CARMIL3 (capping protein regulator and myosin 1 linker 3) - Rat Genome Database
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Gene: CARMIL3 (capping protein regulator and myosin 1 linker 3) Homo sapiens
Analyze
Symbol: CARMIL3
Name: capping protein regulator and myosin 1 linker 3
RGD ID: 1349280
HGNC Page HGNC
Description: Localizes to plasma membrane; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; aflatoxin B1; benzo[a]pyrene.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: C14orf121; capping protein regulator and myosin 1 linker protein 3; capping protein, Arp2/3 and myosin-I linker protein 3; crml-1; leucine rich repeat containing 16B; leucine-rich repeat-containing protein 16B; LRRC16B
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1424,052,009 - 24,069,729 (+)EnsemblGRCh38hg38GRCh38
GRCh381424,052,009 - 24,069,729 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371424,521,218 - 24,538,938 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361423,591,046 - 23,608,777 (+)NCBINCBI36hg18NCBI36
Celera144,385,685 - 4,403,416 (+)NCBI
Cytogenetic Map14q11.2NCBI
HuRef144,636,144 - 4,653,872 (+)NCBIHuRef
CHM1_11424,519,882 - 24,537,614 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

References

Additional References at PubMed
PMID:10737800   PMID:12477932   PMID:15028280   PMID:16344560   PMID:19846667   PMID:21102520   PMID:22810586   PMID:26578515   PMID:29987050   PMID:31694931  


Genomics

Comparative Map Data
CARMIL3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1424,052,009 - 24,069,729 (+)EnsemblGRCh38hg38GRCh38
GRCh381424,052,009 - 24,069,729 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371424,521,218 - 24,538,938 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361423,591,046 - 23,608,777 (+)NCBINCBI36hg18NCBI36
Celera144,385,685 - 4,403,416 (+)NCBI
Cytogenetic Map14q11.2NCBI
HuRef144,636,144 - 4,653,872 (+)NCBIHuRef
CHM1_11424,519,882 - 24,537,614 (+)NCBICHM1_1
Carmil3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391455,728,108 - 55,745,729 (+)NCBIGRCm39mm39
GRCm39 Ensembl1455,728,108 - 55,745,729 (+)Ensembl
GRCm381455,490,651 - 55,508,272 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1455,490,651 - 55,508,272 (+)EnsemblGRCm38mm10GRCm38
MGSCv371456,109,930 - 56,127,101 (+)NCBIGRCm37mm9NCBIm37
MGSCv361454,445,164 - 54,462,335 (+)NCBImm8
Celera1453,296,005 - 53,313,185 (+)NCBICelera
Cytogenetic Map14C3NCBI
Carmil3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21528,978,440 - 28,995,865 (+)NCBI
Rnor_6.0 Ensembl1534,167,945 - 34,184,799 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01534,167,146 - 34,184,799 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01538,057,562 - 38,075,771 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41533,622,020 - 33,639,257 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11533,645,651 - 33,654,958 (+)NCBI
Celera1528,555,021 - 28,571,875 (+)NCBICelera
Cytogenetic Map15p13NCBI
Carmil3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540936,324,474 - 36,340,931 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540936,324,141 - 36,341,648 (-)NCBIChiLan1.0ChiLan1.0
CARMIL3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11422,954,274 - 22,971,981 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1422,954,274 - 22,971,981 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0144,830,041 - 4,847,897 (+)NCBIMhudiblu_PPA_v0panPan3
CARMIL3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.184,059,154 - 4,076,385 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl84,059,133 - 4,076,396 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha83,981,155 - 3,998,261 (+)NCBI
ROS_Cfam_1.084,169,943 - 4,187,054 (+)NCBI
UMICH_Zoey_3.183,860,706 - 3,877,810 (+)NCBI
UNSW_CanFamBas_1.083,922,469 - 3,939,569 (+)NCBI
UU_Cfam_GSD_1.084,184,546 - 4,201,662 (+)NCBI
Carmil3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_ltri_2NW_02440864035,908,398 - 35,925,866 (+)NCBI
SpeTri2.0NW_004936722463,791 - 480,594 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CARMIL3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl775,222,528 - 75,241,243 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1775,222,528 - 75,241,243 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2780,492,975 - 80,511,400 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CARMIL3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1241,034,790 - 1,053,169 (+)NCBI
ChlSab1.1 Ensembl241,035,947 - 1,052,844 (+)Ensembl
Carmil3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046248208,460,032 - 8,477,298 (-)NCBI

Position Markers
RH120783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371424,531,018 - 24,531,290UniSTSGRCh37
Build 361423,600,858 - 23,601,130RGDNCBI36
Celera144,395,497 - 4,395,769RGD
Cytogenetic Map14q11.2UniSTS
HuRef144,645,956 - 4,646,228UniSTS
TNG Radiation Hybrid Map142055.0UniSTS
STS-F02322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371424,538,807 - 24,538,882UniSTSGRCh37
Build 361423,608,647 - 23,608,722RGDNCBI36
Celera144,403,286 - 4,403,361RGD
Cytogenetic Map14q11.2UniSTS
HuRef144,653,742 - 4,653,817UniSTS
GeneMap99-GB4 RH Map1420.64UniSTS
NCBI RH Map1438.0UniSTS
SHGC-32365  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371424,538,785 - 24,538,917UniSTSGRCh37
Build 361423,608,625 - 23,608,757RGDNCBI36
Celera144,403,264 - 4,403,396RGD
Cytogenetic Map14q11.2UniSTS
HuRef144,653,720 - 4,653,852UniSTS
Stanford-G3 RH Map14376.0UniSTS
NCBI RH Map1436.7UniSTS
GeneMap99-G3 RH Map14376.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1674
Count of miRNA genes:586
Interacting mature miRNAs:653
Transcripts:ENST00000334420, ENST00000342740, ENST00000559694, ENST00000560349, ENST00000561354
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.


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
High
Medium 4 4 255 24 505 2 943 3 76 52 249
Low 1681 600 1124 434 1204 278 2008 399 2704 261 1043 1299 161 1 515 1098 1
Below cutoff 747 2372 340 185 679 183 1826 1777 76 143 323 230 12 689 1437 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_138360 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AI017934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI631690 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074167 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL834197 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG913168 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG977591 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU102125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA121863 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DT932621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ821284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ821285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ821286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  FJ821287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF584331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000342740   ⟹   ENSP00000340467
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1424,052,009 - 24,069,729 (+)Ensembl
RefSeq Acc Id: ENST00000559694
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1424,057,215 - 24,069,726 (+)Ensembl
RefSeq Acc Id: ENST00000560349
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1424,061,919 - 24,069,724 (+)Ensembl
RefSeq Acc Id: ENST00000561354
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1424,060,741 - 24,061,930 (+)Ensembl
RefSeq Acc Id: NM_138360   ⟹   NP_612369
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381424,052,009 - 24,069,729 (+)NCBI
GRCh371424,521,206 - 24,538,937 (+)RGD
Build 361423,591,046 - 23,608,777 (+)NCBI Archive
Celera144,385,685 - 4,403,416 (+)RGD
HuRef144,636,144 - 4,653,872 (+)RGD
CHM1_11424,519,882 - 24,537,614 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_612369   ⟸   NM_138360
- UniProtKB: Q8ND23 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000340467   ⟸   ENST00000342740

Promoters
RGD ID:6791487
Promoter ID:HG_KWN:19056
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:ENST00000334420,   NM_138360
Position:
Human AssemblyChrPosition (strand)Source
Build 361423,590,791 - 23,591,502 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q11.2-12(chr14:20151149-27723796)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051484]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051484]|See cases [RCV000051484] Chr14:20151149..27723796 [GRCh38]
Chr14:20619308..28193002 [GRCh37]
Chr14:19689148..27262842 [NCBI36]
Chr14:14q11.2-12
pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20196945-45284802)x1 copy number loss See cases [RCV000051485] Chr14:20196945..45284802 [GRCh38]
Chr14:20665104..45754005 [GRCh37]
Chr14:19734944..44823755 [NCBI36]
Chr14:14q11.2-21.2
pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:23548960-41983402)x1 copy number loss See cases [RCV000051490] Chr14:23548960..41983402 [GRCh38]
Chr14:24018169..42452605 [GRCh37]
Chr14:23088009..41522355 [NCBI36]
Chr14:14q11.2-21.1
pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20000611-38984415)x3 copy number gain See cases [RCV000053803] Chr14:20000611..38984415 [GRCh38]
Chr14:20468770..39453619 [GRCh37]
Chr14:19538610..38523370 [NCBI36]
Chr14:14q11.2-21.1
pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20150949-39746154)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]|See cases [RCV000053806] Chr14:20150949..39746154 [GRCh38]
Chr14:20619108..40215358 [GRCh37]
Chr14:19688948..39285109 [NCBI36]
Chr14:14q11.2-21.1
pathogenic
NM_138360.3(LRRC16B):c.482C>T (p.Ala161Val) single nucleotide variant Malignant melanoma [RCV000070505] Chr14:24055087 [GRCh38]
Chr14:24524296 [GRCh37]
Chr14:23594136 [NCBI36]
Chr14:14q11.2
not provided
NM_138360.3(LRRC16B):c.843C>T (p.Ser281=) single nucleotide variant Malignant melanoma [RCV000070506] Chr14:24056371 [GRCh38]
Chr14:24525580 [GRCh37]
Chr14:23595420 [NCBI36]
Chr14:14q11.2
not provided
NM_138360.3(LRRC16B):c.844C>T (p.His282Tyr) single nucleotide variant Malignant melanoma [RCV000070507] Chr14:24056372 [GRCh38]
Chr14:24525581 [GRCh37]
Chr14:23595421 [NCBI36]
Chr14:14q11.2
not provided
NM_006032.3(CPNE6):c.229C>T (p.Leu77Phe) single nucleotide variant Malignant melanoma [RCV000062737] Chr14:24073559 [GRCh38]
Chr14:24542768 [GRCh37]
Chr14:23612608 [NCBI36]
Chr14:14q11.2
not provided
NM_006032.3(CPNE6):c.228C>T (p.Ala76=) single nucleotide variant Malignant melanoma [RCV000062736] Chr14:24073558 [GRCh38]
Chr14:24542767 [GRCh37]
Chr14:23612607 [NCBI36]
Chr14:14q11.2
not provided
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33
pathogenic
GRCh38/hg38 14q11.2-12(chr14:20412587-25018120)x3 copy number gain See cases [RCV000137725] Chr14:20412587..25018120 [GRCh38]
Chr14:20880746..25487326 [GRCh37]
Chr14:19950586..24557166 [NCBI36]
Chr14:14q11.2-12
likely pathogenic
GRCh38/hg38 14q11.2-12(chr14:23984065-25374494)x1 copy number loss See cases [RCV000142873] Chr14:23984065..25374494 [GRCh38]
Chr14:24453274..25843700 [GRCh37]
Chr14:23523114..24913540 [NCBI36]
Chr14:14q11.2-12
pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33
pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20022693-44093672)x3 copy number gain See cases [RCV000143186] Chr14:20022693..44093672 [GRCh38]
Chr14:20490852..44562875 [GRCh37]
Chr14:19560692..43632625 [NCBI36]
Chr14:14q11.2-21.2
pathogenic
GRCh38/hg38 14q11.2-21.3(chr14:20043513-48642042)x3 copy number gain See cases [RCV000143748] Chr14:20043513..48642042 [GRCh38]
Chr14:20511672..49111245 [GRCh37]
Chr14:19581512..48180995 [NCBI36]
Chr14:14q11.2-21.3
pathogenic
GRCh37/hg19 14q11.2-12(chr14:19100682-28730087) copy number gain not provided [RCV000767822] Chr14:19100682..28730087 [GRCh37]
Chr14:14q11.2-12
pathogenic
GRCh37/hg19 14q11.2-12(chr14:19794561-27768254)x3 copy number gain See cases [RCV000240285] Chr14:19794561..27768254 [GRCh37]
Chr14:14q11.2-12
pathogenic
GRCh37/hg19 14q11.2-22.2(chr14:23164384-54733411)x3 copy number gain See cases [RCV000447658] Chr14:23164384..54733411 [GRCh37]
Chr14:14q11.2-22.2
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q11.2-13.1(chr14:19794561-34049214)x3 copy number gain See cases [RCV000448273] Chr14:19794561..34049214 [GRCh37]
Chr14:14q11.2-13.1
pathogenic
GRCh37/hg19 14q11.2-12(chr14:24233721-31377083)x1 copy number loss See cases [RCV000510673] Chr14:24233721..31377083 [GRCh37]
Chr14:14q11.2-12
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33
pathogenic
GRCh37/hg19 14q11.2-12(chr14:24505708-24601038)x1 copy number loss not provided [RCV000995269] Chr14:24505708..24601038 [GRCh37]
Chr14:14q11.2-12
uncertain significance
GRCh37/hg19 14q11.2-21.2(chr14:20511672-44829030)x3 copy number gain not provided [RCV001006605] Chr14:20511672..44829030 [GRCh37]
Chr14:14q11.2-21.2
pathogenic
GRCh37/hg19 14q11.2-21.1(chr14:20511672-42881888)x3 copy number gain not provided [RCV001249358] Chr14:20511672..42881888 [GRCh37]
Chr14:14q11.2-21.1
not provided
GRCh37/hg19 14q11.2-12(chr14:24163771-24818728)x3 copy number gain not provided [RCV001259179] Chr14:24163771..24818728 [GRCh37]
Chr14:14q11.2-12
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20272 AgrOrtholog
COSMIC CARMIL3 COSMIC
Ensembl Genes ENSG00000186648 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000284765 UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000340467 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000493710 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000342740 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000646442 UniProtKB/Swiss-Prot
Gene3D-CATH 2.30.29.30 UniProtKB/Swiss-Prot
  3.80.10.10 UniProtKB/Swiss-Prot
GTEx ENSG00000186648 GTEx
  ENSG00000284765 GTEx
HGNC ID HGNC:20272 ENTREZGENE
Human Proteome Map CARMIL3 Human Proteome Map
InterPro CARMIL3 UniProtKB/Swiss-Prot
  CARMIL_C UniProtKB/Swiss-Prot
  CARMIL_PH UniProtKB/Swiss-Prot
  Leu-rich_rpt UniProtKB/Swiss-Prot
  LRR_dom_sf UniProtKB/Swiss-Prot
  PH-like_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:90668 UniProtKB/Swiss-Prot
NCBI Gene 90668 ENTREZGENE
OMIM 614716 OMIM
PANTHER PTHR24112:SF43 UniProtKB/Swiss-Prot
Pfam Carm_PH UniProtKB/Swiss-Prot
  CARMIL_C UniProtKB/Swiss-Prot
  LRR_6 UniProtKB/Swiss-Prot
PharmGKB PA162394445 PharmGKB
UniProt CARL3_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary Q8TEF7 UniProtKB/Swiss-Prot
  Q96HS9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-26 CARMIL3  capping protein regulator and myosin 1 linker 3  LRRC16B  leucine rich repeat containing 16B  Symbol and/or name change 5135510 APPROVED