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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_086037.1 Reference GRCr8
- Range
-
41746732..41855924 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
XM_039097678.2 → XP_038953606.1 TBC1 domain family member 9 isoform X1
- UniProtKB/TrEMBL
-
A0A0G2K9K0
- Related
- ENSRNOP00000079826.2, ENSRNOT00000113408.2
- Conserved Domains (5) summary
-
- smart00164
Location:504 → 714
- TBC; Domain in Tre-2, BUB2p, and Cdc16p. Probable Rab-GAPs
- cd13354
Location:298 → 393
- PH-GRAM2_TCB1D9_TCB1D9B; TBC1 domain family members 9 and 9B (TBC1D9 and TBC1D9B) Pleckstrin Homology-Glucosyltransferases, Rab-like GTPase activators and Myotubularins (PH-GRAM) domain, repeat 2
- cd13351
Location:151 → 249
- PH-GRAM1_TCB1D9_TCB1D9B; TBC1 domain family members 9 and 9B (TBC1D9 and TBC1D9B) Pleckstrin Homology-Glucosyltransferases, Rab-like GTPase activators and Myotubularins (PH-GRAM) domain, repeat 1
- cl08302
Location:885 → 915
- EFh; EF-hand, calcium binding motif; A diverse superfamily of calcium sensors and calcium signal modulators; most examples in this alignment model have 2 active canonical EF hands. Ca2+ binding induces a conformational change in the EF-hand motif, leading to ...
- cl17169
Location:938 → 1002
- RRM_SF; RNA recognition motif (RRM) superfamily
-
XM_039097679.2 → XP_038953607.2 TBC1 domain family member 9 isoform X2
- UniProtKB/TrEMBL
-
A0A0G2K9K0
- Related
- ENSRNOP00000103191.1, ENSRNOT00000130407.1
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_001134539.2: Suppressed sequence
- Description
- NM_001134539.2: This RefSeq was removed because currently there is insufficient support for the transcript and the protein.