![]() |
||||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Fusion gene ID: 19385 |
FusionGeneSummary for LAMB1_PARP14 |
![]() |
Fusion gene information | Fusion gene name: LAMB1_PARP14 | Fusion gene ID: 19385 | Hgene | Tgene | Gene symbol | LAMB1 | PARP14 | Gene ID | 3912 | 54625 |
Gene name | laminin subunit beta 1 | poly(ADP-ribose) polymerase family member 14 | |
Synonyms | CLM|LIS5 | ARTD8|BAL2|PARP-14|pART8 | |
Cytomap | 7q31.1 | 3q21.1 | |
Type of gene | protein-coding | protein-coding | |
Description | laminin subunit beta-1laminin B1 chainlaminin, beta 1 | poly [ADP-ribose] polymerase 14ADP-ribosyltransferase diphtheria toxin-like 8B-aggressive lymphoma 2b aggressive lymphoma protein 2collaborator of STAT6 | |
Modification date | 20180522 | 20180519 | |
UniProtAcc | P07942 | Q460N5 | |
Ensembl transtripts involved in fusion gene | ENST00000393561, ENST00000222399, ENST00000393560, ENST00000474380, | ENST00000474629, ENST00000475640, | |
Fusion gene scores | * DoF score | 10 X 8 X 4=320 | 5 X 6 X 2=60 |
# samples | 10 | 6 | |
** MAII score | log2(10/320*10)=-1.67807190511264 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(6/60*10)=0 | |
Context | PubMed: LAMB1 [Title/Abstract] AND PARP14 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | LAMB1 | GO:0030335 | positive regulation of cell migration | 16289578 |
Hgene | LAMB1 | GO:0031175 | neuron projection development | 15894315 |
Hgene | LAMB1 | GO:0034446 | substrate adhesion-dependent cell spreading | 16236823 |
Hgene | LAMB1 | GO:0042476 | odontogenesis | 15894315 |
Tgene | PARP14 | GO:0006471 | protein ADP-ribosylation | 27796300 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | LD | BRCA | TCGA-C8-A134-01A | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
In-frame | ENST00000393561 | ENST00000474629 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
5CDS-intron | ENST00000393561 | ENST00000475640 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
Frame-shift | ENST00000222399 | ENST00000474629 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
5CDS-intron | ENST00000222399 | ENST00000475640 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
Frame-shift | ENST00000393560 | ENST00000474629 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
5CDS-intron | ENST00000393560 | ENST00000475640 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
intron-3CDS | ENST00000474380 | ENST00000474629 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
intron-intron | ENST00000474380 | ENST00000475640 | LAMB1 | chr7 | 107635332 | - | PARP14 | chr3 | 122446659 | + |
Top |
FusionProtFeatures for LAMB1_PARP14 |
![]() |
Hgene | Tgene |
LAMB1 | PARP14 |
Binding to cells via a high affinity receptor, lamininis thought to mediate the attachment, migration and organizationof cells into tissues during embryonic development by interactingwith other extracellular matrix components. Involved in theorganization of the laminar architecture of cerebral cortex. It isprobably required for the integrity of the basement membrane/glialimitans that serves as an anchor point for the endfeet of radialglial cells and as a physical barrier to migrating neurons. Radialglial cells play a central role in cerebral cortical development,where they act both as the proliferative unit of the cerebralcortex and a scaffold for neurons migrating toward the pialsurface. {ECO:0000269|PubMed:23472759}. | ADP-ribosyltransferase (PubMed:16061477,PubMed:27796300). By mono-ADP-ribosylating STAT1 at 'Glu-657' and'Glu-705' and thus decreasing STAT1 phosphorylation, negativelyregulates pro-inflammatory cytokines production in macrophages inresponse to IFNG stimulation (PubMed:27796300). Mono-ADP-ribosylates STAT6 (By similarity). Enhances STAT6-dependenttranscription (By similarity). In macrophages, positivelyregulates MRC1 expression in response to IL4 stimulation bypromoting STAT6 phosphorylation (PubMed:27796300). Mono-ADP-ribosylates PARP9 (PubMed:27796300).{ECO:0000250|UniProtKB:Q2EMV9, ECO:0000269|PubMed:16061477,ECO:0000269|PubMed:27796300}. |
![]() * Minus value of BPloci means that the break pointn is located before the CDS. |
- In-frame and retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1216_1315 | 141 | 1787 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1353_1388 | 141 | 1787 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1442_1781 | 141 | 1787 | Coiled coil | Ontology_term=ECO:0000255 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1028_1083 | 141 | 1787 | Domain | Laminin EGF-like 11 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1084_1131 | 141 | 1787 | Domain | Laminin EGF-like 12 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1132_1178 | 141 | 1787 | Domain | Laminin EGF-like 13 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 271_334 | 141 | 1787 | Domain | Laminin EGF-like 1 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 31_270 | 141 | 1787 | Domain | Laminin N-terminal |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 335_397 | 141 | 1787 | Domain | Laminin EGF-like 2 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 398_457 | 141 | 1787 | Domain | Laminin EGF-like 3 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 458_509 | 141 | 1787 | Domain | Laminin EGF-like 4 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 510_540 | 141 | 1787 | Domain | Laminin EGF-like 5%3B truncated |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 549_767 | 141 | 1787 | Domain | Laminin IV type B |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 773_820 | 141 | 1787 | Domain | Laminin EGF-like 6 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 821_866 | 141 | 1787 | Domain | Laminin EGF-like 7 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 867_916 | 141 | 1787 | Domain | Laminin EGF-like 8 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 917_975 | 141 | 1787 | Domain | Laminin EGF-like 9 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 976_1027 | 141 | 1787 | Domain | Laminin EGF-like 10 |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1179_1397 | 141 | 1787 | Region | Note=Domain II |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1398_1430 | 141 | 1787 | Region | Note=Domain alpha |
Hgene | >LAMB1 | chr7:107635332 | chr3:122446659 | ENST00000222399 | - | 5 | 34 | 1431_1786 | 141 | 1787 | Region | Note=Domain I |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1003_1190 | 1647 | 1802 | Domain | Macro 2 |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1216_1387 | 1647 | 1802 | Domain | Macro 3 |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1523_1601 | 1647 | 1802 | Domain | WWE |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1605_1801 | 1647 | 1802 | Domain | PARP catalytic |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 791_978 | 1647 | 1802 | Domain | Macro 1 |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1023_1024 | 1647 | 1802 | Region | Substrate 2 binding |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1046_1049 | 1647 | 1802 | Region | Substrate 2 binding |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1133_1137 | 1647 | 1802 | Region | Substrate 2 binding |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1175_1178 | 1647 | 1802 | Region | Substrate 2 binding |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1235_1236 | 1647 | 1802 | Region | Substrate 3 binding |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 1332_1336 | 1647 | 1802 | Region | Substrate 3 binding |
Tgene | PARP14 | chr7:107635332 | chr3:122446659 | ENST00000474629 | + | 14 | 17 | 922_926 | 1647 | 1802 | Region | Substrate 1 binding |
Top |
FusionGeneSequence for LAMB1_PARP14 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_LAMB1_ENST00000393561_chr7_107635332_-_PARP14_ENST00000474629_chr3_122446659_+_320aa MDCPLSAPTPPPPLVRFFRAPLPACVPPTLLPVLPAALCRARVRAQEPEFSYGCAEGSCYPATGDLLIGRAQKLSVTSTCGLHKPEPYCI VSHLQEDKKCFICNSQDPYHETLNPDSHLIENVVTTFAPNRLKIWWQSENGVENVTIQLDLEAEFHFTHLIMTFKIERIQNPDLWNSYQA KKKTMDAKNGQTMNEKQLFHGTDAGSVPHVNRNGFNRSYAGKNAVAYGKGTYFAVNANYSANDTYSRPDANGRKHVYYVRVLTGIYTHGN |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_LAMB1_ENST00000393561_chr7_107635332_-_PARP14_ENST00000474629_chr3_122446659_+_960nt ATGGACTGTCCTCTCTCCGCACCCACTCCCCCGCCCCCGCTTGTTCGTTTTTTTCGGGCTCCACTCCCTGCTTGTGTCCCCCCAACTCTG TTGCCTGTCCTTCCCGCAGCCCTGTGCAGAGCCCGAGTGCGCGCTCAGGAACCCGAGTTCAGCTACGGCTGCGCAGAAGGCAGCTGCTAT CCCGCCACGGGCGACCTTCTCATCGGCCGAGCACAGAAGCTTTCGGTGACCTCGACGTGCGGGCTGCACAAGCCCGAACCCTACTGTATC GTCAGCCACTTGCAGGAGGACAAAAAATGCTTCATATGCAATTCCCAAGATCCTTATCATGAGACCCTGAATCCTGACAGCCATCTCATT GAAAATGTGGTCACTACATTTGCTCCAAACCGCCTTAAGATTTGGTGGCAATCTGAAAATGGTGTGGAAAATGTAACTATCCAACTGGAT TTGGAAGCAGAATTCCATTTTACTCATCTCATAATGACTTTCAAGATTGAGAGGATCCAGAATCCAGATCTCTGGAATAGCTACCAGGCA AAGAAAAAAACTATGGATGCCAAGAATGGCCAGACAATGAATGAGAAGCAACTCTTCCATGGGACAGATGCCGGCTCCGTGCCACACGTC AATCGAAATGGCTTTAACCGCAGCTATGCCGGAAAGAATGCTGTGGCATATGGAAAGGGAACCTATTTTGCTGTCAATGCCAATTATTCT GCCAATGATACGTACTCCAGACCAGATGCAAATGGGAGAAAGCATGTGTATTATGTGCGAGTACTTACTGGAATCTATACACATGGAAAT CATTCATTAATTGTGCCTCCTTCAAAGAACCCTCAAAATCCTACTGACCTGTATGACACTGTCACAGATAATGTGCACCATCCAAGTTTA |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_LAMB1_ENST00000393561_chr7_107635332_-_PARP14_ENST00000474629_chr3_122446659_+_3388nt GGGGCTGATCAGGGTGGGCGCGAGCGTCGGTGGGTTTCCCGGGAGGGAGGCTCTCGCTGCTGGACAGACCTGATGACGTGTGTGGGTTTC TTTCCGTGTCCTTCTCCTTTCGGAGTCCCTGCCTTCCCAGCCTCTCCTGCGCTCATCTCTCCATTGTCTTTTCTGTGCATTTTGCTTTCT TCCGAATGGACTGTCCTCTCTCCGCACCCACTCCCCCGCCCCCGCTTGTTCGTTTTTTTCGGGCTCCACTCCCTGCTTGTGTCCCCCCAA CTCTGTTGCCTGTCCTTCCCGCAGCCCTGTGCAGAGCCCGAGTGCGCGCTCAGGAACCCGAGTTCAGCTACGGCTGCGCAGAAGGCAGCT GCTATCCCGCCACGGGCGACCTTCTCATCGGCCGAGCACAGAAGCTTTCGGTGACCTCGACGTGCGGGCTGCACAAGCCCGAACCCTACT GTATCGTCAGCCACTTGCAGGAGGACAAAAAATGCTTCATATGCAATTCCCAAGATCCTTATCATGAGACCCTGAATCCTGACAGCCATC TCATTGAAAATGTGGTCACTACATTTGCTCCAAACCGCCTTAAGATTTGGTGGCAATCTGAAAATGGTGTGGAAAATGTAACTATCCAAC TGGATTTGGAAGCAGAATTCCATTTTACTCATCTCATAATGACTTTCAAGATTGAGAGGATCCAGAATCCAGATCTCTGGAATAGCTACC AGGCAAAGAAAAAAACTATGGATGCCAAGAATGGCCAGACAATGAATGAGAAGCAACTCTTCCATGGGACAGATGCCGGCTCCGTGCCAC ACGTCAATCGAAATGGCTTTAACCGCAGCTATGCCGGAAAGAATGCTGTGGCATATGGAAAGGGAACCTATTTTGCTGTCAATGCCAATT ATTCTGCCAATGATACGTACTCCAGACCAGATGCAAATGGGAGAAAGCATGTGTATTATGTGCGAGTACTTACTGGAATCTATACACATG GAAATCATTCATTAATTGTGCCTCCTTCAAAGAACCCTCAAAATCCTACTGACCTGTATGACACTGTCACAGATAATGTGCACCATCCAA GTTTATTTGTGGCATTTTATGACTACCAAGCATACCCAGAGTACCTTATTACGTTTAGAAAATAACACTTTGGTATCCTTCCCACAAAAT TATTCTCCATTTGTACATATCTAGTTGTAAAACAAGTTTTAGCTTTTTTTTTTAATTCCTCTTAACAGATTTTTCTAATATCCAAGGATC ATTCTTTGTCGCTGAAGTCAGTCTTTCTTCAGCTTCCCTTTCATAATGGAAATGAACTTATTATCTTGAGAGCAAATAACTTGGAAAATT TAAATGAGATAATGCAGTTGCAACTGTGTGTCCACAAGTATGGACATCAAATCTGTGGGAAAAGAACAGGTTTGTATTTTCAGGAAGGAG AGAATAACAGTCTTATAGACAGAGGGCACAGCTAAGCACAGCTGCCACTGCAGGAGACAGGCCCCATGTCAGGATGCCATAGTGCTGTGG GGAGCACAGTATTACCCAGTGGGTAGGGCTTCTGTCTTCCCTGGGAGCAGGGATGGTATCTTAGTCAATTTTTTTCCCTTGAGATGAGGT CTGTGCCTGATGTACAACGGATACTCCATAAATGTTTGACAAACCAACGAAGAATGAAAAAAAGCCTAGTCAGACTCCCATCCAAAGTAG GAACTATCTCTTTAACATTCTTGACTCACTATCACTTTACCTCAAATTGAACAGATTCCATGACGGAACTTCATTCTTCACAAACTAGCC AGTGACATGTGGGACAGCTCTGGCCAGGGCTCTGGGACTGCAGTGTACTTGCGCTCTGCACGGTCCAGGAGCTGTGATGTGGCTGTGGTC TAGGGGAATCCTGCCTGCCCCATGGAGTTGCGCAGCACAACCCTGGCTCCAATTGCCAGAAGGCTCTTTTTAATGCTGAACCAAAATGTG CCTTTTTTTTTTTTTTTTTGAGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCACTGCAGCCACTGC CTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCTAACACACCCAGCTAATTTTGTATTTT TAGTAGAGACGAGGTTTCTCCATGTTCGACAGGCTGGTCTCGAACTCCCACCTCAGCCTCCCAAACTGCTGGGATTACAGGTGTGAGCCA CCGTGACCAGCCAATGTGCCTTCTTATAGTGTCTACTCATTGGTCTTTGTTCTGCCCAGTGATAACAATGGGATAACGCCTGCTACACAT CTTCATTGTGAAACCCTTCCCCTGTGCTGAGATTAAATGAACTCTAAGATTATTAAATAGTATATTTTCCTTGACAGCCTAGCGTTTGAT GATTTTAAAGCCTTATGTATAAATAAACCAAAGGAAGTAAGCAGTCATATTGCTAATTTGCTAACTCCTATCTATTGAATGGTGAAGTTT TAAAAATTTCCCCAGGTAAGTTTAAGATTCAAACACCATCTATTGAGCACCTACATTGTGTGCCAGGTAGTAAAATAGGTGCTTTCATAC ACATTGTCTCAATTCCTGTGAGGTCAGAATTATCTCTGCATTTGAAACTTGAGGAAACATGCTCAGAGTGCAAGAAGCTTCCTTGCCTGA GATCACCTAGAAAGGAACCCTCAGAGCCGGCAACTGAATCTTGGTCCCTGTGATGTCAAGCCCATTGCTCTCCCACTGCAGAACATGGCC TCTAGATTAATGCCACCGATTCAGGAACACCTCCGACAGTCTTGAAATACCCCCATGTTGCCTTGTTTGTTTTTTCCTTCTGGCTTCTTC TATTACAGTCTCTTCATTGGAAGCTCTGTAGGCCAAGGCCAGAGCTGATACTGACACGGAGCCAATGCAGATAGCACATCAGATGCTAGG GGTCGCTGGGAGGATTAAGGGACTTAATCTGCTAGGAACACCTGTACTTGAAGTGGAGGAGGCTAGGGGGCCACAGTTGCTGCTTCATTA ACATAGAGGTTTTGGATTTTTTTCTCTTGTGGTTTGTTTTTTAAGTGGATTGGCAGACTCCTTGTTGCTTAAGAGTGGCTTTCTAGGCAG GCCACTGGCATCTGAATTCATCATTGACAATAAATGTAAGAAATTGGAATAAAAAAGAGAGACCTGCTGTTATTCGCTTTTGTTCTCCAG TGATTTGATTAACTCAGGGCAAGGCTGAATATCAGAGTGTATCGCACTGAAGAATAATAATCCATTCAGTAATGTTATAGTTATCCTCAA |
Top |
FusionGenePPI for LAMB1_PARP14 |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
LAMB1 | TGFB1, ATXN7, CACNA1A, LAMC1, UBC, ATXN7L2, GFI1B, FBXO6, NQO1, DPY30, HSPD1, PDIA3, ERBB2IP, HECW2, KIAA1033, POLR2E, ANTXR2, PA2G4, LGALS3, NTF3, OGN, LGALS9, TMEM25, PTPRK, CD96, PSMD5, NTRK1, PSMC5, KIF11, FGFR1OP, SERPINA12, OS9, DEFA1, COLEC12, CRP, LYZL2, PSG8, BCAM, LMNA | PARP14 | GPI, STAT6, FCER2, HDAC2, HDAC3, CUL2, IKBKG, RPA1, RPA2, RPA3, DTX3L, PARP9, GAN, PARP10 |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
RelatedDrugs for LAMB1_PARP14 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Top |
RelatedDiseases for LAMB1_PARP14 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | LAMB1 | C0004352 | Autistic Disorder | 1 | CTD_human |
Hgene | LAMB1 | C0009324 | Ulcerative Colitis | 1 | CTD_human |
Hgene | LAMB1 | C0009363 | Congenital ocular coloboma (disorder) | 1 | CTD_human |
Hgene | LAMB1 | C0014175 | Endometriosis | 1 | CTD_human |