LASP1NB
gene geneOn this page
Summary
LASP1NB (LASP1 neighbor, HGNC:44353) is a protein-coding gene on chromosome 17q12, encoding LASP1 neighbor protein (A0A1B0GWH6). May play a key role in the skin fibroblasts (FBs)-keratinocyte-like cells (KLCs).
Predicted to be located in membrane.
Source: NCBI Gene 100505576 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 1 total
- MANE Select transcript:
NM_001414697
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:44353 |
| Approved symbol | LASP1NB |
| Name | LASP1 neighbor |
| Location | 17q12 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000263874 |
| Ensembl biotype | protein_coding |
| OMIM | 617544 |
| Entrez | 100505576 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000583195
RefSeq mRNA: 1 — MANE Select: NM_001414697
NM_001414697
Canonical transcript exons
ENST00000583195 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002690625 | 38926417 | 38929381 |
| ENSE00002700748 | 38925614 | 38925891 |
Expression profiles
Bgee: expression breadth ubiquitous, 192 present calls, max score 88.36.
FANTOM5 (CAGE): breadth broad, TPM avg 1.4268 / max 100.4753, expressed in 332 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 160545 | 1.1655 | 297 |
| 160544 | 0.2613 | 107 |
Top tissues by expression
252 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| pancreatic ductal cell | CL:0002079 | 88.36 | silver quality |
| prefrontal cortex | UBERON:0000451 | 86.04 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 83.41 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 83.33 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 82.84 | gold quality |
| frontal cortex | UBERON:0001870 | 82.81 | gold quality |
| Brodmann (1909) area 46 | UBERON:0006483 | 82.80 | gold quality |
| neocortex | UBERON:0001950 | 82.15 | gold quality |
| right frontal lobe | UBERON:0002810 | 81.35 | gold quality |
| hypothalamus | UBERON:0001898 | 80.55 | gold quality |
| cerebral cortex | UBERON:0000956 | 80.42 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 79.19 | gold quality |
| amygdala | UBERON:0001876 | 78.90 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 78.77 | gold quality |
| substantia nigra | UBERON:0002038 | 78.34 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 78.34 | gold quality |
| cerebellar cortex | UBERON:0002129 | 78.28 | gold quality |
| postcentral gyrus | UBERON:0002581 | 78.12 | gold quality |
| cerebellum | UBERON:0002037 | 77.62 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 77.59 | gold quality |
| Ammon’s horn | UBERON:0001954 | 77.39 | gold quality |
| forebrain | UBERON:0001890 | 77.06 | gold quality |
| brain | UBERON:0000955 | 76.91 | gold quality |
| caudate nucleus | UBERON:0001873 | 76.20 | gold quality |
| putamen | UBERON:0001874 | 76.19 | gold quality |
| spinal cord | UBERON:0002240 | 76.16 | gold quality |
| midbrain | UBERON:0001891 | 76.15 | gold quality |
| nucleus accumbens | UBERON:0001882 | 76.12 | gold quality |
| temporal lobe | UBERON:0001871 | 75.93 | gold quality |
| cortical plate | UBERON:0005343 | 75.44 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-36552 | no | 17.49 |
| E-ANND-3 | no | 2.90 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 1)
- These findings indicate that LINC00672 can influence LASP1 expression as a locus-restricted cofactor for p53-mediated gene suppression, thus impacting endometrial cancer and chemosensitivity to paclitaxel. (PMID:28232485)
Cross-species orthologs
0 orthologs
Protein
Protein identifiers
LASP1 neighbor protein — A0A1B0GWH6 (reviewed: A0A1B0GWH6)
Alternative names: Long intergenic non-protein coding RNA 672
All UniProt accessions (1): A0A1B0GWH6
UniProt curated annotations — full annotation on UniProt →
Function. May play a key role in the skin fibroblasts (FBs)-keratinocyte-like cells (KLCs).
Subcellular location. Membrane.
RefSeq proteins (1): NP_001401626* (*=MANE)
Domains & families (InterPro)
UniProt features (2 total): chain 1, transmembrane region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A0A1B0GWH6-F1 | 97.60 | 1.00 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 16 (showing top):
GAUSSMANN_MLL_AF4_FUSION_TARGETS_G_UP, MIKKELSEN_ES_ICP_WITH_H3K4ME3, MIKKELSEN_NPC_ICP_WITH_H3K4ME3, WARTERS_RESPONSE_TO_IR_SKIN, GSE14000_TRANSLATED_RNA_VS_MRNA_4H_LPS_DC_DN, BLANCO_MELO_INFLUENZA_A_INFECTION_A594_CELLS_UP, chr17q12, FAN_EMBRYONIC_CTX_OLIG, HE_LIM_SUN_FETAL_LUNG_C0_ACTC_POS_SMC_CELL, HE_LIM_SUN_FETAL_LUNG_C0_MESENCHYMAL_1_CELL, HE_LIM_SUN_FETAL_LUNG_C0_VASCULAR_SMC_1_CELL, HE_LIM_SUN_FETAL_LUNG_C0_VASCULAR_SMC_2_CELL, GSE25087_FETAL_VS_ADULT_TREG_DN, IZADPANAH_STEM_CELL_ADIPOSE_VS_BONE_DN, GSE21927_EL4_VS_MCA203_TUMOR_MONOCYTES_DN
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (1): membrane (GO:0016020)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A1B0GWH6, A0A7H0DN68, A0A7H0DNB3, A0T0B1, A0T0B4, A0T0P6, A2BVK2, A4ZUB9, A4ZUC7, A5A617, B7K767, C0HJH3, C0HJH4, C7J0R5, O00631, O78448, P0C2G8, P0CAJ2, P0CAJ3, P0CAJ4, P0CK21, P0CK22, P0DN84, P0DPN0, P0DPO4, P0DPO8, P0DTF1, P0DTI0, P11339, P15911, P30396, P37256, P48109, P49487, P49516, P64442, P64443, P64444, P9WEJ6, Q06J23
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
1 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
157 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 17:38925733:G:C | G14R | 0.974 |
| 17:38925737:T:C | L15P | 0.972 |
| 17:38925737:T:G | L15R | 0.959 |
| 17:38925746:T:G | L18R | 0.950 |
| 17:38925725:C:A | A11D | 0.946 |
| 17:38925764:T:C | L24P | 0.937 |
| 17:38925740:T:A | V16D | 0.935 |
| 17:38925737:T:A | L15Q | 0.932 |
| 17:38925700:G:C | D3H | 0.929 |
| 17:38925746:T:C | L18P | 0.926 |
| 17:38925724:G:C | A11P | 0.912 |
| 17:38925713:T:G | L7R | 0.905 |
| 17:38925734:G:A | G14D | 0.901 |
| 17:38925746:T:A | L18Q | 0.899 |
| 17:38925713:T:C | L7P | 0.894 |
| 17:38925767:T:A | L25H | 0.894 |
| 17:38925731:T:A | I13K | 0.884 |
| 17:38925767:T:G | L25R | 0.878 |
| 17:38925716:T:A | M8K | 0.874 |
| 17:38925731:T:G | I13R | 0.871 |
| 17:38925716:T:G | M8R | 0.869 |
| 17:38925701:A:T | D3V | 0.868 |
| 17:38925713:T:A | L7Q | 0.864 |
| 17:38925707:T:G | F5C | 0.844 |
| 17:38925767:T:C | L25P | 0.840 |
| 17:38925706:T:C | F5L | 0.821 |
| 17:38925708:C:A | F5L | 0.821 |
| 17:38925708:C:G | F5L | 0.821 |
| 17:38925701:A:C | D3A | 0.820 |
| 17:38925748:T:C | S19P | 0.809 |
dbSNP variants (sampled 300 via entrez): RS1000367858 (17:38923798 A>G), RS1000900916 (17:38928373 C>G), RS1000969853 (17:38925115 T>C,G), RS1001907631 (17:38929763 A>G), RS1002087905 (17:38924094 A>T), RS1002374339 (17:38926631 A>G), RS1002988992 (17:38927721 C>T), RS1003682710 (17:38926593 T>C), RS1003844861 (17:38926513 C>A,T), RS1004370790 (17:38929498 T>C), RS1004514976 (17:38925487 T>A), RS1004837488 (17:38925195 T>A), RS1004848851 (17:38927665 A>G), RS1004968139 (17:38927484 G>A,T), RS1005790617 (17:38926282 C>G,T)
Disease associations
OMIM: gene MIM:617544 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
13 total (human), top 13 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| (+)-JQ1 compound | increases expression | 2 |
| Phenylmercuric Acetate | affects cotreatment, decreases expression | 2 |
| Particulate Matter | decreases expression, increases expression | 2 |
| aristolochic acid I | increases expression | 1 |
| sodium arsenite | decreases expression | 1 |
| fipronil | affects cotreatment, decreases expression | 1 |
| pifithrin | decreases expression | 1 |
| 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide | affects cotreatment, decreases expression | 1 |
| dorsomorphin | affects cotreatment, decreases expression | 1 |
| DEET | affects cotreatment, decreases expression | 1 |
| Tobacco Smoke Pollution | increases expression | 1 |
| Paclitaxel | increases response to substance | 1 |
| Okadaic Acid | decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.