NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 4

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 0.0 Mos 8 MOS 8q11 87
b 0.0 Lyn(g) 8 LYN 8q13 R SHGC-12792 66-69 87
a 0.5 Penk1 8 PENK 8q11.23-q12 R,G SGC35617 66-69 87
2.6 Gem 8 GEM 8 87
4.4 Cbfa2t1h 8 CBFA2T1 8q21.3-q22.1(g) 87
7.7(g) Cals 8 CA8 8 87
10.5(g) Calb 8 CALB1 8q21.3-q22.1(g) 87
6.3 Pou3f2 6 POU3F2 6q16 65
b 10.5 Cga 6 CGA 6q12-21 G 65
a 10.5 Gabrr1 6 GABRR1 6q14-q21 R SHGC-11156 91-96 65
10.5 Gabrr2 6 GABRR2 6q14-q21 R WI-7717 93-99 65
13.9(g) Cnr1 6 CNR1 6q14-q15 65
S Rmrp 9 RMRP 9p21-p12 93
12.7 Etl2 9 IL11RA 9p13 R SGC35540 53-57 93
15.9 D4H9S3E 9 D9S3 9p21 93
18.6 Ggtb 9 GGTB2 9p13 93
19.9 Galt 9 GALT 9p13 G 93
19.9 Cntfr 9 CNTFR 9p13 93
20.7 Pax5 9 PAX5 9p13 R WI-7677 57-59 93
20.9 Aco1 9 ACO1 9p22-q32 93
21.5 Tmod 9* TMOD 9q22 97
c 21.5 Xpa 9* XPA 9q22.3 R WI-9212 103-104 97
22.3 Aldo2 9* ALDOB 9q22.3-q31 R stSG1311 104-109 97
22.5 Cd72 9* CD72 9p 97
23.1 Abc1 9* ABC1 9q22-q31 97
a 24.6 Txn(g) 9* TXN(g) 9q31(g) 97
b 24.7 Tal2 9* TAL2 9q32 97
30.6 Ambp 9* AMBP 9q32-q33 97
30.6 Lv 9* ALAD 9q32-q34 97
30.6 Zfp37 9* TZN 9q 97
31.4 Orm1 9* ORM1 9q32 97
31.4 Orm2 9* ORM2 9q32 97
31.4 Orm3 9* ORM3 9q32 97
32.2 Pappa 9* PAPPA 9q33.1 R SGC35708 124-125 97
b 32.2 Tnc 9* HXB 9q G 97
b 32.2 Cd30l 9* CD30LG 9q33 R WI-9258 124-125 97
42.6 Cdkn2a 9 CDKN2A 9p21 R SGC31294 77-93 95
42.6 Cdkn2b 9 CDKN2B 9p21 95
b 38(g) Tyrp1 9* TYRP1 9p23 R SGC35386 16-20 92
a, b, c 42.6 Ifa 9* IFNA 9p22 R WI-9020 27-32 92
42.6 Ifb 9* IFNB 9p22 G 92
b 43.6 Tek 9* TEK 9p21 92
a 43(g) AA107359(a) 1 12172(u) 1 R SHGC-15189 97-99 1
47.6(g) Ak3 9* AK3 9p24-p13 92
a, b 44.6 Jun 1 JUN 1p32-p31 1
b 45.4 Cyp4a 1 CYP4B1 1p34-p12 1
b 45.5 Pgm2 1 PGM1 1p32-33 R,G WI-9183 95-102 1
46.3 Jak1 1 JAK1 1p32.3-31.3 1
46.8 Pde4b(g) 1 PDE4B 1p31 1
48.1 D4H1S85 1 D1S85 1p32-p22.1 1
b 49.4 C8b 1 C8B 1p31 R 1
b 49.5 Tal1 1 TAL1 1p31 1
S Ak2 1 AK2 1p34 1
50.6 Urod 1 UROD 1p34 1
51.5 Ipp 1 IPP 1p32-p22 1
b 52.0 Ssbp 1 SSBP 1 1
a, b, 52.0 Glut1 1 SLC2A1 1p35-p31.3 G 1
52.9 Guca2 1 GUCA2 1p35-p34 1
53.0 Col9a2 1 COL9A2 1p32.3-p33 R SGC35672 66-73 1
a, b 55.0 Lmyc1 1 MYCL 1p34 R,G WI-7196 63-73 1
c 56.5 Mpl 1 MPL 1p34 1
b 57.5 Csfgr 1 CSFGR 1p35-p34.3 1
b 57.6 Gja4 1 GJA4 1p36-q12 1
a 57.7 Grik3 1 GRIK3 1p33-34 1
a 57.2 Col8a2 1 COL8A2 1p34.3-p32.3 1
a, b, 59.0 Lck 1 LCK 1p35-p32 1
a 59.0 Il14 1 IL14 1p 1
61.0 Fabph1 1 FABP3 1p36-q31 1
62.2 Hmg17 1 HMG17 1p36.1-p35 G 1
64.6 Slc9a1 1 SLC9A1 1p36.2-p35 1
b 64.6 Fgr 1 FGR 1p36.1 C,G 1
S Magp 1 MFAP2 1p36.1-p35 1
64.8 Oprd1 1 OPRD1 1p36.1-1p34.3 1
65.0 Plod 1 PLOD 1p36.3-p36.2 1
S Agrn 1 AGRN 1p36.3-p32 1
65.6 Hmgcl 1 HMGCL 1p36.1-p35 R SHGC-11459 50-54 1
65.7 Erk 1 ERK 1p36.1 R SHGC-9621 52-54 1
65.7 Cbfa3 1 AML2 1p36 1
b 65.7 Lag 1 LAP18 1p36.1-p35 C 1
b 66.0 Idb3 1 ID3 1p36.1 1
66.1 C1qa 1 C1QA 1 R SHGC-13801 50-52 1
66.1 C1qc 1 C1QC 1 R stSG8106 49-52 1
66.1 C1qb 1 C1QB 1p36.3-p34.1 R WI-16767 49-52 1
66.2 Htr1da 1 HTR1D 1p36.3-p34.3 1
66.6 Pla2g5 1 PLA2G5 1p35 1
66.6 Pla2g2c 1 PLA2G2C 1p35 1
66.6 Pla2g2a 1 PLA2G2A 1p35 R WI-7909 39-54 1
67.2 Elp1 1 ELP1 1p35 1
67.2 Fuca 1 FUCA1 1p35-p34 G 1
69.0 Pax7 1 PAX7 1p36.1 C,P 1
a 70.2 Akp2 1 ALPL 1p35 G 1
71.4 Hspg2 1 HSPG2 1p36.1 C 1
73.2 Eck 1 ECK 1 R M59371 36-49 1
76.5 Nppb 1 NPPB 1p36.3-p36.2 1
a, b 76.5 Nppa 1 NPPA 1p36.2 C,P,G 1
76.5 Plod 1 PLOD 1p36.3-p36.2 R SHGC-30062 22-32 1
75.8 Cd30 1 CD30 1p36.2 R,P SHGC-9861 22-36 1
b 75.5 Tnfr2(b) 1 TNFR2(b) 1p36.3-p36.2 R,C,P SHGC31494 22-36 1
77.6 Pgd 1 PGD 1p36.3 C,G 1
a 78.8 AA165858(a) 1 10958(u) 1 R WI-12099 16-22 1
a, b 78.9 Ski 1 SKV 1q22-24 ?
79.0 Eno1 1 ENO1 1p36.3 C,P,G 1
79.4 Cdc2l1 1 CDC2L1 1p36.3 C 1
b 79.4 Gnb1 1 GNB1 1p36-p31.2 R stSG1939 0-6 1
b 79.4 Ox40 1 TXGP1 1p36 1

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.