1. Gene
  2. STAG3 - stromal antigen 3 Gene

STAG3 - stromal antigen 3 Gene

Homo sapiens

Also known as SPGF61

Gene ID: 10734 | Gene type: protein coding

About STAG3

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:100,177,724-100,219,334 (from NCBI)

This gene has 19 transcripts (splice variants), 205 orthologues, 2 paralogues and is associated with 3 phenotypes. Biased expression in testis (RPKM 44.6), brain (RPKM 6.1) and 2 other tissues.

Summary

The protein encoded by this gene is expressed in the nucleus and is a subunit of the cohesin complex which regulates the cohesion of sister chromatids during cell division. A mutation in this gene is associated with premature ovarian failure. Alternate splicing results in multiple transcript variants encoding distinct isoforms. This gene has multiple pseudogenes. [provided by RefSeq, Apr 2014]

STAG3 Products(5)

mRNA Protein Name
NM_001282716.1 NP_001269645.1 cohesin subunit SA-3 isoform 1
NM_001282717.2 NP_001269646.1 cohesin subunit SA-3 isoform 2
NM_001282718.2 NP_001269647.1 cohesin subunit SA-3 isoform 3
NM_001375438.1 NP_001362367.1 cohesin subunit SA-3 isoform 2
NM_012447.4 NP_036579.2 cohesin subunit SA-3 isoform 1

STAG3 Protein Structure

STAG

STAG: STAG domain (170 - 289)

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  • 1225 a.a.
Protein Preferred Names Protein Names

cohesin subunit SA-3

SCC3 homolog 3

Related Diseases

Diseases Alias
Premature Ovarian Failure 8

POF8

Ovarian Failure, Premature, Type 8

Spermatogenic Failure 61

SPGF61

Premature Menopause

Primary Ovarian Insufficiency

Premature Ovarian Failure

Hypergonadotropic Hypogonadism

Premature Ovarian Insufficiency

Menopause - Premature

Menopause Praecox

Menopause Premature

Menopause, Premature

Female Hypergonadotropic Hypogonadism

Hypergonadotrophic Ovarian Failure

Primary Female Hypogonadism

Pof - [Premature Ovarian Failure]

Ovarian Failure

Ovarian Secretion Suppression

Ovary Hyposecretion

Ovary Secretion Deficiency

Premature Menopause Nos

Male Infertility

Infertility, Male

Infertility Male

Male Sterility

Absolute Infertility

Infertility
46 Xx Gonadal Dysgenesis

Ovarian Dysgenesis

Gonadal Dysgenesis, 46,Xx

Dysgenesis, Ovarian

Amenorrhea

Absence Of Menstruation

Amenia

Cornelia De Lange Syndrome

De Lange Syndrome

Brachmann De Lange Syndrome

Brachmann-De Lange Syndrome

Cdls

Bdls

Typus Degenerativus Amstelodamensis

Spermatogenic Failure

Azoospermia

Spgf

Spermatogenic Failure, Susceptibility To

Absent Sperm

Aspermatogenesis

Infertility Due To Azoospermia

Hypospermatogenesis

Azoospermatism

Orofacial Cleft 8

OFC8

Cleft Lip With Or Without Cleft Palate, Nonsyndromic, 8

Non-Syndromic Cleft Lip/Palate 8

Non-Syndromic Cleft Lip With Or Without Cleft Palate 8

Orofacial Cleft, Type 8

Bardet-Biedl Syndrome 12

BBS12

Bardet-Biedl Syndrome

Bbs

Bardet-Biedl Syndrome, Type 12

Fanconi Anemia, Complementation Group A

Fanconi Anemia

Fanconi Pancytopenia

Fanconi Anemia Complementation Group A

FANCA

Fa

Fanconi Panmyelopathy

Fanconi'S Anemia

Fanconi Anaemia

Fanconi'S Anaemia

Fanconi Hypoplastic Anemia

Estren-Dameshek Variant Of Fanconi Anemia

Estren-Dameshek Variant Of Fanconi Pancytopenia

Fanconi Anemia Estren-Dameshek Variant

Fanconis Anemia

Disorder Of Sexual Development

Disorder Of Sex Development

Disorders Of Sex Development

Sex Development Disorder

Sex Differentiation Disease

Dsd

Sex Differentiation Disorders

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus STAG3 RGD RGD:621333
Canis familiaris STAG3 VGNC VGNC:54072
Macaca mulatta STAG3 VGNC VGNC:81766
Mus musculus STAG3 MGD MGI:1355311
Felis catus STAG3 VGNC VGNC:80685
Bos taurus STAG3 VGNC VGNC:97313