NAA35 (N-alpha-acetyltransferase 35, NatC auxiliary subunit) - Rat Genome Database

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Gene: NAA35 (N-alpha-acetyltransferase 35, NatC auxiliary subunit) Homo sapiens
Analyze
Symbol: NAA35
Name: N-alpha-acetyltransferase 35, NatC auxiliary subunit
RGD ID: 1347911
HGNC Page HGNC:24340
Description: Predicted to enable transferase activity. Involved in negative regulation of apoptotic process. Located in cytosol; nucleoplasm; and plasma membrane. Part of NatC complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: bA379P1.1; corneal wound healing-related protein; EGAP; embryonic growth-associated protein homolog; FLJ21613; FLJ22643; MAK10; MAK10 homolog, amino-acid N-acetyltransferase subunit; MAK10P; N(alpha)-acetyltransferase 35, NatC auxiliary subunit; protein MAK10 homolog; RP11-379P1.1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38985,941,146 - 86,025,462 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl985,941,146 - 86,025,462 (+)EnsemblGRCh38hg38GRCh38
GRCh37988,556,061 - 88,640,377 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36987,745,877 - 87,827,037 (+)NCBINCBI36Build 36hg18NCBI36
Build 34985,785,614 - 85,866,757NCBI
Celera959,127,997 - 59,209,159 (+)NCBICelera
Cytogenetic Map9q21.33NCBI
HuRef958,381,341 - 58,462,508 (+)NCBIHuRef
CHM1_1988,702,594 - 88,783,747 (+)NCBICHM1_1
T2T-CHM13v2.0998,091,659 - 98,175,989 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IDA,IEA,ISS,NAS)
cytosol  (IDA)
NatC complex  (IBA,IDA,IEA,IPI)
nucleoplasm  (IDA)
plasma membrane  (IDA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:8889548   PMID:10855038   PMID:12477932   PMID:14702039   PMID:16344560   PMID:18029348   PMID:19398576   PMID:19660095   PMID:21873635   PMID:24243830   PMID:25921289  
PMID:26186194   PMID:26344197   PMID:27376574   PMID:27432908   PMID:28514442   PMID:28561026   PMID:29180619   PMID:29467282   PMID:29507755   PMID:29778605   PMID:30575818   PMID:30745298  
PMID:31073040   PMID:31091453   PMID:31753913   PMID:32296183   PMID:32694731   PMID:33545068   PMID:33957083   PMID:33961781   PMID:34079125   PMID:35256949   PMID:35271311   PMID:35439318  
PMID:35831314   PMID:36215168   PMID:36949045   PMID:37827155   PMID:38496616  


Genomics

Comparative Map Data
NAA35
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38985,941,146 - 86,025,462 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl985,941,146 - 86,025,462 (+)EnsemblGRCh38hg38GRCh38
GRCh37988,556,061 - 88,640,377 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36987,745,877 - 87,827,037 (+)NCBINCBI36Build 36hg18NCBI36
Build 34985,785,614 - 85,866,757NCBI
Celera959,127,997 - 59,209,159 (+)NCBICelera
Cytogenetic Map9q21.33NCBI
HuRef958,381,341 - 58,462,508 (+)NCBIHuRef
CHM1_1988,702,594 - 88,783,747 (+)NCBICHM1_1
T2T-CHM13v2.0998,091,659 - 98,175,989 (+)NCBIT2T-CHM13v2.0
Naa35
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391359,733,147 - 59,782,612 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1359,733,073 - 59,783,736 (+)EnsemblGRCm39 Ensembl
GRCm381359,585,333 - 59,634,798 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1359,585,259 - 59,635,922 (+)EnsemblGRCm38mm10GRCm38
MGSCv371359,686,694 - 59,736,159 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361359,595,034 - 59,644,421 (+)NCBIMGSCv36mm8
Celera1360,641,585 - 60,690,974 (+)NCBICelera
Cytogenetic Map13B2NCBI
cM Map1331.87NCBI
Naa35
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8175,039,897 - 5,091,916 (-)NCBIGRCr8
mRatBN7.2175,034,360 - 5,086,456 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl175,034,356 - 5,086,386 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx175,053,684 - 5,105,792 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0176,595,718 - 6,647,848 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0175,050,124 - 5,102,227 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0175,411,479 - 5,463,898 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl175,411,506 - 5,463,898 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0177,636,147 - 7,688,566 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41710,940,980 - 10,992,992 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11710,940,980 - 10,992,992 (-)NCBI
Celera175,155,110 - 5,207,156 (-)NCBICelera
Cytogenetic Map17p14NCBI
Naa35
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554321,503,093 - 1,573,012 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554321,503,093 - 1,572,655 (-)NCBIChiLan1.0ChiLan1.0
NAA35
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21185,053,821 - 85,135,600 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1985,059,782 - 85,141,540 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0938,899,667 - 38,984,257 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1983,080,870 - 83,165,485 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl983,084,045 - 83,165,099 (-)Ensemblpanpan1.1panPan2
NAA35
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1173,654,258 - 73,762,268 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl173,655,869 - 73,762,054 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha174,417,076 - 74,524,846 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0173,962,498 - 74,070,030 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl173,963,771 - 74,069,748 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1173,769,789 - 73,878,883 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0173,537,783 - 73,645,488 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0174,242,728 - 74,350,451 (-)NCBIUU_Cfam_GSD_1.0
Naa35
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947120,278,375 - 120,370,609 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366801,367,278 - 1,459,704 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366801,367,487 - 1,459,704 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
NAA35
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1029,202,990 - 29,322,663 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11029,221,531 - 29,322,709 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21033,267,122 - 33,402,800 (-)NCBISscrofa10.2Sscrofa10.2susScr3
NAA35
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11296,617,122 - 96,704,164 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1296,617,969 - 96,702,687 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603884,971,536 - 85,058,976 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Naa35
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248099,415,902 - 9,480,243 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248099,415,071 - 9,481,515 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in NAA35
97 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
NM_024635.3(NAA35):c.406C>T (p.His136Tyr) single nucleotide variant Malignant melanoma [RCV000068727] Chr9:85962070 [GRCh38]
Chr9:88576985 [GRCh37]
Chr9:87766805 [NCBI36]
Chr9:9q21.33		 not provided
NM_024635.3(NAA35):c.1688C>A (p.Thr563Lys) single nucleotide variant Malignant melanoma [RCV000061967] Chr9:86016658 [GRCh38]
Chr9:88631573 [GRCh37]
Chr9:87821393 [NCBI36]
Chr9:9q21.33		 not provided
NM_024635.3(NAA35):c.1692G>A (p.Lys564=) single nucleotide variant Malignant melanoma [RCV000061968] Chr9:86016662 [GRCh38]
Chr9:88631577 [GRCh37]
Chr9:87821397 [NCBI36]
Chr9:9q21.33		 not provided
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 copy number gain See cases [RCV000136788] Chr9:68420430..106579493 [GRCh38]
Chr9:71130848..109341774 [GRCh37]
Chr9:70225166..108381595 [NCBI36]
Chr9:9q21.11-31.2		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3		 pathogenic
GRCh38/hg38 9q21.33(chr9:84861055-86784049)x1 copy number loss See cases [RCV000139131] Chr9:84861055..86784049 [GRCh38]
Chr9:87475970..89398964 [GRCh37]
Chr9:86665790..88588784 [NCBI36]
Chr9:9q21.33		 uncertain significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3 copy number gain See cases [RCV000139789] Chr9:69627642..111454304 [GRCh38]
Chr9:72242558..114216584 [GRCh37]
Chr9:71432378..113256405 [NCBI36]
Chr9:9q21.12-31.3		 pathogenic
GRCh38/hg38 9p24.3-q22.1(chr9:203861-88130444)x4 copy number gain See cases [RCV000141904] Chr9:203861..88130444 [GRCh38]
Chr9:203861..90745359 [GRCh37]
Chr9:193861..89935179 [NCBI36]
Chr9:9p24.3-q22.1		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain not specified [RCV003986800] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-22.1(chr9:70966262-90761254)x4 copy number gain See cases [RCV000512280] Chr9:70966262..90761254 [GRCh37]
Chr9:9q21.11-22.1		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.2-22.32(chr9:79520825-97201274) copy number gain not provided [RCV000767645] Chr9:79520825..97201274 [GRCh37]
Chr9:9q21.2-22.32		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.33(chr9:88622823-88951838)x3 copy number gain not provided [RCV001006242] Chr9:88622823..88951838 [GRCh37]
Chr9:9q21.33		 uncertain significance
NC_000009.11:g.12246100_101559378inv inversion Recurrent spontaneous abortion [RCV000999471] Chr9:12246100..101559378 [GRCh37]
Chr9:9p23-q22.33		 likely pathogenic
GRCh37/hg19 9q21.33(chr9:87881345-88749247) copy number gain not specified [RCV002052819] Chr9:87881345..88749247 [GRCh37]
Chr9:9q21.33		 uncertain significance
GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410) copy number gain not specified [RCV002053853] Chr9:71349994..122603410 [GRCh37]
Chr9:9q21.11-33.2		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 copy number gain See cases [RCV002292402] Chr9:203861..131603223 [GRCh37]
Chr9:9p24.3-q34.11		 pathogenic
GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311) copy number loss Distal tetrasomy 15q [RCV002280776] Chr9:19356861..119513311 [GRCh37]
Chr9:9p22.1-q33.1		 uncertain significance
NM_024635.4(NAA35):c.30C>G (p.Asp10Glu) single nucleotide variant not provided [RCV002730827] Chr9:85942189 [GRCh38]
Chr9:88557104 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1915-14C>T single nucleotide variant not provided [RCV002839288] Chr9:86018685 [GRCh38]
Chr9:88633600 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1914+9G>A single nucleotide variant not provided [RCV002690075] Chr9:86018404 [GRCh38]
Chr9:88633319 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.877+12A>G single nucleotide variant not provided [RCV002750191] Chr9:85978393 [GRCh38]
Chr9:88593308 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.1193C>G (p.Ser398Cys) single nucleotide variant not provided [RCV002842451] Chr9:86007434 [GRCh38]
Chr9:88622349 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.436A>G (p.Met146Val) single nucleotide variant Inborn genetic diseases [RCV003087684]|not provided [RCV003076051] Chr9:85962100 [GRCh38]
Chr9:88577015 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1569-11T>G single nucleotide variant not provided [RCV002750111] Chr9:86016528 [GRCh38]
Chr9:88631443 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.886A>G (p.Ile296Val) single nucleotide variant not provided [RCV002971677] Chr9:85996407 [GRCh38]
Chr9:88611322 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.4G>A (p.Val2Ile) single nucleotide variant not provided [RCV002974791] Chr9:85942163 [GRCh38]
Chr9:88557078 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1797C>T (p.Asp599=) single nucleotide variant not provided [RCV002947110] Chr9:86018278 [GRCh38]
Chr9:88633193 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.347T>G (p.Leu116Trp) single nucleotide variant not provided [RCV002904111] Chr9:85959866 [GRCh38]
Chr9:88574781 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1235A>G (p.Tyr412Cys) single nucleotide variant Inborn genetic diseases [RCV002757197] Chr9:86009876 [GRCh38]
Chr9:88624791 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.81A>C (p.Thr27=) single nucleotide variant not provided [RCV002912470] Chr9:85942240 [GRCh38]
Chr9:88557155 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1833T>G (p.Ser611Arg) single nucleotide variant Inborn genetic diseases [RCV002951413]|not provided [RCV003542464] Chr9:86018314 [GRCh38]
Chr9:88633229 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1569-20A>G single nucleotide variant not provided [RCV002886365] Chr9:86016519 [GRCh38]
Chr9:88631434 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1705+4C>T single nucleotide variant not provided [RCV002886232] Chr9:86016679 [GRCh38]
Chr9:88631594 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.124+3G>A single nucleotide variant not provided [RCV003077623] Chr9:85942286 [GRCh38]
Chr9:88557201 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.679-19T>A single nucleotide variant not provided [RCV003035522] Chr9:85977344 [GRCh38]
Chr9:88592259 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1789G>C (p.Asp597His) single nucleotide variant not provided [RCV002591827] Chr9:86018270 [GRCh38]
Chr9:88633185 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1957C>T (p.Pro653Ser) single nucleotide variant not provided [RCV002910070] Chr9:86018741 [GRCh38]
Chr9:88633656 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.1698A>G (p.Lys566=) single nucleotide variant not provided [RCV002760872] Chr9:86016668 [GRCh38]
Chr9:88631583 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.804A>G (p.Ala268=) single nucleotide variant not provided [RCV003080750] Chr9:85978308 [GRCh38]
Chr9:88593223 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1134T>A (p.Asp378Glu) single nucleotide variant Inborn genetic diseases [RCV002884621] Chr9:86007375 [GRCh38]
Chr9:88622290 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.856C>A (p.Gln286Lys) single nucleotide variant not provided [RCV002913573] Chr9:85978360 [GRCh38]
Chr9:88593275 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.1569-16T>A single nucleotide variant not provided [RCV002848342] Chr9:86016523 [GRCh38]
Chr9:88631438 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.724G>T (p.Val242Leu) single nucleotide variant not provided [RCV003037914] Chr9:85977408 [GRCh38]
Chr9:88592323 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.2091G>A (p.Leu697=) single nucleotide variant not provided [RCV002591893] Chr9:86020942 [GRCh38]
Chr9:88635857 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.802G>A (p.Ala268Thr) single nucleotide variant Inborn genetic diseases [RCV002910471] Chr9:85978306 [GRCh38]
Chr9:88593221 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1124T>C (p.Phe375Ser) single nucleotide variant not provided [RCV002625257] Chr9:86007365 [GRCh38]
Chr9:88622280 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.678+10C>T single nucleotide variant not provided [RCV002875873] Chr9:85976745 [GRCh38]
Chr9:88591660 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.818C>G (p.Ser273Cys) single nucleotide variant not provided [RCV002932204] Chr9:85978322 [GRCh38]
Chr9:88593237 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.124+13T>C single nucleotide variant not provided [RCV002740942] Chr9:85942296 [GRCh38]
Chr9:88557211 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.2118+15G>A single nucleotide variant not provided [RCV002740552] Chr9:86020984 [GRCh38]
Chr9:88635899 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.1621G>A (p.Asp541Asn) single nucleotide variant Inborn genetic diseases [RCV002763329] Chr9:86016591 [GRCh38]
Chr9:88631506 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.2119-15G>A single nucleotide variant not provided [RCV002741512] Chr9:86021886 [GRCh38]
Chr9:88636801 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.2045G>C (p.Arg682Thr) single nucleotide variant not provided [RCV002828251] Chr9:86020896 [GRCh38]
Chr9:88635811 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1021G>A (p.Glu341Lys) single nucleotide variant Inborn genetic diseases [RCV002916189] Chr9:85996542 [GRCh38]
Chr9:88611457 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.584-16T>C single nucleotide variant not provided [RCV002741286] Chr9:85975098 [GRCh38]
Chr9:88590013 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.465A>G (p.Lys155=) single nucleotide variant not provided [RCV002741425] Chr9:85962129 [GRCh38]
Chr9:88577044 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.185C>T (p.Ala62Val) single nucleotide variant not provided [RCV003023070] Chr9:85958498 [GRCh38]
Chr9:88573413 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.384A>G (p.Thr128=) single nucleotide variant not provided [RCV002628676] Chr9:85962048 [GRCh38]
Chr9:88576963 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1001A>G (p.Asp334Gly) single nucleotide variant not provided [RCV002967389] Chr9:85996522 [GRCh38]
Chr9:88611437 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1409C>T (p.Ala470Val) single nucleotide variant Inborn genetic diseases [RCV002878183] Chr9:86013738 [GRCh38]
Chr9:88628653 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1374C>T (p.Ala458=) single nucleotide variant not provided [RCV002922225] Chr9:86013129 [GRCh38]
Chr9:88628044 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.1057-11A>G single nucleotide variant not provided [RCV002746016] Chr9:86003574 [GRCh38]
Chr9:88618489 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.1815G>A (p.Pro605=) single nucleotide variant not provided [RCV002938064] Chr9:86018296 [GRCh38]
Chr9:88633211 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1706-19T>C single nucleotide variant not provided [RCV003027363] Chr9:86017479 [GRCh38]
Chr9:88632394 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.349-4A>G single nucleotide variant not provided [RCV002937768] Chr9:85962009 [GRCh38]
Chr9:88576924 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.976G>A (p.Val326Met) single nucleotide variant not provided [RCV002579381] Chr9:85996497 [GRCh38]
Chr9:88611412 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1807C>T (p.Arg603Cys) single nucleotide variant not provided [RCV002899934] Chr9:86018288 [GRCh38]
Chr9:88633203 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1611G>A (p.Leu537=) single nucleotide variant not provided [RCV002900145] Chr9:86016581 [GRCh38]
Chr9:88631496 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.349-8C>G single nucleotide variant not provided [RCV003047059] Chr9:85962005 [GRCh38]
Chr9:88576920 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1086A>C (p.Ser362=) single nucleotide variant not provided [RCV003089799] Chr9:86003614 [GRCh38]
Chr9:88618529 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.273+3A>G single nucleotide variant not provided [RCV002942177] Chr9:85958589 [GRCh38]
Chr9:88573504 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.516+10C>T single nucleotide variant not provided [RCV002633945] Chr9:85962190 [GRCh38]
Chr9:88577105 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1245C>G (p.His415Gln) single nucleotide variant Inborn genetic diseases [RCV003195332] Chr9:86009886 [GRCh38]
Chr9:88624801 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.733A>T (p.Thr245Ser) single nucleotide variant Inborn genetic diseases [RCV003347986] Chr9:85977417 [GRCh38]
Chr9:88592332 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.957A>C (p.Ile319=) single nucleotide variant not provided [RCV003874071] Chr9:85996478 [GRCh38]
Chr9:88611393 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.877+4A>G single nucleotide variant not provided [RCV003715104] Chr9:85978385 [GRCh38]
Chr9:88593300 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.2038-15A>G single nucleotide variant not provided [RCV003686870] Chr9:86020874 [GRCh38]
Chr9:88635789 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1798G>A (p.Gly600Ser) single nucleotide variant not provided [RCV003739103] Chr9:86018279 [GRCh38]
Chr9:88633194 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1984C>T (p.His662Tyr) single nucleotide variant not provided [RCV003545736] Chr9:86018768 [GRCh38]
Chr9:88633683 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1389+16C>T single nucleotide variant not provided [RCV003547486] Chr9:86013160 [GRCh38]
Chr9:88628075 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1575C>T (p.Leu525=) single nucleotide variant not provided [RCV003691642] Chr9:86016545 [GRCh38]
Chr9:88631460 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1914+7C>T single nucleotide variant not provided [RCV003695614] Chr9:86018402 [GRCh38]
Chr9:88633317 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1563A>T (p.Ile521=) single nucleotide variant not provided [RCV003693695] Chr9:86013892 [GRCh38]
Chr9:88628807 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1492C>T (p.Arg498Cys) single nucleotide variant not provided [RCV003714835] Chr9:86013821 [GRCh38]
Chr9:88628736 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1773+16_1773+17del deletion not provided [RCV003698510] Chr9:86017580..86017581 [GRCh38]
Chr9:88632495..88632496 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.842A>G (p.His281Arg) single nucleotide variant not provided [RCV003664540] Chr9:85978346 [GRCh38]
Chr9:88593261 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.877+12A>T single nucleotide variant not provided [RCV003698060] Chr9:85978393 [GRCh38]
Chr9:88593308 [GRCh37]
Chr9:9q21.33		 benign
NM_024635.4(NAA35):c.560G>T (p.Ser187Ile) single nucleotide variant not provided [RCV003659606] Chr9:85975010 [GRCh38]
Chr9:88589925 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.316A>G (p.Ile106Val) single nucleotide variant not provided [RCV003548337] Chr9:85959835 [GRCh38]
Chr9:88574750 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.516+11G>A single nucleotide variant not provided [RCV003698136] Chr9:85962191 [GRCh38]
Chr9:88577106 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1272T>C (p.Phe424=) single nucleotide variant not provided [RCV003673970] Chr9:86009913 [GRCh38]
Chr9:88624828 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.627+13T>C single nucleotide variant not provided [RCV003560665] Chr9:85975170 [GRCh38]
Chr9:88590085 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.403A>G (p.Ile135Val) single nucleotide variant not provided [RCV003700178] Chr9:85962067 [GRCh38]
Chr9:88576982 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1914+6C>T single nucleotide variant not provided [RCV003549739] Chr9:86018401 [GRCh38]
Chr9:88633316 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.349-8C>A single nucleotide variant not provided [RCV003553280] Chr9:85962005 [GRCh38]
Chr9:88576920 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1884C>T (p.Thr628=) single nucleotide variant not provided [RCV003733809] Chr9:86018365 [GRCh38]
Chr9:88633280 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.679-14dup duplication not provided [RCV003710595] Chr9:85977346..85977347 [GRCh38]
Chr9:88592261..88592262 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.225T>G (p.Ile75Met) single nucleotide variant not provided [RCV003736045] Chr9:85958538 [GRCh38]
Chr9:88573453 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.393G>A (p.Thr131=) single nucleotide variant not provided [RCV003705788] Chr9:85962057 [GRCh38]
Chr9:88576972 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.2026C>G (p.Pro676Ala) single nucleotide variant not provided [RCV003734147] Chr9:86018810 [GRCh38]
Chr9:88633725 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1915-9T>C single nucleotide variant not provided [RCV003720958] Chr9:86018690 [GRCh38]
Chr9:88633605 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.930A>G (p.Pro310=) single nucleotide variant not provided [RCV003720402] Chr9:85996451 [GRCh38]
Chr9:88611366 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1110G>A (p.Leu370=) single nucleotide variant not provided [RCV003722484] Chr9:86003638 [GRCh38]
Chr9:88618553 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.678+7G>T single nucleotide variant not provided [RCV003737779] Chr9:85976742 [GRCh38]
Chr9:88591657 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.880C>G (p.His294Asp) single nucleotide variant not provided [RCV003733965] Chr9:85996401 [GRCh38]
Chr9:88611316 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.231C>G (p.Asn77Lys) single nucleotide variant not provided [RCV003680396] Chr9:85958544 [GRCh38]
Chr9:88573459 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1890G>A (p.Pro630=) single nucleotide variant not provided [RCV003705277] Chr9:86018371 [GRCh38]
Chr9:88633286 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1389+7G>A single nucleotide variant not provided [RCV003728898] Chr9:86013151 [GRCh38]
Chr9:88628066 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1837C>G (p.Gln613Glu) single nucleotide variant not provided [RCV003707103] Chr9:86018318 [GRCh38]
Chr9:88633233 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.349-16T>C single nucleotide variant not provided [RCV003707049] Chr9:85961997 [GRCh38]
Chr9:88576912 [GRCh37]
Chr9:9q21.33		 likely benign
NM_024635.4(NAA35):c.1548C>T (p.His516=) single nucleotide variant not provided [RCV003705639] Chr9:86013877 [GRCh38]
Chr9:88628792 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1844G>A (p.Arg615Gln) single nucleotide variant not provided [RCV003567750] Chr9:86018325 [GRCh38]
Chr9:88633240 [GRCh37]
Chr9:9q21.33		 uncertain significance
NM_024635.4(NAA35):c.1494C>G (p.Arg498=) single nucleotide variant not provided [RCV003821370] Chr9:86013823 [GRCh38]
Chr9:88628738 [GRCh37]
Chr9:9q21.33		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:402
Count of miRNA genes:326
Interacting mature miRNAs:342
Transcripts:ENST00000361671, ENST00000376040, ENST00000416045
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
G63197  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,611,345 - 88,611,625UniSTSGRCh37
Build 36987,801,165 - 87,801,445RGDNCBI36
Celera959,183,288 - 59,183,568RGD
Cytogenetic Map9q21.33UniSTS
HuRef958,436,636 - 58,436,916UniSTS
D9S1649E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37988,596,822 - 88,596,898UniSTSGRCh37
Build 36987,786,642 - 87,786,718RGDNCBI36
Celera959,168,765 - 59,168,841RGD
Cytogenetic Map9q21.33UniSTS
HuRef958,422,112 - 58,422,188UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1771 1097 1270 209 876 91 3280 1115 1488 247 1384 1437 131 693 2099 4
Low 668 1852 456 415 1038 374 1076 1077 2246 171 76 176 44 1 511 689 2 2
Below cutoff 42 37 5 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001321881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001321882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_024635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005252127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518903 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011518904 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017015012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024447649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047423710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363505 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054363506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AK025266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK026296 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL161447 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL161453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL353743 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC117429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA945233 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB023442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000361671   ⟹   ENSP00000354972
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl985,941,146 - 86,025,462 (+)Ensembl
RefSeq Acc Id: ENST00000376040   ⟹   ENSP00000365208
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl985,941,529 - 85,987,041 (+)Ensembl
RefSeq Acc Id: ENST00000416045
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl985,941,182 - 85,966,672 (+)Ensembl
RefSeq Acc Id: NM_001321881   ⟹   NP_001308810
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,941,146 - 86,025,462 (+)NCBI
CHM1_1988,702,594 - 88,783,743 (+)NCBI
T2T-CHM13v2.0998,091,673 - 98,175,989 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001321882   ⟹   NP_001308811
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,941,604 - 86,025,462 (+)NCBI
CHM1_1988,702,981 - 88,786,907 (+)NCBI
T2T-CHM13v2.0998,092,131 - 98,175,989 (+)NCBI
Sequence:
RefSeq Acc Id: NM_024635   ⟹   NP_078911
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,941,146 - 86,025,462 (+)NCBI
GRCh37988,556,009 - 88,638,350 (+)NCBI
Build 36987,745,877 - 87,827,037 (+)NCBI Archive
Celera959,127,997 - 59,209,159 (+)RGD
HuRef958,381,341 - 58,462,508 (+)RGD
CHM1_1988,702,594 - 88,783,747 (+)NCBI
T2T-CHM13v2.0998,091,673 - 98,175,989 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005252127   ⟹   XP_005252184
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,941,146 - 86,025,462 (+)NCBI
GRCh37988,556,009 - 88,638,350 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024447648   ⟹   XP_024303416
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,976,685 - 86,025,462 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024447649   ⟹   XP_024303417
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,977,363 - 86,025,462 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047423710   ⟹   XP_047279666
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,966,596 - 86,025,462 (+)NCBI
RefSeq Acc Id: XM_054363503   ⟹   XP_054219478
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0998,091,659 - 98,175,989 (+)NCBI
RefSeq Acc Id: XM_054363504   ⟹   XP_054219479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0998,117,124 - 98,175,989 (+)NCBI
RefSeq Acc Id: XM_054363505   ⟹   XP_054219480
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0998,127,212 - 98,175,989 (+)NCBI
RefSeq Acc Id: XM_054363506   ⟹   XP_054219481
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0998,127,890 - 98,175,989 (+)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_078911   ⟸   NM_024635
- UniProtKB: Q9H631 (UniProtKB/Swiss-Prot),   Q5VZE6 (UniProtKB/Swiss-Prot),   Q9H703 (UniProtKB/Swiss-Prot),   Q5VZE5 (UniProtKB/Swiss-Prot),   A8K874 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005252184   ⟸   XM_005252127
- Peptide Label: isoform X1
- UniProtKB: Q9H631 (UniProtKB/Swiss-Prot),   Q5VZE6 (UniProtKB/Swiss-Prot),   Q9H703 (UniProtKB/Swiss-Prot),   Q5VZE5 (UniProtKB/Swiss-Prot),   A8K874 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308810   ⟸   NM_001321881
- UniProtKB: Q9H631 (UniProtKB/Swiss-Prot),   Q5VZE6 (UniProtKB/Swiss-Prot),   Q9H703 (UniProtKB/Swiss-Prot),   Q5VZE5 (UniProtKB/Swiss-Prot),   A8K874 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001308811   ⟸   NM_001321882
- UniProtKB: Q9H631 (UniProtKB/Swiss-Prot),   Q5VZE6 (UniProtKB/Swiss-Prot),   Q9H703 (UniProtKB/Swiss-Prot),   Q5VZE5 (UniProtKB/Swiss-Prot),   A8K874 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024303416   ⟸   XM_024447648
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_024303417   ⟸   XM_024447649
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: ENSP00000354972   ⟸   ENST00000361671
RefSeq Acc Id: ENSP00000365208   ⟸   ENST00000376040
RefSeq Acc Id: XP_047279666   ⟸   XM_047423710
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054219478   ⟸   XM_054363503
- Peptide Label: isoform X1
- UniProtKB: Q9H631 (UniProtKB/Swiss-Prot),   Q5VZE6 (UniProtKB/Swiss-Prot),   Q5VZE5 (UniProtKB/Swiss-Prot),   Q9H703 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054219479   ⟸   XM_054363504
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054219480   ⟸   XM_054363505
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054219481   ⟸   XM_054363506
- Peptide Label: isoform X4

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5VZE5-F1-model_v2 AlphaFold Q5VZE5 1-725 view protein structure

Promoters
RGD ID:7215381
Promoter ID:EPDNEW_H13430
Type:initiation region
Name:NAA35_1
Description:N-acetyltransferase 35, NatC auxiliary subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13429  EPDNEW_H13431  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,941,146 - 85,941,206EPDNEW
RGD ID:7215369
Promoter ID:EPDNEW_H13431
Type:initiation region
Name:NAA35_2
Description:N-acetyltransferase 35, NatC auxiliary subunit
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H13429  EPDNEW_H13430  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38985,941,289 - 85,941,349EPDNEW
RGD ID:6807874
Promoter ID:HG_KWN:63878
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000376040,   NM_024635,   OTTHUMT00000052908,   UC004AOJ.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36987,745,496 - 87,746,417 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:24340 AgrOrtholog
COSMIC NAA35 COSMIC
Ensembl Genes ENSG00000135040 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000361671 ENTREZGENE
  ENST00000361671.10 UniProtKB/Swiss-Prot
  ENST00000376040.2 UniProtKB/Swiss-Prot
GTEx ENSG00000135040 GTEx
HGNC ID HGNC:24340 ENTREZGENE
Human Proteome Map NAA35 Human Proteome Map
InterPro Naa35/Mak10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:60560 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 60560 ENTREZGENE
OMIM 619438 OMIM
PANTHER N-ALPHA-ACETYLTRANSFERASE 35, NATC AUXILIARY SUBUNIT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR21373 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Mak10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA165585932 PharmGKB
UniProt A8K874 ENTREZGENE, UniProtKB/TrEMBL
  NAA35_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q5VZE6 ENTREZGENE
  Q9H631 ENTREZGENE
  Q9H703 ENTREZGENE
UniProt Secondary Q5VZE6 UniProtKB/Swiss-Prot
  Q9H631 UniProtKB/Swiss-Prot
  Q9H703 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-12-03 NAA35  N-alpha-acetyltransferase 35, NatC auxiliary subunit  NAA35  N(alpha)-acetyltransferase 35, NatC auxiliary subunit  Symbol and/or name change 5135510 APPROVED
2011-07-27 NAA35  N(alpha)-acetyltransferase 35, NatC auxiliary subunit  MAK10  MAK10 homolog, amino-acid N-acetyltransferase subunit (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED