NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 9

How to use this Resource

Cross Mouse Locus Mouse Gene Human Chr. Human Gene In Situ Method RH Map Genethon Map Homology Group
b 1.0 Il1bc 11 IL1BC 11q23 116
b 1.0 Mmel 11 MMEL 11q22-q23 116
3.0 Fut4 11 FUT4 11q21 116
S Pgr 11 PGR 11q22.1-q22.3 R,G PGR 103 116
S Pde4a 19 PDE4A 19 X 166
a, b 5.0 Ldlr 19 LDLR 19p13.2 R,X.G SHGC-15376 24-35 166
b 5.0 Epor 19 EPOR 19p13.2 R,X WI-14932 31-35 166
b 5.0 Dnmt 19 DNMT 19p13.2-p13.3 X 166
6.0 Acp5 19 ACP5 19p13.2-13.3 X 166
a 7.0 Icam1 19 ICAM1 19p13.2 X,G 166
a 8.0 Gria4 11* GRIA4 11q22 119
a 13.0 Girk4 11* GIRK4 11q23-qter 119
b 15.0 Ets1 11* ETS1 11q23.3 G 119
16.0 Fli1 11* FLI1 11q24.1-q24.3 R SHGC-13607 136-143 119
22.0 Es17 11* ESA4 11q 119
b 26(g) Cbl 11* CBL2 11q23.3-qter R WI-8978 >152 119
23.0 Grik4 11 GRIK4 11q23 R SHGC-31826 102-106 117
26.0 Hist5-2ax 11* H2AX 11q23.2-q23.3 R A004Z11 118-120 118
26.0 Hmbs 11* HMBS 11q23.3 G 118
a, b 26.0 Thy1 11* THY1 11q22.3-q23 R,G stSG1489 118-120 118
26.0 Cd3d 11* CD3D 11q23.3 G 118
b 26.0 Cd3g 11* CD3G 11q23 R,G SHGC-12712 118-120 118
a 26.0 Cd3e 11* CD3E 11q23 R,G WI-9069 118-120 118
26.0 All1 11* ALL1 11q23 R MLL1 118-120 118
26.0 Il10r 11* IL10R 11 R WI-7357 117-118 118
b S Mll 11* MLL 11q23 118
a 27.0 Apoa1 11* APOA1 11q23.3 R,G stSG86 112-117 118
27.0 Apoc3 11* APOC3 11q23-qter R WI-8564 110-117 118
27.0 Apoa4 11* APOA4 11q23-qter G 118
a 28.0 Ncam 11* NCAM 11q23.1 R,G WI-9123 110-112 118
a, b 28.0 Drd2 11* DRD2 11q23.1 R,G SGC31507 110-112 118
29.0 Crya2 11* CRYA2 11q22.3-q23.1 R S45630 108-110 118
30.0 Atm 11* ATM 11q22-q23 118
a 29(g) Hexa 15 HEXA 15q23-q24 R SGC33452 71 136
a 30.0 Sin3a 15 SIN3A 15 136
31.0 Cyp19 15 CYP19 15q21 R,G SHGC-10061 32-47 136
31.0 Cyp1a1 15 CYP1A1 15q22-q24 G 136
b 31.0 Cyp1a2 15 CYP1A2 15 R SGC35304 71-72 136
b 31.0 Crabp1 15 CRABP1 15q22-qter 136
31.0 Cyp11a 15 CYP11A 15q23-q24 G 136
32.0 Acra5 15 CHRNA5 15q24 G 136
32.0 Acra5 15 ACRA4 15q24 136
32.0 Mpi1 15 MPI 15q22-qter R stSG3911 70-72 136
b 32.0 Csk 15 CSK 15q23-q25 136
32.0 Pml 15 PML 15q R SGC31521 71-72 136
36.0 Pk3 15 PKM2 15q24-q25 136
39.0 Hpl 15 LIPC 15q21-q23 G 136
40.0 Tpm1 15 TPM1 15q22 136
40.0 Tcf12 15 TCF12 15q21 136
b 42.0 Myo5a 15 MYH12 15 136
40(g) Htr1b 6 HTR1B 6q13 R SHGC-11206 91-96 64
b 42.0 Bmp5 6 BMP5 6 64
a, b 43.0 Col12a1 6 COL12A1 6 64
44.0 Gst2-2 6 GST2(?) 6 R WI-9141 73-77 64
48.0 Pgm3 6 PGM3 6q12 64
48.0 Mod1 6 ME1 6q12 64
50.0 Grf1 15* GRF1 15q24 137
S Acrb4 15* CHRNB4 15q24 137
51.0 Acra3 15* CHRNA3 15q24 137
50(g) Rbp1 3 RBP1 3q21-q22 R SHGC9745 154-156 32
a, b 56.0 Trf(g) 3 TF 3q21 P,G 32
55(g) Cp 3 CP 3q23-q25 G,P 32
57.0 Gpx 3 GSHPX1 3 32
57.0 Rbp2 3 RBP2 3p11-qter 32
61(g) Ryk 3 RYK 3q22 R stSG1549 148-156 32
S D9H3S92 3* D3S92 3p21.1 25
S D9H3S93 3* D3S93 3p21.1 25
a 58.0 Pthr 3* PTHR 3p22-p21.1 25
b 59.0 Gnat1 3* GNAT1 3p21 25
b 59.0 Gnai2 3* GNAI2 3p21.3-p21.2 P 25
60.0 Acy1 3* ACY1 3p21.1 R stSB1354 35-36 25
b 60.0 Lamb2 3* LAMB2 3p21-q21 R WI-8710 35-36 25
60.0 Apeh 3* APEH 3p21.3-p21.2 25
b 60.0 Hgfl 3* MST1 3p21.3 G 25
60.0 Dag1 3* DAG1 3p21 25
61.0 Ltf 3* LTF 3p21 R 25
b 61.0 Col7a1 3* COL7A1 3p21 25
61.0 Mylc 3* MYL3 3p21.3-p21.2 R 25
a 62.0 Tgfbr2 3* TGFBR2 3p22 25
62.0 Mlh1 3* MLH1 3p23-p22 25
66.0 Bg1 3* GLB1 3p22-p21.3 R M34423 49-55 25
70.0 Scn5a 3* SCN5A 3p21 25
a, b 71.0 Cck 3* CCK 3p22-p21.3 R stSG4228 63-67 25
b 71.0 Nktr 3* NKTR 3p23-p21 R L17326 63-67 25
71.0 Tna 3* TNA 3 R SGC32929 63-67 25
72.0 Cmkbr1 3* CMKBR1 3p21 25
72.0 Catnb 3* CATNB 3p21 25

Human/Mouse Homology Mapping Methods

MethodDescription
CHigh-resolution cytogenetic methods
GGenetic linkage mapping
G*Genetic mapping, with disagreements between genetic and physical map resolved in favor of physical map
LLong-range restriction site mapping
PMultiple physical methods, including YAC and cosmid contigs
RRadiation hybrid mapping
XMultiple sources of high-resolution data

Gene Notes:

KeyDescription
aGene Bank Accession Number for Mouse EST
bGene order has been changed from that shown in the chromosome committee reports or online databases, as required by high-resolution human physical mapping data; these data also indicate a probable difference between human and mouse organization, e.g. a small inversion in one species
gMouse gene order has been changed slightly to conform with human gene order in the absence of conflicting high resolution data
yPosition has been changed from that reported in chromosome committee report or or Mouse Genome Database based on additional data or review of previous data
pDifferent sources of high resolution mapping data give conflicting positions
rDifference between position in inbred mice vs. Mus spretus
uThis is a UniGene designation, given since no gene symbol has been assigned. Note: some of these designations may be retired.

Mouse Locus Notes

The notation S in the Mouse Locus column indicates a gene that is syntenic, but for which there is not enough data to assign a precise position.

Cross Information

The cross column indicates which laboratory mapped a given cross.

a - Duke/Davis cross

b - Frederick cross

c - Jackson Lab cross

RH Notes

This field contains the marker identification used in Radiation Hybrid Mapping. These hyperlinks will connect the user to the Gene Map of the Human Genome. Subsequent hyperlinks on the marker will provide marker details and hyperlink to the actual Human Gene Map region (by selecting the interval defined by the Genethon Map loci intervals). Therefore the user can rapidly obtain information on ESTs that have

Color Key for Homology Map

Human Chr. Human Chr. Human Chr. Human Chr. Human Chr. Human Chr.
1 2 3 4 5 6
7 8 9 10 11 12
13 14 15 16 17 18
19 X

The asterisk character ('*') is used to indicate a different region of homology on the same human chromosome.

A question mark ('?') indicates that the authors are uncertain that this region is truly homologous.