DISP1
Protein dispatched homolog 1
Also known as: DISP1_HUMAN, DISPA, DKFZP434I0428, MGC13130, MGC16796
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96F81
- Gene
- DISP1
- Ensembl
- ENSG00000154309
- Chromosome
- 1
- Canonical length
- 1524 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Plasma membrane
OverviewNCBI Gene
The pattern of cellular proliferation and differentiation that leads to normal development of embryonic structures often depends upon the localized production of secreted protein signals. Cells surrounding the source of a particular signal respond in a graded manner according to the effective concentration of the signal, and this response produces the pattern of cell types constituting the mature structure. A novel segment-polarity gene known as dispatched has been identified in Drosophila and its protein product is required for normal Hedgehog (Hh) signaling. This gene is one of two human homologs of Drosophila dispatched and, based on sequence identity to its mouse counterpart, the encoded protein may play an essential role in Hh patterning activities in the early embryo. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1524 residues, UniProt reviewed canonical sequence.
>Q96F81|DISP1
1 MAMSNGNNDF VVLSNSSIAT SAANPSPLTP CDGDHAAQQL TPKEATRTKV SPNGCLQLNG
61 TVKSSFLPLD NQRMPQMLPQ CCHPCPYHHP LTSHSSHQEC HPEAGPAAPS ALASCCMQPH
121 SEYSASLCPN HSPVYQTTCC LQPSPSFCLH HPWPDHFQHQ PVQQHIANIR PSRPFKLPKS
181 YAALIADWPV VVLGMCTMFI VVCALVGVLV PELPDFSDPL LGFEPRGTAI GQRLVTWNNM
241 VKNTGYKATL ANYPFKYADE QAKSHRDDRW SDDHYEREKR EVDWNFHKDS FFCDVPSDRY
301 SRVVFTSSGG ETLWNLPAIK SMCNVDNSRI RSHPQFGDLC QRTTAASCCP SWTLGNYIAI
361 LNNRSSCQKI VERDVSHTLK LLRTCAKHYQ NGTLGPDCWD MAARRKDQLK CTNVPRKCTK
421 YNAVYQILHY LVDKDFMTPK TADYATPALK YSMLFSPTEK GESMMNIYLD NFENWNSSDG
481 VTTITGIEFG IKHSLFQDYL LMDTVYPAIA IVIVLLVMCV YTKSMFITLM TMFAIISSLI
541 VSYFLYRVVF HFEFFPFMNL TALIILVGIG ADDAFVLCDV WNYTKFDKPH AETSETVSIT
601 LQHAALSMFV TSFTTAAAFY ANYVSNITAI RCFGVYAGTA ILVNYVLMVT WLPAVVVLHE
661 RYLLNIFTCF KKPQQQIYDN KSCWTVACQK CHKVLFAISE ASRIFFEKVL PCIVIKFRYL
721 WLFWFLALTV GGAYIVCINP KMKLPSLELS EFQVFRSSHP FERYDAEYKK LFMFERVHHG
781 EELHMPITVI WGVSPEDNGN PLNPKSKGKL TLDSSFNIAS PASQAWILHF CQKLRNQTFF
841 YQTDEQDFTS CFIETFKQWM ENQDCDEPAL YPCCSHWSFP YKQEIFELCI KRAIMELERS
901 TGYHLDSKTP GPRFDINDTI RAVVLEFQST YLFTLAYEKM HQFYKEVDSW ISSELSSAPE
961 GLSNGWFVSN LEFYDLQDSL SDGTLIAMGL SVAVAFSVML LTTWNIIISL YAIISIAGTI
1021 FVTVGSLVLL GWELNVLESV TISVAVGLSV DFAVHYGVAY RLAPDPDREG KVIFSLSRVG
1081 SAMAMAALTT FVAGAMMMPS TVLAYTQLGT FMMLIMCISW AFATFFFQCM CRCLGPQGTC
1141 GQIPLPKKLQ CSAFSHALST SPSDKGQSKT HTINAYHLDP RGPKSELEHE FYELEPLASH
1201 SCTAPEKTTY EETHICSEFF NSQAKNLGMP VHAAYNSELS KSTESDAGSA LLQPPLEQHT
1261 VCHFFSLNQR CSCPDAYKHL NYGPHSCQQM GDCLCHQCSP TTSSFVQIQN GVAPLKATHQ
1321 AVEGFVHPIT HIHHCPCLQG RVKPAGMQNS LPRNFFLHPV QHIQAQEKIG KTNVHSLQRS
1381 IEEHLPKMAE PSSFVCRSTG SLLKTCCDPE NKQRELCKNR DVSNLESSGG TENKAGGKVE
1441 LSLSQTDASV NSEHFNQNEP KVLFNHLMGE AGCRSCPNNS QSCGRIVRVK CNSVDCQMPN
1501 MEANVPAVLT HSELSGESLL IKTLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DISP1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 12
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 8.5 nTPM
Expression across tissuesHPA
Tissue
- lung: 8.5 nTPM
- testis: 6.1 nTPM
- colon: 5.2 nTPM
- stomach: 5 nTPM
- thyroid gland: 4.9 nTPM
- parathyroid gland: 4.8 nTPM
Single-cell type
- sertoli cells: 713 nCPM
- choroid plexus epithelial cells: 698 nCPM
- microglia: 606 nCPM
- mesothelial cells: 330 nCPM
- foveolar cells: 272 nCPM
- oligodendrocyte progenitor cells: 269 nCPM
Immune cell
- MAIT T-cell: 1.6 nTPM
- NK-cell: 1 nTPM
- naive B-cell: 0.9 nTPM
- gdT-cell: 0.7 nTPM
- memory CD8 T-cell: 0.7 nTPM
- memory CD4 T-cell: 0.6 nTPM
Brain region
- cerebellum: 15 nTPM
- choroid plexus: 15 nTPM
- white matter: 10 nTPM
- basal ganglia: 10 nTPM
- cerebral cortex: 9.8 nTPM
- hypothalamus: 9.7 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about DISP1.
Disease | AllUniProt
Conditions DISP1 is implicated in, by any mechanism.
- Holoprosencephaly 10 (HPE10) MIM:621143
Disease | GeneticClinVar
8 pathogenic / likely-pathogenic of 490 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Holoprosencephaly 10
- See cases
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.6
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.93
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- determination of left/right symmetry
- diaphragm development
- dorsal/ventral pattern formation
- embryonic pattern specification
- peptide transport
- regulation of protein secretion
- smoothened signaling pathway
- patched ligand maturation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DISP1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DISP1 as an antibody target. Whether an autoantibody or antibody against DISP1 could matter depends on whether native DISP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DISP1 is annotated at the cell surface, where native DISP1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label DISP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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