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Gene: MRPL32 (mitochondrial ribosomal protein L32) Homo sapiens

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Symbol:

MRPL32

Name:

mitochondrial ribosomal protein L32

RGD ID:

1321503

HGNC Page

HGNC:14035

Description:

Enables RNA binding activity. Predicted to be involved in mitochondrial translation. Located in mitochondrion. Part of mitochondrial large ribosomal subunit.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

39S ribosomal protein L32, mitochondrial; bL32m; bMRP-59b; HSPC283; L32mt; large ribosomal subunit protein bL32m; mitochondrial large ribosomal subunit protein bL32m; MRP-L32

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Mrpl32 (mitochondrial ribosomal protein L32)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Mrpl32 (mitochondrial ribosomal protein L32)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Mrpl32 (mitochondrial ribosomal protein L32)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	MRPL32 (mitochondrial ribosomal protein L32)	NCBI	Ortholog
Canis lupus familiaris (dog):	MRPL32 (mitochondrial ribosomal protein L32)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, OrthoMCL, Panther, PhylomeDB, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Mrpl32 (mitochondrial ribosomal protein L32)	NCBI	Ortholog
Sus scrofa (pig):	MRPL32 (mitochondrial ribosomal protein L32)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	MRPL32 (mitochondrial ribosomal protein L32)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Mrpl32 (mitochondrial ribosomal protein L32)	NCBI	Ortholog
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Mrpl32 (mitochondrial ribosomal protein L32)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Mrpl32 (mitochondrial ribosomal protein L32)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	mrpl32 (mitochondrial ribosomal protein L32)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Saccharomyces cerevisiae (baker's yeast):	MRPL32	Alliance	DIOPT (Ensembl Compara\|InParanoid\|OrthoFinder\|PANTHER\|PhylomeDB\|SonicParanoid)
Drosophila melanogaster (fruit fly):	mRpL32	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Caenorhabditis elegans (roundworm):	mrpl-32	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	mrpl32	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Xenopus laevis (African clawed frog):	mrpl32.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	mrpl32.S	Alliance	DIOPT (Xenbase)

Related Pseudogenes:

MRPL32P1 MRPL32P2

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	42,932,376 - 42,937,857 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	42,932,376 - 42,948,958 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	42,971,975 - 42,977,456 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	42,938,464 - 42,943,981 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	42,745,178 - 42,750,691	NCBI
Celera	7	42,962,246 - 42,967,760 (+)	NCBI		Celera
Cytogenetic Map	7	p14.1	NCBI
HuRef	7	42,856,743 - 42,862,257 (+)	NCBI		HuRef
CHM1_1	7	42,975,485 - 42,981,003 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	7	43,090,506 - 43,095,986 (+)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	43,011,437 - 43,016,951 (+)	NCBI

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

pleomorphic xanthoastrocytoma (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

2,6-dinitrotoluene (ISO)

2-methylcholine (EXP)

3-chloropropane-1,2-diol (ISO)

4,4'-diaminodiphenylmethane (ISO)

4,4'-sulfonyldiphenol (ISO)

6-propyl-2-thiouracil (ISO)

amitrole (ISO)

arsenite(3-) (ISO)

atrazine (EXP)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

butan-1-ol (EXP)

carbon nanotube (ISO)

chromium(6+) (ISO)

cyclosporin A (EXP)

diclofenac (ISO)

disodium selenite (EXP)

finasteride (ISO)

flutamide (ISO)

folic acid (ISO)

gentamycin (ISO)

hydrogen peroxide (EXP)

ibuprofen (ISO)

isobutanol (EXP)

ketoconazole (EXP)

lipopolysaccharide (EXP)

methamphetamine (ISO)

methimazole (ISO)

mono(2-ethylhexyl) phthalate (EXP)

ozone (ISO)

p-toluidine (ISO)

paracetamol (EXP)

resveratrol (EXP)

sodium arsenite (EXP)

sulfadimethoxine (ISO)

sulindac (ISO)

temozolomide (EXP)

thalidomide (ISO)

titanium dioxide (ISO)

tolcapone (ISO)

trichloroethene (ISO)

valproic acid (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

mitochondrial translation (NAS)

translation (IEA,NAS)

Cellular Component

large ribosomal subunit (IEA)

mitochondrial inner membrane (NAS,TAS)

mitochondrial large ribosomal subunit (IBA,IDA,NAS)

mitochondrial matrix (TAS)

mitochondrial ribosome (NAS)

mitochondrion (HTP,IDA,IEA)

ribonucleoprotein complex (IEA)

ribosome (IEA)

Molecular Function

protein binding (IPI)

RNA binding (HDA)

structural constituent of ribosome (IBA,IEA,NAS)

Phenotype Annotations Click to see Annotation Detail View

Human Phenotype

Pleomorphic xanthoastrocytoma (IAGP)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:8889548	PMID:11279069	PMID:11543634	PMID:11551941	PMID:12446740	PMID:12477932	PMID:12690205	PMID:12706105	PMID:14702039	PMID:15489334	PMID:16341674	PMID:17207965
PMID:20186120	PMID:20877624	PMID:21873635	PMID:22658674	PMID:22939629	PMID:25278503	PMID:25544563	PMID:26186194	PMID:26344197	PMID:26496610	PMID:27023846	PMID:27499296
PMID:28514442	PMID:28892042	PMID:29568061	PMID:29845934	PMID:30033366	PMID:30251372	PMID:31980649	PMID:32296183	PMID:32877691	PMID:33961781	PMID:34578187	PMID:34800366
PMID:35013218	PMID:35235311	PMID:35271311	PMID:35831314	PMID:35944360	PMID:36244648

Genomics

Comparative Map Data

MRPL32
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	7	42,932,376 - 42,937,857 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	7	42,932,376 - 42,948,958 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	7	42,971,975 - 42,977,456 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	7	42,938,464 - 42,943,981 (+)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	7	42,745,178 - 42,750,691	NCBI
Celera	7	42,962,246 - 42,967,760 (+)	NCBI		Celera
Cytogenetic Map	7	p14.1	NCBI
HuRef	7	42,856,743 - 42,862,257 (+)	NCBI		HuRef
CHM1_1	7	42,975,485 - 42,981,003 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	7	43,090,506 - 43,095,986 (+)	NCBI		T2T-CHM13v2.0
CRA_TCAGchr7v2	7	43,011,437 - 43,016,951 (+)	NCBI

Mrpl32
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	13	14,784,886 - 14,787,622 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	13	14,782,769 - 14,787,750 (-)	Ensembl		GRCm39 Ensembl
GRCm38	13	14,610,301 - 14,613,037 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	13	14,608,184 - 14,613,165 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	13	14,702,568 - 14,705,304 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	13	14,402,427 - 14,405,163 (-)	NCBI		MGSCv36	mm8
Celera	13	14,916,683 - 14,919,423 (-)	NCBI		Celera
Cytogenetic Map	13	A1	NCBI
cM Map	13	5.36	NCBI

Mrpl32
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	17	55,260,651 - 55,263,517 (+)	NCBI		GRCr8
mRatBN7.2	17	50,565,133 - 50,568,000 (+)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	17	50,565,055 - 50,568,010 (+)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	17	53,738,050 - 53,740,918 (+)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	17	57,740,969 - 57,743,837 (+)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	17	51,842,088 - 51,844,958 (+)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	17	53,102,534 - 53,105,400 (+)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	17	53,102,534 - 53,105,400 (+)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	17	50,802,293 - 50,805,159 (+)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	17	58,747,047 - 58,749,913 (+)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	17	58,749,915 - 58,752,752 (+)	NCBI
Celera	17	46,597,658 - 46,600,524 (+)	NCBI		Celera
Cytogenetic Map	17	q12.1	NCBI

Mrpl32
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955460	874,769 - 880,694 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955460	875,154 - 880,663 (-)	NCBI	ChiLan1.0	ChiLan1.0

MRPL32
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	6	45,498,032 - 45,503,522 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	7	93,822,745 - 93,828,278 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	7	41,299,092 - 41,304,647 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	7	41,342,701 - 41,348,266 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	7	41,342,706 - 41,348,266 (-)	Ensembl	panpan1.1		panPan2

MRPL32
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	18	7,212,604 - 7,218,051 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	18	7,172,790 - 7,218,036 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	18	7,063,888 - 7,068,898 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	18	7,259,534 - 7,264,990 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	18	7,253,600 - 7,264,977 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	18	7,242,598 - 7,248,043 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	18	7,211,848 - 7,217,297 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	18	7,324,691 - 7,330,096 (-)	NCBI		UU_Cfam_GSD_1.0

Mrpl32
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405118	98,883,494 - 98,887,202 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936478	18,095,154 - 18,099,107 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936478	18,095,227 - 18,098,925 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

MRPL32
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1	18	51,865,077 - 51,909,291 (-)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	18	56,851,935 - 56,857,590 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

MRPL32
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	21	15,666,490 - 15,671,994 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666062	6,816,712 - 6,822,332 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Mrpl32
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624740	18,226,294 - 18,231,090 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624740	18,226,296 - 18,231,120 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in MRPL32
18 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
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 7p14.1-12.3(chr7:39814159-45749735)x1	copy number loss	See cases [RCV000053132]	Chr7:39814159..45749735 [GRCh38] Chr7:39853758..45789334 [GRCh37] Chr7:39820283..45755859 [NCBI36] Chr7:7p14.1-12.3	pathogenic
GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3	copy number gain	See cases [RCV000053532]	Chr7:33328312..62377476 [GRCh38] Chr7:33367924..61831899 [GRCh37] Chr7:33334449..61469334 [NCBI36] Chr7:7p14.3-q11.21	pathogenic
GRCh38/hg38 7p14.1-13(chr7:42388724-43606751)x3	copy number gain	See cases [RCV000053533]	Chr7:42388724..43606751 [GRCh38] Chr7:42428323..43646350 [GRCh37] Chr7:42394848..43612875 [NCBI36] Chr7:7p14.1-13	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 7p14.1-11.2(chr7:40534157-56107122)x1	copy number loss	See cases [RCV000136092]	Chr7:40534157..56107122 [GRCh38] Chr7:40573756..56174815 [GRCh37] Chr7:40540281..56142309 [NCBI36] Chr7:7p14.1-11.2	pathogenic
GRCh38/hg38 7p14.1-12.1(chr7:40020598-50543500)x1	copy number loss	See cases [RCV000136904]	Chr7:40020598..50543500 [GRCh38] Chr7:40060197..50611198 [GRCh37] Chr7:40026722..50578692 [NCBI36] Chr7:7p14.1-12.1	pathogenic
GRCh38/hg38 7p14.1-12.3(chr7:37303478-48660738)x1	copy number loss	See cases [RCV000137139]	Chr7:37303478..48660738 [GRCh38] Chr7:37343082..48700334 [GRCh37] Chr7:37309607..48670880 [NCBI36] Chr7:7p14.1-12.3	pathogenic
GRCh38/hg38 7p14.1-13(chr7:39063400-45363096)x1	copy number loss	See cases [RCV000137305]	Chr7:39063400..45363096 [GRCh38] Chr7:39103000..45402695 [GRCh37] Chr7:39069525..45369220 [NCBI36] Chr7:7p14.1-13	pathogenic
GRCh38/hg38 7p14.1-13(chr7:42452844-43608265)x3	copy number gain	See cases [RCV000139756]	Chr7:42452844..43608265 [GRCh38] Chr7:42492443..43647864 [GRCh37] Chr7:42458968..43614389 [NCBI36] Chr7:7p14.1-13	uncertain significance
GRCh38/hg38 7p14.1-13(chr7:38177999-45304100)x1	copy number loss	See cases [RCV000142297]	Chr7:38177999..45304100 [GRCh38] Chr7:38217601..45343699 [GRCh37] Chr7:38184126..45310224 [NCBI36] Chr7:7p14.1-13	pathogenic
TMEM106B-BRAF fusion	deletion	Pleomorphic xanthoastrocytoma [RCV000454357]	Chr7:12258147..140494267 [GRCh37] Chr7:7p21.3-q34	pathogenic
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 7p14.1-12.3(chr7:40350383-47034422)x1	copy number loss	See cases [RCV000446941]	Chr7:40350383..47034422 [GRCh37] Chr7:7p14.1-12.3	pathogenic
GRCh37/hg19 7p14.3-13(chr7:32911003-44576005)x1	copy number loss	See cases [RCV000446955]	Chr7:32911003..44576005 [GRCh37] Chr7:7p14.3-13	pathogenic
GRCh37/hg19 7p14.1-13(chr7:42417642-43664280)x3	copy number gain	See cases [RCV000448875]	Chr7:42417642..43664280 [GRCh37] Chr7:7p14.1-13	uncertain significance
GRCh37/hg19 7p21.3-12.1(chr7:11048840-52863626)x3	copy number gain	See cases [RCV000512091]	Chr7:11048840..52863626 [GRCh37] Chr7:7p21.3-12.1	pathogenic
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 7p22.3-q36.3(chr7:43361-159119707)x3	copy number gain	See cases [RCV000511549]	Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p14.3-13(chr7:30463886-43470805)x3	copy number gain	not provided [RCV000682909]	Chr7:30463886..43470805 [GRCh37] Chr7:7p14.3-13	pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv	inversion	Childhood apraxia of speech [RCV000234948]	Chr7:21001537..114528369 [GRCh37] Chr7:7p15.3-q31.1	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 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 7p14.1-13(chr7:42417642-43658492)x3	copy number gain	not provided [RCV000848300]	Chr7:42417642..43658492 [GRCh37] Chr7:7p14.1-13	uncertain significance
GRCh37/hg19 7p14.1(chr7:40198215-43252984)x3	copy number gain	not provided [RCV000849081]	Chr7:40198215..43252984 [GRCh37] Chr7:7p14.1	uncertain significance
GRCh37/hg19 7p14.1-13(chr7:42421780-43664397)x3	copy number gain	not provided [RCV000848239]	Chr7:42421780..43664397 [GRCh37] Chr7:7p14.1-13	uncertain significance
GRCh37/hg19 7p14.1-13(chr7:42417642-43658492)x3	copy number gain	not provided [RCV000848253]	Chr7:42417642..43658492 [GRCh37] Chr7:7p14.1-13	uncertain significance
NM_031903.3(MRPL32):c.53G>A (p.Gly18Glu)	single nucleotide variant	not specified [RCV004322267]	Chr7:42932439 [GRCh38] Chr7:42972038 [GRCh37] Chr7:7p14.1	uncertain significance
Single allele	complex	Ring chromosome 7 [RCV002280646]	Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3	pathogenic
GRCh37/hg19 7p14.1-12.3(chr7:41124364-47945566)	copy number loss	Syndactyly [RCV001352654]	Chr7:41124364..47945566 [GRCh37] Chr7:7p14.1-12.3	pathogenic
GRCh37/hg19 7p14.1-12.2(chr7:40778439-50228656)	copy number loss	not specified [RCV002053688]	Chr7:40778439..50228656 [GRCh37] Chr7:7p14.1-12.2	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_031903.3(MRPL32):c.377G>A (p.Cys126Tyr)	single nucleotide variant	not specified [RCV004182688]	Chr7:42937386 [GRCh38] Chr7:42976985 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.187A>C (p.Ser63Arg)	single nucleotide variant	not specified [RCV004207035]	Chr7:42935011 [GRCh38] Chr7:42974610 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.494C>T (p.Pro165Leu)	single nucleotide variant	not specified [RCV004077170]	Chr7:42937503 [GRCh38] Chr7:42977102 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.271C>T (p.Arg91Trp)	single nucleotide variant	not specified [RCV004099144]	Chr7:42935095 [GRCh38] Chr7:42974694 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.122C>T (p.Pro41Leu)	single nucleotide variant	not specified [RCV004176832]	Chr7:42932508 [GRCh38] Chr7:42972107 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.151G>A (p.Gly51Ser)	single nucleotide variant	not specified [RCV004223927]	Chr7:42934975 [GRCh38] Chr7:42974574 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.328T>C (p.Cys110Arg)	single nucleotide variant	not specified [RCV004135265]	Chr7:42937337 [GRCh38] Chr7:42976936 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.41C>T (p.Ser14Phe)	single nucleotide variant	not specified [RCV004345257]	Chr7:42932427 [GRCh38] Chr7:42972026 [GRCh37] Chr7:7p14.1	uncertain significance
GRCh37/hg19 7p14.1-12.3(chr7:42516660-46202495)x1	copy number loss	not provided [RCV003482956]	Chr7:42516660..46202495 [GRCh37] Chr7:7p14.1-12.3	pathogenic
NM_031903.3(MRPL32):c.461T>C (p.Ile154Thr)	single nucleotide variant	not specified [RCV004504810]	Chr7:42937470 [GRCh38] Chr7:42977069 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.68A>G (p.Tyr23Cys)	single nucleotide variant	not specified [RCV004504820]	Chr7:42932454 [GRCh38] Chr7:42972053 [GRCh37] Chr7:7p14.1	likely benign
NM_031903.3(MRPL32):c.209G>T (p.Ser70Ile)	single nucleotide variant	not specified [RCV004504787]	Chr7:42935033 [GRCh38] Chr7:42974632 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.74A>G (p.Glu25Gly)	single nucleotide variant	not specified [RCV004504824]	Chr7:42932460 [GRCh38] Chr7:42972059 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.44C>G (p.Ala15Gly)	single nucleotide variant	not specified [RCV004631649]	Chr7:42932430 [GRCh38] Chr7:42972029 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.470T>C (p.Val157Ala)	single nucleotide variant	not specified [RCV004631650]	Chr7:42937479 [GRCh38] Chr7:42977078 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.443C>A (p.Pro148His)	single nucleotide variant	not specified [RCV004638175]	Chr7:42937452 [GRCh38] Chr7:42977051 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.254G>A (p.Arg85His)	single nucleotide variant	not specified [RCV004638173]	Chr7:42935078 [GRCh38] Chr7:42974677 [GRCh37] Chr7:7p14.1	uncertain significance
NM_031903.3(MRPL32):c.275G>A (p.Cys92Tyr)	single nucleotide variant	not specified [RCV004638174]	Chr7:42935099 [GRCh38] Chr7:42974698 [GRCh37] Chr7:7p14.1	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1533
Count of miRNA genes:	728
Interacting mature miRNAs:	826
Transcripts:	ENST00000223324, ENST00000413995, ENST00000432845, ENST00000496564
Prediction methods:	Microtar, 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.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
1558711	BP56_H	Blood pressure QTL 56 (human)	2.24	0.000002	Blood pressure	systolic	7	36349371	62349371	Human
1559132	SAPOB3_H	Serum apolipoprotein B level QTL 3 (human)	2	0.4	Apolipoprotein level	apolipoprotein B	7	32891074	58891074	Human
2302781	MAMTS16_H	Mammary tumor susceptibility QTL 16 (human)		0.033	Mammary tumor susceptibility		7	36349371	62349371	Human
2289453	BW297_H	Body weight QTL 297 (human)	3.83		Body weight	body mass index	7	23349464	49349464	Human

Markers in Region

RH65255

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	X	53,835,080 - 53,835,211	UniSTS	GRCh37
GRCh37	7	42,977,134 - 42,977,264	UniSTS	GRCh37
Build 36	X	53,851,805 - 53,851,936	RGD	NCBI36
Celera	X	57,670,465 - 57,670,596	RGD
Celera	7	42,967,438 - 42,967,568	UniSTS
Cytogenetic Map	7	p14	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
HuRef	7	42,861,935 - 42,862,065	UniSTS
CRA_TCAGchr7v2	7	43,016,629 - 43,016,759	UniSTS

SHGC-173382

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,974,639 - 42,974,965	UniSTS	GRCh37
Build 36	7	42,941,164 - 42,941,490	RGD	NCBI36
Celera	7	42,964,943 - 42,965,269	RGD
Cytogenetic Map	7	p14	UniSTS
HuRef	7	42,859,440 - 42,859,766	UniSTS
CRA_TCAGchr7v2	7	43,014,134 - 43,014,460	UniSTS

SHGC-2621

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,977,131 - 42,977,317	UniSTS	GRCh37
GRCh37	X	53,835,077 - 53,835,263	UniSTS	GRCh37
Build 36	X	53,851,802 - 53,851,988	RGD	NCBI36
Celera	7	42,967,435 - 42,967,621	UniSTS
Celera	X	57,670,462 - 57,670,648	RGD
Cytogenetic Map	7	p14	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
HuRef	7	42,861,932 - 42,862,118	UniSTS
CRA_TCAGchr7v2	7	43,016,626 - 43,016,812	UniSTS
TNG Radiation Hybrid Map	7	21031.0	UniSTS
GeneMap99-G3 RH Map	7	1890.0	UniSTS

SHGC-2530

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,977,130 - 42,977,376	UniSTS	GRCh37
Build 36	7	42,943,655 - 42,943,901	RGD	NCBI36
Celera	7	42,967,434 - 42,967,680	RGD
Cytogenetic Map	7	p14	UniSTS
HuRef	7	42,861,931 - 42,862,177	UniSTS
CRA_TCAGchr7v2	7	43,016,625 - 43,016,871	UniSTS
TNG Radiation Hybrid Map	7	21031.0	UniSTS
GeneMap99-G3 RH Map	7	1890.0	UniSTS

GDB:6028662

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,977,130 - 42,977,376	UniSTS	GRCh37
Build 36	7	42,943,655 - 42,943,901	RGD	NCBI36
Celera	7	42,967,434 - 42,967,680	RGD
Cytogenetic Map	7	p14	UniSTS
HuRef	7	42,861,931 - 42,862,177	UniSTS
CRA_TCAGchr7v2	7	43,016,625 - 43,016,871	UniSTS

SHGC-32690

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,977,134 - 42,977,266	UniSTS	GRCh37
GRCh37	X	53,835,080 - 53,835,213	UniSTS	GRCh37
Build 36	X	53,851,805 - 53,851,938	RGD	NCBI36
Celera	X	57,670,465 - 57,670,598	RGD
Celera	7	42,967,438 - 42,967,570	UniSTS
Cytogenetic Map	X	p11.22	UniSTS
Cytogenetic Map	7	p14	UniSTS
HuRef	7	42,861,935 - 42,862,067	UniSTS
CRA_TCAGchr7v2	7	43,016,629 - 43,016,761	UniSTS
TNG Radiation Hybrid Map	7	21048.0	UniSTS
GeneMap99-GB4 RH Map	7	209.62	UniSTS
Whitehead-RH Map	7	166.5	UniSTS
NCBI RH Map	7	653.3	UniSTS
GeneMap99-G3 RH Map	7	1919.0	UniSTS

SHGC-32714

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,977,127 - 42,977,251	UniSTS	GRCh37
Build 36	7	42,943,652 - 42,943,776	RGD	NCBI36
Celera	7	42,967,431 - 42,967,555	RGD
Cytogenetic Map	X	p11.22	UniSTS
Cytogenetic Map	7	p14	UniSTS
HuRef	7	42,861,928 - 42,862,052	UniSTS
HuRef	X	50,890,459 - 50,890,584	UniSTS
CRA_TCAGchr7v2	7	43,016,622 - 43,016,746	UniSTS
GeneMap99-GB4 RH Map	7	199.56	UniSTS
Whitehead-RH Map	7	168.1	UniSTS
NCBI RH Map	7	653.3	UniSTS
GeneMap99-G3 RH Map	7	1919.0	UniSTS

MRPL33_3249

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	7	42,976,918 - 42,977,548	UniSTS	GRCh37
Build 36	7	42,943,443 - 42,944,073	RGD	NCBI36
Celera	7	42,967,222 - 42,967,852	RGD
HuRef	7	42,861,719 - 42,862,349	UniSTS
CRA_TCAGchr7v2	7	43,016,413 - 43,017,043	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

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
1204	2439	2788	2253	4974	1726	2351	6	624	1951	465	2270	7306	6472	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_031903	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_156497	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB049649	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB051343	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC010132	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF161401	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK090551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK313393	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AW379023	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC013147	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BM833110	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BU687817	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH236951	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471073	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068271	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB456673	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000223324 ⟹ ENSP00000223324

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	42,932,376 - 42,937,857 (+)	Ensembl

Ensembl Acc Id:

ENST00000413995 ⟹ ENSP00000391562

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	42,935,021 - 42,937,857 (+)	Ensembl

Ensembl Acc Id:

ENST00000432845 ⟹ ENSP00000415581

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	42,932,376 - 42,937,627 (+)	Ensembl

Ensembl Acc Id:

ENST00000496564

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	7	42,935,043 - 42,948,958 (+)	Ensembl

RefSeq Acc Id:

NM_031903 ⟹ NP_114109

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	42,932,376 - 42,937,857 (+)	NCBI
GRCh37	7	42,971,804 - 42,977,456 (+)	NCBI
Build 36	7	42,938,464 - 42,943,981 (+)	NCBI Archive
Celera	7	42,962,246 - 42,967,760 (+)	RGD
HuRef	7	42,856,743 - 42,862,257 (+)	RGD
CHM1_1	7	42,975,485 - 42,981,003 (+)	NCBI
T2T-CHM13v2.0	7	43,090,506 - 43,095,986 (+)	NCBI
CRA_TCAGchr7v2	7	43,011,437 - 43,016,951 (+)	ENTREZGENE

Sequence:

show sequence

CAGCAGGGAAAATGGCGCTGGCCATGCTGGTCTTGGTGGTTTCGCCGTGGTCTGCGGCCCGGGG
AGTGCTTCGAAACTACTGGGAGCGACTGCTACGGAAGCTTCCGCAGAGCCGGCCGGGCTTTCCC
AGTCCTCCGTGGGGACCAGCATTAGCAGTACAGGGCCCAGCCATGTTTACAGAGCCAGCAAATG
ATACCAGTGGAAGTAAAGAGAATTCCAGCCTTTTGGACAGTATCTTTTGGATGGCAGCTCCCAA
AAATAGACGCACCATTGAAGTTAACCGGTGTAGGAGAAGAAATCCGCAGAAGCTTATTAAAGTT
AAGAACAACATAGACGTTTGTCCTGAATGTGGTCACCTGAAACAGAAACATGTCCTTTGTGCCT
ACTGCTATGAAAAGGTGTGCAAGGAGACTGCAGAAATCAGACGACAGATAGGGAAGCAAGAAGG
GGGCCCTTTTAAGGCTCCCACCATAGAGACTGTGGTGCTGTACACGGGAGAGACACCGTCTGAA
CAAGATCAGGGCAAGAGGATCATTGAACGAGACAGAAAGCGACCATCCTGGTTCACCCAGAATT
GACACCAAAGATGTTAAAAGGGTAACTTCACAGTAAATCATTTCTCCTGAAATAGAGGAAGATT
CTTTATGTTGTTGTGCTTGTTTTTAAATCATCAGTATAGTTTAACACATTCTTTCTAAGCAGTT
TTGTGTGGGATAATTTGAAGAATATATTATGAGTAAACTCCGAAAATTTTGTTTATCCAAAGGC
TCAATGGATTATGTTTCTATTATATACAAGGTTTTAAGTAAACATAAAATTTCCAGAACAAAAA
TAAAAAATTTAAAATTCATAGCAAAAA

hide sequence

RefSeq Acc Id:

NR_156497

RefSeq Status:

REVIEWED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	42,932,376 - 42,937,857 (+)	NCBI
T2T-CHM13v2.0	7	43,090,506 - 43,095,986 (+)	NCBI

Sequence:

show sequence

CAGCAGGGAAAATGGCGCTGGCCATGCTGGTCTTGGTGGTTTCGCCGTGGTCTGCGGCCCGGGG
AGTGCTTCGAAACTACTGGGAGCGACTGCTACGGAAGCTTCCGCAGAGCCGGCCGGGCTTTCCC
AGTCCTCCGTGGGGACCAGCATTAGCAGTACAGGGCCCAGCCATGTTTACAGAGCCAGCAAATG
ATACCAGTGGAAGTAAAGAGAATTCCAGCCTTTTGGACAGTATCTTTTGGATGGCAGCTCCCAA
AAATAGACGCACCATTGAAGTTAACCGGTGTAGGAGAAGAAATCCGCAGAAGCTTATTAAAGTT
AAGTCTTCCTGTTAAAGTGAGGTGGAACTAGATGGTGTATGATGACCTCATGTAGCCTGAACAT
CCTAAGAAAGTTAAAATAACAACATAGACGTTTGTCCTGAATGTGGTCACCTGAAACAGAAACA
TGTCCTTTGTGCCTACTGCTATGAAAAGGTGTGCAAGGAGACTGCAGAAATCAGACGACAGATA
GGGAAGCAAGAAGGGGGCCCTTTTAAGGCTCCCACCATAGAGACTGTGGTGCTGTACACGGGAG
AGACACCGTCTGAACAAGATCAGGGCAAGAGGATCATTGAACGAGACAGAAAGCGACCATCCTG
GTTCACCCAGAATTGACACCAAAGATGTTAAAAGGGTAACTTCACAGTAAATCATTTCTCCTGA
AATAGAGGAAGATTCTTTATGTTGTTGTGCTTGTTTTTAAATCATCAGTATAGTTTAACACATT
CTTTCTAAGCAGTTTTGTGTGGGATAATTTGAAGAATATATTATGAGTAAACTCCGAAAATTTT
GTTTATCCAAAGGCTCAATGGATTATGTTTCTATTATATACAAGGTTTTAAGTAAACATAAAAT
TTCCAGAACAAAAATAAAAAATTTAAAATTCATAGCAAAAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_114109	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAF28961	(Get FASTA)	NCBI Sequence Viewer
	AAH13147	(Get FASTA)	NCBI Sequence Viewer
	BAB40854	(Get FASTA)	NCBI Sequence Viewer
	BAB54933	(Get FASTA)	NCBI Sequence Viewer
	BAG36191	(Get FASTA)	NCBI Sequence Viewer
	BAG52183	(Get FASTA)	NCBI Sequence Viewer
	EAL24006	(Get FASTA)	NCBI Sequence Viewer
	EAW94154	(Get FASTA)	NCBI Sequence Viewer
	EAW94155	(Get FASTA)	NCBI Sequence Viewer
	EAW94156	(Get FASTA)	NCBI Sequence Viewer
	EAW94157	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000223324
	ENSP00000223324.2
	ENSP00000391562.1
	ENSP00000415581.1
GenBank Protein	Q9BYC8	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_114109 ⟸ NM_031903
- Peptide Label:	precursor
- UniProtKB:	Q9BYC8 (UniProtKB/Swiss-Prot), Q96Q68 (UniProtKB/Swiss-Prot), Q9P098 (UniProtKB/Swiss-Prot), A4D1V4 (UniProtKB/TrEMBL)
- Sequence:	show sequence MALAMLVLVVSPWSAARGVLRNYWERLLRKLPQSRPGFPSPPWGPALAVQGPAMFTEPANDTSG SKENSSLLDSIFWMAAPKNRRTIEVNRCRRRNPQKLIKVKNNIDVCPECGHLKQKHVLCAYCYE KVCKETAEIRRQIGKQEGGPFKAPTIETVVLYTGETPSEQDQGKRIIERDRKRPSWFTQN hide sequence

Ensembl Acc Id:

ENSP00000391562 ⟸ ENST00000413995

Ensembl Acc Id:

ENSP00000415581 ⟸ ENST00000432845

Ensembl Acc Id:

ENSP00000223324 ⟸ ENST00000223324

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9BYC8-F1-model_v2	AlphaFold	Q9BYC8	1-188	view protein structure

Promoters

RGD ID:

7210455

Promoter ID:

EPDNEW_H10971

Type:

initiation region

Name:

MRPL32_1

Description:

mitochondrial ribosomal protein L32

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	7	42,932,377 - 42,932,437	EPDNEW

RGD ID:

6805929

Promoter ID:

HG_KWN:57156

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:

OTTHUMT00000338669, UC003TIB.1, UC003TIC.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	7	42,938,109 - 42,938,609 (+)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:14035	AgrOrtholog
COSMIC	MRPL32	COSMIC
Ensembl Genes	ENSG00000106591	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000223324	ENTREZGENE
	ENST00000223324.3	UniProtKB/Swiss-Prot
	ENST00000413995.1	UniProtKB/TrEMBL
	ENST00000432845.1	UniProtKB/TrEMBL
GTEx	ENSG00000106591	GTEx
HGNC ID	HGNC:14035	ENTREZGENE
Human Proteome Map	MRPL32	Human Proteome Map
InterPro	Mitoribosomal_protein_bL32	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Ribosomal_L32p	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	Ribosomal_zn-bd	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:64983	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	64983	ENTREZGENE
OMIM	611839	OMIM
PANTHER	39S RIBOSOMAL PROTEIN L32, MITOCHONDRIAL	UniProtKB/Swiss-Prot
	39S RIBOSOMAL PROTEIN L32, MITOCHONDRIAL	UniProtKB/Swiss-Prot
	39S RIBOSOMAL PROTEIN L32, MITOCHONDRIAL	UniProtKB/TrEMBL
	39S RIBOSOMAL PROTEIN L32, MITOCHONDRIAL	UniProtKB/TrEMBL
Pfam	Ribosomal_L32p	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA30963	PharmGKB
Superfamily-SCOP	SSF57829	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A4D1V4	ENTREZGENE, UniProtKB/TrEMBL
	B3KQX1_HUMAN	UniProtKB/TrEMBL
	H7BZU9_HUMAN	UniProtKB/TrEMBL
	Q96Q68	ENTREZGENE
	Q9BYC8	ENTREZGENE
	Q9P098	ENTREZGENE
	RM32_HUMAN	UniProtKB/Swiss-Prot
UniProt Secondary	Q96Q68	UniProtKB/Swiss-Prot
	Q9P098	UniProtKB/Swiss-Prot

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar

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Imported Disease Annotations - ClinVar

Imported Human Phenotype Annotations - ClinVar