Mouse To Human Homology Region Map, Chromosome 8

Mouse To Human Homology Region Map, Chromosome 8

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

0.4 Fcer2a 19 FCER2 19p13.2 X 165

a, b 1.0 Insr 19 INSR 19p13.3-p13.2 X,G 165

1.0 Lamp1 13 LAMP1 13q34 130

2.0 Epl5 13 EPLG5 13q33 130

4.0 Atp4b 13 ATP4B 13q34 R 130

5.0 Col4a1 13 COL4A1 13q34 R,G WI9114 95-117 130

10(g) Atp7b 13 ATP7B 13q14.3-q21.1 130

9(g) Ram1 8 MLVAR 8p12-q21 84

b 8.0 Polb 8 POLB 8p12-p11 G 84

b 9.5(g) Ank1 8 ANK 8p21.1-p11.2 R,G WI-9207 62-65 84

a, b 9.0 Plat 8 PLAT 8p12-q11.2 R,G NIB234 64-65 84

a 8.0 Fnta 8 FNTA 8p22-q11 R WI6045 65-66 84

10.0 Fgfr1 8 FGFR1 8p12-p11.2 R SHGC-11130 62-64 84

a 10.0 Adrb3 8 ADRB3 8p11.1-p12 R WI-9207 62-64 84

11.0 Defcr 8 DEF1 8p23-p22 84

18.0 Gr1 8* GSR 8p21.1 83

b 20.0 Scvr 8* MSR1 8p22 R WI-7228 30-44 83

S Aga 4 AGA 4q34-q35 43

S Mntria 4 MTNR1A 4q35 43

22.5 Klk3 4 KLK3 4q35 R SHGC-9749 199-211 43

25.0 Cf11 4 FXI 4q35 R WI-9131 199-211 43

25.0 Ant1 4 ANT1 4q35 43

32.0 Cpe 4 CPE 4q28 43

32.5 Clc3 4 CLC3 4q32 R H68066 169-178 43

32.5 Tll 4 TLL 4q32-q33 43

33.0 Npy1r 4 NYPY1R 4q31.3-q32 R SHGC-12458 160-170 43

a 32(g) W10357(a) 4 11736(u) 4 R A007J08 169-170 43

35(g) Mlr 4 MLR 4q31.3-q32 43

33.0 Comp 19* COMP 19p13.1 X 168

a, b 33.0 Jund1 19* JUND 19p13.1 X,G 168

a 33.0 Mel 19* MEL 19p13.1 X,G 168

33.0 Sin3b 19* SIN3B 19p13 168

S Nfix 19* NFIX 19q13 168

32.5(g) Pde4c 19* PDE4C 19 168

33.0 Scl18a1 8 SLC18A1 8p21.3 83

33.0 Lpl 8 LPL 8p22 R,G WI-9031 35-40 83

36.0 Gypa 4* GYPA 4q28-q31 R,G SHGC-12331 143-145 41

a, b 37.0 Ucp 4* UCP 4q28-q31 G 41

37.0 Il15 4* IL15 4q31 R WI-93555 139-143 41

a, b 38.0 Junb 19 JUNB 19p13.2 X 167

b 38.0 Lyl1 19 LYL1 19p13.2 X,G 167

a 38.0 Ptgerep1 19 PTGER1 19p13.1 167

38.0 Rfx1 19 RFX1 19p13.1 X 167

40.0 Adcy7 16 ADCY7 16q12-q13 146

43.0 Ces1 16 CES1 16q13-q22.1 R stSG1404 65-72 146

43.2 Es6 16 ESB3 16 146

45.0 Mt3 16 MT3 16q13 R 146

a, b 45.0 Mt1 16 MT1A 16q13 R WI-6072 72-75 146

45.0 Mt2 16 MT2A 16q13 G 146

46.0 Got2 16 GOT2 16q12-q22 R 146

46.0 Gnao 16 GNAO1 16q13 146

42(g) Mov34 16 PSMD7 16q22.2 146

a 50.0 Has3 16 HAS3 16q22.1 146

51.0 Cbfb 16 CBFB 16q22 146

52.0 Cdh1 16 CDH1 16q22.1 146

b 52.0 Cdh3 16 CDH3 16q22.1 146

53.0 Lcat 16 LCAT 16q22.1 R 146

53.0 Ctra 16 CTRA 16 R WI-7891 84-88 146

S Mov34 16 MOV34 16q23-q24 R 146

b 55.0 Hp 16 HP 16q22 R,G 146

55.0 Tat 16 TAT 16q22.1 R SHGC-11957 84-86 146

55.0 Ctrb 16 CTRB 16q23-q24.1 G 146

60.0 Cox4 16 COX4 16q24.1 146

62(g) Plcg2 16 PLCG2 16q24.1 R 146

b 61.0 Maf 16 MAF 16q22-q23 R 146

64.0 Mf1 16 MF1 16q22-q24 146

67.0 Cdh3 16 CDH3 16q24.1-qter R 146

b 67.0 Aprt 16 APRT 16q24.2-qter R,G 146

67.0 Hfh8 16 FKHL5 16q24 146

72(g) Fkh6 16 FKHL6 16q22-q24 146

68(g) Mc1r 16 MC1R 16q24.3 R 146

a, b, c 67.0 Actsk 1 ACTA1 1q42.1-q42.3 R,P SHGC-12727 246-256 7

67.5 Rab4a 1 RAB4A 1q42-43 7

68.0 Agt 1 AGT 1q41-qter R.P WI-8965 249-251 7

S Rn5s 1 RN5S 1q42.11-q42.13 7

Cross	Mouse Locus	Mouse Gene	Human Chr.	Human Gene	In Situ	Method	RH Map	Genethon Map	Homology Group
	0.4	Fcer2a	19	FCER2	19p13.2	X			165
a, b	1.0	Insr	19	INSR	19p13.3-p13.2	X,G			165
	1.0	Lamp1	13	LAMP1	13q34				130
	2.0	Epl5	13	EPLG5	13q33				130
	4.0	Atp4b	13	ATP4B	13q34	R			130
	5.0	Col4a1	13	COL4A1	13q34	R,G	WI9114	95-117	130
	10(g)	Atp7b	13	ATP7B	13q14.3-q21.1				130
	9(g)	Ram1	8	MLVAR	8p12-q21				84
b	8.0	Polb	8	POLB	8p12-p11	G			84
b	9.5(g)	Ank1	8	ANK	8p21.1-p11.2	R,G	WI-9207	62-65	84
a, b	9.0	Plat	8	PLAT	8p12-q11.2	R,G	NIB234	64-65	84
a	8.0	Fnta	8	FNTA	8p22-q11	R	WI6045	65-66	84
	10.0	Fgfr1	8	FGFR1	8p12-p11.2	R	SHGC-11130	62-64	84
a	10.0	Adrb3	8	ADRB3	8p11.1-p12	R	WI-9207	62-64	84
	11.0	Defcr	8	DEF1	8p23-p22				84
	18.0	Gr1	8*	GSR	8p21.1				83
b	20.0	Scvr	8*	MSR1	8p22	R	WI-7228	30-44	83
	S	Aga	4	AGA	4q34-q35				43
	S	Mntria	4	MTNR1A	4q35				43
	22.5	Klk3	4	KLK3	4q35	R	SHGC-9749	199-211	43
	25.0	Cf11	4	FXI	4q35	R	WI-9131	199-211	43
	25.0	Ant1	4	ANT1	4q35				43
	32.0	Cpe	4	CPE	4q28				43
	32.5	Clc3	4	CLC3	4q32	R	H68066	169-178	43
	32.5	Tll	4	TLL	4q32-q33				43
	33.0	Npy1r	4	NYPY1R	4q31.3-q32	R	SHGC-12458	160-170	43
a	32(g)	W10357(a)	4	11736(u)	4	R	A007J08	169-170	43
	35(g)	Mlr	4	MLR	4q31.3-q32				43
	33.0	Comp	19*	COMP	19p13.1	X			168
a, b	33.0	Jund1	19*	JUND	19p13.1	X,G			168
a	33.0	Mel	19*	MEL	19p13.1	X,G			168
	33.0	Sin3b	19*	SIN3B	19p13				168
	S	Nfix	19*	NFIX	19q13				168
	32.5(g)	Pde4c	19*	PDE4C	19				168
	33.0	Scl18a1	8	SLC18A1	8p21.3				83
	33.0	Lpl	8	LPL	8p22	R,G	WI-9031	35-40	83
	36.0	Gypa	4*	GYPA	4q28-q31	R,G	SHGC-12331	143-145	41
a, b	37.0	Ucp	4*	UCP	4q28-q31	G			41
	37.0	Il15	4*	IL15	4q31	R	WI-93555	139-143	41
a, b	38.0	Junb	19	JUNB	19p13.2	X			167
b	38.0	Lyl1	19	LYL1	19p13.2	X,G			167
a	38.0	Ptgerep1	19	PTGER1	19p13.1				167
	38.0	Rfx1	19	RFX1	19p13.1	X			167
	40.0	Adcy7	16	ADCY7	16q12-q13				146
	43.0	Ces1	16	CES1	16q13-q22.1	R	stSG1404	65-72	146
	43.2	Es6	16	ESB3	16				146
	45.0	Mt3	16	MT3	16q13	R			146
a, b	45.0	Mt1	16	MT1A	16q13	R	WI-6072	72-75	146
	45.0	Mt2	16	MT2A	16q13	G			146
	46.0	Got2	16	GOT2	16q12-q22	R			146
	46.0	Gnao	16	GNAO1	16q13				146
	42(g)	Mov34	16	PSMD7	16q22.2				146
a	50.0	Has3	16	HAS3	16q22.1				146
	51.0	Cbfb	16	CBFB	16q22				146
	52.0	Cdh1	16	CDH1	16q22.1				146
b	52.0	Cdh3	16	CDH3	16q22.1				146
	53.0	Lcat	16	LCAT	16q22.1	R			146
	53.0	Ctra	16	CTRA	16	R	WI-7891	84-88	146
	S	Mov34	16	MOV34	16q23-q24	R			146
b	55.0	Hp	16	HP	16q22	R,G			146
	55.0	Tat	16	TAT	16q22.1	R	SHGC-11957	84-86	146
	55.0	Ctrb	16	CTRB	16q23-q24.1	G			146
	60.0	Cox4	16	COX4	16q24.1				146
	62(g)	Plcg2	16	PLCG2	16q24.1	R			146
b	61.0	Maf	16	MAF	16q22-q23	R			146
	64.0	Mf1	16	MF1	16q22-q24				146
	67.0	Cdh3	16	CDH3	16q24.1-qter	R			146
b	67.0	Aprt	16	APRT	16q24.2-qter	R,G			146
	67.0	Hfh8	16	FKHL5	16q24				146
	72(g)	Fkh6	16	FKHL6	16q22-q24				146
	68(g)	Mc1r	16	MC1R	16q24.3	R			146
a, b, c	67.0	Actsk	1	ACTA1	1q42.1-q42.3	R,P	SHGC-12727	246-256	7
	67.5	Rab4a	1	RAB4A	1q42-43				7
	68.0	Agt	1	AGT	1q41-qter	R.P	WI-8965	249-251	7
	S	Rn5s	1	RN5S	1q42.11-q42.13				7

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

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.