ENST00000531114.5 NHERF4
Information
- Transcript ID
- ENST00000531114.5
- Genome
- hg19
- Position
- chr11:119,056,184-119,060,932
- Strand
- +
- CDS length
- 1,716
- Amino acid length
- 572
- Gene symbol
- NHERF4
- Gene type
- protein-coding
- Gene description
- NHERF family PDZ scaffold protein 4
- Gene Entrez Gene ID
- 79849
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 |
---|---|---|
1 | 119,056,184 | 119,056,661 |
2 | 119,056,801 | 119,057,399 |
3 | 119,057,979 | 119,058,168 |
4 | 119,058,273 | 119,058,409 |
5 | 119,058,649 | 119,058,853 |
6 | 119,059,064 | 119,059,260 |
7 | 119,059,349 | 119,059,576 |
8 | 119,059,714 | 119,059,914 |
9 | 119,060,172 | 119,060,932 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
2 | CDS | 119,056,872 | 119,057,399 |
3 | CDS | 119,057,979 | 119,058,168 |
4 | CDS | 119,058,273 | 119,058,409 |
5 | CDS | 119,058,649 | 119,058,853 |
6 | CDS | 119,059,064 | 119,059,260 |
7 | CDS | 119,059,349 | 119,059,576 |
8 | CDS | 119,059,714 | 119,059,914 |
9 | CDS | 119,060,172 | 119,060,201 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr11 | 119,185,475 | 119,190,223 | Link |
CDS sequence
ATGGTAACTCCCTCACCCCCTGGCAACCATTCCCTATCCCTGGAGGCACCACGGCTCCACACGGCCTCCGATCTCCTTGGTAACCACTCACTCGGTCTCCCTCTGATAACAGCCTTGGTTGGGAGTAGAGATAGGAGGGGCCGGGTGTTTTCTCCTGTCCCAGTCCCTCTGCCCACGAACCCCACCACCCAACACCCAACCAGGCAGAAACTGCCCAGCACCCTATCAGGACACAGGGTCTGCCAGGCACACGGCGAACCTGTACTTGGGCTGTGCCCTCTCCTCCCCCTTTTCTGCTGCCCACCTCACCCTCCAGATCCCTGGAGCCTGGAGCGGCCTCGCTTCTGTTTACTGAGCAAAGAGGAGGGCAAGAGTTTTGGCTTCCACCTGCAGCAGGAGCTGGGCAGGGCTGGGCATGTGGTGTGCAGGGTGGACCCAGGCACCTCTGCCCAGCGCCAGGGTCTTCAGGAAGGAGACAGGATCCTGGCGGTGAACAATGATGTTGTGGAACACGAAGACTATGCGGTGGTGGTACGCCGCATCCGGGCCAGCAGCCCTCGGGTGTTGCTGACAGTATTGGCACGGCATGCACATGACGTGGCCCGAGCTCAGCTGGGAGAAGATGCCCACCTCTGTCCCACCCTAGGCCCAGGGGTCCGGCCCCGGCTGTGCCACATAGTGAAAGATGAGGGTGGTTTTGGCTTCAGTGTCACCCATGGCAATCAGGGTCCTTTCTGGTTGGTGCTAAGTACTGGAGGAGCAGCTGAGCGGGCAGGGGTGCCCCCCGGGGCCCGGCTGCTGGAAGTGAATGGGGTCAGTGTGGAGAAGTTCACTCACAACCAACTCACCAGGAAGCTTTGGCAGAGTGGACAGCAGGTGACCTTGCTGGTGGCAGGGCCAGAGGTGGAAGAACAGTGTCGCCAGCTGGGATTGCCCCTGGCTGCACCCCTGGCAGAGGGCTGGGCACTGCCCACCAAGCCCCGCTGCCTGCACCTGGAGAAAGGGCCCCAGGGTTTTGGGTTCCTGCTCCGGGAGGAAAAGGGCCTTGACGGTCGCCCTGGACAGTTCCTGTGGGAGGTGGACCCGGGACTGCCAGCCAAGAAGGCTGGGATGCAGGCTGGGGACCGGCTGGTGGCTGTGGCTGGGGAGAGCGTGGAGGGGCTGGGCCATGAGGAGACAGTGTCCAGGATCCAGGGGCAGGGCTCCTGTGTCTCCCTCACTGTCGTCGACCCTGAGGCGGACCGCTTCTTCAGCATGGTTCGCCTGTCCCCACTCCTCTTCTTGGAGAACACAGAGGCTCCCGCCTCGCCCCGGGGCAGCAGCTCAGCCTCACTGGTTGAGACAGAGGACCCTTCACTTGAAGACACAAGCGTGCCTTCTGTCCCTCTTGGCTCCCGACAGTGCTTCCTGTACCCTGGGCCTGGTGGCAGCTATGGCTTCCGACTCAGTTGTGTGGCCAGTGGGCCTCGTCTCTTCATCTCCCAGGTGACTCCAGGAGGCTCAGCTGCCCGGGCTGGGCTGCAAGTGGGAGACGTGATTCTGGAAGTGAACGGGTATCCTGTTGGGGGACAGAATGACCTGGAGAGGCTTCAGCAGCTGCCTGAGGCTGAGCCACCCCTCTGCCTGAAGCTGGCAGCCAGGTCTCTGCGGGGCTTGGAAGCCTGGATTCCCCCTGGGGCTGCAGAGGACTGGGCTCTGGCCTCGGATCTACTGTAG
Amino sequence
MVTPSPPGNHSLSLEAPRLHTASDLLGNHSLGLPLITALVGSRDRRGRVFSPVPVPLPTNPTTQHPTRQKLPSTLSGHRVCQAHGEPVLGLCPLLPLFCCPPHPPDPWSLERPRFCLLSKEEGKSFGFHLQQELGRAGHVVCRVDPGTSAQRQGLQEGDRILAVNNDVVEHEDYAVVVRRIRASSPRVLLTVLARHAHDVARAQLGEDAHLCPTLGPGVRPRLCHIVKDEGGFGFSVTHGNQGPFWLVLSTGGAAERAGVPPGARLLEVNGVSVEKFTHNQLTRKLWQSGQQVTLLVAGPEVEEQCRQLGLPLAAPLAEGWALPTKPRCLHLEKGPQGFGFLLREEKGLDGRPGQFLWEVDPGLPAKKAGMQAGDRLVAVAGESVEGLGHEETVSRIQGQGSCVSLTVVDPEADRFFSMVRLSPLLFLENTEAPASPRGSSSASLVETEDPSLEDTSVPSVPLGSRQCFLYPGPGGSYGFRLSCVASGPRLFISQVTPGGSAARAGLQVGDVILEVNGYPVGGQNDLERLQQLPEAEPPLCLKLAARSLRGLEAWIPPGAAEDWALASDLL*