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Molecular Function
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Analyze GeneStrainQTL List |
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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 |
FAM131B (Homo sapiens - human) |
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Fam131b (Mus musculus - house mouse) |
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Fam131b (Rattus norvegicus - Norway rat) |
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Fam131b (Chinchilla lanigera - long-tailed chinchilla) |
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FAM131B (Pan paniscus - bonobo/pygmy chimpanzee) |
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FAM131B (Canis lupus familiaris - dog) |
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Fam131b (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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FAM131B (Sus scrofa - pig) |
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RH46942 |
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D1S3694 |
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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. |
RefSeq Transcripts | NM_001031690 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001278297 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001371248 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001371249 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001371250 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001371251 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001371252 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001371253 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_014690 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AB018316 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC092214 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AC093673 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK124557 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK291470 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL832579 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC045611 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC050543 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH236959 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471198 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA226407 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DA334424 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_001031690 ⟹ NP_001026860 | |||||||||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | |||||||||||||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
GGGATGGAGAGGGGAGGGGGGAGCGGAGCCGAGCGGAGACAGCCGCGGCGCTGCAGAGCGGCTGhide sequence |
RefSeq Acc Id: | NM_001278297 ⟹ NP_001265226 | ||||||||||||||||||||||||
RefSeq Status: | VALIDATED | ||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||
Position: |
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Sequence: |
GGGATGGAGAGGGGAGGGGGGAGCGGAGCCGAGCGGAGACAGCCGCGGCGCTGCAGAGCGGCTGhide sequence |
RefSeq Acc Id: | NM_001371248 ⟹ NP_001358177 | |||||||||
RefSeq Status: | VALIDATED | |||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | NM_001371249 ⟹ NP_001358178 | |||||||||
RefSeq Status: | VALIDATED | |||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | NM_001371250 ⟹ NP_001358179 | |||||||||
RefSeq Status: | VALIDATED | |||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | NM_001371251 ⟹ NP_001358180 | |||||||||
RefSeq Status: | VALIDATED | |||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | NM_001371252 ⟹ NP_001358181 | |||||||||
RefSeq Status: | VALIDATED | |||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | NM_001371253 ⟹ NP_001358182 | |||||||||
RefSeq Status: | VALIDATED | |||||||||
Type: | CODING | |||||||||
Position: |
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RefSeq Acc Id: | NM_014690 ⟹ NP_055505 | |||||||||||||||||||||||||||||||||||||||
RefSeq Status: | VALIDATED | |||||||||||||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
ATCTCTCTCTCCCTCTCCGTTGCCTTTTACTGTCGTTCCTGCCTCCTCCGATTCGCTTTGTTCAhide sequence |
Protein RefSeqs | NP_001026860 | (Get FASTA) | NCBI Sequence Viewer |
NP_001265226 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001358177 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001358178 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001358179 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001358180 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001358181 | (Get FASTA) | NCBI Sequence Viewer | |
NP_001358182 | (Get FASTA) | NCBI Sequence Viewer | |
NP_055505 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH45611 | (Get FASTA) | NCBI Sequence Viewer |
AAH50543 | (Get FASTA) | NCBI Sequence Viewer | |
AAS07501 | (Get FASTA) | NCBI Sequence Viewer | |
BAA34493 | (Get FASTA) | NCBI Sequence Viewer | |
BAF84159 | (Get FASTA) | NCBI Sequence Viewer | |
CAD89938 | (Get FASTA) | NCBI Sequence Viewer | |
EAL23787 | (Get FASTA) | NCBI Sequence Viewer | |
EAW51853 | (Get FASTA) | NCBI Sequence Viewer | |
EAW51854 | (Get FASTA) | NCBI Sequence Viewer | |
EAW51855 | (Get FASTA) | NCBI Sequence Viewer | |
EAW51856 | (Get FASTA) | NCBI Sequence Viewer | |
EAW51857 | (Get FASTA) | NCBI Sequence Viewer | |
Q86XD5 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_055505 ⟸ NM_014690 |
- Peptide Label: | isoform b |
- UniProtKB: | Q86XD5 (UniProtKB/Swiss-Prot) |
- Sequence: |
MDSTSSLHGSSLHRPSTEQTRTDFSWDGINLSMEDTTSILPKLKRNSNAYGIGALAKSSFSGIShide sequence |
RefSeq Acc Id: | NP_001026860 ⟸ NM_001031690 |
- Peptide Label: | isoform a |
- UniProtKB: | Q86XD5 (UniProtKB/Swiss-Prot) |
- Sequence: |
MGCIGSRTVGNEVIAVDWKGLKDVDQINMDSTSSLHGSSLHRPSTEQTRTDFSWDGINLSMEDThide sequence |
RefSeq Acc Id: | NP_001265226 ⟸ NM_001278297 |
- Peptide Label: | isoform c |
- UniProtKB: | Q86XD5 (UniProtKB/Swiss-Prot), O94871 (UniProtKB/TrEMBL) |
- Sequence: |
MKDHVTKPTAMGQGRVAHMIEWQGWGKTPAVQPQHSHESVRRDTDAYSDLSDGEKEARFLAGVMhide sequence |
RefSeq Acc Id: | NP_001358179 ⟸ NM_001371250 |
- Peptide Label: | isoform b |
RefSeq Acc Id: | NP_001358177 ⟸ NM_001371248 |
- Peptide Label: | isoform d |
RefSeq Acc Id: | NP_001358180 ⟸ NM_001371251 |
- Peptide Label: | isoform f |
RefSeq Acc Id: | NP_001358181 ⟸ NM_001371252 |
- Peptide Label: | isoform f |
RefSeq Acc Id: | NP_001358178 ⟸ NM_001371249 |
- Peptide Label: | isoform e |
RefSeq Acc Id: | NP_001358182 ⟸ NM_001371253 |
- Peptide Label: | isoform f |
RGD ID: | 7212165 | |||||||||
Promoter ID: | EPDNEW_H11829 | |||||||||
Type: | initiation region | |||||||||
Name: | FAM131B_3 | |||||||||
Description: | family with sequence similarity 131 member B | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
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RGD ID: | 7212167 | |||||||||
Promoter ID: | EPDNEW_H11830 | |||||||||
Type: | initiation region | |||||||||
Name: | FAM131B_1 | |||||||||
Description: | family with sequence similarity 131 member B | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
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RGD ID: | 7212175 | |||||||||
Promoter ID: | EPDNEW_H11834 | |||||||||
Type: | initiation region | |||||||||
Name: | FAM131B_2 | |||||||||
Description: | family with sequence similarity 131 member B | |||||||||
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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Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 | copy number gain | Cleft palate, isolated [RCV000050876]|See cases [RCV000050876] | Chr7:129310166..159282390 [GRCh38] Chr7:128950007..159075079 [GRCh37] Chr7:128737243..158767840 [NCBI36] Chr7:7q32.1-36.3 |
pathogenic |
GRCh38/hg38 7q34-35(chr7:142578948-144254897)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050639]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050639]|See cases [RCV000050639] | Chr7:142578948..144254897 [GRCh38] Chr7:142528609..143951990 [GRCh37] Chr7:141967554..143582923 [NCBI36] Chr7:7q34-35 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|See cases [RCV000051101] | Chr7:132850196..159325876 [GRCh38] Chr7:132534956..159118566 [GRCh37] Chr7:132185496..158811327 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 | copy number loss | Ambiguous genitalia [RCV000052250]|See cases [RCV000052250] | Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 | copy number gain | Global developmental delay [RCV000053576]|See cases [RCV000053576] | Chr7:136309982..159307523 [GRCh38] Chr7:135994730..159100212 [GRCh37] Chr7:135645270..158792973 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:142021716-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|See cases [RCV000053577] | Chr7:142021716..159325876 [GRCh38] Chr7:142528609..159118566 [GRCh37] Chr7:141367985..158811327 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.1(chr7:132023155-149309794)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|See cases [RCV000054172] | Chr7:132023155..149309794 [GRCh38] Chr7:131707914..149006885 [GRCh37] Chr7:131358454..148637818 [NCBI36] Chr7:7q32.3-36.1 |
pathogenic |
GRCh38/hg38 7q33-35(chr7:135414108-144140219)x1 | copy number loss | Obesity [RCV000054173]|See cases [RCV000054173] | Chr7:135414108..144140219 [GRCh38] Chr7:135098857..143837312 [GRCh37] Chr7:134749397..143468245 [NCBI36] Chr7:7q33-35 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] | Chr7:139365967..159282531 [GRCh38] Chr7:139050713..159075220 [GRCh37] Chr7:138701253..158767981 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1 | copy number loss | Corpus callosum agenesis [RCV000054176]|See cases [RCV000054176] | Chr7:140754198..159307523 [GRCh38] Chr7:140453998..159100212 [GRCh37] Chr7:140100467..158792973 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:142358524-159282531)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054177]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054177]|See cases [RCV000054177] | Chr7:142358524..159282531 [GRCh38] Chr7:142528609..159075220 [GRCh37] Chr7:141726947..158767981 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
NM_001031690.2(FAM131B):c.937G>A (p.Glu313Lys) | single nucleotide variant | Malignant melanoma [RCV000067717] | Chr7:143356696 [GRCh38] Chr7:143053789 [GRCh37] Chr7:142763911 [NCBI36] Chr7:7q34 |
not provided |
NM_001031690.2(FAM131B):c.247C>T (p.Leu83=) | single nucleotide variant | Malignant melanoma [RCV000067718] | Chr7:143359347 [GRCh38] Chr7:143056440 [GRCh37] Chr7:142766562 [NCBI36] Chr7:7q34 |
not provided |
NM_001031690.2(FAM131B):c.246C>T (p.Ala82=) | single nucleotide variant | Malignant melanoma [RCV000067719] | Chr7:143359348 [GRCh38] Chr7:143056441 [GRCh37] Chr7:142766563 [NCBI36] Chr7:7q34 |
not provided |
GRCh38/hg38 7q34-35(chr7:141126407-145652221)x3 | copy number gain | See cases [RCV000133645] | Chr7:141126407..145652221 [GRCh38] Chr7:140826207..145349314 [GRCh37] Chr7:140472676..144980247 [NCBI36] Chr7:7q34-35 |
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 7q33-36.2(chr7:137751200-154815582)x3 | copy number gain | See cases [RCV000136592] | Chr7:137751200..154815582 [GRCh38] Chr7:137435946..154607292 [GRCh37] Chr7:137086486..154238225 [NCBI36] Chr7:7q33-36.2 |
pathogenic |
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 | copy number gain | See cases [RCV000136717] | Chr7:97419852..158923762 [GRCh38] Chr7:97049164..158716453 [GRCh37] Chr7:96887100..158409214 [NCBI36] Chr7:7q21.3-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1 | copy number loss | See cases [RCV000137256] | Chr7:141960861..159335866 [GRCh38] Chr7:142528609..159128556 [GRCh37] Chr7:141307130..158821317 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 | copy number loss | See cases [RCV000138120] | Chr7:134666829..158591882 [GRCh38] Chr7:134351581..158384574 [GRCh37] Chr7:134002121..158077335 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 | copy number gain | See cases [RCV000138847] | Chr7:121863759..159335865 [GRCh38] Chr7:121503813..159128555 [GRCh37] Chr7:121291049..158821316 [NCBI36] Chr7:7q31.32-36.3 |
pathogenic |
GRCh38/hg38 7q33-36.1(chr7:135017687-148807400)x1 | copy number loss | See cases [RCV000138903] | Chr7:135017687..148807400 [GRCh38] Chr7:134702438..148504492 [GRCh37] Chr7:134352978..148135425 [NCBI36] Chr7:7q33-36.1 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 | copy number gain | See cases [RCV000139654] | Chr7:132444095..159335866 [GRCh38] Chr7:132128854..159128556 [GRCh37] Chr7:131779394..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 | copy number gain | See cases [RCV000141413] | Chr7:115459015..159325817 [GRCh38] Chr7:115099069..159118507 [GRCh37] Chr7:114886305..158811268 [NCBI36] Chr7:7q31.2-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 | copy number gain | See cases [RCV000142802] | Chr7:131228764..159335866 [GRCh38] Chr7:130913523..159128556 [GRCh37] Chr7:130564063..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 | copy number gain | See cases [RCV000143754] | Chr7:131171478..159327017 [GRCh38] Chr7:130856237..159119707 [GRCh37] Chr7:130506777..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q34-35(chr7:140061285-144622893)x3 | copy number gain | See cases [RCV000143724] | Chr7:140061285..144622893 [GRCh38] Chr7:139761085..144319986 [GRCh37] Chr7:139407554..143950919 [NCBI36] Chr7:7q34-35 |
uncertain significance |
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 | copy number gain | See cases [RCV000143707] | Chr7:132438072..159327017 [GRCh38] Chr7:132122831..159119707 [GRCh37] Chr7:131773371..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 | copy number gain | See cases [RCV000449264] | Chr7:137589621..159119707 [GRCh37] Chr7:7q33-36.3 |
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 7q33-36.3(chr7:133799185-159119707)x1 | copy number loss | See cases [RCV000448836] | Chr7:133799185..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 | copy number gain | See cases [RCV000447709] | Chr7:98969247..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 | copy number gain | See cases [RCV000447956] | Chr7:128276078..159119707 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:140636858-159119707)x1 | copy number loss | See cases [RCV000510250] | Chr7:140636858..159119707 [GRCh37] Chr7:7q34-36.3 |
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 7q33-36.3(chr7:136758593-159119707)x3 | copy number gain | See cases [RCV000510490] | Chr7:136758593..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1 | copy number loss | See cases [RCV000511889] | Chr7:137917376..159119707 [GRCh37] Chr7:7q33-36.3 |
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 7q34-36.3(chr7:140133025-158982771)x1 | copy number loss | not provided [RCV000682910] | Chr7:140133025..158982771 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 | copy number gain | not provided [RCV000682911] | Chr7:98693388..159119707 [GRCh37] Chr7:7q22.1-36.3 |
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 7q34-35(chr7:139623170-143710268)x3 | copy number gain | not provided [RCV000747069] | Chr7:139623170..143710268 [GRCh37] Chr7:7q34-35 |
benign |
GRCh37/hg19 7q34-36.3(chr7:139623170-158329903)x3 | copy number gain | not provided [RCV000747070] | Chr7:139623170..158329903 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1 | copy number loss | not provided [RCV000747083] | Chr7:141938235..159126310 [GRCh37] Chr7:7q34-36.3 |
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 7q32.1-36.3(chr7:128312450-159119220) | copy number gain | not provided [RCV000767558] | Chr7:128312450..159119220 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
GRCh37/hg19 7q34-35(chr7:141751875-147105208)x3 | copy number gain | not provided [RCV000848670] | Chr7:141751875..147105208 [GRCh37] Chr7:7q34-35 |
uncertain significance |
GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 | copy number gain | not provided [RCV000849569] | Chr7:130592554..159119707 [GRCh37] Chr7:7q32.3-36.3 |
pathogenic |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:22202 | AgrOrtholog |
COSMIC | FAM131B | COSMIC |
Ensembl Genes | ENSG00000159784 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000386396 | UniProtKB/TrEMBL |
ENSP00000386568 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000386984 | UniProtKB/Swiss-Prot | |
ENSP00000387017 | UniProtKB/Swiss-Prot | |
ENSP00000387147 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000410603 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000430601 | UniProtKB/TrEMBL | |
ENSP00000430805 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000409222 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENST00000409346 | UniProtKB/Swiss-Prot | |
ENST00000409408 | UniProtKB/Swiss-Prot | |
ENST00000409578 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000410085 | UniProtKB/TrEMBL | |
ENST00000443739 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000519279 | UniProtKB/TrEMBL | |
ENST00000521347 | UniProtKB/TrEMBL | |
GTEx | ENSG00000159784 | GTEx |
HGNC ID | HGNC:22202 | ENTREZGENE |
Human Proteome Map | FAM131B | Human Proteome Map |
InterPro | FAM131 | UniProtKB/Swiss-Prot |
KEGG Report | hsa:9715 | UniProtKB/Swiss-Prot |
NCBI Gene | 9715 | ENTREZGENE |
PANTHER | PTHR15736 | UniProtKB/Swiss-Prot |
Pfam | FAM131 | UniProtKB/Swiss-Prot |
PharmGKB | PA162386065 | PharmGKB |
UniGene | Hs.648908 | ENTREZGENE |
UniProt | E5RI17_HUMAN | UniProtKB/TrEMBL |
E5RJ60_HUMAN | UniProtKB/TrEMBL | |
F131B_HUMAN | UniProtKB/Swiss-Prot | |
H0Y3V6_HUMAN | UniProtKB/TrEMBL | |
O94871 | ENTREZGENE, UniProtKB/TrEMBL | |
Q86XD5 | ENTREZGENE | |
UniProt Secondary | A4D2H6 | UniProtKB/Swiss-Prot |
A6NDW3 | UniProtKB/Swiss-Prot | |
A8K605 | UniProtKB/Swiss-Prot | |
B8ZZN2 | UniProtKB/Swiss-Prot | |
D3DXE3 | UniProtKB/Swiss-Prot | |
J3KQX2 | UniProtKB/Swiss-Prot | |
Q7L0D6 | UniProtKB/Swiss-Prot | |
Q86T97 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2015-11-24 | FAM131B | family with sequence similarity 131 member B | family with sequence similarity 131, member B | Symbol and/or name change | 5135510 | APPROVED |
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More on FAM131B | |
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Alliance Gene |
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NCBI Gene |
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Ensembl Gene |
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JBrowse: hg19 hg38 |
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HGNC Report |
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NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1605421 |
Created: | 2007-04-28 |
Species: | Homo sapiens |
Last Modified: | 2019-11-26 |
Status: | ACTIVE |
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.