MC0 UniProtKB/Swiss-Prot
  Q53TW1 UniProtKB/Swiss-Prot
  Q9NP41 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 CYP26B1  cytochrome P450 family 26 subfamily B member 1  CYP26B1  cytochrome P450, family 26, subfamily B, polypeptide 1  Symbol and/or name change 5135510 APPROVED