ENST00000604395.5 NXF2B
Information
- Transcript ID
- ENST00000604395.5
- Genome
- hg38
- Position
- chrX:102,360,396-102,380,093
- 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 | 102,360,396 | 102,360,645 |
20 | 102,360,792 | 102,360,852 |
19 | 102,363,263 | 102,363,445 |
18 | 102,363,980 | 102,364,052 |
17 | 102,364,653 | 102,364,695 |
16 | 102,364,791 | 102,364,906 |
15 | 102,365,045 | 102,365,103 |
14 | 102,365,224 | 102,365,331 |
13 | 102,365,463 | 102,365,518 |
12 | 102,365,605 | 102,365,673 |
11 | 102,366,054 | 102,366,090 |
10 | 102,367,769 | 102,367,878 |
9 | 102,368,058 | 102,368,165 |
8 | 102,368,286 | 102,368,374 |
7 | 102,368,531 | 102,368,600 |
6 | 102,368,787 | 102,368,867 |
5 | 102,368,983 | 102,369,087 |
4 | 102,369,199 | 102,369,282 |
3 | 102,369,586 | 102,369,736 |
2 | 102,369,963 | 102,370,152 |
1 | 102,379,994 | 102,380,093 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
21 | CDS | 102,360,601 | 102,360,645 |
20 | CDS | 102,360,792 | 102,360,852 |
19 | CDS | 102,363,263 | 102,363,445 |
18 | CDS | 102,363,980 | 102,364,052 |
17 | CDS | 102,364,653 | 102,364,695 |
16 | CDS | 102,364,791 | 102,364,906 |
15 | CDS | 102,365,045 | 102,365,103 |
14 | CDS | 102,365,224 | 102,365,331 |
13 | CDS | 102,365,463 | 102,365,518 |
12 | CDS | 102,365,605 | 102,365,673 |
11 | CDS | 102,366,054 | 102,366,090 |
10 | CDS | 102,367,769 | 102,367,878 |
9 | CDS | 102,368,058 | 102,368,165 |
8 | CDS | 102,368,286 | 102,368,374 |
7 | CDS | 102,368,531 | 102,368,600 |
6 | CDS | 102,368,787 | 102,368,867 |
5 | CDS | 102,368,983 | 102,369,087 |
4 | CDS | 102,369,199 | 102,369,282 |
3 | CDS | 102,369,586 | 102,369,736 |
2 | CDS | 102,369,963 | 102,370,152 |
1 | CDS | 102,379,994 | 102,380,036 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chrX | 101,615,317 | 101,635,014 | Link |
CDS sequence
ATGTGCTCTACTCTAAAGAAGTGTGGGACATACAGAACTGAAGTTGCAGAATGCCATGACCATGGTAGCACTTTTCAAGGAAGAAAGAAAGGTGGGAGTTCTTTCCGGGATAATTTTGACAAGAGGAGCTGTCATTATGAACATGGTGGGTATGAGCGCCCGCCTTCACACTGCCAGGAGAATGATGGAAGCGTGGAGATGAGGGATGTCCACAAGGACCAACAACTAAGACACACTCCTTATAGCATCCGATGCGAAAGAAGAATGAAATGGCATAGTGAAGACGAAATCCGTATTACCACGTGGAGAAATAGAAAACCTCCGGAGAGAAAAATGAGTCAGAACACACAGGATGGATACACAAGGAACTGGTTTAAGGTCACAATTCCTTACGGGATAAAGTATGACAAGGCATGGCTAATGAATTCAATCCAGAGCCATTGCAGTGACCGCTTCACTCCGGTTGATTTCCACTACGTCCGAAATCGGGCATGCTTCTTTGTCCAGGATGCTAGCGCTGCCTCCGCATTGAAGGATGTCAGTTATAAGATTTATGATGATGAGAACCAAAAGATATGTATATTTGTCAATCATTCTACTGCGCCCTACTCTGTGAAGAATAAGTTGAAGCCAGGCCAAATGGAGATGCTAAAGCTGACCATGAACAAACGGTACAATGTCTCCCAGCAAGCTCTTGATCTCCAGAATCTCCGCTTTGACCCAGACTTGATGGGCCGTGACATTGATATAATCCTGAATCGAAGAAACTGCATGGCTGCCACCCTGAAGATCATTGAAAGAAATTTCCCTGAGCTGTTGTCTTTGAACTTGTGCAACAACAAGCTGTACCAGCTGGATGGCCTTTCTGACATTACAGAGAAGGCTCCCAAAGTCAAGACCCTGAATCTCTCCAAAAATAAGCTGGAGTCGGCGTGGGAGTTGGGCAAGGTGAAAGGGCTGAAGCTCGAAGAGCTATGGCTAGAAGGGAACCCGTTGTGCAGCACCTTCTCGGACCAGTCCGCCTATGTAAGTGCCATCCGGGATTGTTTCCCCAAGTTGTTACGCCTGGACGGCCGAGAGTTATCCGCACCAGTGATTGTTGACATTGACAGCTCTGAGACAATGAAACCCTGCAAGGAAAACTTTACTGGATCTGAGACCCTAAAGCATTTAGTCCTGCAATTCCTGCAGCAGTATTACTCGATCTATGACTCTGGAGATCGACAGGGTCTCCTCGGTGCTTACCACGATGAGGCCTGCTTCTCCTTGGCTATTCCCTTCGACCCCAAGGACTCAGCCCCGAGCAGCTTGTGCAAGTACTTTGAGGATAGCAGGAATATGAAAACACTCAAGGACCCCTACCTGAAGGGGGAACTGCTGAGGCGCACAAAACGTGACATTGTGGACTCCCTCAGTGCGTTGCCCAAAACTCAGCATGACCTCAGCTCCATCCTGGTGGACGTGTGGTGCCAGACGGAAAGGATGCTCTGCTTTTCTGTCAATGGGGTTTTCAAGGAAGTGGAAGGACAGTCTCAGGGTTCTGTTCTCGCCTTCACCCGGACCTTCATTGCTACCCCTGGCAGCAGTTCCAGTCTGTGCATCGTGAATGACGAGCTGTTTGTGAGGGATGCCAGCCCCCAAGAGACTCAGAGTGCCTTCTCCATCCCAGTGTCCACACTCTCCTCCAGCTCTGAGCCCTCCCTCTCCCAGGAGCAGCAGGAAATGGTGCAGGCTTTCTCTGCCCAGTCTGGGATGAAACTGGAGTGGTCTCAGAAGTGCCTTCAGGACAATGAGTGGAACTACACTAGAGCTGGCCAGGCCTTCACTATGCTCCAGACCGAGGGCAAGATCCCCGCGGAGGCCTTCAAGCAAATCTCCTAA
Amino sequence
MCSTLKKCGTYRTEVAECHDHGSTFQGRKKGGSSFRDNFDKRSCHYEHGGYERPPSHCQENDGSVEMRDVHKDQQLRHTPYSIRCERRMKWHSEDEIRITTWRNRKPPERKMSQNTQDGYTRNWFKVTIPYGIKYDKAWLMNSIQSHCSDRFTPVDFHYVRNRACFFVQDASAASALKDVSYKIYDDENQKICIFVNHSTAPYSVKNKLKPGQMEMLKLTMNKRYNVSQQALDLQNLRFDPDLMGRDIDIILNRRNCMAATLKIIERNFPELLSLNLCNNKLYQLDGLSDITEKAPKVKTLNLSKNKLESAWELGKVKGLKLEELWLEGNPLCSTFSDQSAYVSAIRDCFPKLLRLDGRELSAPVIVDIDSSETMKPCKENFTGSETLKHLVLQFLQQYYSIYDSGDRQGLLGAYHDEACFSLAIPFDPKDSAPSSLCKYFEDSRNMKTLKDPYLKGELLRRTKRDIVDSLSALPKTQHDLSSILVDVWCQTERMLCFSVNGVFKEVEGQSQGSVLAFTRTFIATPGSSSSLCIVNDELFVRDASPQETQSAFSIPVSTLSSSSEPSLSQEQQEMVQAFSAQSGMKLEWSQKCLQDNEWNYTRAGQAFTMLQTEGKIPAEAFKQIS*