Summary Statistics:
ASD Reports: 8
Recent Reports: 1
Annotated variants: 147
Associated CNVs: 3
Evidence score: 4
Gene Score: 4
Relevance to Autism
Rare inherited loss-of-function and damaging missense variants in the DNAH3 gene were identified in ASD probands from the Simons Simplex Collection (Krumm et al., 2015) and in Chinese ASD probands (Guo et al., 2017). Transmission and De Novo Association (TADA) analysis of a cohort of 536 Chinese ASD probands and 1457 Chinese controls in Guo et al., 2017 identified the DNAH3 gene as an ASD candidate gene with a PTADA between 0.001 and 0.005 (0.00758); however, PTADA for this gene failed to reach significance (P < 0.01) following TADA analysis using a combined cohort of Chinese ASD probands and controls, as well as ASD probands and controls from the Simons Simplex Collection and the Autism Sequencing Consortium.
Molecular Function
This gene belongs to the dynein family, whose members encode large proteins that are constituents of the microtubule-associated motor protein complex. This complex is composed of dynein heavy, intermediate and light chains, which can be axonemal or cytoplasmic. This protein is an axonemal dynein heavy chain. It is involved in producing force for ciliary beating by using energy from ATP hydrolysis.
References
Primary
Excess of rare, inherited truncating mutations in autism.
ASD
Support
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing
ASD
Support
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
ASD
Support
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks.
ASD
Support
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.
ASD
Support
Integrating de novo and inherited variants in 42
ASD
Recent Recommendation
Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.
ASD
GEN966R001
missense_variant
c.11519T>C
p.Leu3840Pro
Familial
Paternal
Simplex
GEN966R002
missense_variant
c.11093G>A
p.Arg3698Gln
Familial
Maternal
Simplex
GEN966R003
missense_variant
c.10723C>G
p.Pro3575Ala
Familial
Paternal
Simplex
GEN966R004
missense_variant
c.10579G>A
p.Gly3527Arg
Familial
Paternal
Simplex
GEN966R005
missense_variant
c.10454C>T
p.Pro3485Leu
Familial
Maternal
Simplex
GEN966R006
missense_variant
c.9637G>T
p.Ala3213Ser
Familial
Paternal
Simplex
GEN966R007
missense_variant
c.9470A>G
p.Asp3157Gly
Familial
Paternal
Simplex
GEN966R008
missense_variant
c.8441G>A
p.Arg2814Gln
Familial
Paternal
Simplex
GEN966R009
missense_variant
c.8143G>C
p.Ala2715Pro
Familial
Paternal
Simplex
GEN966R010
missense_variant
C>G
p.Glu2757Gln
Familial
Paternal
Simplex
GEN966R011
missense_variant
C>G
p.Glu2757Gln
Familial
Maternal
Simplex
GEN966R012
missense_variant
C>G
p.Glu2757Gln
Familial
Paternal
Simplex
GEN966R013
frameshift_variant
c.8113_8114del
p.Gly2705AsnfsTer6
Familial
Paternal
Simplex
GEN966R014
missense_variant
c.7619G>A
p.Cys2540Tyr
Familial
Maternal
Simplex
GEN966R015
missense_variant
c.7619G>A
p.Cys2540Tyr
Familial
Paternal
Simplex
GEN966R016
missense_variant
c.7604C>T
p.Pro2535Leu
Familial
Maternal
Simplex
GEN966R017
missense_variant
c.7603C>T
p.Pro2535Ser
Familial
Maternal
Simplex
GEN966R018
missense_variant
c.7339G>A
p.Asp2447Asn
Familial
Paternal
Simplex
GEN966R019
missense_variant
c.7172G>A
p.Gly2391Asp
Familial
Paternal
Simplex
GEN966R020
missense_variant
c.6791T>A
p.Val2264Asp
Familial
Paternal
Simplex
GEN966R021
missense_variant
c.6689G>A
p.Arg2230Gln
Familial
Paternal
Simplex
GEN966R022
missense_variant
c.6635C>G
p.Ala2212Gly
Familial
Maternal
Simplex
GEN966R023
missense_variant
c.6635C>G
p.Ala2212Gly
Familial
Paternal
Simplex
GEN966R024
missense_variant
C>T
p.Gly2193Arg
Familial
Paternal
Simplex
GEN966R025
missense_variant
C>T
p.Gly2193Arg
Familial
Maternal
Simplex
GEN966R026
missense_variant
c.6439G>A
p.Gly2147Arg
Familial
Maternal
Simplex
GEN966R027
missense_variant
c.6439G>A
p.Gly2147Arg
Familial
Maternal
Simplex
GEN966R028
missense_variant
c.6406G>A
p.Asp2136Asn
Familial
Maternal
Simplex
GEN966R029
frameshift_variant
c.5884_5884+1del
Familial
Maternal
Simplex
GEN966R030
missense_variant
C>T
p.Arg1972Lys
Familial
Paternal
Simplex
GEN966R031
missense_variant
C>T
p.Arg1972Lys
Familial
Paternal
Simplex
GEN966R032
missense_variant
c.5434C>A
p.Leu1812Ile
Familial
Paternal
Simplex
GEN966R033
missense_variant
c.5359G>A
p.Glu1787Lys
Familial
Paternal
Simplex
GEN966R034
missense_variant
G>A
p.Ala1780Val
Familial
Maternal
Simplex
GEN966R035
missense_variant
G>A
p.Ala1780Val
Familial
Maternal
Simplex
GEN966R036
missense_variant
G>A
p.Ala1780Val
Familial
Paternal
Simplex
GEN966R037
missense_variant
c.5152A>G
p.Ser1718Gly
Familial
Paternal
Simplex
GEN966R038
missense_variant
G>A
p.Thr1752Met
Familial
Paternal
Simplex
GEN966R039
missense_variant
c.4753C>T
p.Arg1585Trp
Familial
Paternal
Simplex
GEN966R040
missense_variant
c.4655A>G
p.His1552Arg
Familial
Paternal
Simplex
GEN966R041
missense_variant
c.4631C>T
p.Ser1544Leu
Familial
Maternal
Simplex
GEN966R042
missense_variant
c.4510C>T
p.Arg1504Trp
Familial
Paternal
Simplex
GEN966R043
missense_variant
c.4321G>A
p.Glu1441Lys
Familial
Maternal
Simplex
GEN966R044
missense_variant
c.4312A>G
p.Asn1438Asp
Familial
Maternal
Simplex
GEN966R045
missense_variant
c.4286G>C
p.Gly1429Ala
Familial
Maternal
Simplex
GEN966R046
missense_variant
c.4154C>A
p.Ala1385Asp
Familial
Maternal
Simplex
GEN966R047
missense_variant
c.4154C>A
p.Ala1385Asp
Familial
Paternal
Simplex
GEN966R048
missense_variant
c.4126A>G
p.Asn1376Asp
Familial
Maternal
Simplex
GEN966R049
missense_variant
c.3987G>T
p.Trp1329Cys
Familial
Maternal
Simplex
GEN966R050
missense_variant
c.3907G>A
p.Asp1303Asn
Familial
Paternal
Simplex
GEN966R051
missense_variant
c.3594A>C
p.Glu1198Asp
Familial
Paternal
Simplex
GEN966R052
missense_variant
c.3594A>C
p.Glu1198Asp
Familial
Maternal
Simplex
GEN966R053
missense_variant
c.3594A>C
p.Glu1198Asp
Familial
Maternal
Simplex
GEN966R054
missense_variant
c.3530C>T
p.Ser1177Leu
Familial
Maternal
Simplex
GEN966R055
stop_gained
c.3442C>T
p.Arg1148Ter
Familial
Paternal
Simplex
GEN966R056
missense_variant
c.2069G>A
p.Arg690Gln
Familial
Paternal
Simplex
GEN966R057
splice_site_variant
c.1919+1G>A
Familial
Paternal
Simplex
GEN966R058
missense_variant
c.883C>T
p.Arg295Trp
Familial
Maternal
Simplex
GEN966R059
frameshift_variant
c.708_709del
p.Leu237AlafsTer20
Familial
Maternal
Simplex
GEN966R060
frameshift_variant
c.105del
p.Ser36ValfsTer14
Familial
Paternal
Simplex
GEN966R061
missense_variant
c.12071A>G
p.Tyr4024Cys
Familial
Paternal
Simplex
GEN966R062
missense_variant
c.11519T>C
p.Leu3840Pro
Familial
Maternal
Simplex
GEN966R063
missense_variant
c.11093G>A
p.Arg3698Gln
Familial
Maternal
Simplex
GEN966R064
missense_variant
c.10322C>T
p.Ala3441Val
Familial
Paternal
Simplex
GEN966R065
missense_variant
c.9950G>A
p.Arg3317His
Familial
Maternal
Simplex
GEN966R066
missense_variant
c.9734G>A
p.Arg3245Gln
Familial
Paternal
Simplex
GEN966R067
missense_variant
c.9494C>T
p.Ala3165Val
Familial
Maternal
Simplex
GEN966R068
stop_gained
c.9135G>A
p.Trp3045Ter
Familial
Paternal
Simplex
GEN966R069
stop_gained
c.8934G>A
p.Trp2978Ter
Familial
Paternal
Simplex
GEN966R070
stop_gained
c.8934G>A
p.Trp2978Ter
Familial
Maternal
Simplex
GEN966R071
missense_variant
c.8320G>A
p.Gly2774Ser
Familial
Maternal
Simplex
GEN966R072
missense_variant
c.8131G>C
p.Glu2711Gln
Familial
Paternal
Simplex
GEN966R073
missense_variant
c.8131G>C
p.Glu2711Gln
Familial
Paternal
Simplex
GEN966R074
missense_variant
c.8131G>C
p.Glu2711Gln
Familial
Maternal
Simplex
GEN966R075
stop_gained
c.7972C>T
p.Gln2658Ter
Familial
Maternal
Simplex
GEN966R076
missense_variant
c.7931C>T
p.Ala2644Val
Familial
Maternal
Simplex
GEN966R077
missense_variant
c.7739A>G
p.Lys2580Arg
Familial
Maternal
Simplex
GEN966R078
missense_variant
c.7619G>A
p.Cys2540Tyr
Familial
Paternal
Simplex
GEN966R079
stop_gained
c.6675C>G
p.Tyr2225Ter
Familial
Maternal
Simplex
GEN966R080
missense_variant
c.6662C>T
p.Ser2221Leu
Familial
Paternal
Simplex
GEN966R081
missense_variant
c.6439G>A
p.Gly2147Arg
Familial
Maternal
Simplex
GEN966R082
missense_variant
C>T
p.Arg1972Lys
Familial
Paternal
Simplex
GEN966R083
missense_variant
C>T
p.Arg1972Lys
Familial
Paternal
Simplex
GEN966R084
missense_variant
C>T
p.Arg1972Lys
Familial
Maternal
Simplex
GEN966R085
missense_variant
C>T
p.Arg1972Lys
Familial
Maternal
Simplex
GEN966R086
missense_variant
c.5777G>A
p.Arg1926Lys
Familial
Maternal
Simplex
GEN966R087
missense_variant
c.5777G>A
p.Arg1926Lys
Familial
Paternal
Simplex
GEN966R088
missense_variant
c.5777G>A
p.Arg1926Lys
Familial
Paternal
Simplex
GEN966R089
missense_variant
c.5459C>T
p.Ser1820Phe
Familial
Paternal
Simplex
GEN966R090
missense_variant
G>A
p.Ala1780Val
Familial
Paternal
Simplex
GEN966R091
missense_variant
c.5201C>T
p.Ala1734Val
Familial
Paternal
Simplex
GEN966R092
missense_variant
c.5201C>T
p.Ala1734Val
Familial
Paternal
Simplex
GEN966R093
missense_variant
c.5201C>T
p.Ala1734Val
Familial
Maternal
Simplex
GEN966R094
missense_variant
c.5117C>T
p.Thr1706Met
Familial
Maternal
Simplex
GEN966R095
missense_variant
c.5117C>T
p.Thr1706Met
Familial
Maternal
Simplex
GEN966R096
missense_variant
c.5117C>T
p.Thr1706Met
Familial
Maternal
Simplex
GEN966R097
missense_variant
c.5104C>T
p.Pro1702Ser
Familial
Paternal
Simplex
GEN966R098
missense_variant
c.5005G>A
p.Gly1669Ser
Familial
Paternal
Simplex
GEN966R099
missense_variant
c.4753C>T
p.Arg1585Trp
Familial
Paternal
Simplex
GEN966R100
missense_variant
c.4286G>C
p.Gly1429Ala
Familial
Maternal
Simplex
GEN966R101
missense_variant
c.4286G>C
p.Gly1429Ala
Familial
Maternal
Simplex
GEN966R102
missense_variant
c.4231G>A
p.Asp1411Asn
Familial
Paternal
Simplex
GEN966R103
stop_gained
c.3442C>T
p.Arg1148Ter
Familial
Paternal
Simplex
GEN966R104
missense_variant
c.3436C>G
p.Pro1146Ala
Familial
Paternal
Simplex
GEN966R105
missense_variant
c.3148A>G
p.Ile1050Val
Familial
Paternal
Simplex
GEN966R106
missense_variant
c.2842A>C
p.Ile948Leu
Familial
Paternal
Simplex
GEN966R107
stop_gained
c.2595T>G
p.Tyr865Ter
Familial
Maternal
Simplex
GEN966R108
missense_variant
c.2069G>A
p.Arg690Gln
Familial
Maternal
Simplex
GEN966R109
missense_variant
c.233G>A
p.Ser78Asn
Familial
Paternal
Simplex
GEN966R110
frameshift_variant
c.232del
p.Ser78ValfsTer10
Familial
Maternal
Simplex
GEN966R111
stop_gained
c.10725G>A
p.Trp3575Ter
Familial
GEN966R112
frameshift_variant
c.9289_9290insT
p.Lys3097IlefsTer4
Familial
GEN966R113
splice_site_variant
c.6744+1G>A
Familial
GEN966R114
frameshift_variant
c.2460del
p.Val821TyrfsTer21
Familial
GEN966R115
splice_site_variant
c.1497+2T>C
Familial
GEN966R116
missense_variant
c.11018G>A
p.Gly3673Asp
Familial
GEN966R117
missense_variant
c.10769C>A
p.Pro3590His
Familial
GEN966R118
missense_variant
c.10907C>A
p.Pro3636His
Familial
GEN966R119
missense_variant
c.10907C>A
p.Pro3636His
Familial
GEN966R120
missense_variant
c.8369A>C
p.Asn2790Thr
Familial
GEN966R121
missense_variant
c.7530C>A
p.Asn2510Lys
Familial
GEN966R122
missense_variant
c.6163C>T
p.Arg2055Trp
Familial
GEN966R123
missense_variant
c.5281G>C
p.Asp1761His
Familial
GEN966R124
missense_variant
c.5164G>C
p.Val1722Leu
Familial
GEN966R125
missense_variant
c.4768T>C
p.Ser1590Pro
Familial
GEN966R126
missense_variant
c.2864G>A
p.Arg955Gln
Familial
GEN966R127
synonymous_variant
c.7692T>C
p.Asp2564=
De novo
Simplex
GEN966R128
frameshift_variant
c.10769_10770insT
p.Lys3591GlnfsTer14
Familial
Maternal
Multiplex
GEN966R129
splice_site_variant
c.4210-2A>C
Familial
Paternal
Multiplex
GEN966R130
frameshift_variant
c.3226del
p.Ser1076HisfsTer7
Familial
Maternal
Multiplex
GEN966R131
stop_gained
c.1207C>T
p.Arg403Ter
Familial
Paternal
Multiplex
GEN966R132
frameshift_variant
c.104_107del
p.Gly35ValfsTer14
Familial
Maternal
Multiplex
GEN966R133
missense_variant
c.7786A>G
p.Lys2596Glu
De novo
GEN966R134
missense_variant
c.8578G>A
p.Glu2860Lys
De novo
GEN966R135
missense_variant
c.10487T>C
p.Met3496Thr
De novo
GEN966R136
missense_variant
c.9775G>A
p.Ala3259Thr
De novo
GEN966R137
missense_variant
c.9554T>C
p.Val3185Ala
De novo
GEN966R138
splice_region_variant
c.3582+8C>G
De novo
GEN966R139
synonymous_variant
c.7530C>T
p.Asn2510%3D
De novo
GEN966R140
missense_variant
c.7261C>T
p.Arg2421Cys
De novo
GEN966R141
synonymous_variant
c.3267C>G
p.Thr1089%3D
De novo
GEN966R142
missense_variant
c.7261C>T
p.Arg2421Cys
De novo
Simplex
GEN966R143
synonymous_variant
c.5496C>T
p.Phe1832%3D
De novo
Simplex
GEN966R144
frameshift_variant
c.12260_12263del
p.Asn4087MetfsTer17
Familial
Paternal
Multiplex
GEN966R145
stop_gained
c.11943G>A
p.Trp3981Ter
Familial
Paternal
Multiplex
GEN966R146
frameshift_variant
c.4057_4058del
p.Lys1353ValfsTer3
Familial
Maternal
Multiplex
GEN966R147
stop_gained
c.3442C>T
p.Arg1148Ter
Familial
Maternal
Multiplex
No Common Variants Available
16
Deletion-Duplication
25
16
Deletion-Duplication
19
No Animal Model Data Available
No Interactions Available