Human Gene SH2B1 (ENST00000337120.9) from GENCODE V44
  Description: Homo sapiens SH2B adaptor protein 1 (SH2B1), transcript variant 2, mRNA. (from RefSeq NM_015503)
RefSeq Summary (NM_015503): This gene encodes a member of the SH2-domain containing mediators family. The encoded protein mediates activation of various kinases and may function in cytokine and growth factor receptor signaling and cellular transformation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2009].
Gencode Transcript: ENST00000337120.9
Gencode Gene: ENSG00000178188.16
Transcript (Including UTRs)
   Position: hg38 chr16:28,862,804-28,874,201 Size: 11,398 Total Exon Count: 9 Strand: +
Coding Region
   Position: hg38 chr16:28,866,095-28,873,465 Size: 7,371 Coding Exon Count: 9 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesMethods
Data last updated at UCSC: 2023-08-18 00:09:47

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr16:28,862,804-28,874,201)mRNA (may differ from genome)Protein (671 aa)
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HGNCHPRDLynxMalacardsMGIneXtProt
OMIMPubMedReactomeUniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: SH2B1_HUMAN
DESCRIPTION: RecName: Full=SH2B adapter protein 1; AltName: Full=Pro-rich, PH and SH2 domain-containing signaling mediator; Short=PSM; AltName: Full=SH2 domain-containing protein 1B;
FUNCTION: Adapter protein for several members of the tyrosine kinase receptor family. Involved in multiple signaling pathways mediated by Janus kinase (JAK) and receptor tyrosine kinases, including the receptors of insulin (INS), insulin-like growth factor I (IGF1), nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), platelet-derived growth factor (PDGF) and fibroblast growth factors (FGFs). In growth hormone (GH) signaling, autophosphorylated ('Tyr-813') JAK2 recruits SH2B1, which in turn is phosphorylated by JAK2 on tyrosine residues. These phosphotyrosines form potential binding sites for other signaling proteins. GH also promotes serine/threonine phosphorylation of SH2B1 and these phosphorylated residues may serve to recruit other proteins to the GHR-JAK2-SH2B1 complexes, such as RAC1. In leptin (LEP) signaling, binds to and potentiates the activation of JAK2 by globally enhancing downstream pathways. In response to leptin, binds simultaneously to both, JAK2 and IRS1 or IRS2, thus mediating formation of a complex of JAK2, SH2B1 and IRS1 or IRS2. Mediates tyrosine phosphorylation of IRS1 and IRS2, resulting in activation of the PI 3-kinase pathway. Acts as positive regulator of NGF-mediated activation of the Akt/Forkhead pathway; prolongs NGF-induced phosphorylation of AKT1 on 'Ser-473' and AKT1 enzymatic activity. Enhances the kinase activity of the cytokine receptor-associated tyrosine kinase JAK2 and of other receptor tyrosine kinases, such as FGFR3 and NTRK1. For JAK2, the mechanism seems to involve dimerization of both, SH2B1 and JAK2. Enhances RET phosphorylation and kinase activity. Isoforms seem to be differentially involved in IGF-I and PDGF-induced mitogenesis (By similarity).
SUBUNIT: Self-associates. Homopentamer (By similarity). Forms a heteromultimeric complex with SH2B2 (By similarity). Interacts with SH2B2. Isoform 1 interacts via its SH2 domain with JAK2. Isoform 2 interacts via its SH2 domain and its N-terminus with JAK2; the SH2 domain is required for the major interaction with JAK2 phosphorylated on tyrosine residues; the N-terminus provides a low-affinity binding to JAK2 independent of JAK2 phosphorylation. Isoform 3 interacts via its SH2 domain with JAK2. Isoform 1 interacts via its SH2 domain with INSR; the interaction requires receptor activation. Isoform 3 interacts via its SH2 domain with INSR; the interaction requires receptor activation and requires INSR phosphorylation at 'Tyr-1185'. Isoform 1 interacts with IGF1R; the interaction requires receptor activation. Isoform 2 interacts with PRKAR1A/RET (PTC2) fusion protein; the interaction requires RET 'Tyr-905' and Tyr-981'. Isoform 2 interacts via its SH2 domain with FGFR3; the interaction requires FGFR3 'Tyr-724' and 'Tyr-760'. Isoform 2 interacts with RET; the interaction requires RET kinase activity and RET 'Tyr-981'. Isoform 2 interacts with RAC1. Isoform 2 interacts with PDGFRA and/or PDGFRB; the interaction requires receptor activation. Interacts with ISR1 and ISR2. Isoform 3 is probably part of a complex consisting of INSR, ISR1 and SH2B1. Probably part of a ternary complex consisting of SH2B1, JAK2 and ISR1 or ISR2. May interact with FCER1G (By similarity). Interacts (via SH2 domain) with NTRK1 (phosphorylated) (By similarity).
SUBCELLULAR LOCATION: Cytoplasm (By similarity). Membrane (Probable). Nucleus (By similarity). Note=Shuttles between the nucleus and the cytoplasm (By similarity).
TISSUE SPECIFICITY: Widely expressed with highest levels in skeletal muscle and ovary.
PTM: Phosphorylated on tyrosine residues in response to receptor kinase stimulation. Phosphorylated by RET.
SIMILARITY: Belongs to the SH2B adapter family.
SIMILARITY: Contains 1 PH domain.
SIMILARITY: Contains 1 SH2 domain.
SEQUENCE CAUTION: Sequence=AAH10704.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=BAA92537.1; Type=Erroneous initiation; Note=Translation N-terminally shortened; Sequence=BAB55148.1; Type=Erroneous initiation; Note=Translation N-terminally extended;

-  Primer design for this transcript
 

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Click here to load the transcript sequence and exon structure into Primer3Plus

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Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: SH2B1
Diseases sorted by gene-association score: severe early-onset obesity-insulin resistance syndrome due to sh2b1 deficiency* (350), chromosome 16p11.2 deletion syndrome, 220-kb* (42), chromosome 16p11.2 deletion syndrome, 593-kb* (25)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 29.96 RPKM in Brain - Cerebellum
Total median expression: 781.17 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -1406.203291-0.427 Picture PostScript Text
3' UTR -311.60736-0.423 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR011993 - PH_like_dom
IPR015012 - Phe_ZIP
IPR001849 - Pleckstrin_homology
IPR000980 - SH2

Pfam Domains:
PF00169 - PH domain
PF08916 - Phenylalanine zipper
PF00017 - SH2 domain

ModBase Predicted Comparative 3D Structure on Q9NRF2
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserGenome BrowserNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
MGIRGD    
Protein SequenceProtein Sequence    
AlignmentAlignment    

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0005515 protein binding
GO:0035591 signaling adaptor activity

Biological Process:
GO:0007165 signal transduction
GO:0007596 blood coagulation
GO:0009967 positive regulation of signal transduction
GO:0030032 lamellipodium assembly
GO:0045840 positive regulation of mitotic nuclear division
GO:2000278 regulation of DNA biosynthetic process

Cellular Component:
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0016020 membrane


-  Descriptions from all associated GenBank mRNAs
  AK055104 - Homo sapiens cDNA FLJ30542 fis, clone BRAWH2001378, highly similar to Rattus norvegicus SH2-B PH domain containing signaling mediator 1 (Sh2bpsm1), transcript variant 1, mRNA.
AB037720 - Homo sapiens KIAA1299 mRNA for KIAA1299 protein.
JD505636 - Sequence 486660 from Patent EP1572962.
AK298569 - Homo sapiens cDNA FLJ59376 complete cds, highly similar to Mus musculus SH2B adaptor protein 1 (Sh2b1), mRNA.
AK297080 - Homo sapiens cDNA FLJ59336 complete cds, highly similar to Homo sapiens SH2-B homolog (SH2B), mRNA.
AF227967 - Homo sapiens SH2-B alpha signaling protein (SH2B) mRNA, complete cds, alternatively spliced.
AF227968 - Homo sapiens SH2-B beta signaling protein (SH2B) mRNA, complete cds, alternatively spliced.
AF227969 - Homo sapiens SH2-B gamma signaling protein (SH2B) mRNA, complete cds, alternatively spliced.
AK290332 - Homo sapiens cDNA FLJ75160 complete cds, highly similar to Homo sapiens SH2-B homolog (SH2B), mRNA.
AL713760 - Homo sapiens mRNA; cDNA DKFZp727I201 (from clone DKFZp727I201).
JD391627 - Sequence 372651 from Patent EP1572962.
JD185518 - Sequence 166542 from Patent EP1572962.
JD065180 - Sequence 46204 from Patent EP1572962.
JD046821 - Sequence 27845 from Patent EP1572962.
JD340197 - Sequence 321221 from Patent EP1572962.
JD255378 - Sequence 236402 from Patent EP1572962.
JD185997 - Sequence 167021 from Patent EP1572962.
JD227525 - Sequence 208549 from Patent EP1572962.
JD184103 - Sequence 165127 from Patent EP1572962.
JD295520 - Sequence 276544 from Patent EP1572962.
JD487810 - Sequence 468834 from Patent EP1572962.
JD487867 - Sequence 468891 from Patent EP1572962.
JD433639 - Sequence 414663 from Patent EP1572962.
JD122360 - Sequence 103384 from Patent EP1572962.
JD426212 - Sequence 407236 from Patent EP1572962.
JD484679 - Sequence 465703 from Patent EP1572962.
JD501595 - Sequence 482619 from Patent EP1572962.
JD470583 - Sequence 451607 from Patent EP1572962.
JD393399 - Sequence 374423 from Patent EP1572962.
JD138118 - Sequence 119142 from Patent EP1572962.
JD563581 - Sequence 544605 from Patent EP1572962.
JD038529 - Sequence 19553 from Patent EP1572962.
JD484496 - Sequence 465520 from Patent EP1572962.
JD426229 - Sequence 407253 from Patent EP1572962.
JD230188 - Sequence 211212 from Patent EP1572962.
JD353675 - Sequence 334699 from Patent EP1572962.
JD144919 - Sequence 125943 from Patent EP1572962.
JD341629 - Sequence 322653 from Patent EP1572962.
JD389501 - Sequence 370525 from Patent EP1572962.
AB385445 - Synthetic construct DNA, clone: pF1KA1299, Homo sapiens SH2B1 gene for SH2B adaptor protein 1, complete cds, without stop codon, in Flexi system.
BC010704 - Homo sapiens SH2B adaptor protein 1, mRNA (cDNA clone MGC:16976 IMAGE:3866324), complete cds.
AL049924 - Homo sapiens mRNA; cDNA DKFZp564G1182 (from clone DKFZp564G1182); partial cds.
AK027488 - Homo sapiens cDNA FLJ14582 fis, clone NT2RM4001411, highly similar to Mus musculus Pro-rich, PH, SH2 domain-containing signaling mediator (PSM) mRNA.
CU679801 - Synthetic construct Homo sapiens gateway clone IMAGE:100017245 5' read SH2B1 mRNA.
KJ902399 - Synthetic construct Homo sapiens clone ccsbBroadEn_11793 SH2B1 gene, encodes complete protein.
JD154832 - Sequence 135856 from Patent EP1572962.
JD076626 - Sequence 57650 from Patent EP1572962.
JD445745 - Sequence 426769 from Patent EP1572962.
JD478125 - Sequence 459149 from Patent EP1572962.
JD545862 - Sequence 526886 from Patent EP1572962.
JD101293 - Sequence 82317 from Patent EP1572962.
JD209155 - Sequence 190179 from Patent EP1572962.
JD113022 - Sequence 94046 from Patent EP1572962.
JD402616 - Sequence 383640 from Patent EP1572962.
JD257839 - Sequence 238863 from Patent EP1572962.
JD045483 - Sequence 26507 from Patent EP1572962.
JD089207 - Sequence 70231 from Patent EP1572962.
JD077204 - Sequence 58228 from Patent EP1572962.
JD479309 - Sequence 460333 from Patent EP1572962.
JD284462 - Sequence 265486 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa04722 - Neurotrophin signaling pathway

Reactome (by CSHL, EBI, and GO)

Protein Q9NRF2 (Reactome details) participates in the following event(s):

R-HSA-997237 SH2B proteins bind JAK2
R-HSA-983231 Factors involved in megakaryocyte development and platelet production
R-HSA-109582 Hemostasis
R-HSA-1675473 SH2B binds JAK2
R-HSA-2671872 Phosphorylated LEP:LEPR:JAK2 Binds SH2B1
R-HSA-2671862 JAK2 Phosphorylates IRS in Response to Leptin
R-HSA-2671873 Phosphorylated LEP:LEPR:JAK2:SH2B1 Binds IRS1/2
R-HSA-1170546 Prolactin receptor signaling
R-HSA-2586552 Signaling by Leptin
R-HSA-1280215 Cytokine Signaling in Immune system
R-HSA-162582 Signal Transduction
R-HSA-168256 Immune System

-  Other Names for This Gene
  Alternate Gene Symbols: A8K2R7, ENST00000337120.1, ENST00000337120.2, ENST00000337120.3, ENST00000337120.4, ENST00000337120.5, ENST00000337120.6, ENST00000337120.7, ENST00000337120.8, KIAA1299, NM_015503, Q96FK3, Q96SX3, Q9NRF1, Q9NRF2, Q9NRF3, Q9P2P7, Q9Y3Y3, SH2B, SH2B1_HUMAN, uc002drm.1, uc002drm.2, uc002drm.3, uc002drm.4
UCSC ID: ENST00000337120.9
RefSeq Accession: NM_015503
Protein: Q9NRF2 (aka SH2B1_HUMAN)
CCDS: CCDS32424.1, CCDS53997.1

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.