Version: 8.0.0
Date: Tue Jan 28 2025
1,718 results for rspry1

rspry1

(Danio rerio)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: si:ch211-257c9.1
Source: ZFIN:ZDB-GENE-061026-2
Biotype: protein coding gene
Symbol: rspry1 (Dre)
Symbol: rspry1
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Strict Orthology Symbols: rspry1

Rspry1

(Rattus norvegicus)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: LOC291860, similar to F16A11.1, LOC689249, MGC156751, similar to SPla/RYanodine receptor SPRY (1J970), RING finger and SPRY domain-containing protein 1, RGD1308847
Source: RGD:1308847
Biotype: protein coding gene
Symbol: Rspry1 (Rno)
Symbol: Rspry1
Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1); INTERACTS WITH 3-chloropropane
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Strict Orthology Symbols: rspry1

Rspry1

(Mus musculus)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: AI608258, expressed sequence AI608258, RGD1308847, 4930470D19Rik, RIKEN cDNA 4930470D19 gene
Source: MGI:1914860
Biotype: protein coding gene
Symbol: Rspry1 (Mmu)
Symbol: Rspry1
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Strict Orthology Symbols: rspry1
Alleles: Rspry1 (Mmu)...Rspry1 (Mmu)

RSPRY1

(Homo sapiens)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: KIAA1972, SEMDFA, RING finger and SPRY domain-containing protein 1
Source: HGNC:29420
Biotype: protein coding gene
Symbol: RSPRY1 (Hsa)
Symbol: RSPRY1
Strict Orthology Symbols: rspry1

rspry1

(Xenopus tropicalis)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: ring finger and SPRY domain containing 1, rspry1
Source: Xenbase:XB-GENE-1002344
Biotype: gene
Symbol: rspry1
Symbol: rspry1 (Xtr)
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Synonyms: rspry1...rspry1...rspry1
Strict Orthology Symbols: rspry1

rspry1.L

(Xenopus laevis)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: rspry1.L, ring finger and SPRY domain containing 1
Source: Xenbase:XB-GENE-17345261
Biotype: gene
Symbol: rspry1.L (Xla)
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Strict Orthology Symbols: rspry1
Symbol: rspry1.L

rspry1.S

(Xenopus laevis)
Gene
Name: ring finger and SPRY domain containing 1
Synonyms: ring finger and SPRY domain containing 1, rspry1.S
Source: Xenbase:XB-GENE-1002350
Biotype: gene
Symbol: rspry1.S (Xla)
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Strict Orthology Symbols: rspry1
Symbol: rspry1.S

Rspry1tm1Lex

(Mus musculus)
Allele/Variant
Source: MGI:5007310
Genes: Rspry1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Rspry1 (Mmu)
Genes: Rspry1 (Mmu)
Symbol: Rspry1tm1Lex

Rspry1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305642
Genes: Rspry1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Rspry1 (Mmu)
Genes: Rspry1 (Mmu)
Symbol: Rspry1em1Gpt

F16A11.1

(Caenorhabditis elegans)
Gene
Name: RING finger and SPRY domain-containing protein 1
Synonyms: CELE_F16A11.1
Source: WB:WBGene00008876
Biotype: protein coding gene
Gene Synopsis: Is an ortholog of human RSPRY1 (ring finger and SPRY domain containing 1).
Automated Gene Synopsis: Orthologous to human RSPRY1 (ring finger and SPRY domain containing 1).
Strict Orthology Symbols: rspry1

proteolysis involved in protein catabolic process

Gene Ontology
Source: GO:0051603
Synonyms:
  • peptidolysis during cellular protein catabolic process
  • peptidolysis during cellular protein catabolism
Branch: biological process
Genes: Rspry1 (Rno)...RSPRY1 (Hsa)...Rspry1 (Mmu)...rspry1 (Dre)

ubiquitin-protein transferase activity

Gene Ontology
Source: GO:0004842
Synonyms:
  • E2
  • E3
Branch: molecular function
Genes: rspry1 (Dre)...Rspry1 (Rno)...RSPRY1 (Hsa)...Rspry1 (Mmu)

sa32199

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-1518
Genes: rspry1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: rspry1 (Dre)

sa23276

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-17004
Genes: rspry1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: rspry1 (Dre)

sa16314

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-4804
Genes: rspry1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: rspry1 (Dre)

sa23277

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-11662
Genes: rspry1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: rspry1 (Dre)

sa43079

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-8702
Genes: rspry1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: rspry1 (Dre)

extracellular region

Gene Ontology
Source: GO:0005576
Synonyms:
  • extracellular
Branch: cellular component
Genes: Rspry1 (Mmu)...RSPRY1 (Hsa)

metal ion binding

Gene Ontology
Source: GO:0046872
Synonyms:
  • heavy metal binding
  • metal binding
Branch: molecular function
Genes: Rspry1 (Mmu)...rspry1 (Dre)...RSPRY1 (Hsa)

cytoplasm

Gene Ontology
Source: GO:0005737
Synonyms: Not Available
Branch: cellular component
Genes: rspry1 (Dre)...Rspry1 (Mmu)...Rspry1 (Rno)...RSPRY1 (Hsa)

(GRCh38)16:57238875C>G

(Homo sapiens)
Allele/Variant
Source: rs1468419280
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57238875C>G

(GRCh38)16:57216148C>T

(Homo sapiens)
Allele/Variant
Source: rs777991006
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57216148C>T

(GRCh38)16:57227371C>T

(Homo sapiens)
Allele/Variant
Source: rs60653561
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57227371C>T

(GRCh38)16:57227380G>A

(Homo sapiens)
Allele/Variant
Source: rs759791177
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57227380G>A

(GRCh38)16:57238928C>T

(Homo sapiens)
Allele/Variant
Source: rs1327464943
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57238928C>T

(GRCh38)16:57230748G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.57230748G>A
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57230748G>A

(GRCh38)16:57231212T>A

(Homo sapiens)
Allele/Variant
Source: rs2075214464
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57231212T>A

(GRCh38)16:57216945C>T

(Homo sapiens)
Allele/Variant
Source: rs1025369477
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57216945C>T

(GRCh38)16:57209070C>T

(Homo sapiens)
Allele/Variant
Source: rs375654242
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57209070C>T

(GRCh38)16:57235194G>A

(Homo sapiens)
Allele/Variant
Source: rs765218951
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57235194G>A

(GRCh38)16:57204890C>A

(Homo sapiens)
Allele/Variant
Source: rs755475021
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57204890C>A

(GRCh38)16:57209057T>A

(Homo sapiens)
Allele/Variant
Source: rs147902966
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57209057T>A

(GRCh38)16:57230828T>C

(Homo sapiens)
Allele/Variant
Source: rs2075205929
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57230828T>C

(GRCh38)16:57221367C>T

(Homo sapiens)
Allele/Variant
Source: rs150201254
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57221367C>T

(GRCh38)16:57216994G>A

(Homo sapiens)
Allele/Variant
Source: rs760353400
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57216994G>A

(GRCh38)16:57209198A>G

(Homo sapiens)
Allele/Variant
Source: rs371561971
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57209198A>G

(GRCh38)16:57221434T>C

(Homo sapiens)
Allele/Variant
Source: rs753112705
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57221434T>C

(GRCh38)16:57204834A>G

(Homo sapiens)
Allele/Variant
Source: rs377663780
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57204834A>G

(GRCh38)16:57204705G>T

(Homo sapiens)
Allele/Variant
Source: rs758306925
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57204705G>T

(GRCh38)16:57212959T>G

(Homo sapiens)
Allele/Variant
Source: rs766875613
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57212959T>G

(GRCh38)16:57217009G>C

(Homo sapiens)
Allele/Variant
Source: rs776059388
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57217009G>C

(GRCh38)16:57209079A>C

(Homo sapiens)
Allele/Variant
Source: rs146849995
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57209079A>C

(GRCh38)16:57212985A>G

(Homo sapiens)
Allele/Variant
Source: rs746592167
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57212985A>G

(GRCh38)16:57230704C>T

(Homo sapiens)
Allele/Variant
Source: rs775579081
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57230704C>T

(GRCh38)16:57208065G>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.57208065G>T
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57208065G>T

(GRCh38)16:57227234A>C

(Homo sapiens)
Allele/Variant
Source: rs11643790
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57227234A>C

(GRCh38)16:57231206A>G

(Homo sapiens)
Allele/Variant
Source: rs2075214282
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57231206A>G

(GRCh38)16:57216946G>A

(Homo sapiens)
Allele/Variant
Source: rs375513384
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57216946G>A

(GRCh38)16:57204992C>A

(Homo sapiens)
Allele/Variant
Source: rs767390490
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57204992C>A

(GRCh38)16:57230707C>T

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.57230707C>T
Genes: RSPRY1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:57230707C>T