HBQ1 protein (Homo sapiens) - STRING network view

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Score

HBQ1

hemoglobin, theta 1 (142 aa)

Predicted Functional Partners:

HBD

0.889

LUC7L

0.813

GABRQ

0.802

AHSP

0.771

CYB5R3

0.762

HBB

0.732

HBE1

0.732

HBZ

0.727

HBA2

0.726

HBA1

0.726

Your Current Organism:

Homo sapiens

NCBI taxonomy Id: 9606
Other names: H. sapiens, Homo, Homo sapiens, human, man

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Browse interactions in tabular form:

node1	node2	node1 accession	node2 accession	node1 annotation	node2 annotation	score
AHSP	CYB5R3	ENSP00000307199	ENSP00000354468	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	cytochrome b5 reductase 3	0.720
AHSP	HBA1	ENSP00000307199	ENSP00000322421	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, alpha 1; Involved in oxygen transport from the lung to the various peripheral tissues (By similarity)	0.973
AHSP	HBA2	ENSP00000307199	ENSP00000251595	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, alpha 2	0.996
AHSP	HBB	ENSP00000307199	ENSP00000333994	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, beta	0.951
AHSP	HBD	ENSP00000307199	ENSP00000369654	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, delta; Involved in oxygen transport from the lung to the various peripheral tissues	0.858
AHSP	HBE1	ENSP00000307199	ENSP00000292896	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, epsilon 1; The epsilon chain is a beta-type chain of early mammalian embryonic hemoglobin	0.907
AHSP	HBQ1	ENSP00000307199	ENSP00000199708	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, theta 1	0.771
AHSP	HBZ	ENSP00000307199	ENSP00000252951	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	hemoglobin, zeta; The zeta chain is an alpha-type chain of mammalian embryonic hemoglobin, synthesized primarily in the yolk sac	0.748
CYB5R3	AHSP	ENSP00000354468	ENSP00000307199	cytochrome b5 reductase 3	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	0.720
CYB5R3	HBA1	ENSP00000354468	ENSP00000322421	cytochrome b5 reductase 3	hemoglobin, alpha 1; Involved in oxygen transport from the lung to the various peripheral tissues (By similarity)	0.887
CYB5R3	HBA2	ENSP00000354468	ENSP00000251595	cytochrome b5 reductase 3	hemoglobin, alpha 2	0.899
CYB5R3	HBB	ENSP00000354468	ENSP00000333994	cytochrome b5 reductase 3	hemoglobin, beta	0.841
CYB5R3	HBD	ENSP00000354468	ENSP00000369654	cytochrome b5 reductase 3	hemoglobin, delta; Involved in oxygen transport from the lung to the various peripheral tissues	0.846
CYB5R3	HBE1	ENSP00000354468	ENSP00000292896	cytochrome b5 reductase 3	hemoglobin, epsilon 1; The epsilon chain is a beta-type chain of early mammalian embryonic hemoglobin	0.762
CYB5R3	HBQ1	ENSP00000354468	ENSP00000199708	cytochrome b5 reductase 3	hemoglobin, theta 1	0.762
CYB5R3	HBZ	ENSP00000354468	ENSP00000252951	cytochrome b5 reductase 3	hemoglobin, zeta; The zeta chain is an alpha-type chain of mammalian embryonic hemoglobin, synthesized primarily in the yolk sac	0.762
GABRQ	HBQ1	ENSP00000359329	ENSP00000199708	gamma-aminobutyric acid (GABA) A receptor, theta; GABA, the major inhibitory neurotransmitter in the vertebrate brain, mediates neuronal inhibition by binding to the GABA/benzodiazepine receptor and opening an integral chloride channel	hemoglobin, theta 1	0.802
HBA1	AHSP	ENSP00000322421	ENSP00000307199	hemoglobin, alpha 1; Involved in oxygen transport from the lung to the various peripheral tissues (By similarity)	alpha hemoglobin stabilizing protein; Acts as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia	0.973
HBA1	CYB5R3	ENSP00000322421	ENSP00000354468	hemoglobin, alpha 1; Involved in oxygen transport from the lung to the various peripheral tissues (By similarity)	cytochrome b5 reductase 3	0.887
HBA1	HBA2	ENSP00000322421	ENSP00000251595	hemoglobin, alpha 1; Involved in oxygen transport from the lung to the various peripheral tissues (By similarity)	hemoglobin, alpha 2	0.900

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