Version: 8.0.0
Date: Tue Jan 28 2025
33 results for tnni2b.2

tnni2b.2

(Danio rerio)
Gene
Name: troponin I type 2b (skeletal, fast), tandem duplicate 2
Synonyms: tropI-2b, zgc:92191
Source: ZFIN:ZDB-GENE-040801-9
Biotype: protein coding gene
Symbol: tnni2b.2 (Dre)
Symbol: tnni2b.2

TNNI2

(Homo sapiens)
Gene
Name: troponin I2, fast skeletal type
Synonyms: fsTnI, FSSV, troponin I, fast-twitch isoform, DA2B, troponin I, fast skeletal muscle, fast-twitch skeletal muscle troponin I, DA2B1, troponin I type 2 (skeletal, fast), troponin I fast twitch 2, AMCD2B, troponin I, skeletal, fast, troponin I, fast-twitch skeletal muscle isoform
Source: HGNC:11946
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

TNNI3

(Homo sapiens)
Gene
Name: troponin I3, cardiac type
Synonyms: cTnI, MGC116817, CMD1FF, TNNC1, CMH7, troponin I type 3 (cardiac), cardiac troponin I, RCM1, familial hypertrophic cardiomyopathy 7, troponin I, cardiac muscle, cardiomyopathy, dilated 2A (autosomal recessive), troponin 1, type 3, CMD2A
Source: HGNC:11947
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

Tnni2

(Rattus norvegicus)
Gene
Name: troponin I2, fast skeletal type
Synonyms: troponin I, fast-twitch isoform, troponin I, fast skeletal muscle, troponin I skeletal fast 2, troponin I type 2 (skeletal, fast), troponin I, skeletal, fast 2, troponin 1, type 2
Source: RGD:62050
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

unc-27

(Caenorhabditis elegans)
Gene
Name: UNCoordinated 27
Synonyms: unc-99, tni-2, ZK721.2, CELE_ZK721.2
Source: WB:WBGene00006764
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

tni-4

(Caenorhabditis elegans)
Gene
Name: TropoNin I 4
Synonyms: W03F8.b, W03F8.1, CELE_W03F8.1
Source: WB:WBGene00006586
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

Tnni3

(Mus musculus)
Gene
Name: troponin I, cardiac 3
Synonyms: cTnI, cTNI, Tn1, TnI, cardiac troponin I
Source: MGI:98783
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

Tnni2

(Mus musculus)
Gene
Name: troponin I, skeletal, fast 2
Synonyms: Not Available
Source: MGI:105070
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

wupA

(Drosophila melanogaster)
Gene
Name: wings up A
Synonyms: HLI, wup-A, DROTROPONI, CG7178, troponin I, haplo-lethal region I, HL08042, flightless-H, hdp2, TpnI, chrX:17947374..17947524, DmTpnI, HDP, Hdp, troponin-I, wings up, hdp-a, HL-I, Tn I, WupA, Troponin-I, wings-up A, held up, heldup, held-up2, TnI, held-up, troponin, Troponin I, fliH, hdp, heldup-a, wupa, flightless H
Source: FB:FBgn0283471
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

Tnni3

(Rattus norvegicus)
Gene
Name: troponin I3, cardiac type
Synonyms: troponin I, cardiac, cTNI, Troponin I, troponin I, cardiac muscle, troponin I cardiac, troponin 1, type 3, TnI, troponin I type 3 (cardiac), cardiac troponin I
Source: RGD:62052
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

tni-1

(Caenorhabditis elegans)
Gene
Name: TropoNin I 1
Synonyms: CELE_F42E11.4, F42E11.4
Source: WB:WBGene00006584
Biotype: protein coding gene
Strict Orthology Symbols: tnni2b.2

tnni2

(Xenopus tropicalis)
Gene
Name: troponin I2, fast skeletal type
Synonyms: TnIf, fssv, fstni, da2b, troponin I2, fast skeletal type, amcd2b, tnni2, fast troponin I
Source: Xenbase:XB-GENE-478629
Biotype: gene
Strict Orthology Symbols: tnni2b.2

distal arthrogryposis type 2B1

Disease
Source: DOID:0111600
Definition: A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in the TNNI2 gene on chromosome 11p15.5.
Genes: tnni2b.2 (Dre)

restrictive cardiomyopathy 1

Disease
Source: DOID:0111425
Definition: A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.42.
Genes: tnni2b.2 (Dre)

dilated cardiomyopathy 2A

Disease
Source: DOID:0110460
Definition: A dilated cardiomyopathy that has_material_basis_in mutation in the TNNI3 gene on chromosome 19q13.
Genes: tnni2b.2 (Dre)

dilated cardiomyopathy 1FF

Disease
Source: DOID:0110459
Definition: A dilated cardiomyopathy that has_material_basis_in mutation in the TNNI3 gene on chromosome 19q13.42.
Genes: tnni2b.2 (Dre)

hypertrophic cardiomyopathy 7

Disease
Source: DOID:0110313
Definition: A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
Genes: tnni2b.2 (Dre)

arthrogryposis multiplex congenita

Disease
Source: DOID:0080954
Definition: A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth.
Genes: tnni2b.2 (Dre)

troponin complex

Gene Ontology
Source: GO:0005861
Synonyms: Not Available
Branch: cellular component
Genes: tnni2b.2 (Dre)

skeletal muscle contraction

Gene Ontology
Source: GO:0003009
Synonyms: Not Available
Branch: biological process
Genes: tnni2b.2 (Dre)

adenocarcinoma

Disease
Source: DOID:299
Definition: A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from epithelial cells, which originate in glandular tissue.
Genes: tnni2b.2 (Dre)

restrictive cardiomyopathy

Disease
Source: DOID:397
Definition: An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium.
Genes: tnni2b.2 (Dre)

distal arthrogryposis

Disease
Source: DOID:0050646
Definition: A muscle tissue disease characterized by congenital joint contractures of hand and feet.
Genes: tnni2b.2 (Dre)

cardiac muscle contraction

Gene Ontology
Source: GO:0060048
Synonyms:
  • heart muscle contraction
Branch: biological process
Genes: tnni2b.2 (Dre)

heart disease

Disease
Source: DOID:114
Definition: A cardiovascular system disease that involves the heart.
Genes: tnni2b.2 (Dre)

hypertrophic cardiomyopathy

Disease
Source: DOID:11984
Definition: An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause.
Genes: tnni2b.2 (Dre)

cardiomyopathy

Disease
Source: DOID:0050700
Definition: A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle.
Genes: tnni2b.2 (Dre)

dilated cardiomyopathy

Disease
Source: DOID:12930
Definition: An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently.
Genes: tnni2b.2 (Dre)

coronary artery disease

Disease
Source: DOID:3393
Definition: An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles.
Genes: tnni2b.2 (Dre)

sa17285

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-13421
Genes: tnni2b.2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: tnni2b.2 (Dre)

sa38632

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-16084
Genes: tnni2b.2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: tnni2b.2 (Dre)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: tnni2b.2 (Dre)

actin binding

Gene Ontology
Source: GO:0003779
Synonyms:
  • membrane associated actin binding
Branch: molecular function
Genes: tnni2b.2 (Dre)