Location |
Symbol |
Title |
MIM # |
Disorder |
Comments |
Method |
Mouse |
7q35-q36 |
SMARCD3, BAF60C |
SWI/SNF related, matrix-associated, actin-dependent regulator of chromatin, subfamily D, member 3 |
601737 |
|
|
Psh, R |
|
7q35-q36 |
TAS2R38, T2R61, PTC |
Taste receptor, type 2, member 38 |
607751 |
[Phenylthiocarbamide tasting], 171200 (3) |
|
Fd, REc |
|
7q36 |
ABCF2, HUSSY18 |
ATP-binding cassette, subfamily F, member 2 |
612510 |
|
|
Psh, R, REc |
|
7q36 |
ACRPS |
Acropectoral syndrome |
605967 |
Acropectoral syndrome (2) |
|
Fd |
|
7q36 |
AD10 |
Alzheimer disease-10 |
609636 |
Alzheimer disease-10, 104300 (2) |
max lod with D7S798 |
Fd |
|
7q36 |
ATP6V0E2 |
ATPase, H+ transporting, lysosomal, 9kD, V- subunit E2 |
611019 |
|
|
REc |
|
7q36 |
FLACE |
B-cell acute lymphoblastic leukemia-expressed gene |
608450 |
|
|
R |
|
7q36 |
CDK5 |
Cyclin-dependent kinase 5 |
123831 |
|
|
A |
5(cdk5) |
7q36 |
EN2, AUTS10 |
Engrailed-2 |
131310 |
{Autism, susceptibility to, 10}, 611016 (3) |
|
REa, A, Fd |
5(En2) |
7q36 |
GBX1 |
Gastrulatin brain homeo box 1 |
603354 |
|
|
A |
5(Gbx1) |
7q36 |
HLXB9, HOXHB9, SCRA1 |
Homeo box-HB9 |
142994 |
Currarino syndrome, 176450 (3) |
|
Fd, REc |
|
7q36 |
HPFH2 |
Hereditary persistence of fetal hemoglobin, heterocellular, Indian type |
142335 |
?Hereditary persistence of fetal hemoglobin, heterocellular,Indian type (2) |
|
Fd |
|
7q36 |
INSIG1 |
Insulin-induced gene 1 |
602055 |
|
|
A |
|
7q36 |
LMBR1, ACHP, C7orf2, PPD2 |
Limb region 1, mouse, homolog of |
605522 |
Acheiropody, 200500 (3); Polydactyly, preaxial type II, 174500 (3);Triphalangeal thumb, type I, 174500 (3); Triphalangeal thumb-polysyndactyly syndrome, 174500 (3); Syndactyly, type IV, 186200 (3) |
|
Fd, HZ, Fd |
5(Lmbr1) |
7q36 |
MLL3, KIAA1506 |
Myeloid/lymphoid or mixed-lineage leukemia 3 |
606833 |
|
|
A |
|
7q36 |
MYP4 |
Myopia 4 |
608367 |
Myopia 4 (2) |
|
Fd |
|
7q36 |
NOS3 |
Nitric oxide synthase 3, endothelial cell |
163729 |
{Coronary spasms, susceptibility to} (3); {Alzheimer disease,late-onset, susceptibility to}, 104300 (3); {Hypertension, susceptibility to}, 145500 (3); {Hypertension, pregnancy-induced}, 189800 (3); {Placentalabruption} (3); {Ischemic stroke, susceptibility to}, 601367 (3) |
|
REa, A, Psh |
5(Nos3) |
7q36 |
PACIP1, PAXIP1L, PTIP |
PAX transcription activation domain-interacting protein 1 |
608254 |
{Alzheimer disease, susceptibility to}, 104300 (3) |
|
R, A |
|
7q36 |
PRKAG2, WPWS, CMH6 |
Protein kinase, AMP-activated, noncatalytic, gamma-2 |
602743 |
Wolff-Parkinson-White syndrome, 194200 (3); Cardiomyopathy,hypertrophic 6, with WPW, 600858 (3); Glycogen storage disease of heart, lethal congenital, 261740 (3) |
|
REc, R, Fd |
|
7q36 |
PTPRN2, IAR, ICAAR |
Protein-tyrosine phosphatase, receptor-type, N, polypeptide 2 |
601698 |
|
|
A, R |
|
7q36 |
RHEB2 |
Ras homolog enriched in brain 2 |
601293 |
|
|
A |
|