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Table 1 Shows the names of genes located in chromosome Y with the amount of respective mutations alongside with the frequency of GO terms

From: Human Chromosome Y and Haplogroups; introducing YDHS Database

Ensembl ID

Gene name HGNC

No. ISOGG mutations

Positive selection?

No. Gene Ontologies

Gene length (bp)

MIM Gene Accession(s)

Orphanet Ids

ENSG00000012817

KDM5D

861

No

55

41,074

426,000

1646

ENSG00000067048

DDX3Y

320

No

21

16,371

400,010

-

ENSG00000114374

USP9Y

250

No

12

159,604

400,005

1646

ENSG00000129873

CDY2B

-

No

8

2810

400,018

-

ENSG00000131002

Cyorf15A / Cyorf15B

-

No

0

38,961

400,031

-

ENSG00000157828

RPS4Y2

12

No

6

24,868

400,030

-

ENSG00000169789

PRY

-

No

0

24,240

400,019,400,041

-

ENSG00000169807

PRY2

-

No

0

24,251

400,019,400,041

-

ENSG00000169953

HSFY2

-

No

18

42,295

400,029

-

ENSG00000172288

CDY1

-

No

10

2785

400,016

-

ENSG00000172468

HSFY1

-

No

24

42,292

400,029

-

ENSG00000182415

CDY2A

-

No

8

2810

400,016,400,018

-

ENSG00000183753

BPY2

-

No

10

31,646

400,013

-

ENSG00000183795

BPY2B

-

No

5

31,647

400,013

-

ENSG00000185894

BPY2C

-

No

5

31,647

400,013

-

ENSG00000187191

DAZ3

-

No

16

50,410

400,027

1646

ENSG00000188120

DAZ1

-

No

23

69,739

400,003

1646

ENSG00000198692

EIF1AY

108

No

7

17,429

400,014

-

ENSG00000205916

DAZ4

-

No

27

73,175

400,003,400,026

1646

ENSG00000205944

DAZ2

-

No

48

71,909

400,026

1646

ENSG00000234414

RBMY1A1

1

No

19

37,954

400,006

1646

ENSG00000244646

XKRY2

-

No

0

8417

-

-

ENSG00000250868

XKRY

-

No

0

8418

-

-

  1. If the gene has a very high number of GO terms associated, it can be argued that the gene is functionally active and probably part of a signaling network. It can be stated that genes having a lot of mutations also have a very high number of ontologies, except for EIF1AY. Table 1 reveals also the length of the gene so that the density of mutations per gene can be addressed. The MIM and OrphaNet codes are also included to show how the genes are linked to various medical conditions