Version: 8.2.0
Date: Wed Aug 27 2025
1,652 results for Samd3

SAMD3

(Homo sapiens)
Gene
Name: sterile alpha motif domain containing 3
Synonyms: MGC35163, SAM domain-containing protein 3, FLJ34563, sterile alpha motif domain-containing protein 3
Source: HGNC:21574
Biotype: protein coding gene
Symbol: SAMD3 (Hsa)
Symbol: SAMD3
Strict Orthology Symbols: Samd3

Samd3

(Mus musculus)
Gene
Name: sterile alpha motif domain containing 3
Synonyms: gene model 623, (NCBI), LOC268288, Gm623
Source: MGI:2685469
Biotype: protein coding gene
Symbol: Samd3 (Mmu)
Symbol: Samd3
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: Samd3
Alleles: Samd3 (Mmu)...Samd3 (Mmu)...Samd3 (Mmu)...Samd3 (Mmu)

Samd3

(Rattus norvegicus)
Gene
Name: sterile alpha motif domain containing 3
Synonyms: LOC685940, similar to sterile alpha motif domain containing 3 isoform a, sterile alpha motif domain-containing protein 3
Source: RGD:1587834
Biotype: protein coding gene
Symbol: Samd3 (Rno)
Symbol: Samd3
Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3); INTERACTS WITH bisphenol A; vinclozolin
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: Samd3

Samd3tm1(HBEGF)Wfkr

(Mus musculus)
Allele/Variant
Source: MGI:7260137
Genes: Samd3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Samd3 (Mmu)
Genes: Samd3 (Mmu)
Symbol: Samd3tm1(HBEGF)Wfkr
Constructs: Samd3< construct

Samd3em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305747
Genes: Samd3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Samd3 (Mmu)
Genes: Samd3 (Mmu)
Symbol: Samd3em1Gpt

Samd3em1(IMPC)H

(Mus musculus)
Allele/Variant
Source: MGI:6293846
Genes: Samd3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Samd3 (Mmu)
Genes: Samd3 (Mmu)
Symbol: Samd3em1(IMPC)H

Samd3tm1.1(HBEGF)Wfkr

(Mus musculus)
Allele/Variant
Source: MGI:7260138
Genes: Samd3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Samd3 (Mmu)
Genes: Samd3 (Mmu)
Symbol: Samd3tm1.1(HBEGF)Wfkr
Constructs: Samd3< construct

Samd3em1(IMPC)H/Samd3em1(IMPC)H [background:] C57BL/6N-Samd3em1(IMPC)H/H

(Mus musculus)
Model
Id: MGI:6731432
Synonyms: Not Available
Symbol: Samd3/Samd3 [background:] C57BL/6N-Samd3/H (Mmu)
Genes: Samd3 (Mmu)
Alleles: Samd3 (Mmu)
Name: Samd3/Samd3 [background:] C57BL/6N-Samd3/H

Samd3-ps1

(Rattus norvegicus)
Gene
Name: sterile alpha motif domain containing 3, pseudogene 1
Synonyms: LOC100361725, rCG57360-like
Source: RGD:2319549
Biotype: pseudogene
Symbol: Samd3-ps1 (Rno)
Symbol: Samd3-ps1

Samd3tm1.1(HBEGF)Wfkr/Samd3+ [background:] C57BL/6J-Samd3tm1.1(HBEGF)Wfkr

(Mus musculus)
Model
Id: MGI:7261153
Synonyms: Not Available
Symbol: Samd3/Samd3<+> [background:] C57BL/6J-Samd3 (Mmu)
Genes: Samd3 (Mmu)
Alleles: Samd3 (Mmu)
Name: Samd3/Samd3<+> [background:] C57BL/6J-Samd3

Samd3tm1.1(HBEGF)Wfkr/Samd3tm1.1(HBEGF)Wfkr [background:] C57BL/6J-Samd3tm1.1(HBEGF)Wfkr

(Mus musculus)
Model
Id: MGI:7261152
Synonyms: Not Available
Symbol: Samd3/Samd3 [background:] C57BL/6J-Samd3 (Mmu)
Genes: Samd3 (Mmu)
Alleles: Samd3 (Mmu)
Name: Samd3/Samd3 [background:] C57BL/6J-Samd3

si:dkeyp-2c8.3

(Danio rerio)
Gene
Name: si:dkeyp-2c8.3
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-081031-97
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: Samd3

si:ch73-42k18.1

(Danio rerio)
Gene
Name: si:ch73-42k18.1
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-141215-12
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: Samd3

si:dkey-34k9.3

(Danio rerio)
Gene
Name: si:dkey-34k9.3
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-070705-460
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: Samd3

si:dkey-21n10.3

(Danio rerio)
Gene
Name: si:dkey-21n10.3
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-070912-444
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: SAMD3

LOC116407561

(Xenopus tropicalis)
Gene
Name: uncharacterized LOC116407561
Synonyms: uncharacterized LOC116407561, LOC116407561
Source: Xenbase:XB-GENE-29092715
Biotype: gene
Automated Gene Synopsis: Orthologous to human SAMD3 (sterile alpha motif domain containing 3).
Strict Orthology Symbols: Samd3

si:ch211-182e10.4

(Danio rerio)
Gene
Name: si:ch211-182e10.4
Synonyms: CH211-182E10.5
Source: ZFIN:ZDB-GENE-041014-76
Biotype: protein coding gene
Strict Orthology Symbols: Samd3

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Samd3 (Mmu)

cellular_component

Gene Ontology
Source: GO:0005575
Synonyms:
  • cell or subcellular entity
  • cellular component
Branch: cellular component
Genes: Samd3 (Mmu)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Samd3 (Mmu)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: SAMD3 (Hsa)

(GRCh38)6:130209536G>A

(Homo sapiens)
Allele/Variant
Source: rs267600802
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130209536G>A

(GRCh38)6:130144771T>G

(Homo sapiens)
Allele/Variant
Source: rs369863649
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144771T>G

(GRCh38)6:130209568C>T

(Homo sapiens)
Allele/Variant
Source: rs371148224
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130209568C>T

(GRCh38)6:130145380A>G

(Homo sapiens)
Allele/Variant
Source: rs1788527354
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130145380A>G

(GRCh38)6:130146115A>G

(Homo sapiens)
Allele/Variant
Source: rs1000039284
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130146115A>G

(GRCh38)6:130214506C>T

(Homo sapiens)
Allele/Variant
Source: rs193004422
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130214506C>T

(GRCh38)6:130184126G>C

(Homo sapiens)
Allele/Variant
Source: rs144450186
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130184126G>C

(GRCh38)6:130144705C>T

(Homo sapiens)
Allele/Variant
Source: rs140284624
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144705C>T

(GRCh38)6:130144677A>G

(Homo sapiens)
Allele/Variant
Source: rs368648301
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144677A>G

(GRCh38)6:130146133T>G

(Homo sapiens)
Allele/Variant
Source: rs749467124
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130146133T>G

(GRCh38)6:130184159C>T

(Homo sapiens)
Allele/Variant
Source: rs746454475
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130184159C>T

(GRCh38)6:130209508C>A

(Homo sapiens)
Allele/Variant
Source: rs112197738
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130209508C>A

(GRCh38)6:130209575C>A

(Homo sapiens)
Allele/Variant
Source: rs138130162
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130209575C>A

(GRCh38)6:130214457A>G

(Homo sapiens)
Allele/Variant
Source: rs143580700
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130214457A>G

(GRCh38)6:130144702C>T

(Homo sapiens)
Allele/Variant
Source: rs201831635
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144702C>T

(GRCh38)6:130184465T>C

(Homo sapiens)
Allele/Variant
Source: rs956208350
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130184465T>C

(GRCh38)6:130175902C>T

(Homo sapiens)
Allele/Variant
Source: rs200849847
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130175902C>T

(GRCh38)6:130209601C>T

(Homo sapiens)
Allele/Variant
Source: rs267600803
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130209601C>T

(GRCh38)6:130144546C>T

(Homo sapiens)
Allele/Variant
Source: rs367601593
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144546C>T

(GRCh38)6:130184534C>G

(Homo sapiens)
Allele/Variant
Source: rs758222319
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130184534C>G

(GRCh38)6:130184615A>G

(Homo sapiens)
Allele/Variant
Source: rs930859093
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130184615A>G

(GRCh38)6:130146035A>T

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.130146035A>T
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130146035A>T

(GRCh38)6:130146036T>A

(Homo sapiens)
Allele/Variant
Source: NC_000006.12:g.130146036T>A
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130146036T>A

(GRCh38)6:130154844A>G

(Homo sapiens)
Allele/Variant
Source: rs775960481
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130154844A>G

(GRCh38)6:130209603C>G

(Homo sapiens)
Allele/Variant
Source: rs1010788005
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130209603C>G

(GRCh38)6:130214400C>T

(Homo sapiens)
Allele/Variant
Source: rs143283725
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130214400C>T

(GRCh38)6:130144542C>T

(Homo sapiens)
Allele/Variant
Source: rs773652776
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144542C>T

(GRCh38)6:130144666A>G

(Homo sapiens)
Allele/Variant
Source: rs767707486
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130144666A>G

(GRCh38)6:130214406G>A

(Homo sapiens)
Allele/Variant
Source: rs139187903
Genes: SAMD3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:130214406G>A