Version: 8.2.0Date: Wed Aug 27 2025
Category
NCMAP
(Homo sapiens)Gene
Name: non-compact myelin associated protein
Synonyms: noncompact myelin-associated protein, myelin protein of 11 kDa, uncharacterized protein C1orf130, C1orf130, MP11, myelin glycoprotein 11, FLJ42528
Source: HGNC:29332
Biotype: protein coding gene
Symbol: NCMAP (Hsa)
Symbol: NCMAP
Strict Orthology Symbols: Ncmap
Ncmap
(Rattus norvegicus)Gene
Name: noncompact myelin associated protein
Synonyms: hypothetical protein LOC689826, noncompact myelin-associated protein, LOC689826, myelin protein of 11 kDa, Mp11
Source: RGD:1587554
Biotype: protein coding gene
Symbol: Ncmap (Rno)
Symbol: Ncmap
Gene Synopsis: Orthologous to human NCMAP (non-compact myelin associated protein); INTERACTS WITH 1-naphthyl isothiocyanate
Automated Gene Synopsis: Orthologous to human NCMAP (non-compact myelin associated protein).
Strict Orthology Symbols: Ncmap
Ncmap
(Mus musculus)Gene
Name: noncompact myelin associated protein
Synonyms: A330049M08Rik, RIKEN cDNA A330049M08 gene, Mp11
Source: MGI:2444888
Biotype: protein coding gene
Symbol: Ncmap (Mmu)
Symbol: Ncmap
Automated Gene Synopsis: Orthologous to human NCMAP (non-compact myelin associated protein).
Strict Orthology Symbols: Ncmap
Alleles: Ncmap
ncmap
(Xenopus tropicalis)Gene
Name: non-compact myelin associated protein
Synonyms: ncmap, non-compact myelin associated protein
Source: Xenbase:XB-GENE-5800493
Biotype: gene
Symbol: ncmap (Xtr)
Symbol: ncmap
Automated Gene Synopsis: Orthologous to human NCMAP (non-compact myelin associated protein).
Synonyms: ncmap...ncmap
Strict Orthology Symbols: Ncmap
NCMAP-DT
(Homo sapiens)Gene
Name: NCMAP divergent transcript
Synonyms: Not Available
Source: HGNC:54327
Biotype: ncRNA gene
Symbol: NCMAP-DT (Hsa)
Symbol: NCMAP-DT
ncmap.L
(Xenopus laevis)Gene
Name: non-compact myelin associated protein
Synonyms: non-compact myelin associated protein, ncmap.L
Source: Xenbase:XB-GENE-6486691
Biotype: gene
Symbol: ncmap.L (Xla)
Symbol: ncmap.L
ncmap.S
(Xenopus laevis)Gene
Name: non-compact myelin associated protein
Synonyms: ncmap.S, non-compact myelin associated protein
Source: Xenbase:XB-GENE-17340636
Biotype: gene
Symbol: ncmap.S (Xla)
Symbol: ncmap.S
Ncmapem1(IMPC)J
(Mus musculus)Allele/Variant
Source: MGI:6295411
Genes: Ncmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ncmap
Genes: Ncmap (Mmu)
Symbol: Ncmapem1(IMPC)J
Ncmapem2Gpt
(Mus musculus)Allele/Variant
Source: MGI:7302856
Genes: Ncmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ncmap
Genes: Ncmap (Mmu)
Symbol: Ncmapem2Gpt
Ncmapem1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7302855
Genes: Ncmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ncmap
Genes: Ncmap (Mmu)
Symbol: Ncmapem1Gpt
si:dkey-221l4.10
(Danio rerio)Gene
Name: si:dkey-221l4.10
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-131121-493
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human NCMAP (non-compact myelin associated protein).
Strict Orthology Symbols: Ncmap
Gene Ontology
Source: GO:0032290
Synonyms:
- myelin formation in peripheral nervous system
- peripheral nervous system myelin sheath formation
Branch: biological process
Genes: NCMAP (Hsa)...Ncmap (Mmu)...Ncmap (Rno)
Gene Ontology
Source: GO:0033270
Synonyms:
- paranode
Branch: cellular component
Genes: NCMAP (Hsa)...Ncmap (Rno)...Ncmap (Mmu)
Gene Ontology
Source: GO:0019911
Synonyms: Not Available
Branch: molecular function
Genes: NCMAP (Hsa)...Ncmap (Rno)...Ncmap (Mmu)
Gene Ontology
Source: GO:0043220
Synonyms:
- Schmidt-Lanterman cleft
Branch: cellular component
Genes: NCMAP (Hsa)...Ncmap (Rno)...Ncmap (Mmu)
Gene Ontology
Source: GO:0031641
Synonyms: Not Available
Branch: biological process
Genes: NCMAP (Hsa)...Ncmap (Rno)...Ncmap (Mmu)
Gene Ontology
Source: GO:0031643
Synonyms:
- activation of myelination
- stimulation of myelination
Branch: biological process
Genes: NCMAP (Hsa)...Ncmap (Rno)...Ncmap (Mmu)
Gene Ontology
Source: GO:0005886
Synonyms:
- bacterial inner membrane
- cell membrane
Branch: cellular component
Genes: Ncmap (Mmu)...NCMAP (Hsa)...Ncmap (Rno)
Gene Ontology
Source: GO:0016020
Synonyms:
- integral component of membrane
- integral to membrane
Branch: cellular component
Genes: Ncmap (Mmu)...NCMAP (Hsa)...Ncmap (Rno)
(GRCh38)1:24595462C>A
(Homo sapiens)Allele/Variant
Source: rs200084084
Genes: NCMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:24595462C>A
(GRCh38)1:24595441C>T
(Homo sapiens)Allele/Variant
Source: rs763387308
Genes: NCMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:24595441C>T
(GRCh38)1:24605647A>G
(Homo sapiens)Allele/Variant
Source: rs758735853
Genes: NCMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:24605647A>G
(GRCh38)1:24605680G>A
(Homo sapiens)Allele/Variant
Source: rs1004778042
Genes: NCMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:24605680G>A
(GRCh38)1:24594839C>A
(Homo sapiens)Allele/Variant
Source: rs207460059
Genes: NCMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:24594839C>A
(GRCh38)1:24605685G>A
(Homo sapiens)Allele/Variant
Source: rs1224868158
Genes: NCMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:24605685G>A
(mRatBN7.2)5:147609371T>A
(Rattus norvegicus)Allele/Variant
Source: rs3320721992
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147609371T>A
(mRatBN7.2)5:147610233T>C
(Rattus norvegicus)Allele/Variant
Source: rs199258704
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147610233T>C
(mRatBN7.2)5:147610433G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051340.1:g.147610433G>T
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147610433G>T
(mRatBN7.2)5:147620964A>G
(Rattus norvegicus)Allele/Variant
Source: rs3320615882
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147620964A>G
(mRatBN7.2)5:147608852A>G
(Rattus norvegicus)Allele/Variant
Source: rs3320546575
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147608852A>G
(mRatBN7.2)5:147609464G>A
(Rattus norvegicus)Allele/Variant
Source: rs3320721959
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147609464G>A
(mRatBN7.2)5:147617435A>G
(Rattus norvegicus)Allele/Variant
Source: rs197077026
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147617435A>G
(mRatBN7.2)5:147608371A>C
(Rattus norvegicus)Allele/Variant
Source: rs3320692832
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147608371A>C
(mRatBN7.2)5:147621268T>C
(Rattus norvegicus)Allele/Variant
Source: rs198600323
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147621268T>C
(mRatBN7.2)5:147621294T>C
(Rattus norvegicus)Allele/Variant
Source: rs198927794
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147621294T>C
(mRatBN7.2)5:147608524C>T
(Rattus norvegicus)Allele/Variant
Source: rs3320688009
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147608524C>T
(mRatBN7.2)5:147610213C>T
(Rattus norvegicus)Allele/Variant
Source: rs3320718087
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147610213C>T
(mRatBN7.2)5:147614984A>C
(Rattus norvegicus)Allele/Variant
Source: rs3320690838
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147614984A>C
(mRatBN7.2)5:147616844C>T
(Rattus norvegicus)Allele/Variant
Source: rs198015009
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147616844C>T
(mRatBN7.2)5:147609354T>C
(Rattus norvegicus)Allele/Variant
Source: rs3320715694
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147609354T>C
(mRatBN7.2)5:147610124C>T
(Rattus norvegicus)Allele/Variant
Source: rs3320715725
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147610124C>T
(mRatBN7.2)5:147610435G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051340.1:g.147610435G>T
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147610435G>T
(mRatBN7.2)5:147617711T>C
(Rattus norvegicus)Allele/Variant
Source: rs198017489
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147617711T>C
(mRatBN7.2)5:147618066G>A
(Rattus norvegicus)Allele/Variant
Source: rs199174900
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147618066G>A
(mRatBN7.2)5:147618698G>A
(Rattus norvegicus)Allele/Variant
Source: rs198526835
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147618698G>A
(mRatBN7.2)5:147611888G>A
(Rattus norvegicus)Allele/Variant
Source: rs3320546509
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147611888G>A
(mRatBN7.2)5:147612467A>G
(Rattus norvegicus)Allele/Variant
Source: rs198377252
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147612467A>G
(mRatBN7.2)5:147612528A>G
(Rattus norvegicus)Allele/Variant
Source: rs3320715749
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147612528A>G
(mRatBN7.2)5:147611095A>G
(Rattus norvegicus)Allele/Variant
Source: rs3320692916
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147611095A>G
(mRatBN7.2)5:147609891C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051340.1:g.147609891C>T
Genes: Ncmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:147609891C>T