Human to Mouse Homology Region Map, Chromosome 14

Human to Mouse Homology Region Map, Chromosome 14

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

SHGC-153 2-8 R 14q11-q12 DAD1 14 Dad1 36.5(g) a 131

14 BMP4 14* Bmp4 14(g) b 132

14q11.2-q12 APE 14* Apex 18.5 b 132

stSG1642 2-8 R 14q11 NRL 14* Nrl 19.5 132

14q11.2 NP1 14* Np 19.5 132

SHGC-11082 2-8 R,G 14q11.2 TCRA 14* Tcra 19.5 a, b 132

SHGC-9765 2-8 R 14q11.2 TCRD 14* Tcrd 19.5 132

stSG1614 0-1 R 14q11 ANG 14* Ang 20.0 132

G 14q11.2 CTSG 14* Ctsg 20.0 b 132

14q11.2-q13 MYH6 14* Myhca 20.0 b 132

G 14q11.2-q13 MYH7 14* Myhcb 20.0 132

14q21-q22 OTX2 14* Otx2 20.5 132

14q11.2 ADCY4 14* Adcy4 S 132

14q11.2 CMA1 14* Mcpt5 20(g) 132

G 14q12 CTLA1 14* Ctla1 20.5 a, b 132

14q12-q13 PAX9 12 Pax9 27.0 133

G 14q11.2-q24.3 PYGL 12 Pygl 30.0 133

14q21.3 SOS2 12 Sos2 30.0 133

14q21-q24 HIF1A 12 Hif1a 31.0 133

14q22-q24 MAX 12 Max 33.0 a, b 133

WI-7536 58-59 R,G 14q23-q24.2 SPTB 12 Spnb1 33.0 b 133

14q22-q24 HSPA2 12 Hsp70-2 34.0 133

14q24.1 GPX2 12 Gpx2 36.0 133

WI-9215 58-65 R 14q23-q24 FNTB 12 Fntb 37.0 a 133

14q31 TSHR 12 Tshr 37.0 133

14q24.3 CHX10 12 Chx10 38.0 133

14q31 PGF 12 Pgf 39.0 133

14q24.3 FOS 12 Fos 40.0 b 133

SGC30624 73-76 R 14q24 TGFB3 12 Tgfb3 41.0 b 133

14q24.3-q32.1 GALC 12 Galc 48.0 133

14q32 CHGA 12 Chga 48.0 133

14q32.1 CBG 12 Cbg 51.0 c 133

G 14q32.1 P1 12 Spi1 51.0 a, b 133

G 14q32.1 AACT 12 Pre2 52.0 133

14q32.1 GSC 12 Gsc 52.0 133

14q31-q32.1 BDKRB2 12 Bdkrb2 53.0 133

14 YY1 12 Yy1 53.0 133

14q32.3 D14S17 12 D12H14S17 55.0 133

WI-8982 116-124 R 14q32.3 CKB 12 Ckb 55.0 133

14q32.3-qter DNCL 12 Dncgc1 55.0 133

14q32 TNFAIP2 12 Tnfip2 56.0 a 133

G 14q32.33 AKT1 12 Akt 58.0 133

SHGC-11760 >124 R,G 14q32.33 IGH 12 Igh-C 58.0 a, b 133

14q32.33 IGHE 12 Igh-7 58.0 133

RH Map	Genethon Map	Method	In Situ	Human Gene	Mouse Chr.	Mouse Gene	Mouse Locus	Cross	Homology Group
SHGC-153	2-8	R	14q11-q12	DAD1	14	Dad1	36.5(g)	a	131
			14	BMP4	14*	Bmp4	14(g)	b	132
			14q11.2-q12	APE	14*	Apex	18.5	b	132
stSG1642	2-8	R	14q11	NRL	14*	Nrl	19.5		132
			14q11.2	NP1	14*	Np	19.5		132
SHGC-11082	2-8	R,G	14q11.2	TCRA	14*	Tcra	19.5	a, b	132
SHGC-9765	2-8	R	14q11.2	TCRD	14*	Tcrd	19.5		132
stSG1614	0-1	R	14q11	ANG	14*	Ang	20.0		132
		G	14q11.2	CTSG	14*	Ctsg	20.0	b	132
			14q11.2-q13	MYH6	14*	Myhca	20.0	b	132
		G	14q11.2-q13	MYH7	14*	Myhcb	20.0		132
			14q21-q22	OTX2	14*	Otx2	20.5		132
			14q11.2	ADCY4	14*	Adcy4	S		132
			14q11.2	CMA1	14*	Mcpt5	20(g)		132
		G	14q12	CTLA1	14*	Ctla1	20.5	a, b	132
			14q12-q13	PAX9	12	Pax9	27.0		133
		G	14q11.2-q24.3	PYGL	12	Pygl	30.0		133
			14q21.3	SOS2	12	Sos2	30.0		133
			14q21-q24	HIF1A	12	Hif1a	31.0		133
			14q22-q24	MAX	12	Max	33.0	a, b	133
WI-7536	58-59	R,G	14q23-q24.2	SPTB	12	Spnb1	33.0	b	133
			14q22-q24	HSPA2	12	Hsp70-2	34.0		133
			14q24.1	GPX2	12	Gpx2	36.0		133
WI-9215	58-65	R	14q23-q24	FNTB	12	Fntb	37.0	a	133
			14q31	TSHR	12	Tshr	37.0		133
			14q24.3	CHX10	12	Chx10	38.0		133
			14q31	PGF	12	Pgf	39.0		133
			14q24.3	FOS	12	Fos	40.0	b	133
SGC30624	73-76	R	14q24	TGFB3	12	Tgfb3	41.0	b	133
			14q24.3-q32.1	GALC	12	Galc	48.0		133
			14q32	CHGA	12	Chga	48.0		133
			14q32.1	CBG	12	Cbg	51.0	c	133
		G	14q32.1	P1	12	Spi1	51.0	a, b	133
		G	14q32.1	AACT	12	Pre2	52.0		133
			14q32.1	GSC	12	Gsc	52.0		133
			14q31-q32.1	BDKRB2	12	Bdkrb2	53.0		133
			14	YY1	12	Yy1	53.0		133
			14q32.3	D14S17	12	D12H14S17	55.0		133
WI-8982	116-124	R	14q32.3	CKB	12	Ckb	55.0		133
			14q32.3-qter	DNCL	12	Dncgc1	55.0		133
			14q32	TNFAIP2	12	Tnfip2	56.0	a	133
		G	14q32.33	AKT1	12	Akt	58.0		133
SHGC-11760	>124	R,G	14q32.33	IGH	12	Igh-C	58.0	a, b	133
			14q32.33	IGHE	12	Igh-7	58.0		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