LASP1NB

gene
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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

FieldValue
HGNC IDHGNC:44353
Approved symbolLASP1NB
NameLASP1 neighbor
Location17q12
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000263874
Ensembl biotypeprotein_coding
OMIM617544
Entrez100505576

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

ExonStartEnd
ENSE000026906253892641738929381
ENSE000027007483892561438925891

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 IDTPM avgSamples expressed
1605451.1655297
1605440.2613107

Top tissues by expression

252 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
pancreatic ductal cellCL:000207988.36silver quality
prefrontal cortexUBERON:000045186.04gold quality
dorsolateral prefrontal cortexUBERON:000983483.41gold quality
Brodmann (1909) area 9UBERON:001354083.33gold quality
anterior cingulate cortexUBERON:000983582.84gold quality
frontal cortexUBERON:000187082.81gold quality
Brodmann (1909) area 46UBERON:000648382.80gold quality
neocortexUBERON:000195082.15gold quality
right frontal lobeUBERON:000281081.35gold quality
hypothalamusUBERON:000189880.55gold quality
cerebral cortexUBERON:000095680.42gold quality
C1 segment of cervical spinal cordUBERON:000646979.19gold quality
amygdalaUBERON:000187678.90gold quality
superior frontal gyrusUBERON:000266178.77gold quality
substantia nigraUBERON:000203878.34gold quality
cerebellar hemisphereUBERON:000224578.34gold quality
cerebellar cortexUBERON:000212978.28gold quality
postcentral gyrusUBERON:000258178.12gold quality
cerebellumUBERON:000203777.62gold quality
right hemisphere of cerebellumUBERON:001489077.59gold quality
Ammon’s hornUBERON:000195477.39gold quality
forebrainUBERON:000189077.06gold quality
brainUBERON:000095576.91gold quality
caudate nucleusUBERON:000187376.20gold quality
putamenUBERON:000187476.19gold quality
spinal cordUBERON:000224076.16gold quality
midbrainUBERON:000189176.15gold quality
nucleus accumbensUBERON:000188276.12gold quality
temporal lobeUBERON:000187175.93gold quality
cortical plateUBERON:000534375.44gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-GEOD-36552no17.49
E-ANND-3no2.90

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 proteinA0A1B0GWH6 (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)

ModelpLDDTFraction very-high
AF-A0A1B0GWH6-F197.601.00

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:

CategoryTerms
cellular anatomical structure1

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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

157 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
17:38925733:G:CG14R0.974
17:38925737:T:CL15P0.972
17:38925737:T:GL15R0.959
17:38925746:T:GL18R0.950
17:38925725:C:AA11D0.946
17:38925764:T:CL24P0.937
17:38925740:T:AV16D0.935
17:38925737:T:AL15Q0.932
17:38925700:G:CD3H0.929
17:38925746:T:CL18P0.926
17:38925724:G:CA11P0.912
17:38925713:T:GL7R0.905
17:38925734:G:AG14D0.901
17:38925746:T:AL18Q0.899
17:38925713:T:CL7P0.894
17:38925767:T:AL25H0.894
17:38925731:T:AI13K0.884
17:38925767:T:GL25R0.878
17:38925716:T:AM8K0.874
17:38925731:T:GI13R0.871
17:38925716:T:GM8R0.869
17:38925701:A:TD3V0.868
17:38925713:T:AL7Q0.864
17:38925707:T:GF5C0.844
17:38925767:T:CL25P0.840
17:38925706:T:CF5L0.821
17:38925708:C:AF5L0.821
17:38925708:C:GF5L0.821
17:38925701:A:CD3A0.820
17:38925748:T:CS19P0.809

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.

ChemicalActions (top 5)PubMed papers
(+)-JQ1 compoundincreases expression2
Phenylmercuric Acetateaffects cotreatment, decreases expression2
Particulate Matterdecreases expression, increases expression2
aristolochic acid Iincreases expression1
sodium arsenitedecreases expression1
fipronilaffects cotreatment, decreases expression1
pifithrindecreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphinaffects cotreatment, decreases expression1
DEETaffects cotreatment, decreases expression1
Tobacco Smoke Pollutionincreases expression1
Paclitaxelincreases response to substance1
Okadaic Aciddecreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.