Version: 8.0.0
Date: Tue Jan 28 2025
5,299 results for fam134b

retreg1

(Danio rerio)
Gene
Name: reticulophagy regulator 1
Synonyms: fam134b
Source: ZFIN:ZDB-GENE-130221-1
Biotype: protein coding gene
Synonyms: fam134b...fam134b...fam134b

RETREG1-AS1

(Homo sapiens)
Gene
Name: RETREG1 antisense RNA 1
Synonyms: LOC101929524, uncharacterized LOC101929524, AC024588.1, novel transcript, antisense to FAM134B
Source: HGNC:55551
Biotype: ncRNA gene
Synonyms: novel transcript, antisense to FAM134B

RETREG1

(Homo sapiens)
Gene
Name: reticulophagy regulator 1
Synonyms: family with sequence similarity 134 member B, JK1, FAM134B, FLJ22179, FLJ20152, family with sequence similarity 134, member B, JK-1, FLJ22155, reticulophagy receptor 1, reticulophagy receptor FAM134B
Source: HGNC:25964
Biotype: protein coding gene
Synonyms: FAM134B...FAM134B...reticulophagy receptor FAM134B

Retreg1

(Rattus norvegicus)
Gene
Name: reticulophagy regulator 1
Synonyms: Fam134b, LOC103689968, family with sequence similarity 134, member B, LOC619558, reticulophagy receptor 1, hypothetical protein LOC619558, reticulophagy receptor FAM134B, protein FAM134B
Source: RGD:1565003
Biotype: protein coding gene
Synonyms: Fam134b...Fam134b...reticulophagy receptor FAM134B...protein FAM134B

retreg1.S

(Xenopus laevis)
Gene
Name: reticulophagy regulator 1
Synonyms: retreg1.S, reticulophagy regulator 1, fam134b
Source: Xenbase:XB-GENE-6488772
Biotype: gene
Synonyms: fam134b...fam134b...fam134b

retreg1.L

(Xenopus laevis)
Gene
Name: reticulophagy regulator 1
Synonyms: retreg1.L, reticulophagy regulator 1, fam134b
Source: Xenbase:XB-GENE-17331251
Biotype: gene
Synonyms: fam134b...fam134b...fam134b

retreg1

(Xenopus tropicalis)
Gene
Name: reticulophagy regulator 1
Synonyms: retreg1, reticulophagy regulator 1, fam134b
Source: Xenbase:XB-GENE-982868
Biotype: gene
Synonyms: fam134b...fam134b...fam134b

Retreg1

(Mus musculus)
Gene
Name: reticulophagy regulator 1
Synonyms: Fam134b, RIKEN cDNA 1810015C04 gene, family with sequence similarity 134, member B, expressed sequence AU015349, AU015349, 1810015C04Rik
Source: MGI:1913520
Biotype: protein coding gene
Synonyms: Fam134b...Fam134b

Retreg1em2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586192
Genes: Retreg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam134b

Retreg1em5Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305364
Genes: Retreg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam134b

Retreg1em1(IMPC)J

(Mus musculus)
Allele/Variant
Source: MGI:6304302
Genes: Retreg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam134b

hereditary sensory and autonomic neuropathy type 2B

Disease
Source: DOID:0070150
Definition: A hereditary sensory and autonomic neuropathy type 2 characterized by early childhood onset of distal sensory impairment that has_material_basis_in homozygous mutation in the FAM134B gene on chromosome 5p15.

Retreg1tm1.1Cahb

(Mus musculus)
Allele/Variant
Source: MGI:5774849
Genes: Retreg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam134b

Retreg1tm1.2Myz

(Mus musculus)
Allele/Variant
Source: MGI:6450915
Genes: Retreg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam134b

Retreg1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305363
Genes: Retreg1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Fam134b

(GRCh38)5:16474855C>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.16474855C>A
Genes: RETREG1 (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)5:16474855C>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475017A>G

(Homo sapiens)
Allele/Variant
Source: rs372629414
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16475017A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475125G>A

(Homo sapiens)
Allele/Variant
Source: rs373322680
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16475125G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475144T>A

(Homo sapiens)
Allele/Variant
Source: rs2126505973
Genes: RETREG1 (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)5:16475144T>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475226G>A

(Homo sapiens)
Allele/Variant
Source: rs750575538
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16475226G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16477657C>G

(Homo sapiens)
Allele/Variant
Source: rs2126510439
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16477657C>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16616764A>T

(Homo sapiens)
Allele/Variant
Source: rs1579736280
Genes: RETREG1-AS1 (Hsa), RETREG1 (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)5:16616764A>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16616811C>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.16616811C>T
Genes: RETREG1-AS1 (Hsa), RETREG1 (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)5:16616811C>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16616792G>A

(Homo sapiens)
Allele/Variant
Source: rs1012745104
Genes: RETREG1-AS1 (Hsa), RETREG1 (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)5:16616792G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16616686G>A

(Homo sapiens)
Allele/Variant
Source: rs776560421
Genes: RETREG1-AS1 (Hsa), RETREG1 (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)5:16616686G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16474801T>C

(Homo sapiens)
Allele/Variant
Source: rs1474211875
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16474801T>C
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475146A>G

(Homo sapiens)
Allele/Variant
Source: rs200156015
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16475146A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475162C>A

(Homo sapiens)
Allele/Variant
Source: rs772681100
Genes: RETREG1 (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)5:16475162C>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16478106G>A

(Homo sapiens)
Allele/Variant
Source: rs953507650
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16478106G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16478986T>G

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.16478986T>G
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16478986T>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16481055C>T

(Homo sapiens)
Allele/Variant
Source: rs759194355
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16481055C>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475227G>A

(Homo sapiens)
Allele/Variant
Source: rs751914179
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16475227G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16478032A>G

(Homo sapiens)
Allele/Variant
Source: rs137852738
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16478032A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16481243A>G

(Homo sapiens)
Allele/Variant
Source: rs148364715
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16481243A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16477694T>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.16477694T>A
Genes: RETREG1 (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)5:16477694T>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16474986T>A

(Homo sapiens)
Allele/Variant
Source: rs780084870
Genes: RETREG1 (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)5:16474986T>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475053A>G

(Homo sapiens)
Allele/Variant
Source: rs886043753
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16475053A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16478947A>G

(Homo sapiens)
Allele/Variant
Source: rs200070690
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16478947A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16478048C>T

(Homo sapiens)
Allele/Variant
Source: rs2126511545
Genes: RETREG1 (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)5:16478048C>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16478866C>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.16478866C>T
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16478866C>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16477736G>C

(Homo sapiens)
Allele/Variant
Source: rs137852739
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16477736G>C
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16477738G>C

(Homo sapiens)
Allele/Variant
Source: rs778481043
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16477738G>C
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16508311A>C

(Homo sapiens)
Allele/Variant
Source: rs72744178
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16508311A>C
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16616954A>G

(Homo sapiens)
Allele/Variant
Source: rs773314283
Genes: RETREG1-AS1 (Hsa), RETREG1 (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)5:16616954A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16616957C>A

(Homo sapiens)
Allele/Variant
Source: rs1419565672
Genes: RETREG1-AS1 (Hsa), RETREG1 (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)5:16616957C>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16474999C>G

(Homo sapiens)
Allele/Variant
Source: rs150705378
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16474999C>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475009A>G

(Homo sapiens)
Allele/Variant
Source: rs1057518317
Genes: RETREG1 (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)5:16475009A>G
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16475028C>T

(Homo sapiens)
Allele/Variant
Source: rs753136289
Genes: RETREG1 (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)5:16475028C>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16477755C>T

(Homo sapiens)
Allele/Variant
Source: rs1202823800
Genes: RETREG1 (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)5:16477755C>T
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B

(GRCh38)5:16477780G>A

(Homo sapiens)
Allele/Variant
Source: rs2126510926
Genes: RETREG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:16477780G>A
Gene Synonyms: FAM134B...reticulophagy receptor FAM134B