SPEM2 (SPEM family member 2) - Rat Genome Database

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Gene: SPEM2 (SPEM family member 2) Homo sapiens
Analyze
Symbol: SPEM2
Name: SPEM family member 2
RGD ID: 1604207
HGNC Page HGNC:27315
Description: Predicted to be located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C17orf74; chromosome 17 open reading frame 74; hypothetical protein LOC201243; uncharacterized protein C17orf74; uncharacterized protein SPEM2
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
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
GRCh38177,425,616 - 7,427,568 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl177,425,616 - 7,427,568 (+)EnsemblGRCh38hg38GRCh38
GRCh37177,328,935 - 7,330,887 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36177,269,659 - 7,271,611 (+)NCBINCBI36Build 36hg18NCBI36
Celera177,354,821 - 7,356,773 (+)NCBICelera
Cytogenetic Map17p13.1NCBI
HuRef177,222,961 - 7,224,913 (+)NCBIHuRef
CHM1_1177,338,027 - 7,339,979 (+)NCBICHM1_1
T2T-CHM13v2.0177,329,669 - 7,331,621 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Cellular Component
membrane  (IEA)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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  


Genomics

Comparative Map Data
SPEM2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38177,425,616 - 7,427,568 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl177,425,616 - 7,427,568 (+)EnsemblGRCh38hg38GRCh38
GRCh37177,328,935 - 7,330,887 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36177,269,659 - 7,271,611 (+)NCBINCBI36Build 36hg18NCBI36
Celera177,354,821 - 7,356,773 (+)NCBICelera
Cytogenetic Map17p13.1NCBI
HuRef177,222,961 - 7,224,913 (+)NCBIHuRef
CHM1_1177,338,027 - 7,339,979 (+)NCBICHM1_1
T2T-CHM13v2.0177,329,669 - 7,331,621 (+)NCBIT2T-CHM13v2.0
Spem2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391169,707,386 - 69,709,313 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1169,707,392 - 69,709,291 (-)EnsemblGRCm39 Ensembl
GRCm381169,816,560 - 69,818,487 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1169,816,566 - 69,818,465 (-)EnsemblGRCm38mm10GRCm38
MGSCv371169,630,068 - 69,631,942 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361169,632,761 - 69,634,635 (-)NCBIMGSCv36mm8
Celera1177,377,527 - 77,379,401 (-)NCBICelera
Cytogenetic Map11B3NCBI
cM Map1142.89NCBI
Spem2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81055,035,892 - 55,037,790 (-)NCBIGRCr8
mRatBN7.21054,537,168 - 54,539,026 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1054,537,174 - 54,539,058 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1059,199,677 - 59,201,528 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01058,688,243 - 58,690,094 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01054,195,894 - 54,197,745 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01056,424,164 - 56,426,012 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1056,424,164 - 56,426,012 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01056,169,247 - 56,171,081 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41056,638,639 - 56,640,472 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1053,691,427 - 53,693,278 (-)NCBICelera
Cytogenetic Map10q24NCBI
Spem2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554679,498,541 - 9,500,466 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554679,493,708 - 9,500,466 (-)NCBIChiLan1.0ChiLan1.0
SPEM2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21915,019,413 - 15,024,166 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11716,985,222 - 16,989,970 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0177,458,605 - 7,461,545 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1177,445,958 - 7,447,907 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl177,449,092 - 7,453,041 (+)Ensemblpanpan1.1panPan2
PanPan1.1 Ensembl177,445,958 - 7,447,907 (+)Ensemblpanpan1.1panPan2
SPEM2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1532,357,302 - 32,359,197 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl532,357,336 - 32,359,129 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha532,495,333 - 32,497,293 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0532,462,905 - 32,464,865 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl532,462,999 - 32,464,797 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1532,428,139 - 32,430,099 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0532,386,871 - 32,388,831 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0532,564,139 - 32,566,099 (+)NCBIUU_Cfam_GSD_1.0
Spem2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560247,232,222 - 47,236,485 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936595708,799 - 710,604 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936595708,694 - 710,810 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SPEM2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1252,728,826 - 52,730,822 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11252,729,001 - 52,731,131 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21255,021,617 - 55,023,538 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SPEM2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1166,800,970 - 6,803,726 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl166,801,835 - 6,803,655 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605914,604,873 - 14,607,257 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17p13.2-13.1(chr17:5732977-8038822)x1 copy number loss See cases [RCV000051043] Chr17:5732977..8038822 [GRCh38]
Chr17:5636297..7942140 [GRCh37]
Chr17:5577021..7882865 [NCBI36]
Chr17:17p13.2-13.1		 pathogenic
GRCh38/hg38 17p13.1(chr17:6958978-8335684)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052457]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052457]|See cases [RCV000052457] Chr17:6958978..8335684 [GRCh38]
Chr17:6862297..8239002 [GRCh37]
Chr17:6803021..8179727 [NCBI36]
Chr17:17p13.1		 pathogenic
GRCh38/hg38 17p13.2-13.1(chr17:6307904-8842949)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053407]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053407]|See cases [RCV000053407] Chr17:6307904..8842949 [GRCh38]
Chr17:6211224..8746266 [GRCh37]
Chr17:6151948..8686991 [NCBI36]
Chr17:17p13.2-13.1		 pathogenic
GRCh38/hg38 17p13.1(chr17:7210345-7496934)x1 copy number loss See cases [RCV000053425] Chr17:7210345..7496934 [GRCh38]
Chr17:7113664..7400253 [GRCh37]
Chr17:7054388..7340977 [NCBI36]
Chr17:17p13.1		 pathogenic
NM_199339.2(SPEM1):c.839C>T (p.Ala280Val) single nucleotide variant Malignant melanoma [RCV000071688] Chr17:7421514 [GRCh38]
Chr17:7324833 [GRCh37]
Chr17:7265557 [NCBI36]
Chr17:17p13.1		 not provided
GRCh38/hg38 17p13.1(chr17:6958978-7491129)x3 copy number gain See cases [RCV000133763] Chr17:6958978..7491129 [GRCh38]
Chr17:6862297..7394448 [GRCh37]
Chr17:6803021..7335172 [NCBI36]
Chr17:17p13.1		 uncertain significance
GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3 copy number gain See cases [RCV000134970] Chr17:198748..7491129 [GRCh38]
Chr17:50690..7394448 [GRCh37]
Chr17:48539..7335172 [NCBI36]
Chr17:17p13.3-13.1		 pathogenic
GRCh38/hg38 17p13.2-12(chr17:5732953-12095349)x3 copy number gain See cases [RCV000134851] Chr17:5732953..12095349 [GRCh38]
Chr17:5636273..11998666 [GRCh37]
Chr17:5576997..11939391 [NCBI36]
Chr17:17p13.2-12		 pathogenic
GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1 copy number loss See cases [RCV000138214] Chr17:162016..7697012 [GRCh38]
Chr17:45835..7600330 [GRCh37]
Chr17:11807..7541055 [NCBI36]
Chr17:17p13.3-13.1		 pathogenic
GRCh38/hg38 17p13.2-13.1(chr17:6361393-7750863)x3 copy number gain See cases [RCV000138220] Chr17:6361393..7750863 [GRCh38]
Chr17:6264713..7654181 [GRCh37]
Chr17:6205437..7594906 [NCBI36]
Chr17:17p13.2-13.1		 likely pathogenic
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3 copy number gain See cases [RCV000138531] Chr17:162016..12343901 [GRCh38]
Chr17:45835..12247218 [GRCh37]
Chr17:11807..12187943 [NCBI36]
Chr17:17p13.3-12		 pathogenic
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3 copy number gain See cases [RCV000142236] Chr17:150732..14764202 [GRCh38]
Chr17:525..14667519 [GRCh37]
Chr17:525..14608244 [NCBI36]
Chr17:17p13.3-12		 pathogenic
GRCh37/hg19 17p13.1(chr17:7241916-8692213)x1 copy number loss See cases [RCV000445992] Chr17:7241916..8692213 [GRCh37]
Chr17:17p13.1		 pathogenic
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3 copy number gain See cases [RCV000511786] Chr17:525..15027737 [GRCh37]
Chr17:17p13.3-12		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.1(chr17:6934163-8217978)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626431] Chr17:6934163..8217978 [GRCh37]
Chr17:17p13.1		 drug response
GRCh37/hg19 17p13.1(chr17:7094070-7414448)x1 copy number loss See cases [RCV000512276] Chr17:7094070..7414448 [GRCh37]
Chr17:17p13.1		 likely pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NC_000017.10:g.7124585_7400253dup duplication Robin sequence [RCV000677112] Chr17:7124585..7400253 [GRCh37]
Chr17:17p13.1		 uncertain significance
Single allele duplication Isolated Pierre-Robin syndrome [RCV000677112] Chr17:7124585..7400253 [GRCh37]
Chr17:17p13.1		 likely pathogenic
GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3 copy number gain not provided [RCV000683866] Chr17:525..11186432 [GRCh37]
Chr17:17p13.3-12		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.1(chr17:7269373-7390669)x1 copy number loss not provided [RCV000739395] Chr17:7269373..7390669 [GRCh37]
Chr17:17p13.1		 benign
NC_000017.10:g.(?_7123304)_(7606804_?)del deletion Common variable immunodeficiency [RCV003107751] Chr17:7123304..7606804 [GRCh37]
Chr17:17p13.1		 uncertain significance
NC_000017.10:g.(?_6589506)_(8151374_?)dup duplication Common variable immunodeficiency [RCV001338841]|Dyskeratosis congenita [RCV001031775] Chr17:6589506..8151374 [GRCh37]
Chr17:17p13.1		 uncertain significance
GRCh37/hg19 17p13.1(chr17:6650649-8040151)x3 copy number gain not provided [RCV001259299] Chr17:6650649..8040151 [GRCh37]
Chr17:17p13.1		 pathogenic
NC_000017.10:g.(?_6328780)_(7606804_?)dup duplication Congenital myasthenic syndrome 2A [RCV003109217]|Very long chain acyl-CoA dehydrogenase deficiency [RCV003119078] Chr17:6328780..7606804 [GRCh37]
Chr17:17p13.2-13.1		 uncertain significance
GRCh37/hg19 17p13.1(chr17:7241916-8692213) copy number loss not specified [RCV002052586] Chr17:7241916..8692213 [GRCh37]
Chr17:17p13.1		 pathogenic
GRCh37/hg19 17p13.1(chr17:7020054-8086290) copy number loss not specified [RCV002052585] Chr17:7020054..8086290 [GRCh37]
Chr17:17p13.1		 pathogenic
NC_000017.10:g.(?_7120455)_(8151423_?)del deletion Li-Fraumeni syndrome [RCV003111420] Chr17:7120455..8151423 [GRCh37]
Chr17:17p13.1		 pathogenic
NC_000017.10:g.(?_7123304)_(8193254_?)del deletion Very long chain acyl-CoA dehydrogenase deficiency [RCV003119081] Chr17:7123304..8193254 [GRCh37]
Chr17:17p13.1		 pathogenic
GRCh37/hg19 17p13.1(chr17:7004894-7766789)x1 copy number loss not provided [RCV003222936] Chr17:7004894..7766789 [GRCh37]
Chr17:17p13.1		 pathogenic
GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3 copy number gain Chromosome 17p13.3 duplication syndrome [RCV003327726] Chr17:165730..11404096 [GRCh38]
Chr17:17p13.3-12		 pathogenic
GRCh37/hg19 17p13.1(chr17:7002380-7469251)x1 copy number loss not specified [RCV003987240] Chr17:7002380..7469251 [GRCh37]
Chr17:17p13.1		 pathogenic
GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3 copy number gain not specified [RCV003987215] Chr17:525..21510992 [GRCh37]
Chr17:17p13.3-11.2		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1083
Count of miRNA genes:536
Interacting mature miRNAs:611
Transcripts:ENST00000333870, ENST00000574034
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
RH98448  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37177,330,674 - 7,330,812UniSTSGRCh37
Build 36177,271,398 - 7,271,536RGDNCBI36
Celera177,356,560 - 7,356,698RGD
Cytogenetic Map17p13.1UniSTS
HuRef177,224,700 - 7,224,838UniSTS
GeneMap99-GB4 RH Map1753.8UniSTS


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 adipose tissue appendage
High
Medium 1 1 2 2 362 1 2
Low 19 9 18 4 6 3 47 19 68 2 46 18 1 8 30
Below cutoff 1380 1563 960 275 679 168 2825 1389 2903 150 631 853 110 742 1902

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000333870   ⟹   ENSP00000328061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,425,616 - 7,427,568 (+)Ensembl
RefSeq Acc Id: ENST00000574034   ⟹   ENSP00000458799
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl177,425,641 - 7,427,568 (+)Ensembl
RefSeq Acc Id: NM_175734   ⟹   NP_783861
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,425,616 - 7,427,568 (+)NCBI
GRCh37177,328,851 - 7,330,887 (+)NCBI
Build 36177,269,659 - 7,271,611 (+)NCBI Archive
Celera177,354,821 - 7,356,773 (+)RGD
HuRef177,222,961 - 7,224,913 (+)RGD
CHM1_1177,338,027 - 7,339,979 (+)NCBI
T2T-CHM13v2.0177,329,669 - 7,331,621 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006721471   ⟹   XP_006721534
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38177,425,616 - 7,427,568 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054315367   ⟹   XP_054171342
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0177,329,669 - 7,331,621 (+)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_783861   ⟸   NM_175734
- UniProtKB: Q0P670 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006721534   ⟸   XM_006721471
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000328061   ⟸   ENST00000333870
RefSeq Acc Id: ENSP00000458799   ⟸   ENST00000574034
RefSeq Acc Id: XP_054171342   ⟸   XM_054315367
- Peptide Label: isoform X1
Protein Domains
Spermatid maturation protein 1 N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q0P670-F1-model_v2 AlphaFold Q0P670 1-501 view protein structure

Promoters
RGD ID:7233743
Promoter ID:EPDNEW_H22617
Type:initiation region
Name:C17orf74_1
Description:chromosome 17 open reading frame 74
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
GRCh38177,425,616 - 7,425,676EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:27315 AgrOrtholog
COSMIC SPEM2 COSMIC
Ensembl Genes ENSG00000184560 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000283714 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000333870 ENTREZGENE
  ENST00000333870.8 UniProtKB/Swiss-Prot
  ENST00000574034.1 UniProtKB/TrEMBL
  ENST00000639609.2 UniProtKB/Swiss-Prot
GTEx ENSG00000184560 GTEx
  ENSG00000283714 GTEx
HGNC ID HGNC:27315 ENTREZGENE
Human Proteome Map SPEM2 Human Proteome Map
InterPro SPEM1_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:201243 UniProtKB/Swiss-Prot
NCBI Gene 201243 ENTREZGENE
PANTHER SPEM FAMILY MEMBER 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SPERMATID MATURATION PROTEIN 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Spem1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142672222 PharmGKB
UniProt I3L1F6_HUMAN UniProtKB/TrEMBL
  Q0P670 ENTREZGENE, UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-08-01 SPEM2  SPEM family member 2  C17orf74  chromosome 17 open reading frame 74  Symbol and/or name change 5135510 APPROVED