ABHD8 (abhydrolase domain containing 8) - Rat Genome Database

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Gene: ABHD8 (abhydrolase domain containing 8) Homo sapiens
Analyze
Symbol: ABHD8
Name: abhydrolase domain containing 8
RGD ID: 1313870
HGNC Page HGNC:23759
Description: Predicted to enable hydrolase activity. Located in extracellular exosome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: abhydrolase domain-containing protein 8; alpha/beta hydrolase domain-containing protein 8; FLJ11743; MGC14280; MGC2512
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
GRCh381917,292,131 - 17,303,425 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1917,292,131 - 17,310,236 (-)EnsemblGRCh38hg38GRCh38
GRCh371917,402,940 - 17,414,234 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361917,263,940 - 17,275,282 (-)NCBINCBI36Build 36hg18NCBI36
Build 341917,263,940 - 17,275,234NCBI
Celera1917,304,682 - 17,316,010 (-)NCBICelera
Cytogenetic Map19p13.11NCBI
HuRef1916,969,585 - 16,980,841 (-)NCBIHuRef
CHM1_11917,402,410 - 17,413,755 (-)NCBICHM1_1
T2T-CHM13v2.01917,427,016 - 17,438,315 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:8125298   PMID:14702039   PMID:15489334   PMID:16344560   PMID:18570454   PMID:20852631   PMID:21873635   PMID:28514442   PMID:31586073   PMID:31741433   PMID:31753913   PMID:32296183  
PMID:33961781  


Genomics

Comparative Map Data
ABHD8
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381917,292,131 - 17,303,425 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1917,292,131 - 17,310,236 (-)EnsemblGRCh38hg38GRCh38
GRCh371917,402,940 - 17,414,234 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361917,263,940 - 17,275,282 (-)NCBINCBI36Build 36hg18NCBI36
Build 341917,263,940 - 17,275,234NCBI
Celera1917,304,682 - 17,316,010 (-)NCBICelera
Cytogenetic Map19p13.11NCBI
HuRef1916,969,585 - 16,980,841 (-)NCBIHuRef
CHM1_11917,402,410 - 17,413,755 (-)NCBICHM1_1
T2T-CHM13v2.01917,427,016 - 17,438,315 (-)NCBIT2T-CHM13v2.0
Abhd8
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39871,909,344 - 71,917,351 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl871,909,349 - 71,916,299 (-)EnsemblGRCm39 Ensembl
GRCm38871,456,700 - 71,464,707 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl871,456,705 - 71,463,655 (-)EnsemblGRCm38mm10GRCm38
MGSCv37873,980,599 - 73,987,556 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36874,385,694 - 74,392,635 (-)NCBIMGSCv36mm8
Celera873,975,916 - 73,982,874 (-)NCBICelera
Cytogenetic Map8B3.3NCBI
cM Map834.43NCBI
Abhd8
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81618,178,441 - 18,185,178 (-)NCBIGRCr8
mRatBN7.21618,144,464 - 18,151,201 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1618,144,464 - 18,157,667 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1618,195,456 - 18,202,192 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01619,328,097 - 19,334,828 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01618,248,386 - 18,255,122 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01619,866,028 - 19,872,765 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1619,866,022 - 19,872,774 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01619,727,394 - 19,734,131 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41618,628,138 - 18,634,875 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11618,628,150 - 18,634,815 (-)NCBI
Celera1618,349,543 - 18,356,280 (-)NCBICelera
Cytogenetic Map16p14NCBI
Abhd8
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955524925,102 - 930,270 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955524924,128 - 932,046 (+)NCBIChiLan1.0ChiLan1.0
ABHD8
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22022,163,225 - 22,174,254 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11921,169,828 - 21,180,856 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01916,780,132 - 16,791,233 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11917,755,973 - 17,765,502 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1917,755,973 - 17,765,502 (-)Ensemblpanpan1.1panPan2
ABHD8
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12045,448,457 - 45,459,507 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2045,449,871 - 45,459,506 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2045,361,602 - 45,372,692 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02045,934,667 - 45,945,756 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2045,938,590 - 45,945,756 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12045,171,316 - 45,182,397 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02045,581,102 - 45,592,179 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02045,856,948 - 45,868,041 (+)NCBIUU_Cfam_GSD_1.0
Abhd8
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118204,010,015 - 204,018,487 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365963,560,636 - 3,567,678 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365963,559,139 - 3,567,626 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ABHD8
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl260,380,705 - 60,388,983 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1260,380,691 - 60,388,986 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
ABHD8
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1615,798,462 - 15,810,012 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl615,798,256 - 15,810,036 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660743,632,121 - 3,643,774 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Abhd8
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624908641,841 - 647,877 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624908641,181 - 648,366 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in ABHD8
15 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3 copy number gain See cases [RCV000050635] Chr19:17176767..34924150 [GRCh38]
Chr19:17287576..35415054 [GRCh37]
Chr19:17148576..40106894 [NCBI36]
Chr19:19p13.11-q13.11		 pathogenic
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3 copy number gain See cases [RCV000052912] Chr19:13974677..27839676 [GRCh38]
Chr19:14085489..28330584 [GRCh37]
Chr19:13946489..33022424 [NCBI36]
Chr19:19p13.12-q11		 pathogenic
NM_024527.5(ABHD8):c.780C>G (p.Phe260Leu) single nucleotide variant Inborn genetic diseases [RCV003183365] Chr19:17294827 [GRCh38]
Chr19:17405636 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.367G>T (p.Asp123Tyr) single nucleotide variant Inborn genetic diseases [RCV003185125] Chr19:17301250 [GRCh38]
Chr19:17412059 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.1262A>C (p.Glu421Ala) single nucleotide variant Inborn genetic diseases [RCV003190158] Chr19:17292719 [GRCh38]
Chr19:17403528 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3 copy number gain See cases [RCV000136696] Chr19:15133594..24193591 [GRCh38]
Chr19:15244405..24376393 [GRCh37]
Chr19:15105405..24168233 [NCBI36]
Chr19:19p13.12-12		 pathogenic|likely pathogenic
GRCh38/hg38 19p13.11(chr19:17246895-17730147)x1 copy number loss See cases [RCV000143571] Chr19:17246895..17730147 [GRCh38]
Chr19:17357704..17840956 [GRCh37]
Chr19:17218704..17701956 [NCBI36]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.11(chr19:17001280-17536087)x3 copy number gain See cases [RCV000240162] Chr19:17001280..17536087 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.11(chr19:17392434-17449187)x1 copy number loss See cases [RCV000240063] Chr19:17392434..17449187 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.11-11(chr19:16526787-24631604)x3 copy number gain not provided [RCV000752593] Chr19:16526787..24631604 [GRCh37]
Chr19:19p13.11-11		 pathogenic
GRCh37/hg19 19p13.12-13.11(chr19:15970389-17893528)x1 copy number loss not provided [RCV000487468] Chr19:15970389..17893528 [GRCh37]
Chr19:19p13.12-13.11		 pathogenic
GRCh37/hg19 19p13.12-13.11(chr19:15921132-17479860)x1 copy number loss See cases [RCV000511230] Chr19:15921132..17479860 [GRCh37]
Chr19:19p13.12-13.11		 likely pathogenic
GRCh37/hg19 19p13.11(chr19:17325373-17840956)x1 copy number loss See cases [RCV000511154] Chr19:17325373..17840956 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_024527.5(ABHD8):c.706G>A (p.Ala236Thr) single nucleotide variant Inborn genetic diseases [RCV003276397] Chr19:17300911 [GRCh38]
Chr19:17411720 [GRCh37]
Chr19:19p13.11		 uncertain significance
Single allele duplication not provided [RCV000678022] Chr19:17001280..17536087 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_024527.5(ABHD8):c.60C>T (p.Ala20=) single nucleotide variant not provided [RCV001724581] Chr19:17301557 [GRCh38]
Chr19:17412366 [GRCh37]
Chr19:19p13.11		 benign
GRCh37/hg19 19p13.11(chr19:16875725-17477318)x1 copy number loss not provided [RCV000848728] Chr19:16875725..17477318 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.415G>A (p.Gly139Ser) single nucleotide variant Inborn genetic diseases [RCV003254719] Chr19:17301202 [GRCh38]
Chr19:17412011 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.406G>A (p.Ala136Thr) single nucleotide variant Inborn genetic diseases [RCV003265429] Chr19:17301211 [GRCh38]
Chr19:17412020 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.12-12(chr19:14286624-20956753)x3 copy number gain not provided [RCV001259370] Chr19:14286624..20956753 [GRCh37]
Chr19:19p13.12-12		 pathogenic
NM_024527.5(ABHD8):c.1030G>A (p.Gly344Ser) single nucleotide variant Inborn genetic diseases [RCV002687753] Chr19:17294407 [GRCh38]
Chr19:17405216 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.401G>A (p.Gly134Asp) single nucleotide variant Inborn genetic diseases [RCV002767851] Chr19:17301216 [GRCh38]
Chr19:17412025 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.644C>T (p.Ala215Val) single nucleotide variant Inborn genetic diseases [RCV002768229] Chr19:17300973 [GRCh38]
Chr19:17411782 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.32G>C (p.Cys11Ser) single nucleotide variant Inborn genetic diseases [RCV002803213] Chr19:17301585 [GRCh38]
Chr19:17412394 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.946C>A (p.Arg316Ser) single nucleotide variant Inborn genetic diseases [RCV002941110] Chr19:17294491 [GRCh38]
Chr19:17405300 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.1121C>T (p.Pro374Leu) single nucleotide variant Inborn genetic diseases [RCV002936810] Chr19:17294316 [GRCh38]
Chr19:17405125 [GRCh37]
Chr19:19p13.11		 uncertain significance
NM_024527.5(ABHD8):c.127G>C (p.Val43Leu) single nucleotide variant Inborn genetic diseases [RCV003383651] Chr19:17301490 [GRCh38]
Chr19:17412299 [GRCh37]
Chr19:19p13.11		 uncertain significance
GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3 copy number gain not specified [RCV003986122] Chr19:13970692..18139376 [GRCh37]
Chr19:19p13.13-13.11		 uncertain significance
GRCh37/hg19 19p13.11(chr19:16857649-17423590)x3 copy number gain not specified [RCV003986116] Chr19:16857649..17423590 [GRCh37]
Chr19:19p13.11		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:918
Count of miRNA genes:577
Interacting mature miRNAs:649
Transcripts:ENST00000247706, ENST00000593489, ENST00000594194
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
ABHD8__4234  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371917,402,945 - 17,403,626UniSTSGRCh37
Build 361917,263,945 - 17,264,626RGDNCBI36
Celera1917,304,687 - 17,305,368RGD
HuRef1916,969,590 - 16,970,271UniSTS


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 1796 1629 1578 476 1021 340 3217 1261 3570 262 1373 1489 147 654 2078 2
Low 630 1353 145 146 910 124 1137 932 137 156 75 119 24 550 710 2
Below cutoff 6 2 13 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000247706   ⟹   ENSP00000247706
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1917,292,131 - 17,303,425 (-)Ensembl
RefSeq Acc Id: ENST00000593489   ⟹   ENSP00000468883
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1917,301,140 - 17,310,236 (-)Ensembl
RefSeq Acc Id: ENST00000594194   ⟹   ENSP00000470413
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1917,301,289 - 17,303,425 (-)Ensembl
RefSeq Acc Id: NM_024527   ⟹   NP_078803
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381917,292,131 - 17,303,425 (-)NCBI
GRCh371917,402,940 - 17,414,282 (-)RGD
Build 361917,263,940 - 17,275,282 (-)NCBI Archive
Celera1917,304,682 - 17,316,010 (-)RGD
HuRef1916,969,585 - 16,980,841 (-)RGD
CHM1_11917,402,410 - 17,413,755 (-)NCBI
T2T-CHM13v2.01917,427,016 - 17,438,315 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_078803   ⟸   NM_024527
- UniProtKB: Q9HAE9 (UniProtKB/Swiss-Prot),   Q96I13 (UniProtKB/Swiss-Prot),   B2C6G3 (UniProtKB/TrEMBL),   B2RD12 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000247706   ⟸   ENST00000247706
RefSeq Acc Id: ENSP00000468883   ⟸   ENST00000593489
RefSeq Acc Id: ENSP00000470413   ⟸   ENST00000594194
Protein Domains
AB hydrolase-1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96I13-F1-model_v2 AlphaFold Q96I13 1-439 view protein structure

Promoters
RGD ID:6795079
Promoter ID:HG_KWN:29238
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid
Transcripts:NM_024527
Position:
Human AssemblyChrPosition (strand)Source
Build 361917,275,139 - 17,275,639 (-)MPROMDB
RGD ID:7239021
Promoter ID:EPDNEW_H25256
Type:initiation region
Name:ABHD8_1
Description:abhydrolase domain containing 8
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
GRCh381917,303,399 - 17,303,459EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23759 AgrOrtholog
COSMIC ABHD8 COSMIC
Ensembl Genes ENSG00000127220 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000247706 ENTREZGENE
  ENST00000247706.4 UniProtKB/Swiss-Prot
  ENST00000593489.1 UniProtKB/TrEMBL
  ENST00000594194.1 UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.1820 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000127220 GTEx
HGNC ID HGNC:23759 ENTREZGENE
Human Proteome Map ABHD8 Human Proteome Map
InterPro AB_hydrolase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AB_hydrolase_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Epox_hydrolase-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:79575 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 79575 ENTREZGENE
PANTHER PROTEIN ABHD8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RE40534P-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Abhydrolase_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134994313 PharmGKB
PRINTS ABHYDROLASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EPOXHYDRLASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF53474 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt ABHD8_HUMAN UniProtKB/Swiss-Prot
  B2C6G3 ENTREZGENE, UniProtKB/TrEMBL
  B2RD12 ENTREZGENE, UniProtKB/TrEMBL
  M0QX40_HUMAN UniProtKB/TrEMBL
  M0QZA8_HUMAN UniProtKB/TrEMBL
  Q96I13 ENTREZGENE
  Q9HAE9 ENTREZGENE
UniProt Secondary Q9HAE9 UniProtKB/Swiss-Prot