Evidence Details for SLC9A10


Gene Symbol: | SLC9A10 ( - ) |
---|---|
Gene Full Name: | solute carrier family 9, member 10 |
Band: | 3q13.2 |
Quick Links | Entrez ID:285335; OMIM: 612738; Uniprot ID:S9A10_HUMAN; ENSEMBL ID: ENSG00000172139; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |


>SLC9A10|285335|nucleotide
ATGGCTGGAATATTTAAGGAGTTTTTTTTCAGTACTGAGGACCTCCCTGAAGTCATTCTAACATTGTCTTTGATCAGCTCCATTGGAGCATTTTTGAACCGGCAC
TTGGAAGACTTTCCAATTCCTGTCCCTGTGATATTATTTTTACTTGGATGCAGTTTTGAAGTATTAAGCTTTACATCTTCACAGGTCCAAAGATACGCAAACGCC
ATACAATGGATGAGTCCAGACTTATTTTTTCGTATATTTACACCAGTAGTTTTCTTTACTACTGCATTTGACATGGATACGTACATGCTTCAAAAGTTATTTTGG
CAGATACTTTTAATTTCAATTCCCGGCTTTTTGGTTAATTATATCTTAGTTCTTTGGCATCTGGCATCTGTAAATCAATTACTTTTGAAGCCTACCCAATGGTTA
TTATTTTCAGCTATCCTTGTGAGTTCAGATCCCATGCTAACCGCAGCTGCTATAAGAGACCTTGGGCTTTCTAGAAGCCTCATCAGTTTAATTAATGGAGAAAGT
CTGATGACCTCTGTTATATCATTAATTACATTTACTAGTATTATGGATTTTGACCAAAGACTACAAAGTAAAAGAAACCATACCTTAGCTGAAGAGATCGTGGGT
GGAATTTGTTCATATATTATAGCAAGTTTCTTGTTTGGAATTCTAAGTTCAAAACTGATTCAATTTTGGATGTCAACTGTTTTTGGTGATGATGTCAATCATATA
AGTCTCATCTTTTCAATTCTGTATCTCATCTTTTATATTTGTGAGTTAGTTGGAATGTCAGGAATATTTACTCTGGCCATTGTGGGACTTCTTTTAAATTCTACA
AGTTTTAAAGCAGCAATTGAAGAAACACTTCTTCTTGAATTCTGGACTTTTCTATCACGTATTGCTTTTCTCATGGTGTTTACTTTCTTTGGACTTCTAATTCCT
GCACATACATATTTGTATATAGAATTTGTTGATATATACTATTCATTAAATATCTACTTAACATTGATTGTTTTAAGATTTCTGACCCTTCTTTTAATAAGCCCT
GTTTTGTCTCGAGTTGGTCATGAGTTCAGTTGGCGCTGGATATTCATAATGGTCTGTAGTGAAATGAAGGGGATGCCTAATATAAACATGGCCCTTCTGCTTGCC
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ATGGCTGGAATATTTAAGGAGTTTTTTTTCAGTACTGAGGACCTCCCTGAAGTCATTCTAACATTGTCTTTGATCAGCTCCATTGGAGCATTTTTGAACCGGCAC
TTGGAAGACTTTCCAATTCCTGTCCCTGTGATATTATTTTTACTTGGATGCAGTTTTGAAGTATTAAGCTTTACATCTTCACAGGTCCAAAGATACGCAAACGCC
ATACAATGGATGAGTCCAGACTTATTTTTTCGTATATTTACACCAGTAGTTTTCTTTACTACTGCATTTGACATGGATACGTACATGCTTCAAAAGTTATTTTGG
CAGATACTTTTAATTTCAATTCCCGGCTTTTTGGTTAATTATATCTTAGTTCTTTGGCATCTGGCATCTGTAAATCAATTACTTTTGAAGCCTACCCAATGGTTA
TTATTTTCAGCTATCCTTGTGAGTTCAGATCCCATGCTAACCGCAGCTGCTATAAGAGACCTTGGGCTTTCTAGAAGCCTCATCAGTTTAATTAATGGAGAAAGT
CTGATGACCTCTGTTATATCATTAATTACATTTACTAGTATTATGGATTTTGACCAAAGACTACAAAGTAAAAGAAACCATACCTTAGCTGAAGAGATCGTGGGT
GGAATTTGTTCATATATTATAGCAAGTTTCTTGTTTGGAATTCTAAGTTCAAAACTGATTCAATTTTGGATGTCAACTGTTTTTGGTGATGATGTCAATCATATA
AGTCTCATCTTTTCAATTCTGTATCTCATCTTTTATATTTGTGAGTTAGTTGGAATGTCAGGAATATTTACTCTGGCCATTGTGGGACTTCTTTTAAATTCTACA
AGTTTTAAAGCAGCAATTGAAGAAACACTTCTTCTTGAATTCTGGACTTTTCTATCACGTATTGCTTTTCTCATGGTGTTTACTTTCTTTGGACTTCTAATTCCT
GCACATACATATTTGTATATAGAATTTGTTGATATATACTATTCATTAAATATCTACTTAACATTGATTGTTTTAAGATTTCTGACCCTTCTTTTAATAAGCCCT
GTTTTGTCTCGAGTTGGTCATGAGTTCAGTTGGCGCTGGATATTCATAATGGTCTGTAGTGAAATGAAGGGGATGCCTAATATAAACATGGCCCTTCTGCTTGCC
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>SLC9A10|285335|protein
MAGIFKEFFFSTEDLPEVILTLSLISSIGAFLNRHLEDFPIPVPVILFLLGCSFEVLSFTSSQVQRYANAIQWMSPDLFFRIFTPVVFFTTAFDMDTYMLQKLFW
QILLISIPGFLVNYILVLWHLASVNQLLLKPTQWLLFSAILVSSDPMLTAAAIRDLGLSRSLISLINGESLMTSVISLITFTSIMDFDQRLQSKRNHTLAEEIVG
GICSYIIASFLFGILSSKLIQFWMSTVFGDDVNHISLIFSILYLIFYICELVGMSGIFTLAIVGLLLNSTSFKAAIEETLLLEFWTFLSRIAFLMVFTFFGLLIP
AHTYLYIEFVDIYYSLNIYLTLIVLRFLTLLLISPVLSRVGHEFSWRWIFIMVCSEMKGMPNINMALLLAYSDLYFGSDKEKSQILFHGVLVCLITLVVNRFILP
VAVTILGLRDATSTKYKSVCCTFQHFQELTKSAASALKFDKDLANADWNMIEKAITLENPYMLNEEETTEHQKVKCPHCNKEIDEIFNTEAMELANRRLLSAQIA
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MAGIFKEFFFSTEDLPEVILTLSLISSIGAFLNRHLEDFPIPVPVILFLLGCSFEVLSFTSSQVQRYANAIQWMSPDLFFRIFTPVVFFTTAFDMDTYMLQKLFW
QILLISIPGFLVNYILVLWHLASVNQLLLKPTQWLLFSAILVSSDPMLTAAAIRDLGLSRSLISLINGESLMTSVISLITFTSIMDFDQRLQSKRNHTLAEEIVG
GICSYIIASFLFGILSSKLIQFWMSTVFGDDVNHISLIFSILYLIFYICELVGMSGIFTLAIVGLLLNSTSFKAAIEETLLLEFWTFLSRIAFLMVFTFFGLLIP
AHTYLYIEFVDIYYSLNIYLTLIVLRFLTLLLISPVLSRVGHEFSWRWIFIMVCSEMKGMPNINMALLLAYSDLYFGSDKEKSQILFHGVLVCLITLVVNRFILP
VAVTILGLRDATSTKYKSVCCTFQHFQELTKSAASALKFDKDLANADWNMIEKAITLENPYMLNEEETTEHQKVKCPHCNKEIDEIFNTEAMELANRRLLSAQIA
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Click 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) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 6 (3) |




Family Based Association Studies: 1
Reference | Stage | Platform | #Families | Affecteds | Result | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|
#Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
||||||
CAUCASIAN | |||||||||||
Ma, 2009_1 | Discovery | Illumina's Human 1M v1 Beadchip | 438 | - (-) | ![]() | ![]() | ASD | - - |
- - |
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. |




Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Allen-Brady, 2008 | - | SNP-based genomic screen | ![]() | ![]() | ASD | 1 | - | 1 | - | 7 | 22 | 29 |






Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |






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