ACTR3C (actin related protein 3C) - Rat Genome Database

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Gene: ACTR3C (actin related protein 3C) Homo sapiens
Analyze
Symbol: ACTR3C
Name: actin related protein 3C
RGD ID: 2923209
HGNC Page HGNC:37282
Description: Predicted to enable ATP binding activity and actin binding activity. Predicted to contribute to actin filament binding activity. Located in extracellular exosome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: actin-related Arp11; actin-related protein 11; actin-related protein 3C; ARP11; ARP3 actin related protein 3 homolog C; ARP3 actin-related protein 3 homolog C; ARP3 actin-related protein 3 homolog C (yeast)
RGD Orthologs
Bonobo
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
GRCh387149,881,360 - 150,323,545 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7150,243,916 - 150,323,725 (-)Ensemblhg38GRCh38
GRCh377149,578,449 - 150,020,634 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367149,575,234 - 149,651,741 (-)NCBIBuild 36Build 36hg18NCBI36
Celera7147,954,920 - 147,965,656 (+)NCBICelera
Celera7144,543,643 - 144,577,847 (-)NCBICelera
Cytogenetic Map7q36.1NCBI
HuRef7143,760,344 - 143,837,262 (-)NCBIHuRef
CHM1_17149,951,119 - 150,027,600 (-)NCBICHM1_1
T2T-CHM13v2.07151,063,321 - 151,501,798 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27149,282,168 - 149,358,608 (-)NCBI
JBrowse:




Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8889548   PMID:11162478   PMID:14651955   PMID:16344560   PMID:21873635   PMID:23533145   PMID:26186194   PMID:27926873   PMID:28514442   PMID:28611215   PMID:33961781   PMID:34537242  
PMID:40593736  


Genomics

Comparative Map Data
ACTR3C
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh387149,881,360 - 150,323,545 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl7150,243,916 - 150,323,725 (-)Ensemblhg38GRCh38
GRCh377149,578,449 - 150,020,634 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 367149,575,234 - 149,651,741 (-)NCBIBuild 36Build 36hg18NCBI36
Celera7147,954,920 - 147,965,656 (+)NCBICelera
Celera7144,543,643 - 144,577,847 (-)NCBICelera
Cytogenetic Map7q36.1NCBI
HuRef7143,760,344 - 143,837,262 (-)NCBIHuRef
CHM1_17149,951,119 - 150,027,600 (-)NCBICHM1_1
T2T-CHM13v2.07151,063,321 - 151,501,798 (-)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v27149,282,168 - 149,358,608 (-)NCBI
ACTR3C
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v26186,445,034 - 186,771,854 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1738,455,298 - 38,752,225 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v07141,591,399 - 141,910,646 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.17154,063,876 - 154,066,458 (-)NCBIPanPan1.1PanPan1.1panPan2

Variants

.
Variants in ACTR3C
32 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q35-36.1(chr7:147345844-150426340)x1 copy number loss See cases [RCV000050838] Chr7:147345844..150426340 [GRCh38]
Chr7:147042936..150123428 [GRCh37]
Chr7:146673869..149754361 [NCBI36]
Chr7:7q35-36.1		 pathogenic
GRCh38/hg38 7q36.1(chr7:150319864-152674271)x1 copy number loss See cases [RCV000050552] Chr7:150319864..152674271 [GRCh38]
Chr7:150016953..152371356 [GRCh37]
Chr7:149647886..152002289 [NCBI36]
Chr7:7q36.1		 pathogenic
GRCh38/hg38 7q35-36.1(chr7:143884559-152674271)x1 copy number loss See cases [RCV000050750] Chr7:143884559..152674271 [GRCh38]
Chr7:143581652..152371356 [GRCh37]
Chr7:143212585..152002289 [NCBI36]
Chr7:7q35-36.1		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:147250465-159325876)x1 copy number loss See cases [RCV000051108] Chr7:147250465..159325876 [GRCh38]
Chr7:146947557..159118566 [GRCh37]
Chr7:146578490..158811327 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 copy number gain See cases [RCV000053576] Chr7:136309982..159307523 [GRCh38]
Chr7:135994730..159100212 [GRCh37]
Chr7:135645270..158792973 [NCBI36]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:142021716-159325876)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|See cases [RCV000053577] Chr7:142021716..159325876 [GRCh38]
Chr7:142528609..159118566 [GRCh37]
Chr7:141367985..158811327 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:142358524-159282531)x1 copy number loss See cases [RCV000054177] Chr7:142358524..159282531 [GRCh38]
Chr7:142528609..159075220 [GRCh37]
Chr7:141726947..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:143884559-159282390)x1 copy number loss See cases [RCV000054178] Chr7:143884559..159282390 [GRCh38]
Chr7:143581652..159075079 [GRCh37]
Chr7:143212585..158767840 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 copy number gain See cases [RCV000050876] Chr7:129310166..159282390 [GRCh38]
Chr7:128950007..159075079 [GRCh37]
Chr7:128737243..158767840 [NCBI36]
Chr7:7q32.1-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 copy number gain See cases [RCV000051101] Chr7:132850196..159325876 [GRCh38]
Chr7:132534956..159118566 [GRCh37]
Chr7:132185496..158811327 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:145699944-159296617)x1 copy number loss See cases [RCV000054188] Chr7:145699944..159296617 [GRCh38]
Chr7:145397037..159089306 [GRCh37]
Chr7:145027970..158782067 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q36.1(chr7:148256584-152332535)x1 copy number loss See cases [RCV000054189] Chr7:148256584..152332535 [GRCh38]
Chr7:147953676..152029620 [GRCh37]
Chr7:147584609..151660553 [NCBI36]
Chr7:7q36.1		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] Chr7:139365967..159282531 [GRCh38]
Chr7:139050713..159075220 [GRCh37]
Chr7:138701253..158767981 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1 copy number loss See cases [RCV000054176] Chr7:140754198..159307523 [GRCh38]
Chr7:140453998..159100212 [GRCh37]
Chr7:140100467..158792973 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 copy number gain See cases [RCV000136717] Chr7:97419852..158923762 [GRCh38]
Chr7:97049164..158716453 [GRCh37]
Chr7:96887100..158409214 [NCBI36]
Chr7:7q21.3-36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1 copy number loss See cases [RCV000137256] Chr7:141960861..159335866 [GRCh38]
Chr7:142528609..159128556 [GRCh37]
Chr7:141307130..158821317 [NCBI36]
Chr7:7q34-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:145436544-159331441)x1 copy number loss See cases [RCV000137338] Chr7:145436544..159331441 [GRCh38]
Chr7:145133637..159124131 [GRCh37]
Chr7:144764570..158816892 [NCBI36]
Chr7:7q35-36.3		 pathogenic|likely pathogenic
GRCh38/hg38 7q35-36.3(chr7:145250254-159335866)x1 copy number loss See cases [RCV000138005] Chr7:145250254..159335866 [GRCh38]
Chr7:144947347..159128556 [GRCh37]
Chr7:144578280..158821317 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q35-36.2(chr7:147345844-153833351)x3 copy number gain See cases [RCV000135825] Chr7:147345844..153833351 [GRCh38]
Chr7:147042936..153530436 [GRCh37]
Chr7:146673869..153161369 [NCBI36]
Chr7:7q35-36.2		 pathogenic
GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3 copy number gain See cases [RCV000136592] Chr7:137751200..154815582 [GRCh38]
Chr7:137435946..154607292 [GRCh37]
Chr7:137086486..154238225 [NCBI36]
Chr7:7q33-36.2		 pathogenic
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 copy number loss See cases [RCV000138120] Chr7:134666829..158591882 [GRCh38]
Chr7:134351581..158384574 [GRCh37]
Chr7:134002121..158077335 [NCBI36]
Chr7:7q33-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:146047157-157522158)x1 copy number loss See cases [RCV000137781] Chr7:146047157..157522158 [GRCh38]
Chr7:145744250..157314852 [GRCh37]
Chr7:145375183..157007613 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:150113232-154162779)x3 copy number gain See cases [RCV000138566] Chr7:150113232..154162779 [GRCh38]
Chr7:149810321..153859864 [GRCh37]
Chr7:149441254..153490797 [NCBI36]
Chr7:7q36.1-36.2		 likely pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 copy number gain See cases [RCV000139654] Chr7:132444095..159335866 [GRCh38]
Chr7:132128854..159128556 [GRCh37]
Chr7:131779394..158821317 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.2(chr7:150275734-153342804)x3 copy number gain See cases [RCV000139660] Chr7:150275734..153342804 [GRCh38]
Chr7:149972823..153039889 [GRCh37]
Chr7:149603756..152670822 [NCBI36]
Chr7:7q36.1-36.2		 uncertain significance
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 copy number gain See cases [RCV000142802] Chr7:131228764..159335866 [GRCh38]
Chr7:130913523..159128556 [GRCh37]
Chr7:130564063..158821317 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q36.1-36.3(chr7:150260297-159325876)x1 copy number loss See cases [RCV000142592] Chr7:150260297..159325876 [GRCh38]
Chr7:149957386..159118566 [GRCh37]
Chr7:149588319..158811327 [NCBI36]
Chr7:7q36.1-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 copy number gain See cases [RCV000143754] Chr7:131171478..159327017 [GRCh38]
Chr7:130856237..159119707 [GRCh37]
Chr7:130506777..158812468 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 copy number gain See cases [RCV000143707] Chr7:132438072..159327017 [GRCh38]
Chr7:132122831..159119707 [GRCh37]
Chr7:131773371..158812468 [NCBI36]
Chr7:7q32.3-36.3		 pathogenic
GRCh38/hg38 7q35-36.3(chr7:147144002-159327017)x1 copy number loss See cases [RCV000143503] Chr7:147144002..159327017 [GRCh38]
Chr7:146841094..159119707 [GRCh37]
Chr7:146472027..158812468 [NCBI36]
Chr7:7q35-36.3		 pathogenic
GRCh38/hg38 7q35-36.1(chr7:143596735-150089125)x4 copy number gain See cases [RCV000138555] Chr7:143596735..150089125 [GRCh38]
Chr7:143293828..149786214 [GRCh37]
Chr7:143003950..149417147 [NCBI36]
Chr7:7q35-36.1		 likely pathogenic
GRCh38/hg38 7q36.1(chr7:149666954-149906059)x3 copy number gain See cases [RCV000134324] Chr7:149666954..149906059 [GRCh38]
Chr7:149364045..149603148 [GRCh37]
Chr7:148994978..149234081 [NCBI36]
Chr7:7q36.1		 benign
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 copy number gain See cases [RCV000447709] Chr7:98969247..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:143839360-159138663) copy number loss Abnormal esophagus morphology [RCV000416719] Chr7:143839360..159138663 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:133799185-159119707)x1 copy number loss See cases [RCV000448836] Chr7:133799185..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:149261179-159075020)x3 copy number gain See cases [RCV000447776] Chr7:149261179..159075020 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 copy number gain See cases [RCV000447956] Chr7:128276078..159119707 [GRCh37]
Chr7:7q32.1-36.3		 pathogenic
NM_001164458.2(ACTR3C):c.361C>T (p.Gln121Ter) single nucleotide variant not provided [RCV004711098]|not specified [RCV000454558] Chr7:150286477 [GRCh38]
Chr7:149983566 [GRCh37]
Chr7:7q36.1		 benign
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:148189771-150867270)x4 copy number gain See cases [RCV000511618] Chr7:148189771..150867270 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) copy number gain not provided [RCV000767558] Chr7:128312450..159119220 [GRCh37]
Chr7:7q32.1-36.3		 pathogenic
NM_001164458.2(ACTR3C):c.34A>G (p.Ile12Val) single nucleotide variant not specified [RCV004296376] Chr7:150295263 [GRCh38]
Chr7:149992352 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q34-36.3(chr7:140133025-158982771)x1 copy number loss not provided [RCV000682910] Chr7:140133025..158982771 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:139623170-158329903)x3 copy number gain not provided [RCV000747070] Chr7:139623170..158329903 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q35-36.1(chr7:143711059-152573935)x3 copy number gain not provided [RCV000747094] Chr7:143711059..152573935 [GRCh37]
Chr7:7q35-36.1		 benign
GRCh37/hg19 7q36.1-36.3(chr7:148238976-159126310)x1 copy number loss not provided [RCV000747115] Chr7:148238976..159126310 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:149964361-150163624)x3 copy number gain not provided [RCV000849576] Chr7:149964361..150163624 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1(chr7:149968222-152539376)x3 copy number gain not provided [RCV000847582] Chr7:149968222..152539376 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3 copy number gain not provided [RCV001005994] Chr7:109251060..159119707 [GRCh37]
Chr7:7q31.1-36.3		 pathogenic
GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 copy number gain not provided [RCV000849569] Chr7:130592554..159119707 [GRCh37]
Chr7:7q32.3-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:145962558-159119707)x1 copy number loss not provided [RCV001006022] Chr7:145962558..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:143107740-156886246)x3 copy number gain not provided [RCV001249383] Chr7:143107740..156886246 [GRCh37]
Chr7:7q35-36.3		 not provided
GRCh37/hg19 7q33-36.3(chr7:133851002-159119707)x3 copy number gain not provided [RCV001834520] Chr7:133851002..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:148153261-157543640)x3 copy number gain not provided [RCV001827941] Chr7:148153261..157543640 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:146927174-159128556)x3 copy number gain not provided [RCV002279740] Chr7:146927174..159128556 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:149332630-151498689)x1 copy number loss not provided [RCV002472413] Chr7:149332630..151498689 [GRCh37]
Chr7:7q36.1		 pathogenic
GRCh37/hg19 7q36.1(chr7:150018908-150591382)x1 copy number loss not provided [RCV002474835] Chr7:150018908..150591382 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.322G>A (p.Asp108Asn) single nucleotide variant not specified [RCV004193959] Chr7:150286516 [GRCh38]
Chr7:149983605 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.395C>T (p.Ala132Val) single nucleotide variant not specified [RCV004206562] Chr7:150286443 [GRCh38]
Chr7:149983532 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.518A>C (p.Glu173Ala) single nucleotide variant not specified [RCV004247259] Chr7:150284799 [GRCh38]
Chr7:149981888 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.194C>T (p.Pro65Leu) single nucleotide variant not specified [RCV004207685] Chr7:150289553 [GRCh38]
Chr7:149986642 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.492G>A (p.Met164Ile) single nucleotide variant not specified [RCV004172875] Chr7:150284825 [GRCh38]
Chr7:149981914 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.553C>T (p.Pro185Ser) single nucleotide variant not specified [RCV004146405] Chr7:150284764 [GRCh38]
Chr7:149981853 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.266A>G (p.Glu89Gly) single nucleotide variant not specified [RCV004269007] Chr7:150289481 [GRCh38]
Chr7:149986570 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3 copy number gain Neurodevelopmental disorder [RCV003327609] Chr7:137463392..159345973 [GRCh38]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q34-36.1(chr7:140154317-152551638)x1 copy number loss not provided [RCV003334300] Chr7:140154317..152551638 [GRCh37]
Chr7:7q34-36.1		 pathogenic
NM_001164458.2(ACTR3C):c.95G>C (p.Arg32Pro) single nucleotide variant not specified [RCV004348718] Chr7:150293370 [GRCh38]
Chr7:149990459 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q33-36.3(chr7:135639005-159119707)x1 copy number loss not provided [RCV003482988] Chr7:135639005..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:142099013-159119707)x1 copy number loss not provided [RCV003482989] Chr7:142099013..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q36.1(chr7:148896264-150963866)x1 copy number loss not specified [RCV003986691] Chr7:148896264..150963866 [GRCh37]
Chr7:7q36.1		 pathogenic
NM_001164458.2(ACTR3C):c.548G>A (p.Arg183Gln) single nucleotide variant not specified [RCV004435879] Chr7:150284769 [GRCh38]
Chr7:149981858 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.554C>T (p.Pro185Leu) single nucleotide variant not specified [RCV004435889] Chr7:150284763 [GRCh38]
Chr7:149981852 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.562A>C (p.Lys188Gln) single nucleotide variant not specified [RCV004435894] Chr7:150284755 [GRCh38]
Chr7:149981844 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.260C>T (p.Pro87Leu) single nucleotide variant not specified [RCV004433873] Chr7:150289487 [GRCh38]
Chr7:149986576 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.212T>C (p.Ile71Thr) single nucleotide variant not specified [RCV004433869] Chr7:150289535 [GRCh38]
Chr7:149986624 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.322G>C (p.Asp108His) single nucleotide variant not specified [RCV004433881] Chr7:150286516 [GRCh38]
Chr7:149983605 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.62C>T (p.Ala21Val) single nucleotide variant not specified [RCV004606425] Chr7:150293403 [GRCh38]
Chr7:149990492 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q35-36.3(chr7:147773827-159119707)x1 copy number loss not provided [RCV004819356] Chr7:147773827..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:142491993-159119707)x3 copy number gain not provided [RCV004819304] Chr7:142491993..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q31.32-36.1(chr7:122190535-149944340)x1 copy number loss not provided [RCV004819354] Chr7:122190535..149944340 [GRCh37]
Chr7:7q31.32-36.1		 pathogenic
NM_001164458.2(ACTR3C):c.214A>G (p.Thr72Ala) single nucleotide variant not specified [RCV004898323] Chr7:150289533 [GRCh38]
Chr7:149986622 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.268C>G (p.Gln90Glu) single nucleotide variant not specified [RCV004898327] Chr7:150289479 [GRCh38]
Chr7:149986568 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.142G>A (p.Val48Ile) single nucleotide variant not specified [RCV004898316] Chr7:150293323 [GRCh38]
Chr7:149990412 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 copy number gain See cases [RCV000138847] Chr7:121863759..159335865 [GRCh38]
Chr7:121503813..159128555 [GRCh37]
Chr7:121291049..158821316 [NCBI36]
Chr7:7q31.32-36.3		 pathogenic
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 copy number gain See cases [RCV000141413] Chr7:115459015..159325817 [GRCh38]
Chr7:115099069..159118507 [GRCh37]
Chr7:114886305..158811268 [NCBI36]
Chr7:7q31.2-36.3		 pathogenic
NC_000007.14:g.150205357T>C single nucleotide variant Lung cancer [RCV000105820] Chr7:150205357 [GRCh38]
Chr7:149902446 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 copy number gain See cases [RCV000449264] Chr7:137589621..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:140636858-159119707)x1 copy number loss See cases [RCV000510250] Chr7:140636858..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:136758593-159119707)x3 copy number gain See cases [RCV000510490] Chr7:136758593..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1 copy number loss See cases [RCV000511889] Chr7:137917376..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3 copy number gain Neurodevelopmental disorder [RCV003327610] Chr7:138620939..159233475 [GRCh38]
Chr7:7q34-36.3		 likely pathogenic
NM_001164458.2(ACTR3C):c.479A>T (p.Asn160Ile) single nucleotide variant not specified [RCV004286326] Chr7:150284838 [GRCh38]
Chr7:149981927 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 copy number gain not provided [RCV000682911] Chr7:98693388..159119707 [GRCh37]
Chr7:7q22.1-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1 copy number loss not provided [RCV000747083] Chr7:141938235..159126310 [GRCh37]
Chr7:7q34-36.3		 pathogenic
GRCh37/hg19 7q32.3-36.3(chr7:131414604-159126310)x1 copy number loss See cases [RCV001007432] Chr7:131414604..159126310 [GRCh37]
Chr7:7q32.3-36.3		 pathogenic
Single allele complex Ring chromosome 7 [RCV002280646] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:148695373-159119707)x1 copy number loss not provided [RCV001832910] Chr7:148695373..159119707 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
NC_000007.13:g.(?_130781014)_(150301047_?)del deletion not provided [RCV003116360] Chr7:130781014..150301047 [GRCh37]
Chr7:7q32.3-36.1		 pathogenic
GRCh37/hg19 7q36.1-36.3(chr7:149062717-159124131)x1 copy number loss not provided [RCV002279756] Chr7:149062717..159124131 [GRCh37]
Chr7:7q36.1-36.3		 pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:56604613-96692931)x1 copy number loss See cases [RCV002287832] Chr7:56604613..96692931 [GRCh37]
Chr7:7p22.3-q36.3		 uncertain significance
NM_001164458.2(ACTR3C):c.94C>T (p.Arg32Cys) single nucleotide variant not specified [RCV004188546] Chr7:150293371 [GRCh38]
Chr7:149990460 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.494A>G (p.Glu165Gly) single nucleotide variant not specified [RCV004121072] Chr7:150284823 [GRCh38]
Chr7:149981912 [GRCh37]
Chr7:7q36.1		 uncertain significance
NM_001164458.2(ACTR3C):c.19G>C (p.Val7Leu) single nucleotide variant not specified [RCV004091955] Chr7:150295278 [GRCh38]
Chr7:149992367 [GRCh37]
Chr7:7q36.1		 uncertain significance
GRCh37/hg19 7q36.1(chr7:148538593-150967829)x1 copy number loss not provided [RCV003482992] Chr7:148538593..150967829 [GRCh37]
Chr7:7q36.1		 pathogenic
GRCh37/hg19 7q35-36.3(chr7:144940098-159119707)x1 copy number loss not provided [RCV003482991] Chr7:144940098..159119707 [GRCh37]
Chr7:7q35-36.3		 pathogenic
GRCh37/hg19 7q33-36.3(chr7:137456457-159119707)x3 copy number gain not specified [RCV003986713] Chr7:137456457..159119707 [GRCh37]
Chr7:7q33-36.3		 pathogenic
GRCh37/hg19 7q34-36.3(chr7:141690279-159119707)x3 copy number gain See cases [RCV004442845] Chr7:141690279..159119707 [GRCh37]
Chr7:7q34-36.3		 pathogenic
NM_001164458.2(ACTR3C):c.35T>C (p.Ile12Thr) single nucleotide variant not specified [RCV004435874] Chr7:150295262 [GRCh38]
Chr7:149992351 [GRCh37]
Chr7:7q36.1		 uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:2514
Count of miRNA genes:1095
Interacting mature miRNAs:1345
Transcripts:ENST00000252071, ENST00000477367, ENST00000477871, ENST00000478393, ENST00000539352
Prediction methods:Miranda, Rnahybrid
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
597493404GWAS1589478_Hpulse pressure measurement QTL GWAS1589478 (human)0.000003pulse pressure measurement7149949337149949338Human
597488029GWAS1584103_HCleft palate, cleft lip QTL GWAS1584103 (human)0.000005Cleft palate, cleft lip7150067074150067075Human
406923842GWAS572818_Hpulse pressure measurement QTL GWAS572818 (human)0.000003pulse pressure measurement7149949337149949338Human
617107404GWAS2124903_HAlzheimer disease, family history of Alzheimer’s disease QTL GWAS2124903 (human)4e-09Alzheimer disease, family history of Alzheimer’s disease7149904512149904514Human
597130515GWAS1226589_Hwellbeing measurement, alcohol consumption measurement QTL GWAS1226589 (human)9e-09wellbeing measurement, alcohol consumption measurement7150184579150184580Human
617029827GWAS2047326_Hchemerin measurement QTL GWAS2047326 (human)4e-35chemerin measurement7150323292150323293Human
629028218GWAS2922393_Hchemerin measurement QTL GWAS2922393 (human)4e-35chemerin measurement7150323292150323293Human
407233481GWAS882457_Hlate-onset Alzheimers disease QTL GWAS882457 (human)0.000006late-onset Alzheimers disease7149924921149924922Human
597206294GWAS1302368_Hglucagon measurement QTL GWAS1302368 (human)4e-08glucagon measurement7150023746150023747Human
617195994GWAS2176434_Hlevel of GTPase IMAP family member 7 in blood QTL GWAS2176434 (human)3e-31level of GTPase IMAP family member 7 in blood7150302919150302920Human
407347923GWAS996899_Hresponse to angiotensin-converting enzyme inhibitor QTL GWAS996899 (human)0.000006response to angiotensin-converting enzyme inhibitor7149900188149900189Human
407371090GWAS1020066_Hadolescent idiopathic scoliosis QTL GWAS1020066 (human)4e-08adolescent idiopathic scoliosis7150055152150055153Human
616998864GWAS2016363_Hlate-onset Alzheimers disease QTL GWAS2016363 (human)0.000006late-onset Alzheimers disease7149924921149924922Human
407068377GWAS717353_Hvisual perception measurement QTL GWAS717353 (human)3e-23visual perception measurement7150169025150169026Human
628623846GWAS2532075_Hresponse to angiotensin-converting enzyme inhibitor QTL GWAS2532075 (human)0.000006response to angiotensin-converting enzyme inhibitor7149900188149900189Human
407346265GWAS995241_Hretinoic acid receptor responder protein 2 measurement QTL GWAS995241 (human)4e-17retinoic acid receptor responder protein 2 measurement7150197525150197526Human
628413035GWAS2321264_Hvisual perception quality QTL GWAS2321264 (human)3e-23visual perception quality7150169025150169026Human
597400452GWAS1496526_Hchemerin measurement QTL GWAS1496526 (human)4e-35chemerin measurement7150323292150323293Human
407349350GWAS998326_Hcoronary artery calcification QTL GWAS998326 (human)0.000001coronary artery calcification7149941248149941249Human
1559221SCL67_HSerum cholesterol level QTL 67 (human)2.980.002Lipid leveltriglyceride7141776251159345973Human
597411263GWAS1507337_Hadolescent idiopathic scoliosis QTL GWAS1507337 (human)4e-08adolescent idiopathic scoliosis7150055152150055153Human
597485496GWAS1581570_HCleft palate, cleft lip QTL GWAS1581570 (human)0.0000002Cleft palate, cleft lip7150067074150067075Human
1559218SCL69_HSerum cholesterol level QTL 69 (human)3.410.002Lipid leveltriglyceride7141776251159345973Human
407199980GWAS848956_Hwellbeing measurement, alcohol consumption measurement QTL GWAS848956 (human)9e-09wellbeing measurement, alcohol consumption measurement7150184579150184580Human
628904277GWAS2812506_Hretinoic acid receptor responder protein 2 measurement QTL GWAS2812506 (human)4e-17retinoic acid receptor responder protein 2 measurement7150197525150197526Human
597307307GWAS1403381_Hplatelet count QTL GWAS1403381 (human)9e-10platelet count7150322539150322540Human
597460910GWAS1556984_Hresponse to angiotensin-converting enzyme inhibitor QTL GWAS1556984 (human)0.000006response to angiotensin-converting enzyme inhibitor7149900188149900189Human
617035509GWAS2053008_Hpulse pressure measurement QTL GWAS2053008 (human)0.000003pulse pressure measurement7149949337149949338Human
628430534GWAS2338763_Hadolescent idiopathic scoliosis QTL GWAS2338763 (human)4e-08adolescent idiopathic scoliosis7150055152150055153Human
1559213SCL71_HSerum cholesterol level QTL 71 (human)3.46Lipid leveltriglyceride7141776251159345973Human
628479817GWAS2388046_Hlate-onset Alzheimers disease QTL GWAS2388046 (human)0.000006brain integrity trait (VT:0010579)7149924921149924922Human
628561224GWAS2469453_Hgalectin-3 measurement QTL GWAS2469453 (human)7e-14galectin-3 measurement7150305430150305431Human
617126409GWAS2143908_Hlevel of GTPase IMAP family member 7 in blood serum QTL GWAS2143908 (human)3e-31level of GTPase IMAP family member 7 in blood serum7150302919150302920Human
407343108GWAS992084_Hplatelet count QTL GWAS992084 (human)9e-10platelet count7150322539150322540Human
597999586GWAS1718885_Hwellbeing measurement, alcohol consumption quality QTL GWAS1718885 (human)9e-09wellbeing measurement, alcohol consumption quality7150184579150184580Human
1559263SCL72_HSerum cholesterol level QTL 72 (human)3.25Lipid leveltriglyceride7141776251159345973Human
597394641GWAS1490715_Hvisual perception measurement QTL GWAS1490715 (human)3e-23visual perception measurement7150169025150169026Human
617090565GWAS2108064_HCleft palate, cleft lip QTL GWAS2108064 (human)0.0000002Cleft palate, cleft lip7150067074150067075Human
617004041GWAS2021540_Hglucagon measurement QTL GWAS2021540 (human)4e-08glucagon measurement7150023746150023747Human
1559237SCL70_HSerum cholesterol level QTL 70 (human)3.520.002Lipid leveltriglyceride7141776251159345973Human
597075136GWAS1171210_Hcoronary artery calcification QTL GWAS1171210 (human)0.000001coronary artery calcification7149941248149941249Human
597077056GWAS1173130_Hchemerin measurement QTL GWAS1173130 (human)8e-14chemerin measurement7150316304150316305Human
1559232SCL66_HSerum cholesterol level QTL 66 (human)2.980.002Lipid leveltriglyceride7141776251159345973Human
616994078GWAS2011577_Hresponse to angiotensin-converting enzyme inhibitor QTL GWAS2011577 (human)0.000006response to angiotensin-converting enzyme inhibitor7149900188149900189Human
617090576GWAS2108075_HCleft palate, cleft lip QTL GWAS2108075 (human)0.000005Cleft palate, cleft lip7150067074150067075Human
628940068GWAS2848297_Hplatelet count QTL GWAS2848297 (human)4e-08platelet quantity (VT:0003179)platelet count (CMO:0000029)7150316211150316212Human
628830241GWAS2738470_HCleft palate, cleft lip QTL GWAS2738470 (human)0.000005Cleft palate, cleft lip7150067074150067075Human
616997530GWAS2015029_Hcoronary artery calcification QTL GWAS2015029 (human)0.000001coronary artery integrity trait (VT:0010746)7149941248149941249Human
628708775GWAS2617004_Hlevel of GTPase IMAP family member 7 in blood QTL GWAS2617004 (human)3e-31level of GTPase IMAP family member 7 in blood7150302919150302920Human
407207963GWAS856939_Hchemerin measurement QTL GWAS856939 (human)4e-35chemerin measurement7150323292150323293Human
626463671GWAS2277604_Hplatelet count QTL GWAS2277604 (human)4e-08platelet count7150316211150316212Human
1578618SCL127_HSerum cholesterol level QTL 127 (human)3.7Lipid leveltriglyceride7141776251159345973Human
407211175GWAS860151_Hglucagon measurement QTL GWAS860151 (human)4e-08glucagon measurement7150023746150023747Human
628546452GWAS2454681_Hplatelet count QTL GWAS2454681 (human)9e-10platelet quantity (VT:0003179)platelet count (CMO:0000029)7150322539150322540Human
616561884GWAS1958467_Hgalectin-3 measurement QTL GWAS1958467 (human)7e-14galectin-3 measurement7150305430150305431Human
597140592GWAS1236666_Hretinoic acid receptor responder protein 2 measurement QTL GWAS1236666 (human)4e-17retinoic acid receptor responder protein 2 measurement7150197525150197526Human
628829715GWAS2737944_HCleft palate, cleft lip QTL GWAS2737944 (human)0.0000002Cleft palate, cleft lip7150067074150067075Human
1578610SCL128_HSerum cholesterol level QTL 128 (human)2.2Lipid levelLDL cholesterol7141776251159345973Human
407078953GWAS727929_Hchemerin measurement QTL GWAS727929 (human)8e-14chemerin measurement7150316304150316305Human
597824078GWAS1691469_Hwellbeing measurement QTL GWAS1691469 (human)9e-09wellbeing measurement7150184579150184580Human
628785559GWAS2693788_Hwellbeing measurement, alcohol consumption quality QTL GWAS2693788 (human)9e-09wellness/fitness trait (VT:1000152)7150184579150184580Human
628653833GWAS2562062_Hpulse pressure measurement QTL GWAS2562062 (human)0.000003arterial blood pressure trait (VT:2000000)pulse pressure (CMO:0000292)7149949337149949338Human
617013427GWAS2030926_Hadolescent idiopathic scoliosis QTL GWAS2030926 (human)4e-08adolescent idiopathic scoliosis7150055152150055153Human
598006097GWAS1725396_Hvisual perception quality QTL GWAS1725396 (human)3e-23visual perception quality7150169025150169026Human
1559264SCL68_HSerum cholesterol level QTL 68 (human)3.10.002Lipid leveltriglyceride7141776251159345973Human
616544712GWAS1941295_Hlevel of GTPase IMAP family member 7 in blood serum QTL GWAS1941295 (human)3e-31level of GTPase IMAP family member 7 in blood serum7150302919150302920Human
597075950GWAS1172024_Hlate-onset Alzheimers disease QTL GWAS1172024 (human)0.000006late-onset Alzheimers disease7149924921149924922Human
628904454GWAS2812683_HAlzheimer disease, family history of Alzheimer’s disease QTL GWAS2812683 (human)4e-09Alzheimer disease, family history of Alzheimer’s disease7149904512149904514Human
628454794GWAS2363023_Hglucagon measurement QTL GWAS2363023 (human)4e-08blood glucagon amount (VT:0002695)blood glucagon level (CMO:0001294)7150023746150023747Human

Markers in Region
SHGC-147571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377149,978,428 - 149,978,726UniSTSGRCh37
GRCh377152,525,323 - 152,525,621UniSTSGRCh37
Build 367149,609,361 - 149,609,659RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7143,794,399 - 143,794,697UniSTS
CRA_TCAGchr7v27151,852,403 - 151,852,701UniSTS
CRA_TCAGchr7v27149,316,295 - 149,316,593UniSTS
TNG Radiation Hybrid Map768950.0UniSTS
GDB:4585543  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377150,019,093 - 150,019,200UniSTSGRCh37
Build 367149,650,026 - 149,650,133RGDNCBI36
Celera7144,576,182 - 144,576,289RGD
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map7q31-q35UniSTS
HuRef7143,835,597 - 143,835,704UniSTS
CRA_TCAGchr7v27149,356,943 - 149,357,050UniSTS
GDB:1318002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,531,003 - 152,531,144UniSTSGRCh37
GRCh377149,972,902 - 149,973,043UniSTSGRCh37
Build 367149,603,835 - 149,603,976RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7143,788,937 - 143,789,078UniSTS
HuRef7146,337,461 - 146,337,602UniSTS
CRA_TCAGchr7v27149,310,769 - 149,310,910UniSTS
CRA_TCAGchr7v27151,858,083 - 151,858,224UniSTS
GDB:1318182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,524,232 - 152,524,351UniSTSGRCh37
GRCh377149,979,698 - 149,979,817UniSTSGRCh37
Build 367149,610,631 - 149,610,750RGDNCBI36
Cytogenetic Map7q36.1UniSTS
HuRef7143,795,669 - 143,795,788UniSTS
CRA_TCAGchr7v27149,317,565 - 149,317,684UniSTS
CRA_TCAGchr7v27151,851,312 - 151,851,431UniSTS
D7S3198  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh377152,503,164 - 152,503,345UniSTSGRCh37
GRCh377150,000,738 - 150,000,919UniSTSGRCh37
Build 367149,631,671 - 149,631,852RGDNCBI36
Celera7144,557,827 - 144,558,008RGD
Cytogenetic Map7q36.1UniSTS
HuRef7146,315,547 - 146,315,728UniSTS
HuRef7143,816,682 - 143,816,863UniSTS
CRA_TCAGchr7v27149,338,590 - 149,338,771UniSTS
CRA_TCAGchr7v27151,830,244 - 151,830,425UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map6p25.1-p23UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map13q12.1UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map12p13.1-p12.3UniSTS
Cytogenetic Map3p25.2UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map3p21.2UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic MapXp21.2UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map15q23UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map14q32.12UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map2q24.3UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map15q22.2UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map6p21UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map12p13-p12UniSTS
Cytogenetic Map9p13.2UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map9q22.2UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p22.1UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map9q13-q21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic MapXp11.2UniSTS
Cytogenetic Map19pUniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map18p11.31-p11.21UniSTS
Cytogenetic Map11p15.3-p15.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map8q22UniSTS
Cytogenetic Map4p15.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map2p16.3UniSTS
Cytogenetic Map16p13.12UniSTS
Cytogenetic Map7p21.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map6q24.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map10q23.2UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map6q22.1UniSTS
Cytogenetic Map1q42.1UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map3p21-p12UniSTS
Cytogenetic Map4q35UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3p22-p21.33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map3q22.1UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map9q22UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map20q11.2-q13.2UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map2q31.3UniSTS
Cytogenetic Map1q31UniSTS
Cytogenetic Map7q32-q33UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map14q23-q24.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map2p24-p21UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map12p11UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map20q13UniSTS
Cytogenetic Map17q25.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic MapXq25-q26UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map15q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p36.22UniSTS
Cytogenetic Map3q26.31UniSTS
Cytogenetic Map17q22-q23UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map16q12.2UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map3q26.2-q27UniSTS
Cytogenetic Map1q25.1-q25.2UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map9q21.13UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map22q13.31UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map5q21.3UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map10q22.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic MapXp22UniSTS
Cytogenetic MapXq23UniSTS
Cytogenetic Map20p12.3-p11.21UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map4q32-q34UniSTS
Cytogenetic MapXq25-q26.1UniSTS
Cytogenetic Map2p25-p24UniSTS
Cytogenetic Map2p25UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic MapXp22.2-p22.1UniSTS
Cytogenetic MapXq22.1UniSTS
Cytogenetic Map4q25UniSTS
Cytogenetic Map3p24.2UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map20q11.22-q12UniSTS
Cytogenetic Map4q34.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map22q13.1-q13.2UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map12q13-q14UniSTS
Cytogenetic Map6q14.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q31.2UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map12q13UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map21q21.2UniSTS
Cytogenetic Map10q24.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map8q21.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map1q32.2UniSTS
Cytogenetic Map4q21.3UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map3q26.2UniSTS
Cytogenetic Map2q36.3UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map11q22.1UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map4p15.32UniSTS
Cytogenetic Map18q12.2UniSTS
Cytogenetic Map15q15.2UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map12q14.1UniSTS
Cytogenetic Map6p22.3-p22.1UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map6q15UniSTS
Cytogenetic Map6q23.3UniSTS
Cytogenetic Map13q14UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map1p35UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic MapXp11UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map20p12UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXp22.3UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map19p13.3-p13.2UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map7q22.3UniSTS
Cytogenetic Map9p22UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q23.2UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map2p22.3UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map22q13.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map11p14UniSTS
Cytogenetic Map1p32.1UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map4q34.3UniSTS
Cytogenetic Map9p12UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map13q34UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map11q23.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3p13UniSTS
Cytogenetic Map4p13UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map15q22-q24UniSTS
Cytogenetic Map8q23UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map4q31.3UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map13q12.11UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map3q21.1UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic Map21q22.13UniSTS
Cytogenetic Map15q22.1-q22.31UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic MapXq13UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map14q32.1UniSTS
Cytogenetic Map16q12-q13UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map12q11-q12UniSTS
Cytogenetic Map1q42.1-q43UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map12q24UniSTS
Cytogenetic MapXp22.11UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map8q24.21UniSTS
Cytogenetic Map12q13.1UniSTS
Cytogenetic Map12q22-q23.1UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map5q31.2-q34UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map6q24.2UniSTS
Cytogenetic Map22qUniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map7p11UniSTS
Cytogenetic MapXp22.12-p22.11UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map8q24.22UniSTS
Cytogenetic Map8p22-p21.3UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map1p36.12UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map6q25.2-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic Map3q28-q29UniSTS
Cytogenetic Map7p14-p13UniSTS
Cytogenetic Map12q24.2UniSTS
Cytogenetic Map6p22.2UniSTS
Cytogenetic Map7q22-qterUniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map1p21UniSTS
Cytogenetic Map1q32.2-q41UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map3q26.33UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map5p15.1-p14.3UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map6q22-q23UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map14q21UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map2q24UniSTS
Cytogenetic Map12p13UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic MapXq22.2UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map7p15.1UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map14q32.13UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map16p13.1UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic Map20q13.2-q13.3UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map13q13.3UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1202 2437 2764 2225 4953 1726 2347 6 624 1941 465 2256 7253 6428 50 3726 1 850 1741 1612 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001164458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001164459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351027 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351028 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001351030 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147015 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147017 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147018 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147020 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_147022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005250043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516507 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516508 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011516511 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012550 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446882 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446883 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420748 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047420751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007060141 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007060142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007060143 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007060144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007060145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB039791 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005586 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006008 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092666 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC092681 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC093458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC099647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM674900 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX640643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA868104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DN992136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR004860 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000252071   ⟹   ENSP00000252071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,302,980 (-)Ensembl
Ensembl Acc Id: ENST00000477367   ⟹   ENSP00000417997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,293,312 - 150,323,163 (-)Ensembl
Ensembl Acc Id: ENST00000477871   ⟹   ENSP00000418635
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,286,468 - 150,323,725 (-)Ensembl
Ensembl Acc Id: ENST00000478393   ⟹   ENSP00000417426
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,243,916 - 150,323,573 (-)Ensembl
Ensembl Acc Id: ENST00000539352   ⟹   ENSP00000440990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,284,747 - 150,295,296 (-)Ensembl
Ensembl Acc Id: ENST00000613959   ⟹   ENSP00000481447
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,243,919 - 150,249,060 (-)Ensembl
Ensembl Acc Id: ENST00000683684   ⟹   ENSP00000507618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,212 - 150,323,545 (-)Ensembl
Ensembl Acc Id: ENST00000865059   ⟹   ENSP00000535118
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,246,810 - 150,323,707 (-)Ensembl
Ensembl Acc Id: ENST00000865060   ⟹   ENSP00000535119
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,212 - 150,323,712 (-)Ensembl
Ensembl Acc Id: ENST00000865061   ⟹   ENSP00000535120
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,132 - 150,323,529 (-)Ensembl
Ensembl Acc Id: ENST00000865062   ⟹   ENSP00000535121
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,600 (-)Ensembl
Ensembl Acc Id: ENST00000865063   ⟹   ENSP00000535122
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,139 - 150,323,508 (-)Ensembl
Ensembl Acc Id: ENST00000865064   ⟹   ENSP00000535123
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,542 (-)Ensembl
Ensembl Acc Id: ENST00000865065   ⟹   ENSP00000535124
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,212 - 150,323,537 (-)Ensembl
Ensembl Acc Id: ENST00000865066   ⟹   ENSP00000535125
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,508 (-)Ensembl
Ensembl Acc Id: ENST00000865067   ⟹   ENSP00000535126
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,495 (-)Ensembl
Ensembl Acc Id: ENST00000865068   ⟹   ENSP00000535127
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,211 - 150,323,395 (-)Ensembl
Ensembl Acc Id: ENST00000865069   ⟹   ENSP00000535128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,157 (-)Ensembl
Ensembl Acc Id: ENST00000865070   ⟹   ENSP00000535129
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,149 (-)Ensembl
Ensembl Acc Id: ENST00000916821   ⟹   ENSP00000586880
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,248,811 - 150,323,545 (-)Ensembl
Ensembl Acc Id: ENST00000944427   ⟹   ENSP00000614486
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,215 - 150,323,644 (-)Ensembl
Ensembl Acc Id: ENST00000944428   ⟹   ENSP00000614487
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,216 - 150,323,573 (-)Ensembl
Ensembl Acc Id: ENST00000944429   ⟹   ENSP00000614488
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,212 - 150,323,535 (-)Ensembl
Ensembl Acc Id: ENST00000944430   ⟹   ENSP00000614489
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,213 - 150,323,535 (-)Ensembl
Ensembl Acc Id: ENST00000944431   ⟹   ENSP00000614490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,247,215 - 150,323,201 (-)Ensembl
Ensembl Acc Id: ENST00000944432   ⟹   ENSP00000614491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl7150,248,972 - 150,308,267 (-)Ensembl
RefSeq Acc Id: NM_001164458   ⟹   NP_001157930
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,247,212 - 150,323,545 (-)NCBI
GRCh377149,944,301 - 150,020,758 (-)RGD
Celera7144,543,643 - 144,577,847 (-)RGD
HuRef7143,760,344 - 143,837,262 (-)ENTREZGENE
CHM1_17149,951,119 - 150,027,600 (-)NCBI
T2T-CHM13v2.07151,425,468 - 151,501,798 (-)NCBI
CRA_TCAGchr7v27149,282,168 - 149,358,608 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001164459   ⟹   NP_001157931
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,247,212 - 150,303,063 (-)NCBI
GRCh377149,944,301 - 150,020,758 (-)RGD
Celera7144,543,643 - 144,577,847 (-)RGD
HuRef7143,760,344 - 143,837,262 (-)ENTREZGENE
CHM1_17149,951,119 - 150,006,911 (-)NCBI
T2T-CHM13v2.07151,425,468 - 151,481,322 (-)NCBI
CRA_TCAGchr7v27149,282,168 - 149,358,608 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_001351027   ⟹   NP_001337956
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,047,715 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,225,949 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351028   ⟹   NP_001337957
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,323,545 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,501,798 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351029   ⟹   NP_001337958
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001351030   ⟹   NP_001337959
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147012
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,323,545 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,501,798 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147013
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,243,916 - 150,323,545 (-)NCBI
T2T-CHM13v2.07151,422,172 - 151,501,798 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147014
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147015
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147016
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147017
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147018
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147019
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,221,100 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,399,353 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147020
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,047,715 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,225,949 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147021
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,047,715 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,225,949 (-)NCBI
Sequence:
RefSeq Acc Id: NR_147022
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,047,715 (-)NCBI
T2T-CHM13v2.07151,063,321 - 151,225,949 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005250043   ⟹   XP_005250100
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,263,888 - 150,323,545 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516506   ⟹   XP_011514808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,247,212 - 150,323,545 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516507   ⟹   XP_011514809
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,235,261 - 150,323,545 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516508   ⟹   XP_011514810
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,235,174 - 150,323,545 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011516511   ⟹   XP_011514813
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,266,153 - 150,323,545 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024446884   ⟹   XP_024302652
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,887,178 - 150,047,715 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047420748   ⟹   XP_047276704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,214,302 - 150,323,545 (-)NCBI
RefSeq Acc Id: XM_047420749   ⟹   XP_047276705
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,892,332 - 150,323,545 (-)NCBI
RefSeq Acc Id: XM_047420750   ⟹   XP_047276706
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,887,178 - 150,047,715 (-)NCBI
RefSeq Acc Id: XM_047420751   ⟹   XP_047276707
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,887,178 - 150,047,715 (-)NCBI
RefSeq Acc Id: XR_007060141
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,230,223 - 150,323,545 (-)NCBI
RefSeq Acc Id: XR_007060142
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,230,223 - 150,323,545 (-)NCBI
RefSeq Acc Id: XR_007060143
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,887,178 - 150,323,545 (-)NCBI
RefSeq Acc Id: XR_007060144
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,887,178 - 150,323,545 (-)NCBI
RefSeq Acc Id: XR_007060145
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh387149,881,360 - 150,323,545 (-)NCBI
RefSeq Acc Id: NP_001157930   ⟸   NM_001164458
- Peptide Label: isoform a precursor
- UniProtKB: Q5CZI4 (UniProtKB/Swiss-Prot),   Q9C0K3 (UniProtKB/Swiss-Prot),   A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001157931   ⟸   NM_001164459
- Peptide Label: isoform a precursor
- UniProtKB: Q5CZI4 (UniProtKB/Swiss-Prot),   Q9C0K3 (UniProtKB/Swiss-Prot),   A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005250100   ⟸   XM_005250043
- Peptide Label: isoform X3
- UniProtKB: A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514810   ⟸   XM_011516508
- Peptide Label: isoform X2
- UniProtKB: Q5CZI4 (UniProtKB/Swiss-Prot),   Q9C0K3 (UniProtKB/Swiss-Prot),   A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514809   ⟸   XM_011516507
- Peptide Label: isoform X2
- UniProtKB: Q5CZI4 (UniProtKB/Swiss-Prot),   Q9C0K3 (UniProtKB/Swiss-Prot),   A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514808   ⟸   XM_011516506
- Peptide Label: isoform X2
- UniProtKB: Q5CZI4 (UniProtKB/Swiss-Prot),   Q9C0K3 (UniProtKB/Swiss-Prot),   A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011514813   ⟸   XM_011516511
- Peptide Label: isoform X5
- UniProtKB: A0A0A0MTI9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001337957   ⟸   NM_001351028
- Peptide Label: isoform c
- Sequence:
RefSeq Acc Id: NP_001337958   ⟸   NM_001351029
- Peptide Label: isoform d
- Sequence:
RefSeq Acc Id: NP_001337959   ⟸   NM_001351030
- Peptide Label: isoform d
- Sequence:
RefSeq Acc Id: NP_001337956   ⟸   NM_001351027
- Peptide Label: isoform b
- Sequence:
RefSeq Acc Id: XP_024302652   ⟸   XM_024446884
- Peptide Label: isoform X6
- Sequence:
Ensembl Acc Id: ENSP00000252071   ⟸   ENST00000252071
Ensembl Acc Id: ENSP00000418635   ⟸   ENST00000477871
Ensembl Acc Id: ENSP00000417997   ⟸   ENST00000477367
Ensembl Acc Id: ENSP00000417426   ⟸   ENST00000478393
Ensembl Acc Id: ENSP00000481447   ⟸   ENST00000613959
Ensembl Acc Id: ENSP00000440990   ⟸   ENST00000539352
Ensembl Acc Id: ENSP00000507618   ⟸   ENST00000683684
RefSeq Acc Id: XP_047276706   ⟸   XM_047420750
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047276707   ⟸   XM_047420751
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047276705   ⟸   XM_047420749
- Peptide Label: isoform X4
- UniProtKB: A0A0A0MTI9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047276704   ⟸   XM_047420748
- Peptide Label: isoform X1
Ensembl Acc Id: ENSP00000535118   ⟸   ENST00000865059
Ensembl Acc Id: ENSP00000614486   ⟸   ENST00000944427
Ensembl Acc Id: ENSP00000535122   ⟸   ENST00000865063
Ensembl Acc Id: ENSP00000535125   ⟸   ENST00000865066
Ensembl Acc Id: ENSP00000535128   ⟸   ENST00000865069
Ensembl Acc Id: ENSP00000535119   ⟸   ENST00000865060
Ensembl Acc Id: ENSP00000535124   ⟸   ENST00000865065
Ensembl Acc Id: ENSP00000535127   ⟸   ENST00000865068
Ensembl Acc Id: ENSP00000586880   ⟸   ENST00000916821
Ensembl Acc Id: ENSP00000614488   ⟸   ENST00000944429
Ensembl Acc Id: ENSP00000614491   ⟸   ENST00000944432
Ensembl Acc Id: ENSP00000535126   ⟸   ENST00000865067
Ensembl Acc Id: ENSP00000614490   ⟸   ENST00000944431
Ensembl Acc Id: ENSP00000614489   ⟸   ENST00000944430
Ensembl Acc Id: ENSP00000535121   ⟸   ENST00000865062
Ensembl Acc Id: ENSP00000614487   ⟸   ENST00000944428
Ensembl Acc Id: ENSP00000535123   ⟸   ENST00000865064
Ensembl Acc Id: ENSP00000535129   ⟸   ENST00000865070
Ensembl Acc Id: ENSP00000535120   ⟸   ENST00000865061

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9C0K3-F1-model_v2 AlphaFold Q9C0K3 1-210 view protein structure

Promoters
RGD ID:6805199
Promoter ID:HG_KWN:60236
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:NM_001164459
Position:
Human AssemblyChrPosition (strand)Source
Build 367149,630,676 - 149,631,176 (-)MPROMDB
RGD ID:6805197
Promoter ID:HG_KWN:60239
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid
Transcripts:NM_001164458
Position:
Human AssemblyChrPosition (strand)Source
Build 367149,651,551 - 149,652,437 (-)MPROMDB
RGD ID:7212255
Promoter ID:EPDNEW_H11874
Type:initiation region
Name:ACTR3C_2
Description:ARP3 actin-related protein 3 homolog C
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11876  EPDNEW_H11877  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,303,063 - 150,303,123EPDNEW
RGD ID:7212259
Promoter ID:EPDNEW_H11876
Type:initiation region
Name:ACTR3C_1
Description:ARP3 actin-related protein 3 homolog C
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11874  EPDNEW_H11877  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,323,522 - 150,323,582EPDNEW
RGD ID:7212261
Promoter ID:EPDNEW_H11877
Type:initiation region
Name:ACTR3C_3
Description:ARP3 actin-related protein 3 homolog C
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11874  EPDNEW_H11876  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh387150,323,751 - 150,323,811EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:37282 AgrOrtholog
COSMIC ACTR3C COSMIC
Ensembl Genes ENSG00000106526 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000252071 ENTREZGENE
  ENST00000252071.8 UniProtKB/Swiss-Prot
  ENST00000478393 ENTREZGENE
  ENST00000539352 ENTREZGENE
  ENST00000683684 ENTREZGENE
  ENST00000683684.1 UniProtKB/Swiss-Prot
  ENST00000865060 ENTREZGENE
  ENST00000916821 ENTREZGENE
Gene3D-CATH 3.30.420.40 UniProtKB/Swiss-Prot
  Actin, Chain A, domain 4 UniProtKB/Swiss-Prot
GTEx ENSG00000106526 GTEx
HGNC ID HGNC:37282 ENTREZGENE
Human Proteome Map ACTR3C Human Proteome Map
InterPro Actin UniProtKB/Swiss-Prot
  ATPase_NBD UniProtKB/Swiss-Prot
KEGG Report hsa:653857 UniProtKB/Swiss-Prot
NCBI Gene 653857 ENTREZGENE
PANTHER PTHR11937 UniProtKB/Swiss-Prot
Pfam Actin UniProtKB/Swiss-Prot
PharmGKB PA165617588 PharmGKB
SMART ACTIN UniProtKB/Swiss-Prot
Superfamily-SCOP SSF53067 UniProtKB/Swiss-Prot
UniProt A0A0A0MTI9 ENTREZGENE, UniProtKB/TrEMBL
  ARP3C_HUMAN UniProtKB/Swiss-Prot
  C9IZN3_HUMAN UniProtKB/TrEMBL
  C9J580_HUMAN UniProtKB/TrEMBL
  H7C4J1_HUMAN UniProtKB/TrEMBL
  Q5CZI4 ENTREZGENE
  Q9C0K3 ENTREZGENE
UniProt Secondary Q5CZI4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-01-15 ACTR3C  actin related protein 3C    ARP3 actin related protein 3 homolog C  Symbol and/or name change 5135510 APPROVED
2017-05-02 ACTR3C  ARP3 actin related protein 3 homolog C    ARP3 actin-related protein 3 homolog C  Symbol and/or name change 5135510 APPROVED
2016-04-19 ACTR3C  ARP3 actin-related protein 3 homolog C    ARP3 actin-related protein 3 homolog C (yeast)  Symbol and/or name change 5135510 APPROVED