1. Gene
  2. RINT1 - RAD50 interactor 1 Gene

RINT1 - RAD50 interactor 1 Gene

Homo sapiens

Also known as ILFS3; RINT-1

Gene ID: 60561 | Gene type: protein coding

About RINT1

Cytogenetic location: 7q22.3 Genomic coordinates (GRCh38): 7:105,532,201-105,567,677 (from NCBI)

This gene has 8 transcripts (splice variants), 207 orthologues and is associated with 3 phenotypes. Ubiquitous expression in testis (RPKM 8.2), bone marrow (RPKM 7.8) and 25 other tissues.

Summary

This gene encodes a protein first identified for its ability to interact with the RAD50 double strand break repair protein, with the resulting interaction implicated in the regulation of cell cycle progression and telomere length. The encoded protein may also play a role in trafficking of cellular cargo from the endosome to the trans-Golgi network. Mutations in this gene may be associated with breast Cancer in human patients. [provided by RefSeq, Oct 2016]

RINT1 Products(5)

mRNA Protein Name
NM_001346599.2 NP_001333528.1 RAD50-interacting protein 1 isoform 2
NM_001346600.2 NP_001333529.1 RAD50-interacting protein 1 isoform 3
NM_001346601.2 NP_001333530.1 RAD50-interacting protein 1 isoform 4
NM_001346603.2 NP_001333532.1 RAD50-interacting protein 1 isoform 3
NM_021930.6 NP_068749.3 RAD50-interacting protein 1 isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
11096100 GOA
Biological Process GO Annotation Evidence Reference Source
involved in mitotic G2 DNA damage checkpoint signaling IMP
IMP: Inferred from mutant phenotype
11096100 GOA
involved in regulation of ER to Golgi vesicle-mediated transport IMP
IMP: Inferred from mutant phenotype
16571679 GOA
Cellular Component GO Annotation Evidence Reference Source
part of Dsl1/NZR complex IDA
IDA: Inferred from direct assay
20462495 GOA
part of Dsl1/NZR complex IPI
IPI: Inferred from physical interaction
20462495 GOA
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
15029241 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

RINT1 Protein Structure

RINT1_TIP1

RINT1_TIP1: RINT-1 / TIP-1 family (304 - 785)

  • 0
  • 200
  • 400
  • 600
  • 792 a.a.
Protein Preferred Names Protein Names

RAD50-interacting protein 1

RINT1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264 24056303
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264 24056303
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264 20462495
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264
GMS
24056303
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264 20462495
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264 33961781
Intra
RINT1 Q6NUQ1 ZW10 Homo sapiens O43264 28514442
Intra
RINT1 Q6NUQ1 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
RINT1 Q6NUQ1 CEP57L1 Homo sapiens Q8IYX8-2 25416956
Intra
RINT1 Q6NUQ1 FAM107A Homo sapiens O95990-3 25416956
Intra
RINT1 Q6NUQ1 FAM107A Homo sapiens O95990-3 25416956
Intra
RINT1 Q6NUQ1 RTP5 Homo sapiens Q14D33 25416956
Intra
RINT1 Q6NUQ1 RTP5 Homo sapiens Q14D33 25416956
Intra
RINT1 Q6NUQ1 LOC729862 Homo sapiens Q0VAF8 25416956
Intra
RINT1 Q6NUQ1 LOC729862 Homo sapiens Q0VAF8 25416956
Intra
RINT1 Q6NUQ1 LOC729862 Homo sapiens Q0VAF9 25416956
Intra
RINT1 Q6NUQ1 LOC729862 Homo sapiens Q0VAF9 25416956
Intra
RINT1 Q6NUQ1 CCDC146 Homo sapiens Q8IYE0-2 25416956
Intra
RINT1 Q6NUQ1 RSRC2 Homo sapiens Q7L4I2-2 25416956
Intra
RINT1 Q6NUQ1 RSRC2 Homo sapiens Q7L4I2-2 25416956
Intra
RINT1 Q6NUQ1 RSRC2 Homo sapiens Q7L4I2-2 25416956
Intra
RINT1 Q6NUQ1 RIBC1 Homo sapiens Q8N443 25416956
Intra
RINT1 Q6NUQ1 RIBC1 Homo sapiens Q8N443 32296183
Intra
RINT1 Q6NUQ1 ZNF697 Homo sapiens Q8N508 25416956
Intra
RINT1 Q6NUQ1 JMY Homo sapiens Q8N9B5-2 32296183
Intra
RINT1 Q6NUQ1 FAM81B Homo sapiens Q96LP2 25416956
Intra
RINT1 Q6NUQ1 LYSMD1 Homo sapiens Q96S90 32296183
Intra
RINT1 Q6NUQ1 SH2D4A Homo sapiens Q9H788-2 25416956
Intra
RINT1 Q6NUQ1 STRN Homo sapiens O43815 25416956
Intra
RINT1 Q6NUQ1 TSHZ2 Homo sapiens Q9NRE2 32296183
Intra
RINT1 Q6NUQ1 SFR1 Homo sapiens Q86XK3 25416956
Intra
RINT1 Q6NUQ1 CDR2L Homo sapiens Q86X02 32296183
Intra
RINT1 Q6NUQ1 TRIM69 Homo sapiens Q86WT6-2 32296183
Intra
RINT1 Q6NUQ1 C19orf44 Homo sapiens Q9H6X5-2 32296183
Intra
RINT1 Q6NUQ1 RNF39 Homo sapiens Q9H2S5 32296183
Intra
RINT1 Q6NUQ1 MGC50722 Homo sapiens Q8IVT4 32296183
Intra
RINT1 Q6NUQ1 ANKRD11 Homo sapiens X5D778 32296183
Intra
RINT1 Q6NUQ1 FAM110A Homo sapiens Q9BQ89 32296183
Intra
RINT1 Q6NUQ1 MISP Homo sapiens Q8IVT2 32296183
Intra
RINT1 Q6NUQ1 TSEN54 Homo sapiens Q7Z6J9 32296183
Intra
RINT1 Q6NUQ1 PRPF18 Homo sapiens Q99633 32296183
Intra
RINT1 Q6NUQ1 ARHGAP45 Homo sapiens Q92619 32296183
Intra
RINT1 Q6NUQ1 CCDC121 Homo sapiens Q6ZUS5 25416956
Intra
RINT1 Q6NUQ1 UVRAG Homo sapiens Q9P2Y5 24056303
Intra
RINT1 Q6NUQ1 UVRAG Homo sapiens Q9P2Y5
GMS
24056303
Intra
RINT1 Q6NUQ1 UVRAG Homo sapiens Q9P2Y5 24056303
Intra
RINT1 Q6NUQ1 UVRAG Homo sapiens Q9P2Y5 24056303
Intra
RINT1 Q6NUQ1 VAV3 Homo sapiens Q9UKW4 32296183
Intra
RINT1 Q6NUQ1 HDAC4 Homo sapiens P56524 25416956
Intra
RINT1 Q6NUQ1 HDAC4 Homo sapiens P56524 25416956
Intra
RINT1 Q6NUQ1 PIK3R2 Homo sapiens O00459 25416956
Intra
RINT1 Q6NUQ1 PIK3R2 Homo sapiens O00459 25416956
Intra
RINT1 Q6NUQ1 TXLNA Homo sapiens P40222 25416956
Intra
RINT1 Q6NUQ1 DPF2 Homo sapiens Q92785 32296183
Intra
RINT1 Q6NUQ1 SMARCE1 Homo sapiens Q969G3 25416956
Intra
RINT1 Q6NUQ1 BLOC1S6 Homo sapiens Q9UL45 32296183
Intra
RINT1 Q6NUQ1 CWF19L2 Homo sapiens Q2TBE0 25416956
Intra
RINT1 Q6NUQ1 MYOZ3 Homo sapiens Q8TDC0 32296183
Intra
RINT1 Q6NUQ1 ZNF835 Homo sapiens Q9Y2P0 32296183
Intra
RINT1 Q6NUQ1 ZNF655 Homo sapiens Q8N720 25416956
Intra
RINT1 Q6NUQ1 ZNF655 Homo sapiens Q8N720 31515488
Intra
RINT1 Q6NUQ1 ZNF655 Homo sapiens Q8N720 25416956
Intra
RINT1 Q6NUQ1 SNW1 Homo sapiens Q13573 25416956
Intra
RINT1 Q6NUQ1 SNW1 Homo sapiens Q13573 25416956
Intra
RINT1 Q6NUQ1 FAM90A1 Homo sapiens Q86YD7 25416956
Intra
RINT1 Q6NUQ1 FAM90A1 Homo sapiens Q86YD7 25416956
Intra
RINT1 Q6NUQ1 FAM161A Homo sapiens Q3B820 25416956
Intra
RINT1 Q6NUQ1 FAM161A Homo sapiens Q3B820 25416956
Intra
RINT1 Q6NUQ1 FAM161A Homo sapiens Q3B820 25416956
Intra
RINT1 Q6NUQ1 FAM161B Homo sapiens Q96MY7 32296183
Intra
RINT1 Q6NUQ1 LMO2 Homo sapiens P25791 25416956
Intra
RINT1 Q6NUQ1 USHBP1 Homo sapiens Q8N6Y0 32296183
Intra
RINT1 Q6NUQ1 RBM41 Homo sapiens Q96IZ5 32296183
Intra
RINT1 Q6NUQ1 RBM41 Homo sapiens Q96IZ5 25416956
Intra
RINT1 Q6NUQ1 C19orf25 Homo sapiens Q9UFG5 28514442
Intra
RINT1 Q6NUQ1 C19orf25 Homo sapiens Q9UFG5 33961781
Intra
RINT1 Q6NUQ1 C19orf25 Homo sapiens Q9UFG5 32296183
Intra
RINT1 Q6NUQ1 FAM124B Homo sapiens Q9H5Z6 25416956
Intra
RINT1 Q6NUQ1 FAM124B Homo sapiens Q9H5Z6 25416956
Intra
RINT1 Q6NUQ1 EXOC8 Homo sapiens Q8IYI6 32296183
Intra
RINT1 Q6NUQ1 MMTAG2 Homo sapiens Q9BU76 32296183
Intra
RINT1 Q6NUQ1 SGF29 Homo sapiens Q96ES7 32296183
Intra
RINT1 Q6NUQ1 SGF29 Homo sapiens Q96ES7 25416956
Intra
RINT1 Q6NUQ1 RAMAC Homo sapiens Q9BTL3 32296183
Intra
RINT1 Q6NUQ1 CCDC120 Homo sapiens Q96HB5 32296183
Intra
RINT1 Q6NUQ1 SH2D4A Homo sapiens Q9H788 25416956
Intra
RINT1 Q6NUQ1 SH2D4A Homo sapiens Q9H788 32296183
Intra
RINT1 Q6NUQ1 SH2D4A Homo sapiens Q9H788 25416956
Intra
RINT1 Q6NUQ1 TACO1 Homo sapiens Q9BSH4 32296183
Intra
RINT1 Q6NUQ1 SCNM1 Homo sapiens Q9BWG6 27107012
Intra
RINT1 Q6NUQ1 SCNM1 Homo sapiens Q9BWG6 25416956
Intra
RINT1 Q6NUQ1 SCNM1 Homo sapiens Q9BWG6 25416956
Intra
RINT1 Q6NUQ1 SCNM1 Homo sapiens Q9BWG6 25416956
Intra
RINT1 Q6NUQ1 EPC1 Homo sapiens Q9H2F5 25416956
Intra
RINT1 Q6NUQ1 EPC1 Homo sapiens Q9H2F5 25416956
Intra
RINT1 Q6NUQ1 AIRIM Homo sapiens Q9NX04 25416956
Intra
RINT1 Q6NUQ1 AIRIM Homo sapiens Q9NX04 32296183
Intra
RINT1 Q6NUQ1 DCX Homo sapiens O43602 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Infantile Liver Failure Syndrome 3

ILFS3

Acute Liver Failure

Fulminant Hepatic Failure

Acute Hepatic Failure

Liver Failure Acute

Hepatic Failure Fulminant

Liver Failure, Acute

Fever-Associated Acute Infantile Liver Failure Syndrome
Infantile Liver Failure Syndrome

Infantile Liver Failure

Hereditary Breast Ovarian Cancer Syndrome

Hereditary Breast And Ovarian Cancer Syndrome

Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer

Breast And/Or Ovarian Cancer

Breast And Ovarian Cancer Syndrome

Hboc Syndrome

Hereditary Breast And Ovarian Cancer

Brca1- Brca2-Associated Hboc

Pelger-Huet Anomaly

PHA

Pelger-Huët Anomaly

Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy And Skeletal Abnormalities

Pelger Huet Anomaly

Pelger-Huet Nuclear Anomaly

Munchausen By Proxy

Munchausen Syndrome By Proxy

Munchausen By Proxy Syndrome

Münchausen Syndrome By Proxy

Optic Nerve Hypoplasia, Bilateral

Optic Nerve Hypoplasia

Bilateral Optic Nerve Hypoplasia

Optic Nerve Hypoplasia, Familial Bilateral

Familial Bilateral Optic Nerve Hypoplasia

Isolated Optic Nerve Hypoplasia/Aplasia

Optic Nerve Aplasia, Bilateral

Onh

BONH

Bilateral Optic Nerve Aplasia

Hypoplasia, Optic Nerve, Bilateral

Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Breast Cancer, Susceptibility To

Breast Cancer, Early-Onset

Malignant Tumor Of Breast

Carcinoma Of Male Breast

Breast Cancer, Invasive Ductal

Breast Cancer, Protection Against

Breast Cancer, Somatic

Breast Cancer, Male

Breast Cancer, Lobular, Somatic

Breast Tumor

Mammary Cancer

Mammary Tumor

Malignant Neoplasm Of Male Breast

Mammary Carcinoma

Male Breast Carcinoma

Familial Cancer Of Breast

Invasive Ductal Breast Carcinoma

Breast Cancer Susceptibility

Breast Cancer, Male, Susceptibility To

Breast Cancer, Early-Onset, Susceptibility To

Malignant Tumor Of The Breast

Mammary Neoplasm

Primary Breast Cancer

Neoplasm Of Male Breast

Carcinoma Of Breast

Breast Cancer In Men

Familial Breast Cancer

Cancer Of Breast

BC

Breast Cancer Familial

Breast Cancer Familial Male

Breast Cancer, Familial Male

Breast Male Carcinoma

Breast Neoplasms

Breast Neoplasms, Male

Mammary Tumors

Mammary Carcinomas

Cancer, Breast

Cancer, Breast, Susceptibility

Invasive Breast Ductal Carcinoma

Breast Neoplasm

Susceptibility To Breast Cancer

Mammary Neoplasms

Animal Mammary Neoplasms

Primary Malignant Neoplasm Of Breast

Infiltrating Ductal Carcinoma Of Breast

Infiltrating Duct Carcinoma Of Unspecified Site

Infiltrating Ductular Carcinoma Of Unspecified Site

Invasive Breast Carcinoma Of No Special Type

Microinvasive Carcinoma Of Breast

Carcinoma With Apocrine Differentiation

Lynch Syndrome

Hereditary Nonpolyposis Colon Cancer

Hereditary Nonpolyposis Colorectal Cancer

Hereditary Nonpolyposis Colorectal Carcinoma

Hereditary Nonpolyposis Colorectal Neoplasms

Familial Nonpolyposis Colon Cancer

Hnpcc

Coca 1

Hereditary Defective Mismatch Repair Syndrome

Hereditary Non-Polyposis Colon Cancer

Hereditary Non-Polyposis Colon Cancer Syndrome

Hereditary Non-Polyposis Colorectal Cancer

Hereditary Non-Polyposis Colorectal Cancer Syndrome

Hereditary Nonpolyposis Colon Cancer Syndrome

Hereditary Nonpolyposis Colorectal Cancer Syndrome

Hereditary Nonpolyposis Colorectal Neoplasm

Hnpcc - Hereditary Nonpolyposis Colon Cancer

Cancer Family Syndrome

Familial Nonpolyposis Colorectal Cancer

Colon Cancer, Familial Nonpolyposis

Colorectal Neoplasms, Hereditary Nonpolyposis

Cancer, Colorectal, Nonpolyposis, Hereditary

Colorectal Cancer, Hereditary Nonpolyposis, Type 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
Bos taurus RINT1 VGNC VGNC:33979
Rattus norvegicus RINT1 RGD RGD:1560433
Mus musculus RINT1 MGD MGI:1916233
Macaca mulatta RINT1 VGNC VGNC:76802
Felis catus RINT1 VGNC VGNC:64637
Canis familiaris RINT1 VGNC VGNC:45591