1. Gene
  2. FAM168A - family with sequence similarity 168 member A Gene

FAM168A - family with sequence similarity 168 member A Gene

Homo sapiens

Also known as TCRP1; KIAA0280

Gene ID: 23201 | Gene type: protein coding

About FAM168A

Cytogenetic location: 11q13.4 Genomic coordinates (GRCh38): 11:73,400,487-73,598,112 (from NCBI)

This gene has 5 transcripts (splice variants), 223 orthologues and 1 paralogue. Ubiquitous expression in brain (RPKM 45.1), gall bladder (RPKM 10.1) and 24 other tissues.

Summary

Involved in positive regulation of base-excision repair. [provided by Alliance of Genome Resources, Apr 2022]

FAM168A Products(3)

mRNA Protein Name
NM_001286050.2 NP_001272979.1 protein FAM168A isoform 1
NM_001286051.2 NP_001272980.1 protein FAM168A isoform 3
NM_015159.3 NP_055974.1 protein FAM168A isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
21516116 GOA
Biological Process GO Annotation Evidence Reference Source
involved in positive regulation of base-excision repair IDA
IDA: Inferred from direct assay
25260657 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

FAM168A Protein Structure

TCRP1

TCRP1: Tongue Cancer Chemotherapy Resistant Protein 1 (1 - 244)

  • 0
  • 100
  • 200
  • 244 a.a.
Protein Preferred Names Protein Names

protein FAM168A

tongue cancer chemotherapy resistance-associated protein 1

FAM168A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
FAM168A Q92567 PRR20C Homo sapiens P86479 25416956
Intra
FAM168A Q92567 SNRPC Homo sapiens Q5TAL4 25416956
Intra
FAM168A Q92567 SNRPC Homo sapiens Q5TAL4 25416956
Intra
FAM168A Q92567 R3HDM2 Homo sapiens Q9Y2K5-2 25416956
Intra
FAM168A Q92567 R3HDM2 Homo sapiens Q9Y2K5-2 25416956
Intra
FAM168A Q92567 UBE2V1 Homo sapiens Q13404 25416956
Intra
FAM168A Q92567 UBASH3B Homo sapiens Q8TF42 25416956
Intra
FAM168A Q92567 UBASH3B Homo sapiens Q8TF42 25416956
Intra
FAM168A Q92567 UBASH3B Homo sapiens Q8TF42 25416956
Intra
FAM168A Q92567 NAF1 Homo sapiens Q96HR8 25416956
Intra
FAM168A Q92567 NAF1 Homo sapiens Q96HR8 25416956
Intra
FAM168A Q92567 NAF1 Homo sapiens Q96HR8 25416956
Intra
FAM168A Q92567 VPS37C Homo sapiens A5D8V6 25416956
Intra
FAM168A Q92567 SMAP2 Homo sapiens Q8WU79 25416956
Intra
FAM168A Q92567 SMAP2 Homo sapiens Q8WU79 25416956
Intra
FAM168A Q92567 TAX1BP1 Homo sapiens Q86VP1 25416956
Intra
FAM168A Q92567 DAZAP2 Homo sapiens Q15038 25416956
Intra
FAM168A Q92567 KLHL42 Homo sapiens Q9P2K6 25416956
Intra
FAM168A Q92567 RBPMS Homo sapiens Q93062 25416956
Intra
FAM168A Q92567 RBPMS Homo sapiens Q93062 25416956
Intra
FAM168A Q92567 RBPMS Homo sapiens Q93062 25416956
Intra
FAM168A Q92567 DTX2 Homo sapiens Q86UW9 25416956
Intra
FAM168A Q92567 DTX2 Homo sapiens Q86UW9 25416956
Intra
FAM168A Q92567 DTX2 Homo sapiens Q86UW9 25416956
Intra
FAM168A Q92567 SF1 Homo sapiens Q15637 25416956
Intra
FAM168A Q92567 SF1 Homo sapiens Q15637 25416956
Intra
FAM168A Q92567 SF1 Homo sapiens Q15637 25416956
Intra
FAM168A Q92567 SS18L1 Homo sapiens O75177 25416956
Intra
FAM168A Q92567 SS18L1 Homo sapiens O75177 25416956
Intra
FAM168A Q92567 SS18L1 Homo sapiens O75177 25416956
Intra
FAM168A Q92567 OTUB2 Homo sapiens Q96DC9 31515488
Intra
FAM168A Q92567 OTUB2 Homo sapiens Q96DC9 25416956
Intra
FAM168A Q92567 OTULIN Homo sapiens Q96BN8 25416956
Intra
FAM168A Q92567 DAB1 Homo sapiens O75553 25416956
Intra
FAM168A Q92567 DAB1 Homo sapiens O75553 25416956
Intra
FAM168A Q92567 DAB1 Homo sapiens O75553 25416956
Intra
FAM168A Q92567 C1orf94 Homo sapiens Q6P1W5 25416956
Intra
FAM168A Q92567 C1orf94 Homo sapiens Q6P1W5 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Oral Squamous Cell Carcinoma

Mouth Squamous Cell Carcinoma

Squamous Cell Carcinoma Of Mouth

Tongue Carcinoma

Tongue Cancer

Malignant Neoplasm Of Tongue

Tongue Neoplasms

Tongue Neoplasm

Deafness, Autosomal Recessive 63

DFNB63

Autosomal Recessive Nonsyndromic Deafness 63

Autosomal Recessive Deafness 63

Deafness, Autosomal Recessive, 63

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 63

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 63

Deafness, Autosomal Recessive, Type 63

Tongue Disease

Abnormality Of The Tongue

Tongue Diseases

Tongue Disorders

Disorder Of Tongue

Glossopathy

Unspecified Condition Of The Tongue

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
Felis catus FAM168A VGNC VGNC:102881
Mus musculus FAM168A MGD MGI:2442372
Canis familiaris FAM168A VGNC VGNC:40619
Bos taurus FAM168A VGNC VGNC:28752
Rattus norvegicus FAM168A RGD RGD:1308929
Macaca mulatta FAM168A VGNC VGNC:72398