Human to Mouse Homology Region Map, Chromosome 22

Human to Mouse Homology Region Map, Chromosome 22

RH Map Genethon Map Method In Situ Human Gene Mouse Chr. Mouse Gene Mouse Locus Cross Homology Group

stTUPLE1 3-9 R,X 22q11 TUP1 16 Tuple1 17(g) 186

stTOP1P2 9-16 R,G 22q TOP1P2 16 Top1ps2 11.4 186

stCOMT 3-9 R,X,G* 22q11.2 COMT 16 Comt 13.0 186

stVPREB 9-16 R,X 22q11.2 VPREB1 16 Vpreb1 12.0 186

22q11.2 MIF 10 Mif 40.5 a 187

WI-14102 9-16 R,X 22q11 GNAZ 10 Gnaz 40.0 b 187

X,G 22q11 BCR 10 Bcr 40.0 b 187

L22589 9-16 R,X 22q11.2 IGLL1 16* Igl 13.0 a, b 188

stCRYB2A 9-16 R,X,G 22q11.2-q12.1 CRYBB2 5 Crybb2 60.0 189

22q11 ADRBK2 5 Adrbk2 60.0 b 189

X 22q11.2-q12.1 CRYBB3 5 Crybb3 60.0 189

22q11.2-q12.1 CRYBB1 5 Crybb1 59.0 189

X 22q11.2-q12.1 CRYBB4 5 Crybb4 59.0 189

stLIF 23-24 R,X 22q12 LIF 11 Lif 1.0 b 190

X 22q12.2 NF2 11 Nf2 1.0 190

22q12 CAMK2B 11 Camk2b 1.0 b 190

22q12 OSM 11 Osm 1.0 190

SHGC-12522 22-25 R,X 22q12 TCN2 11 Tcn2 3(g) 190

22q12.1-q13.1 NFH 11 Nfh 5(g) 190

SHGC-12911 22-25 R,X 22q12.1-q13.2 TIMP3 10 Timp3 47.0 a, c 191

stMB 31-33 R,X,G 22q12 MB 15 Mb 43.3 192

SHGC-11984 36 R,X 22q12-q13.1 PVALB 15 Pva 43.4 192

M26062 31-40 R,X,G 22q13 IL2RB 15 Il2rb 46(g) b 192

X,G 22q12.3-q13.1 MYH9 15 Myh9 43.3 b 192

WI-8985 40-42 R,X,G 22q12.3-q13.1 PDGFB 15 Pdgfb 43.3 a 192

22q12.3-13.1 SCX 15 Scx 43.3 192

22q12-q13.1 LGALS1 15 Lgals1 44.9 b 192

22q13.31-qter DIA1 15 Dia1 45.2 192

stPPAR 40-45 R 22q12-q13.1 PPAR 15 Ppara 48.8 a 192

22q13 TEF 15 Tef 49.2 c 192

22q13-qter ACR 15 Acr 48.6 192

22q12-qter TST 15 Tst 47.0 192

22q13 CYP2D9 15 Cyp2d9 47.2 192

stCYP2D 40-45 R,X.G 22q11.2-qter CYP2D 15 Cyp2d 47.2 192

stBZRP 40-45 R,X 22q13.3-qter BZRP 15 Bzrp 43.3(g) 192

X 22q13 ECGF1 15 Pdgfec 51.6 b 192

WI-8900 40-45 R 22q11.2-q13.3 ACO2 15 Aco2 S 192

stFIBB 40-45 R 22 FBLN1 15 Fbln1 S 192

22q13 GAD3 15 Gad3 S 192

stARSA 40-45 X 22q13.31-qter ARSA 15 As2 S 192

RH Map	Genethon Map	Method	In Situ	Human Gene	Mouse Chr.	Mouse Gene	Mouse Locus	Cross	Homology Group
stTUPLE1	3-9	R,X	22q11	TUP1	16	Tuple1	17(g)		186
stTOP1P2	9-16	R,G	22q	TOP1P2	16	Top1ps2	11.4		186
stCOMT	3-9	R,X,G*	22q11.2	COMT	16	Comt	13.0		186
stVPREB	9-16	R,X	22q11.2	VPREB1	16	Vpreb1	12.0		186
			22q11.2	MIF	10	Mif	40.5	a	187
WI-14102	9-16	R,X	22q11	GNAZ	10	Gnaz	40.0	b	187
		X,G	22q11	BCR	10	Bcr	40.0	b	187
L22589	9-16	R,X	22q11.2	IGLL1	16*	Igl	13.0	a, b	188
stCRYB2A	9-16	R,X,G	22q11.2-q12.1	CRYBB2	5	Crybb2	60.0		189
			22q11	ADRBK2	5	Adrbk2	60.0	b	189
		X	22q11.2-q12.1	CRYBB3	5	Crybb3	60.0		189
			22q11.2-q12.1	CRYBB1	5	Crybb1	59.0		189
		X	22q11.2-q12.1	CRYBB4	5	Crybb4	59.0		189
stLIF	23-24	R,X	22q12	LIF	11	Lif	1.0	b	190
		X	22q12.2	NF2	11	Nf2	1.0		190
			22q12	CAMK2B	11	Camk2b	1.0	b	190
			22q12	OSM	11	Osm	1.0		190
SHGC-12522	22-25	R,X	22q12	TCN2	11	Tcn2	3(g)		190
			22q12.1-q13.1	NFH	11	Nfh	5(g)		190
SHGC-12911	22-25	R,X	22q12.1-q13.2	TIMP3	10	Timp3	47.0	a, c	191
stMB	31-33	R,X,G	22q12	MB	15	Mb	43.3		192
SHGC-11984	36	R,X	22q12-q13.1	PVALB	15	Pva	43.4		192
M26062	31-40	R,X,G	22q13	IL2RB	15	Il2rb	46(g)	b	192
		X,G	22q12.3-q13.1	MYH9	15	Myh9	43.3	b	192
WI-8985	40-42	R,X,G	22q12.3-q13.1	PDGFB	15	Pdgfb	43.3	a	192
			22q12.3-13.1	SCX	15	Scx	43.3		192
			22q12-q13.1	LGALS1	15	Lgals1	44.9	b	192
			22q13.31-qter	DIA1	15	Dia1	45.2		192
stPPAR	40-45	R	22q12-q13.1	PPAR	15	Ppara	48.8	a	192
			22q13	TEF	15	Tef	49.2	c	192
			22q13-qter	ACR	15	Acr	48.6		192
			22q12-qter	TST	15	Tst	47.0		192
			22q13	CYP2D9	15	Cyp2d9	47.2		192
stCYP2D	40-45	R,X.G	22q11.2-qter	CYP2D	15	Cyp2d	47.2		192
stBZRP	40-45	R,X	22q13.3-qter	BZRP	15	Bzrp	43.3(g)		192
		X	22q13	ECGF1	15	Pdgfec	51.6	b	192
WI-8900	40-45	R	22q11.2-q13.3	ACO2	15	Aco2	S		192
stFIBB	40-45	R	22	FBLN1	15	Fbln1	S		192
			22q13	GAD3	15	Gad3	S		192
stARSA	40-45	X	22q13.31-qter	ARSA	15	As2	S		192

Human/Mouse Homology Mapping Methods

Method	Description
C	High-resolution cytogenetic methods
G	Genetic linkage mapping
G*	Genetic mapping, with disagreements between genetic and physical map resolved in favor of physical map
L	Long-range restriction site mapping
P	Multiple physical methods, including YAC and cosmid contigs
R	Radiation hybrid mapping
X	Multiple sources of high-resolution data

Gene Notes:

Key	Description
a	Gene Bank Accession Number for Mouse EST
b	Gene 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
g	Mouse gene order has been changed slightly to conform with human gene order in the absence of conflicting high resolution data
y	Position has been changed from that reported in chromosome committee report or or Mouse Genome Database based on additional data or review of previous data
p	Different sources of high resolution mapping data give conflicting positions
r	Difference between position in inbred mice vs. Mus spretus
u	This 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