ABHD16A - abhydrolase domain containing 16A, phospholipase Gene

Also Known as BAT5; NG26; PP199; SPG86; hBAT5; D6S82E

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7920

About ABHD16A

Cytogenetic location: 6p21.33 Genomic coordinates (GRCh38): 6:31,686,955-31,703,324 (from NCBI)

This gene has 16 transcripts (splice variants), 1 gene allele, 193 orthologues, 7 paralogues and is associated with 2 phenotypes. Ubiquitous expression in testis (RPKM 19.9), prostate (RPKM 13.9) and 25 other tissues.

Summary

A cluster of genes, BAT1-BAT5, has been localized in the vicinity of the genes for tumor necrosis factor alpha and tumor necrosis factor beta. These genes are all within the human major histocompatibility complex class III region. The protein encoded by this gene is thought to be involved in some aspects of immunity. Alternatively spliced transcript variants have been described. [provided by RefSeq, Apr 2010]

ABHD16A Products (2)

mRNA Protein Name
NM_001177515.2 NP_001170986.1 phosphatidylserine lipase ABHD16A isoform b
NM_021160.3 NP_066983.1 phosphatidylserine lipase ABHD16A isoform a
Molecular Function GO Annotation Evidence References Source
NOT enables lysophospholipase activity IDA
IDA: Inferred from direct assay
25290914 GOA
enables monoacylglycerol lipase activity IDA
IDA: Inferred from direct assay
25290914 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
14667819 GOA
Biological Process GO Annotation Evidence References Source
involved in monoacylglycerol catabolic process IDA
IDA: Inferred from direct assay
25290914 GOA
involved in prostaglandin catabolic process IDA
IDA: Inferred from direct assay
25290914 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ABHD16A Protein Structure

Abhydrolase_5

Abhydrolase_5: Alpha/beta hydrolase family (301 - 444)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 558 a.a.
Protein Preferred Names Protein Names

phosphatidylserine lipase ABHD16A

  • HLA-B associated transcript 5

ABHD16A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ABHD16A O95870 RETREG3 Homo sapiens Q86VR2 25416956
Intra
ABHD16A O95870 RETREG3 Homo sapiens Q86VR2 32296183
Intra
ABHD16A O95870 RETREG3 Homo sapiens Q86VR2 32296183
Intra
ABHD16A O95870 RETREG3 Homo sapiens Q86VR2 25416956
Intra
ABHD16A O95870 RETREG3 Homo sapiens Q86VR2 29892012
Intra
ABHD16A O95870 RETREG3 Homo sapiens Q86VR2 32296183
Intra
ABHD16A O95870 WBP1L Homo sapiens Q9NX94 32296183
Intra
ABHD16A O95870 WBP1L Homo sapiens Q9NX94 32296183
Intra
ABHD16A O95870 WBP1L Homo sapiens Q9NX94 32296183
Intra
ABHD16A O95870 AQP7 Homo sapiens Q6P5T0 32296183
Intra
ABHD16A O95870 AQP7 Homo sapiens Q6P5T0 32296183
Intra
ABHD16A O95870 AQP7 Homo sapiens Q6P5T0 32296183
Intra
ABHD16A O95870 VMA21 Homo sapiens Q3ZAQ7 32296183
Intra
ABHD16A O95870 VMA21 Homo sapiens Q3ZAQ7 32296183
Intra
ABHD16A O95870 VMA21 Homo sapiens Q3ZAQ7 32296183
Intra
ABHD16A O95870 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
ABHD16A O95870 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
ABHD16A O95870 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
ABHD16A O95870 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
ABHD16A O95870 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
ABHD16A O95870 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
ABHD16A O95870 GDAP1 Homo sapiens Q8TB36 32296183
Intra
ABHD16A O95870 GDAP1 Homo sapiens Q8TB36 32296183
Intra
ABHD16A O95870 GDAP1 Homo sapiens Q8TB36 32296183
Intra
ABHD16A O95870 RHBDL1 Homo sapiens O75783 32296183
Intra
ABHD16A O95870 RHBDL1 Homo sapiens O75783 32296183
Intra
ABHD16A O95870 PKMYT1 Homo sapiens Q99640-2 32296183
Intra
ABHD16A O95870 AQP6 Homo sapiens Q13520 32296183
Intra
ABHD16A O95870 AQP6 Homo sapiens Q13520 32296183
Intra
ABHD16A O95870 AQP6 Homo sapiens Q13520 32296183
Intra
ABHD16A O95870 SLC7A8 Homo sapiens Q9UHI5 32296183
Intra
ABHD16A O95870 SLC7A8 Homo sapiens Q9UHI5 32296183
Intra
ABHD16A O95870 SLC7A8 Homo sapiens Q9UHI5 32296183
Intra
ABHD16A O95870 TMEM143 Homo sapiens Q96AN5 32296183
Intra
ABHD16A O95870 GPR152 Homo sapiens Q8TDT2 32296183
Intra
ABHD16A O95870 UNC93A Homo sapiens Q86WB7-2 32296183
Intra
ABHD16A O95870 PERP Homo sapiens Q96FX8 32296183
Intra
ABHD16A O95870 CYP1A2 Homo sapiens P05177 32296183
Intra
ABHD16A O95870 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
ABHD16A O95870 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
ABHD16A O95870 GOLT1A Homo sapiens Q6ZVE7 32296183
Intra
ABHD16A O95870 RHBDD2 Homo sapiens Q6NTF9-3 32296183
Intra
ABHD16A O95870 RHBDD2 Homo sapiens Q6NTF9-3 32296183
Intra
ABHD16A O95870 RHBDD2 Homo sapiens Q6NTF9-3 32296183
Intra
ABHD16A O95870 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
ABHD16A O95870 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
ABHD16A O95870 HSD17B13 Homo sapiens Q7Z5P4 32296183
Intra
ABHD16A O95870 CBARP Homo sapiens Q8N350-4 32296183
Intra
ABHD16A O95870 CBARP Homo sapiens Q8N350-4 32296183
Intra
ABHD16A O95870 CBARP Homo sapiens Q8N350-4 32296183
Intra
ABHD16A O95870 STMN4 Homo sapiens Q9H169-2 32296183
Intra
ABHD16A O95870 STMN4 Homo sapiens Q9H169-2 32296183
Intra
ABHD16A O95870 STMN4 Homo sapiens Q9H169-2 32296183
Intra
ABHD16A O95870 ITGAM Homo sapiens P11215 32296183
Intra
ABHD16A O95870 ATP5PF Homo sapiens P18859 32296183
Intra
ABHD16A O95870 ATP5PF Homo sapiens P18859 32296183
Intra
ABHD16A O95870 ATP5PF Homo sapiens P18859 32296183
Intra
ABHD16A O95870 AGPAT3 Homo sapiens Q9NRZ7 32296183
Intra
ABHD16A O95870 BRI3 Homo sapiens O95415 32296183
Intra
ABHD16A O95870 BRI3 Homo sapiens O95415 32296183
Intra
ABHD16A O95870 RNF5 Homo sapiens Q99942 32296183
Intra
ABHD16A O95870 RNF5 Homo sapiens Q99942 32296183
Intra
ABHD16A O95870 RNF5 Homo sapiens Q99942
Y2H
14667819
Intra
ABHD16A O95870 RNF5 Homo sapiens Q99942 32296183
Intra
ABHD16A O95870 RNF5 Homo sapiens Q99942 25416956
Intra
ABHD16A O95870 POLE Homo sapiens Q07864 32296183
Intra
ABHD16A O95870 POLE Homo sapiens Q07864 32296183
Intra
ABHD16A O95870 POLE Homo sapiens Q07864 32296183
Intra
ABHD16A O95870 TMEM147 Homo sapiens Q9BVK8 32296183
Intra
ABHD16A O95870 TMEM147 Homo sapiens Q9BVK8
Y2H
14667819
Intra
ABHD16A O95870 EBP Homo sapiens Q15125 32296183
Intra
ABHD16A O95870 EBP Homo sapiens Q15125 32296183
Intra
ABHD16A O95870 EBP Homo sapiens Q15125 32296183
Intra
ABHD16A O95870 GORAB Homo sapiens Q5T7V8 32296183
Intra
ABHD16A O95870 GORAB Homo sapiens Q5T7V8 32296183
Intra
ABHD16A O95870 GORAB Homo sapiens Q5T7V8 32296183
Intra
ABHD16A O95870 FKBP7 Homo sapiens Q9Y680 32296183
Intra
ABHD16A O95870 FKBP7 Homo sapiens Q9Y680 32296183
Intra
ABHD16A O95870 FKBP7 Homo sapiens Q9Y680 32296183
Intra
ABHD16A O95870 SLC10A1 Homo sapiens Q14973 32296183
Intra
ABHD16A O95870 SLC10A1 Homo sapiens Q14973 32296183
Intra
ABHD16A O95870 SLC10A1 Homo sapiens Q14973 32296183
Intra
ABHD16A O95870 LTA Homo sapiens P01374 32296183
Intra
ABHD16A O95870 TM4SF19 Homo sapiens Q96DZ7 32296183
Intra
ABHD16A O95870 TM4SF19 Homo sapiens Q96DZ7 32296183
Intra
ABHD16A O95870 TM4SF19 Homo sapiens Q96DZ7 32296183
Intra
ABHD16A O95870 TMEM65 Homo sapiens Q6PI78 32296183
Intra
ABHD16A O95870 CIDEB Homo sapiens Q9UHD4 32296183
Intra
ABHD16A O95870 CIDEB Homo sapiens Q9UHD4 32296183
Intra
ABHD16A O95870 CIDEB Homo sapiens Q9UHD4 32296183
Intra
ABHD16A O95870 TMEM139 Homo sapiens Q8IV31 32296183
Intra
ABHD16A O95870 TMEM139 Homo sapiens Q8IV31 32296183
Intra
ABHD16A O95870 TMEM139 Homo sapiens Q8IV31 32296183
Intra
ABHD16A O95870 DTX2 Homo sapiens Q86UW9 25416956
Intra
ABHD16A O95870 DTX2 Homo sapiens Q86UW9 32296183
Intra
ABHD16A O95870 DTX2 Homo sapiens Q86UW9 32296183
Intra
ABHD16A O95870 DTX2 Homo sapiens Q86UW9 32296183
Intra
ABHD16A O95870 GJA5 Homo sapiens P36382 32296183
Intra
ABHD16A O95870 GJA5 Homo sapiens P36382 32296183
Intra
ABHD16A O95870 GJA5 Homo sapiens P36382 32296183
Intra
ABHD16A O95870 GYPC Homo sapiens P04921 32296183
Intra
ABHD16A O95870 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
ABHD16A O95870 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
ABHD16A O95870 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
ABHD16A O95870 IFITM3 Homo sapiens Q01628 32296183
Intra
ABHD16A O95870 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
ABHD16A O95870 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
ABHD16A O95870 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
ABHD16A O95870 SLC30A2 Homo sapiens Q9BRI3 32296183
Intra
ABHD16A O95870 SLC30A2 Homo sapiens Q9BRI3 32296183
Intra
ABHD16A O95870 SLC30A2 Homo sapiens Q9BRI3 32296183
Intra
ABHD16A O95870 STX1B Homo sapiens P61266 32296183
Intra
ABHD16A O95870 FDPS Homo sapiens P14324 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

ABHD16A Antibodies

Cat. No. Product Name Application Reactivity
HY-P82508 BAT5 Antibody (YA2253) WB Human, Rat
HY-P82508A BAT5 Antibody (YA2253)(PBS only) WB Human, Rat

Related Diseases

Diseases Alias
Spastic Paraplegia 86, Autosomal Recessive
  • SPG86

  • Hereditary Spastic Paraplegia 86

  • Spastic Paraplegia 86 Autosomal Recessive

  • Doid:0112342

Complex Hereditary Spastic Paraplegia
  • Complex Hsp

  • Complex Spg

  • Complex Familial Spastic Paraplegia

  • Complicated Hsp

  • Complicated Spg

  • Complicated Familial Spastic Paraplegia

  • Complicated Hereditary Spastic Paraplegia

Autosomal Recessive Complex Spastic Paraplegia
  • Autosomal Recessive Complex Hsp

  • Autosomal Recessive Complex Spg

  • Autosomal Recessive Complicated Hsp

  • Autosomal Recessive Complicated Spg

  • Autosomal Recessive Complicated Spastic Paraplegia

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract
  • Pharc Syndrome

  • PHARC

  • Polyneyropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract

  • Polyneuropathy-Hearing Loss-Ataxia-Retinitis Pigmentosa-Cataract Syndrome

  • Peripheral Neuropathy, Fiskerstrand Type

  • Polyneuropathy-Deafness-Ataxia-Retinitis Pigmentosa-Cataract Syndrome

  • Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, Cataract

Oliver-Mcfarlane Syndrome
  • Trichomegaly-Retina Pigmentary Degeneration-Dwarfism Syndrome

  • OMCS

  • Long Eyelashes-Intellectual Disability Syndrome

  • Trichomegaly With Mental Retardation, Dwarfism, And Pigmentary Degeneration Of Retina

  • Eyelashes, Long, With Mental Retardation

  • Eyelashes Long Mental Retardation

  • Trichomegaly With Intellectual Disability, Dwarfism And Pigmentary Degeneration

  • Trichomegaly With Intellectual Disability, Dwarfism And Pigmentary Degeneration Of Retina

  • Eyelashes, Long With Intellectual Disability

  • Oliver Mcfarlane Syndrome

  • Congenital Trichomegaly, Pigmentary Retinal Degeneration, And Short Stature

  • Trichomegaly, Retina Pigmentary Degeneration, Dwarfism

  • Trichomegaly Retina Pigmentary Degeneration Dwarfism

Short-Rib Thoracic Dysplasia 6 With Or Without Polydactyly
  • Majewski Syndrome

  • SRTD6

  • Srps2a

  • Short Rib-Polydactyly Syndrome, Majewski Type

  • Polydactyly With Neonatal Chondrodystrophy, Type Ii

  • Short Rib-Polydactyly Syndrome Type Iia

  • Short Rib-Polydactyly Syndrome Type 2

  • Short Rib-Polydactyly Syndrome Type Ii

  • Short Rib-Polydactyly Syndrome, Type Ii

  • Srps, Type Ii

  • Short Rib-Polydactyly Syndrome, Type Iia

  • Polydactyly With Neonatal Chondrodystrophy Type 2

  • Srps Type 2

  • Short Rib-Polydactyly Syndrome Majewski Type

  • Polydactyly With Neonatal Chondrodystrophy Type Ii

  • Short Rib-Polydactyly Syndrome 2a

  • Srps Type Ii

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris ABHD16A VGNC VGNC:37464
Felis catus ABHD16A VGNC VGNC:59481
Bos taurus ABHD16A VGNC VGNC:25495
Macaca mulatta ABHD16A VGNC VGNC:69393
Mus musculus ABHD16A MGD MGI:99476
Rattus norvegicus ABHD16A RGD RGD:1303164
Others ABHD16A NCBI