103 results for tprgl

Tprgl-ps2

(Mus musculus)
Gene
Name: transformation related protein 63 regulated like, pseudogene 2
Synonyms: predicted gene 8018, Gm8018, EG666276, predicted gene, EG666276
Source: MGI:3645629
Biotype: pseudogene
Symbol: Tprgl-ps2 (Mmu)
Symbol: Tprgl-ps2

Tprgl-ps1

(Mus musculus)
Gene
Name: transformation related protein 63 regulated like, pseudogene 1
Synonyms: Gm18958, predicted gene, 18958
Source: MGI:5011143
Biotype: pseudogene
Symbol: Tprgl-ps1 (Mmu)
Symbol: Tprgl-ps1

Tprg1l

(Mus musculus)
Gene
Name: transformation related protein 63 regulated 1 like
Synonyms: 1200015A19Rik, transformation related protein 63 regulated like, mover, RIKEN cDNA 1200015A19 gene, Tprgl
Source: MGI:1915058
Biotype: protein coding gene
Synonyms: Tprgl...Tprgl

TPRG1L

(Homo sapiens)
Gene
Name: tumor protein p63 regulated 1 like
Synonyms: SVAP30, tumor protein p63 regulated 1-like, mover, FAM79A, RP11-46F15.3, mossy fiber terminal-associated vertebrate-specific presynaptic protein, h-mover, tumor protein p63-regulated gene 1-like protein, family with sequence similarity 79, member A, TPRGL, FLJ21811
Source: HGNC:27007
Biotype: protein coding gene
Synonyms: TPRGL...TPRGL

Tprg1lem1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7626958
Genes: Tprg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Tprgl

Tprg1ltm1.1Tdre

(Mus musculus)
Allele/Variant
Source: MGI:6385131
Genes: Tprg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Tprgl

Tprg1lem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7307780
Genes: Tprg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Tprgl

Tprg1lem1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7587245
Genes: Tprg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Tprgl

Tprg1ltm1.2Tdre

(Mus musculus)
Allele/Variant
Source: MGI:6385150
Genes: Tprg1l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Tprgl

(GRCh38)1:3625088G>T

(Homo sapiens)
Allele/Variant
Source: rs1644472793
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625088G>T
Gene Synonyms: TPRGL

(GRCh38)1:3627579A>G

(Homo sapiens)
Allele/Variant
Source: rs1305794677
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3627579A>G
Gene Synonyms: TPRGL

(GRCh38)1:3628538A>T

(Homo sapiens)
Allele/Variant
Source: rs369478316
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3628538A>T
Gene Synonyms: TPRGL

(GRCh38)1:3625757C>T

(Homo sapiens)
Allele/Variant
Source: rs201126720
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625757C>T
Gene Synonyms: TPRGL

(GRCh38)1:3625850C>T

(Homo sapiens)
Allele/Variant
Source: rs144560440
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625850C>T
Gene Synonyms: TPRGL

(GRCh38)1:3627564T>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.3627564T>C
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3627564T>C
Gene Synonyms: TPRGL

(GRCh38)1:3625091T>G

(Homo sapiens)
Allele/Variant
Source: rs928393948
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625091T>G
Gene Synonyms: TPRGL

(GRCh38)1:3628505C>T

(Homo sapiens)
Allele/Variant
Source: rs138694185
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3628505C>T
Gene Synonyms: TPRGL

(GRCh38)1:3627539A>T

(Homo sapiens)
Allele/Variant
Source: rs140484869
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3627539A>T
Gene Synonyms: TPRGL

(GRCh38)1:3625157G>T

(Homo sapiens)
Allele/Variant
Source: rs758658171
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625157G>T
Gene Synonyms: TPRGL

(GRCh38)1:3627585G>A

(Homo sapiens)
Allele/Variant
Source: rs772930439
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3627585G>A
Gene Synonyms: TPRGL

(GRCh38)1:3625199C>T

(Homo sapiens)
Allele/Variant
Source: rs903216951
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625199C>T
Gene Synonyms: TPRGL

(GRCh38)1:3625254A>G

(Homo sapiens)
Allele/Variant
Source: rs1644474784
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625254A>G
Gene Synonyms: TPRGL

(GRCh38)1:3625760A>T

(Homo sapiens)
Allele/Variant
Source: rs1292949014
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625760A>T
Gene Synonyms: TPRGL

(GRCh38)1:3625832A>G

(Homo sapiens)
Allele/Variant
Source: rs1644483678
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625832A>G
Gene Synonyms: TPRGL

(GRCh38)1:3625184G>A

(Homo sapiens)
Allele/Variant
Source: rs894696879
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3625184G>A
Gene Synonyms: TPRGL

(GRCh38)1:3628506G>A

(Homo sapiens)
Allele/Variant
Source: rs1413182628
Genes: TPRG1L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:3628506G>A
Gene Synonyms: TPRGL

Allele/Variant
Source: rs33031651
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154241999G>A
Gene Synonyms: Tprgl

Allele/Variant
Source: rs227469455
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242183G>C
Gene Synonyms: Tprgl

Allele/Variant
Source: rs1135370422
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242351A>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs236206269
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242376C>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs1132041601
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242474G>A
Gene Synonyms: Tprgl

Allele/Variant
Source: rs33033364
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242713T>C
Gene Synonyms: Tprgl

Allele/Variant
Source: rs33034275
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154243440T>C
Gene Synonyms: Tprgl

Allele/Variant
Source: rs266105763
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154243389T>G
Gene Synonyms: Tprgl

Allele/Variant
Source: rs33035174
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154243963A>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs230854745
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154244759T>C
Gene Synonyms: Tprgl

Allele/Variant
Source: rs264378433
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242815G>A
Gene Synonyms: Tprgl

Allele/Variant
Source: rs33033367
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154243046C>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs1133273477
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154244129T>A
Gene Synonyms: Tprgl

Allele/Variant
Source: rs246399650
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
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: (GRCm39)4:154244556C>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs239558066
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154244737G>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs212177694
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154244755C>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs239566408
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154244206G>C
Gene Synonyms: Tprgl

Allele/Variant
Source: rs260406953
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154244750A>G
Gene Synonyms: Tprgl

Allele/Variant
Source: rs33033370
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154243297T>C
Gene Synonyms: Tprgl

Allele/Variant
Source: rs244373327
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242118A>G
Gene Synonyms: Tprgl

Allele/Variant
Source: rs1133822544
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242817G>A
Gene Synonyms: Tprgl

Allele/Variant
Source: rs1135034442
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242875C>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs1132925169
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154242907G>T
Gene Synonyms: Tprgl

Allele/Variant
Source: rs255803751
Genes: Tprg1l (Mmu), Wrap73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:154243075G>A
Gene Synonyms: Tprgl