NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 5

How to use this Resource

Cross Mouse Locus Mouse Gene Human Chr. Human Gene In Situ Method RH Map Genethon Map Homology Group
1.0 Gnai1 7 GNAI1 7q21-q22 77
1.0 Pgy1 7 PGY1 7q21-q22 P,C 77
1.0 Pgy3 7 PGY3 7q21-q22 P,G 77
1.0 Sri 7 SRI 7q21 77
4.0 Cchl2a 7 CCHL2A 7q21-q22 P 77
a, b 4.0 Hgf 7 HGF 7q21.1 P 77
8.0 Rln 7 RELN 7q22 P,R SHGC-32029 114-119 77
c 9.0 Nos3 7* NOS3 7q35-q36 R SHGC-11213 163 81
12.0 Cdk5 7* CDK5 7q36 R SGC30025 167-175 81
12.0 Dpp6 7* DPP6 7 81
14.0 Ae2 7* SLC4A2 7q35-q36 81
15.0 Htr5a 7* HTR5A 7q35-q36 81
b 15.0 En2 7* EN2 7q36 P,G 81
16.0 Shh 7* SHH 7q36 81
a, b 17.0 Il6 7 IL6 7p21-p15 P,R,G SHGC-9784 36-39 70
18.0 Tyms 18 TYMS 18p11.3 153
18.0 Lrpap1 4 LRPAP1 4p16.3 38
20.0 Gprk2l 4 GPRK2L 4p16.3 38
b 20.0 D5H4S43 4 D4S43 4p16.3 38
b 20.0 Fgfr3 4 FGFR3 4p16.3 R X84939 0 38
20.0 Adra2c 4 ADRA2C 4p16.3-p15 R,G SHGC-13378 6-12 38
20.0 Add1 4 ADD1 4p16.3 38
21.0 Hdh 4 HD 4p16.3 38
b 21.0 Msx1 4 MSX1 4p16.3-p16.1 G 38
22.0 D5H4S115 4 D4S115 4p16.3 38
23.0 D5H4S62 4 D4S62 4p16.2-p16.1 38
b 23.0 Drd5 4 DRD5 4p15.3-p15.1 R 38
28.0 Cd38 4 CD38 4 R SGC31590 24-32 38
a 30.0 Qdpr 4 QDPR 4p15.3 38
33.0 D5H4S76 4 D4S76 4p16.2-p15.1 38
33.0 D5H4S80 4 D4S80 4p16.2-p15.1 38
c 34.0 Cckar 4 CCKAR 4 R SHGC12838 38-43 38
38.0 Pgm1 4 PGM2 4p14-q12 38
39.0 Pep7 4 PEPS 4p11-q12 38
39.0 Recc1 4 RFC1 4p13-p14 38
a 40.0 W65100(a) 4 22148(u) 4 R D25250 50-56 38
40.0 Gabra2 4 GABRA2 4p12-p13 R WI-7294 61-62 38
40.0 Gabrb1 4 GABRB1 4p12-p13 G 38
40.0 Txk 4 TXK 4p12 38
a, b 41.0 Cncg 4 CNCG 4p13-p14 R 38
b 41.0 Tec 4 TEC 4p12 R SHGC-9639 60-62 38
41.0 Cenpc 4 CENPC 4q12-q13.3 38
b, c 42.0 Flk1 4 KDR 4q12 38
a, b, c 42.0 Kit 4 KIT 4q12 R,G 38
a, b, c 42.0 Pdgfra 4 PDGFRA 4q11-q12 G* 38
S Ugt2b5 4 UGT2B 4q13 38
c 44.0 Gnrhr 4 GNRHR 4q13.1-q21.1 R L03380 71-77 38
44.0 Ste 4 STE 4q13.1-q21.1 38
a 45.0 Csnb 4 CSN2 4p16.3-q21 R 38
46.0 Ambn 4 AMBN 4q 38
49.0 Amen 4 AMEN 4q 38
a 50.0 Afp 4 AFP 4q11-q13 R SHGC-10695 77-81 38
b, c 50.0 Alb1 4 ALB 4q11-q13 R,G A004G47 77-90 38
50.0 Gc 4 GC 4q12-q13 R,G 38
51.0 Areg 4 AREG 4q13-q21 R D4S3138 77-81 38
51.0 Btc 4 BTC 4q13-q21 38
S Igj 4 IGJ 4q21 R WI-18564 77-90 38
a 51.0 Mgsa 4 GRO1 4q21 G* 38
b 55.0 Bmp3(g) 4 BMP3 4p14-q21 38
b 55.0 Fgf5(g) 4 FGF5 4q21 R M23534 77-90 38
56.0 Dmp1 4 DMP1 4q21 38
56.0 Ibps 4 IBPS 4q21-25 38
56.0 Spp1(g) 4 SPP1 4q11-q21 R,G 38
a 57.0 Pdeb 4* PDE6B 4p16.3 37
57.0 Dagk4 4* DAGK4 4p16.3 37
57.0 Idua 4* IDUA 4p16.3 37
b 56.0 Gfi1 1 GFI1 1p22 3
a 56.0 AA124718(a) 1 1649(u) 1 R WI-9122 129-132 3
a 56.0 AA155193(a) 1 25505(u) 1 R 25505 131 3
59.0 Crybb4 22 CRYBB4 22q11.2-q12.1 X 189
59.0 Crybb1 22 CRYBB1 22q11.2-q12.1 189
60.0 Crybb3 22 CRYBB3 22q11.2-q12.1 X 189
60.0 Crybb2 22 CRYBB2 22q11.2-q12.1 R,X,G stCRYB2A 9-16 189
b 60.0 Adrbk2 22 ADRBK2 22q11 189
65.0 Acads 12 ACADS 12q22-qter 125
65.0 Tcf1 12 TCF1 12q24.3 125
65.0 Dao1 12 DAO 12q24.3 125
S Cenpc 12 CENPC 12 125
70.0 Nos1 12 NOS1 12q24.2-q24.3 R SGC31491 126-133 125
b 72.0 Eln 7* ELN 7q11.23 75
72.0 Gus 7* GUSB 7q22 P,R WI-9137 77-79 75
72.0 Phkg 7* PHKG1 7p12-q21 75
b S Asl 7* ASL 7q21.3-q22.1 P 75
76.0 Ncf1 7* NCF1 7q11.23 P 75
76.0 Gnb2 7* GNB2 7q21.3-q22.1 75
78.0 Lmk1 7* LMK1 7q11.23 75
b, c 79.0 Zp3 7* ZP3 7 P 75
79.0 Ocm 7* OCM 7p13-p11 P 78
a, b 80.0 Epo 7* EPO 7q21.3-q22.1 P,C 78
80.0 Pcolce 7* PCOLCE 7q21.3-q22 78
80.0 Azgp1 7* AZGP1 7q22.1 P 78
80.0 Cutl1 7* CUTL1 7q22.1 P 78
80.0 Mor1 7* MDH2 7p13-q22 78
80.0 Ache 7* ACHE 7q22 C 78
82.0 Cyp3a11 7* CYP3A 7q21.3-q22.1 78
85.0 D5Kyo2 7* PLANH1 7q21.3-q22 C,G 78
a, b 84.0 Pdgfa 7* PDGFA 7p22 R,X SHGC-10715 <1 68
84.0 Prkar1b 7* PRKAR1B 7pter-p22 68
85.0 Pms2 7* PMSL2 7p22 R,X WI-16837 7-10 68
b 85.0 Flt1 13 FLT1 13q12 R 126
b 85.0 Flt3 13 FLT3 13q12 126
88.0 Atrc1 13 ATRC1 13q12.3 G 126

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.