Version: 8.0.0
Date: Tue Jan 28 2025
271 results for ctrb1

Ctrb1

(Mus musculus)
Gene
Name: chymotrypsinogen B1
Synonyms: Ctrb, expressed sequence AI504462, pancreatic proteinase 2, Prt-2, 2200008D09Rik, RIKEN cDNA 2200008D09 gene, AI504462
Source: MGI:88559
Biotype: protein coding gene
Symbol: Ctrb1 (Mmu)
Symbol: Ctrb1
Automated Gene Synopsis: Orthologous to human CTRB1 (chymotrypsinogen B1) and CTRB2 (chymotrypsinogen B2).
Strict Orthology Symbols: ctrb1
Alleles: Ctrb1 (Mmu)...Ctrb1 (Mmu)...Ctrb1 (Mmu)

CTRB1

(Homo sapiens)
Gene
Name: chymotrypsinogen B1
Synonyms: MGC88037, FLJ42412, chymotrypsinogen B, CTRB
Source: HGNC:2521
Biotype: protein coding gene
Symbol: CTRB1 (Hsa)
Symbol: CTRB1
Gene Synopsis: This CTRB1 gene is located head-to-head with the related CTRB2 gene....inverts a 16.6 Kb region containing portions of intron 1, exon 1, and the upstream sequence of the CTRB1...In this inversion haplotype exon 1 and flanking sequence is swapped in CTRB1 and CTRB2....The GRCh38 assembly represents the minor allele for SNP rs8048956 of the CTRB1 gene....This CTRB1 gene encodes distinct isoforms, some or all of which may undergo similar processing to generate
Strict Orthology Symbols: ctrb1

ctrb1

(Xenopus tropicalis)
Gene
Name: chymotrypsinogen B1
Synonyms: chymotrypsinogen B, chymotrypsinogen B1, ctrb1, ctrb
Source: Xenbase:XB-GENE-977509
Biotype: gene
Symbol: ctrb1 (Xtr)
Symbol: ctrb1
Automated Gene Synopsis: Orthologous to human CTRB1 (chymotrypsinogen B1) and CTRB2 (chymotrypsinogen B2).
Synonyms: ctrb1...ctrb1...ctrb1
Strict Orthology Symbols: ctrb1.L...Ctrb1...CTRB1

Ctrb1

(Rattus norvegicus)
Gene
Name: chymotrypsinogen B1
Synonyms: Ctrb, chymotrypsinogen B, Chymotrypsin B, chymotrypsin B1
Source: RGD:2444
Biotype: protein coding gene
Symbol: Ctrb1 (Rno)
Symbol: Ctrb1
Strict Orthology Symbols: ctrb1

ctrb1.L

(Xenopus laevis)
Gene
Name: chymotrypsinogen B1
Synonyms: ctrb1.L, chymotrypsinogen B, chymotrypsinogen B1, ctrb
Source: Xenbase:XB-GENE-977512
Biotype: gene
Symbol: ctrb1.L (Xla)
Automated Gene Synopsis: Orthologous to human CTRB1 (chymotrypsinogen B1).
Strict Orthology Symbols: ctrb1
Symbol: ctrb1.L

Ctrb1Gt(OST27792)Lex

(Mus musculus)
Allele/Variant
Source: MGI:3529453
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ctrb1 (Mmu)
Genes: Ctrb1 (Mmu)
Symbol: Ctrb1Gt(OST27792)Lex

Ctrb1em1Toth

(Mus musculus)
Allele/Variant
Source: MGI:6455002
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ctrb1 (Mmu)
Genes: Ctrb1 (Mmu)
Symbol: Ctrb1em1Toth

Ctrb1em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7289193
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ctrb1 (Mmu)
Genes: Ctrb1 (Mmu)
Symbol: Ctrb1em1Smoc

Ctrb1em1Toth/Ctrb1em1Toth [background:] C57BL/6N-Ctrb1em1Toth

(Mus musculus)
Model
Id: MGI:6455007
Synonyms: Not Available
Symbol: Ctrb1/Ctrb1 [background:] C57BL/6N-Ctrb1 (Mmu)
Genes: Ctrb1 (Mmu)
Alleles: Ctrb1 (Mmu)
Name: Ctrb1/Ctrb1 [background:] C57BL/6N-Ctrb1

ctrb.1

(Danio rerio)
Gene
Name: chymotrypsinogen B, tandem duplicate 1
Synonyms: wu:fb69e12, ctrb1, fb69e12, wu:fb61f07
Source: ZFIN:ZDB-GENE-030131-1171
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human CTRB1 (chymotrypsinogen B1) and CTRB2 (chymotrypsinogen B2).
Synonyms: ctrb1...ctrb1...ctrb1
Strict Orthology Symbols: Ctrb1...CTRB1

ctrb.3

(Danio rerio)
Gene
Name: chymotrypsinogen B, tandem duplicate 3
Synonyms: zgc:112160
Source: ZFIN:ZDB-GENE-050417-229
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human CTRB1 (chymotrypsinogen B1) and CTRB2 (chymotrypsinogen B2).
Strict Orthology Symbols: ctrb1

ctrb.2

(Danio rerio)
Gene
Name: chymotrypsinogen B, tandem duplicate 2
Synonyms: zgc:136461
Source: ZFIN:ZDB-GENE-060519-7
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human CTRB1 (chymotrypsinogen B1) and CTRB2 (chymotrypsinogen B2).
Strict Orthology Symbols: Ctrb1...CTRB1

CTRB2

(Homo sapiens)
Gene
Name: chymotrypsinogen B2
Synonyms: chymotrypsin B2
Source: HGNC:2522
Biotype: protein coding gene
Gene Synopsis: This CTRB2 gene is located head-to-head with the related CTRB1 gene....inverts a 16.6 Kb region containing portions of intron 1, exon 1, and the upstream sequence of the CTRB1...In this inversion haplotype exon 1 and flanking sequence is swapped in CTRB1 and CTRB2....The GRCh38 assembly represents the minor allele for SNP rs8048956 of the CTRB1 gene.
Strict Orthology Symbols: ctrb1

CG11912

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: SP140, anon-WO0140519.112
Source: FB:FBgn0031248
Biotype: protein coding gene
Strict Orthology Symbols: ctrb1

CG6592

(Drosophila melanogaster)
Gene
Name: Not Available
Synonyms: lincRNA.S4213, SP105
Source: FB:FBgn0035669
Biotype: protein coding gene
Strict Orthology Symbols: Ctrb1

Jon74E

(Drosophila melanogaster)
Gene
Name: Jonah 74E
Synonyms: CT19724, CG6298, SP85
Source: FB:FBgn0023197
Biotype: protein coding gene
Strict Orthology Symbols: Ctrb1

zf3439Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-220520-2
Genes: ctrb.1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ctrb1

digestion

Gene Ontology
Source: GO:0007586
Synonyms: Not Available
Branch: biological process
Genes: Ctrb1 (Rno)...CTRB1 (Hsa)...Ctrb1 (Mmu)

pancreatitis

Disease
Source: DOID:4989
Definition: A pancreas disease that is characterized by inflammation of the pancreas.
Genes: Ctrb1 (Rno)...CTRB1 (Hsa)...Ctrb1 (Mmu)...ctrb1 (Xtr)

response to cytokine

Gene Ontology
Source: GO:0034097
Synonyms:
  • response to cytokine stimulus
Branch: biological process
Genes: Ctrb1 (Rno)...Ctrb1 (Mmu)

serine-type peptidase activity

Gene Ontology
Source: GO:0008236
Synonyms:
  • serine protease activity
Branch: molecular function
Genes: Ctrb1 (Mmu)...Ctrb1 (Rno)...CTRB1 (Hsa)

response to food

Gene Ontology
Source: GO:0032094
Synonyms: Not Available
Branch: biological process
Genes: Ctrb1 (Rno)

protein catabolic process

Gene Ontology
Source: GO:0030163
Synonyms:
  • cellular protein breakdown
  • cellular protein catabolic process
Branch: biological process
Genes: Ctrb1 (Mmu)...Ctrb1 (Rno)

response to nutrient

Gene Ontology
Source: GO:0007584
Synonyms:
  • nutritional response pathway
  • response to nutrients
Branch: biological process
Genes: Ctrb1 (Rno)

response to peptide hormone

Gene Ontology
Source: GO:0043434
Synonyms:
  • response to peptide hormone stimulus
  • response to polypeptide hormone stimulus
Branch: biological process
Genes: Ctrb1 (Rno)

serine-type endopeptidase activity

Gene Ontology
Source: GO:0004252
Synonyms:
  • blood coagulation factor activity
  • serine elastase activity
Branch: molecular function
Genes: Ctrb1 (Mmu)...Ctrb1 (Rno)...CTRB1 (Hsa)

response to toxic substance

Gene Ontology
Source: GO:0009636
Synonyms:
  • detoxification response
  • toxin resistance
Branch: biological process
Genes: Ctrb1 (Rno)

positive regulation of apoptotic process

Gene Ontology
Source: GO:0043065
Synonyms:
  • activation of apoptosis
  • positive regulation of apoptosis
Branch: biological process
Genes: Ctrb1 (Mmu)...Ctrb1 (Rno)

proteolysis

Gene Ontology
Source: GO:0006508
Synonyms:
  • ATP-dependent proteolysis
  • peptidolysis
Branch: biological process
Genes: Ctrb1 (Rno)...Ctrb1 (Mmu)...CTRB1 (Hsa)

peptidase activity

Gene Ontology
Source: GO:0008233
Synonyms:
  • hydrolase, acting on peptide bonds
  • peptidase activity, acting on D-amino acid peptides
Branch: molecular function
Genes: Ctrb1 (Mmu)...Ctrb1 (Rno)

sa21002

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-124
Genes: ctrb.1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ctrb1

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: CTRB1 (Hsa)...Ctrb1 (Rno)

(GRCh38)16:75224144G>A

(Homo sapiens)
Allele/Variant
Source: rs1379132184
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224144G>A

(GRCh38)16:75223010C>T

(Homo sapiens)
Allele/Variant
Source: rs988924329
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223010C>T

(GRCh38)16:75223544G>A

(Homo sapiens)
Allele/Variant
Source: rs749947761
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223544G>A

(GRCh38)16:75222788C>A

(Homo sapiens)
Allele/Variant
Source: rs369201413
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222788C>A

(GRCh38)16:75224162G>A

(Homo sapiens)
Allele/Variant
Source: rs772939808
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224162G>A

(GRCh38)16:75224717G>A

(Homo sapiens)
Allele/Variant
Source: rs375112297
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224717G>A

(GRCh38)16:75225312C>G

(Homo sapiens)
Allele/Variant
Source: rs207476166
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75225312C>G

(GRCh38)16:75219026C>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.75219026C>T
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75219026C>T

(GRCh38)16:75222813G>A

(Homo sapiens)
Allele/Variant
Source: rs1460273237
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222813G>A

(GRCh38)16:75222836G>A

(Homo sapiens)
Allele/Variant
Source: rs575650101
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222836G>A

(GRCh38)16:75222837T>C

(Homo sapiens)
Allele/Variant
Source: rs760725877
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222837T>C

(GRCh38)16:75223041G>A

(Homo sapiens)
Allele/Variant
Source: rs1395895685
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223041G>A

(GRCh38)16:75223215C>A

(Homo sapiens)
Allele/Variant
Source: rs2076707794
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223215C>A

(GRCh38)16:75224088C>T

(Homo sapiens)
Allele/Variant
Source: rs922977869
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224088C>T

(GRCh38)16:75224136G>A

(Homo sapiens)
Allele/Variant
Source: rs1468304725
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224136G>A

(GRCh38)16:75224148T>C

(Homo sapiens)
Allele/Variant
Source: rs1941683318
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224148T>C

(GRCh38)16:75224711T>C

(Homo sapiens)
Allele/Variant
Source: rs755026878
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224711T>C

(GRCh38)16:75223580G>T

(Homo sapiens)
Allele/Variant
Source: rs1328058568
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223580G>T