Version: 8.0.0
Date: Tue Jan 28 2025
7,592 results for erc1
Allele/Variant

Erc1tm1a(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:5428652
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1a(EUCOMM)Hmgu

Erc1tm1c(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:6449229
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1c(EUCOMM)Hmgu

Erc1tm1.1Toh

(Mus musculus)
Allele/Variant
Source: MGI:6512418
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1.1Toh

Erc1tm1.1Aakh

(Mus musculus)
Allele/Variant
Source: MGI:7316481
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1.1Aakh

Erc1tm1Ksak

(Mus musculus)
Allele/Variant
Source: MGI:5827582
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1Ksak

Erc1tm1Sud

(Mus musculus)
Allele/Variant
Source: MGI:3763189
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1Sud

Erc1tm1b(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:5692791
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm1b(EUCOMM)Hmgu

Erc1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7298633
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1em1Gpt

Erc1Gt(RRF343)Byg

(Mus musculus)
Allele/Variant
Source: MGI:4127703
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1Gt(RRF343)Byg

Erc1tm2.1Sud

(Mus musculus)
Allele/Variant
Source: MGI:4940381
Genes: Erc1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Erc1 (Mmu)
Genes: Erc1 (Mmu)
Symbol: Erc1tm2.1Sud

erc1-Δ

(Saccharomyces cerevisiae)
Allele/Variant
Source: SGD:S000279253
Genes: ERC1 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: erc1-Δ (Sce)
Genes: ERC1 (Sce)
Symbol: erc1-Δ

la024749Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-12316
Genes: erc1b (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: erc1b (Dre)

Hsap\ERC1UAS.Tag:HA

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0370174
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\ERC1
Construct Expressed Component: ERC1 (Hsa)

sa24673

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-17883
Genes: erc1a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: erc1a (Dre)

sa31376

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-992
Genes: erc1b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: erc1b (Dre)

sa24672

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-17882
Genes: erc1a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: non_coding_transcript_exon_variant, splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: erc1a (Dre)

sa20205

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-15162
Genes: erc1b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: erc1b (Dre)

sa44299

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-9673
Genes: erc1a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
Genes: erc1a (Dre)

sa33386

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-2350
Genes: erc1b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: erc1b (Dre)

(GRCh38)12:1371872C>T

(Homo sapiens)
Allele/Variant
Source: rs35478691
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1371872C>T

(GRCh38)12:1028450A>G

(Homo sapiens)
Allele/Variant
Source: rs372323969
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1028450A>G

(GRCh38)12:1028028C>T

(Homo sapiens)
Allele/Variant
Source: rs775689550
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1028028C>T

(GRCh38)12:1110274G>A

(Homo sapiens)
Allele/Variant
Source: rs147857333
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1110274G>A

(GRCh38)12:1182006G>A

(Homo sapiens)
Allele/Variant
Source: rs1954529888
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1182006G>A

(GRCh38)12:1236864G>A

(Homo sapiens)
Allele/Variant
Source: rs376405419
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1236864G>A

(GRCh38)12:1490097A>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.1490097A>C
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1490097A>C

(GRCh38)12:1236834A>G

(Homo sapiens)
Allele/Variant
Source: rs374319917
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, coding_sequence_variant, incomplete_terminal_codon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1236834A>G

(GRCh38)12:1371874A>G

(Homo sapiens)
Allele/Variant
Source: rs573132476
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1371874A>G

(GRCh38)12:1083520C>T

(Homo sapiens)
Allele/Variant
Source: rs187560506
Genes: ERC1 (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)12:1083520C>T

(GRCh38)12:1027951G>C

(Homo sapiens)
Allele/Variant
Source: rs61740169
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1027951G>C

(GRCh38)12:1028203C>T

(Homo sapiens)
Allele/Variant
Source: rs138791726
Genes: ERC1 (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)12:1028203C>T

(GRCh38)12:1190003G>A

(Homo sapiens)
Allele/Variant
Source: rs998691557
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1190003G>A

(GRCh38)12:1181929G>A

(Homo sapiens)
Allele/Variant
Source: rs377706150
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1181929G>A

(GRCh38)12:1027967C>T

(Homo sapiens)
Allele/Variant
Source: rs749881506
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1027967C>T

(GRCh38)12:1236782C>G

(Homo sapiens)
Allele/Variant
Source: rs370750239
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1236782C>G

(GRCh38)12:1480892G>T

(Homo sapiens)
Allele/Variant
Source: rs112807806
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1480892G>T

(GRCh38)12:1236902C>A

(Homo sapiens)
Allele/Variant
Source: rs201360261
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1236902C>A

(GRCh38)12:1444631A>G

(Homo sapiens)
Allele/Variant
Source: rs12319376
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1444631A>G

(GRCh38)12:1183386G>C

(Homo sapiens)
Allele/Variant
Source: rs61758142
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1183386G>C

(GRCh38)12:1180569C>A

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.1180569C>A
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1180569C>A

(GRCh38)12:1181934A>G

(Homo sapiens)
Allele/Variant
Source: rs141757454
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1181934A>G

(GRCh38)12:1028226G>A

(Homo sapiens)
Allele/Variant
Source: rs770130777
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1028226G>A

(GRCh38)12:1083521G>A

(Homo sapiens)
Allele/Variant
Source: rs912612332
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1083521G>A

(GRCh38)12:1236858C>T

(Homo sapiens)
Allele/Variant
Source: rs776148895
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1236858C>T

(GRCh38)12:1110325A>G

(Homo sapiens)
Allele/Variant
Source: rs372551806
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1110325A>G

(GRCh38)12:1189979C>G

(Homo sapiens)
Allele/Variant
Source: rs757912572
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1189979C>G

(GRCh38)12:1371966C>T

(Homo sapiens)
Allele/Variant
Source: rs1181099489
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1371966C>T

(GRCh38)12:1144549A>T

(Homo sapiens)
Allele/Variant
Source: rs207472607
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1144549A>T

(GRCh38)12:1116006G>T

(Homo sapiens)
Allele/Variant
Source: rs374949092
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1116006G>T

(GRCh38)12:1444700G>A

(Homo sapiens)
Allele/Variant
Source: rs377422276
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1444700G>A