 Gene Ontology Annotations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Gene-Chemical Interaction Annotations
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Gene Ontology AnnotationsReferences - curated| 1. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
| 2. | RGD automated import pipeline for gene-chemical interactions |
| 3. | Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11. |
References - uncurated| PubMed | 11352567 14702039 15177564 15489334 16344560 17207965 18187620 20877624 21873635 23251661 23505323 |
Genomics
Comparative Map Data| NIPSNAP3B (Homo sapiens - human) |
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| NIPSNAP3B (Pan paniscus - bonobo/pygmy chimpanzee) |
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| LOC481650 (Canis lupus familiaris - dog) |
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Position Markers| NIPSNAP3A |
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miRNA Target Status
Predicted Target Of
| 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. |
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Expression
Sequence
Nucleotide Sequences| RefSeq Transcripts | NM_018376 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| NR_130759 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| NR_130760 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| XM_011518839 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| XR_001746344 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| XR_001746345 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| XR_428532 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| GenBank Nucleotide | AF287262 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| AF370389 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK002137 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK090505 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK091667 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK310397 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AL359846 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC005202 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC017914 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BX107655 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BX647652 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| CH471105 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| DA346124 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| HF584099 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
Reference Sequences
| RefSeq Acc Id: | NM_018376 ⟹ NP_060846 | ||||||||||||||||||||||||||||||||||
| RefSeq Status: | VALIDATED | ||||||||||||||||||||||||||||||||||
| Type: | CODING | ||||||||||||||||||||||||||||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
| RefSeq Acc Id: | NR_130759 | ||||||||||||||
| RefSeq Status: | VALIDATED | ||||||||||||||
| Type: | NON-CODING | ||||||||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
| RefSeq Acc Id: | NR_130760 | ||||||||||||||
| RefSeq Status: | VALIDATED | ||||||||||||||
| Type: | NON-CODING | ||||||||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
| RefSeq Acc Id: | XM_011518839 ⟹ XP_011517141 | |||||||||
| RefSeq Status: | ||||||||||
| Type: | CODING | |||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
| RefSeq Acc Id: | XR_001746344 | |||||||||
| RefSeq Status: | ||||||||||
| Type: | NON-CODING | |||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
| RefSeq Acc Id: | XR_001746345 | |||||||||
| RefSeq Status: | ||||||||||
| Type: | NON-CODING | |||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
| RefSeq Acc Id: | XR_428532 | |||||||||
| RefSeq Status: | ||||||||||
| Type: | NON-CODING | |||||||||
| Position: |
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| Sequence: |
AGTGCACTCCAGCCTGGGCGACAGAGCAAGACTACGTCTCAAACAAAGAAACAAGTTAACCCTGhide sequence |
Protein Sequences| Protein RefSeqs | NP_060846 | (Get FASTA) | NCBI Sequence Viewer |
| XP_011517141 | (Get FASTA) | NCBI Sequence Viewer | |
| GenBank Protein | AAH05202 | (Get FASTA) | NCBI Sequence Viewer |
| AAH17914 | (Get FASTA) | NCBI Sequence Viewer | |
| AAK43527 | (Get FASTA) | NCBI Sequence Viewer | |
| AAQ15225 | (Get FASTA) | NCBI Sequence Viewer | |
| BAA92101 | (Get FASTA) | NCBI Sequence Viewer | |
| CCQ43596 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW58991 | (Get FASTA) | NCBI Sequence Viewer | |
| Q9BS92 | (Get FASTA) | NCBI Sequence Viewer |
Reference Sequences
| RefSeq Acc Id: | NP_060846 ⟸ NM_018376 |
| - UniProtKB: | Q9BS92 (UniProtKB/Swiss-Prot), Q71RE8 (UniProtKB/TrEMBL) |
| - Sequence: |
MLVLRSGLTKALASRTLAPQVCSSFATGPRQYDGTFYEFRTYYLKPSNMNAFMENLKKNIHLRThide sequence |
| RefSeq Acc Id: | XP_011517141 ⟸ XM_011518839 |
| - Peptide Label: | isoform X1 |
| - UniProtKB: | F2Z3L7 (UniProtKB/TrEMBL) |
| - Sequence: |
MLVLRSGLTKALASRTLAPQVCSSFATGPRQYDGTFYEFRTYYLKPSNMNAFMENLKKNIHLRThide sequence |
Promoters| RGD ID: | 7215735 | |||||||||
| Promoter ID: | EPDNEW_H13614 | |||||||||
| Type: | initiation region | |||||||||
| Name: | NIPSNAP3B_2 | |||||||||
| Description: | nipsnap homolog 3B | |||||||||
| SO ACC ID: | SO:0000170 | |||||||||
| Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
| Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | |||||||||
| Position: |
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| RGD ID: | 7215737 | |||||||||
| Promoter ID: | EPDNEW_H13615 | |||||||||
| Type: | initiation region | |||||||||
| Name: | NIPSNAP3B_1 | |||||||||
| Description: | nipsnap homolog 3B | |||||||||
| SO ACC ID: | SO:0000170 | |||||||||
| Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
| Experiment Methods: | Single-end sequencing.; Paired-end sequencing. | |||||||||
| Position: |
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| RGD ID: | 6807923 | |||||||||
| Promoter ID: | HG_KWN:64378 | |||||||||
| Type: | CpG-Island | |||||||||
| SO ACC ID: | SO:0000170 | |||||||||
| Source: | MPROMDB | |||||||||
| Tissues & Cell Lines: | K562, Lymphoblastoid, NB4 | |||||||||
| Transcripts: | ENST00000374760, NM_018376, OTTHUMT00000053487, OTTHUMT00000053488, UC004BCJ.1 | |||||||||
| Position: |
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Clinical Variants| Name | Type | Condition(s) | Position(s) | Clinical significance |
| GRCh38/hg38 9q22.33-33.1(chr9:99138048-115011033)x1 | copy number loss | Abnormal facial shape [RCV000050315]|See cases [RCV000050315] | Chr9:99138048..115011033 [GRCh38] Chr9:101900330..117773312 [GRCh37] Chr9:100940151..116813133 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
| GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3 | copy number gain | Global developmental delay [RCV000050347]|Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050348]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050348]|See cases [RCV000050348] | Chr9:193412..138179445 [GRCh38] Chr9:204193..141073897 [GRCh37] Chr9:194193..140193718 [NCBI36] Chr9:9p24.3-q34.3 |
pathogenic |
| GRCh38/hg38 9q22.33-33.1(chr9:99349916-115767475)x1 | copy number loss | Chiari malformation type II [RCV000052921]|See cases [RCV000052921] | Chr9:99349916..115767475 [GRCh38] Chr9:102112198..118529754 [GRCh37] Chr9:101152019..117569575 [NCBI36] Chr9:9q22.33-33.1 |
pathogenic |
| GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124532)x3 | copy number gain | Intrauterine growth retardation [RCV000053745]|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 | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053746]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053746]|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 9q22.32-31.2(chr9:94184266-106730550)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053774]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053774]|See cases [RCV000053774] | Chr9:94184266..106730550 [GRCh38] Chr9:96946548..109492831 [GRCh37] Chr9:95986369..108532652 [NCBI36] Chr9:9q22.32-31.2 |
pathogenic |
| GRCh38/hg38 9q22.1-32(chr9:88522292-113687796)x3 | copy number gain | Global developmental delay [RCV000053752]|See cases [RCV000053752] | Chr9:88522292..113687796 [GRCh38] Chr9:91137207..116450076 [GRCh37] Chr9:90327027..115489897 [NCBI36] Chr9:9q22.1-32 |
pathogenic |
| NM_018376.3(NIPSNAP3B):c.402G>A (p.Trp134Ter) | single nucleotide variant | Malignant melanoma [RCV000068481] | Chr9:104768993 [GRCh38] Chr9:107531274 [GRCh37] Chr9:106571095 [NCBI36] Chr9:9q31.1 |
not provided |
| NM_018376.3(NIPSNAP3B):c.719C>T (p.Pro240Leu) | single nucleotide variant | Malignant melanoma [RCV000061854] | Chr9:104773048 [GRCh38] Chr9:107535329 [GRCh37] Chr9:106575150 [NCBI36] Chr9:9q31.1 |
not provided |
| 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 9q22.32-31.3(chr9:95061030-108695569)x1 | copy number loss | See cases [RCV000134375] | Chr9:95061030..108695569 [GRCh38] Chr9:97823312..111457849 [GRCh37] Chr9:96863133..110497670 [NCBI36] Chr9:9q22.32-31.3 |
pathogenic |
| GRCh38/hg38 9q31.1-32(chr9:103767420-112984794)x1 | copy number loss | See cases [RCV000134976] | Chr9:103767420..112984794 [GRCh38] Chr9:106529701..115747074 [GRCh37] Chr9:105569522..114786895 [NCBI36] Chr9:9q31.1-32 |
pathogenic |
| GRCh38/hg38 9q31.1(chr9:103006145-105161449)x1 | copy number loss | See cases [RCV000135554] | Chr9:103006145..105161449 [GRCh38] Chr9:105768427..107923730 [GRCh37] Chr9:104808248..106963551 [NCBI36] Chr9:9q31.1 |
uncertain significance |
| GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3 | copy number gain | See cases [RCV000136788] | Chr9:68420430..106579493 [GRCh38] Chr9:71130848..109341774 [GRCh37] Chr9:70225166..108381595 [NCBI36] Chr9:9q21.11-31.2 |
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 9q22.33-31.3(chr9:99024205-109947890)x1 | copy number loss | See cases [RCV000138281] | Chr9:99024205..109947890 [GRCh38] Chr9:101786487..112710170 [GRCh37] Chr9:100826308..111749991 [NCBI36] Chr9:9q22.33-31.3 |
pathogenic|likely 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 9q21.12-31.3(chr9:69627642-111454304)x3 | copy number gain | See cases [RCV000139789] | Chr9:69627642..111454304 [GRCh38] Chr9:72242558..114216584 [GRCh37] Chr9:71432378..113256405 [NCBI36] Chr9:9q21.12-31.3 |
pathogenic |
| 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 9q31.1-31.2(chr9:104036284-105935181)x3 | copy number gain | See cases [RCV000143264] | Chr9:104036284..105935181 [GRCh38] Chr9:106798565..108697462 [GRCh37] Chr9:105838386..107737283 [NCBI36] Chr9:9q31.1-31.2 |
uncertain significance |
| 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 9q22.33-33.1(chr9:99138048-115011033)x1 | copy number loss | See cases [RCV000148264] | Chr9:99138048..115011033 [GRCh38] Chr9:101900330..117773312 [GRCh37] Chr9:100940151..116813133 [NCBI36] Chr9:9q22.33-33.1 |
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 | See cases [RCV000447207] | Chr9:203861..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 |
| NC_000009.11:g.(?_102339410)_(109549354_?)del | deletion | Schizophrenia [RCV000416788] | Chr9:102339410..109549354 [GRCh37] Chr9:101379231..108589175 [NCBI36] Chr9:9q22.33-31.2 |
likely pathogenic |
| GRCh37/hg19 9q31.1-31.3(chr9:103271401-113948226)x1 | copy number loss | See cases [RCV000447957] | Chr9:103271401..113948226 [GRCh37] Chr9:9q31.1-31.3 |
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 9q21.11-34.3(chr9:71069743-140999928) | copy number gain | Global developmental delay [RCV000626548]|Seizures [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 9q31.1-31.3(chr9:106487247-114541579)x1 | copy number loss | not provided [RCV000683163] | Chr9:106487247..114541579 [GRCh37] Chr9:9q31.1-31.3 |
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 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 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(chr9:106618735-107897515)x3 | copy number gain | not provided [RCV000848900] | Chr9:106618735..107897515 [GRCh37] Chr9:9q31.1 |
uncertain significance |
| 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 |
Additional Information
External Database Links| Database | Acc Id | Source(s) |
| AGR Gene | HGNC:23641 | AgrOrtholog |
| COSMIC | NIPSNAP3B | COSMIC |
| Ensembl Genes | ENSG00000165028 | ENTREZGENE, UniProtKB/Swiss-Prot |
| Ensembl Protein | ENSP00000363894 | ENTREZGENE, UniProtKB/Swiss-Prot |
| ENSP00000435209 | ENTREZGENE, UniProtKB/TrEMBL | |
| Ensembl Transcript | ENST00000374762 | ENTREZGENE, UniProtKB/Swiss-Prot |
| ENST00000460936 | ENTREZGENE, UniProtKB/TrEMBL | |
| GTEx | ENSG00000165028 | GTEx |
| HGNC ID | HGNC:23641 | ENTREZGENE |
| Human Proteome Map | NIPSNAP3B | Human Proteome Map |
| InterPro | Dimeric_a/b-barrel | UniProtKB/Swiss-Prot |
| NIPSNAP | UniProtKB/Swiss-Prot | |
| KEGG Report | hsa:55335 | UniProtKB/Swiss-Prot |
| NCBI Gene | 55335 | ENTREZGENE |
| OMIM | 608872 | OMIM |
| Pfam | NIPSNAP | UniProtKB/Swiss-Prot |
| PharmGKB | PA134947095 | PharmGKB |
| Superfamily-SCOP | SSF54909 | UniProtKB/Swiss-Prot |
| UniGene | Hs.429294 | ENTREZGENE |
| Hs.720355 | ENTREZGENE | |
| Hs.732606 | ENTREZGENE | |
| UniProt | F2Z3L7 | ENTREZGENE, UniProtKB/TrEMBL |
| L8EA27_HUMAN | UniProtKB/TrEMBL | |
| NPS3B_HUMAN | UniProtKB/Swiss-Prot | |
| Q71RE8 | ENTREZGENE, UniProtKB/TrEMBL | |
| Q9BS92 | ENTREZGENE | |
| UniProt Secondary | Q5VX30 | UniProtKB/Swiss-Prot |
| Q9NUM2 | UniProtKB/Swiss-Prot |
Nomenclature History| Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
|---|---|---|---|---|---|---|---|
| 2016-04-26 | NIPSNAP3B | nipsnap homolog 3B | nipsnap homolog 3B (C. elegans) | Symbol and/or name change | 5135510 | APPROVED | |
| 2011-09-01 | NIPSNAP3B | nipsnap homolog 3B (C. elegans) | NIPSNAP3B | nipsnap homolog 3B (C. elegans) | Symbol and/or name change | 5135510 | APPROVED |
 |
| More on NIPSNAP3B | |
|
Alliance Gene |
|
NCBI Gene |
|
Ensembl Gene |
|
|
JBrowse: hg19 hg38 |
|
HGNC Report |
|
NCBI Genome Data Viewer |
| CRRD Object Information | |
| CRRD ID: | 1348563 |
| Created: | 2005-03-08 |
| Species: | Homo sapiens |
| Last Modified: | 2019-11-26 |
| Status: | ACTIVE |
