NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 7

How to use this Resource

Cross Mouse Locus Mouse Gene Human Chr. Human Gene In Situ Method RH Map Genethon Map Homology Group
2.0(y) Il11 19 IL11 19 181
a 2.0 Pkcc 19 PRKCG 19q13.4 X,G 181
2.0 Zfp132 19 ZFP132 19 181
2.0 Syt3 19 SYT3 19q R,X stSG4046 81-94 181
2.0 Zfp134 19 ZFP134 19 X 181
2.0 Zfp98 19 ZFP98 19 181
2.5 Calm3 19* CALM3 19q13.3 X 176
a, b 2.5 Cea5 19 CEA5 19q13.2 X,G 171
2.5 Cea2 19 CEA2 19 171
2.5 Ptgir 19* PTGIR 13q13.3 R,X SHGC-9630 69-81 174
3.3 D7H19S51 19* D19S51 19q13.3 174
3.3 D7H19S112 19* D19S112 19q13.3 174
a 4.0 Ckmm 19 CKM 19q13.3 X,G 175
4.0 Dm15 19 B15 19q13.3 175
4.0 Dm9 19 D19S539E 19q13.3 X 175
4.0 Ercc1 19* ERCC1 19q13.3 X,G 173
a 4.0 Ercc2 19* ERCC2 19q13.3 G 173
a 4.0 Atp1a3 19* ATP1A3 19q13.2 X,G 173
a 4.0 D7H19S19 19* D19S19 19q13.2 173
4.0 Apoc2 19* APOC2 19q13.2 X,G 173
4.0 Apoc1 19* APOC1 19q13.2 X 173
a 4.0 Apoe 19* APOE 19q13.2 R,X stSG94 69-81 173
a 5.5 Xrcc1 19 XRCC1 19q13.2 R,X SHGC30018 67-69 172
5.5 Cd79a 19 IGA 19q13.2 172
6.0 Zfp94 19 ZFP94 19 172
6.0 Zfp93 19 ZFP93 19 172
a, b 6.0 Pou2f2 19 POU2F2 19q13 X 172
a 6.0 Trsp 19 TRSP 19q13.2-q13.3 G 172
6.5 Bcl3 19 BCL3 19q13.2 X,G 172
8(g) Lig1 19 LIG1 19q13.3 172
a 9(g) Pvs 19 PVS 19q13.2 R,X SHGC-11493 67-69 172
8(g) Bgp 19* BGP 19q13.2 R,X SGC35228 63-69 170
6.5 Cea10 19* CEA10 19 170
c 5.5(g) Lipe 19* LIPE 19q13.1-q13.2 R,X,G SGC34102 63-65 170
a, b 6.5 Tgfb1 19* TGFB1 19q13.1 X 170
6.5 Cyp2f1 19* CYP2F1 19q13.2 X,G 170
6.5 Cyp2b9 19* CYP2B9 19q13.2 170
6.5 Cyp2b13 19* CYP2B13 19q13.2 X 170
a 6.5 Cyp2b9 19* CYP2B113 19q13.2 X,G 170
6.5 Cyp2a5 19* CYP2A5 19q13.2 170
a 6.5 Cyp2a4 19* Cyp2a4 19q13.2 X,G 170
a? 6.5 Grik5 19* GRIK5 19q13.2 170
b 6(g) Hnf3g 19 TCF3G 19p13.3 X 162
9.0 Atp4a 19 ATP4A 19q13.1 162
a 9.0 Zfp36 19* ZFP36 19q13.1 169
9.0 D7H19F11S1 19* D19F11S1 19q13.1 169
10.0 Ryr 19* RYR1 19q13.1 X,G* 169
15(g) Ufo 19* UFO 19q13.1-q13.2 R SHGC-12719 62-65 169
13.0 Coxb 19* COXB 19q13.1 X 169
13.0 Atp4a 19* ATP4A 19q13.1 X 169
b 11(g) Cd22 19* CD22 19q13.1 R,X X59350 49-58 169
a, b 13.0 Mag 19* MAG 19q13.1 R,X WI-15623 58-60 169
a 13(y) Scn1b 19* SCN1B 19q13.1 X 169
a, b 13(y) Gpi1 19* GPI 19q13.1 R,X,G* SHGC-11013 58 169
a, b 13(y) Cebpa 19* CEBPA 19q13.1 X 169
15.0 Pep4 19* PEPD 19q13.1 X 169
15.0 Ccne 19* CCNE 19q12-q13 169
b 23.0 Ntf5 19 NTF5 19 179
23.0 Ngfg 19 NGFG 19q13.3 179
23.0 Lim2 19 LIM2 19 X 179
23.0 Etfb 19 ETFB 19 X 179
23.0 Cd33 19 CD33 19 X 179
a, b, c 23.0 Klk1 19 KLK1 19q13.3 X,G 179
a 23.0 Lhb 19* LHB 19q13.3 X 177
23.0 Dbp 19* DBP 19q13 177
a 23.0 Bax 19* BAX 19q13.3-q13.4 X 177
a 23.0 Gys1 19* GYS1 19q13.3 R,X SHGC-9668 69-81 177
23(y) Hrc 19* HRC 19q13.3 X,G 177
a 23.0 Cd37 19* CD37 19q13.3 R WI-15345 69-97 177
a, b 23.0 Rras 19* RRAS 19q13.3 X 177
a 23.0 Snrp70 19* SNRP70 19q13.3 X 177
P 24.0 Saa1 11 SAA1 11p15.1 R SGC32644 22-24 111
P 24.0 Saa2 11 SAA2 11p15.1 111
P 24.0 Saa3 11 SAA3 11p15.1 R 111
P 24.0 Saa4 11 SAA4 11p15.1 111
a, P 24.0 Saa5 11 SAA5 11p15.1 111
P 24.0 Tph 11 TPH(g) 11p15.3-p14(g) R 111
b, P 24.0 Kcnc1 11 KCNC1 11p14.3-p15.2 R 111
c, P 24.0 Ldh3(b) 11 LDHC(b) 11p15.5-p14.3 R 111
24.0 Ldh1 11 LDHA 11p15.1-p14 R 111
a, b 24.0 Myod1 11 MYOD1 11p15 R 111
27.0 D7H15F37S1 15 D15F37S1 15q11-q13 134
a, b 28.0 p 15 OCA2 15q11.2-q12 134
28.0 Gabra5 15 GABRA5 15q11-q13 R WI-9133 6-14 134
b 28.0 Gabrb3 15 GABRB3 15q11.2-q12 R,G stSG1644 13-17 134
28.0 Gabrg3 15 GABRG3 15q11-q13 134
b 29.0 Snrpn 15 SNRPN 15q11-q12 R SGC31492 14-20 134
29.0 Znf127 15 ZNF127 15q11-q13 134
29.0 Pcsk6 15 PCSK6 15q 134
29.0 Tjp1 15 TJP1 15q13 134
a 30(g) Acra7 15 CHRNA7 15q14 R stSG3316 17-22 134
33.0 Mef2a 15* MEF2A 15q26 140
33.0 Aporp1 15* TFCOUP2 15q26 140
a, b 33.0 Igf1r 15* IGF1R 15q25-qter R SHGC-12341 98-103 140
a, b 39.0 Fes 15* FES 15q26.1 G 140
39.0 Agc 15* AGC1 15q26 140
c 39.0 Pcsk3 15* PACE 15q25-q26 140
39.0 Ntrk3 15* NTRK3 15q24-q25 R SGC30075 80-83 140
39.0 Rlbp1 15* RLBP1 15q26 R J04213 77-80 140
41.0 Idh2 15* IDH2 15q21-qter 140
43.0 Fah 15 FAH 15q23-q25 139
46(g) Mod2 6 ME2 6p25-p24 58
a, b 44.0 Tyr 11* TYR 11q21 R,G WI-9075 92-96 115
46.0 D7H11S833E 11* GARP 11q13.5-q14 115
a 47.0 Ucp2 11* UCP2 11q13 R WI-13873 80-84 115
b 48.0 Omp 11* OMP 11q13.4-q14.1 R 115
a 50.0 Arrb1 11* ARRB1 11q13 115
48.0 Myo7a 11* MYO7A 11q13.5 115
50.0 Rt6-1 11* RT6 11q13 115
50.0 Icln 11* ICLN 11q13.5-q14 115
a, c 50.0 Hbb 11 HBB 11p15.4 R,G 110
S Smpd1 11 SMPD1 11p15.4 R SMD1 6-14 110
b 50.0 Rbtn1 11 RBTN1 11p15 R LMO 16 110
50.0 Rpt1 11 RPT1 11p15 110
52.0 Lmo1 11 LMO1 11p15.3-p14(g) 110
a 53.0 Pth 11 PTH 11p15.2-p15.1 R,G 110
a, b 54.0 Calc 11 CALCA 11p15.2-p15.1 R,G WI-6982 22-28 110
41(g) Sur 11 SUR 11p15.1 110
c 50.0 Cckbr 11 CCKBR 11p15.4 110
56.0 Scnn1b 16 SCNN1B 16p12.1-p11.2 145
56.0 Scnn1g 16 SCNN1G 16p12.1-p11.2 R L36592 31-41 145
b 60.0 Pkcb 16 PRKCB1 16p12 R 145
c 61.0 Stp1 16 STP1 16p12.1-p11.2 R 145
b 62.0 Il4r 16 IL4R 16p12.1-p11.2 R SGC30149 45-50 145
59(g) Cd19 16 CD19 16p11.2 R 145
60(g) Itgal 16 ITGAL 16p13.1-p11 R 145
b 62.0 Spn 16 SPN 16p11.2 R 145
63.0 Oat 10 OAT 10q26 R.G M23204 151-162 108
b 63.0 Fgfr2 10 FGFR2 10q25.3-q26 R SHGC-9871 145-162 108
64.0 Cyp2e1 10 CYP2E1 10q24.3-qter R,G stSG1303 169-182 108
b 66.0 Mgmt 10 MGMT 10q26 108
63(g) Uros3 10 UROS 10q25.2-q26.3 R Cda02c01 158-162 108
68.0 Ptpre 10 PTPRE 10q26 108
72.0 Muc2 11* MUC2 11p15.5 R MUC2B 0-6 109
72.0 Ctsd 11* CTSD 11p15.5 109
72.0 Muc5ac 11* MUC5ac 11p15.5 109
b 70.0 Drd4 11* DRD4 11p15.5 R 109
a 69.0 Hras1 11* HRAS1 11p15.5 R,G 109
a, b 69.0 H19 11* D11S813E 11p15.5-p15.4 R 109
b 69.0 Igf2 11* IGF2 11p15.5 R WI-14149 3-27 109
69.0 Cdkn1c 11* CDKN1C 11p15.5 109
a 67.0 Th 11* TH 11p15.5 R,G 109
a 69.0 Tapa1 11* TAPA1 11p15.5-p11 109
a, b, c 69.0 Ins2 11* INS 11p15.5 R,G 109
S Rrm1 11* RRM1 11p15.5-p15.4 R RRMI 14-16 109
a 69.5 Fis1 11 FIS1 11q24.1-q24.3 114
69.7 D7H11S814 11 D11S814 11q13 114
72.0 Ccnd1 11 CCND1 11q13.1 R WI-16756 70-77 114
72.0 Fgf4 11 FGF4 11q13.3 R FGF4 70-77 114
b 72.0 Fgf3 11 FGF3 11q13.3 R,G 114

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.