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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
Genomic
-
NG_012494.2 RefSeqGene
- Range
-
4782..533158
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001287242.2 → NP_001274171.1 rho GTPase-activating protein 6 isoform 6
Status: REVIEWED
- Description
- Transcript Variant: This variant (6) differs in the 5' UTR and CDS, and uses an alternate downstream translation start, compared to variant 1. The resulting protein (isoform 6) has a shorter N-terminus, compared to isoform 11.
- Source sequence(s)
-
AB208792, AC002366, BC035785, BC150635, HY018118
- UniProtKB/TrEMBL
-
A8KAL3
- Conserved Domains (1) summary
-
- cd04376
Location:222 → 428
- RhoGAP_ARHGAP6; RhoGAP_ARHGAP6: RhoGAP (GTPase-activator protein [GAP] for Rho-like small GTPases) domain of ArhGAP6-like proteins. ArhGAP6 shows GAP activity towards RhoA, but not towards Cdc42 and Rac1. ArhGAP6 is often deleted in microphthalmia with linear skin ...
-
NM_006125.3 → NP_006116.2 rho GTPase-activating protein 6 isoform 3
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) lacks the last two exons but has an alternate 3' segment at the 3' end, as compared to variant 1. The encoded isoform 3 has a distinct and shorter C-terminus, as compared to isoform 1.
- Source sequence(s)
-
AB208792, AC004554, AF012272
- Consensus CDS
-
CCDS14142.1
- UniProtKB/TrEMBL
-
Q59HG6
- Related
- ENSP00000370094.1, ENST00000380718.1
- Conserved Domains (2) summary
-
- cd04376
Location:402 → 608
- RhoGAP_ARHGAP6; RhoGAP_ARHGAP6: RhoGAP (GTPase-activator protein [GAP] for Rho-like small GTPases) domain of ArhGAP6-like proteins. ArhGAP6 shows GAP activity towards RhoA, but not towards Cdc42 and Rac1. ArhGAP6 is often deleted in microphthalmia with linear skin ...
- pfam17093
Location:67 → 137
- PBP_N; Penicillin-binding protein N-terminus
-
NM_013423.3 → NP_038267.1 rho GTPase-activating protein 6 isoform 4
See identical proteins and their annotated locations for NP_038267.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) has an alternate 5' exon and the translation starts with a downstream AUG codon, as compared to variant 1. The encoded isoform 4 has a shorter N-terminus, as compared to isoform 1.
- Source sequence(s)
-
AC002366, AC003657, AF177663
- Consensus CDS
-
CCDS14141.1
- UniProtKB/Swiss-Prot
-
O43182
- Related
- ENSP00000302312.6, ENST00000303025.10
- Conserved Domains (1) summary
-
- cd04376
Location:199 → 405
- RhoGAP_ARHGAP6; RhoGAP_ARHGAP6: RhoGAP (GTPase-activator protein [GAP] for Rho-like small GTPases) domain of ArhGAP6-like proteins. ArhGAP6 shows GAP activity towards RhoA, but not towards Cdc42 and Rac1. ArhGAP6 is often deleted in microphthalmia with linear skin ...
-
NM_013427.3 → NP_038286.2 rho GTPase-activating protein 6 isoform 1
See identical proteins and their annotated locations for NP_038286.2
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) encodes the longest isoform (1).
- Source sequence(s)
-
AC003657, AC004554, AF117067, AF177663
- Consensus CDS
-
CCDS14140.1
- UniProtKB/Swiss-Prot
- B2RWQ0, O43182, O43437, Q9P1B3, Q9UK81, Q9UK82
- UniProtKB/TrEMBL
-
A8KAL3
- Related
- ENSP00000338967.4, ENST00000337414.9
- Conserved Domains (2) summary
-
- cd04376
Location:402 → 608
- RhoGAP_ARHGAP6; RhoGAP_ARHGAP6: RhoGAP (GTPase-activator protein [GAP] for Rho-like small GTPases) domain of ArhGAP6-like proteins. ArhGAP6 shows GAP activity towards RhoA, but not towards Cdc42 and Rac1. ArhGAP6 is often deleted in microphthalmia with linear skin ...
- pfam17093
Location:67 → 121
- PBP_N; Penicillin-binding protein N-terminus
RNA
-
NR_109776.2 RNA Sequence
Status: REVIEWED
- Description
- Transcript Variant: This variant (7) contains an alternate 3' exon, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AB208792, AC004554, AF022212
- Related
-
ENST00000495242.5
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 GRCh38.p14 Primary Assembly
Genomic
-
NC_000023.11 Reference GRCh38.p14 Primary Assembly
- Range
-
11137544..11665920 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060947.1 Alternate T2T-CHM13v2.0
- Range
-
10720022..11248464 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
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_001174.3: Suppressed sequence
- Description
- NM_001174.3: This RefSeq was permanently suppressed because currently there is insufficient support for the protein, and it is a nonsense-mediated mRNA decay (NMD) candidate.
-
NM_013422.2: Suppressed sequence
- Description
- NM_013422.2: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.