ENST00000393600.8 FAM50A
Information
- Transcript ID
- ENST00000393600.8
- Genome
- hg38
- Position
- chrX:154,444,141-154,450,654
- Strand
- +
- CDS length
- 1,020
- Amino acid length
- 340
- Gene symbol
- FAM50A
- Gene type
- protein-coding
- Gene description
- family with sequence similarity 50 member A
- Gene Entrez Gene ID
- 9130
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
Exon
| Exon number | Start | Stop |
|---|---|---|
| 1 | 154,444,141 | 154,444,346 |
| 2 | 154,445,633 | 154,445,717 |
| 3 | 154,445,812 | 154,445,911 |
| 4 | 154,446,415 | 154,446,560 |
| 5 | 154,448,484 | 154,448,560 |
| 6 | 154,448,690 | 154,448,756 |
| 7 | 154,448,893 | 154,448,954 |
| 8 | 154,449,221 | 154,449,297 |
| 9 | 154,449,681 | 154,449,735 |
| 10 | 154,449,883 | 154,449,931 |
| 11 | 154,450,029 | 154,450,099 |
| 12 | 154,450,209 | 154,450,319 |
| 13 | 154,450,424 | 154,450,654 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 154,444,236 | 154,444,346 |
| 2 | CDS | 154,445,633 | 154,445,717 |
| 3 | CDS | 154,445,812 | 154,445,911 |
| 4 | CDS | 154,446,415 | 154,446,560 |
| 5 | CDS | 154,448,484 | 154,448,560 |
| 6 | CDS | 154,448,690 | 154,448,756 |
| 7 | CDS | 154,448,893 | 154,448,954 |
| 8 | CDS | 154,449,221 | 154,449,297 |
| 9 | CDS | 154,449,681 | 154,449,735 |
| 10 | CDS | 154,449,883 | 154,449,931 |
| 11 | CDS | 154,450,029 | 154,450,099 |
| 12 | CDS | 154,450,209 | 154,450,319 |
| 13 | CDS | 154,450,424 | 154,450,432 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chrX | 153,672,488 | 153,679,002 | Link |
CDS sequence
ATGGCTCAATACAAGGGCGCCGCGAGCGAGGCCGGCCGCGCCATGCACCTGATGAAGAAGCGGGAGAAGCAGCGCGAGCAGATGGAGCAGATGAAGCAGCGCATCGCGGAGGAGAACATCATGAAATCCAACATTGACAAGAAGTTCTCTGCGCACTACGACGCGGTGGAGGCAGAGCTCAAGTCCAGCACCGTGGGTCTCGTGACCCTGAATGACATGAAGGCCAAGCAGGAGGCTCTGGTGAAGGAGCGGGAGAAGCAGCTGGCCAAGAAGGAGCAGTCCAAGGAGCTGCAGATGAAGCTGGAGAAGCTTCGAGAGAAGGAGCGTAAGAAGGAAGCCAAGCGGAAGATCTCCAGCCTGTCCTTCACCCTGGAGGAGGAAGAAGAGGGAGGCGAGGAGGAAGAGGAGGCGGCCATGTATGAGGAGGAGATGGAAAGGGAAGAGATCACCACGAAGAAGAGAAAACTGGGGAAGAACCCAGACGTTGACACAAGCTTCTTGCCTGATCGAGACCGTGAGGAGGAGGAGAATCGGCTTCGGGAAGAGCTGCGGCAGGAGTGGGAAGCCAAGCAGGAGAAGATCAAGAGTGAGGAGATCGAGATCACCTTCAGCTACTGGGATGGCTCTGGGCACCGGCGGACAGTCAAGATGAGAAAGGGCAACACCATGCAGCAGTTCCTGCAGAAGGCGCTCGAGATCCTTCGGAAAGACTTCAGTGAGCTGAGGTCCGCAGGGGTGGAGCAGCTCATGTACATCAAGGAGGACTTGATCATCCCTCACCATCACAGCTTCTACGACTTCATCGTCACCAAGGCACGGGGGAAGAGTGGACCACTCTTCAACTTTGATGTTCATGACGATGTGCGGTTGCTCAGTGACGCCACTGTGGAGAAGGATGAGTCCCATGCAGGCAAGGTGGTGCTGAGGAGCTGGTACGAGAAGAACAAGCACATCTTTCCCGCCAGCCGCTGGGAACCCTACGACCCTGAAAAGAAGTGGGACAAGTACACGATCCGCTGA
Amino sequence
MAQYKGAASEAGRAMHLMKKREKQREQMEQMKQRIAEENIMKSNIDKKFSAHYDAVEAELKSSTVGLVTLNDMKAKQEALVKEREKQLAKKEQSKELQMKLEKLREKERKKEAKRKISSLSFTLEEEEEGGEEEEEAAMYEEEMEREEITTKKRKLGKNPDVDTSFLPDRDREEEENRLREELRQEWEAKQEKIKSEEIEITFSYWDGSGHRRTVKMRKGNTMQQFLQKALEILRKDFSELRSAGVEQLMYIKEDLIIPHHHSFYDFIVTKARGKSGPLFNFDVHDDVRLLSDATVEKDESHAGKVVLRSWYEKNKHIFPASRWEPYDPEKKWDKYTIR*