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Category

1,099 results for hdhd2

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HDHD2

(Homo sapiens)

Gene

Name: haloacid dehalogenase like hydrolase domain containing 2

Synonyms: epididymis secretory protein Li 301, haloacid dehalogenase-like hydrolase domain-containing protein 2, HEL-S-301, 3110052N05Rik, DKFZP564D1378

Source: HGNC:25364

Biotype: protein coding gene

Symbol: HDHD2 (Hsa)

Symbol: HDHD2

Strict Orthology Symbols: hdhd2

Allele/Variant (13)

Hdhd2

(Mus musculus)

Gene

Name: haloacid dehalogenase-like hydrolase domain containing 2

Synonyms: RIKEN cDNA 0610039H12 gene, Ier3ip1, LRRG00122, RGD1308579, 3110052N05Rik, 0610039H12Rik, RIKEN cDNA 3110052N05 gene

Source: MGI:1924237

Biotype: protein coding gene

Symbol: Hdhd2 (Mmu)

Symbol: Hdhd2

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Strict Orthology Symbols: hdhd2

Alleles: Hdhd2 (Mmu)...Hdhd2 (Mmu)...Hdhd2 (Mmu)...Hdhd2 (Mmu)

hdhd2

(Danio rerio)

Gene

Name: haloacid dehalogenase-like hydrolase domain containing 2

Synonyms: zgc:110332

Source: ZFIN:ZDB-GENE-050320-37

Biotype: protein coding gene

Symbol: hdhd2 (Dre)

Symbol: hdhd2

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Strict Orthology Symbols: hdhd2

Allele/Variant (1)

Hdhd2

(Rattus norvegicus)

Gene

Name: haloacid dehalogenase-like hydrolase domain containing 2

Synonyms: immediate early response 3-interacting protein 1, haloacid dehalogenase-like hydrolase domain-containing protein 2, Ier3ip1, similar to RIKEN cDNA 3110052N05, LRRG00122, RGD1308579, LOC361351

Source: RGD:1308579

Biotype: protein coding gene

Symbol: Hdhd2 (Rno)

Symbol: Hdhd2

Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2); INTERACTS WITH

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Strict Orthology Symbols: hdhd2

Allele/Variant (108)

hdhd2

(Xenopus tropicalis)

Gene

Name: haloacid dehalogenase like hydrolase domain containing 2

Synonyms: hdhd2, haloacid dehalogenase like hydrolase domain containing 2

Source: Xenbase:XB-GENE-977915

Biotype: gene

Symbol: hdhd2

Symbol: hdhd2 (Xtr)

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Synonyms: hdhd2...hdhd2...hdhd2

Strict Orthology Symbols: hdhd2

hdhd2.L

(Xenopus laevis)

Gene

Name: haloacid dehalogenase like hydrolase domain containing 2

Synonyms: hdhd2.L, haloacid dehalogenase like hydrolase domain containing 2

Source: Xenbase:XB-GENE-6487569

Biotype: gene

Symbol: hdhd2.L (Xla)

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Strict Orthology Symbols: hdhd2

Symbol: hdhd2.L

Hdhd2^em2Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7300193

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hdhd2 (Mmu)

Genes: Hdhd2 (Mmu)

Symbol: Hdhd2^em2Gpt

Gene (1)

Hdhd2^{Tn(sb-Tyr)1799B.CA8Ove}

(Mus musculus)

Allele/Variant

Source: MGI:5300462

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hdhd2 (Mmu)

Genes: Hdhd2 (Mmu)

Symbol: Hdhd2^{Tn(sb-Tyr)1799B.CA8Ove}

Hdhd2^{Gt(OST364697)Lex}

(Mus musculus)

Allele/Variant

Source: MGI:4295178

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hdhd2 (Mmu)

Genes: Hdhd2 (Mmu)

Symbol: Hdhd2^{Gt(OST364697)Lex}

Gene (1)

Hdhd2^em1Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7300192

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hdhd2 (Mmu)

Genes: Hdhd2 (Mmu)

Symbol: Hdhd2^em1Gpt

Gene (1)

Hdhd2^{Tn(sb-Tyr)1799B.CA8Ove}/Hdhd2^{Tn(sb-Tyr)1799B.CA8Ove} [background:] involves: FVB/N

(Mus musculus)

Model

Id: MGI:5300512

Synonyms: Not Available

Symbol: Hdhd2/Hdhd2 [background:] involves: FVB/N (Mmu)

Genes: Hdhd2 (Mmu)

Alleles: Hdhd2 (Mmu)

Name: Hdhd2

/Hdhd2

[background:] involves: FVB/N

Gene (1)

CG17294

(Drosophila melanogaster)

Gene

Name: Not Available

Synonyms: Phos17294, 15010468

Source: FB:FBgn0032032

Biotype: protein coding gene

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Strict Orthology Symbols: hdhd2

Allele/Variant (65)

K08B12.3

(Caenorhabditis elegans)

Gene

Name: Haloacid dehalogenase-like hydrolase domain-containing protein 2

Synonyms: CELE_K08B12.3

Source: WB:WBGene00019522

Biotype: protein coding gene

Gene Synopsis: Is an ortholog of human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Automated Gene Synopsis: Orthologous to human HDHD2 (haloacid dehalogenase like hydrolase domain containing 2).

Strict Orthology Symbols: hdhd2

Allele/Variant (33)

Ier3ip1

(Mus musculus)

Gene

Name: immediate early response 3 interacting protein 1

Synonyms: 1110057H19Rik, expressed sequence AI644142, LRRG00122, RGD1308579, AL022863, RIKEN cDNA 1110057H19 gene, AL022842, expressed sequence AL022863, expressed sequence AL022842, AV026606, expressed sequence AV026606, AI644142

Source: MGI:1913441

Biotype: protein coding gene

Strict Orthology Symbols: Hdhd2

ier3ip1

(Danio rerio)

Gene

Name: immediate early response 3 interacting protein 1

Synonyms: HSPC039, zgc:112367, im:6906551

Source: ZFIN:ZDB-GENE-050506-106

Biotype: protein coding gene

Strict Orthology Symbols: Hdhd2

Model (2)

CG32069

(Drosophila melanogaster)

Gene

Name: Not Available

Synonyms: CG6316

Source: FB:FBgn0052069

Biotype: protein coding gene

Strict Orthology Symbols: Hdhd2

Allele/Variant (21)

W09G3.8

(Caenorhabditis elegans)

Gene

Name: Immediate early response 3-interacting protein 1

Synonyms: CELE_W09G3.8

Source: WB:WBGene00012371

Biotype: protein coding gene

Strict Orthology Symbols: Hdhd2

Allele/Variant (17)

YOS1

(Saccharomyces cerevisiae)

Gene

Name: Yip One Suppressor

Synonyms: YER074W-A

Source: SGD:S000007651

Biotype: protein coding gene

Strict Orthology Symbols: Hdhd2

Allele/Variant (9)

phosphatase activity

Gene Ontology

Source: GO:0016791

Synonyms:

phosphatase
phosphoric monoester hydrolase activity

Branch: molecular function

Genes: hdhd2 (Dre)...Hdhd2 (Mmu)...Hdhd2 (Rno)...HDHD2 (Hsa)

Genes Annotated with this GO Term (1715)

dephosphorylation

Gene Ontology

Source: GO:0016311

Synonyms: Not Available

Branch: biological process

Genes: hdhd2 (Dre)

Genes Annotated with this GO Term (900)

enzyme binding

Gene Ontology

Source: GO:0019899

Synonyms: Not Available

Branch: molecular function

Genes: Hdhd2 (Mmu)...Hdhd2 (Rno)...HDHD2 (Hsa)

Genes Annotated with this GO Term (8435)

sa9783

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-130411-5374

Genes: hdhd2 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: hdhd2 (Dre)

protein transport

Gene Ontology

Source: GO:0015031

Synonyms:

enzyme transport

Branch: biological process

Genes: Hdhd2 (Rno)

Genes Annotated with this GO Term (5253)

extracellular exosome

Gene Ontology

Source: GO:0070062

Synonyms:

exosome
extracellular vesicular exosome

Branch: cellular component

Genes: HDHD2 (Hsa)

Genes Annotated with this GO Term (2517)

metal ion binding

Gene Ontology

Source: GO:0046872

Synonyms:

heavy metal binding
metal binding

Branch: molecular function

Genes: HDHD2 (Hsa)...hdhd2 (Dre)...Hdhd2 (Mmu)...Hdhd2 (Rno)

Genes Annotated with this GO Term (10000)

hydrolase activity

Gene Ontology

Source: GO:0016787

Synonyms: Not Available

Branch: molecular function

Genes: hdhd2 (Dre)

Genes Annotated with this GO Term (10000)

cytoplasm

Gene Ontology

Source: GO:0005737

Synonyms: Not Available

Branch: cellular component

Genes: hdhd2 (Dre)...HDHD2 (Hsa)...Hdhd2 (Mmu)...Hdhd2 (Rno)

Genes Annotated with this GO Term (10000)

cellular_component

Gene Ontology

Source: GO:0005575

Synonyms:

cell or subcellular entity
cellular component

Branch: cellular component

Genes: hdhd2 (Dre)

Genes Annotated with this GO Term (10000)

(GRCh38)18:47136402T>A

(Homo sapiens)

Allele/Variant

Source: rs777403004

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47136402T>A

(GRCh38)18:47115196G>T

(Homo sapiens)

Allele/Variant

Source: rs374879684

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47115196G>T

(GRCh38)18:47130295A>G

(Homo sapiens)

Allele/Variant

Source: rs374727760

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47130295A>G

(GRCh38)18:47136382T>C

(Homo sapiens)

Allele/Variant

Source: rs567505755

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47136382T>C

(GRCh38)18:47115137C>T

(Homo sapiens)

Allele/Variant

Source: NC_000018.10:g.47115137C>T

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47115137C>T

(GRCh38)18:47115215C>T

(Homo sapiens)

Allele/Variant

Source: rs193082755

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47115215C>T

(GRCh38)18:47115284C>T

(Homo sapiens)

Allele/Variant

Source: rs199745448

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47115284C>T

(GRCh38)18:47115218C>T

(Homo sapiens)

Allele/Variant

Source: rs1239085552

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47115218C>T

(GRCh38)18:47130245G>A

(Homo sapiens)

Allele/Variant

Source: rs200669234

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, coding_sequence_variant, incomplete_terminal_codon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47130245G>A

(GRCh38)18:47130304G>A

(Homo sapiens)

Allele/Variant

Source: rs143862755

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47130304G>A

(GRCh38)18:47134588A>G

(Homo sapiens)

Allele/Variant

Source: rs750228968

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47134588A>G

(GRCh38)18:47115242A>G

(Homo sapiens)

Allele/Variant

Source: rs1393699347

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47115242A>G

(GRCh38)18:47134630C>T

(Homo sapiens)

Allele/Variant

Source: rs757468260

Genes: HDHD2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)18:47134630C>T

(GRCm39)18:77032013G>C

(Mus musculus)

Allele/Variant

Source: rs257192527

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 5_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77032013G>C

(GRCm39)18:77059532G>C

(Mus musculus)

Allele/Variant

Source: rs243133462

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77059532G>C

(GRCm39)18:77059590A>G

(Mus musculus)

Allele/Variant

Source: rs864300242

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77059590A>G

(GRCm39)18:77059780A>C

(Mus musculus)

Allele/Variant

Source: rs232414937

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77059780A>C

(GRCm39)18:77061657T>C

(Mus musculus)

Allele/Variant

Source: rs50902924

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77061657T>C

(GRCm39)18:77061958A>G

(Mus musculus)

Allele/Variant

Source: rs48928891

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77061958A>G

(GRCm39)18:77061191G>A

(Mus musculus)

Allele/Variant

Source: rs259536319

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77061191G>A

(GRCm39)18:77061585C>T

(Mus musculus)

Allele/Variant

Source: rs239167036

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77061585C>T

(GRCm39)18:77059415A>G

(Mus musculus)

Allele/Variant

Source: rs219531053

Genes: Hdhd2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCm39)18:77059415A>G

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