TMEM179B (transmembrane protein 179B) - Rat Genome Database

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Gene: TMEM179B (transmembrane protein 179B) Homo sapiens
Analyze
Symbol: TMEM179B
Name: transmembrane protein 179B
RGD ID: 1601691
HGNC Page HGNC:33744
Description: Located in nuclear speck and nucleolus.
Type: protein-coding
RefSeq Status: VALIDATED
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381162,787,402 - 62,790,400 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1162,787,402 - 62,790,400 (+)EnsemblGRCh38hg38GRCh38
GRCh371162,554,874 - 62,557,872 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361162,311,450 - 62,314,448 (+)NCBINCBI36Build 36hg18NCBI36
Celera1159,883,458 - 59,886,456 (+)NCBICelera
Cytogenetic Map11q12.3NCBI
HuRef1158,883,899 - 58,886,898 (+)NCBIHuRef
CHM1_11162,437,956 - 62,440,954 (+)NCBICHM1_1
T2T-CHM13v2.01162,776,793 - 62,779,792 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:11053263   PMID:12477932   PMID:22939629   PMID:26186194   PMID:28514442   PMID:31318583   PMID:32296183   PMID:32393512   PMID:33961781   PMID:35271311   PMID:36949045  


Genomics

Comparative Map Data
TMEM179B
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381162,787,402 - 62,790,400 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1162,787,402 - 62,790,400 (+)EnsemblGRCh38hg38GRCh38
GRCh371162,554,874 - 62,557,872 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361162,311,450 - 62,314,448 (+)NCBINCBI36Build 36hg18NCBI36
Celera1159,883,458 - 59,886,456 (+)NCBICelera
Cytogenetic Map11q12.3NCBI
HuRef1158,883,899 - 58,886,898 (+)NCBIHuRef
CHM1_11162,437,956 - 62,440,954 (+)NCBICHM1_1
T2T-CHM13v2.01162,776,793 - 62,779,792 (+)NCBIT2T-CHM13v2.0
Tmem179b
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39198,749,886 - 8,751,831 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl198,749,889 - 8,751,831 (-)EnsemblGRCm39 Ensembl
GRCm38198,772,522 - 8,774,467 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl198,772,525 - 8,774,467 (-)EnsemblGRCm38mm10GRCm38
MGSCv37198,847,012 - 8,848,957 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36198,839,574 - 8,841,487 (-)NCBIMGSCv36mm8
Celera198,532,413 - 8,534,358 (-)NCBICelera
Cytogenetic Map19ANCBI
cM Map195.55NCBI
Tmem179b
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81215,099,245 - 215,101,231 (-)NCBIGRCr8
mRatBN7.21205,670,126 - 205,672,112 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1205,666,744 - 205,672,112 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1214,078,544 - 214,080,530 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01221,113,677 - 221,115,663 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01213,806,380 - 213,808,366 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01224,972,218 - 224,975,091 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1224,972,218 - 224,974,203 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01231,910,390 - 231,912,736 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41211,443,288 - 211,445,273 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1203,183,056 - 203,185,041 (-)NCBICelera
Cytogenetic Map1q43NCBI
TMEM179B
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2964,012,488 - 64,015,351 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11165,055,181 - 65,058,043 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01158,142,806 - 58,145,668 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11161,498,409 - 61,499,816 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1161,498,409 - 61,499,816 (+)Ensemblpanpan1.1panPan2
TMEM179B
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11853,896,518 - 53,898,716 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1853,896,518 - 53,898,659 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1852,502,559 - 52,504,761 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01854,948,986 - 54,951,188 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1854,946,941 - 54,951,142 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11854,045,602 - 54,047,804 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01853,620,063 - 53,622,265 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01854,416,326 - 54,418,528 (-)NCBIUU_Cfam_GSD_1.0
Tmem179b
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494710,388,816 - 10,390,927 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936581498,178 - 504,853 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936581502,562 - 504,826 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMEM179B
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl28,983,759 - 8,986,080 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.128,983,822 - 8,986,106 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.228,329,062 - 8,331,346 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TMEM179B
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1111,113,066 - 11,115,863 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl111,113,254 - 11,115,771 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038108,456,115 - 108,458,713 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tmem179b
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046249261,244,780 - 1,246,469 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TMEM179B
12 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q12.3(chr11:62433886-63096003)x3 copy number gain See cases [RCV000053620] Chr11:62433886..63096003 [GRCh38]
Chr11:62201358..62863475 [GRCh37]
Chr11:61957934..62620051 [NCBI36]
Chr11:11q12.3		 pathogenic
GRCh38/hg38 11q12.3(chr11:62452571-62862781)x3 copy number gain See cases [RCV000053621] Chr11:62452571..62862781 [GRCh38]
Chr11:62220043..62630253 [GRCh37]
Chr11:61976619..62386829 [NCBI36]
Chr11:11q12.3		 pathogenic
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh38/hg38 11q12.3(chr11:62562836-62840570)x3 copy number gain See cases [RCV000134807] Chr11:62562836..62840570 [GRCh38]
Chr11:62330308..62608042 [GRCh37]
Chr11:62086884..62364618 [NCBI36]
Chr11:11q12.3		 uncertain significance
GRCh38/hg38 11q12.3(chr11:62249520-62946093)x3 copy number gain See cases [RCV000138411] Chr11:62249520..62946093 [GRCh38]
Chr11:62016992..62713565 [GRCh37]
Chr11:61773568..62470141 [NCBI36]
Chr11:11q12.3		 pathogenic
GRCh37/hg19 11q12.3(chr11:61840997-62987330)x1 copy number loss See cases [RCV000448355] Chr11:61840997..62987330 [GRCh37]
Chr11:11q12.3		 likely pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11q12.3(chr11:62314663-62788240)x3 copy number gain not provided [RCV000849841] Chr11:62314663..62788240 [GRCh37]
Chr11:11q12.3		 uncertain significance
GRCh37/hg19 11q12.3(chr11:62487052-62788240)x3 copy number gain not provided [RCV000846292] Chr11:62487052..62788240 [GRCh37]
Chr11:11q12.3		 uncertain significance
NC_000011.9:g.(?_59596957)_(68707199_?)dup duplication Familial temporal lobe epilepsy 8 [RCV001372442] Chr11:59596957..68707199 [GRCh37]
Chr11:11q12.1-13.3		 uncertain significance
NC_000011.9:g.(?_58916346)_(64972349_?)dup duplication Leukocyte adhesion deficiency 3 [RCV003113394]|not provided [RCV003113393] Chr11:58916346..64972349 [GRCh37]
Chr11:11q12.1-13.1		 uncertain significance|no classifications from unflagged records
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
NM_199337.3(TMEM179B):c.644G>A (p.Arg215His) single nucleotide variant not specified [RCV004237804] Chr11:62790031 [GRCh38]
Chr11:62557503 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.304A>G (p.Ile102Val) single nucleotide variant not specified [RCV004125003] Chr11:62789311 [GRCh38]
Chr11:62556783 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.169C>T (p.Pro57Ser) single nucleotide variant not specified [RCV004159952] Chr11:62789095 [GRCh38]
Chr11:62556567 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.31C>G (p.Leu11Val) single nucleotide variant not specified [RCV004218153] Chr11:62787462 [GRCh38]
Chr11:62554934 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.461C>G (p.Thr154Ser) single nucleotide variant not specified [RCV004163223] Chr11:62789642 [GRCh38]
Chr11:62557114 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.286G>C (p.Gly96Arg) single nucleotide variant not specified [RCV004203641] Chr11:62789293 [GRCh38]
Chr11:62556765 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.452C>T (p.Pro151Leu) single nucleotide variant not specified [RCV004131542] Chr11:62789633 [GRCh38]
Chr11:62557105 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.37C>G (p.Leu13Val) single nucleotide variant not specified [RCV004179520] Chr11:62787468 [GRCh38]
Chr11:62554940 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.517T>A (p.Leu173Met) single nucleotide variant not specified [RCV004254830] Chr11:62789904 [GRCh38]
Chr11:62557376 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.549G>C (p.Gln183His) single nucleotide variant not specified [RCV004275020] Chr11:62789936 [GRCh38]
Chr11:62557408 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.22C>A (p.Arg8Ser) single nucleotide variant not specified [RCV004329353] Chr11:62787453 [GRCh38]
Chr11:62554925 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.481A>G (p.Asn161Asp) single nucleotide variant not specified [RCV004354093] Chr11:62789662 [GRCh38]
Chr11:62557134 [GRCh37]
Chr11:11q12.3		 uncertain significance
GRCh37/hg19 11q12.2-13.5(chr11:59923608-76272324)x3 copy number gain not provided [RCV003484842] Chr11:59923608..76272324 [GRCh37]
Chr11:11q12.2-13.5		 pathogenic
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3 copy number gain not specified [RCV003986944] Chr11:56895955..69295402 [GRCh37]
Chr11:11q12.1-13.3		 likely pathogenic
GRCh37/hg19 11p11.12-q13.1(chr11:50398499-63924462)x3 copy number gain not specified [RCV003986918] Chr11:50398499..63924462 [GRCh37]
Chr11:11p11.12-q13.1		 likely pathogenic
NM_199337.3(TMEM179B):c.269T>C (p.Ile90Thr) single nucleotide variant not specified [RCV004475375] Chr11:62789195 [GRCh38]
Chr11:62556667 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.34G>C (p.Ala12Pro) single nucleotide variant not specified [RCV004475376] Chr11:62787465 [GRCh38]
Chr11:62554937 [GRCh37]
Chr11:11q12.3		 uncertain significance
NM_199337.3(TMEM179B):c.509G>C (p.Trp170Ser) single nucleotide variant not specified [RCV004475377] Chr11:62789896 [GRCh38]
Chr11:62557368 [GRCh37]
Chr11:11q12.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1118
Count of miRNA genes:507
Interacting mature miRNAs:568
Transcripts:ENST00000333449, ENST00000526546, ENST00000532345, ENST00000532586, ENST00000533861
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
STS-W92041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371162,553,612 - 62,553,783UniSTSGRCh37
Build 361162,310,188 - 62,310,359RGDNCBI36
Celera1159,882,196 - 59,882,367RGD
Cytogenetic Map11q12.3UniSTS
HuRef1158,882,637 - 58,882,808UniSTS
GeneMap99-GB4 RH Map11230.64UniSTS
NCBI RH Map11563.0UniSTS


Expression


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

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2438 2890 1717 616 1937 457 4265 2019 3512 416 1460 1612 175 1 1204 2696 6 2
Low 1 101 9 8 14 8 92 178 222 3 1 92
Below cutoff

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000333449   ⟹   ENSP00000333697
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,787,402 - 62,790,400 (+)Ensembl
RefSeq Acc Id: ENST00000526546   ⟹   ENSP00000436606
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,789,169 - 62,789,823 (+)Ensembl
RefSeq Acc Id: ENST00000532345
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,789,060 - 62,790,110 (+)Ensembl
RefSeq Acc Id: ENST00000532586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,787,415 - 62,790,167 (+)Ensembl
RefSeq Acc Id: ENST00000533861   ⟹   ENSP00000433055
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1162,787,415 - 62,790,246 (+)Ensembl
RefSeq Acc Id: NM_001363599   ⟹   NP_001350528
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,787,402 - 62,790,400 (+)NCBI
T2T-CHM13v2.01162,776,793 - 62,779,792 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363600   ⟹   NP_001350529
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,787,402 - 62,790,400 (+)NCBI
T2T-CHM13v2.01162,776,793 - 62,779,792 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001363601   ⟹   NP_001350530
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,787,402 - 62,790,400 (+)NCBI
T2T-CHM13v2.01162,776,793 - 62,779,792 (+)NCBI
Sequence:
RefSeq Acc Id: NM_199337   ⟹   NP_955369
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,787,402 - 62,790,400 (+)NCBI
GRCh371162,554,281 - 62,557,872 (+)NCBI
Build 361162,311,450 - 62,314,448 (+)NCBI Archive
Celera1159,883,458 - 59,886,456 (+)RGD
HuRef1158,883,899 - 58,886,898 (+)RGD
CHM1_11162,437,956 - 62,440,954 (+)NCBI
T2T-CHM13v2.01162,776,793 - 62,779,792 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_955369   ⟸   NM_199337
- Peptide Label: isoform 1 precursor
- UniProtKB: Q7Z7N9 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001350530   ⟸   NM_001363601
- Peptide Label: isoform 4
RefSeq Acc Id: NP_001350528   ⟸   NM_001363599
- Peptide Label: isoform 2 precursor
- UniProtKB: G3V185 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001350529   ⟸   NM_001363600
- Peptide Label: isoform 3 precursor
RefSeq Acc Id: ENSP00000333697   ⟸   ENST00000333449
RefSeq Acc Id: ENSP00000433055   ⟸   ENST00000533861
RefSeq Acc Id: ENSP00000436606   ⟸   ENST00000526546

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7Z7N9-F1-model_v2 AlphaFold Q7Z7N9 1-219 view protein structure

Promoters
RGD ID:6789450
Promoter ID:HG_KWN:13135
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_199337
Position:
Human AssemblyChrPosition (strand)Source
Build 361162,310,621 - 62,311,707 (+)MPROMDB
RGD ID:7220725
Promoter ID:EPDNEW_H16108
Type:initiation region
Name:TMEM179B_1
Description:transmembrane protein 179B
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381162,787,402 - 62,787,462EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:33744 AgrOrtholog
COSMIC TMEM179B COSMIC
Ensembl Genes ENSG00000185475 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000333449 ENTREZGENE
  ENST00000333449.9 UniProtKB/Swiss-Prot
  ENST00000526546.1 UniProtKB/TrEMBL
  ENST00000533861 ENTREZGENE
  ENST00000533861.5 UniProtKB/TrEMBL
GTEx ENSG00000185475 GTEx
HGNC ID HGNC:33744 ENTREZGENE
Human Proteome Map TMEM179B Human Proteome Map
InterPro TMEM179B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:374395 UniProtKB/Swiss-Prot
NCBI Gene 374395 ENTREZGENE
PANTHER PTHR31056 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TRANSMEMBRANE PROTEIN 179B UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162405996 PharmGKB
UniProt G3V185 ENTREZGENE, UniProtKB/TrEMBL
  H0YEV1_HUMAN UniProtKB/TrEMBL
  Q7Z7N9 ENTREZGENE, UniProtKB/Swiss-Prot