ENST00000604395.5 NXF2B
Information
- Transcript ID
- ENST00000604395.5
- Genome
- hg19
- Position
- chrX:101,615,317-101,635,014
- Strand
- -
- CDS length
- 1,881
- Amino acid length
- 627
- Gene symbol
- NXF2B
- Gene type
- protein-coding
- Gene description
- nuclear RNA export factor 2B
- Gene Entrez Gene ID
- 728343
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
---|---|---|
21 | 101,615,317 | 101,615,566 |
20 | 101,615,713 | 101,615,773 |
19 | 101,618,184 | 101,618,366 |
18 | 101,618,901 | 101,618,973 |
17 | 101,619,574 | 101,619,616 |
16 | 101,619,712 | 101,619,827 |
15 | 101,619,966 | 101,620,024 |
14 | 101,620,145 | 101,620,252 |
13 | 101,620,384 | 101,620,439 |
12 | 101,620,526 | 101,620,594 |
11 | 101,620,975 | 101,621,011 |
10 | 101,622,690 | 101,622,799 |
9 | 101,622,979 | 101,623,086 |
8 | 101,623,207 | 101,623,295 |
7 | 101,623,452 | 101,623,521 |
6 | 101,623,708 | 101,623,788 |
5 | 101,623,904 | 101,624,008 |
4 | 101,624,120 | 101,624,203 |
3 | 101,624,507 | 101,624,657 |
2 | 101,624,884 | 101,625,073 |
1 | 101,634,915 | 101,635,014 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
21 | CDS | 101,615,522 | 101,615,566 |
20 | CDS | 101,615,713 | 101,615,773 |
19 | CDS | 101,618,184 | 101,618,366 |
18 | CDS | 101,618,901 | 101,618,973 |
17 | CDS | 101,619,574 | 101,619,616 |
16 | CDS | 101,619,712 | 101,619,827 |
15 | CDS | 101,619,966 | 101,620,024 |
14 | CDS | 101,620,145 | 101,620,252 |
13 | CDS | 101,620,384 | 101,620,439 |
12 | CDS | 101,620,526 | 101,620,594 |
11 | CDS | 101,620,975 | 101,621,011 |
10 | CDS | 101,622,690 | 101,622,799 |
9 | CDS | 101,622,979 | 101,623,086 |
8 | CDS | 101,623,207 | 101,623,295 |
7 | CDS | 101,623,452 | 101,623,521 |
6 | CDS | 101,623,708 | 101,623,788 |
5 | CDS | 101,623,904 | 101,624,008 |
4 | CDS | 101,624,120 | 101,624,203 |
3 | CDS | 101,624,507 | 101,624,657 |
2 | CDS | 101,624,884 | 101,625,073 |
1 | CDS | 101,634,915 | 101,634,957 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chrX | 102,360,396 | 102,380,093 | Link |
CDS sequence
ATGTGCTCTACTCTAAAGAAGTGTGGGACATACAGAACTGAAGTTGCAGAATGCCATGACCATGGTAGCACTTTTCAAGGAAGAAAGAAAGGTGGGAGTTCTTTCCGGGATAATTTTGACAAGAGGAGCTGTCATTATGAACATGGTGGGTATGAGCGCCCGCCTTCACACTGCCAGGAGAATGATGGAAGCGTGGAGATGAGGGATGTCCACAAGGACCAACAACTAAGACACACTCCTTATAGCATCCGATGCGAAAGAAGAATGAAATGGCATAGTGAAGACGAAATCCGTATTACCACGTGGAGAAATAGAAAACCTCCGGAGAGAAAAATGAGTCAGAACACACAGGATGGATACACAAGGAACTGGTTTAAGGTCACAATTCCTTACGGGATAAAGTATGACAAGGCATGGCTAATGAATTCAATCCAGAGCCATTGCAGTGACCGCTTCACTCCGGTTGATTTCCACTACGTCCGAAATCGGGCATGCTTCTTTGTCCAGGATGCTAGCGCTGCCTCCGCATTGAAGGATGTCAGTTATAAGATTTATGATGATGAGAACCAAAAGATATGTATATTTGTCAATCATTCTACTGCGCCCTACTCTGTGAAGAATAAGTTGAAGCCAGGCCAAATGGAGATGCTAAAGCTGACCATGAACAAACGGTACAATGTCTCCCAGCAAGCTCTTGATCTCCAGAATCTCCGCTTTGACCCAGACTTGATGGGCCGTGACATTGATATAATCCTGAATCGAAGAAACTGCATGGCTGCCACCCTGAAGATCATTGAAAGAAATTTCCCTGAGCTGTTGTCTTTGAACTTGTGCAACAACAAGCTGTACCAGCTGGATGGCCTTTCTGACATTACAGAGAAGGCTCCCAAAGTCAAGACCCTGAATCTCTCCAAAAATAAGCTGGAGTCGGCGTGGGAGTTGGGCAAGGTGAAAGGGCTGAAGCTCGAAGAGCTATGGCTAGAAGGGAACCCGTTGTGCAGCACCTTCTCGGACCAGTCCGCCTATGTAAGTGCCATCCGGGATTGTTTCCCCAAGTTGTTACGCCTGGACGGCCGAGAGTTATCCGCACCAGTGATTGTTGACATTGACAGCTCTGAGACAATGAAACCCTGCAAGGAAAACTTTACTGGATCTGAGACCCTAAAGCATTTAGTCCTGCAATTCCTGCAGCAGTATTACTCGATCTATGACTCTGGAGATCGACAGGGTCTCCTCGGTGCTTACCACGATGAGGCCTGCTTCTCCTTGGCTATTCCCTTCGACCCCAAGGACTCAGCCCCGAGCAGCTTGTGCAAGTACTTTGAGGATAGCAGGAATATGAAAACACTCAAGGACCCCTACCTGAAGGGGGAACTGCTGAGGCGCACAAAACGTGACATTGTGGACTCCCTCAGTGCGTTGCCCAAAACTCAGCATGACCTCAGCTCCATCCTGGTGGACGTGTGGTGCCAGACGGAAAGGATGCTCTGCTTTTCTGTCAATGGGGTTTTCAAGGAAGTGGAAGGACAGTCTCAGGGTTCTGTTCTCGCCTTCACCCGGACCTTCATTGCTACCCCTGGCAGCAGTTCCAGTCTGTGCATCGTGAATGACGAGCTGTTTGTGAGGGATGCCAGCCCCCAAGAGACTCAGAGTGCCTTCTCCATCCCAGTGTCCACACTCTCCTCCAGCTCTGAGCCCTCCCTCTCCCAGGAGCAGCAGGAAATGGTGCAGGCTTTCTCTGCCCAGTCTGGGATGAAACTGGAGTGGTCTCAGAAGTGCCTTCAGGACAATGAGTGGAACTACACTAGAGCTGGCCAGGCCTTCACTATGCTCCAGACCGAGGGCAAGATCCCCGCGGAGGCCTTCAAGCAAATCTCCTAA
Amino sequence
MCSTLKKCGTYRTEVAECHDHGSTFQGRKKGGSSFRDNFDKRSCHYEHGGYERPPSHCQENDGSVEMRDVHKDQQLRHTPYSIRCERRMKWHSEDEIRITTWRNRKPPERKMSQNTQDGYTRNWFKVTIPYGIKYDKAWLMNSIQSHCSDRFTPVDFHYVRNRACFFVQDASAASALKDVSYKIYDDENQKICIFVNHSTAPYSVKNKLKPGQMEMLKLTMNKRYNVSQQALDLQNLRFDPDLMGRDIDIILNRRNCMAATLKIIERNFPELLSLNLCNNKLYQLDGLSDITEKAPKVKTLNLSKNKLESAWELGKVKGLKLEELWLEGNPLCSTFSDQSAYVSAIRDCFPKLLRLDGRELSAPVIVDIDSSETMKPCKENFTGSETLKHLVLQFLQQYYSIYDSGDRQGLLGAYHDEACFSLAIPFDPKDSAPSSLCKYFEDSRNMKTLKDPYLKGELLRRTKRDIVDSLSALPKTQHDLSSILVDVWCQTERMLCFSVNGVFKEVEGQSQGSVLAFTRTFIATPGSSSSLCIVNDELFVRDASPQETQSAFSIPVSTLSSSSEPSLSQEQQEMVQAFSAQSGMKLEWSQKCLQDNEWNYTRAGQAFTMLQTEGKIPAEAFKQIS*