Evidence Details for STMN4
Basic Information Top
| Gene Symbol: | STMN4 ( MGC111012,RB3 ) |
|---|---|
| Gene Full Name: | stathmin-like 4 |
| Band: | 8p21.2 |
| Quick Links | Entrez ID:81551; OMIM: NA; Uniprot ID:STMN4_HUMAN; ENSEMBL ID: ENSG00000015592; HGNC ID: 16078 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>STMN4|81551|nucleotide
ATGACCCTTGCTGCCTACAAAGAGAAGATGAAGGAGCTCCCGCTGGTGTCCTTGTTCTGCTCCTGCTTCCTGGCCGATCCCCTGAATAAGTCGTCCTACAAATAT
GAAGGCTGGTGTGGGAGACAGTGTAGGAGGAAGGATGAAAGCCAGCGGAAAGACAGTGCTGACTGGAGAGAAAGAAGAGCTCAGGCAGACACGGTGGACCTGAAT
TGGTGCGTCATTTCCGACATGGAAGTCATCGAGCTGAACAAATGCACCTCGGGCCAATCCTTTGAAGTCATCCTGAAGCCACCCTCCTTTGATGGGGTTCCCGAG
TTCAACGCCTCCCTGCCAAGGCGGCGAGACCCATCCCTGGAAGAGATCCAGAAGAAACTAGAAGCGGCTGAGGAGCGAAGGAAGTACCAGGAAGCGGAGCTCCTG
AAACACCTAGCAGAGAAACGGGAACATGAGAGAGAGGTGATCCAAAAGGCCATTGAGGAAAACAACAACTTCATCAAGATGGCTAAGGAAAAACTGGCCCAGAAG
ATGGAATCCAACAAGGAGAACAGGGAGGCCCACCTCGCCGCCATGTTGGAACGGCTGCAAGAGAAGGACAAGCACGCCGAGGAGGTGCGGAAAAACAAGGAGCTG
AAGGAAGAGGCCTCCAGGTAA
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ATGACCCTTGCTGCCTACAAAGAGAAGATGAAGGAGCTCCCGCTGGTGTCCTTGTTCTGCTCCTGCTTCCTGGCCGATCCCCTGAATAAGTCGTCCTACAAATAT
GAAGGCTGGTGTGGGAGACAGTGTAGGAGGAAGGATGAAAGCCAGCGGAAAGACAGTGCTGACTGGAGAGAAAGAAGAGCTCAGGCAGACACGGTGGACCTGAAT
TGGTGCGTCATTTCCGACATGGAAGTCATCGAGCTGAACAAATGCACCTCGGGCCAATCCTTTGAAGTCATCCTGAAGCCACCCTCCTTTGATGGGGTTCCCGAG
TTCAACGCCTCCCTGCCAAGGCGGCGAGACCCATCCCTGGAAGAGATCCAGAAGAAACTAGAAGCGGCTGAGGAGCGAAGGAAGTACCAGGAAGCGGAGCTCCTG
AAACACCTAGCAGAGAAACGGGAACATGAGAGAGAGGTGATCCAAAAGGCCATTGAGGAAAACAACAACTTCATCAAGATGGCTAAGGAAAAACTGGCCCAGAAG
ATGGAATCCAACAAGGAGAACAGGGAGGCCCACCTCGCCGCCATGTTGGAACGGCTGCAAGAGAAGGACAAGCACGCCGAGGAGGTGCGGAAAAACAAGGAGCTG
AAGGAAGAGGCCTCCAGGTAA
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>STMN4|81551|protein
MTLAAYKEKMKELPLVSLFCSCFLADPLNKSSYKYEGWCGRQCRRKDESQRKDSADWRERRAQADTVDLNWCVISDMEVIELNKCTSGQSFEVILKPPSFDGVPE
FNASLPRRRDPSLEEIQKKLEAAEERRKYQEAELLKHLAEKREHEREVIQKAIEENNNFIKMAKEKLAQKMESNKENREAHLAAMLERLQEKDKHAEEVRKNKEL
KEEASR
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MTLAAYKEKMKELPLVSLFCSCFLADPLNKSSYKYEGWCGRQCRRKDESQRKDSADWRERRAQADTVDLNWCVISDMEVIELNKCTSGQSFEVILKPPSFDGVPE
FNASLPRRRDPSLEEIQKKLEAAEERRKYQEAELLKHLAEKREHEREVIQKAIEENNNFIKMAKEKLAQKMESNKENREAHLAAMLERLQEKDKHAEEVRKNKEL
KEEASR
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Evidence summary TopClick the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Score (No. of Studies) | No | 1 (1) | 1 (2) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 8 (5) |
Syndromic Autism Gene TopGenome-Wide Association Studies (By Ethnic Group) Top Family Based Association Studies: 1
| Reference | Stage | Platform | #Families | Affecteds | Result | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
||||||
| MIXED/OTHERS | |||||||||||
| Tao Y, 2016_2 | replication | Illumina HumanHap550 BeadChip | 2591 | 2588 (13.33%) |  |  | ASD | - from 1 to 108 years |
- - | ||
Case Control Based Association Studies: 0
| Reference | Stage | Platform | ASD Cases | Normal Controls | Result | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ | #Subjects (% Women) |
Age (range) |
|||||
| No Evidence. | ||||||||||||
CNV Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Papanikolaou, 2006 | - | FISH | | | autism | - | - | - | - | 1 | - | 1 |
| Berkel, 2010 | Canada | SNP microarray | | | ASD | - | - | - | - | 396 | 5023 | 5419 |
Linkage Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Lauritsen, 2006 | Faroe Islands | microsatellite-based genomic screen | | | autism | - | - | - | - | 12 | 44 | 56 |
Low Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies TopNGS de novo Mutation Studies Top| Reference | Case Number | Family Number | de novo Number | Title |
|---|---|---|---|---|
| De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
NGS Mosaic SNV Studies TopNGS Other Studies Top Low Scale Gene Studies TopContact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.