ITGB1P1 (integrin beta 1 pseudogene 1)

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Keyword

Gene: ITGB1P1 (integrin beta 1 pseudogene 1) Homo sapiens

Symbol:

ITGB1P1

Name:

integrin beta 1 pseudogene 1

Description:

Type:

pseudo

RefSeq Status:

VALIDATED

Also known as:

FNRBL; ITGB1L

Related Functional Gene:

ITGB1

Latest Assembly:

Human Genome Assembly GRCh37

Position:

Map	Chr	Position	Strand	Source
Human Genome Assembly HuRef	19	32,910,012 - 32,920,030	-	NCBI
Human Genome Assembly GRCh37	19	14,732,331 - 14,734,100	-	NCBI
Human Celera Assembly	19	14,625,602 - 14,626,210	-	NCBI
Human Cytogenetic Map	19	p		NCBI

Model

Launch Genome Browser (GBrowse) : build 37 (hg19)

Annotation (Toggle Detail/Summary View)

References - uncurated

Genomics

Position Markers

RH47472

Map	Chr	Position	Source
Human Genome Assembly HuRef	10	32,908,943 - 32,909,035	UniSTS
Human Genome Assembly GRCh37	10	33,189,433 - 33,189,525	UniSTS
Human Genome Assembly GRCh37	19	14,733,900 - 14,733,992	UniSTS
Human Celera Assembly	19	14,627,056 - 14,627,148	UniSTS
Human Celera Assembly	10	32,954,767 - 32,954,859	RGD
Human Genome Assembly Build 36	10	33,229,439 - 33,229,531	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	19	p13.1	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

RH47140

Map	Chr	Position	Source
Human Genome Assembly HuRef	10	32,909,209 - 32,909,399	UniSTS
Human Genome Assembly GRCh37	10	33,189,699 - 33,189,889	UniSTS
Human Genome Assembly GRCh37	19	14,733,536 - 14,733,726	UniSTS
Human Celera Assembly	19	14,626,692 - 14,626,882	UniSTS
Human Celera Assembly	10	32,955,033 - 32,955,223	RGD
Human Genome Assembly Build 36	10	33,229,705 - 33,229,895	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	19	p13.1	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

RH40308

Map	Chr	Position	Source
Human Genome Assembly HuRef	10	32,909,024 - 32,909,239	UniSTS
Human Genome Assembly GRCh37	10	33,189,514 - 33,189,729	UniSTS
Human Genome Assembly GRCh37	19	14,733,696 - 14,733,911	UniSTS
Human Celera Assembly	19	14,626,852 - 14,627,067	UniSTS
Human Celera Assembly	10	32,954,848 - 32,955,063	RGD
Human Genome Assembly Build 36	10	33,229,520 - 33,229,735	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	19	p13.1	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

GDB:181546

Map	Chr	Position	Source
Human Genome Assembly HuRef	10	32,908,923 - 32,909,505	UniSTS
Human Genome Assembly GRCh37	10	33,189,413 - 33,189,995	UniSTS
Human Genome Assembly GRCh37	19	14,733,430 - 14,734,012	UniSTS
Human Celera Assembly	19	14,626,586 - 14,627,168	UniSTS
Human Celera Assembly	10	32,954,747 - 32,955,329	RGD
Human Genome Assembly Build 36	10	33,229,419 - 33,230,001	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	19	p13.1	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

SHGC-32719

Map	Chr	Position	Source
Human TNG Radiation Hybrid Map	10	17460.0	UniSTS
Human Genome Assembly HuRef	10	32,909,321 - 32,909,449	UniSTS
Human Genome Assembly GRCh37	10	33,189,811 - 33,189,939	UniSTS
Human Genome Assembly GRCh37	19	14,733,486 - 14,733,614	UniSTS
Human Celera Assembly	10	32,955,145 - 32,955,273	RGD
Human Celera Assembly	19	14,626,642 - 14,626,770	UniSTS
Human Genome Assembly Build 36	10	33,229,817 - 33,229,945	RGD
Human Cytogenetic Map	19	p13.1	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS
Human Cytogenetic Map	19	p	UniSTS

PMC59887P1

Map	Chr	Position	Source
Human Genome Assembly GRCh37	19	14,732,383 - 14,732,844	UniSTS
Human Celera Assembly	19	14,625,539 - 14,626,000	RGD
Human Genome Assembly Build 36	19	14,593,383 - 14,593,844	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	19	p13.1	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

D10S2370

Map	Chr	Position	Source
Human GeneMap99-G3 RH Map	10	1976.0	UniSTS
Human Stanford-G3 RH Map	10	1976.0	UniSTS
Human Genome Assembly HuRef	10	32,909,737 - 32,909,998	UniSTS
Human Genome Assembly GRCh37	10	33,190,227 - 33,190,488	UniSTS
Human Celera Assembly	10	32,955,561 - 32,955,822	RGD
Human Genome Assembly Build 36	10	33,230,233 - 33,230,494	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

D10S2354

Map	Chr	Position	Source
Human Genome Assembly HuRef	10	32,916,370 - 32,916,476	UniSTS
Human Genome Assembly GRCh37	10	33,196,862 - 33,196,968	UniSTS
Human Celera Assembly	10	32,962,198 - 32,962,304	RGD
Human Genome Assembly Build 36	10	33,236,868 - 33,236,974	RGD
Human Cytogenetic Map	19	p	UniSTS
Human Cytogenetic Map	10	p11.2	UniSTS

QTLs in Region (Human Genome Assembly GRCh37)

The following QTLs overlap with this region.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1298499	UAE1_H	Urinary albumin excretion QTL 1 (human)	2.73	.0009	Urinary albumin excretion	urine albumin:creatinine ratio (ACR)	19	1	16075900	Human
1331657	COPD9_H	Chronic obstructive pulmonary disease QTL 9 (human)	1.94		Chronic airflow obstruction	post-bronchodilator FEV1	19	12712793	57533128	Human
1331639	COPD3_H	Chronic obstructive pulmonary disease QTL 3 (human)	1.54		Chronic airflow obstruction	FEV1 <80% predicted and FEV/FVC<90% predicted	19	2682318	28682318	Human
1358846	MULTSCL30_H	Multiple sclerosis susceptibility QTL 30 (human)	.89		Multiple sclerosis susceptibility		19	3314332	29911216	Human
1559347	SCL92_H	Serum cholesterol level QTL 92 (human)	2.15	.0008	Lipid level	LDL cholesterol	19	1	25712901	Human
1559400	SCL97_H	Serum cholesterol level QTL97 (human)	3.89	.00002	Lipid level	total cholesterol	19	1	19113369	Human
1559404	SCL117_H	Serum cholesterol level QTL 117 (human)	2.05		Lipid level	triglyceride-HDL ratio	19	1	16140092	Human
2289238	BW148_H	Body weight QTL 148 (human)	2.13	.0009	Body weight	BMI	19	12712793	31914947	Human
2289216	BW367_H	Body weight QTL 367 (human)		.0469	Body fat amount	percent fat	19	10652925	36652925	Human
1643248	BW138_H	Body weight QTL 138 (human)	1.47		Body weight		19	1	22804918	Human
2289557	SLIPL22_H	Serum lipid level QTL 22 (human)			Lipid level	cholesterol level	19	4857757	30857757	Human
2293449	PRSTS270_H	Prostate tumor susceptibility QTL 270 (human)			Prostate tumor susceptibility		19	1	15567316	Human
2293432	PRSTS269_H	Prostate tumor susceptibility QTL 269 (human)			Prostate tumor susceptibility		19	1	15567316	Human
2300113	PRSTS337_H	Prostate tumor susceptibility QTL 337 (human)			Prostate tumor susceptibility		19	1	17392514	Human
2301145	PRSTS371_H	Prostate tumor susceptibility QTL 371 (human)	2.91	.0001	Prostate tumor susceptibility		19	1	31914947	Human
2301170	PRSTS375_H	Prostate tumor susceptibility QTL 375 (human)	1.87		Prostate tumor susceptibility		19	1	16314463	Human
2301168	PRSTS378_H	Prostate tumor susceptibility QTL 378 (human)	1.09		Prostate tumor susceptibility		19	1	16314463	Human
2301163	PRSTS377_H	Prostate tumor susceptibility QTL 377 (human)	1.59		Prostate tumor susceptibility		19	1	16314463	Human
2301152	PRSTS373_H	Prostate tumor susceptibility QTL 373 (human)	2.94		Prostate tumor susceptibility		19	1	16314463	Human
2314744	GLUCO92_H	Glucose level QTL 92 (human)	.86	.005	Glucose level	non-insulin dependent	19	1	22178483	Human
2315824	GLUCO176_H	Glucose level QTL 176 (human)	1.37	.006	Glucose level		19	14633401	30417232	Human
2316728	GLUCO279_H	Glucose level QTL 279 (human)	1.26	.01358	Glucose level		19	1	25712901	Human

Sequence

Nucleotide Sequences

Additional Information

External Database Links

Nomenclature History

More on ITGB1P1

Entrez Gene

Ensembl Gene

Genome Browser:

(hg19)

RGD Object Information
RGD ID:	1352514
Created:	2005-03-08
Species:	Homo sapiens
Last Modified:	2013-03-06
Status:	ACTIVE