NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 19

How to use this Resource

Cross Mouse Locus Mouse Gene Human Chr. Human Gene In Situ Method RH Map Genethon Map Homology Group
0 Catf1 11 SMBP2 11q13.2-q13.4 113
0.0 Gstp1 11 GSTP1 11q13 R SHGC-11734 70-77 113
b 4(g) Adrbk1 11 ADRBK1 11q13 R WI-15244 70-72 113
a 0.0 Pcx 11 PC 11q R PC 70-77 113
a 0.0 Seao 11 SEA 11q13 R,G 113
2(g) Pygm 11 PYGM 11q13.1 R,G 113
2(g) Ltbp2 11 LTBP2 11q13 113
a 0.0 Mdu1 11 MDU1 11q12-q13 R J02939 62-70 113
a 2.0 Fth 11 FTH1 11q13 R 113
3.0 Emk 11 EMK 11q13 113
3.0 Fau 11 FAU 11q13 113
a 4.0 Cd20 11 CD20 11q12-q13.1 R 113
a, b 5.0 Cd5 11 CD5 11q13 R,G SHCG-12715 64-70 113
8(g) Fcer1b 11 FCER1B 11q13 R SGC35231 62-65 113
a 7.0 Osbp 11 OSBP 11q12-q13 R stSG1375 62-65 113
b 7.0 Cntf 11 CNTF 11q12 R 113
8(g) Rom1 11 ROM1 11q13 113
S Fen1 11 FEN1 11q12 113
c 18.0 Lpc1 9 ANX1 9q11-q22 R SHGC-12349 57-68 94
21(y) Aldh1 9 ALDH1 9q21 R stSG4572 65-68 94
S(y) Rln 9 RLN1 9q21 94
c 20.0 Vldlr 9* VLDLR 9p24 R SHGC-12535 0 91
S(y) Snf2l2 9* SNF2L2 9p24-p23 91
24.0 Jak2 9* JAK2 9p24 91
a, b 23.0 Fas 10 APT1 10q24.1 R D29201 111-123 107
a 25.0 Ide 10 IDE 10q23-q25 R D10S2141 114-122 107
S Ifi54 10 IFI54 10q23-q24 107
S Ifi56 10 IFI56 10q23-q24 R T90506 111-123 107
S Lip1 10 LIPA 10q23.2-q23.3 107
a, b 27.0 Cyp2c 10 CYP2C 10q24.1-q24.3 107
29.0 Pnlip 10 PNLIP 10q24-q26 107
37.0 Got1 10 GOT1 10q24.1-q25.1 107
38.0 Rbp4 10 RBP4 10q23-q24 R SHGC-10696 131-134 107
b 39.5 Tdt 10 DNTT 10q23-24 107
c 43.0 Tlx1 10 HOX11 10q24 M62626 131 107
43.0 Pax2 10 PAX2 10q24 107
45.0 Fgf8 10 FGF8 10q25-q26 107
46.0 Cyp17 10 CYP17 10q24-q25 107
49.0 Col17a1 10 BPAG2 10q24.3 107
a 49.5 Mxi1 10 MXI1 10q25 107
a 50.0 Adra2a 10 ADRA2A 10q24-q26 107
50.0 Aop1 10 AOP1 10 107
a 51.0 Adrb1 10 ADRB1 10q24-q26 107
S Pgam1 10 PGAM1 10q25.3 107
b 51.0 Csfgmra X CSF2RA Xp22.32 194

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.