MORN5 (MORN repeat containing 5) - Rat Genome Database

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Gene: MORN5 (MORN repeat containing 5) Homo sapiens
Analyze
Symbol: MORN5
Name: MORN repeat containing 5
RGD ID: 1317107
HGNC Page HGNC:17841
Description: Predicted to be located in sperm flagellum; INTERACTS WITH amiodarone; butanal; entinostat.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C9orf113; C9orf18; FLJ46909; FLJ50034; MORN repeat-containing protein 5; RP11-498E2.5
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
GRCh389122,159,908 - 122,200,083 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9122,159,908 - 122,200,088 (+)EnsemblGRCh38hg38GRCh38
GRCh379124,922,187 - 124,962,362 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369123,962,011 - 124,002,182 (+)NCBINCBI36Build 36hg18NCBI36
Build 349122,001,743 - 122,041,915NCBI
Celera995,570,479 - 95,610,667 (+)NCBICelera
Cytogenetic Map9q33.2NCBI
HuRef994,536,958 - 94,577,149 (+)NCBIHuRef
CHM1_19125,070,254 - 125,110,422 (+)NCBICHM1_1
T2T-CHM13v2.09134,357,378 - 134,397,571 (+)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
motile cilium  (IEA)
sperm flagellum  (IEA,ISS)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:20583170   PMID:24665060   PMID:28514442   PMID:32296183   PMID:33961781  


Genomics

Comparative Map Data
MORN5
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389122,159,908 - 122,200,083 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl9122,159,908 - 122,200,088 (+)EnsemblGRCh38hg38GRCh38
GRCh379124,922,187 - 124,962,362 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 369123,962,011 - 124,002,182 (+)NCBINCBI36Build 36hg18NCBI36
Build 349122,001,743 - 122,041,915NCBI
Celera995,570,479 - 95,610,667 (+)NCBICelera
Cytogenetic Map9q33.2NCBI
HuRef994,536,958 - 94,577,149 (+)NCBIHuRef
CHM1_19125,070,254 - 125,110,422 (+)NCBICHM1_1
T2T-CHM13v2.09134,357,378 - 134,397,571 (+)NCBIT2T-CHM13v2.0
Morn5
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39235,939,485 - 35,969,721 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl235,939,470 - 35,969,730 (+)EnsemblGRCm39 Ensembl
GRCm38236,049,473 - 36,079,709 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl236,049,458 - 36,079,718 (+)EnsemblGRCm38mm10GRCm38
MGSCv37235,904,993 - 35,935,229 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36235,871,482 - 35,901,718 (+)NCBIMGSCv36mm8
Celera235,753,180 - 35,783,430 (+)NCBICelera
Cytogenetic Map2BNCBI
cM Map224.15NCBI
Morn5
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8339,799,531 - 39,827,482 (+)NCBIGRCr8
mRatBN7.2319,402,221 - 19,430,075 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl319,401,801 - 19,430,083 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx322,480,719 - 22,508,543 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0331,065,643 - 31,093,468 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0329,312,911 - 29,340,721 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0315,379,109 - 15,407,252 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl315,379,109 - 15,407,252 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0320,688,321 - 20,716,464 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4315,161,871 - 15,190,016 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1315,058,636 - 15,086,516 (+)NCBI
Celera314,114,197 - 14,142,356 (+)NCBICelera
Cytogenetic Map3p11NCBI
Morn5
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554195,859,718 - 5,903,198 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554195,859,596 - 5,903,296 (-)NCBIChiLan1.0ChiLan1.0
MORN5
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21117,146,722 - 17,187,412 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1917,149,068 - 17,189,761 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0993,284,583 - 93,325,008 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.19121,625,783 - 121,665,725 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl9121,625,783 - 121,665,725 (+)Ensemblpanpan1.1panPan2
MORN5
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1960,367,298 - 60,405,075 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl960,375,742 - 60,405,188 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha959,562,692 - 59,599,608 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0961,282,406 - 61,319,312 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl961,290,859 - 61,320,054 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1960,056,537 - 60,093,673 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0960,372,884 - 60,410,136 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0960,461,909 - 60,499,172 (-)NCBIUU_Cfam_GSD_1.0
Morn5
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404947190,788,741 - 190,866,460 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648710,556,968 - 10,589,813 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648710,557,296 - 10,589,529 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MORN5
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1262,258,298 - 262,295,533 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11262,258,133 - 262,295,132 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21294,559,787 - 294,594,852 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MORN5
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11217,395,246 - 17,434,466 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1217,395,065 - 17,434,438 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603525,614,770 - 25,654,121 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Morn5
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462476013,089,138 - 13,131,599 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462476013,093,161 - 13,131,698 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MORN5
6 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000050348] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121112395-138075224)x3 copy number gain See cases [RCV000051009] Chr9:121112395..138075224 [GRCh38]
Chr9:123874673..140969676 [GRCh37]
Chr9:122914494..140089497 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9q33.2-33.3(chr9:120938041-123469664)x1 copy number loss See cases [RCV000052922] Chr9:120938041..123469664 [GRCh38]
Chr9:123700319..126231943 [GRCh37]
Chr9:122740140..125271764 [NCBI36]
Chr9:9q33.2-33.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 copy number gain See cases [RCV000053745] Chr9:193412..138124532 [GRCh38]
Chr9:204193..141018984 [GRCh37]
Chr9:194193..140138805 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3 copy number gain See cases [RCV000053746] Chr9:193412..138114463 [GRCh38]
Chr9:214367..141008915 [GRCh37]
Chr9:204367..140128736 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053748]|See cases [RCV000053748] Chr9:193412..138179445 [GRCh38]
Chr9:266045..141073897 [GRCh37]
Chr9:256045..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121586837-138179445)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053776]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053776]|See cases [RCV000053776] Chr9:121586837..138179445 [GRCh38]
Chr9:124349116..141073897 [GRCh37]
Chr9:123388937..140193718 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
NM_001286828.1(MORN5):c.*36+9800G>A single nucleotide variant Lung cancer [RCV000108160] Chr9:122184427 [GRCh38]
Chr9:124946706 [GRCh37]
Chr9:9q33.2		 uncertain significance
GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445) copy number gain See cases [RCV000133791] Chr9:204193..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3 copy number gain See cases [RCV000134920] Chr9:121073102..138179445 [GRCh38]
Chr9:123835380..141073897 [GRCh37]
Chr9:122875201..140193718 [NCBI36]
Chr9:9q33.2-34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3 copy number gain See cases [RCV000138783] Chr9:193412..138124524 [GRCh38]
Chr9:204090..141018976 [GRCh37]
Chr9:194090..140138797 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000139207] Chr9:193412..138159073 [GRCh38]
Chr9:68420641..141053525 [GRCh37]
Chr9:67910461..140173346 [NCBI36]
Chr9:9p11.2-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3 copy number gain See cases [RCV000138962] Chr9:193412..138159073 [GRCh38]
Chr9:204104..141053525 [GRCh37]
Chr9:194104..140173346 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic|conflicting data from submitters
GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 copy number gain See cases [RCV000141876] Chr9:203861..138125937 [GRCh38]
Chr9:203861..141020389 [GRCh37]
Chr9:193861..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3 copy number gain See cases [RCV000143476] Chr9:203862..138125937 [GRCh38]
Chr9:203862..141020389 [GRCh37]
Chr9:193862..140140210 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 copy number gain See cases [RCV000148113] Chr9:193412..138179445 [GRCh38]
Chr9:204193..141073897 [GRCh37]
Chr9:194193..140193718 [NCBI36]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3 copy number gain See cases [RCV000240081] Chr9:163131..141122114 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407) copy number gain See cases [RCV000449375] Chr9:62525..141006407 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3 copy number gain not specified [RCV003986800] Chr9:203861..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203864-141020389)x3 copy number gain See cases [RCV000448978] Chr9:203864..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q31.1-33.3(chr9:104604851-126253089)x1 copy number loss See cases [RCV000447763] Chr9:104604851..126253089 [GRCh37]
Chr9:9q31.1-33.3		 pathogenic
GRCh37/hg19 9q33.2-34.3(chr9:124642754-141146461)x3 copy number gain See cases [RCV000448784] Chr9:124642754..141146461 [GRCh37]
Chr9:9q33.2-34.3		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928) copy number gain Global developmental delay [RCV000626548] Chr9:71069743..140999928 [GRCh37]
Chr9:9q21.11-34.3		 likely pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389) copy number gain See cases [RCV000512392] Chr9:203862..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141122247)x3 copy number gain not provided [RCV000748055] Chr9:10590..141122247 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q31.3-33.3(chr9:113083182-126779494)x1 copy number loss not provided [RCV000748606] Chr9:113083182..126779494 [GRCh37]
Chr9:9q31.3-33.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141107672)x3 copy number gain not provided [RCV000748053] Chr9:10590..141107672 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:46587-141066491)x3 copy number gain not provided [RCV000748063] Chr9:46587..141066491 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:10590-141114095)x2 copy number gain not provided [RCV000748054] Chr9:10590..141114095 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3 copy number gain not provided [RCV000847808] Chr9:71416475..141020389 [GRCh37]
Chr9:9q21.11-34.3		 pathogenic
GRCh37/hg19 9q33.2-33.3(chr9:124604592-126306080)x1 copy number loss not provided [RCV001006270] Chr9:124604592..126306080 [GRCh37]
Chr9:9q33.2-33.3		 uncertain significance
GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3 copy number gain not provided [RCV000845900] Chr9:203861..141020388 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q31.1-33.3(chr9:104604851-126253089) copy number loss not specified [RCV002052825] Chr9:104604851..126253089 [GRCh37]
Chr9:9q31.1-33.3		 pathogenic
GRCh37/hg19 9q33.1-33.3(chr9:120045175-127335905)x1 copy number loss not provided [RCV001834516] Chr9:120045175..127335905 [GRCh37]
Chr9:9q33.1-33.3		 pathogenic
GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389) copy number gain not specified [RCV002053823] Chr9:353349..141020389 [GRCh37]
Chr9:9p24.3-q34.3		 pathogenic
GRCh37/hg19 9q32-34.11(chr9:116422275-131713233) copy number gain not specified [RCV002052831] Chr9:116422275..131713233 [GRCh37]
Chr9:9q32-34.11		 pathogenic
GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3 copy number gain See cases [RCV002292402] Chr9:203861..131603223 [GRCh37]
Chr9:9p24.3-q34.11		 pathogenic
GRCh37/hg19 9q33.2-33.3(chr9:124018736-129995568)x1 copy number loss not provided [RCV002474540] Chr9:124018736..129995568 [GRCh37]
Chr9:9q33.2-33.3		 pathogenic
NM_198469.4(MORN5):c.-2C>T single nucleotide variant not provided [RCV002512387] Chr9:122159971 [GRCh38]
Chr9:124922250 [GRCh37]
Chr9:9q33.2		 benign
NM_198469.4(MORN5):c.5A>G (p.Glu2Gly) single nucleotide variant Inborn genetic diseases [RCV002845130] Chr9:122159977 [GRCh38]
Chr9:124922256 [GRCh37]
Chr9:9q33.2		 uncertain significance
NM_198469.4(MORN5):c.151G>C (p.Gly51Arg) single nucleotide variant Inborn genetic diseases [RCV002915453] Chr9:122166871 [GRCh38]
Chr9:124929150 [GRCh37]
Chr9:9q33.2		 uncertain significance
NM_198469.4(MORN5):c.326A>G (p.Asn109Ser) single nucleotide variant Inborn genetic diseases [RCV002986072] Chr9:122174514 [GRCh38]
Chr9:124936793 [GRCh37]
Chr9:9q33.2		 uncertain significance
NM_198469.4(MORN5):c.395C>A (p.Thr132Lys) single nucleotide variant Inborn genetic diseases [RCV003308696] Chr9:122174583 [GRCh38]
Chr9:124936862 [GRCh37]
Chr9:9q33.2		 uncertain significance
GRCh37/hg19 9q33.2-33.3(chr9:122755951-127551056)x1 copy number loss not specified [RCV003986827] Chr9:122755951..127551056 [GRCh37]
Chr9:9q33.2-33.3		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:947
Count of miRNA genes:649
Interacting mature miRNAs:729
Transcripts:ENST00000373764, ENST00000418632, ENST00000477017, ENST00000486801, ENST00000536616
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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

Markers in Region
SHGC-145840  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh379124,949,362 - 124,949,701UniSTSGRCh37
Build 369123,989,183 - 123,989,522RGDNCBI36
Celera995,597,647 - 95,597,986RGD
Cytogenetic Map9q33.2UniSTS
HuRef994,564,129 - 94,564,468UniSTS


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 pharyngeal arch
High
Medium 716 1 6 30 73 132 7 438 117
Low 1057 40 345 13 44 8 79 759 2758 195 650 428 7 1 12 54 2
Below cutoff 412 1272 698 213 380 106 2065 553 613 135 258 657 113 685 1282

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000373764   ⟹   ENSP00000362869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9122,159,908 - 122,200,083 (+)Ensembl
RefSeq Acc Id: ENST00000418632   ⟹   ENSP00000409949
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9122,164,615 - 122,174,568 (+)Ensembl
RefSeq Acc Id: ENST00000477017
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9122,169,661 - 122,174,754 (+)Ensembl
RefSeq Acc Id: ENST00000486801
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9122,166,768 - 122,200,083 (+)Ensembl
RefSeq Acc Id: ENST00000536616   ⟹   ENSP00000437483
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl9122,159,908 - 122,200,088 (+)Ensembl
RefSeq Acc Id: NM_001286828   ⟹   NP_001273757
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389122,159,908 - 122,200,083 (+)NCBI
HuRef994,536,955 - 94,577,149 (+)NCBI
CHM1_19125,070,251 - 125,110,422 (+)NCBI
T2T-CHM13v2.09134,357,378 - 134,397,571 (+)NCBI
Sequence:
RefSeq Acc Id: NM_198469   ⟹   NP_940871
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh389122,159,908 - 122,200,083 (+)NCBI
GRCh379124,922,190 - 124,962,368 (+)NCBI
Build 369123,962,011 - 124,002,182 (+)NCBI Archive
Celera995,570,479 - 95,610,667 (+)RGD
HuRef994,536,955 - 94,577,149 (+)NCBI
CHM1_19125,070,251 - 125,110,422 (+)NCBI
T2T-CHM13v2.09134,357,378 - 134,397,571 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_940871   ⟸   NM_198469
- Peptide Label: isoform a
- UniProtKB: B7Z7I5 (UniProtKB/Swiss-Prot),   Q6ZQN1 (UniProtKB/Swiss-Prot),   Q5VZ52 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001273757   ⟸   NM_001286828
- Peptide Label: isoform b
- UniProtKB: A0A0A0MTF6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000362869   ⟸   ENST00000373764
RefSeq Acc Id: ENSP00000437483   ⟸   ENST00000536616
RefSeq Acc Id: ENSP00000409949   ⟸   ENST00000418632

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5VZ52-F1-model_v2 AlphaFold Q5VZ52 1-161 view protein structure

Promoters
RGD ID:7216057
Promoter ID:EPDNEW_H13775
Type:initiation region
Name:MORN5_1
Description:MORN repeat containing 5
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh389122,159,908 - 122,159,968EPDNEW
RGD ID:6807885
Promoter ID:HG_KWN:64795
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_198469,   OTTHUMT00000053909
Position:
Human AssemblyChrPosition (strand)Source
Build 369123,961,151 - 123,961,957 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:17841 AgrOrtholog
COSMIC MORN5 COSMIC
Ensembl Genes ENSG00000185681 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000373764 ENTREZGENE
  ENST00000373764.8 UniProtKB/Swiss-Prot
  ENST00000418632.1 UniProtKB/TrEMBL
  ENST00000536616 ENTREZGENE
  ENST00000536616.5 UniProtKB/TrEMBL
Gene3D-CATH Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000185681 GTEx
HGNC ID HGNC:17841 ENTREZGENE
Human Proteome Map MORN5 Human Proteome Map
InterPro MORN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Morn5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:254956 UniProtKB/Swiss-Prot
NCBI Gene 254956 ENTREZGENE
OMIM 619837 OMIM
PANTHER MORN REPEAT-CONTAINING PROTEIN 5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR46437 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MORN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25975 PharmGKB
SMART MORN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Histone H3 K4-specific methyltransferase SET7/9 N-terminal domain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A0MTF6 ENTREZGENE, UniProtKB/TrEMBL
  B7Z7I5 ENTREZGENE
  MORN5_HUMAN UniProtKB/Swiss-Prot
  Q5T7S4_HUMAN UniProtKB/TrEMBL
  Q5VZ52 ENTREZGENE
  Q6ZQN1 ENTREZGENE
UniProt Secondary B7Z7I5 UniProtKB/Swiss-Prot
  Q6ZQN1 UniProtKB/Swiss-Prot