1. Gene
  2. QRICH1 - glutamine rich 1 Gene

QRICH1 - glutamine rich 1 Gene

Homo sapiens

Also known as AB-DIP; VERBRAS

Gene ID: 54870 | Gene type: protein coding

About QRICH1

Cytogenetic location: 3p21.31 Genomic coordinates (GRCh38): 3:49,029,707-49,094,373 (from NCBI)

This gene has 22 transcripts (splice variants), 263 orthologues, 18 paralogues and is associated with 3 phenotypes. Ubiquitous expression in testis (RPKM 28.0), bone marrow (RPKM 21.2) and 25 other tissues.

Summary

Enables DNA binding activity. Involved in several processes, including PERK-mediated unfolded protein response; intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress; and positive regulation of transcription, DNA-templated. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

QRICH1 Products(8)

mRNA Protein Name
NM_001320580.2 NP_001307509.1 transcriptional regulator QRICH1
NM_001320581.2 NP_001307510.1 transcriptional regulator QRICH1
NM_001320582.2 NP_001307511.1 transcriptional regulator QRICH1
NM_001320583.2 NP_001307512.1 transcriptional regulator QRICH1
NM_001320584.1 NP_001307513.1 transcriptional regulator QRICH1
NM_001320585.1 NP_001307514.1 transcriptional regulator QRICH1
NM_017730.4 NP_060200.2 transcriptional regulator QRICH1
NM_198880.3 NP_942581.1 transcriptional regulator QRICH1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables DNA binding IMP
IMP: Inferred from mutant phenotype
33384352 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence Reference Source
involved in PERK-mediated unfolded protein response IMP
IMP: Inferred from mutant phenotype
33384352 GOA
involved in endoplasmic reticulum unfolded protein response IMP
IMP: Inferred from mutant phenotype
33384352 GOA
involved in integrated stress response signaling IMP
IMP: Inferred from mutant phenotype
33384352 GOA
involved in intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress IMP
IMP: Inferred from mutant phenotype
33384352 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
33384352 GOA
involved in positive regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
33384352 GOA
involved in response to endoplasmic reticulum stress IMP
IMP: Inferred from mutant phenotype
33384352 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nucleus IDA
IDA: Inferred from direct assay
33384352 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

QRICH1 Protein Structure

DUF3504

DUF3504: Domain of unknown function (DUF3504) (596 - 759)

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

transcriptional regulator QRICH1

glutamine-rich protein 1

QRICH1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
QRICH1 Q2TAL8 BICRAL Homo sapiens Q6AI39 32296183
Intra
QRICH1 Q2TAL8 BICRAL Homo sapiens Q6AI39 32296183
Intra
QRICH1 Q2TAL8 BICRAL Homo sapiens Q6AI39 32296183
Intra
QRICH1 Q2TAL8 FLJ13057 Homo sapiens Q53SE7 25416956
Intra
QRICH1 Q2TAL8 FLJ13057 Homo sapiens Q53SE7 25416956
Intra
QRICH1 Q2TAL8 SELENOV Homo sapiens P59797 32296183
Intra
QRICH1 Q2TAL8 SELENOV Homo sapiens P59797 32296183
Intra
QRICH1 Q2TAL8 DNAAF6 Homo sapiens Q9NQM4 32296183
Intra
QRICH1 Q2TAL8 DNAAF6 Homo sapiens Q9NQM4 32296183
Intra
QRICH1 Q2TAL8 DNAAF6 Homo sapiens Q9NQM4 32296183
Intra
QRICH1 Q2TAL8 TEKT5 Homo sapiens Q96M29 32296183
Intra
QRICH1 Q2TAL8 TEKT5 Homo sapiens Q96M29 32296183
Intra
QRICH1 Q2TAL8 TEKT5 Homo sapiens Q96M29 32296183
Intra
QRICH1 Q2TAL8 PUF60 Homo sapiens Q9UHX1 25416956
Intra
QRICH1 Q2TAL8 PUF60 Homo sapiens Q9UHX1 25416956
Intra
QRICH1 Q2TAL8 PUF60 Homo sapiens Q9UHX1 25416956
Intra
QRICH1 Q2TAL8 NFYA Homo sapiens P23511-2 32296183
Intra
QRICH1 Q2TAL8 NFYA Homo sapiens P23511-2 32296183
Intra
QRICH1 Q2TAL8 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
QRICH1 Q2TAL8 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
QRICH1 Q2TAL8 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
QRICH1 Q2TAL8 USP54 Homo sapiens Q70EL1-9 32296183
Intra
QRICH1 Q2TAL8 USP54 Homo sapiens Q70EL1-9 32296183
Intra
QRICH1 Q2TAL8 USP54 Homo sapiens Q70EL1-9 32296183
Intra
QRICH1 Q2TAL8 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
QRICH1 Q2TAL8 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
QRICH1 Q2TAL8 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
QRICH1 Q2TAL8 NFIX Homo sapiens Q14938-5 32296183
Intra
QRICH1 Q2TAL8 NFIX Homo sapiens Q14938-5 32296183
Intra
QRICH1 Q2TAL8 POU6F2 Homo sapiens P78424 32296183
Intra
QRICH1 Q2TAL8 POU6F2 Homo sapiens P78424 32296183
Intra
QRICH1 Q2TAL8 LHX3 Homo sapiens Q9UBR4-2 32296183
Intra
QRICH1 Q2TAL8 LHX3 Homo sapiens Q9UBR4-2 32296183
Intra
QRICH1 Q2TAL8 LHX3 Homo sapiens Q9UBR4-2 32296183
Intra
QRICH1 Q2TAL8 SMAP1 Homo sapiens Q8IYB5-2 32296183
Intra
QRICH1 Q2TAL8 SMAP1 Homo sapiens Q8IYB5-2 32296183
Intra
QRICH1 Q2TAL8 SMAP1 Homo sapiens Q8IYB5-2 32296183
Intra
QRICH1 Q2TAL8 CIMIP2B Homo sapiens A8MTA8-2 32296183
Intra
QRICH1 Q2TAL8 CIMIP2B Homo sapiens A8MTA8-2 32296183
Intra
QRICH1 Q2TAL8 MYH7B Homo sapiens A7E2Y1-2 32296183
Intra
QRICH1 Q2TAL8 MYH7B Homo sapiens A7E2Y1-2 32296183
Intra
QRICH1 Q2TAL8 POGZ Homo sapiens Q7Z3K3 32296183
Intra
QRICH1 Q2TAL8 POGZ Homo sapiens Q7Z3K3 27107012
Intra
QRICH1 Q2TAL8 POGZ Homo sapiens Q7Z3K3 32296183
Intra
QRICH1 Q2TAL8 SRARP Homo sapiens Q8NEQ6 32296183
Intra
QRICH1 Q2TAL8 SRARP Homo sapiens Q8NEQ6 32296183
Intra
QRICH1 Q2TAL8 SRARP Homo sapiens Q8NEQ6 32296183
Intra
QRICH1 Q2TAL8 PIERCE2 Homo sapiens H3BRN8 32296183
Intra
QRICH1 Q2TAL8 PIERCE2 Homo sapiens H3BRN8 32296183
Intra
QRICH1 Q2TAL8 LBX1 Homo sapiens P52954 32296183
Intra
QRICH1 Q2TAL8 LBX1 Homo sapiens P52954 32296183
Intra
QRICH1 Q2TAL8 GMCL1 Homo sapiens Q96IK5 27107012
Intra
QRICH1 Q2TAL8 GMCL1 Homo sapiens Q96IK5 32296183
Intra
QRICH1 Q2TAL8 GMCL1 Homo sapiens Q96IK5 27107012
Intra
QRICH1 Q2TAL8 GMCL1 Homo sapiens Q96IK5 32296183
Intra
QRICH1 Q2TAL8 GMCL1 Homo sapiens Q96IK5 32296183
Intra
QRICH1 Q2TAL8 LMO4 Homo sapiens P61968 32296183
Intra
QRICH1 Q2TAL8 LMO4 Homo sapiens P61968 32296183
Intra
QRICH1 Q2TAL8 PRKAR1B Homo sapiens P31321 32296183
Intra
QRICH1 Q2TAL8 PRKAR1B Homo sapiens P31321 32296183
Intra
QRICH1 Q2TAL8 MEOX1 Homo sapiens P50221 25416956
Intra
QRICH1 Q2TAL8 LHX4 Homo sapiens Q969G2 32296183
Intra
QRICH1 Q2TAL8 LHX4 Homo sapiens Q969G2 32296183
Intra
QRICH1 Q2TAL8 LHX4 Homo sapiens Q969G2 32296183
Intra
QRICH1 Q2TAL8 TRAF2 Homo sapiens Q12933 32296183
Intra
QRICH1 Q2TAL8 TRAF2 Homo sapiens Q12933 32296183
Intra
QRICH1 Q2TAL8 TRAF1 Homo sapiens Q13077 32296183
Intra
QRICH1 Q2TAL8 TRAF1 Homo sapiens Q13077 25416956
Intra
QRICH1 Q2TAL8 TRAF1 Homo sapiens Q13077 32296183
Intra
QRICH1 Q2TAL8 TRAF1 Homo sapiens Q13077 25416956
Intra
QRICH1 Q2TAL8 NLK Homo sapiens Q9UBE8 25416956
Intra
QRICH1 Q2TAL8 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
QRICH1 Q2TAL8 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
QRICH1 Q2TAL8 HSFY1 Homo sapiens Q96LI6 25416956
Intra
QRICH1 Q2TAL8 HSFY1 Homo sapiens Q96LI6 25416956
Intra
QRICH1 Q2TAL8 HSFY1 Homo sapiens Q96LI6 25416956
Intra
QRICH1 Q2TAL8 CEACAM6 Homo sapiens P40199 32296183
Intra
QRICH1 Q2TAL8 CEACAM6 Homo sapiens P40199 32296183
Intra
QRICH1 Q2TAL8 ZYX Homo sapiens Q15942 32296183
Intra
QRICH1 Q2TAL8 ZYX Homo sapiens Q15942 32296183
Intra
QRICH1 Q2TAL8 FHL2 Homo sapiens Q14192 32296183
Intra
QRICH1 Q2TAL8 FHL2 Homo sapiens Q14192 32296183
Intra
QRICH1 Q2TAL8 SEPHS1 Homo sapiens P49903 25416956
Intra
QRICH1 Q2TAL8 SEPHS1 Homo sapiens P49903 25416956
Intra
QRICH1 Q2TAL8 SEPHS1 Homo sapiens P49903 25416956
Intra
QRICH1 Q2TAL8 HSPB8 Homo sapiens Q9UJY1 25416956
Intra
QRICH1 Q2TAL8 HSPB8 Homo sapiens Q9UJY1 32296183
Intra
QRICH1 Q2TAL8 HSPB8 Homo sapiens Q9UJY1 25416956
Intra
QRICH1 Q2TAL8 HSPB8 Homo sapiens Q9UJY1 32296183
Intra
QRICH1 Q2TAL8 HSPB8 Homo sapiens Q9UJY1 25416956
Intra
QRICH1 Q2TAL8 HSPB8 Homo sapiens Q9UJY1 32296183
Intra
QRICH1 Q2TAL8 RBM17 Homo sapiens Q96I25 31515488
Intra
QRICH1 Q2TAL8 RBM17 Homo sapiens Q96I25 25416956
Intra
QRICH1 Q2TAL8 FHL3 Homo sapiens Q13643 32296183
Intra
QRICH1 Q2TAL8 FHL3 Homo sapiens Q13643 25416956
Intra
QRICH1 Q2TAL8 FHL3 Homo sapiens Q13643 32296183
Intra
QRICH1 Q2TAL8 PAX6 Homo sapiens P26367 32296183
Intra
QRICH1 Q2TAL8 PAX6 Homo sapiens P26367 32296183
Intra
QRICH1 Q2TAL8 CRX Homo sapiens O43186 25416956
Intra
QRICH1 Q2TAL8 CRX Homo sapiens O43186 25416956
Intra
QRICH1 Q2TAL8 CRX Homo sapiens O43186 32296183
Intra
QRICH1 Q2TAL8 CRX Homo sapiens O43186 25416956
Intra
QRICH1 Q2TAL8 CRX Homo sapiens O43186 32296183
Intra
QRICH1 Q2TAL8 FHL5 Homo sapiens Q5TD97 32296183
Intra
QRICH1 Q2TAL8 FHL5 Homo sapiens Q5TD97 32296183
Intra
QRICH1 Q2TAL8 FHL5 Homo sapiens Q5TD97 32296183
Intra
QRICH1 Q2TAL8 NFIX Homo sapiens Q14938 25416956
Intra
QRICH1 Q2TAL8 SP2 Homo sapiens Q02086-2 32296183
Intra
QRICH1 Q2TAL8 SP2 Homo sapiens Q02086-2 32296183
Intra
QRICH1 Q2TAL8 LASP1 Homo sapiens Q14847-2 32296183
Intra
QRICH1 Q2TAL8 LASP1 Homo sapiens Q14847-2 32296183
Intra
QRICH1 Q2TAL8 KHDC4 Homo sapiens Q7Z7F0-4 32296183
Intra
QRICH1 Q2TAL8 KHDC4 Homo sapiens Q7Z7F0-4 32296183
Intra
QRICH1 Q2TAL8 KHDC4 Homo sapiens Q7Z7F0-4 32296183
Intra
QRICH1 Q2TAL8 KLHDC7B Homo sapiens Q96G42 32296183
Intra
QRICH1 Q2TAL8 KLHDC7B Homo sapiens Q96G42 32296183
Intra
QRICH1 Q2TAL8 KLHDC7B Homo sapiens Q96G42 32296183
Intra
QRICH1 Q2TAL8 ARID5A Homo sapiens Q03989 32296183
Intra
QRICH1 Q2TAL8 ARID5A Homo sapiens Q03989 32296183
Intra
QRICH1 Q2TAL8 TOX4 Homo sapiens O94842 32296183
Intra
QRICH1 Q2TAL8 TOX4 Homo sapiens O94842 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Ververi-Brady Syndrome

VERBRAS

Qrich1-Related Intellectual Disability-Chondrodysplasia Syndrome

Cerebellofaciodental Syndrome

Cerebellar-Facial-Dental Syndrome

CFDS

Floating-Harbor Syndrome

FLHS

Fhs

Pelletier-Leisti Syndrome

Short Stature With Delayed Bone Age, Expressive Language Delay, A Triangular Face With A Prominent Nose And Deep-Set Eyes

Leisti-Hollander-Rimoin Syndrome

Three M Syndrome 1

3-M Syndrome

Yakut Short Stature Syndrome

3m Syndrome

Le Merrer Syndrome

Dolichospondylic Dysplasia

Gloomy Face Syndrome

Three M Syndrome

3M1

3m Syndrome 1

Miller-Mckusick-Malvaux Syndrome

3-Msbn

Three-M Slender-Boned Nanism

Miller-Mckusick-Malvaux-Syndrome

3-M Syndrome 1

3m Syndrome-1

3m Syndrome, Type 1

Dwarfism

Dwarfism Tall Vertebrae

Mowat-Wilson Syndrome

MOWS

Microcephaly, Mental Retardation, And Distinct Facial Features, With Or Without Hirschsprung Disease

Hirschsprung Disease-Mental Retardation Syndrome

Mowat-Wilson Syndrome Due To Monosomy 2q22

Hirschsprung Disease Mental Retardation Syndrome

Microcephaly, Mental Retardation, And Distinct Facial Featrues, With Or Without Hirschprung Disease

Hirschsprung Disease - Intellectual Disability Syndrome

Hirschsprung Disease Intellectual Disability Syndrome

Intellectual Disability, Microcephaly, And Distinct Facial Features With Or Without Hirschsprung Disease

Mws

Hirschsprung Disease-Intellectual Disability Syndrome

Hirschsprung Disease And Intellectual Disability Due To 2q22 Microdeletion

Hirschsprung Disease And Intellectual Disability Due To Del(2)(Q22)

Hirschsprung Disease And Intellectual Disability Due To Monosomy 2q22

Mowat-Wilson Syndrome Due To 2q22 Microdeletion

Mowat-Wilson Syndrome Due To Del(2)Q(22)

Mowat-Wilson Syndrome Due To A Zeb2 Point Mutation

Hirschsprung Disease And Intellectual Disability Due To A Zeb2 Point Mutation

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 QRICH1 VGNC VGNC:64459
Bos taurus QRICH1 VGNC VGNC:33602
Canis familiaris QRICH1 VGNC VGNC:45236
Macaca mulatta QRICH1 VGNC VGNC:76530
Rattus norvegicus QRICH1 RGD RGD:1311095
Mus musculus QRICH1 MGD MGI:1916482