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RMND5B (Required For Meiotic Nuclear Division 5 Homolog B) is a Protein Coding gene. Diseases associated with RMND5B include Dyskeratosis Congenita, Autosomal Recessive 2 and Dyskeratosis Congenita, Autosomal Recessive 1. An important paralog of this gene is RMND5A.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0004842 | contributes_to ubiquitin-protein transferase activity | IBA | 21873635 |
GO:0005515 | protein binding | IEA | -- |
GO:0016740 | transferase activity | IEA | -- |
GO:0046872 | metal ion binding | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IBA | 21873635 |
GO:0005737 | cytoplasm | IBA | 21873635 |
GO:0005829 | cytosol | IDA,IEA | 25793641 |
GO:0034657 | GID complex | IBA | 21873635 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006511 | ubiquitin-dependent protein catabolic process | IBA | 21873635 |
GO:0016567 | protein ubiquitination | IEA | -- |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | IBA | 21873635 |
ExUns: | 1 | ^ | 2 | ^ | 3a | · | 3b | ^ | 4 | ^ | 5a | · | 5b | · | 5c | ^ | 6a | · | 6b | ^ | 7a | · | 7b | · | 7c | ^ | 8a | · | 8b | ^ | 9 | ^ | 10a | · | 10b | · | 10c | ^ | 11a | · | 11b | ^ | 12 | ^ | 13 | ^ | 14a | · | 14b | · | 14c | · |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | - | - | - | - | - | - | |||||||||||||||||||||||||||||||||||||||||||||
SP2: | - | - | - | - | - | - | - | |||||||||||||||||||||||||||||||||||||||||||||
SP3: | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||||
SP4: | - | - | - | - | - | - | - | |||||||||||||||||||||||||||||||||||||||||||||
SP5: | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||||
SP6: | - | - | - | - | - | |||||||||||||||||||||||||||||||||||||||||||||||
SP7: | - | - | - | - | - | - | ||||||||||||||||||||||||||||||||||||||||||||||
SP8: | - | - | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||
SP9: | - | - | - | - | ||||||||||||||||||||||||||||||||||||||||||||||||
SP10: | - | |||||||||||||||||||||||||||||||||||||||||||||||||||
SP11: | ||||||||||||||||||||||||||||||||||||||||||||||||||||
SP12: | - |
ExUns: | 14d |
---|---|
SP1: | |
SP2: | |
SP3: | |
SP4: | |
SP5: | |
SP6: | |
SP7: | |
SP8: | |
SP9: | |
SP10: | |
SP11: | |
SP12: |
This gene was present in the common ancestor of animals and fungi.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
chimpanzee (Pan troglodytes) |
Mammalia | RMND5B 33 32 |
|
OneToOne | |
dog (Canis familiaris) |
Mammalia | RMND5B 33 32 |
|
OneToOne | |
cow (Bos Taurus) |
Mammalia | RMND5B 33 32 |
|
OneToOne | |
mouse (Mus musculus) |
Mammalia | Rmnd5b 17 33 32 |
|
||
rat (Rattus norvegicus) |
Mammalia | Rmnd5b 32 |
|
||
platypus (Ornithorhynchus anatinus) |
Mammalia | RMND5B 33 |
|
OneToOne | |
lizard (Anolis carolinensis) |
Reptilia | RMND5B 33 |
|
OneToOne | |
zebrafish (Danio rerio) |
Actinopterygii | rmnd5b 33 32 |
|
OneToOne | |
zgc73277 32 |
|
||||
fruit fly (Drosophila melanogaster) |
Insecta | CG3295 33 |
|
OneToMany | |
worm (Caenorhabditis elegans) |
Secernentea | T07D1.2 33 32 |
|
OneToMany | |
baker's yeast (Saccharomyces cerevisiae) |
Saccharomycetes | RMD5 33 |
|
OneToMany | |
sea squirt (Ciona savignyi) |
Ascidiacea | CSA.7116 33 |
|
OneToMany |
SNP ID | Clin | Chr 05 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
rs115334254 | benign, likely-benign, Dyskeratosis congenita, Dyskeratosis Congenita, Recessive | 178,149,824(+) | G/A | 3_prime_UTR_variant, genic_downstream_transcript_variant | |
rs121908089 | pathogenic, Dyskeratosis congenita, autosomal recessive 2, Dyskeratosis congenita autosomal recessive 1 | 178,149,760(+) | A/G | 3_prime_UTR_variant, genic_downstream_transcript_variant | |
rs121908090 | pathogenic, Dyskeratosis congenita, autosomal recessive 2, Dyskeratosis congenita autosomal recessive 1 | 178,149,799(+) | C/T | 3_prime_UTR_variant, genic_downstream_transcript_variant | |
rs121908091 | pathogenic, Dyskeratosis congenita, autosomal recessive 2, Dyskeratosis congenita autosomal recessive 1 | 178,149,715(+) | A/T | 3_prime_UTR_variant, genic_downstream_transcript_variant | |
rs139588879 | benign, likely-benign, Dyskeratosis congenita, not specified | 178,149,823(+) | C/T | 3_prime_UTR_variant, genic_downstream_transcript_variant |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv5844n100 | CNV | gain | 25217958 |
esv3352132 | CNV | duplication | 20981092 |
esv3607706 | CNV | loss | 21293372 |
nsv1019404 | CNV | gain | 25217958 |
nsv1120062 | OTHER | inversion | 24896259 |
nsv462567 | CNV | loss | 19166990 |
nsv471058 | CNV | loss | 18288195 |
nsv600392 | CNV | loss | 21841781 |
nsv600394 | CNV | loss | 21841781 |
Disorder | Aliases | PubMed IDs |
---|---|---|
dyskeratosis congenita, autosomal recessive 2 |
|
|
dyskeratosis congenita, autosomal recessive 1 |
|
|
dyskeratosis congenita autosomal recessive |
|
|
dyskeratosis congenita |
|
|