Location |
Symbol |
Title |
MIM # |
Disorder |
Comments |
Method |
Mouse |
17q23 |
ACE, DCP1, ACE1, MVCD3 |
Angiotensin I converting enzyme (dipeptidyl carboxypeptidase-1) |
106180 |
{Myocardial infarction, susceptibility to} (3); {Alzheimer disease,susceptibility to}, 104300 (3); {Microvascular complications of diabetes 3, 612624 (3); [Angiotensin I-converting enzyme, benign serum increase] (3);{SARS, progression of} (3); Renal tubular dysgenesis, 267430 (3) |
|
A, H, Fd |
|
17q23 |
BSZQTL |
Bone size quantitative trait locus 1 |
609656 |
{Bone size QTL} (2) |
|
Fd |
|
17q23 |
CA4, RP17 |
Carbonic anhydrase IV |
114760 |
Retinitis pigmentosa-17, 600852 (3) |
|
REa, A, Fd |
|
17q23 |
CD79B, IGB, B29 |
Immunoglobulin-associated protein (B29) |
147245 |
|
|
A |
|
17q23 |
CLTC |
Clathrin, heavy polypeptide (Hc) |
118955 |
|
fusion gene with TFE3 in renal adenocarcinoma |
REc, Ch |
|
17q23 |
MKS1, MKS, BBS13 |
MKS1 gene |
609883 |
Meckel syndrome, type 1, 249000 (3); Bardet-Biedl syndrome 13,209900 (3) |
frequent in Finland |
Fd, REc |
|
17q23 |
PECAM1 |
Platelet/endothelial cell adhesion molecule (CD31 antigen) |
173445 |
|
|
Psh, A |
6(Pecam1) |
17q23 |
SEPT4, PNUTL2 |
Septin 4 |
603696 |
|
|
A, REc |
11(Sept4) |
17q23 |
TBX2 |
T-box 2 |
600747 |
|
|
A, H |
11(Tbx2) |
17q23-q24 |
KPNA2, RCH1, QIP2 |
Karyopherin alpha-2 |
600685 |
|
|
REc |
|
17q23-q24 |
POLG2, POLGB, PEOA4 |
Polymerase, DNA, gamma-2 |
604983 |
Progressive external ophthalmoplegia with mitochondrial DNAdeletions, autosomal dominant 4, 610131 (3) |
|
REc |
|
17q23-q24 |
PRKAR1A, TSE1, CNC1, CAR, PPNAD1 |
Protein kinase, cAMP-dependent, regulatory, type I, alpha |
188830 |
Carney complex, type 1, 160980 (3); Myxoma, intracardiac, 255960 (3);Thyroid carcinoma, papillary, 188550 (3); Pigmented adrenocortical disease, primary, 1, 610489 (3); Adrenocortical tumor, somatic (3) |
fused with RET to form PTC2 |
S, M, REa, RE, Fd |
11(Tse1) |
17q23-q24 |
RGS9, PERRS |
Regulator of G protein signaling 9 |
604067 |
Bradyopsia, 608415 (3) |
|
R, A |
|
17q23-q24 |
SMARCD2, BAF60B |
SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin, subfamily d, member 2 |
601736 |
|
|
Psh, R |
|
17q23-q25 |
DDX5, HLR1, G17P1 |
DEAD/H box-5 (RNA helicase, 68kD) |
180630 |
|
near BRCA1 |
REa, REn |
|
17q23-q25 |
ICAM2 |
Intercellular adhesion molecule-2 |
146630 |
|
|
REa, C |
|
17q23-q25 |
MRPL38 |
Mitodhondrial ribosomal protein L38 |
611844 |
|
|
R, REc |
|
17q23-q25 |
MRPS7 |
Mitochondrial ribosomal protein S7 |
611974 |
|
|
R, REc |
|
17q23-q25 |
NT5C, UMPH2, DNT1 |
5', 3' nucleotidase, cytosolic |
191720 |
|
|
REa |
11(Umph2) |
17q23-qter |
APOH |
Apolipoprotein H (beta-2-glycoprotein I) |
138700 |
[Apolipoprotein H deficiency] (3) |
|
Fd, REa |
11(Apoh) |
17q23-qter |
PEPE |
Peptidase E |
170200 |
|
|
S |
|