A0N9R6 (A0N9R6_HUMAN) Unreviewed, UniProtKB/TrEMBL

Names and origin

Protein names

Submitted name:
Insulin-like growth factor type 2 receptor EMBL CAA62977.1

Submitted name:
Insulin-like growth factor type II receptor EMBL CAA58672.1

Gene names

Name:	IGF2R EMBL CAA58672.1
Synonyms:	igf2R EMBL CAA62977.1

Organism

Homo sapiens (Human) EMBL CAA58672.1

Taxonomic identifier

9606 [NCBI]

Taxonomic lineage

cellular organisms › Eukaryota › Opisthokonta › Metazoa › Eumetazoa › Bilateria › Deuterostomia › Chordata › Craniata › Vertebrata › Gnathostomata › Teleostomi › Euteleostomi › Sarcopterygii › Tetrapoda › Amniota › Mammalia › Theria › Eutheria › Euarchontoglires › Primates › Haplorrhini › Simiiformes › Catarrhini › Hominoidea › Hominidae › Homininae › Homo

Protein attributes

Sequence length	49 AA.
Sequence status	Fragment.
Protein existence	Evidence at transcript level

Ontologies

Keywords
Molecular function	Receptor EMBL CAA58672.1
Gene Ontology (GO)
Cellular_component	membrane Inferred from electronic annotation. Source: Compara nuclear envelope lumen Inferred from electronic annotation. Source: Compara
Molecular_function	mannose binding Inferred from electronic annotation. Source: Compara
Complete GO annotation...

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view	Feature identifier
Experimental info
	Non-terminal residue	49	1	EMBL CAA58672.1

Sequences

	Sequence		Length	Mass (Da)
	A0N9R6 [UniParc]. Last modified December 12, 2006. Version 1. Checksum: C0824C7F0946FEBA	FASTA	49	5,015
	10 20 30 40 MGAAAGRSPH LGPAPARRPQ RSLLLLQLLL LVAAPGSTQA QAAPFPELC

References

[1]	"Insulin-like growth factor II receptor as a multifunctional binding protein." Morgan D.O., Edman J.C., Standring D.N., Fried V.A., Smith M.C., Roth R.A., Rutter W.J. Nature 329:301-307(1987) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE. Tissue: PBL EMBL CAA58672.1.
[2]	"The human cation-independent mannose 6-phosphate receptor. Cloning and sequence of the full-length cDNA and expression of functional receptor in COS cells." Oshima A., Nolan C.M., Kyle J.W., Grubb J.H., Sly W.S. J. Biol. Chem. 263:2553-2562(1988) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE. Tissue: PBL EMBL CAA58672.1.
[3]	"Conservation of a methylation imprint and a putative imprinting box at the human IGF2R locus." Smrzka O.W., Fae I., Stoger R., Kurzbauer R., Fischer G.F., Henn T., Weith A., Barlow D.P. Hum. Mol. Genet. 4:1945-1952(1995) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE. Tissue: PBL EMBL CAA58672.1.
[4]	Kalscheuer V.M.M. Submitted (SEP-1995) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.
[5]	"Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription." Riesewijk A.M., Schepens M.T., Welch T.R., van den Berg-Loonen E.M., Mariman E.M., Ropers H.H., Kalscheuer V.M. Genomics 31:158-166(1996) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE.

Cross-references

Sequence databases
EMBL GenBank DDBJ	X83699 Genomic DNA. Translation: CAA58672.1. X91875 Genomic DNA. Translation: CAA62977.1.
IPI	IPI00289819.
3D structure databases
ModBase	Search...
Protein-protein interaction databases
STRING	A0N9R6.
Protocols and materials databases
StructuralBiologyKnowledgebase	Search...
Organism-specific databases
H-InvDB	HIX0033007.
Gene expression databases
ArrayExpress	A0N9R6.
Bgee	A0N9R6.
Family and domain databases
ProtoNet	Search...
Other
ChiTaRS	IGF2R. human.
NextBio	35460098.

Entry information

Entry name

A0N9R6_HUMAN

Accession

Primary (citable) accession number: A0N9R6

Entry history

Integrated into UniProtKB/TrEMBL:	December 12, 2006
Last sequence update:	December 12, 2006
Last modified:	April 3, 2013
This is version 25 of the entry and version 1 of the sequence. [Complete history]

Entry status

Unreviewed (UniProtKB/TrEMBL)

Disclaimer

Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.