Entry Search - 608256 611819 - OMIM
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Search: '608256 611819 (Search in: MIM number)'
Results: 2 entries.

1:
* 608256. SODIUM VOLTAGE-GATED CHANNEL, BETA SUBUNIT 4; SCN4B
Cytogenetic location: 11q23.3, Genomic coordinates (GRCh38): 11:118,133,377-118,152,823
Matching terms: 608256
► Gene-Phenotype Relationships  ► Links 
Gene-Phenotype Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key
11q23.3 Atrial fibrillation, familial, 17 611819 AD 3
Long QT syndrome 10 611819 AD 3
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2:
# 611819. LONG QT SYNDROME 10; LQT10
ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED
Cytogenetic locations: 11q23.3,
Matching terms: 611819
► Phenotype-Gene Relationships  ► Phenotypic Series  ► ICD+  ► Links 
Phenotype-Gene Relationships
Location Phenotype Phenotype
MIM number 		Inheritance Phenotype
mapping key 		Gene/Locus Gene/Locus
MIM number
11q23.3 Long QT syndrome 10 611819 AD 3 SCN4B 608256
11q23.3 Atrial fibrillation, familial, 17 611819 AD 3 SCN4B 608256
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Long QT syndrome - PS192500 - 21 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
2p21 Long QT syndrome 15 AD 3 616249 CALM2 114182
3p25.3 Long QT syndrome 9 AD 3 611818 CAV3 601253
3p22.2 Long QT syndrome 3 AD 3 603830 SCN5A 600163
4q25-q26 Cardiac arrhythmia, ankyrin-B-related AD 3 600919 ANK2 106410
4q25-q26 Long QT syndrome 4 AD 3 600919 ANK2 106410
7q21.2 ?Long QT syndrome 11 AD 3 611820 AKAP9 604001
7q36.1 Long QT syndrome 2 AD 3 613688 KCNH2 152427
11p15.5-p15.4 Long QT syndrome 1 AD 3 192500 KCNQ1 607542
11p15.5-p15.4 {Long QT syndrome 1, acquired, susceptibility to} AD 3 192500 KCNQ1 607542
11q23.3 Long QT syndrome 10 AD 3 611819 SCN4B 608256
11q23.3 Atrial fibrillation, familial, 17 AD 3 611819 SCN4B 608256
11q24.3 Long QT syndrome 13 AD 3 613485 KCNJ5 600734
12p13.33 Long QT syndrome 8 AD 3 618447 CACNA1C 114205
12q12 {Long QT syndrome, acquired, reduced susceptibility to} AD 3 613688 ALG10B 603313
14q32.11 Long QT syndrome 14 AD 3 616247 CALM1 114180
17q24.3 Andersen syndrome AD 3 170390 KCNJ2 600681
19q13.32 ?Ventricular tachycardia, catecholaminergic polymorphic 6 AD 3 618782 CALM3 114183
19q13.32 Long QT syndrome 16 AD 3 618782 CALM3 114183
20q11.21 Long QT syndrome 12 AD 3 612955 SNTA1 601017
21q22.11 Long QT syndrome 6 AD 3 613693 KCNE2 603796
21q22.12 Long QT syndrome 5 AD 3 613695 KCNE1 176261
Atrial fibrillation, familial - PS608583 - 20 Entries
Location Phenotype Inheritance Phenotype
mapping key 		Phenotype
MIM number 		Gene/Locus Gene/Locus
MIM number
1p36.22 Atrial fibrillation, familial, 6 AD 3 612201 NPPA 108780
1q21.2 Atrial fibrillation, familial, 11 AD 3 614049 GJA5 121013
3p22.2 Atrial fibrillation, familial, 10 AD 3 614022 SCN5A 600163
4q25 {Atrial fibrillation, familial, 5} 2 611494 ATFB5 611494
5p13.2 ?Atrial fibrillation 15 AR 3 615770 NUP155 606694
6q14-q16 Atrial fibrillation, familial, 2 2 608988 ATFB2 608988
10q22-q24 Atrial fibrillation, familial, 1 AD 2 608583 ATFB1 608583
11p15.5-p15.4 Atrial fibrillation, familial, 3 AD 3 607554 KCNQ1 607542
11q23.3 Long QT syndrome 10 AD 3 611819 SCN4B 608256
11q23.3 Atrial fibrillation, familial, 17 AD 3 611819 SCN4B 608256
11q23.3 Atrial fibrillation, familial, 14 AD 3 615378 SCN2B 601327
11q24.1 Atrial fibrillation, familial, 16 AD 3 613120 SCN3B 608214
11q24.1 Brugada syndrome 7 AD 3 613120 SCN3B 608214
12p13.32 Atrial fibrillation, familial, 7 AD 3 612240 KCNA5 176267
12p12.1 ?Atrial fibrillation, familial, 12 AD 3 614050 ABCC9 601439
16q22.2-q22.3 {Atrial fibrillation 8, susceptibility to} AD 3 613055 ZFHX3 104155
17q21.32 ?Atrial fibrillation, familial, 18 AD 3 617280 MYL4 160770
17q24.3 Atrial fibrillation, familial, 9 AD 3 613980 KCNJ2 600681
19q13.11 Atrial fibrillation, familial, 13 AD 3 615377 SCN1B 600235
21q22.11 Atrial fibrillation, familial, 4 3 611493 KCNE2 603796
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ICD+
ORPHA: 101016, 334, 768
DO: 0110651
▲ Close
Search: 608256 611819 (Search in: MIM number)
Results: 2 entries.

1:
* 608256. SODIUM VOLTAGE-GATED CHANNEL, BETA SUBUNIT 4; SCN4B
Cytogenetic location: 11q23.3, Genomic coordinates (GRCh38): 11:118,133,377-118,152,823
Matching terms: 608256

2:
# 611819. LONG QT SYNDROME 10; LQT10
ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED
Cytogenetic locations: 11q23.3,
Matching terms: 611819


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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: April 25, 2024