SLIT2 (slit guidance ligand 2)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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9353 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Slit guidance ligand 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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SLIT2 |
SynonymsGene synonyms aliases
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SLIL3, Slit-2 |
ChromosomeChromosome number
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4 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4p15.31 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the slit family of secreted glycoproteins, which are ligands for the Robo family of immunoglobulin receptors. Slit proteins play highly conserved roles in axon guidance and neuronal migration and may also have functions durin |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs200151302 |
G>A |
Pathogenic, uncertain-significance |
Coding sequence variant, missense variant |
rs1008555507 |
A>C,T |
Pathogenic |
Missense variant, coding sequence variant |
rs1577330805 |
G>A |
Pathogenic |
Missense variant, coding sequence variant, genic upstream transcript variant |
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miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Transcription factor |
Regulation |
Reference |
HDAC5 |
Repression |
19351956 |
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
O94813 |
Protein name |
Slit homolog 2 protein (Slit-2) [Cleaved into: Slit homolog 2 protein N-product; Slit homolog 2 protein C-product] |
Protein function |
Thought to act as molecular guidance cue in cellular migration, and function appears to be mediated by interaction with roundabout homolog receptors. During neural development involved in axonal navigation at the ventral midline of the neural tu |
PDB |
2V70
,
2V9S
,
2V9T
,
2WFH
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF01462 |
LRRNT |
27 → 54 |
Leucine rich repeat N-terminal domain |
Family |
PF13855 |
LRR_8 |
55 → 115 |
Leucine rich repeat |
Repeat |
PF13855 |
LRR_8 |
104 → 163 |
Leucine rich repeat |
Repeat |
PF13855 |
LRR_8 |
127 → 187 |
Leucine rich repeat |
Repeat |
PF13855 |
LRR_8 |
152 → 211 |
Leucine rich repeat |
Repeat |
PF01463 |
LRRCT |
234 → 258 |
Leucine rich repeat C-terminal domain |
Family |
PF01462 |
LRRNT |
272 → 299 |
Leucine rich repeat N-terminal domain |
Family |
PF13855 |
LRR_8 |
300 → 360 |
Leucine rich repeat |
Repeat |
PF13855 |
LRR_8 |
372 → 432 |
Leucine rich repeat |
Repeat |
PF01463 |
LRRCT |
454 → 479 |
Leucine rich repeat C-terminal domain |
Family |
PF13855 |
LRR_8 |
534 → 587 |
Leucine rich repeat |
Repeat |
PF13855 |
LRR_8 |
607 → 666 |
Leucine rich repeat |
Repeat |
PF01463 |
LRRCT |
688 → 713 |
Leucine rich repeat C-terminal domain |
Family |
PF01462 |
LRRNT |
726 → 753 |
Leucine rich repeat N-terminal domain |
Family |
PF13855 |
LRR_8 |
754 → 813 |
Leucine rich repeat |
Repeat |
PF13855 |
LRR_8 |
803 → 861 |
Leucine rich repeat |
Repeat |
PF01463 |
LRRCT |
883 → 908 |
Leucine rich repeat C-terminal domain |
Family |
PF00008 |
EGF |
922 → 953 |
EGF-like domain |
Domain |
PF00008 |
EGF |
961 → 994 |
EGF-like domain |
Domain |
PF00008 |
EGF |
1002 → 1032 |
EGF-like domain |
Domain |
PF00008 |
EGF |
1040 → 1072 |
EGF-like domain |
Domain |
PF00008 |
EGF |
1080 → 1110 |
EGF-like domain |
Domain |
PF12661 |
hEGF |
1130 → 1151 |
Human growth factor-like EGF |
Domain |
PF02210 |
Laminin_G_2 |
1188 → 1316 |
Laminin G domain |
Domain |
PF12661 |
hEGF |
1341 → 1362 |
Human growth factor-like EGF |
Domain |
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Sequence |
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Sequence length |
1529 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Epilepsy |
Epilepsy, Temporal Lobe, Uncinate Epilepsy, Epilepsy, Benign Psychomotor, Childhood, Epilepsy, Lateral Temporal |
rs113994140, rs119454947, rs28937874, rs1589762127, rs104894166, rs28939075, rs2134001459, rs104894167, rs119488099, rs119488100, rs1805032, rs387906420, rs121917752, rs121918622, rs121434579, rs1581220270, rs281865564, rs387907313, rs397514564, rs397514670, rs768241563, rs587776973, rs587776974, rs587776975, rs879255234, rs587776976, rs587776977, rs121917993, rs398123588, rs13306758, rs587777363, rs587777364, rs587777458, rs587777459, rs541024038, rs797044545, rs730882240, rs786205703, rs794726859, rs796053126, rs796053035, rs796053216, rs796052839, rs869025201, rs797044999, rs797044998, rs797045045, rs794726762, rs869312971, rs869312972, rs879255652, rs886037938, rs886037958, rs886037959, rs886037960, rs886037961, rs886037962, rs886037965, rs886037966, rs886039245, rs886039246, rs886039251, rs886039252, rs772872014, rs886039253, rs886039256, rs757511744, rs886039261, rs886039263, rs578185749, rs886039266, rs886039268, rs886039269, rs886039273, rs368820286, rs1057518801, rs1057518688, rs1057519107, rs1057519273, rs752753379, rs767795673, rs1057519424, rs755946598, rs760609867, rs1057521066, rs1057524233, rs1060501488, rs1060501487, rs755127868, rs751533302, rs771373457, rs1475605360, rs1555401942, rs1553567864, rs200661329, rs766667249, rs1556607762, rs1555882921, rs1555882867, rs1555900914, rs1553546836, rs77216276, rs755595256, rs1554169267, rs747661902, rs2105890565, rs1021001959, rs1555441032, rs1555439541, rs1556526609, rs1315483224, rs759952667, rs1555885023, rs1553456695, rs1555942720, rs1569083500, rs1559127505, rs1206309859, rs1567139896, rs1567134495, rs1431914212, rs1569166925, rs1569255443, rs1568955379, rs1567152003, rs374158137, rs1567129567, rs1569523728, rs1568991466, rs1569186093, rs1569254004, rs1372605067, rs1569067939, rs1568963062, rs1563959514, rs1569012755, rs1559118914, rs1602338615, rs1596522356, rs1364913665, rs1596522300, rs1596526976, rs1229740428, rs1596385588, rs1596500172, rs1596505517, rs1601925213, rs1601970168, rs1602010382, rs1602903591, rs1603014297, rs1603014708, rs1601875057, rs1601970824, rs1601755632, rs1587393982, rs1592977444, rs1575562076, rs1570998206, rs1588057922, rs1596528731, rs1602349641, rs1587401875, rs2065899210, rs1596526915, rs2093486364, rs2056165149, rs2056100951, rs781482552, rs1899868619, rs1900088045, rs1898675878, rs1898686157, rs1898837245, rs1898844513, rs2082841677, rs2085727988, rs2092933941, rs2091657024, rs1899864955, rs1898844907, rs2083056830, rs2084070588, rs1899713412, rs2082695884, rs1977106116, rs1977105425, rs1443687532 |
20153733 |
Lung carcinoma |
Small cell carcinoma of lung |
rs1805076, rs121909071, rs121913530, rs112445441, rs121913529, rs121913535, rs121913297, rs121913279, rs104886003, rs397516975, rs11554290, rs121913364, rs121913351, rs121913369, rs121913355, rs121912470, rs121913273, rs121913281, rs121913348, rs727503093, rs121913353, rs397516890, rs397516896, rs121913378, rs397516897, rs397516977, rs397516978, rs397516979, rs397516980, rs397516981, rs397516982, rs121913240, rs17851045, rs397517086, rs121913428, rs397517094, rs397517098, rs397517106, rs121913465, rs397517108, rs397517111, rs397517112, rs397517114, rs397517116, rs1554350366, rs397517127, rs397517200, rs397517202, rs121913283, rs121913370, rs121913357, rs727503106, rs121913238, rs727503108, rs397517040, rs397516976, rs1555618025, rs1057519729, rs1584238193 |
22941188 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Liver carcinoma |
Liver carcinoma |
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19100240 |
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