FKBP6 - FKBP prolyl isomerase family member 6 (inactive) Gene

Also Known as FKBP36; SPGF77

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8468

About FKBP6

Cytogenetic location: 7q11.23 Genomic coordinates (GRCh38): 7:73,328,161-73,358,625 (from NCBI)

This gene has 8 transcripts (splice variants), 197 orthologues, 18 paralogues and is associated with 1 phenotype. Restricted expression toward testis (RPKM 29.4).

Summary

The protein encoded by this gene is a cis-trans peptidyl-prolyl isomerase that may function in immunoregulation and basic cellular processes involving protein folding and trafficking. This gene is located in a chromosomal region that is deleted in Williams-Beuren syndrome. Defects in this gene may cause male infertility. There are multiple pseudogenes for this gene located nearby on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

FKBP6 Products (4)

mRNA Protein Name
NM_001135211.3 NP_001128683.1 inactive peptidyl-prolyl cis-trans isomerase FKBP6 isoform b
NM_001281304.2 NP_001268233.1 inactive peptidyl-prolyl cis-trans isomerase FKBP6 isoform c
NM_001362789.2 NP_001349718.1 inactive peptidyl-prolyl cis-trans isomerase FKBP6 isoform d
NM_003602.5 NP_003593.3 inactive peptidyl-prolyl cis-trans isomerase FKBP6 isoform a
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
26567527 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence References Source
involved in positive regulation of viral genome replication IMP
IMP: Inferred from mutant phenotype
26567527 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

FKBP6 Protein Structure

FKBP_C

FKBP_C: FKBP-type peptidyl-prolyl cis-trans isomerase (53 - 140)

  • 0
  • 100
  • 200
  • 300
  • 327 a.a.
Protein Preferred Names Protein Names

inactive peptidyl-prolyl cis-trans isomerase FKBP6

  • 36 kDa FKBP

FKBP6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
FKBP6 O75344 SUMO1P1 Homo sapiens G2XKQ0 25910212
Intra
FKBP6 O75344 SUMO1P1 Homo sapiens G2XKQ0 25910212
Intra
FKBP6 O75344 SUMO1P1 Homo sapiens G2XKQ0 25416956
Intra
FKBP6 O75344 SUMO1P1 Homo sapiens G2XKQ0 25910212
Intra
FKBP6 O75344 RAB11FIP2 Homo sapiens Q7L804 32296183
Intra
FKBP6 O75344 RAB11FIP2 Homo sapiens Q7L804 32296183
Intra
FKBP6 O75344 RAB11FIP2 Homo sapiens Q7L804 32296183
Intra
FKBP6 O75344 TEPSIN Homo sapiens Q96N21 32296183
Intra
FKBP6 O75344 TEPSIN Homo sapiens Q96N21 32296183
Intra
FKBP6 O75344 TEPSIN Homo sapiens Q96N21 32296183
Intra
FKBP6 O75344 DLGAP4 Homo sapiens Q9Y2H0-1 32296183
Intra
FKBP6 O75344 DLGAP4 Homo sapiens Q9Y2H0-1 32296183
Intra
FKBP6 O75344 DLGAP4 Homo sapiens Q9Y2H0-1 32296183
Intra
FKBP6 O75344 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
FKBP6 O75344 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
FKBP6 O75344 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
FKBP6 O75344 BDNF Homo sapiens P23560-2 32814053
Intra
FKBP6 O75344 BDNF Homo sapiens P23560-2 32814053
Intra
FKBP6 O75344 BDNF Homo sapiens P23560-2 32814053
Intra
FKBP6 O75344 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
FKBP6 O75344 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
FKBP6 O75344 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
FKBP6 O75344 MEI4 Homo sapiens A8MW99 32296183
Intra
FKBP6 O75344 MEI4 Homo sapiens A8MW99 32296183
Intra
FKBP6 O75344 GSC2 Homo sapiens O15499 32296183
Intra
FKBP6 O75344 GSC2 Homo sapiens O15499 32296183
Intra
FKBP6 O75344 RNF4 Homo sapiens P78317 32296183
Intra
FKBP6 O75344 RNF4 Homo sapiens P78317 32296183
Intra
FKBP6 O75344 RNF4 Homo sapiens P78317 32296183
Intra
FKBP6 O75344 KANK2 Homo sapiens Q63ZY3 32296183
Intra
FKBP6 O75344 OSBP Homo sapiens P22059 33961781
Intra
FKBP6 O75344 OSBP Homo sapiens P22059 28514442
Intra
FKBP6 O75344 OSBP Homo sapiens P22059 25036637
Intra
FKBP6 O75344 KRT75 Homo sapiens O95678 32296183
Intra
FKBP6 O75344 KRT75 Homo sapiens O95678 32296183
Intra
FKBP6 O75344 KRT75 Homo sapiens O95678 32296183
Intra
FKBP6 O75344 PIAS2 Homo sapiens O75928-2 32296183
Intra
FKBP6 O75344 PIAS2 Homo sapiens O75928-2 32296183
Intra
FKBP6 O75344 PIAS2 Homo sapiens O75928-2 32296183
Intra
FKBP6 O75344 CFTR Homo sapiens P13569 35156780
Intra
FKBP6 O75344 GAPDH Homo sapiens P04406 32814053
Intra
FKBP6 O75344 GAPDH Homo sapiens P04406 32814053
Intra
FKBP6 O75344 GAPDH Homo sapiens P04406 32814053
Intra
FKBP6 O75344 STUB1 Homo sapiens Q9UNE7 32814053
Intra
FKBP6 O75344 STUB1 Homo sapiens Q9UNE7 32814053
Intra
FKBP6 O75344 STUB1 Homo sapiens Q9UNE7 32814053
Intra
FKBP6 O75344 ALDH3A1 Homo sapiens P30838 32296183
Intra
FKBP6 O75344 ALDH3A1 Homo sapiens P30838 32296183
Intra
FKBP6 O75344 ALDH3A1 Homo sapiens P30838 32296183
Intra
FKBP6 O75344 EEF1D Homo sapiens P29692-2 32296183
Intra
FKBP6 O75344 EEF1D Homo sapiens P29692-2 32296183
Intra
FKBP6 O75344 EEF1D Homo sapiens P29692-2 32296183
Intra
FKBP6 O75344 ZNF655 Homo sapiens Q8N720 32296183
Intra
FKBP6 O75344 ZNF655 Homo sapiens Q8N720 32296183
Intra
FKBP6 O75344 ZNF655 Homo sapiens Q8N720 32296183
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 32296183
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 32296183
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 25910212
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 31515488
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 25910212
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 25910212
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 25416956
Intra
FKBP6 O75344 CDK5RAP3 Homo sapiens Q96JB5 32296183
Intra
FKBP6 O75344 TMEM9B Homo sapiens Q9NQ34 32296183
Intra
FKBP6 O75344 FKBP8 Homo sapiens Q14318 26567527
Intra
FKBP6 O75344 CRACR2A Homo sapiens Q9BSW2 32296183
Intra
FKBP6 O75344 CBS Homo sapiens P35520 32814053
Intra
FKBP6 O75344 CBS Homo sapiens P35520 32814053
Intra
FKBP6 O75344 CBS Homo sapiens P35520 32814053
Intra
FKBP6 O75344 LZTS2 Homo sapiens Q9BRK4 25910212
Intra
FKBP6 O75344 LZTS2 Homo sapiens Q9BRK4 25910212
Intra
FKBP6 O75344 LZTS2 Homo sapiens Q9BRK4 25416956
Intra
FKBP6 O75344 LZTS2 Homo sapiens Q9BRK4 25910212
Intra
FKBP6 O75344 NTAQ1 Homo sapiens Q96HA8 32296183
Intra
FKBP6 O75344 DDIT4L Homo sapiens Q96D03 32296183
Intra
FKBP6 O75344 DDIT4L Homo sapiens Q96D03 32296183
Intra
FKBP6 O75344 DDIT4L Homo sapiens Q96D03 32296183
Intra
FKBP6 O75344 ENKD1 Homo sapiens Q9H0I2 32296183
Intra
FKBP6 O75344 IHO1 Homo sapiens Q8IYA8 25910212
Intra
FKBP6 O75344 IHO1 Homo sapiens Q8IYA8 25416956
Intra
FKBP6 O75344 IHO1 Homo sapiens Q8IYA8 25910212
Intra
FKBP6 O75344 IHO1 Homo sapiens Q8IYA8 25910212
Intra
FKBP6 O75344 IHO1 Homo sapiens Q8IYA8 25416956
Intra
FKBP6 O75344 NME7 Homo sapiens Q9Y5B8 16189514
Intra
FKBP6 O75344 NME7 Homo sapiens Q9Y5B8 32296183
Intra
FKBP6 O75344 MEOX2 Homo sapiens P50222 25910212
Intra
FKBP6 O75344 MEOX2 Homo sapiens P50222 25910212
Intra
FKBP6 O75344 MEOX2 Homo sapiens P50222 25910212
Intra
FKBP6 O75344 PICK1 Homo sapiens Q9NRD5 32296183
Intra
FKBP6 O75344 PICK1 Homo sapiens Q9NRD5 32296183
Intra
FKBP6 O75344 PICK1 Homo sapiens Q9NRD5 32296183
Intra
FKBP6 O75344 CFP Homo sapiens P27918 32296183
Intra
FKBP6 O75344 CFP Homo sapiens P27918 32296183
Intra
FKBP6 O75344 CFP Homo sapiens P27918 32296183
Cross
FKBP6 O75344 Usp19 Mus musculus Q3UJD6-2 25036637
Intra
FKBP6 O75344 ECM1 Homo sapiens Q16610 32296183
Intra
FKBP6 O75344 ECM1 Homo sapiens Q16610 32296183
Intra
FKBP6 O75344 ECM1 Homo sapiens Q16610 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

FKBP6 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83175 FKBP6 Antibody (YA2920) WB, IHC-P Human, Mouse, Rat
HY-P83175A FKBP6 Antibody (YA2920)(PBS only) WB, IHC-P Human, Mouse, Rat

Related Diseases

Diseases Alias
Williams-Beuren Syndrome
  • Williams Syndrome

  • WBS

  • Wms

  • Deletion 7q11.23

  • Monosomy 7q11.23

  • Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb

  • Fanconi Schlesinger Syndrome

  • Beuren Syndrome

  • Elfin Facies Syndrome

  • Elfin Facies With Hypercalcemia

  • Hypercalcemia-Supravalvar Aortic Stenosis

  • Ws

Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 2
  • Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss

  • EDSKSCL2

  • Edskmh

  • Ehlers-Danlos Syndrome Kyphoscoliotic Type 2

  • Kyphoscoliotic Ehlers-Danlos Syndrome Due To Fkbp22 Deficiency

  • Ehlers-Danlos Syndrome With Kyphoscoliosis, Myopathy, And Deafness

  • Ehlers-Danlos Syndrome With Kyphoscoliosis, Myopathy, And Hearing Loss

  • Fkbp14-Related Eds

  • Fkbp22-Deficient Eds

  • Kyphoscoliotic Eds Due To Fkbp22 Deficiency

  • Keds-Fkbp14

  • Ehlers-Danlos Syndrome, With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss

  • Ehlers-Danlos Syndrome, Kyphoscoliotic, Type 2

Spermatogenic Failure
  • Azoospermia

  • Spgf

  • Spermatogenic Failure, Susceptibility To

  • Absent Sperm

  • Aspermatogenesis

  • Infertility Due To Azoospermia

  • Hypospermatogenesis

  • Azoospermatism

Supravalvular Aortic Stenosis
  • SVAS

  • Supravalvar Aortic Stenosis

  • Supravalvar Aortic Stenosis, Eisenberg Type

  • Aortic Supravalvular Stenosis

  • Aortic Stenosis, Supravalvular

  • Supra-Valvular Aortic Stenosis

  • Stenosis, Aortic Supravalvular

  • Stenosis, Supravalvular Aortic

  • Supravalvular Stenosis, Aortic

  • Aortic Stenosis Supravalvular

Williams-Beuren Region Duplication Syndrome
  • 7q11.23 Duplication Syndrome

  • 7q11.23 Microduplication Syndrome

  • Chromosome 7q11.23 Duplication Syndrome

  • Wbs Duplication Syndrome

  • Somerville-Van Der Aa Syndrome

  • Dup(7)(Q11.23)

  • Trisomy 7q11.23

  • William-Beuren Region Duplication Syndrome

  • Chromosome 7q11.23 Duplication

Male Infertility
  • Infertility, Male

  • Infertility Male

  • Male Sterility

  • Absolute Infertility

Chromosome 17q12 Deletion Syndrome
  • 17q12 Microdeletion Syndrome

  • Del(17)(Q12)

  • Monosomy 17q12

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
Rattus norvegicus FKBP6 RGD RGD:1308926
Macaca mulatta FKBP6 VGNC VGNC:72666
Mus musculus FKBP6 MGD MGI:2137612
Felis catus FKBP6 VGNC VGNC:62282
Bos taurus FKBP6 VGNC VGNC:29025
Canis familiaris FKBP6 VGNC VGNC:40892
Others FKBP6 NCBI