Mouse To Human Homology Region Map, Chromosome 12

Mouse To Human Homology Region Map, Chromosome 12

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

S Reg1a 2 REG1A(g) 2p12(g) 9

b 1.0 Synd1 2 SDC 2p R stSG9345 40-48 9

2.0 Apob 2 APOB 2p24-p23 R,G SGC34591 40-48 9

S Adcy3 2 ADCY3 2p24-p2 9

4.0 Kif3c 2 KIF3C(?) 2 R stSG4510 48-50 9

4.0 Nmyc1 2 MYCN 2p24.1 R WI-7056 36-40 9

a, b 4.0 Pomc1 2 POMC 2p23 9

b 6.0 Odc 2 ODC1 2p25 R stSG1950 22-32 9

7.0 Rrm2 2 RRM2 2p24-p25 R NIB787 12-17 9

7.0 Idb2 2 ID2 2p25 9

S Acp1 2 ACP1 2p25 G 9

a 9 AA163387(a) 2 32438(u) 2 R WI-15103 0-3 9

15.0 Tpo 2 TPO 2p25-p24 G 9

18.0 Ahr 7 AHR 7p21 X SHGC-12907 10-29 69

20.0 Meox2 7 MEOX2 7p22.1-p21.3 X SHGC-12960 10-21 69

15(g) Dld 7* DLD 7q31-q32 P 79

a, b, c 21.0 Lamb1-1 7* LAMB1 7q22-q31 P 79

a 21.0 AA177420(a) 7* PRKAR2A 7 P 79

22.0 Nrcam 7* NRCAM 7q22-q31 79

27.0 Pax9 14 PAX9 14q12-q13 133

30.0 Pygl 14 PYGL 14q11.2-q24.3 G 133

30.0 Sos2 14 SOS2 14q21.3 133

31.0 Hif1a 14 HIF1A 14q21-q24 133

a, b 33.0 Max 14 MAX 14q22-q24 133

b 33.0 Spnb1 14 SPTB 14q23-q24.2 R,G WI-7536 58-59 133

34.0 Hsp70-2 14 HSPA2 14q22-q24 133

36.0 Gpx2 14 GPX2 14q24.1 133

a 37.0 Fntb 14 FNTB 14q23-q24 R WI-9215 58-65 133

37.0 Tshr 14 TSHR 14q31 133

38.0 Chx10 14 CHX10 14q24.3 133

39.0 Pgf 14 PGF 14q31 133

b 40.0 Fos 14 FOS 14q24.3 133

b 41.0 Tgfb3 14 TGFB3 14q24 R SGC30624 73-76 133

48.0 Galc 14 GALC 14q24.3-q32.1 133

48.0 Chga 14 CHGA 14q32 133

c 51.0 Cbg 14 CBG 14q32.1 133

a, b 51.0 Spi1 14 P1 14q32.1 G 133

52.0 Pre2 14 AACT 14q32.1 G 133

52.0 Gsc 14 GSC 14q32.1 133

53.0 Bdkrb2 14 BDKRB2 14q31-q32.1 133

53.0 Yy1 14 YY1 14 133

55.0 D12H14S17 14 D14S17 14q32.3 133

55.0 Ckb 14 CKB 14q32.3 R WI-8982 116-124 133

55.0 Dncgc1 14 DNCL 14q32.3-qter 133

a 56.0 Tnfip2 14 TNFAIP2 14q32 133

58.0 Akt 14 AKT1 14q32.33 G 133

a, b 58.0 Igh-C 14 IGH 14q32.33 R,G SHGC-11760 >124 133

58.0 Igh-7 14 IGHE 14q32.33 133

Cross	Mouse Locus	Mouse Gene	Human Chr.	Human Gene	In Situ	Method	RH Map	Genethon Map	Homology Group
	S	Reg1a	2	REG1A(g)	2p12(g)				9
b	1.0	Synd1	2	SDC	2p	R	stSG9345	40-48	9
	2.0	Apob	2	APOB	2p24-p23	R,G	SGC34591	40-48	9
	S	Adcy3	2	ADCY3	2p24-p2				9
	4.0	Kif3c	2	KIF3C(?)	2	R	stSG4510	48-50	9
	4.0	Nmyc1	2	MYCN	2p24.1	R	WI-7056	36-40	9
a, b	4.0	Pomc1	2	POMC	2p23				9
b	6.0	Odc	2	ODC1	2p25	R	stSG1950	22-32	9
	7.0	Rrm2	2	RRM2	2p24-p25	R	NIB787	12-17	9
	7.0	Idb2	2	ID2	2p25				9
	S	Acp1	2	ACP1	2p25	G			9
a	9	AA163387(a)	2	32438(u)	2	R	WI-15103	0-3	9
	15.0	Tpo	2	TPO	2p25-p24	G			9
	18.0	Ahr	7	AHR	7p21	X	SHGC-12907	10-29	69
	20.0	Meox2	7	MEOX2	7p22.1-p21.3	X	SHGC-12960	10-21	69
	15(g)	Dld	7*	DLD	7q31-q32	P			79
a, b, c	21.0	Lamb1-1	7*	LAMB1	7q22-q31	P			79
a	21.0	AA177420(a)	7*	PRKAR2A	7	P			79
	22.0	Nrcam	7*	NRCAM	7q22-q31				79
	27.0	Pax9	14	PAX9	14q12-q13				133
	30.0	Pygl	14	PYGL	14q11.2-q24.3	G			133
	30.0	Sos2	14	SOS2	14q21.3				133
	31.0	Hif1a	14	HIF1A	14q21-q24				133
a, b	33.0	Max	14	MAX	14q22-q24				133
b	33.0	Spnb1	14	SPTB	14q23-q24.2	R,G	WI-7536	58-59	133
	34.0	Hsp70-2	14	HSPA2	14q22-q24				133
	36.0	Gpx2	14	GPX2	14q24.1				133
a	37.0	Fntb	14	FNTB	14q23-q24	R	WI-9215	58-65	133
	37.0	Tshr	14	TSHR	14q31				133
	38.0	Chx10	14	CHX10	14q24.3				133
	39.0	Pgf	14	PGF	14q31				133
b	40.0	Fos	14	FOS	14q24.3				133
b	41.0	Tgfb3	14	TGFB3	14q24	R	SGC30624	73-76	133
	48.0	Galc	14	GALC	14q24.3-q32.1				133
	48.0	Chga	14	CHGA	14q32				133
c	51.0	Cbg	14	CBG	14q32.1				133
a, b	51.0	Spi1	14	P1	14q32.1	G			133
	52.0	Pre2	14	AACT	14q32.1	G			133
	52.0	Gsc	14	GSC	14q32.1				133
	53.0	Bdkrb2	14	BDKRB2	14q31-q32.1				133
	53.0	Yy1	14	YY1	14				133
	55.0	D12H14S17	14	D14S17	14q32.3				133
	55.0	Ckb	14	CKB	14q32.3	R	WI-8982	116-124	133
	55.0	Dncgc1	14	DNCL	14q32.3-qter				133
a	56.0	Tnfip2	14	TNFAIP2	14q32				133
	58.0	Akt	14	AKT1	14q32.33	G			133
a, b	58.0	Igh-C	14	IGH	14q32.33	R,G	SHGC-11760	>124	133
	58.0	Igh-7	14	IGHE	14q32.33				133

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