NCBI GenBank

Mouse To Human Homology Region Map, Chromosome 14

How to use this Resource

Cross Mouse Locus Mouse Gene Human Chr. Human Gene In Situ Method RH Map Genethon Map Homology Group
b 1.3 Il3ra X IL3RA Xp22.32 193
a, b 1.5 Rarb 3 RARB 3p24.3-p24.2 P 23
2(g) Ptprg 3* PTPRG 3p14.2 P,R 27
a 2.5 AA144896(a) 3* 1922(u) 3 R WI-9056 80-85 27
1.5 Anx7 10 ANX7 10q21.1-q21.2 R SHGC-12519 93-98 104
S Camkg 10 CAMK 10q22 104
a, b, c 2.5 Plau 10 PLAU 10q24 G* 104
b 2.5 Vcl 10 VCL 10q11.2-qter 104
8.0 Cchl1a2 3 CACNL1A2 3p14.3 R 24
b 8.0 Wnt5a 3 WNT5A 3p14-p21 24
b 13.0 Rbp3 10* RBP3 10q11.2 G 105
b 14.0 Sftp1 10* SFTP1 10q21-q24 R WI-7219 105-109 105
14.0 Sftp4 10* SFTP4 10q22.2-q23.1 105
15.5 Glud 10* GLUD 10q23-q24 R SHGC-9763 105-109 105
10(g) Adk 10 ADK 10q11-q24 103
c 15.5 Chat 10 CHAT 10q11.2 103
15.0 Mbl1 10 MBL 10q11.2 R SHGC-10740 72-74 103
S Itih1 3* ITIH1 3p21.1-p21.2 R SHGC-11985 65-67 26
c 15.5 Prkcd 3* PRKCD 3 R stSG3839 63-77 26
S Itih3 3* ITIH3 3p13-p12 R SHGC-11985 63-67 26
19.5 Gjb2 13 GJB2 13 127
19.7 Gja3 13 GJA3 13 127
b 14(g) Bmp4 14 BMP4 14 132
b 18.5 Apex 14 APE 14q11.2-q12 132
19.5 Nrl 14 NRL 14q11 R stSG1642 2-8 132
19.5 Np 14 NP1 14q11.2 132
a, b 19.5 Tcra 14 TCRA 14q11.2 R,G SHGC-11082 2-8 132
19.5 Tcrd 14 TCRD 14q11.2 R SHGC-9765 2-8 132
20.0 Ang 14 ANG 14q11 R stSG1614 0-1 132
b 20.0 Ctsg 14 CTSG 14q11.2 G 132
b 20.0 Myhca 14 MYH6 14q11.2-q13 132
20.0 Myhcb 14 MYH7 14q11.2-q13 G 132
20.5 Otx2 14 OTX2 14q21-q22 132
S Adcy4 14 ADCY4 14q11.2 132
20(g) Mcpt5 14 CMA1 14q11.2 132
a, b 20.5 Ctla1 14 CTLA1 14q12 G 132
20(g) Acra2 8 CHRNA2 8 82
27.0 Gata4 8 GATA4 8pter-p21.2 82
28.0 Blk 8 BLK 8p23-p22 82
28.5 Ctsb 8 CTSB 8p22 R WI-8953 6-25 82
28.5 Clu 8 CLU 8p21 82
b 28.5 Nfl 8 NEFL 8p21 G 82
b 32.5 Sftp2 8 SFTP2 8p 82
b 32.5 Bmp1 8 BMP1 8p21 82
38.0 Epb4.9 8 EBP49 8p21.1 82
39.5 Gnrh 8 GNRH 8p21-p11.2 82
39.5 Lhr 8 LHRH 8p21-p11.2 82
a 36.5(g) Dad1 14* DAD1 14q11-q12 R SHGC-153 2-8 131
41.0 Es10 13* ESD 13q14.1-q14.2 G 128
41.0 Rb1 13* RB1 13q14.2 R,G L11910 40-49 128
a 41.0 Htr2 13* HTR2 13q14-q21 R,G* SGC31576 40-46 128
47.6 D14H13S26 13* D13S25 13q21 R 46 128
51.0 Ednrb 13* EDNRB 13q22-q31 128
S Pou4f1 13* POU4F1 13q14-q22 R L20433 62-65 128
58.0 Dct 13* TYRP2 13q22 128
b 59.0 Rap2a 13* RAP2A 13q34 128
64.0 Pcca 13* PCCA 13q32 R,G 128

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.