NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 15

How to use this Resource

Cross Mouse Locus Mouse Gene Human Chr. Human Gene In Situ Method RH Map Genethon Map Homology Group
a, b 4.6 Ghr 5 GHR 5p14-p13 45
b 4.6 Mlvi2 5 MLVI2 5p14-p13 45
b 4.6 Il7r 5 IL7R 5p13 R SHGC-1118 46-51 45
4.6 Prlr 5 PRLR 5p14-p13 R SHGC-11126 46-51 45
b 4.6 Lifr 5 LIFR 5p13-p12 45
3(g) C6(g) 5 C6 5p13 R WI-8877 54-61 45
3(g) C7(g) 5 C7 5p13 45
5.0 Slc1a3 5 SLC1A3 5p13 45
a 6.4 Ptgerep2 5 PTGER2 5p13.1 R WI-6043 54-61 45
6.7 Slc1a3 5 SLC1A3 5p13 45
9.2 Myo10 5 MYO10 5p15,1-p14.3 45
b 14.5 Hspg1 8 SDC2 8q22-q23 R stSG3816 102-122 90
14.7 Rpl30 8 RPL30 8 90
c 22.4 Trhs 8 TRHS 8 90
a 31.0 Has2 8 HAS2 8q24.12 90
32.0 Mlvi4 8 MLVI4 8q24 90
a, b 32.0 Myc 8 MYC 8q24 R,G WI-7052 136-142 90
b 32.0 Mlvi1 8 MLVI1 8q 90
b 32.0 Pvt1 8 PVT1 8q24 90
b 36.4 Tgn 8 TG 8q24 G 90
40.3 Gpt1 8 GPT 8q24.2-qter G 90
42.0 Fadk 8 PTK2 8q24-qter R WI-7711 161-166 90
36.4(g) Slap 8* SLA 8q22.3 89
44.9(g) Cypb11b1 8* CYPB11B1 8q21-q22 89
44.9(g) Cypb11b2 8* CYPB11B2 8q21-q22 89
43.3 Mb 22 MB 22q12 R,X,G stMB 31-33 192
43.4 Pva 22 PVALB 22q12-q13.1 R,X SHGC-11984 36 192
b 46(g) Il2rb 22 IL2RB 22q13 R,X,G M26062 31-40 192
b 43.3 Myh9 22 MYH9 22q12.3-q13.1 X,G 192
a 43.3 Pdgfb 22 PDGFB 22q12.3-q13.1 R,X,G WI-8985 40-42 192
43.3 Scx 22 SCX 22q12.3-13.1 192
b 44.9 Lgals1 22 LGALS1 22q12-q13.1 192
45.2 Dia1 22 DIA1 22q13.31-qter 192
a 48.8 Ppara 22 PPAR 22q12-q13.1 R stPPAR 40-45 192
c 49.2 Tef 22 TEF 22q13 192
48.6 Acr 22 ACR 22q13-qter 192
47.0 Tst 22 TST 22q12-qter 192
47.2 Cyp2d9 22 CYP2D9 22q13 192
47.2 Cyp2d 22 CYP2D 22q11.2-qter R,X.G stCYP2D 40-45 192
43.3(g) Bzrp 22 BZRP 22q13.3-qter R,X stBZRP 40-45 192
b 51.6 Pdgfec 22 ECGF1 22q13 X 192
S Aco2 22 ACO2 22q11.2-q13.3 R WI-8900 40-45 192
S Fbln1 22 FBLN1 22 R stFIBB 40-45 192
S Gad3 22 GAD3 22q13 192
S As2 22 ARSA 22q13.31-qter X stARSA 40-45 192
56.8 Aqp5 12 AQP5 12q13 122
56.8 Cchb3 12 CACLNB3 12q13 122
a, c 56.8 Col2a1 12 COL2AI 12q12-q13.1 R,X,G WI-6991 65-67 122
b 56.8 Ela1 12 ELA1 12 G 122
b 56.8 Wnt1 12 WNT1 12q13 R 122
56.8 D15Kz1 12 D15KZ1M 12 122
a, b 56.8 Gdc1 12 GPD1 12 X 122
56.8 Tegt 12 TEGT 12q12-q13 122
58.7(g) Krt2-4 12 KRT4 12p12.2-q11 R.X X67683 67-70 122
58.7(g) Krt2-8 12 KRT8 12p13.2-q24.1 122
a, b 57.4(g) Rarg 12 RARG 12q13 X 122
56.8 Tcfc[2 12 TCFCP2 12 122
61.1(g) Itgb7 12 ITGB7 12q13 R WI-7746 65-67 122
59.8(g) Nramp2 12 NRAMP2 12q13 R WI-11374 65-67 122
58.7(g) Spl1 12 SP1 12q13 R,X SHGC-10996 70-72 122
57.4 Hoxc13 12 HOXC13 12q12-q13 122
b, c 57.4 Itga5 12 ITGA5 12q11-q13 122
b 57.4 Hoxc4 12 HOXC4 12q12-q13 X 122
57.4 Hoxc5 12 HOXC5 12q12-q13 122
57.4 Hoxc6 12 HOXC6 12q12-q13 122
57.4 Hoxc8 12 HOXC8 12q12-q13 122
57.4 Hoxc9 12 HOXC9 12q12-q13 122
57.4 Hoxc10 12 HOXC10 12q12-q13 122
57.4 Hoxc11 12 HOXC11 12q12-q13 122
57.4 Hoxc12 12 HOXC12 12q12-q13 122
57.6 Cntn1 12 CNTN1 12q11-q12 122
S Hbr1 12 HMR 12q13 122
S Prph 12 PRPH 12q12-q13 122
S Pfk4 12 PFKX 12 122
S Lrp 12 LRP1 12q13-q14 122
S A2mr 12 A2MR 12q13-q14 R 122
61.7 Nfe2 12 NFE2 12q13 122
64.0 Scn8a 12 SCN8A 12q13 122

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.