Gene Map - Chromosome: 21 - OMIM - (OMIM.ORG)

OMIM Gene/Loci: 1 - 10 of 185 on Chromosome 21 (All Entries)
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Phenotype Only Entries All Entries

Location
(from NCBI, GRCh38) 		Gene/Locus Gene/Locus name Gene/Locus
MIM number 		Phenotype Phenotype
MIM number 		Inheritance Pheno
map
key 		Comments Mouse
symbol
(from MGI)
21:1
21p13-q11 		AUTS12 Autism, susceptibility to, 12 610838 {Autism susceptibility 12} 610838 2 max lod at D21S1437
21:3,100,001
21p12 		RNR4 Ribosomal RNA-4 180453
21:7,000,001
21p11.2 		BAGE1, BAGE BAGE family, member 1 605167 previously assigned to chr.13
21:7,000,001
21p11.2 		BAGE3 BAGE family, member 3 617777
21:10,413,497
21p11.2 		BAGE2 BAGE family, member 2 617776
21:10,521,583
21p11.2 		TPTE Transmembrane phosphatase with tensin homology 604336 Tpte
21:13,000,001
21q11.2 		NRCLP3 Narcolepsy 3 609039 Narcolepsy 3 609039 AD 2 max lod at D21S1245
21:13,000,001
21q11.2 		TAM, MST Myeloproliferative syndrome, transient (transient abnormal myelopoiesis) 159595 Leukemia, transient, of Down syndrome 159595 2
21:13,609,777
21q11.2 		POTED, ANKRD21, POTE POTE ankyrin domain family, member D 607549
21:14,108,812
21q11.2 		LIPI, LPDL, PRED5 Lipase I 609252 Lipi

« pter  |  ‹ Towards pter  |  Towards qter ›  |  qter »
OMIM Gene/Loci: 1 - 10 of 185 on Chromosome 21 (All Entries)

Location
(from NCBI, GRCh38) 		Gene/Locus Gene/Locus name Gene/Locus
MIM
number 		Phenotype Phenotype
MIM
number 		Inheritance Pheno
map
key 		Comments Mouse
symbol
(from MGI)
21:1-15,000,000
21p13-q11 		AUTS12 Autism, susceptibility to, 12 610838 {Autism susceptibility 12} 610838 2 max lod at D21S1437
21:3,100,001-7,000,000
21p12 		RNR4 Ribosomal RNA-4 180453
21:7,000,001-10,900,000
21p11.2 		BAGE1, BAGE BAGE family, member 1 605167 previously assigned to chr.13
21:7,000,001-10,900,000
21p11.2 		BAGE3 BAGE family, member 3 617777
21:10,413,497-10,518,274
21p11.2 		BAGE2 BAGE family, member 2 617776
21:10,521,583-10,605,716
21p11.2 		TPTE Transmembrane phosphatase with tensin homology 604336 Tpte
21:13,000,001-15,000,000
21q11.2 		NRCLP3 Narcolepsy 3 609039 Narcolepsy 3 609039 Autosomal dominant 2 max lod at D21S1245
21:13,000,001-15,000,000
21q11.2 		TAM, MST Myeloproliferative syndrome, transient (transient abnormal myelopoiesis) 159595 Leukemia, transient, of Down syndrome 159595 2
21:13,609,777-13,645,823
21q11.2 		POTED, ANKRD21, POTE POTE ankyrin domain family, member D 607549
21:14,108,812-14,210,955
21q11.2 		LIPI, LPDL, PRED5 Lipase I 609252 Lipi


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2026 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2026 Johns Hopkins University.
Printed: May 27, 2026