Version: 8.0.0Date: Tue Jan 28 2025
Category
SCMH1
(Homo sapiens)Gene
Name: Scm polycomb group protein homolog 1
Synonyms: sex comb on midleg homolog 1, Scml3, sex comb on midleg homolog 1 (Drosophila), polycomb protein SCMH1
Source: HGNC:19003
Biotype: protein coding gene
Symbol: SCMH1 (Hsa)
Symbol: SCMH1
Synonyms: polycomb protein SCMH1
Strict Orthology Symbols: scmh1
scmh1
(Danio rerio)Gene
Name: Scm polycomb group protein homolog 1
Synonyms: zgc:162582
Source: ZFIN:ZDB-GENE-070410-82
Biotype: protein coding gene
Symbol: scmh1 (Dre)
Symbol: scmh1
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1).
Strict Orthology Symbols: Scmh1...SCMH1
Scmh1
(Mus musculus)Gene
Name: Scm polycomb group homolog 1
Synonyms: expressed sequence AI315320, Scml3, AI851618, AI315320, expressed sequence AI851618, sex comb on midleg-like 3 (Drosophila)
Source: MGI:1352762
Biotype: protein coding gene
Symbol: Scmh1 (Mmu)
Symbol: Scmh1
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1).
Strict Orthology Symbols: scmh1
Alleles: Scmh1
Scmh1
(Rattus norvegicus)Gene
Name: Scm polycomb group protein homolog 1
Synonyms: sex comb on midleg homolog 1, sex comb on midleg 1, sex comb on midleg homolog 1 (Drosophila), LOC362581, polycomb protein SCMH1
Source: RGD:1305788
Biotype: protein coding gene
Symbol: Scmh1 (Rno)
Symbol: Scmh1
Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1); INTERACTS WITH acetamide; amphetamine
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1).
Synonyms: polycomb protein SCMH1
Strict Orthology Symbols: scmh1
scmh1
(Xenopus tropicalis)Gene
Name: Scm polycomb group protein homolog 1
Synonyms: Scm polycomb group protein homolog 1, scmh1
Source: Xenbase:XB-GENE-968911
Biotype: gene
Symbol: scmh1 (Xtr)
Symbol: scmh1
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1).
Synonyms: scmh1...scmh1...scmh1
Strict Orthology Symbols: Scmh1...scmh1.S...SCMH1...scmh1.L
SCMH1-DT
(Homo sapiens)Gene
Name: SCMH1 divergent transcript
Synonyms: translation initiation factor IF-2, uncharacterized LOC102723924, LOC102723924
Source: HGNC:55675
Biotype: ncRNA gene
Symbol: SCMH1-DT (Hsa)
Symbol: SCMH1-DT
scmh1.S
(Xenopus laevis)Gene
Name: Scm polycomb group protein homolog 1
Synonyms: Scm polycomb group protein homolog 1, scmh1.S
Source: Xenbase:XB-GENE-17336467
Biotype: gene
Symbol: scmh1.S (Xla)
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1).
Strict Orthology Symbols: scmh1
Symbol: scmh1.S
scmh1.L
(Xenopus laevis)Gene
Name: Scm polycomb group protein homolog 1
Synonyms: Scm polycomb group protein homolog 1, scmh1.L
Source: Xenbase:XB-GENE-968916
Biotype: gene
Symbol: scmh1.L (Xla)
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1).
Strict Orthology Symbols: scmh1
Symbol: scmh1.L
Scmh1tm1e(EUCOMM)Hmgu
(Mus musculus)Allele/Variant
Source: MGI:4458794
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1tm1e(EUCOMM)Hmgu
Scmh1em2Cya
(Mus musculus)Allele/Variant
Source: MGI:7586381
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1em2Cya
Scmh1tm1e.1(EUCOMM)Hmgu
(Mus musculus)Allele/Variant
Source: MGI:6324158
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1tm1e.1(EUCOMM)Hmgu
Scmh1tm1Hko
(Mus musculus)Allele/Variant
Source: MGI:3706668
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1tm1Hko
Scmh1tm1Yota
(Mus musculus)Allele/Variant
Source: MGI:5475146
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1tm1Yota
Scmh1em1Smoc
(Mus musculus)Allele/Variant
Source: MGI:7766645
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1em1Smoc
Scmh1tm1a(EUCOMM)Hmgu
(Mus musculus)Allele/Variant
Source: MGI:4456695
Genes: Scmh1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Scmh1
Genes: Scmh1 (Mmu)
Symbol: Scmh1tm1a(EUCOMM)Hmgu
Model
Id: MGI:5475148
Synonyms: Not Available
Symbol: Scmh1/Scmh1 [background:] involves: 129X1/SvJ * C57BL/6 (Mmu)
Genes: Scmh1 (Mmu)
Alleles: Scmh1
Name: Scmh1/Scmh1 [background:] involves: 129X1/SvJ * C57BL/6
Id: MGI:3707449
Synonyms: Not Available
Symbol: Scmh1/Scmh1 [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 (Mmu)
Genes: Scmh1 (Mmu)
Alleles: Scmh1
Name: Scmh1/Scmh1 [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Scmh1tm1e.1(EUCOMM)Hmgu/Scmh1tm1e.1(EUCOMM)Hmgu [background:] C57BL/6N-Scmh1tm1e.1(EUCOMM)Hmgu/Ieg
(Mus musculus)Model
Id: MGI:6408638
Synonyms: Not Available
Symbol: Scmh1/Scmh1 [background:] C57BL/6N-Scmh1
Genes: Scmh1 (Mmu)
Alleles: Scmh1
Name: Scmh1/Scmh1 [background:] C57BL/6N-Scmh1
Scm
(Drosophila melanogaster)Gene
Name: Sex comb on midleg
Synonyms: Sex combs on midleg, Sex combs on midlegs, Su(z)302, Sex Comb on Midleg, sex comb on midleg, l(3)85Ef, scm, CG9495, SCM, Sex Comb on the Midleg
Source: FB:FBgn0003334
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human SCMH1 (Scm polycomb group protein homolog 1) and SCML2 (Scm polycomb group protein
Strict Orthology Symbols: scmh1
Phc2tm1Hko/Phc2tm1Hko Scmh1tm1Hko/Scmh1tm1Hko [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6
(Mus musculus)Model
Id: MGI:3707450
Synonyms: Not Available
Genes: Scmh1 (Mmu)
Alleles: Scmh1
Name: Phc2/Phc2 Scmh1/Scmh1 [background:] involves: 129S1/Sv * 129X1/SvJ *
Symbol: Phc2/Phc2 Scmh1/Scmh1 [background:] involves: 129S1/Sv * 129X1/SvJ *
Phc2tm1Hko/Phc2+ Scmh1tm1Hko/Scmh1tm1Hko [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6
(Mus musculus)Model
Id: MGI:3707451
Synonyms: Not Available
Genes: Scmh1 (Mmu)
Alleles: Scmh1
Name: Phc2/Phc2<+> Scmh1/Scmh1 [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL
Symbol: Phc2/Phc2<+> Scmh1/Scmh1 [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL
Gene Ontology
Source: GO:0010369
Synonyms: Not Available
Branch: cellular component
Genes: Scmh1 (Mmu)...Scmh1 (Rno)...SCMH1 (Hsa)
Gene Ontology
Source: GO:0001673
Synonyms:
- male germ-cell nucleus
Branch: cellular component
Genes: Scmh1 (Rno)...Scmh1 (Mmu)...SCMH1 (Hsa)
Gene Ontology
Source: GO:0009952
Synonyms:
- anterior/posterior pattern formation
Branch: biological process
Genes: Scmh1 (Mmu)...SCMH1 (Hsa)...Scmh1 (Rno)
Gene Ontology
Source: GO:0031507
Synonyms:
- TGS
- chromatin silencing
Branch: biological process
Genes: Scmh1 (Mmu)...SCMH1 (Hsa)
Gene Ontology
Source: GO:0042393
Synonyms:
- histone-specific chaperone activity
Branch: molecular function
Genes: Scmh1 (Mmu)...SCMH1 (Hsa)
Gene Ontology
Source: GO:0007283
Synonyms:
- generation of spermatozoa
Branch: biological process
Genes: SCMH1 (Hsa)...Scmh1 (Rno)...Scmh1 (Mmu)
(GRCh38)1:41075449C>A
(Homo sapiens)Allele/Variant
Source: rs759220732
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41075449C>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41116949C>A
(Homo sapiens)Allele/Variant
Source: rs771472375
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41116949C>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41028318T>C
(Homo sapiens)Allele/Variant
Source: rs780713552
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41028318T>C
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41075335C>T
(Homo sapiens)Allele/Variant
Source: rs1657945029
Genes: SCMH1 (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)1:41075335C>T
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41113360C>T
(Homo sapiens)Allele/Variant
Source: rs373257448
Genes: SCMH1 (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)1:41113360C>T
Gene Synonyms: polycomb protein SCMH1
Gene Ontology
Source: GO:0045892
Synonyms:
- down regulation of gene-specific transcription
- down regulation of transcription, DNA-dependent
Branch: biological process
Genes: SCMH1 (Hsa)...Scmh1 (Mmu)
(GRCh38)1:41037541C>A
(Homo sapiens)Allele/Variant
Source: rs755215679
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41037541C>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41116995G>A
(Homo sapiens)Allele/Variant
Source: rs140656390
Genes: SCMH1 (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)1:41116995G>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41028707C>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.41028707C>A
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)1:41028707C>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41037427G>A
(Homo sapiens)Allele/Variant
Source: rs780097526
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41037427G>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41045911A>C
(Homo sapiens)Allele/Variant
Source: rs207460094
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41045911A>C
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41046461G>A
(Homo sapiens)Allele/Variant
Source: rs191253318
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41046461G>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41046539C>T
(Homo sapiens)Allele/Variant
Source: rs753695456
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41046539C>T
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41070688C>T
(Homo sapiens)Allele/Variant
Source: rs755833243
Genes: SCMH1 (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)1:41070688C>T
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41028702C>A
(Homo sapiens)Allele/Variant
Source: rs747407979
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41028702C>A
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41075451A>G
(Homo sapiens)Allele/Variant
Source: rs140590267
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41075451A>G
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41048720T>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.41048720T>G
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41048720T>G
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41070697G>C
(Homo sapiens)Allele/Variant
Source: rs760590161
Genes: SCMH1 (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)1:41070697G>C
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41152632C>G
(Homo sapiens)Allele/Variant
Source: rs545395137
Genes: SCMH1 (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)1:41152632C>G
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41037397C>T
(Homo sapiens)Allele/Variant
Source: rs1380677081
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41037397C>T
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41142917T>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.41142917T>C
Genes: SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41142917T>C
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41037372T>C
(Homo sapiens)Allele/Variant
Source: rs148897535
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41037372T>C
Gene Synonyms: polycomb protein SCMH1
(GRCh38)1:41037482T>C
(Homo sapiens)Allele/Variant
Source: rs561244725
Genes: SLFNL1-AS1 (Hsa), SCMH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:41037482T>C
Gene Synonyms: polycomb protein SCMH1