1. Gene
  2. CRLF3 - cytokine receptor like factor 3 Gene

CRLF3 - cytokine receptor like factor 3 Gene

Homo sapiens

Also known as FRWS; CRLM9; p48.2; CREME9; CYTOR4; CREME-9

Gene ID: 51379 | Gene type: protein coding

About CRLF3

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:30,782,684-30,824,692 (from NCBI)

This gene has 6 transcripts (splice variants), 203 orthologues and 1 paralogue. Broad expression in lymph node (RPKM 15.5), appendix (RPKM 12.1) and 24 other tissues.

Summary

This gene encodes a cytokine receptor-like factor that may negatively regulate cell cycle progression at the G0/G1 phase. Studies of the related rat protein suggest that it may regulate neuronal morphology and synaptic vesicle biogenesis. This gene is one of several genes located in the neurofibromatosis type I tumor suppressor region on the q arm of chromosome 17, a region that is subject to microdeletions, duplications, chromosomal breaks and rearrangements. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2 and 5. [provided by RefSeq, Aug 2012]

CRLF3 Products(1)

mRNA Protein Name
NM_015986.4 NP_057070.3 cytokine receptor-like factor 3
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of G1/S transition of mitotic cell cycle IMP
IMP: Inferred from mutant phenotype
19427400 GOA
involved in negative regulation of cell growth IDA
IDA: Inferred from direct assay
19427400 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
19427400 GOA
involved in positive regulation of receptor signaling pathway via JAK-STAT IDA
IDA: Inferred from direct assay
19427400 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
19427400 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
19427400 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
Protein Preferred Names Protein Names

cytokine receptor-like factor 3

cytokine receptor-like molecule 9

CRLF3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CRLF3 Q8IUI8 LGALS14 Homo sapiens Q8TCE9 25416956
Intra
CRLF3 Q8IUI8 LGALS14 Homo sapiens Q8TCE9 32296183
Intra
CRLF3 Q8IUI8 LGALS14 Homo sapiens Q8TCE9 25416956
Intra
CRLF3 Q8IUI8 MAT2A Homo sapiens P31153 32814053
Intra
CRLF3 Q8IUI8 MAT2A Homo sapiens P31153 32814053
Intra
CRLF3 Q8IUI8 MAT2A Homo sapiens P31153 32814053
Intra
CRLF3 Q8IUI8 JPH3 Homo sapiens Q8WXH2 32814053
Intra
CRLF3 Q8IUI8 JPH3 Homo sapiens Q8WXH2 32814053
Intra
CRLF3 Q8IUI8 JPH3 Homo sapiens Q8WXH2 32814053
Intra
CRLF3 Q8IUI8 KIF1B Homo sapiens O60333-2 32814053
Intra
CRLF3 Q8IUI8 KIF1B Homo sapiens O60333-2 32814053
Intra
CRLF3 Q8IUI8 KIF1B Homo sapiens O60333-2 32814053
Intra
CRLF3 Q8IUI8 DMWD Homo sapiens G5E9A7 32814053
Intra
CRLF3 Q8IUI8 DMWD Homo sapiens G5E9A7 32814053
Intra
CRLF3 Q8IUI8 DMWD Homo sapiens G5E9A7 32814053
Intra
CRLF3 Q8IUI8 BAG6 Homo sapiens P46379-2 32814053
Intra
CRLF3 Q8IUI8 BAG6 Homo sapiens P46379-2 32814053
Intra
CRLF3 Q8IUI8 BAG6 Homo sapiens P46379-2 32814053
Intra
CRLF3 Q8IUI8 KCTD21 Homo sapiens Q4G0X4 32296183
Intra
CRLF3 Q8IUI8 KCTD21 Homo sapiens Q4G0X4 32296183
Intra
CRLF3 Q8IUI8 L3MBTL3 Homo sapiens Q96JM7-2 32296183
Intra
CRLF3 Q8IUI8 L3MBTL3 Homo sapiens Q96JM7-2 32296183
Intra
CRLF3 Q8IUI8 L3MBTL3 Homo sapiens Q96JM7-2 32296183
Intra
CRLF3 Q8IUI8 TSC1 Homo sapiens Q86WV8 32814053
Intra
CRLF3 Q8IUI8 TSC1 Homo sapiens Q86WV8 32814053
Intra
CRLF3 Q8IUI8 TSC1 Homo sapiens Q86WV8 32814053
Intra
CRLF3 Q8IUI8 NOS3 Homo sapiens P29474 32814053
Intra
CRLF3 Q8IUI8 NOS3 Homo sapiens P29474 32814053
Intra
CRLF3 Q8IUI8 NOS3 Homo sapiens P29474 32814053
Intra
CRLF3 Q8IUI8 VPS25 Homo sapiens Q9BRG1 32296183
Intra
CRLF3 Q8IUI8 VPS25 Homo sapiens Q9BRG1 25416956
Intra
CRLF3 Q8IUI8 CRLF3 Homo sapiens Q8IUI8 32296183
Intra
CRLF3 Q8IUI8 VPS25 Homo sapiens Q9BRG1 32296183
Intra
CRLF3 Q8IUI8 CRLF3 Homo sapiens Q8IUI8 32296183
Intra
CRLF3 Q8IUI8 VPS25 Homo sapiens Q9BRG1 29892012
Intra
CRLF3 Q8IUI8 CRLF3 Homo sapiens Q8IUI8 25416956
Intra
CRLF3 Q8IUI8 VPS25 Homo sapiens Q9BRG1 32296183
Intra
CRLF3 Q8IUI8 CRLF3 Homo sapiens Q8IUI8 32296183
Intra
CRLF3 Q8IUI8 HSPB1 Homo sapiens P04792 32814053
Intra
CRLF3 Q8IUI8 HSPB1 Homo sapiens P04792 32814053
Intra
CRLF3 Q8IUI8 HSPB1 Homo sapiens P04792 32814053
Intra
CRLF3 Q8IUI8 SNRPB Homo sapiens P14678-2 32814053
Intra
CRLF3 Q8IUI8 SNRPB Homo sapiens P14678-2 32814053
Intra
CRLF3 Q8IUI8 SNRPB Homo sapiens P14678-2 32814053
Intra
CRLF3 Q8IUI8 NEFL Homo sapiens P07196 32814053
Intra
CRLF3 Q8IUI8 NEFL Homo sapiens P07196 32814053
Intra
CRLF3 Q8IUI8 NEFL Homo sapiens P07196 32814053
Intra
CRLF3 Q8IUI8 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
CRLF3 Q8IUI8 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
CRLF3 Q8IUI8 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
CRLF3 Q8IUI8 SPRED1 Homo sapiens Q7Z699 32814053
Intra
CRLF3 Q8IUI8 SPRED1 Homo sapiens Q7Z699 32814053
Intra
CRLF3 Q8IUI8 SPRED1 Homo sapiens Q7Z699 32814053
Intra
CRLF3 Q8IUI8 MYOZ3 Homo sapiens Q8TDC0 32296183
Intra
CRLF3 Q8IUI8 MYOZ3 Homo sapiens Q8TDC0 32296183
Intra
CRLF3 Q8IUI8 MYOZ3 Homo sapiens Q8TDC0 32296183
Intra
CRLF3 Q8IUI8 ICAM5 Homo sapiens Q9UMF0 32814053
Intra
CRLF3 Q8IUI8 ICAM5 Homo sapiens Q9UMF0 32814053
Intra
CRLF3 Q8IUI8 ICAM5 Homo sapiens Q9UMF0 32814053
Intra
CRLF3 Q8IUI8 NDUFV2 Homo sapiens P19404 32814053
Intra
CRLF3 Q8IUI8 NDUFV2 Homo sapiens P19404 32814053
Intra
CRLF3 Q8IUI8 NDUFV2 Homo sapiens P19404 32814053
Intra
CRLF3 Q8IUI8 PHYH Homo sapiens O14832 32814053
Intra
CRLF3 Q8IUI8 PHYH Homo sapiens O14832 32814053
Intra
CRLF3 Q8IUI8 PHYH Homo sapiens O14832 32814053
Intra
CRLF3 Q8IUI8 DDIT4L Homo sapiens Q96D03 32296183
Intra
CRLF3 Q8IUI8 DDIT4L Homo sapiens Q96D03 32296183
Intra
CRLF3 Q8IUI8 DDIT4L Homo sapiens Q96D03 32296183
Intra
CRLF3 Q8IUI8 GFAP Homo sapiens P14136 32814053
Intra
CRLF3 Q8IUI8 GFAP Homo sapiens P14136 32814053
Intra
CRLF3 Q8IUI8 GFAP Homo sapiens P14136 32814053
Intra
CRLF3 Q8IUI8 PRPS1 Homo sapiens P60891 32814053
Intra
CRLF3 Q8IUI8 PRPS1 Homo sapiens P60891 32814053
Intra
CRLF3 Q8IUI8 PRPS1 Homo sapiens P60891 32814053
Intra
CRLF3 Q8IUI8 RBM14 Homo sapiens Q96PK6 26871637
Intra
CRLF3 Q8IUI8 FLNA Homo sapiens P21333-2 32814053
Intra
CRLF3 Q8IUI8 FLNA Homo sapiens P21333-2 32814053
Intra
CRLF3 Q8IUI8 FLNA Homo sapiens P21333-2 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Neurofibromatosis

Neurofibromatoses

Acoustic Neurofibromatosis

Central Neurofibromatosis

Peripheral Neurofibromatosis

Recklinghausen'S Neurofibromatosis

Von Reklinghausen Disease

Neurofibromatosis Type 1

Actinic Keratosis

Solar Keratosis

Actinic Keratosis

Senile Hyperkeratosis

Sk - Solar Keratosis

Keratosis, Actinic

Seborrheic Keratosis

Ak - [Actinic Keratosis]

Sk - [Solar Keratosis]

Neurofibromatosis, Type I

Von Recklinghausen Disease

Neurofibromatosis 1

Neurofibromatosis, Type 1

NF1

Neurofibromatosis, Peripheral Type

Neurofibromatosis Type I

Neurofibromatosis Type 1 Due To Nf1 Mutation Or Intragenic Deletion

Familial Spinal Neurofibromatosis

Fsnf

Peripheral Neurofibromatosis

Von Recklinghausen'S Neurofibromatosis

Von Recklinghausen Disease Due To Nf1 Mutation Or Intragenic Deletion

Neurofibromatosis Peripheral Type

Von Recklinghausen Syndrome

Neurofibromatosis Type 1

Von Recklinghausen Neuropathy

Nf1 - [Neurofibromatosis Type 1]

Recklinghausen Disease

Chromosome 17q11.2 Deletion Syndrome

Nf1 Microdeletion Syndrome

17q11 Microdeletion Syndrome

Neurofibromatosis Type 1 Microdeletion Syndrome

Van Asperen Syndrome

Del(17)(Q11)

Monosomy 17q11

Chromosome 17q11.2 Deletion Syndrome, 1.4mb

Chromosome 15q26-Qter Deletion Syndrome

Drayer Syndrome

15q26 Deletion Syndrome

Distal 15q Deletion Syndrome

Distal Monosomy 15q

Telomeric 15q Deletion Syndrome

Monosomy 15q26

Epiphyseal Dysplasia, Multiple, 5

EDM5

Multiple Epiphyseal Dysplasia 5

Bhmed

Multiple Epiphyseal Dysplasia Type 5

Multiple Epiphyseal Dysplasia, Matn3-Related

Microepiphyseal Dysplasia, Bilateral Hereditary

Bilateral Hereditary Microepiphyseal Dysplasia

Multiple Epiphyseal Dysplasia Matn3-Related

Epiphyseal Dysplasia Multiple 5

Multiple Epiphyseal Dysplasia, Matn3 Related

Bilateral Hereditary Micro-Epiphyseal Dysplasia

Med5

Polyepiphyseal Dysplasia Type 5

Dysplasia, Epiphyseal, Multiple, Type 5

Dysgraphia

Agraphia

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 CRLF3 VGNC VGNC:39622
Felis catus CRLF3 VGNC VGNC:61184
Macaca mulatta CRLF3 VGNC VGNC:71428
Rattus norvegicus CRLF3 RGD RGD:621517
Mus musculus CRLF3 MGD MGI:1860086
Bos taurus CRLF3 VGNC VGNC:27718