H2-D1 MGI Mouse Gene Detail - MGI:95896 - histocompatibility 2, D region locus 1

Symbol

H2-D1
Name

histocompatibility 2, D region locus 1
Synonyms

H-2D

Feature Type

protein coding gene
IDs

MGI:95896
NCBI Gene: 14964
Alliance

gene page
Transcription Start Sites

20 TSS
Candidate for QTL

1 QTL

Sequence Map

Chr17:35482070-35486473 bp, + strand
From NCBI annotation of GRCm39
View this region in JBrowse
Genome Browsers

Ensembl | UCSC | NCBI

Genetic Map

Chromosome 17, 18.61 cM
Mapping Data

59 experiments

Strain Annotations

12
RFLP

20

For selected strains:

Strain	Gene Model ID	Feature Type	Coordinates
C57BL/6J	MGI_C57BL6J_95896	protein coding gene	Chr17:35481706-35486475 (+)
129S1/SvImJ	MGP_129S1SvImJ_G0023634	protein coding gene	Chr17:35417236-35422003 (+)
A/J	MGP_AJ_G0023627	protein coding gene	Chr17:35304678-35308941 (-)
AKR/J	MGP_AKRJ_G0023562	protein coding gene	Chr17:34732244-34951224 (+)
BALB/cJ	MGP_BALBcJ_G0023515	protein coding gene	Chr17:32956396-32961399 (-)
C3H/HeJ	MGP_C3HHeJ_G0023361	protein coding gene	Chr17:35118094-35300641 (+)
C57BL/6NJ	no annotation
CAROLI/EiJ	no annotation
CAST/EiJ	no annotation
CBA/J	MGP_CBAJ_G0023339	protein coding gene	Chr17:38271082-38643035 (+)
DBA/2J	no annotation
FVB/NJ	MGP_FVBNJ_G0023434	protein coding gene	Chr17:33406139-33408496 (+)
LP/J	MGP_LPJ_G0023544	protein coding gene	Chr17:35744980-35751057 (+)
NOD/ShiLtJ	MGP_NODShiLtJ_G0023456	protein coding gene	Chr17:37198906-37205360 (+)
NZO/HlLtJ	MGP_NZOHlLtJ_G0023998	protein coding gene	Chr17:33533763-33540308 (-)
PWK/PhJ	no annotation
SPRET/EiJ	no annotation
WSB/EiJ	MGP_WSBEiJ_G0022837	protein coding gene	Chr17:33523155-33547904 (-)

Human Ortholog

HLA-A, major histocompatibility complex, class I, A

Vertebrate Orthologs

24

Vertebrate Orthology Source

Alliance of Genome Resources

Human Ortholog

HLA-A, major histocompatibility complex, class I, A
Synonyms

HLAA
Links

HGNC:4931

NCBI Gene ID: 3105

neXtProt AC: NX_P04439

UniProt: P04439
Chr Location

6p22.1; chr6:29941260-29949572 (+) GRCh38

Human Ortholog

HLA-B, major histocompatibility complex, class I, B
Synonyms

AS, B-4901, HLAB
Links

HGNC:4932

NCBI Gene ID: 3106

neXtProt AC: NX_P01889

UniProt: P01889
Chr Location

6p21.33; chr6:31353872-31367067 (-) GRCh38

Human Ortholog

HLA-C, major histocompatibility complex, class I, C
Synonyms

D6S204, HLAC, HLA-JY3, HLC-C, MHC, PSORS1
Links

HGNC:4933

NCBI Gene ID: 3107

neXtProt AC: NX_P10321

UniProt: P10321
Chr Location

6p21.33; chr6:31268749-31272130 (-) GRCh38

Human Ortholog

HLA-E, major histocompatibility complex, class I, E
Synonyms

HLA-6.2, QA1
Links

HGNC:4962

NCBI Gene ID: 3133

neXtProt AC: NX_P13747

UniProt: P13747
Chr Location

6p22.1; chr6:30489509-30494194 (+) GRCh38

Human Ortholog

HLA-F, major histocompatibility complex, class I, F
Synonyms

CDA12, HLA-5.4, HLA-CDA12, HLAF
Links

HGNC:4963

NCBI Gene ID: 3134

neXtProt AC: NX_P30511

UniProt: P30511
Chr Location

6p22.1; chr6:29722775-29738532 (+) GRCh38

Human Ortholog

HLA-G, major histocompatibility complex, class I, G
Synonyms

MHC-G
Links

HGNC:4964

NCBI Gene ID: 3135

neXtProt AC: NX_P17693

UniProt: P17693
Chr Location

6p22.1; chr6:29826474-29831125 (+) GRCh38

Human Ortholog

HLA-H, major histocompatibility complex, class I, H (pseudogene)
Synonyms

HLAHP
Links

HGNC:4965

NCBI Gene ID: 3136

UniProt: P01893
Chr Location

6p22.1; chr6:29887573-29891079 (+) GRCh38

MGI Vertebrate Homology

H2-D1 stringent orthology
7 human;1 mouse;9 rat;8 zebrafish
HCOP

vertebrate homology predictions: HLA-A, HLA-B, HLA-C, HLA-E, HLA-F, HLA-G, HLA-H
Gene Tree

H2-D1

Diseases

45 with human HLA-A,HLA-B,HLA-C,HLA-E,HLA-G associations

				Human Disease	Mouse Models
				acquired immunodeficiency syndrome IDs acquired immunodeficiency syndrome DOID:635 EFO:0000765 ICD10CM:B20 MESH:D000163 NCI:C2851 UMLS_CUI:C0001175
				acute retinal necrosis syndrome IDs acute retinal necrosis syndrome DOID:3611 MESH:D015882 UMLS_CUI:C0035319
				allergic asthma IDs allergic asthma DOID:9415 DOID:9416 DOID:9417 ICD10CM:J45 ICD9CM:493.0 UMLS_CUI:C0155877
				alopecia IDs alopecia DOID:987 ICD10CM:L65.9 ICD9CM:704.0 ICD9CM:704.00 MESH:D000505 NCI:C50575 OMIM:PS203655 UMLS_CUI:C0002170
				ankylosing spondylitis IDs ankylosing spondylitis DOID:7147 EFO:0003898 ICD10CM:M45 ICD9CM:720.0 MESH:D013167 NCI:C84564 OMIM:PS106300 ORDO:825 UMLS_CUI:C0038013
				anterior uveitis IDs anterior uveitis DOID:1407 MESH:D014606 NCI:C35109 UMLS_CUI:C0042165
				asthma IDs asthma DOID:2841 DOID:12703 DOID:13829 DOID:13830 DOID:2840 DOID:5783 ICD10CM:J45 ICD9CM:493 ICD9CM:493.9 KEGG:05310 MESH:D001249 NCI:C28397 OMIM:600807 UMLS_CUI:C0004096
				Behcet's disease IDs Behcet's disease DOID:13241 EFO:0003780 ICD10CM:M35.2 ICD9CM:136.1 ICD9CM_2006:136.1 MESH:D001528 NCI:C34416 OMIM:109650 UMLS_CUI:C0004943
				birdshot chorioretinopathy IDs birdshot chorioretinopathy DOID:0111079 MESH:D000080365 OMIM:605808 ORDO:179 UMLS_CUI:C1853959
				central nervous system vasculitis IDs central nervous system vasculitis DOID:525 MESH:D020293 NCI:C84622 UMLS_CUI:C0751878
				cerebral infarction IDs cerebral infarction DOID:3526 ICD10CM:I63 MESH:D002544 NCI:C50486 OMIM:601367 UMLS_CUI:C0007785
				cervical cancer IDs cervical cancer DOID:4362 DOID:4361 ICD10CM:C53 ICD9CM:180 ICD9CM:180.9 MESH:D002583 NCI:C2940 NCI:C9311 OMIM:603956 UMLS_CUI:C0007847 UMLS_CUI:C0007873
				colitis IDs colitis DOID:0060180 EFO:0003872 ICD10CM:K52.9 MESH:D003092 NCI:C26723 UMLS_CUI:C0009319
				COVID-19 IDs COVID-19 DOID:0080600 ICD10CM:U07.1 MESH:D000086382 NCI:C171133 UMLS_CUI:C5203670
				Cytomegalovirus retinitis IDs Cytomegalovirus retinitis DOID:0080160 MESH:D017726
				dermatitis IDs dermatitis DOID:2723 DOID:8614 DOID:8917 ICD10CM:L30.9 MESH:D003872 NCI:C2983 UMLS_CUI:C0011603
				diabetic retinopathy IDs diabetic retinopathy DOID:8947 ICD9CM:362.0 MESH:D003930 NCI:C34538 UMLS_CUI:C0011884
				erythema nodosum IDs erythema nodosum DOID:0080750 MESH:D004893
				Graves' disease IDs Graves' disease DOID:12361 EFO:0004237 ICD10CM:E05.0 MESH:D006111 NCI:C3071 OMIM:275000 UMLS_CUI:C0018213
				hepatitis C IDs hepatitis C DOID:1883 DOID:12430 DOID:12432 DOID:2049 EFO:0003047 ICD10CM:B19.20 ICD9CM:070.7 MESH:D006526 NCI:C3098 UMLS_CUI:C0019196
				human immunodeficiency virus infectious disease IDs human immunodeficiency virus infectious disease DOID:526 ICD10CM:B20 ICD9CM:042 ICD9CM:042-042.99 MESH:D015658 NCI:C3108 UMLS_CUI:C0019693
				Meniere's disease IDs Meniere's disease DOID:9849 ICD10CM:H81.0 ICD9CM:386.0 ICD9CM:386.00 MESH:D008575 NCI:C185243 OMIM:156000 UMLS_CUI:C0025281
				mitral valve prolapse IDs mitral valve prolapse DOID:988 MESH:D008945 NCI:C50655 OMIM:157700 OMIM:607829 OMIM:610840 UMLS_CUI:C0026267
				Moyamoya disease IDs Moyamoya disease DOID:13099 ICD10CM:I67.5 ICD9CM:437.5 MESH:D009072 NCI:C84895 OMIM:252350 OMIM:300845 OMIM:607151 OMIM:608796 OMIM:614042 OMIM:615750 ORDO:2573 ORDO:280679 ORDO:401945 UMLS_CUI:C0026654
				occupational asthma IDs occupational asthma DOID:0080820
				otosclerosis IDs otosclerosis DOID:12185 EFO:0004213 ICD10CM:H80.80 ICD9CM:387.8 OMIM:PS166800 ORDO:2794 UMLS_CUI:C0029696
				pre-eclampsia IDs pre-eclampsia DOID:10591 DOID:12684 ICD10CM:O14 MESH:D011225 NCI:C85021 OMIM:189800 OMIM:609402 OMIM:609403 OMIM:609404 OMIM:614592 ORDO:275555 UMLS_CUI:C0032914
				psoriasis 1 IDs psoriasis 1 DOID:0111286 OMIM:177900
				reactive arthritis IDs reactive arthritis DOID:6196 DOID:10148 DOID:11891 DOID:13318 DOID:13519 DOID:13782 DOID:13783 DOID:13784 DOID:13785 DOID:6194 DOID:9760 ICD10CM:M02.10 ICD10CM:M02.3 ICD9CM:099.3 ICD9CM:711.3 ICD9CM:711.30 MESH:D016918 NCI:C34975 UMLS_CUI:C0035012 UMLS_CUI:C0152085
				retinal vasculitis IDs retinal vasculitis DOID:11563 ICD10CM:H35.06 ICD9CM:362.18 MESH:D031300 UMLS_CUI:C0152026
				retinopathy of prematurity IDs retinopathy of prematurity DOID:13025 ICD10CM:H35.1 ICD9CM_2006:362.21 ICD9CM:362.20 ICD9CM:362.21 MESH:D012178 NCI:C34982 UMLS_CUI:C0035344
				sarcoidosis IDs sarcoidosis DOID:11335 ICD10CM:D86 ICD9CM:135 MESH:D012507 NCI:C34995 ORDO:797 UMLS_CUI:C0036202
				scleroderma IDs scleroderma DOID:419 MESH:D012594 NCI:C26746 UMLS_CUI:C0011644
				sensorineural hearing loss IDs sensorineural hearing loss DOID:10003 DOID:11053 DOID:12112 DOID:12114 ICD10CM:H90.5 ICD9CM_2006:389.11 ICD9CM_2006:389.14 ICD9CM:389.1 ICD9CM:389.10 ICD9CM:389.14 MESH:D006319 NCI:C26739 UMLS_CUI:C0018784
				severe acute respiratory syndrome IDs severe acute respiratory syndrome DOID:2945 ICD10CM:J12.81 ICD9CM:079.82 MESH:D045169 NCI:C85064 UMLS_CUI:C1175175
				spondyloarthropathy IDs spondyloarthropathy DOID:1123 MESH:D025242 UMLS_CUI:C0949691
				Stevens-Johnson syndrome IDs Stevens-Johnson syndrome DOID:0050426 EFO:0004276 ICD10CM:L51.1 ICD9CM:695.13 ICD9CM:695.15 MESH:D013262 NCI:C79484 UMLS_CUI:C0038325
				synovitis IDs synovitis DOID:2703 MESH:D013585 NCI:C50766 UMLS_CUI:C0039103
				Takayasu's arteritis IDs Takayasu's arteritis DOID:2508 DOID:13377 ICD10CM:M31.4 ICD9CM:446.7 MESH:D001015 MESH:D013625 NCI:C34391 NCI:C35062 OMIM:207600 UMLS_CUI:C0003490 UMLS_CUI:C0039263
				thromboangiitis obliterans IDs thromboangiitis obliterans DOID:12918 ICD10CM:I73.1 ICD9CM:443.1 MESH:D013919 NCI:C35070 OMIM:211480 UMLS_CUI:C0040021
				thrombophlebitis IDs thrombophlebitis DOID:3875 DOID:1146 ICD10CM:I80.0 ICD9CM_2006:451.0 ICD9CM:451.0 MESH:D013924 NCI:C3410 UMLS_CUI:C0040046 UMLS_CUI:C0265057
				trachoma IDs trachoma DOID:11265 DOID:13013 DOID:13264 ICD10CM:A71 ICD10CM:A71.0 ICD10CM:A71.1 ICD9CM:076 ICD9CM:076.0 ICD9CM:076.1 ICD9CM:076.9 MESH:D014141 UMLS_CUI:C0040592 UMLS_CUI:C0153107 UMLS_CUI:C0153108
				tuberculosis IDs tuberculosis DOID:399 DOID:10096 DOID:12688 DOID:12691 DOID:415 DOID:9901 DOID:9902 MESH:D014375 UMLS_CUI:C0041295
				uveitis IDs uveitis DOID:13141 ICD10CM:H20.9 MESH:D014605 NCI:C26909 UMLS_CUI:C0042164
				vulva cancer IDs vulva cancer DOID:1245 DOID:1282 ICD10CM:C51 ICD9CM:184.4 MESH:D014846 NCI:C3443 NCI:C7502 UMLS_CUI:C0042995 UMLS_CUI:C0375071

Click on a disease name to see all genes associated with that disease.

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Phenotype Summary

5 phenotypes from 5 alleles in 5 genetic backgrounds
21 phenotypes from multigenic genotypes
193 phenotype references

Phenotype Overview

Blue squares indicate phenotypes directly attributed to mutations/alleles of this gene.

adipose tissue	behavior/neurological	cardiovascular system	cellular	craniofacial	digestive/alimentary system	embryo	endocrine/exocrine glands	growth/size/body	hearing/vestibular/ear	hematopoietic system	homeostasis/metabolism	integument	immune system	limbs/digits/tail	liver/biliary system	mortality/aging	muscle	nervous system	pigmentation	renal/urinary system	reproductive system	respiratory system	skeleton	taste/olfaction	neoplasm	vision/eye

Click cells to view annotations.

All Mutations and Alleles

21
Endonuclease-mediated

15
Spontaneous

2
Targeted

3
Transgenic

1
Genomic Mutations

1 involving H2-D1
Incidental Mutations

Mutagenetix , APF
Find Mice (IMSR)

47 strains or lines available
Comparison Matrix

Gene Expression + Phenotype

Mice homozygous for a spontaneous allele are susceptible to chronic Theiler's Murine Encephalomyelitis Virus (TMEV) infection and demyelination, and lack the ability to respond to the viral peptide VP2121-130, the single Ag driving the protective CD8 T cell response in wild-type B6 mice.

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All GO Annotations

86
GO References

10

Molecular Function

carbohydrate derivative binding	cytoskeletal protein binding	DNA binding	enzyme regulator	hydrolase	ligase	lipid binding	oxidoreductase	RNA binding	signaling receptor activity	signaling receptor binding	transcription	transferase	transporter

Biological Process

carbohydrate derivative metabolism	cell differentiation	cell population proliferation	cellular component organization	DNA-templated transcription	establishment of localization	homeostatic process	immune system process	lipid metabolic process	programmed cell death	protein metabolic process	response to stimulus	signaling	system development

Cellular Component

cell projection	cytoplasmic vesicle	cytoskeleton	cytosol	endoplasmic reticulum	endosome	extracellular region	Golgi apparatus	mitochondrion	membraneless organelle	nucleus	organelle envelope	organelle lumen	plasma membrane	protein-containing complex	synapse	vacuole

Click cells to view annotations.

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Expression Overview

GXD's primary emphasis is on endogenous gene expression during development. Click on grid cells to view annotations.

Blue cells = expressed in wild-type.
Gray triangles = other expression annotations only
(e.g. absence of expression or data from mutants).

early conceptus	embryo ectoderm	embryo endoderm	embryo mesoderm	embryo mesenchyme	extraembryonic component	alimentary system	auditory system	branchial arches	cardiovascular system	connective tissue	endocrine system	exocrine system	hemolymphoid system	integumental system	limbs	liver and biliary system	musculoskeletal system	nervous system	olfactory system	reproductive system	respiratory system	urinary system	visual system

Click cells to view annotations.

Assay Results

809
Tissues

77
cDNA Data

16
Literature Summary

8

Images

Tissue x Stage Matrix

Comparison Matrix

Gene Expression + Phenotype

Other Mouse Links

Allen Institute

GENSAT

GEO

Expression Atlas

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All Sequences

93
RefSeq

2
UniProt

28
CCDS

CCDS57074.1

Ensembl

ENSMUSG00000073411 (Evidence)
NCBI Gene

14964

			Length	Strain/Species	Flank
genomic	14964	NCBI Gene Model \| MGI Sequence Detail	4404	C57BL/6J	± kb
transcript	NM_010380	RefSeq \| MGI Sequence Detail	1736	ZRU/MplStud
polypeptide	P14427	UniProt \| EBI \| MGI Sequence Detail	368	Not Applicable

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UniProt

28 Sequences
Protein Ontology

PR:000002006 H-2 class I histocompatibility antigen D1 alpha chain

(term hierarchy)
PDB

1BII, 1BZ9, 1CE6, 1DDH, 1FFN, 1FFO, 1FFP, 1FG2, 1HOC, 1INQ, 1JPF, 1JPG, 1JUF, 1N3N, 1N5A, 1QLF, 1QO3, 1S7U, 1S7V, 1S7W, 1S7X, 1WBX, 1WBY, 1YN6, 1YN7, 1ZHB, 2CII, 2F74, 2VE6, 2ZOK, 2ZOL, 3BUY, 3CC5, 3CCH, 3CH1, 3CPL, 3DMM, 3E6F, 3E6H, 3ECB, 3FTG, 3L3H, 3PQY, 3QUK, 3QUL, 3TBS, 3TBT, 3TBV, 3TBW, 3TBY, 3WS3, 3WS6, 4HUU, 4HUV, 4HUW, 4HUX, 4HV8, 4IHO, 4L8B, 4L8C, 4L8D, 4NSK, 4PG2, 5E8N, 5E8O, 5E8P, 5IVX, 5JWD, 5JWE, 5KD4, 5KD7, 5M00, 5M01, 5M02, 5MZM, 5OPI, 5SWS, 5SWZ, 5T7G, 5TIL, 5TJE, 5WER, 5WES, 5WET, 5WEU, 5WLG, 5WLI, 6G9Q, 6G9R, 6GB5, 6GB7, 6H6D, 6H6H, 6MP0, 6MP1, 6NPR, 6WZY, 6X00, 7JWI, 7JWJ, 7N4K, 7N5C, 7N5P, 7N5Q, 7N9J, 7NA5, 7P0A, 7P0T, 7QNG, 8D5E, 8D5F, 8FHL, 8FHU, 8TQ7, 8TQ8, 8TQ9, 8TQA
InterPro Domains

IPR050208 Antigen-presenting and immune regulatory MHC class I-related

IPR003597 Immunoglobulin C1-set

IPR007110 Immunoglobulin-like domain

IPR036179 Immunoglobulin-like domain superfamily

IPR013783 Immunoglobulin-like fold

IPR003006 Immunoglobulin/major histocompatibility complex, conserved site

IPR011162 MHC classes I/II-like antigen recognition protein

IPR001039 MHC class I alpha chain, alpha1 alpha2 domains

IPR010579 MHC class I, alpha chain, C-terminal

IPR011161 MHC class I-like antigen recognition-like

IPR037055 MHC class I-like antigen recognition-like superfamily
GlyGen

P14427 7 sites, 3 N-linked glycans (3 sites), 1 O-linked glycan (1 site)

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All nucleic 118

Genomic 92

cDNA 19

Primer pair 5

Other 2

Microarray probesets 11

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MGD-MRK-10379, MGD-MRK-10492

Summaries

All 315

Developmental Gene Expression 8

Gene Ontology 10

Phenotypes 193
Earliest

J:106349 Melvold RW, et al., Eight new histocompatibility mutations associated with the H-2 complex. Immunogenetics. 1976;3:185-191
Latest

J:354545 Dong H, et al., Targeting PRMT9-mediated arginine methylation suppresses cancer stem cell maintenance and elicits cGAS-mediated anticancer immunity. Nat Cancer. 2024 Apr;5(4):601-624

TSS for H2-D1:

(View these features in JBrowse)

Transcription Start Site	Location	Distance from Gene 5'-end
Tssr144334	Chr17:35481702-35481752 (+)	-343 bp
Tssr144335	Chr17:35481778-35481799 (+)	-281 bp
Tssr144336	Chr17:35482039-35482050 (+)	-25 bp
Tssr144337	Chr17:35482063-35482076 (+)	0 bp
Tssr144338	Chr17:35482267-35482286 (+)	207 bp
Tssr144339	Chr17:35482401-35482433 (+)	347 bp
Tssr144340	Chr17:35482735-35482744 (+)	670 bp
Tssr144341	Chr17:35482840-35482861 (+)	781 bp
Tssr144342	Chr17:35482937-35482966 (+)	882 bp
Tssr144343	Chr17:35483022-35483034 (+)	958 bp
Tssr144344	Chr17:35483373-35483394 (+)	1,314 bp
Tssr144345	Chr17:35483752-35483763 (+)	1,688 bp
Tssr144346	Chr17:35483812-35483826 (+)	1,749 bp
Tssr144347	Chr17:35483867-35483871 (+)	1,799 bp
Tssr144348	Chr17:35484766-35484788 (+)	2,707 bp
Tssr144349	Chr17:35485155-35485228 (+)	3,122 bp
Tssr144350	Chr17:35485980-35486018 (+)	3,929 bp
Tssr144351	Chr17:35486069-35486084 (+)	4,007 bp
Tssr144352	Chr17:35486115-35486169 (+)	4,072 bp
Tssr144353	Chr17:35486227-35486255 (+)	4,171 bp

H2-D1 is Candidate Gene for:

QTL	Genetic Location*	Genome Location (GRCm39)	Reference	QTL Note
Blmpf1	Chr17, 17.25 cM	Chr17:32061652-37644775	J:100369	Gene expression analysis was used to identify candidate genes for bleomycin-induced pulmonary fibrorsis QTLs Blmpf1 and Blmpf2. These loci were previously mapped in an F2 cross between susceptible strain C57BL/6J and resistant strain C3Hf/Kam. Blmpf1 maps to 17.4 cM on mouse Chromosome 17 and Blmpf2 maps to 28 cM on mouse Chromosome 11. Genes mapping to the Blmpf1 interval on mouse Chromosome 17 were evaluated for lung mRNA expression in C57BL/6J and C3Hf/Kam animals with and without bleomycin treatment. Genes showing significant expression differences with P<0.001 are H2-D1 (19.09 cM), C4 (18.8 cM), Glo1 (16 cM), H2-Q7 (19.19 cM), H2-K (18.65 cM), Gabbr1 (20.4 cM), Tff2 (17 cM), Notch4 (18.72 cM), and Fkbp5 (13 cM). Genes mapping to the Blmpf2 interval on mouse Chromosome 11 were evaluated for lung mRNA expression in C57BL/6J and C3Hf/Kam animals with and without bleomycin treatment. Genes showing significant expression differences with P<0.001 are Scgb3a1 (25 cM), Trim16, Pttg1, and Gria1 (31 cM).

*cM position of peak correlated region/marker

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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