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Category

389 results for mansc4

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Mansc4

(Mus musculus)

Gene

Name: MANSC domain containing 4

Synonyms: predicted gene, EG545893, Gm5887, predicted gene 5887, EG545893

Source: MGI:3645619

Biotype: protein coding gene

Symbol: Mansc4 (Mmu)

Symbol: Mansc4

Automated Gene Synopsis: Orthologous to human MANSC4 (MANSC domain containing 4).

Strict Orthology Symbols: mansc4

Alleles: Mansc4 (Mmu)...Mansc4 (Mmu)

Mansc4

(Rattus norvegicus)

Gene

Name: MANSC domain containing 4

Synonyms: hypothetical protein LOC691362, MANSC domain-containing protein 4, LOC691362

Source: RGD:1585055

Biotype: protein coding gene

Symbol: Mansc4 (Rno)

Symbol: Mansc4

Gene Synopsis: Orthologous to human MANSC4 (MANSC domain containing 4); INTERACTS WITH 6-propyl-2-thiouracil; bisphenol

Automated Gene Synopsis: Orthologous to human MANSC4 (MANSC domain containing 4).

Strict Orthology Symbols: mansc4

Allele/Variant (40)

MANSC4

(Homo sapiens)

Gene

Name: MANSC domain containing 4

Synonyms: MANSC domain-containing protein ENSP00000370673, MANSC domain-containing protein 4

Source: HGNC:40023

Biotype: protein coding gene

Symbol: MANSC4 (Hsa)

Symbol: MANSC4

Strict Orthology Symbols: mansc4

Allele/Variant (18)

mansc4

(Xenopus tropicalis)

Gene

Name: MANSC domain containing 4

Synonyms: mansc4, MANSC domain containing 4

Source: Xenbase:XB-GENE-22068717

Biotype: gene

Symbol: mansc4 (Xtr)

Symbol: mansc4

Automated Gene Synopsis: Orthologous to human MANSC4 (MANSC domain containing 4).

Synonyms: mansc4...mansc4...mansc4

Strict Orthology Symbols: Mansc4...MANSC4

Mansc4^{tm1a(KOMP)Wtsi}

(Mus musculus)

Allele/Variant

Source: MGI:4947759

Genes: Mansc4 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Mansc4 (Mmu)

Genes: Mansc4 (Mmu)

Symbol: Mansc4^{tm1a(KOMP)Wtsi}

Gene (1)

Mansc4^{tm1b(KOMP)Wtsi}

(Mus musculus)

Allele/Variant

Source: MGI:6120810

Genes: Mansc4 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Mansc4 (Mmu)

Genes: Mansc4 (Mmu)

Symbol: Mansc4^{tm1b(KOMP)Wtsi}

Mansc4^{tm1b(KOMP)Wtsi}/Mansc4^{tm1b(KOMP)Wtsi} [background:] C57BL/6N-Mansc4^{tm1b(KOMP)Wtsi}/Wtsi

(Mus musculus)

Model

Id: MGI:6461419

Synonyms: Not Available

Symbol: Mansc4/Mansc4 [background:] C57BL/6N-Mansc4/Wtsi (Mmu

Genes: Mansc4 (Mmu)

Alleles: Mansc4 (Mmu)

Name: Mansc4/Mansc4 [background:] C57BL/6N-Mansc4/Wtsi

Gene (1)

epithelium development

Gene Ontology

Source: GO:0060429

Synonyms: Not Available

Branch: biological process

Genes: Mansc4 (Mmu)...Mansc4 (Rno)...MANSC4 (Hsa)

Genes Annotated with this GO Term (5641)

epidermis development

Gene Ontology

Source: GO:0008544

Synonyms:

hypodermis development

Branch: biological process

Genes: Mansc4 (Mmu)...Mansc4 (Rno)...MANSC4 (Hsa)

Genes Annotated with this GO Term (1323)

serine-type endopeptidase inhibitor activity

Gene Ontology

Source: GO:0004867

Synonyms:

serine protease inhibitor activity
serine proteinase inhibitor activity

Branch: molecular function

Genes: Mansc4 (Mmu)...Mansc4 (Rno)...MANSC4 (Hsa)

Genes Annotated with this GO Term (581)

extracellular matrix organization

Gene Ontology

Source: GO:0030198

Synonyms:

extracellular matrix organisation
extracellular matrix organization and biogenesis

Branch: biological process

Genes: Mansc4 (Mmu)...Mansc4 (Rno)...MANSC4 (Hsa)

Genes Annotated with this GO Term (1188)

plasma membrane

Gene Ontology

Source: GO:0005886

Synonyms:

bacterial inner membrane
cell membrane

Branch: cellular component

Genes: Mansc4 (Mmu)...MANSC4 (Hsa)...Mansc4 (Rno)

Genes Annotated with this GO Term (10000)

membrane

Gene Ontology

Source: GO:0016020

Synonyms:

integral component of membrane
integral to membrane

Branch: cellular component

Genes: MANSC4 (Hsa)...Mansc4 (Mmu)

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: Mansc4 (Mmu)

Genes Annotated with this GO Term (10000)

biological_process

Gene Ontology

Source: GO:0008150

Synonyms:

biological process
physiological process

Branch: biological process

Genes: Mansc4 (Mmu)

Genes Annotated with this GO Term (10000)

molecular_function

Gene Ontology

Source: GO:0003674

Synonyms:

molecular function

Branch: molecular function

Genes: Mansc4 (Mmu)

Genes Annotated with this GO Term (10000)

(GRCh38)12:27763043C>T

(Homo sapiens)

Allele/Variant

Source: rs796592150

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763043C>T

(GRCh38)12:27762866C>T

(Homo sapiens)

Allele/Variant

Source: rs943061681

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27762866C>T

(GRCh38)12:27763022G>T

(Homo sapiens)

Allele/Variant

Source: NC_000012.12:g.27763022G>T

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763022G>T

(GRCh38)12:27771107T>C

(Homo sapiens)

Allele/Variant

Source: rs1317155701

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27771107T>C

(GRCh38)12:27762817C>G

(Homo sapiens)

Allele/Variant

Source: rs369103921

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27762817C>G

(GRCh38)12:27762920T>C

(Homo sapiens)

Allele/Variant

Source: rs934253899

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27762920T>C

(GRCh38)12:27762979T>C

(Homo sapiens)

Allele/Variant

Source: rs187627523

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27762979T>C

(GRCh38)12:27763309A>G

(Homo sapiens)

Allele/Variant

Source: rs778736951

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763309A>G

(GRCh38)12:27763022G>A

(Homo sapiens)

Allele/Variant

Source: rs527342988

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763022G>A

(GRCh38)12:27763228G>A

(Homo sapiens)

Allele/Variant

Source: rs376492706

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763228G>A

(GRCh38)12:27771215T>A

(Homo sapiens)

Allele/Variant

Source: rs1304474569

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27771215T>A

(GRCh38)12:27762802C>T

(Homo sapiens)

Allele/Variant

Source: rs2062052972

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27762802C>T

(GRCh38)12:27762829C>A

(Homo sapiens)

Allele/Variant

Source: rs979159128

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27762829C>A

(GRCh38)12:27763231G>A

(Homo sapiens)

Allele/Variant

Source: rs371286460

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763231G>A

(GRCh38)12:27763325A>G

(Homo sapiens)

Allele/Variant

Source: NC_000012.12:g.27763325A>G

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763325A>G

(GRCh38)12:27763342C>T

(Homo sapiens)

Allele/Variant

Source: rs367849450

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27763342C>T

(GRCh38)12:27766751A>G

(Homo sapiens)

Allele/Variant

Source: rs1466416424

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27766751A>G

(GRCh38)12:27771082C>G

(Homo sapiens)

Allele/Variant

Source: rs1356918768

Genes: MANSC4 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (GRCh38)12:27771082C>G

(mRatBN7.2)4:179999777A>C

(Rattus norvegicus)

Allele/Variant

Source: rs198007281

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179999777A>C

(mRatBN7.2)4:179991916C>A

(Rattus norvegicus)

Allele/Variant

Source: rs197183955

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179991916C>A

(mRatBN7.2)4:179996101G>A

(Rattus norvegicus)

Allele/Variant

Source: rs197203328

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179996101G>A

(mRatBN7.2)4:180000026T>C

(Rattus norvegicus)

Allele/Variant

Source: rs105400734

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:180000026T>C

(mRatBN7.2)4:180000057A>G

(Rattus norvegicus)

Allele/Variant

Source: rs3320430961

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:180000057A>G

(mRatBN7.2)4:179996762C>A

(Rattus norvegicus)

Allele/Variant

Source: rs106715106

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179996762C>A

(mRatBN7.2)4:179997208G>A

(Rattus norvegicus)

Allele/Variant

Source: rs105103423

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179997208G>A

(mRatBN7.2)4:179992484T>C

(Rattus norvegicus)

Allele/Variant

Source: rs197839116

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179992484T>C

(mRatBN7.2)4:179992965A>G

(Rattus norvegicus)

Allele/Variant

Source: rs197104284

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179992965A>G

(mRatBN7.2)4:179993626G>T

(Rattus norvegicus)

Allele/Variant

Source: rs198765534

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179993626G>T

(mRatBN7.2)4:179997661T>C

(Rattus norvegicus)

Allele/Variant

Source: rs3320443530

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179997661T>C

(mRatBN7.2)4:179993996G>A

(Rattus norvegicus)

Allele/Variant

Source: rs197517876

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179993996G>A

(mRatBN7.2)4:179997062G>A

(Rattus norvegicus)

Allele/Variant

Source: rs105871962

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179997062G>A

(mRatBN7.2)4:179997415G>A

(Rattus norvegicus)

Allele/Variant

Source: rs3320421913

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179997415G>A

(mRatBN7.2)4:179999694G>T

(Rattus norvegicus)

Allele/Variant

Source: rs3320447989

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:179999694G>T

(mRatBN7.2)4:180001009A>G

(Rattus norvegicus)

Allele/Variant

Source: rs3320421947

Genes: Mansc4 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 5_prime_UTR_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)4:180001009A>G

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