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Category

97 results for hspb2

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HSPB2

(Homo sapiens)

Gene

Name: heat shock protein family B (small) member 2

Synonyms: LOH11CR1K, heat shock 27kD protein 2, heat shock protein family B member 2, MGC133245, HSP27, Hs.78846, MKBP, heat shock 27kDa protein 2, heat shock protein beta-2, DMPK-binding protein, heat-shock protein beta-2

Source: HGNC:5247

Biotype: protein coding gene

Symbol: HSPB2 (Hsa)

Symbol: HSPB2

Strict Orthology Symbols: hspb2

Allele/Variant (8)

hspb2

(Danio rerio)

Gene

Name: heat shock protein, alpha-crystallin-related, b2

Synonyms: zgc:112532

Source: ZFIN:ZDB-GENE-050417-260

Biotype: protein coding gene

Symbol: hspb2 (Dre)

Symbol: hspb2

Automated Gene Synopsis: Orthologous to human HSPB2 (heat shock protein family B (small) member 2).

Strict Orthology Symbols: hspb2

Hspb2

(Mus musculus)

Gene

Name: heat shock protein 2

Synonyms: 2810021G24Rik, RIKEN cDNA 2810021G24 gene, HSP27, MKBP, 27kDa

Source: MGI:1916503

Biotype: protein coding gene

Symbol: Hspb2 (Mmu)

Symbol: Hspb2

Automated Gene Synopsis: Orthologous to human HSPB2 (heat shock protein family B (small) member 2).

Strict Orthology Symbols: hspb2

Alleles: Hspb2 (Mmu)...Hspb2 (Mmu)...Hspb2 (Mmu)...Hspb2 (Mmu)...Hspb2 (Mmu)

Hspb2

(Rattus norvegicus)

Gene

Name: heat shock protein family B (small) member 2

Synonyms: heat shock protein beta 2, heat shock 27kD protein 2, heat shock protein 2, heat shock protein B2, heat shock 27kDa protein 2, heat shock protein beta-2

Source: RGD:70914

Biotype: protein coding gene

Symbol: Hspb2 (Rno)

Symbol: Hspb2

Gene Synopsis: Orthologous to human HSPB2 (heat shock protein family B (small) member 2); INTERACTS WITH 1-naphthyl

Automated Gene Synopsis: Orthologous to human HSPB2 (heat shock protein family B (small) member 2).

Strict Orthology Symbols: hspb2

Allele/Variant (30)

hspb2

(Xenopus tropicalis)

Gene

Name: heat shock protein family B (small) member 2

Synonyms: heat shock protein family B (small) member 2, hspb2

Source: Xenbase:XB-GENE-940436

Biotype: gene

Symbol: hspb2

Symbol: hspb2 (Xtr)

Automated Gene Synopsis: Orthologous to human HSPB2 (heat shock protein family B (small) member 2).

Synonyms: hspb2...hspb2...hspb2

Strict Orthology Symbols: hspb2

HSPB2-C11orf52

(Homo sapiens)

Gene

Name: HSPB2-C11orf52 readthrough (NMD candidate)

Synonyms: C11orf52, FLJ77220, MGC131888

Source: HGNC:41996

Biotype: ncRNA gene

Symbol: HSPB2-C11orf52 (Hsa)

Gene Synopsis: transcript is a candidate for nonsense-mediated mRNA decay (NMD) based on the use of the supported HSPB2

Symbol: HSPB2-C11orf52

Allele/Variant (9)

hspb2.L

(Xenopus laevis)

Gene

Name: heat shock protein family B (small) member 2

Synonyms: heat shock protein family B (small) member 2, hspb2.L

Source: Xenbase:XB-GENE-6488821

Biotype: gene

Symbol: hspb2.L (Xla)

Automated Gene Synopsis: Orthologous to human HSPB2 (heat shock protein family B (small) member 2).

Strict Orthology Symbols: hspb2

Symbol: hspb2.L

Hspb2^{tm1(KOMP)Vlcg}

(Mus musculus)

Allele/Variant

Source: MGI:4452922

Genes: Hspb2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hspb2 (Mmu)

Genes: Hspb2 (Mmu)

Symbol: Hspb2^{tm1(KOMP)Vlcg}

Gene (1)

Hspb2^{tm1.1(KOMP)Vlcg}

(Mus musculus)

Allele/Variant

Source: MGI:5445926

Genes: Hspb2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hspb2 (Mmu)

Genes: Hspb2 (Mmu)

Symbol: Hspb2^{tm1.1(KOMP)Vlcg}

Hspb2^tm1.1Ijb

(Mus musculus)

Allele/Variant

Source: MGI:5447475

Genes: Hspb2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hspb2 (Mmu)

Genes: Hspb2 (Mmu)

Symbol: Hspb2^tm1.1Ijb

Hspb2^emSmoc

(Mus musculus)

Allele/Variant

Source: MGI:7290269

Genes: Hspb2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hspb2 (Mmu)

Genes: Hspb2 (Mmu)

Symbol: Hspb2^emSmoc

Gene (1)

Hspb2^em1Cya

(Mus musculus)

Allele/Variant

Source: MGI:7584373

Genes: Hspb2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hspb2 (Mmu)

Genes: Hspb2 (Mmu)

Symbol: Hspb2^em1Cya

Gene (1)

Hspb2^em1Smoc

(Mus musculus)

Allele/Variant

Source: MGI:7766196

Genes: Hspb2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hspb2 (Mmu)

Genes: Hspb2 (Mmu)

Symbol: Hspb2^em1Smoc

Gene (1)

Hspb2^{tm1.1(KOMP)Vlcg}/Hspb2^{tm1.1(KOMP)Vlcg} [background:] C57BL/6N-Hspb2^{tm1.1(KOMP)Vlcg}/J

(Mus musculus)

Model

Id: MGI:5631209

Synonyms: Not Available

Symbol: Hspb2/Hspb2 [background:] C57BL/6N-Hspb2/J (Mmu)

Genes: Hspb2 (Mmu)

Alleles: Hspb2 (Mmu)

Name: Hspb2/Hspb2 [background:] C57BL/6N-Hspb2/J

Gene (1)

Hspb2^tm1.1Ijb/Hspb2^tm1.1Ijb [background:] involves: 129S4/SvJaeSor * FVB

(Mus musculus)

Model

Id: MGI:5447480

Synonyms: Not Available

Symbol: Hspb2/Hspb2 [background:] involves: 129S4/SvJaeSor * FVB (Mmu)

Genes: Hspb2 (Mmu)

Alleles: Hspb2 (Mmu)

Name: Hspb2/Hspb2 [background:] involves: 129S4/SvJaeSor * FVB

Gene (1)

hsp-12.2

(Caenorhabditis elegans)

Gene

Name: Heat Shock Protein 12.2

Synonyms: CELE_C14B9.1, C14B9.1

Source: WB:WBGene00002011

Biotype: protein coding gene

Strict Orthology Symbols: hspb2

hsp-12.1

(Caenorhabditis elegans)

Gene

Name: Heat Shock Protein 12.1

Synonyms: T22A3.2, CELE_T22A3.2

Source: WB:WBGene00011906

Biotype: protein coding gene

Strict Orthology Symbols: hspb2

somatic muscle development

Gene Ontology

Source: GO:0007525

Synonyms: Not Available

Branch: biological process

Genes: HSPB2 (Hsa)...Hspb2 (Mmu)...Hspb2 (Rno)

Genes Annotated with this GO Term (130)

structural constituent of eye lens

Gene Ontology

Source: GO:0005212

Synonyms: Not Available

Branch: molecular function

Genes: HSPB2 (Hsa)...Hspb2 (Mmu)...hspb2 (Dre)...Hspb2 (Rno)

Genes Annotated with this GO Term (143)

protein refolding

Gene Ontology

Source: GO:0042026

Synonyms:

heat shock protein activity

Branch: biological process

Genes: HSPB2 (Hsa)...Hspb2 (Mmu)...hspb2 (Dre)...Hspb2 (Rno)

Genes Annotated with this GO Term (186)

response to heat

Gene Ontology

Source: GO:0009408

Synonyms:

response to heat shock

Branch: biological process

Genes: Hspb2 (Mmu)...hspb2 (Dre)...HSPB2 (Hsa)...Hspb2 (Rno)

Genes Annotated with this GO Term (577)

unfolded protein binding

Gene Ontology

Source: GO:0051082

Synonyms:

chaperone activity

Branch: molecular function

Genes: hspb2 (Dre)...HSPB2 (Hsa)...Hspb2 (Rno)...Hspb2 (Mmu)

Genes Annotated with this GO Term (599)

response to unfolded protein

Gene Ontology

Source: GO:0006986

Synonyms:

heat shock protein activity

Branch: biological process

Genes: HSPB2 (Hsa)

Genes Annotated with this GO Term (659)

enzyme activator activity

Gene Ontology

Source: GO:0008047

Synonyms:

metalloenzyme activator activity

Branch: molecular function

Genes: HSPB2 (Hsa)

Genes Annotated with this GO Term (2644)

negative regulation of apoptotic process

Gene Ontology

Source: GO:0043066

Synonyms:

anti-apoptosis
apoptosis inhibitor activity

Branch: biological process

Genes: HSPB2 (Hsa)...Hspb2 (Mmu)...Hspb2 (Rno)...hspb2 (Dre)

Genes Annotated with this GO Term (3523)

nucleus

Gene Ontology

Source: GO:0005634

Synonyms:

cell nucleus
horsetail nucleus

Branch: cellular component

Genes: Hspb2 (Mmu)...HSPB2 (Hsa)...hspb2 (Dre)...Hspb2 (Rno)

Genes Annotated with this GO Term (10000)

cytoplasm

Gene Ontology

Source: GO:0005737

Synonyms: Not Available

Branch: cellular component

Genes: Hspb2 (Mmu)...HSPB2 (Hsa)...hspb2 (Dre)...Hspb2 (Rno)

Genes Annotated with this GO Term (10000)

molecular_function

Gene Ontology

Source: GO:0003674

Synonyms:

molecular function

Branch: molecular function

Genes: hspb2 (Dre)

Genes Annotated with this GO Term (10000)

(mRatBN7.2)8:51089802C>A

(Rattus norvegicus)

Allele/Variant

Source: rs197125222

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51089802C>A

(mRatBN7.2)8:51090222C>A

(Rattus norvegicus)

Allele/Variant

Source: rs3321377343

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51090222C>A

(mRatBN7.2)8:51092852C>T

(Rattus norvegicus)

Allele/Variant

Source: rs105170591

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51092852C>T

(mRatBN7.2)8:51089221A>G

(Rattus norvegicus)

Allele/Variant

Source: rs107030812

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51089221A>G

(mRatBN7.2)8:51091367T>C

(Rattus norvegicus)

Allele/Variant

Source: rs197906051

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51091367T>C

(mRatBN7.2)8:51092854A>C

(Rattus norvegicus)

Allele/Variant

Source: rs106901041

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51092854A>C

(mRatBN7.2)8:51090219C>G

(Rattus norvegicus)

Allele/Variant

Source: rs3321266045

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51090219C>G

(mRatBN7.2)8:51093411G>A

(Rattus norvegicus)

Allele/Variant

Source: rs8146269

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51093411G>A

(mRatBN7.2)8:51092844T>C

(Rattus norvegicus)

Allele/Variant

Source: rs105387827

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51092844T>C

(mRatBN7.2)8:51088957C>T

(Rattus norvegicus)

Allele/Variant

Source: rs197719194

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51088957C>T

(mRatBN7.2)8:51090019C>T

(Rattus norvegicus)

Allele/Variant

Source: rs3321313915

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51090019C>T

(mRatBN7.2)8:51092446G>A

(Rattus norvegicus)

Allele/Variant

Source: rs105084582

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51092446G>A

(mRatBN7.2)8:51093267G>C

(Rattus norvegicus)

Allele/Variant

Source: rs8152074

Genes: Hspb2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51093267G>C

(GRCh38)11:111913878G>A

(Homo sapiens)

Allele/Variant

Source: rs146155375

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111913878G>A

(GRCh38)11:111913650C>T

(Homo sapiens)

Allele/Variant

Source: rs782717759

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111913650C>T

(GRCh38)11:111912851C>T

(Homo sapiens)

Allele/Variant

Source: rs1965509398

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111912851C>T

(GRCh38)11:111912852A>G

(Homo sapiens)

Allele/Variant

Source: rs782199553

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111912852A>G

(GRCh38)11:111913677G>A

(Homo sapiens)

Allele/Variant

Source: rs4252589

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111913677G>A

(GRCh38)11:111913683G>A

(Homo sapiens)

Allele/Variant

Source: rs781794984

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111913683G>A

(GRCh38)11:111913801A>G

(Homo sapiens)

Allele/Variant

Source: rs782241905

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111913801A>G

(GRCh38)11:111912839C>A

(Homo sapiens)

Allele/Variant

Source: rs1965509144

Genes: CRYAB (Hsa), HSPB2 (Hsa), HSPB2-C11orf52 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)11:111912839C>A

(mRatBN7.2)8:51087185T>C

(Rattus norvegicus)

Allele/Variant

Source: rs198408263

Genes: Hspb2 (Rno), C8h11orf52 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)8:51087185T>C

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