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The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCr8
Genomic
-
NC_086030.1 Reference GRCr8
- Range
-
6192958..6300997
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_063271243.1 → XP_063127313.1 rho guanine nucleotide exchange factor 18 isoform X1
- UniProtKB/TrEMBL
-
A0A8I5ZLL3
- Related
- ENSRNOP00000062255.3, ENSRNOT00000066281.4
-
XM_063271244.1 → XP_063127314.1 rho guanine nucleotide exchange factor 18 isoform X2
- UniProtKB/TrEMBL
-
A0A8I5ZLL3
- Related
- ENSRNOP00000099512.1, ENSRNOT00000148939.1
-
XM_063271245.1 → XP_063127315.1 rho guanine nucleotide exchange factor 18 isoform X3
-
XM_039089307.2 → XP_038945235.1 rho guanine nucleotide exchange factor 18 isoform X3
- UniProtKB/TrEMBL
-
A0A8I5ZLL3
- Conserved Domains (4) summary
-
- cd00160
Location:102 → 296
- RhoGEF; Guanine nucleotide exchange factor for Rho/Rac/Cdc42-like GTPases; Also called Dbl-homologous (DH) domain. It appears that PH domains invariably occur C-terminal to RhoGEF/DH domains.
- cd15794
Location:336 → 454
- PH_ARHGEF18; Rho guanine nucleotide exchange factor 18 Pleckstrin homology (PH) domain
- pfam17380
Location:661 → 784
- DUF5401; Family of unknown function (DUF5401)
- cl28929
Location:741 → 956
- VirB10_like; VirB10 and similar proteins form part of core complex in Type IV secretion system (T4SS)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NM_001107115.1: Suppressed sequence
- Description
- NM_001107115.1: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.