BCAT1 (branched chain amino acid transaminase 1) - Rat Genome Database
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Gene: BCAT1 (branched chain amino acid transaminase 1) Homo sapiens
Analyze
Symbol: BCAT1
Name: branched chain amino acid transaminase 1
RGD ID: 1345403
HGNC Page HGNC
Description: Predicted to have branched-chain-amino-acid transaminase activity. Predicted to be involved in leucine biosynthetic process and valine biosynthetic process. Predicted to localize to mitochondrion.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: BCATC; BCT1; branched chain amino-acid transaminase 1, cytosolic; branched chain aminotransferase 1, cytosolic; branched-chain-amino-acid aminotransferase, cytosolic; DKFZp686E12175; ECA39; MECA39; placental protein 18; PNAS-121; PNAS121; PP18
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
GRCh38.p13 Ensembl1224,810,024 - 24,949,101 (-)EnsemblGRCh38hg38GRCh38
GRCh381224,810,024 - 24,949,101 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371224,962,958 - 25,102,035 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361224,855,545 - 24,993,499 (-)NCBINCBI36hg18NCBI36
Build 341224,855,561 - 24,993,499NCBI
Celera1230,109,823 - 30,249,287 (-)NCBI
Cytogenetic Map12p12.1NCBI
HuRef1224,732,841 - 24,872,358 (-)NCBIHuRef
CHM1_11224,928,106 - 25,067,454 (-)NCBICHM1_1
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
(-)-demecolcine  (EXP)
17alpha-ethynylestradiol  (ISO)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2,3-dimethoxynaphthalene-1,4-dione  (EXP)
3,3',4,4',5-pentachlorobiphenyl  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-azacytidine  (EXP)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
acetamide  (ISO)
aflatoxin B1  (EXP)
aflatoxin B2  (EXP)
aflatoxin M1  (EXP)
all-trans-retinoic acid  (EXP)
allyl alcohol  (ISO)
ammonium chloride  (ISO)
arsenite(3-)  (EXP)
atrazine  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
benzo[e]pyrene  (EXP)
beta-naphthoflavone  (EXP)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (EXP,ISO)
bucladesine  (EXP)
Butylbenzyl phthalate  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
calcidiol  (ISO)
carbamazepine  (EXP)
carbofuran  (ISO)
carbon nanotube  (ISO)
chloroacetaldehyde  (EXP)
cisplatin  (EXP,ISO)
clodronic acid  (EXP)
cobalt dichloride  (EXP)
cocaine  (ISO)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP,ISO)
DDT  (ISO)
dexamethasone  (ISO)
dibutyl phthalate  (ISO)
dieldrin  (ISO)
diethyl phthalate  (ISO)
diethylstilbestrol  (ISO)
diisobutyl phthalate  (ISO)
diisononyl phthalate  (ISO)
dioxygen  (EXP)
doxorubicin  (EXP,ISO)
endosulfan  (ISO)
enzyme inhibitor  (EXP)
ethanol  (ISO)
ethyl methanesulfonate  (EXP)
fenofibrate  (EXP)
folic acid  (ISO)
formaldehyde  (EXP)
furan  (ISO)
genistein  (ISO)
heptachlor  (ISO)
ifosfamide  (EXP)
isoprenaline  (ISO)
lead diacetate  (ISO)
medroxyprogesterone acetate  (EXP)
metacetamol  (ISO)
metaproterenol  (ISO)
methapyrilene  (EXP,ISO)
methyl methanesulfonate  (EXP)
mirex  (ISO)
mitoxantrone  (ISO)
N-methyl-4-phenylpyridinium  (EXP)
neomycin  (ISO)
nickel atom  (EXP)
orciprenaline  (ISO)
paracetamol  (EXP,ISO)
pentane-2,3-dione  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
phenylbutazone  (ISO)
potassium chromate  (EXP)
progesterone  (EXP)
quercetin  (EXP)
scopolamine  (ISO)
silicon dioxide  (EXP)
Soman  (ISO)
sunitinib  (EXP)
tamibarotene  (EXP)
tamoxifen  (ISO)
testosterone  (ISO)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
titanium dioxide  (ISO)
triamterene  (ISO)
tributylstannane  (ISO)
Tributyltin oxide  (ISO)
trimellitic anhydride  (ISO)
tunicamycin  (EXP)
urethane  (EXP)
valproic acid  (EXP,ISO)
vincristine  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (ISO)
cytosol  (TAS)
mitochondrion  (IBA)

References

Additional References at PubMed
PMID:6933702   PMID:7566098   PMID:8692959   PMID:8889548   PMID:9657861   PMID:10471790   PMID:12477932   PMID:14702039   PMID:15231748   PMID:16141215   PMID:17007058   PMID:17846126  
PMID:18074675   PMID:18419134   PMID:19119849   PMID:19260141   PMID:19913121   PMID:20062060   PMID:20339536   PMID:20379614   PMID:20628086   PMID:20639392   PMID:20734064   PMID:20877624  
PMID:21873635   PMID:22107788   PMID:22863883   PMID:23043456   PMID:23400010   PMID:23455924   PMID:23758864   PMID:23793099   PMID:24463277   PMID:25261097   PMID:26173071   PMID:26186194  
PMID:26372729   PMID:26783998   PMID:27246112   PMID:28005267   PMID:28052414   PMID:28235484   PMID:28319069   PMID:28514442   PMID:28699638   PMID:29053956   PMID:29144447   PMID:29211698  
PMID:29447920   PMID:29540532   PMID:29791485   PMID:29796114   PMID:29915159   PMID:29955894   PMID:30113684   PMID:30230527   PMID:30265706   PMID:30310175   PMID:30378334   PMID:31048545  
PMID:31391242   PMID:31536960   PMID:32296183   PMID:32571264   PMID:32694827  


Genomics

Comparative Map Data
BCAT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1224,810,024 - 24,949,101 (-)EnsemblGRCh38hg38GRCh38
GRCh381224,810,024 - 24,949,101 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371224,962,958 - 25,102,035 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361224,855,545 - 24,993,499 (-)NCBINCBI36hg18NCBI36
Build 341224,855,561 - 24,993,499NCBI
Celera1230,109,823 - 30,249,287 (-)NCBI
Cytogenetic Map12p12.1NCBI
HuRef1224,732,841 - 24,872,358 (-)NCBIHuRef
CHM1_11224,928,106 - 25,067,454 (-)NCBICHM1_1
Bcat1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm396144,939,561 - 145,021,883 (-)NCBIGRCm39mm39
GRCm39 Ensembl6144,939,561 - 145,021,910 (-)Ensembl
GRCm386144,993,835 - 145,076,157 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl6144,993,835 - 145,076,184 (-)EnsemblGRCm38mm10GRCm38
MGSCv376144,942,355 - 145,024,677 (-)NCBIGRCm37mm9NCBIm37
MGSCv366144,956,312 - 145,033,242 (-)NCBImm8
Celera6148,047,506 - 148,145,066 (-)NCBICelera
Cytogenetic Map6G3NCBI
cM Map677.27NCBI
Bcat1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.24177,964,834 - 178,046,573 (-)NCBI
Rnor_6.0 Ensembl4179,259,308 - 179,339,795 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.04179,259,305 - 179,340,021 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.04243,463,299 - 243,491,574 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.04243,444,839 - 243,460,481 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44182,641,517 - 182,692,917 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.14182,886,640 - 182,938,041 (-)NCBI
Celera4166,483,269 - 166,533,125 (-)NCBICelera
Cytogenetic Map4q44NCBI
Bcat1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541319,981,328 - 20,087,638 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541319,975,395 - 20,087,656 (-)NCBIChiLan1.0ChiLan1.0
BCAT1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11263,978,116 - 64,114,127 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1263,978,116 - 64,107,463 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01261,364,154 - 61,500,827 (+)NCBIMhudiblu_PPA_v0panPan3
BCAT1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12722,536,297 - 22,643,350 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2722,535,254 - 22,636,959 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2723,725,637 - 23,832,733 (-)NCBI
ROS_Cfam_1.02722,769,835 - 22,843,576 (+)NCBI
UMICH_Zoey_3.12722,584,192 - 22,657,415 (+)NCBI
UNSW_CanFamBas_1.02722,569,213 - 22,676,273 (+)NCBI
UU_Cfam_GSD_1.02723,897,853 - 24,005,177 (-)NCBI
Bcat1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494584,462,896 - 84,532,986 (+)NCBI
SpeTri2.0NW_0049365482,385,756 - 2,454,423 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
BCAT1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl548,814,300 - 48,925,976 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1548,814,212 - 48,925,632 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2552,534,770 - 52,624,453 (+)NCBISscrofa10.2Sscrofa10.2susScr3
BCAT1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11124,578,760 - 24,709,541 (-)NCBI
ChlSab1.1 Ensembl1124,579,487 - 24,709,132 (-)Ensembl
Bcat1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462475214,074,701 - 14,166,075 (+)NCBI

Position Markers
D12S1617  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371225,100,032 - 25,100,288UniSTSGRCh37
Build 361224,991,299 - 24,991,555RGDNCBI36
Celera1230,246,926 - 30,247,182RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,869,996 - 24,870,254UniSTS
Marshfield Genetic Map1244.03RGD
Marshfield Genetic Map1244.03UniSTS
Genethon Genetic Map1245.1UniSTS
deCODE Assembly Map1245.91UniSTS
Whitehead-YAC Contig Map12 UniSTS
RH44650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,964,370 - 24,964,515UniSTSGRCh37
Build 361224,855,637 - 24,855,782RGDNCBI36
Celera1230,111,235 - 30,111,380RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,734,253 - 24,734,398UniSTS
GeneMap99-GB4 RH Map1292.63UniSTS
D12S1956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,982,837 - 24,983,062UniSTSGRCh37
Build 361224,874,104 - 24,874,329RGDNCBI36
Celera1230,129,667 - 30,129,892RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,752,701 - 24,752,926UniSTS
Whitehead-RH Map12172.6UniSTS
Whitehead-YAC Contig Map12 UniSTS
RH103298  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,963,059 - 24,963,183UniSTSGRCh37
Build 361224,854,326 - 24,854,450RGDNCBI36
Celera1230,109,924 - 30,110,048RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,732,942 - 24,733,066UniSTS
GeneMap99-GB4 RH Map1292.63UniSTS
G60541  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371225,100,043 - 25,100,289UniSTSGRCh37
Build 361224,991,310 - 24,991,556RGDNCBI36
Celera1230,246,937 - 30,247,183RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,870,007 - 24,870,255UniSTS
TNG Radiation Hybrid Map1211179.0UniSTS
TNG Radiation Hybrid Map1518199.0UniSTS
BCAT1_8225  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,964,187 - 24,964,948UniSTSGRCh37
Build 361224,855,454 - 24,856,215RGDNCBI36
Celera1230,111,052 - 30,111,813RGD
HuRef1224,734,070 - 24,734,831UniSTS
SHGC-57548  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371224,963,064 - 24,963,189UniSTSGRCh37
Build 361224,854,331 - 24,854,456RGDNCBI36
Celera1230,109,929 - 30,110,054RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,732,947 - 24,733,072UniSTS
TNG Radiation Hybrid Map1211122.0UniSTS
D12S1435  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371225,053,109 - 25,053,306UniSTSGRCh37
Build 361224,944,376 - 24,944,573RGDNCBI36
Celera1230,200,009 - 30,200,206RGD
Cytogenetic Map12p12.1UniSTS
HuRef1224,822,955 - 24,823,152UniSTS
Whitehead-YAC Contig Map12 UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR155hsa-miR-155-5pMirtarbaseexternal_infoMicroarrayFunctional MTI (Weak)19193853

Predicted Target Of
Summary Value
Count of predictions:4832
Count of miRNA genes:1180
Interacting mature miRNAs:1460
Transcripts:ENST00000261192, ENST00000342945, ENST00000355164, ENST00000538118, ENST00000539282, ENST00000539780, ENST00000543099, ENST00000544418, ENST00000546285
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component
High 5
Medium 157 181 186 28 723 30 408 102 421 90 444 576 8 221 76 3
Low 2164 2431 1271 330 1081 177 2985 1383 3223 253 942 967 156 1 982 2022
Below cutoff 62 372 262 260 144 252 950 708 87 75 50 46 9 1 690 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_008170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001178091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001178092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001178093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001178094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017019768 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001748835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA376058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC023796 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC026310 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF277179 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK024923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK299088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL390172 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC026006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC033864 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM458559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU618839 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU730066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX474651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749308 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC385021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U21551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000261192   ⟹   ENSP00000261192
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,810,024 - 24,949,101 (-)Ensembl
RefSeq Acc Id: ENST00000342945   ⟹   ENSP00000339805
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,814,821 - 24,949,086 (-)Ensembl
RefSeq Acc Id: ENST00000355164
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,945,431 - 24,949,061 (-)Ensembl
RefSeq Acc Id: ENST00000538118   ⟹   ENSP00000440817
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,814,803 - 24,902,296 (-)Ensembl
RefSeq Acc Id: ENST00000539282   ⟹   ENSP00000443459
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,817,481 - 24,903,075 (-)Ensembl
RefSeq Acc Id: ENST00000539780   ⟹   ENSP00000440827
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,817,809 - 24,949,043 (-)Ensembl
RefSeq Acc Id: ENST00000543099
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,817,656 - 24,830,328 (-)Ensembl
RefSeq Acc Id: ENST00000544418
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,833,811 - 24,902,388 (-)Ensembl
RefSeq Acc Id: ENST00000546285   ⟹   ENSP00000438593
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,878,536 - 24,949,049 (-)Ensembl
RefSeq Acc Id: ENST00000612790   ⟹   ENSP00000481749
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1224,836,447 - 24,881,398 (-)Ensembl
RefSeq Acc Id: NM_001178091   ⟹   NP_001171562
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,810,024 - 24,949,101 (-)NCBI
GRCh371224,962,958 - 25,102,393 (-)ENTREZGENE
HuRef1224,732,841 - 24,872,358 (-)ENTREZGENE
CHM1_11224,928,106 - 25,067,454 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001178092   ⟹   NP_001171563
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,810,024 - 24,949,101 (-)NCBI
GRCh371224,962,958 - 25,102,393 (-)NCBI
HuRef1224,732,841 - 24,872,358 (-)ENTREZGENE
CHM1_11224,928,106 - 25,067,454 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001178093   ⟹   NP_001171564
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,810,024 - 24,903,067 (-)NCBI
GRCh371224,962,958 - 25,102,393 (-)ENTREZGENE
HuRef1224,732,841 - 24,872,358 (-)ENTREZGENE
CHM1_11224,928,106 - 25,021,091 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001178094   ⟹   NP_001171565
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,810,024 - 24,902,222 (-)NCBI
GRCh371224,962,958 - 25,102,393 (-)ENTREZGENE
HuRef1224,732,841 - 24,872,358 (-)ENTREZGENE
CHM1_11224,928,106 - 25,020,404 (-)NCBI
Sequence:
RefSeq Acc Id: NM_005504   ⟹   NP_005495
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,810,024 - 24,949,101 (-)NCBI
GRCh371224,962,958 - 25,102,393 (-)ENTREZGENE
Build 361224,855,545 - 24,993,499 (-)NCBI Archive
HuRef1224,732,841 - 24,872,358 (-)ENTREZGENE
CHM1_11224,928,106 - 25,067,454 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017019768   ⟹   XP_016875257
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,811,361 - 24,906,010 (-)NCBI
Sequence:
RefSeq Acc Id: XR_001748835
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,811,361 - 24,906,004 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001171563   ⟸   NM_001178092
- Peptide Label: isoform 3
- UniProtKB: P54687 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001171562   ⟸   NM_001178091
- Peptide Label: isoform 2
- UniProtKB: P54687 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_005495   ⟸   NM_005504
- Peptide Label: isoform 1
- UniProtKB: P54687 (UniProtKB/Swiss-Prot),   A0A024RAV0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001171564   ⟸   NM_001178093
- Peptide Label: isoform 4
- UniProtKB: P54687 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001171565   ⟸   NM_001178094
- Peptide Label: isoform 5
- UniProtKB: P54687 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016875257   ⟸   XM_017019768
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000438593   ⟸   ENST00000546285
RefSeq Acc Id: ENSP00000481749   ⟸   ENST00000612790
RefSeq Acc Id: ENSP00000440817   ⟸   ENST00000538118
RefSeq Acc Id: ENSP00000443459   ⟸   ENST00000539282
RefSeq Acc Id: ENSP00000440827   ⟸   ENST00000539780
RefSeq Acc Id: ENSP00000261192   ⟸   ENST00000261192
RefSeq Acc Id: ENSP00000339805   ⟸   ENST00000342945

Promoters
RGD ID:7223443
Promoter ID:EPDNEW_H17467
Type:initiation region
Name:BCAT1_2
Description:branched chain amino acid transaminase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17468  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,902,222 - 24,902,282EPDNEW
RGD ID:6789904
Promoter ID:HG_KWN:15208
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562,   Lymphoblastoid
Transcripts:ENST00000342945,   NM_001178094
Position:
Human AssemblyChrPosition (strand)Source
Build 361224,946,911 - 24,947,411 (-)MPROMDB
RGD ID:6789710
Promoter ID:HG_KWN:15209
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:NM_001178093
Position:
Human AssemblyChrPosition (strand)Source
Build 361224,946,986 - 24,947,486 (-)MPROMDB
RGD ID:7223445
Promoter ID:EPDNEW_H17468
Type:initiation region
Name:BCAT1_1
Description:branched chain amino acid transaminase 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H17467  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381224,949,053 - 24,949,113EPDNEW
RGD ID:6789711
Promoter ID:HG_KWN:15211
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001178091,   NM_001178092,   NM_005504
Position:
Human AssemblyChrPosition (strand)Source
Build 361224,993,181 - 24,994,112 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12p12.1(chr12:24638349-25193743)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050939]|Macrocephaly [RCV000050940]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050939]|See cases [RCV000050939] Chr12:24638349..25193743 [GRCh38]
Chr12:24791283..25346677 [GRCh37]
Chr12:12p12.1
uncertain significance
GRCh38/hg38 12p12.3-11.23(chr12:19295848-27012560)x1 copy number loss See cases [RCV000052782] Chr12:19295848..27012560 [GRCh38]
Chr12:19448782..27165493 [GRCh37]
Chr12:19340049..27056760 [NCBI36]
Chr12:12p12.3-11.23
pathogenic
GRCh38/hg38 12p12.1-11.21(chr12:21771052-32222232)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052783]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052783]|See cases [RCV000052783] Chr12:21771052..32222232 [GRCh38]
Chr12:21923986..32375166 [GRCh37]
Chr12:21815253..32266433 [NCBI36]
Chr12:12p12.1-11.21
pathogenic
GRCh38/hg38 12p13.33-11.22(chr12:121055-28415184)x1 copy number loss See cases [RCV000052776] Chr12:121055..28415184 [GRCh38]
Chr12:282465..28568117 [GRCh37]
Chr12:100482..28459384 [NCBI36]
Chr12:12p13.33-11.22
pathogenic
GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3 copy number gain See cases [RCV000053662] Chr12:80412..25470329 [GRCh38]
Chr12:282465..25623263 [GRCh37]
Chr12:59839..25514530 [NCBI36]
Chr12:12p13.33-12.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4 copy number gain See cases [RCV000053666] Chr12:212976..33926913 [GRCh38]
Chr12:322142..34079848 [GRCh37]
Chr12:192403..33971115 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p12.3-12.1(chr12:18252085-25696258)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053670]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053670]|See cases [RCV000053670] Chr12:18252085..25696258 [GRCh38]
Chr12:18405019..25849192 [GRCh37]
Chr12:18296286..25740459 [NCBI36]
Chr12:12p12.3-12.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3 copy number gain See cases [RCV000053660] Chr12:77187..34380176 [GRCh38]
Chr12:282465..34533111 [GRCh37]
Chr12:56614..34424378 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
NM_005504.6(BCAT1):c.510+13578C>G single nucleotide variant Lung cancer [RCV000110905] Chr12:24864952 [GRCh38]
Chr12:25017886 [GRCh37]
Chr12:12p12.1
uncertain significance
NM_005504.6(BCAT1):c.78+2868A>T single nucleotide variant Lung cancer [RCV000110906] Chr12:24898946 [GRCh38]
Chr12:25051880 [GRCh37]
Chr12:12p12.1
uncertain significance
GRCh38/hg38 12p12.1(chr12:24638349-25193743)x3 copy number gain See cases [RCV000050939] Chr12:24638349..25193743 [GRCh38]
Chr12:24791283..25346677 [GRCh37]
Chr12:24682550..25237944 [NCBI36]
Chr12:12p12.1
uncertain significance
GRCh38/hg38 12p12.1(chr12:24784088-25101275)x3 copy number gain See cases [RCV000135386] Chr12:24784088..25101275 [GRCh38]
Chr12:24937022..25254209 [GRCh37]
Chr12:24828289..25145476 [NCBI36]
Chr12:12p12.1
uncertain significance
GRCh38/hg38 12p12.3-12.1(chr12:19265334-25482589)x1 copy number loss See cases [RCV000135588] Chr12:19265334..25482589 [GRCh38]
Chr12:19418268..25635523 [GRCh37]
Chr12:19309535..25526790 [NCBI36]
Chr12:12p12.3-12.1
likely pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3 copy number gain See cases [RCV000136611] Chr12:121255..34603274 [GRCh38]
Chr12:282465..34756209 [GRCh37]
Chr12:100682..34647476 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3 copy number gain See cases [RCV000139052] Chr12:121271..34603261 [GRCh38]
Chr12:282465..34756196 [GRCh37]
Chr12:100698..34647463 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4 copy number gain See cases [RCV000139787] Chr12:54427..34608071 [GRCh38]
Chr12:282465..34761006 [GRCh37]
Chr12:33854..34652273 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4 copy number gain See cases [RCV000142149] Chr12:64620..34682902 [GRCh38]
Chr12:173786..34835837 [GRCh37]
Chr12:44047..34727104 [NCBI36]
Chr12:12p13.33-11.1
pathogenic
GRCh38/hg38 12p12.1(chr12:24552217-25193743)x3 copy number gain See cases [RCV000143315] Chr12:24552217..25193743 [GRCh38]
Chr12:24705151..25346677 [GRCh37]
Chr12:24596418..25237944 [NCBI36]
Chr12:12p12.1
uncertain significance
GRCh37/hg19 12p13.33-11.1(chr12:148034-34178799)x4 copy number gain See cases [RCV000240164] Chr12:148034..34178799 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic|likely pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:89061-34178799)x3 copy number gain See cases [RCV000240487] Chr12:89061..34178799 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p12.1(chr12:24970786-25307280)x3 copy number gain not provided [RCV000585303] Chr12:24970786..25307280 [GRCh37]
Chr12:12p12.1
likely benign
GRCh37/hg19 12p12.1(chr12:24686645-25353987)x3 copy number gain See cases [RCV000449381] Chr12:24686645..25353987 [GRCh37]
Chr12:12p12.1
uncertain significance
GRCh37/hg19 12p12.1(chr12:24965813-25225609)x3 copy number gain See cases [RCV000449101] Chr12:24965813..25225609 [GRCh37]
Chr12:12p12.1
benign
GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)x3 copy number gain See cases [RCV000449191] Chr12:173786..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33-12.1(chr12:173786-25286865)x3 copy number gain See cases [RCV000449287] Chr12:173786..25286865 [GRCh37]
Chr12:12p13.33-12.1
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3 copy number gain See cases [RCV000447551] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p12.3-11.23(chr12:18037107-26681362)x3 copy number gain See cases [RCV000446008] Chr12:18037107..26681362 [GRCh37]
Chr12:12p12.3-11.23
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:189578-34756150) copy number gain See cases [RCV000446017] Chr12:189578..34756150 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p12.1(chr12:25097583-25225609)x3 copy number gain See cases [RCV000448318] Chr12:25097583..25225609 [GRCh37]
Chr12:12p12.1
benign
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p12.1(chr12:24687132-25353987)x3 copy number gain See cases [RCV000510169] Chr12:24687132..25353987 [GRCh37]
Chr12:12p12.1
likely benign
GRCh37/hg19 12p13.33-11.1(chr12:565369-34835837)x3 copy number gain See cases [RCV000511580] Chr12:565369..34835837 [GRCh37]
Chr12:12p13.33-11.1
likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-11.22(chr12:173786-28219229)x3 copy number gain See cases [RCV000510961] Chr12:173786..28219229 [GRCh37]
Chr12:12p13.33-11.22
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x2,3 copy number gain not provided [RCV000683478] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3 copy number gain not provided [RCV000683479] Chr12:173786..34835837 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
GRCh37/hg19 12p13.33-q11(chr12:173786-37869107)x3 copy number gain not provided [RCV000683480] Chr12:173786..37869107 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-11.21(chr12:191619-31733044)x3 copy number gain not provided [RCV000750245] Chr12:191619..31733044 [GRCh37]
Chr12:12p13.33-11.21
pathogenic
GRCh37/hg19 12p12.1(chr12:24690628-25356709)x3 copy number gain not provided [RCV000750337] Chr12:24690628..25356709 [GRCh37]
Chr12:12p12.1
likely benign
GRCh37/hg19 12p12.1(chr12:23457173-25177321)x1 copy number loss Lamb-shaffer syndrome [RCV000857286] Chr12:23457173..25177321 [GRCh37]
Chr12:12p12.1
pathogenic
GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4 copy number gain not provided [RCV001006470] Chr12:274676..37869301 [GRCh37]
Chr12:12p13.33-q11
pathogenic
GRCh37/hg19 12p12.1(chr12:22602778-25225668)x1 copy number loss Lamb-shaffer syndrome [RCV000856634] Chr12:22602778..25225668 [GRCh37]
Chr12:12p12.1
pathogenic
NM_005504.7(BCAT1):c.39C>T (p.Thr13=) single nucleotide variant not provided [RCV000891746] Chr12:24901853 [GRCh38]
Chr12:25054787 [GRCh37]
Chr12:12p12.1
benign
GRCh37/hg19 12p12.1(chr12:24692382-25353945)x3 copy number gain not provided [RCV000849877] Chr12:24692382..25353945 [GRCh37]
Chr12:12p12.1
uncertain significance
GRCh37/hg19 12p12.3-11.23(chr12:16141429-27733325)x1 copy number loss not provided [RCV000849815] Chr12:16141429..27733325 [GRCh37]
Chr12:12p12.3-11.23
pathogenic
GRCh37/hg19 12p13.33-11.1(chr12:173786-34496628)x3 copy number gain not provided [RCV000847209] Chr12:173786..34496628 [GRCh37]
Chr12:12p13.33-11.1
pathogenic
NM_005504.7(BCAT1):c.57A>G (p.Lys19=) single nucleotide variant not provided [RCV000927179] Chr12:24901835 [GRCh38]
Chr12:25054769 [GRCh37]
Chr12:12p12.1
likely benign
NM_005504.7(BCAT1):c.963G>A (p.Glu321=) single nucleotide variant not provided [RCV000935137] Chr12:24832804 [GRCh38]
Chr12:24985738 [GRCh37]
Chr12:12p12.1
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:976 AgrOrtholog
COSMIC BCAT1 COSMIC
Ensembl Genes ENSG00000060982 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000261192 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000339805 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000438593 UniProtKB/TrEMBL
  ENSP00000440817 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000440827 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000443459 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000481749 UniProtKB/TrEMBL
Ensembl Transcript ENST00000261192 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000342945 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000538118 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000539282 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000539780 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000546285 UniProtKB/TrEMBL
  ENST00000612790 UniProtKB/TrEMBL
Gene3D-CATH 3.20.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.30.470.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000060982 GTEx
HGNC ID HGNC:976 ENTREZGENE
Human Proteome Map BCAT1 Human Proteome Map
InterPro Aminotrans_IV UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Aminotrans_IV_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Aminotransferase-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  B_amino_transII UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  BCAT-like_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  BCAT-like_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  BCAT_family UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:586 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 586 ENTREZGENE
OMIM 113520 OMIM
Pfam Aminotran_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25288 PharmGKB
PIRSF BCAT1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE AA_TRANSFER_CLASS_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56752 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
TIGRFAMs ilvE_II UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024RAV0 ENTREZGENE, UniProtKB/TrEMBL
  A0A087WYF2_HUMAN UniProtKB/TrEMBL
  BCAT1_HUMAN UniProtKB/Swiss-Prot
  F5H2F2_HUMAN UniProtKB/TrEMBL
  L8E7S9_HUMAN UniProtKB/TrEMBL
  P54687 ENTREZGENE
UniProt Secondary B3KY27 UniProtKB/Swiss-Prot
  B7Z2M5 UniProtKB/Swiss-Prot
  B7Z5L0 UniProtKB/Swiss-Prot
  F5H5E4 UniProtKB/Swiss-Prot
  Q68DQ7 UniProtKB/Swiss-Prot
  Q96MY9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-14 BCAT1  branched chain amino acid transaminase 1  BCAT1  branched chain amino-acid transaminase 1, cytosolic  Symbol and/or name change 5135510 APPROVED
2016-03-14 BCAT1  branched chain amino acid transaminase 1    branched chain amino-acid transaminase 1, cytosolic  Symbol and/or name change 5135510 APPROVED
2011-08-17 BCAT1  branched chain amino-acid transaminase 1, cytosolic  BCAT1  branched chain amino-acid transaminase 1, cytosolic  Symbol and/or name change 5135510 APPROVED
2011-07-27 BCAT1  branched chain amino-acid transaminase 1, cytosolic  BCAT1  branched chain aminotransferase 1, cytosolic  Symbol and/or name change 5135510 APPROVED