ZAN - zonadhesin Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 7455

About ZAN

Cytogenetic location: 7q22.1 Genomic coordinates (GRCh38): 7:100,733,595-100,797,797 (from NCBI)

This gene has 8 transcripts (splice variants), 147 orthologues and 19 paralogues. Low expression observed in reference dataset.

Summary

This gene encodes a protein that functions in the species specificity of sperm adhesion to the egg zona pellucida. The encoded protein is located in the acrosome and may be involved in signaling or gamete recognition. An allelic polymorphism in this gene results in both functional and frameshifted alleles; the reference genome represents the functional allele. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2015]

ZAN Products (2)

mRNA Protein Name
NM_003386.3 NP_003377.2 zonadhesin isoform 3 precursor
NM_173059.3 NP_775082.2 zonadhesin isoform 6 precursor

ZAN Protein Structure

MAM

MAM: MAM domain, meprin/A5/mu (41 - 203)

MAM

MAM: MAM domain, meprin/A5/mu (211 - 367)

MAM

MAM: MAM domain, meprin/A5/mu (373 - 535)

TIL

TIL: Trypsin Inhibitor like cysteine rich domain (1044 - 1093)

TILa

TILa: TILa domain (1094 - 1148)

VWD

VWD: von Willebrand factor type D domain (1156 - 1307)

C8

C8: C8 domain (1353 - 1423)

TIL

TIL: Trypsin Inhibitor like cysteine rich domain (1426 - 1479)

TILa

TILa: TILa domain (1480 - 1535)

VWD

VWD: von Willebrand factor type D domain (1542 - 1695)

C8

C8: C8 domain (1738 - 1809)

TIL

TIL: Trypsin Inhibitor like cysteine rich domain (1812 - 1867)

TILa

TILa: TILa domain (1868 - 1920)

VWD

VWD: von Willebrand factor type D domain (1930 - 2084)

C8

C8: C8 domain (2134 - 2207)

TIL

TIL: Trypsin Inhibitor like cysteine rich domain (2210 - 2266)

TILa

TILa: TILa domain (2267 - 2322)

VWD

VWD: von Willebrand factor type D domain (2330 - 2483)

C8

C8: C8 domain (2541 - 2617)

EGF

EGF: EGF-like domain (2620 - 2648)

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  • 2500
  • 2720 a.a.
Protein Preferred Names Protein Names

zonadhesin

Related Diseases

Diseases Alias
Granulomatous Orchitis
  • Non-Specific Granulomatous Orchitis

Deafness, Autosomal Recessive 21
  • DFNB21

  • Autosomal Recessive Nonsyndromic Deafness 21

  • Autosomal Recessive Deafness 21

  • Deafness, Autosomal Recessive, 21

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 21

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 21

  • Deafness, Autosomal Recessive, Type 21

Von Willebrand Disease, Type 2
  • Von Willebrand Disease Type 2m

  • Von Willebrand Disease Type 2

  • Von Willebrand Disease Type 2a

  • Von Willebrand Disease Type 2b

  • Von Willebrand Disease Type 2n

  • VWD2

  • Von Willebrand'S Disease 2

  • Von Willebrand Disease Type Ii

  • Von Willebrand Disease, Type Ii

  • Vwd, Type 2

  • Von Willebrand Disease, Types 2a, 2b, 2m, And 2n

  • Vwd Type 2

  • Von Willebrand Disease 2

  • Von Willebrand Disease Normandy Variant

  • Von Willebrand Disease Type 2 Malmo

  • Von Willebrand Disease Type I New York

  • Von Willebrand Factor Deficiency Type 2

  • Vwd2a

  • Vwd2b

  • Vwd2m

  • Vwd2n

  • Von Willebrand Disease, Type 2a, 2b, 2m, And 2n

  • Von Willebrand Disease, Type 2a

  • Von Willebrand Disease, Type 2b

  • Von Willebrand Disease, Type 2n

Deafness, Autosomal Dominant 13
  • DFNA13

  • Autosomal Dominant Nonsyndromic Deafness 13

  • Autosomal Dominant Deafness 13

  • Deafness, Autosomal Dominant, 13

  • Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 13

  • Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 13

  • Deafness, Autosomal Dominant, Type 13

Deafness, Autosomal Dominant 44
  • DFNA44

  • Autosomal Dominant Nonsyndromic Deafness 44

  • Autosomal Dominant Deafness 44

  • Deafness, Autosomal Dominant, 44

  • Deafness, Autosomal Dominant, Type 44

Von Willebrand Disease, Type 1
  • Von Willebrand Disease Type 1

  • VWD1

  • Von Willebrand'S Disease 1

  • Von Willebrand Disease Type I

  • Von Willebrand Disease, Type I

  • Vwd, Type 1

  • Vwd Type 1

  • Von Willebrand Disease 1

  • Von Willebrand Factor Deficiency Type 1

  • Von Willebrand Disease, Type 1, Susceptibility To

Von Willebrand Disease, Type 3
  • Von Willebrand Disease Type 3

  • VWD3

  • Von Willebrand'S Disease 3

  • Von Willebrand Disease Type Iii

  • Von Willebrand Disease, Type Iii

  • Vwd, Type 3

  • Vwd Type 3

  • Von Willebrand Disease 3

  • Von Willebrand Disease Recessive Form

  • Von Willebrand Factor Deficiency Type 3

Orchitis
  • Inflammation Of Testis

  • Orchititis

  • Mumps Orchitis

Tick Paralysis
Epididymo-Orchitis
Deafness, Autosomal Dominant 10
  • DFNA10

  • Autosomal Dominant Nonsyndromic Deafness 10

  • Autosomal Dominant Deafness 10

  • Deafness, Autosomal Dominant, 10

  • Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 10

  • Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 10

  • Deafness, Autosomal Dominant, Type 10

Autosomal Recessive Nonsyndromic Deafness
  • Deafness, Autosomal Recessive, Nonsyndromic

Autosomal Dominant Nonsyndromic Deafness
  • Autosomal Dominant Deafness

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 ZAN RGD RGD:1305044
Macaca mulatta ZAN VGNC VGNC:81797
Bos taurus ZAN VGNC VGNC:99806
Felis catus ZAN VGNC VGNC:80703
Mus musculus ZAN MGD MGI:106656
Others ZAN NCBI