CYP3A43 (cytochrome P450 family 3 subfamily A member 43) - Rat Genome Database

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Gene: CYP3A43 (cytochrome P450 family 3 subfamily A member 43) Homo sapiens
Analyze
Symbol: CYP3A43
Name: cytochrome P450 family 3 subfamily A member 43
RGD ID: 1350489
HGNC Page HGNC:17450
Description: Predicted to enable estrogen 16-alpha-hydroxylase activity and testosterone 6-beta-hydroxylase activity. Predicted to be involved in oxidative demethylation and steroid metabolic process. Predicted to be located in endoplasmic reticulum membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cytochrome P450 3A43; cytochrome P450 polypeptide 43; cytochrome P450, family 3, subfamily A, polypeptide 43; cytochrome P450, subfamily IIIA, polypeptide 43; MGC119315; MGC119316
RGD Orthologs
Rat
Bonobo
Green Monkey
Alliance Genes
More Info more info ...
Related Pseudogenes: CYP3A137P  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38799,828,013 - 99,866,093 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl799,828,013 - 99,866,093 (+)EnsemblGRCh38hg38GRCh38
GRCh37799,425,636 - 99,463,716 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36799,263,572 - 99,302,109 (+)NCBINCBI36Build 36hg18NCBI36
Build 34799,070,286 - 99,108,824NCBI
Celera794,159,885 - 94,198,421 (+)NCBICelera
Cytogenetic Map7q22.1NCBI
HuRef794,061,564 - 94,099,614 (+)NCBIHuRef
CHM1_1799,355,683 - 99,393,889 (+)NCBICHM1_1
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
1,2-dimethylhydrazine  (ISO)
1-naphthyl isothiocyanate  (ISO)
17beta-estradiol  (ISO)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,4,6-trinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
2-(3,4-dimethoxyphenyl)-5-\{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino\}-2-(propan-2-yl)pentanenitrile  (ISO)
3H-1,2-dithiole-3-thione  (ISO)
aflatoxin B1  (EXP)
ammonium chloride  (ISO)
arsenous acid  (EXP)
atrazine  (ISO)
benzo[a]pyrene  (EXP)
beta-carotene  (EXP)
bexarotene  (ISO)
bis(2-ethylhexyl) phthalate  (EXP,ISO)
bisphenol A  (ISO)
bosentan  (EXP)
carbamazepine  (EXP)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
cyclosporin A  (EXP)
cyhalothrin  (ISO)
cylindrospermopsin  (EXP)
cyproconazole  (ISO)
dexamethasone  (ISO)
Diallyl sulfide  (ISO)
diarsenic trioxide  (EXP)
diuron  (ISO)
endosulfan  (ISO)
ethoxyquin  (ISO)
fipronil  (EXP,ISO)
flavonoids  (ISO)
flutamide  (ISO)
formaldehyde  (EXP)
furan  (ISO)
Ginkgolide A  (ISO)
glafenine  (ISO)
methapyrilene  (ISO)
N,N-diethyl-m-toluamide  (EXP)
N-nitrosodiethylamine  (ISO)
N-Nitrosopyrrolidine  (EXP)
nefazodone  (ISO)
obeticholic acid  (EXP)
paracetamol  (EXP)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenethyl caffeate  (ISO)
phenformin  (ISO)
phenobarbital  (ISO)
pirinixic acid  (EXP,ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
prochloraz  (ISO)
riddelliine  (ISO)
rotenone  (ISO)
senecionine  (EXP)
tebuconazole  (EXP)
testosterone  (EXP)
tetrachloromethane  (ISO)
thioacetamide  (ISO)
triadimefon  (ISO)
troglitazone  (EXP)
urethane  (EXP)
valdecoxib  (ISO)
valproic acid  (ISO)
verapamil  (ISO)
vinclozolin  (ISO)
zinc atom  (ISO)
zinc(0)  (ISO)

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. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9890157   PMID:11137287   PMID:11160876   PMID:11243885   PMID:11266076   PMID:11726664   PMID:12477932   PMID:12853948   PMID:14695544   PMID:14759258   PMID:15128046   PMID:15548719  
PMID:15894682   PMID:16314882   PMID:16848237   PMID:18566991   PMID:19343046   PMID:19789190   PMID:20529763   PMID:20715157   PMID:21081028   PMID:21533175   PMID:21873635   PMID:22344438  
PMID:24595013   PMID:25150845   PMID:25807282   PMID:26585945   PMID:28673024   PMID:30021884   PMID:32301865   PMID:32461654   PMID:32487729   PMID:33961781   PMID:34299191   PMID:35256949  
PMID:36613552  


Genomics

Comparative Map Data
CYP3A43
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38799,828,013 - 99,866,093 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl799,828,013 - 99,866,093 (+)EnsemblGRCh38hg38GRCh38
GRCh37799,425,636 - 99,463,716 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36799,263,572 - 99,302,109 (+)NCBINCBI36Build 36hg18NCBI36
Build 34799,070,286 - 99,108,824NCBI
Celera794,159,885 - 94,198,421 (+)NCBICelera
Cytogenetic Map7q22.1NCBI
HuRef794,061,564 - 94,099,614 (+)NCBIHuRef
CHM1_1799,355,683 - 99,393,889 (+)NCBICHM1_1
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Cyp3a18
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81213,994,312 - 14,044,185 (+)NCBIGRCr8
mRatBN7.2128,880,509 - 8,930,382 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl128,880,528 - 8,930,381 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx129,678,389 - 9,728,392 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01210,301,584 - 10,351,575 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0129,325,028 - 9,375,015 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01210,636,294 - 10,684,273 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1210,636,275 - 10,684,278 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01212,738,271 - 12,787,784 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4129,086,752 - 9,136,606 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1129,116,679 - 9,166,534 (-)NCBI
Celera1210,707,212 - 10,757,562 (+)NCBICelera
Cytogenetic Map12p11NCBI
CYP3A43
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26117,746,741 - 117,785,619 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan17166,011,375 - 166,050,250 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0791,862,437 - 91,903,033 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17105,296,111 - 105,335,958 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl7105,296,111 - 105,335,958 (+)Ensemblpanpan1.1panPan2
CYP3A43
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12813,217,123 - 13,256,859 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2813,216,548 - 13,257,015 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660703,012,292 - 3,052,631 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in CYP3A43
19 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q21.3-22.1(chr7:98288474-101259804)x3 copy number gain See cases [RCV000053573] Chr7:98288474..101259804 [GRCh38]
Chr7:97917786..100903085 [GRCh37]
Chr7:97755722..100689805 [NCBI36]
Chr7:7q21.3-22.1
pathogenic
GRCh38/hg38 7q22.1(chr7:99219420-100902269)x1 copy number loss See cases [RCV000054154] Chr7:99219420..100902269 [GRCh38]
Chr7:98817043..100499889 [GRCh37]
Chr7:98654979..100337825 [NCBI36]
Chr7:7q22.1
pathogenic
NM_057095.2(CYP3A43):c.829G>A (p.Asp277Asn) single nucleotide variant Malignant melanoma [RCV000061709] Chr7:99856863 [GRCh38]
Chr7:99454486 [GRCh37]
Chr7:99292422 [NCBI36]
Chr7:7q22.1
not provided
NM_057095.2(CYP3A43):c.71+3416T>G single nucleotide variant Lung cancer [RCV000106736] Chr7:99831602 [GRCh38]
Chr7:99429225 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q22.1(chr7:99195836-102258175)x1 copy number loss See cases [RCV000135782] Chr7:99195836..102258175 [GRCh38]
Chr7:98793459..101718950 [GRCh37]
Chr7:98631395..101688175 [NCBI36]
Chr7:7q22.1
pathogenic|uncertain significance
GRCh38/hg38 7q22.1(chr7:99195836-100348063)x3 copy number gain See cases [RCV000135630] Chr7:99195836..100348063 [GRCh38]
Chr7:98793459..99945686 [GRCh37]
Chr7:98631395..99783622 [NCBI36]
Chr7:7q22.1
likely benign
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3
pathogenic
GRCh38/hg38 7q22.1(chr7:99643456-99913142)x3 copy number gain See cases [RCV000140269] Chr7:99643456..99913142 [GRCh38]
Chr7:99241079..99510765 [GRCh37]
Chr7:99079015..99348701 [NCBI36]
Chr7:7q22.1
likely benign
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q21.2-22.1(chr7:92445452-99686985)x1 copy number loss Split hand-foot malformation 1 [RCV000656540] Chr7:92445452..99686985 [GRCh37]
Chr7:7q21.2-22.1
pathogenic
GRCh37/hg19 7q22.1(chr7:98847725-102472176)x1 copy number loss not provided [RCV000682904] Chr7:98847725..102472176 [GRCh37]
Chr7:7q22.1
pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3
pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Childhood apraxia of speech [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q22.1(chr7:99459256-99463380)x1 copy number loss not provided [RCV000746916] Chr7:99459256..99463380 [GRCh37]
Chr7:7q22.1
benign
GRCh37/hg19 7q22.1(chr7:99461483-99466558)x1 copy number loss not provided [RCV000746917] Chr7:99461483..99466558 [GRCh37]
Chr7:7q22.1
benign
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
NM_057095.3(CYP3A43):c.435G>T (p.Met145Ile) single nucleotide variant not provided [RCV000910641] Chr7:99848168 [GRCh38]
Chr7:99445791 [GRCh37]
Chr7:7q22.1
benign
NM_057095.3(CYP3A43):c.340C>T (p.Leu114=) single nucleotide variant not provided [RCV000907323] Chr7:99847509 [GRCh38]
Chr7:99445132 [GRCh37]
Chr7:7q22.1
benign
NM_057095.3(CYP3A43):c.1018C>G (p.Pro340Ala) single nucleotide variant not provided [RCV001694979] Chr7:99859982 [GRCh38]
Chr7:99457605 [GRCh37]
Chr7:7q22.1
benign
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q21.12-22.1(chr7:87477185-100333327) copy number gain Isolated Pierre-Robin syndrome [RCV001352649] Chr7:87477185..100333327 [GRCh37]
Chr7:7q21.12-22.1
pathogenic
GRCh37/hg19 7q22.1-31.1(chr7:99417471-111586308) copy number loss not specified [RCV002053711] Chr7:99417471..111586308 [GRCh37]
Chr7:7q22.1-31.1
pathogenic
GRCh37/hg19 7q22.1(chr7:98755291-99886571)x3 copy number gain not provided [RCV001836489] Chr7:98755291..99886571 [GRCh37]
Chr7:7q22.1
uncertain significance
NC_000007.13:g.(?_98983338)_(100860555_?)del deletion not provided [RCV001877526] Chr7:98983338..100860555 [GRCh37]
Chr7:7q22.1
pathogenic|uncertain significance
NC_000007.13:g.(?_98507659)_(100860555_?)dup duplication not provided [RCV003113282] Chr7:98507659..100860555 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3
uncertain significance
NM_057095.3(CYP3A43):c.1192A>G (p.Ile398Val) single nucleotide variant Inborn genetic diseases [RCV002762397] Chr7:99861778 [GRCh38]
Chr7:99459401 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.757A>G (p.Ile253Val) single nucleotide variant Inborn genetic diseases [RCV002911302] Chr7:99855677 [GRCh38]
Chr7:99453300 [GRCh37]
Chr7:7q22.1
likely benign
NM_057095.3(CYP3A43):c.560C>T (p.Thr187Ile) single nucleotide variant Inborn genetic diseases [RCV003001553] Chr7:99849584 [GRCh38]
Chr7:99447207 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.1006G>A (p.Asp336Asn) single nucleotide variant Inborn genetic diseases [RCV002821453] Chr7:99859970 [GRCh38]
Chr7:99457593 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.1337G>A (p.Arg446Lys) single nucleotide variant Inborn genetic diseases [RCV002762042] Chr7:99863620 [GRCh38]
Chr7:99461243 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.1258A>G (p.Ser420Gly) single nucleotide variant Inborn genetic diseases [RCV002768131] Chr7:99863541 [GRCh38]
Chr7:99461164 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.768G>A (p.Met256Ile) single nucleotide variant Inborn genetic diseases [RCV002709537] Chr7:99855688 [GRCh38]
Chr7:99453311 [GRCh37]
Chr7:7q22.1
likely benign
NM_057095.3(CYP3A43):c.866C>T (p.Ala289Val) single nucleotide variant Inborn genetic diseases [RCV002919332] Chr7:99859830 [GRCh38]
Chr7:99457453 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.223T>C (p.Tyr75His) single nucleotide variant Inborn genetic diseases [RCV003178005] Chr7:99844147 [GRCh38]
Chr7:99441770 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.634A>C (p.Lys212Gln) single nucleotide variant Inborn genetic diseases [RCV003185480] Chr7:99849658 [GRCh38]
Chr7:99447281 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.853A>G (p.Lys285Glu) single nucleotide variant Inborn genetic diseases [RCV003308625] Chr7:99856887 [GRCh38]
Chr7:99454510 [GRCh37]
Chr7:7q22.1
likely benign
GRCh38/hg38 7q22.1(chr7:98454022-100723798)x1 copy number loss Multiple congenital anomalies/dysmorphic syndrome [RCV003327701] Chr7:98454022..100723798 [GRCh38]
Chr7:7q22.1
pathogenic
NM_057095.3(CYP3A43):c.1373G>C (p.Arg458Thr) single nucleotide variant Inborn genetic diseases [RCV003357190] Chr7:99863656 [GRCh38]
Chr7:99461279 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.161T>C (p.Leu54Pro) single nucleotide variant Inborn genetic diseases [RCV003386582] Chr7:99836542 [GRCh38]
Chr7:99434165 [GRCh37]
Chr7:7q22.1
uncertain significance
GRCh37/hg19 7q22.1(chr7:99114000-101878272)x1 copy number loss not provided [RCV003482971] Chr7:99114000..101878272 [GRCh37]
Chr7:7q22.1
pathogenic
GRCh37/hg19 7q22.1(chr7:99263437-100105272)x1 copy number loss not provided [RCV003482973] Chr7:99263437..100105272 [GRCh37]
Chr7:7q22.1
uncertain significance
NM_057095.3(CYP3A43):c.1298T>C (p.Ile433Thr) single nucleotide variant Inborn genetic diseases [RCV003343267] Chr7:99863581 [GRCh38]
Chr7:99461204 [GRCh37]
Chr7:7q22.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1973
Count of miRNA genes:687
Interacting mature miRNAs:743
Transcripts:ENST00000222382, ENST00000312017, ENST00000342499, ENST00000354829, ENST00000415413, ENST00000417625, ENST00000421837, ENST00000433277, ENST00000434806, ENST00000436834, ENST00000444905, ENST00000463915, ENST00000472352, ENST00000477658, ENST00000481362, ENST00000491648, ENST00000495115
Prediction methods: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.

Markers in Region
CYP3A43_1909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37799,463,572 - 99,464,335UniSTSGRCh37
Build 36799,301,508 - 99,302,271RGDNCBI36
Celera794,197,820 - 94,198,583RGD
HuRef794,099,459 - 94,100,222UniSTS
CRA_TCAGchr7v2798,823,391 - 98,824,154UniSTS


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 123 123 123 1 3
Low 24 14 267 231 22 231 183 31 241 26 571 26 20 170
Below cutoff 2150 2237 1163 248 1032 98 3752 1965 3284 319 730 1346 159 1108 2395 4

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001278921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_022820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_057095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_057096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_103868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_103869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446877 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358843 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054358846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA417369 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF280113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF319634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF337813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY390423 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY390424 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY390425 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY390426 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC100981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC100982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236956 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000222382   ⟹   ENSP00000222382
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,116 - 99,866,001 (+)Ensembl
RefSeq Acc Id: ENST00000312017   ⟹   ENSP00000312110
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,116 - 99,866,001 (+)Ensembl
RefSeq Acc Id: ENST00000342499   ⟹   ENSP00000345351
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,013 - 99,866,102 (+)Ensembl
RefSeq Acc Id: ENST00000354829   ⟹   ENSP00000346887
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,013 - 99,866,093 (+)Ensembl
RefSeq Acc Id: ENST00000415413   ⟹   ENSP00000401521
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000417625   ⟹   ENSP00000416581
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,043 - 99,866,001 (+)Ensembl
RefSeq Acc Id: ENST00000433277   ⟹   ENSP00000400316
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000434806   ⟹   ENSP00000411653
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,116 - 99,866,001 (+)Ensembl
RefSeq Acc Id: ENST00000436834   ⟹   ENSP00000415221
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,043 - 99,866,001 (+)Ensembl
RefSeq Acc Id: ENST00000444905   ⟹   ENSP00000405557
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000463915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000472352
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,855,488 - 99,861,840 (+)Ensembl
RefSeq Acc Id: ENST00000477658
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000481362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,116 - 99,866,001 (+)Ensembl
RefSeq Acc Id: ENST00000491648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000495115
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,049 - 99,866,045 (+)Ensembl
RefSeq Acc Id: ENST00000631161   ⟹   ENSP00000486759
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl799,828,013 - 99,839,420 (+)Ensembl
RefSeq Acc Id: NM_001278921   ⟹   NP_001265850
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,866,093 (+)NCBI
HuRef794,061,564 - 94,099,614 (+)NCBI
CHM1_1799,355,683 - 99,393,889 (+)NCBI
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBI
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Sequence:
RefSeq Acc Id: NM_022820   ⟹   NP_073731
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,866,093 (+)NCBI
GRCh37799,425,636 - 99,463,727 (+)NCBI
Build 36799,263,572 - 99,302,109 (+)NCBI Archive
HuRef794,061,564 - 94,099,614 (+)NCBI
CHM1_1799,355,683 - 99,393,889 (+)NCBI
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBI
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Sequence:
RefSeq Acc Id: NM_057095   ⟹   NP_476436
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,866,093 (+)NCBI
GRCh37799,425,636 - 99,463,727 (+)NCBI
Build 36799,263,572 - 99,302,109 (+)NCBI Archive
HuRef794,061,564 - 94,099,614 (+)NCBI
CHM1_1799,355,683 - 99,393,889 (+)NCBI
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBI
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Sequence:
RefSeq Acc Id: NM_057096   ⟹   NP_476437
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,866,093 (+)NCBI
GRCh37799,425,636 - 99,463,727 (+)NCBI
Build 36799,263,572 - 99,302,109 (+)NCBI Archive
HuRef794,061,564 - 94,099,614 (+)NCBI
CHM1_1799,355,683 - 99,393,889 (+)NCBI
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBI
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_103868
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,866,093 (+)NCBI
HuRef794,061,564 - 94,099,614 (+)NCBI
CHM1_1799,355,683 - 99,393,889 (+)NCBI
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBI
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Sequence:
RefSeq Acc Id: NR_103869
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,866,093 (+)NCBI
HuRef794,061,564 - 94,099,614 (+)NCBI
CHM1_1799,355,683 - 99,393,889 (+)NCBI
T2T-CHM13v2.07101,067,527 - 101,105,595 (+)NCBI
CRA_TCAGchr7v2798,785,456 - 98,823,546 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017012544   ⟹   XP_016868033
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,847,571 - 99,866,093 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017012545   ⟹   XP_016868034
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,847,546 - 99,866,093 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047420745   ⟹   XP_047276701
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,836,511 - 99,866,093 (+)NCBI
RefSeq Acc Id: XM_047420746   ⟹   XP_047276702
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,838,926 - 99,866,093 (+)NCBI
RefSeq Acc Id: XM_054358843   ⟹   XP_054214818
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07101,076,025 - 101,105,595 (+)NCBI
RefSeq Acc Id: XM_054358844   ⟹   XP_054214819
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07101,078,440 - 101,105,595 (+)NCBI
RefSeq Acc Id: XM_054358845   ⟹   XP_054214820
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07101,087,085 - 101,105,595 (+)NCBI
RefSeq Acc Id: XM_054358846   ⟹   XP_054214821
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.07101,087,060 - 101,105,595 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001265850 (Get FASTA)   NCBI Sequence Viewer  
  NP_073731 (Get FASTA)   NCBI Sequence Viewer  
  NP_476436 (Get FASTA)   NCBI Sequence Viewer  
  NP_476437 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868033 (Get FASTA)   NCBI Sequence Viewer  
  XP_016868034 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276701 (Get FASTA)   NCBI Sequence Viewer  
  XP_047276702 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214818 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214819 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214820 (Get FASTA)   NCBI Sequence Viewer  
  XP_054214821 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAG32291 (Get FASTA)   NCBI Sequence Viewer  
  AAG33009 (Get FASTA)   NCBI Sequence Viewer  
  AAG33010 (Get FASTA)   NCBI Sequence Viewer  
  AAG33011 (Get FASTA)   NCBI Sequence Viewer  
  AAG33012 (Get FASTA)   NCBI Sequence Viewer  
  AAG33013 (Get FASTA)   NCBI Sequence Viewer  
  AAG33014 (Get FASTA)   NCBI Sequence Viewer  
  AAI00982 (Get FASTA)   NCBI Sequence Viewer  
  AAI00983 (Get FASTA)   NCBI Sequence Viewer  
  AAK00325 (Get FASTA)   NCBI Sequence Viewer  
  AAK38841 (Get FASTA)   NCBI Sequence Viewer  
  AAQ92351 (Get FASTA)   NCBI Sequence Viewer  
  AAQ92352 (Get FASTA)   NCBI Sequence Viewer  
  AAQ92353 (Get FASTA)   NCBI Sequence Viewer  
  AAQ92354 (Get FASTA)   NCBI Sequence Viewer  
  AAS07394 (Get FASTA)   NCBI Sequence Viewer  
  AAS07395 (Get FASTA)   NCBI Sequence Viewer  
  EAW76630 (Get FASTA)   NCBI Sequence Viewer  
  EAW76631 (Get FASTA)   NCBI Sequence Viewer  
  EAW76632 (Get FASTA)   NCBI Sequence Viewer  
  EAW76633 (Get FASTA)   NCBI Sequence Viewer  
  EAW76634 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000222382
  ENSP00000222382.5
  ENSP00000312110
  ENSP00000312110.5
  ENSP00000346887
  ENSP00000346887.3
  ENSP00000400316.1
  ENSP00000401521.1
  ENSP00000405557.1
  ENSP00000411653.1
  ENSP00000415221.1
  ENSP00000416581
  ENSP00000416581.1
  ENSP00000486759.1
GenBank Protein Q9HB55 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_073731   ⟸   NM_022820
- Peptide Label: isoform 1
- UniProtKB: Q9HB55 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_476436   ⟸   NM_057095
- Peptide Label: isoform 2
- UniProtKB: Q9HB54 (UniProtKB/Swiss-Prot),   Q9HB53 (UniProtKB/Swiss-Prot),   Q9HB52 (UniProtKB/Swiss-Prot),   Q75MK3 (UniProtKB/Swiss-Prot),   Q75MK2 (UniProtKB/Swiss-Prot),   Q495Y1 (UniProtKB/Swiss-Prot),   Q9HB57 (UniProtKB/Swiss-Prot),   Q9HB55 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_476437   ⟸   NM_057096
- Peptide Label: isoform 3
- UniProtKB: Q9HB55 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001265850   ⟸   NM_001278921
- Peptide Label: isoform 4
- UniProtKB: Q9HB55 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016868034   ⟸   XM_017012545
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_016868033   ⟸   XM_017012544
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000401521   ⟸   ENST00000415413
RefSeq Acc Id: ENSP00000416581   ⟸   ENST00000417625
RefSeq Acc Id: ENSP00000312110   ⟸   ENST00000312017
RefSeq Acc Id: ENSP00000405557   ⟸   ENST00000444905
RefSeq Acc Id: ENSP00000222382   ⟸   ENST00000222382
RefSeq Acc Id: ENSP00000400316   ⟸   ENST00000433277
RefSeq Acc Id: ENSP00000346887   ⟸   ENST00000354829
RefSeq Acc Id: ENSP00000411653   ⟸   ENST00000434806
RefSeq Acc Id: ENSP00000486759   ⟸   ENST00000631161
RefSeq Acc Id: ENSP00000345351   ⟸   ENST00000342499
RefSeq Acc Id: ENSP00000415221   ⟸   ENST00000436834
RefSeq Acc Id: XP_047276701   ⟸   XM_047420745
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047276702   ⟸   XM_047420746
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054214818   ⟸   XM_054358843
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054214819   ⟸   XM_054358844
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054214821   ⟸   XM_054358846
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054214820   ⟸   XM_054358845
- Peptide Label: isoform X2

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9HB55-F1-model_v2 AlphaFold Q9HB55 1-503 view protein structure

Promoters
RGD ID:7211265
Promoter ID:EPDNEW_H11375
Type:initiation region
Name:CYP3A43_1
Description:cytochrome P450 family 3 subfamily A member 43
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38799,828,013 - 99,828,073EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17450 AgrOrtholog
COSMIC CYP3A43 COSMIC
Ensembl Genes ENSG00000021461 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000222382 ENTREZGENE
  ENST00000222382.5 UniProtKB/Swiss-Prot
  ENST00000312017 ENTREZGENE
  ENST00000312017.9 UniProtKB/Swiss-Prot
  ENST00000354829 ENTREZGENE
  ENST00000354829.7 UniProtKB/Swiss-Prot
  ENST00000415413.5 UniProtKB/TrEMBL
  ENST00000417625 ENTREZGENE
  ENST00000417625.5 UniProtKB/Swiss-Prot
  ENST00000433277.5 UniProtKB/TrEMBL
  ENST00000434806 ENTREZGENE
  ENST00000434806.5 UniProtKB/Swiss-Prot
  ENST00000436834 ENTREZGENE
  ENST00000436834.5 UniProtKB/TrEMBL
  ENST00000444905.5 UniProtKB/TrEMBL
  ENST00000631161.2 UniProtKB/TrEMBL
Gene3D-CATH 1.10.630.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000021461 GTEx
HGNC ID HGNC:17450 ENTREZGENE
Human Proteome Map CYP3A43 Human Proteome Map
InterPro Cyt_P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_P450_E_CYP3A UniProtKB/Swiss-Prot
  Cyt_P450_E_grp-I UniProtKB/TrEMBL
  Cyt_P450_E_grp-II UniProtKB/Swiss-Prot
  Cyt_P450_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:64816 UniProtKB/Swiss-Prot
NCBI Gene 64816 ENTREZGENE
OMIM 606534 OMIM
PANTHER CYTOCHROME P450 3A43 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CYTOCHROME P450 FAMILY 3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam p450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB CYP3A43 RGD, PharmGKB
PRINTS EP450I UniProtKB/TrEMBL
  EP450II UniProtKB/Swiss-Prot
  EP450IICYP3A UniProtKB/Swiss-Prot
  P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CYTOCHROME_P450 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48264 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt C9JA26_HUMAN UniProtKB/TrEMBL
  CP343_HUMAN UniProtKB/Swiss-Prot
  E7EMH4_HUMAN UniProtKB/TrEMBL
  E9PDL8_HUMAN UniProtKB/TrEMBL
  E9PG90_HUMAN UniProtKB/TrEMBL
  Q495Y0_HUMAN UniProtKB/TrEMBL
  Q495Y1 ENTREZGENE
  Q75MK2 ENTREZGENE
  Q75MK3 ENTREZGENE
  Q7Z2G5_HUMAN UniProtKB/TrEMBL
  Q9HB50_HUMAN UniProtKB/TrEMBL
  Q9HB51_HUMAN UniProtKB/TrEMBL
  Q9HB52 ENTREZGENE
  Q9HB53 ENTREZGENE
  Q9HB54 ENTREZGENE
  Q9HB55 ENTREZGENE
  Q9HB57 ENTREZGENE
UniProt Secondary Q495Y1 UniProtKB/Swiss-Prot
  Q75MK2 UniProtKB/Swiss-Prot
  Q75MK3 UniProtKB/Swiss-Prot
  Q9HB52 UniProtKB/Swiss-Prot
  Q9HB53 UniProtKB/Swiss-Prot
  Q9HB54 UniProtKB/Swiss-Prot
  Q9HB57 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 CYP3A43  cytochrome P450 family 3 subfamily A member 43  CYP3A43  cytochrome P450, family 3, subfamily A, polypeptide 43  Symbol and/or name change 5135510 APPROVED