Incidental Mutation 'IGL00310:Dync2h1'
ID 277513
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dync2h1
Ensembl Gene ENSMUSG00000047193
Gene Name dynein cytoplasmic 2 heavy chain 1
Synonyms 4432416O06Rik, DHC2, D030010H02Rik, D330044F14Rik, Dnchc2, DHC1b, b2b414Clo
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL00310
Quality Score
Status
Chromosome 9
Chromosomal Location 6928503-7184446 bp(-) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 7155072 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000116679 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000048417] [ENSMUST00000139115] [ENSMUST00000140466] [ENSMUST00000147193]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000048417
SMART Domains Protein: ENSMUSP00000046733
Gene: ENSMUSG00000047193

DomainStartEndE-ValueType
Pfam:DHC_N1 187 676 1.6e-43 PFAM
Pfam:DHC_N2 1117 1523 4.1e-120 PFAM
AAA 1684 1830 3.72e-2 SMART
AAA 1971 2127 2.18e0 SMART
AAA 2283 2431 1.66e0 SMART
low complexity region 2588 2602 N/A INTRINSIC
Pfam:AAA_8 2618 2881 6.8e-27 PFAM
Pfam:MT 2894 3230 5.4e-28 PFAM
Pfam:AAA_9 3242 3471 1.1e-50 PFAM
Pfam:Dynein_heavy 3605 4304 2.3e-136 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000139115
SMART Domains Protein: ENSMUSP00000120322
Gene: ENSMUSG00000047193

DomainStartEndE-ValueType
Pfam:DHC_N1 188 676 3.2e-45 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000140466
SMART Domains Protein: ENSMUSP00000120007
Gene: ENSMUSG00000047193

DomainStartEndE-ValueType
Pfam:DHC_N1 187 676 1.6e-43 PFAM
Pfam:DHC_N2 1117 1523 4.1e-120 PFAM
AAA 1684 1830 3.72e-2 SMART
AAA 1971 2127 2.18e0 SMART
AAA 2283 2431 1.66e0 SMART
low complexity region 2588 2602 N/A INTRINSIC
Pfam:AAA_8 2618 2881 6.8e-27 PFAM
Pfam:MT 2894 3230 5.4e-28 PFAM
Pfam:AAA_9 3242 3471 1.1e-50 PFAM
Pfam:Dynein_heavy 3605 4304 2.3e-136 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000147056
Predicted Effect probably benign
Transcript: ENSMUST00000147193
SMART Domains Protein: ENSMUSP00000116679
Gene: ENSMUSG00000047193

DomainStartEndE-ValueType
Pfam:DHC_N1 188 674 4e-45 PFAM
Pfam:DHC_N2 1118 1521 5.5e-111 PFAM
AAA 1684 1830 3.72e-2 SMART
AAA 1971 2127 2.18e0 SMART
AAA 2283 2431 1.66e0 SMART
low complexity region 2588 2602 N/A INTRINSIC
Pfam:AAA_8 2618 2880 4.4e-27 PFAM
Pfam:MT 2894 3230 1.3e-27 PFAM
Pfam:AAA_9 3246 3477 1e-79 PFAM
Pfam:Dynein_heavy 3618 4310 8.5e-158 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary cilium function and often involve polydactyly, abnormal skeletogenesis, and polycystic kidneys. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010]
PHENOTYPE: Homozygotes for a gene trap allele show complete embryonic lethality with altered heart looping and brain morphology. Chemically induced mutants show randomized heart looping and polydactyly. Holoprosencephaly or exencephaly, micrognathia, and cardiac, renal, airway and eye defects may be observed. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 10 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agap1 T G 1: 89,887,670 (GRCm38) V573G probably damaging Het
Dpp6 T A 5: 27,723,443 (GRCm38) D786E probably damaging Het
Kcnq4 G A 4: 120,698,016 (GRCm38) Q657* probably null Het
Kif14 G A 1: 136,469,018 (GRCm38) S354N probably benign Het
Mettl25 T C 10: 105,826,434 (GRCm38) H225R probably benign Het
Mocos C T 18: 24,660,044 (GRCm38) T66I possibly damaging Het
Ptprk T A 10: 28,336,510 (GRCm38) D221E possibly damaging Het
Slc13a3 A T 2: 165,411,923 (GRCm38) F437I probably damaging Het
Slc7a15 T C 12: 8,539,121 (GRCm38) Y142C probably damaging Het
Sox4 C A 13: 28,952,973 (GRCm38) G17W probably damaging Het
Other mutations in Dync2h1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Dync2h1 APN 9 7,158,839 (GRCm38) missense probably benign 0.42
IGL00499:Dync2h1 APN 9 7,168,700 (GRCm38) missense possibly damaging 0.95
IGL00579:Dync2h1 APN 9 7,035,728 (GRCm38) splice site probably benign
IGL00660:Dync2h1 APN 9 7,075,797 (GRCm38) missense probably damaging 0.98
IGL00964:Dync2h1 APN 9 7,174,881 (GRCm38) splice site probably benign
IGL01025:Dync2h1 APN 9 7,162,789 (GRCm38) missense probably damaging 1.00
IGL01093:Dync2h1 APN 9 7,145,611 (GRCm38) missense probably benign 0.01
IGL01108:Dync2h1 APN 9 7,176,771 (GRCm38) missense possibly damaging 0.87
IGL01126:Dync2h1 APN 9 7,116,588 (GRCm38) missense probably benign 0.00
IGL01474:Dync2h1 APN 9 7,102,493 (GRCm38) missense probably benign 0.01
IGL01531:Dync2h1 APN 9 7,071,111 (GRCm38) missense probably benign 0.11
IGL01548:Dync2h1 APN 9 7,071,922 (GRCm38) missense probably damaging 1.00
IGL01621:Dync2h1 APN 9 7,140,897 (GRCm38) critical splice donor site probably null
IGL01672:Dync2h1 APN 9 7,118,884 (GRCm38) nonsense probably null
IGL01681:Dync2h1 APN 9 7,142,196 (GRCm38) splice site probably null
IGL01685:Dync2h1 APN 9 7,142,297 (GRCm38) missense probably damaging 1.00
IGL01724:Dync2h1 APN 9 7,081,077 (GRCm38) missense probably benign 0.03
IGL01738:Dync2h1 APN 9 7,114,922 (GRCm38) missense possibly damaging 0.77
IGL01783:Dync2h1 APN 9 7,118,822 (GRCm38) unclassified probably benign
IGL01813:Dync2h1 APN 9 7,122,799 (GRCm38) missense probably damaging 1.00
IGL01931:Dync2h1 APN 9 7,114,973 (GRCm38) missense probably damaging 1.00
IGL01931:Dync2h1 APN 9 7,011,207 (GRCm38) missense probably benign 0.33
IGL02105:Dync2h1 APN 9 7,075,892 (GRCm38) missense probably damaging 1.00
IGL02137:Dync2h1 APN 9 7,134,349 (GRCm38) missense probably benign
IGL02140:Dync2h1 APN 9 7,147,791 (GRCm38) missense probably benign
IGL02175:Dync2h1 APN 9 7,111,548 (GRCm38) missense possibly damaging 0.91
IGL02283:Dync2h1 APN 9 7,125,912 (GRCm38) missense probably damaging 0.99
IGL02305:Dync2h1 APN 9 7,122,678 (GRCm38) missense probably benign
IGL02342:Dync2h1 APN 9 7,142,246 (GRCm38) missense probably damaging 1.00
IGL02367:Dync2h1 APN 9 7,158,926 (GRCm38) missense probably damaging 0.98
IGL02458:Dync2h1 APN 9 7,117,422 (GRCm38) missense probably damaging 1.00
IGL02563:Dync2h1 APN 9 7,035,700 (GRCm38) missense possibly damaging 0.95
IGL02825:Dync2h1 APN 9 6,955,901 (GRCm38) splice site probably benign
IGL02955:Dync2h1 APN 9 7,142,864 (GRCm38) missense probably benign 0.00
IGL02992:Dync2h1 APN 9 7,137,074 (GRCm38) missense probably benign 0.01
IGL02996:Dync2h1 APN 9 6,935,279 (GRCm38) missense probably damaging 0.99
IGL03224:Dync2h1 APN 9 7,076,235 (GRCm38) missense probably benign 0.32
IGL03226:Dync2h1 APN 9 7,125,918 (GRCm38) missense probably benign
IGL03233:Dync2h1 APN 9 7,101,525 (GRCm38) missense possibly damaging 0.90
deinonychus UTSW 9 7,159,478 (GRCm38) splice site probably null
R0016:Dync2h1 UTSW 9 7,144,346 (GRCm38) splice site probably benign
R0016:Dync2h1 UTSW 9 7,144,346 (GRCm38) splice site probably benign
R0043:Dync2h1 UTSW 9 7,005,574 (GRCm38) missense probably benign 0.05
R0109:Dync2h1 UTSW 9 7,111,487 (GRCm38) missense probably damaging 1.00
R0109:Dync2h1 UTSW 9 7,111,487 (GRCm38) missense probably damaging 1.00
R0121:Dync2h1 UTSW 9 7,001,327 (GRCm38) splice site probably benign
R0277:Dync2h1 UTSW 9 7,129,046 (GRCm38) missense probably benign
R0360:Dync2h1 UTSW 9 7,113,182 (GRCm38) missense possibly damaging 0.62
R0362:Dync2h1 UTSW 9 7,005,487 (GRCm38) splice site probably null
R0389:Dync2h1 UTSW 9 7,167,244 (GRCm38) splice site probably null
R0443:Dync2h1 UTSW 9 7,167,244 (GRCm38) splice site probably null
R0496:Dync2h1 UTSW 9 7,155,180 (GRCm38) missense probably benign 0.42
R0506:Dync2h1 UTSW 9 7,113,153 (GRCm38) missense probably benign 0.05
R0511:Dync2h1 UTSW 9 7,122,692 (GRCm38) missense probably benign 0.00
R0540:Dync2h1 UTSW 9 7,051,480 (GRCm38) missense probably benign 0.00
R0550:Dync2h1 UTSW 9 7,120,954 (GRCm38) splice site probably null
R0564:Dync2h1 UTSW 9 7,139,432 (GRCm38) missense probably damaging 1.00
R0607:Dync2h1 UTSW 9 7,051,480 (GRCm38) missense probably benign 0.00
R0699:Dync2h1 UTSW 9 7,103,680 (GRCm38) missense probably benign 0.00
R0725:Dync2h1 UTSW 9 7,015,497 (GRCm38) missense possibly damaging 0.93
R0835:Dync2h1 UTSW 9 7,116,642 (GRCm38) critical splice acceptor site probably null
R0837:Dync2h1 UTSW 9 7,077,979 (GRCm38) missense probably benign 0.07
R0894:Dync2h1 UTSW 9 7,041,734 (GRCm38) splice site probably benign
R0938:Dync2h1 UTSW 9 7,002,658 (GRCm38) missense probably benign 0.02
R1056:Dync2h1 UTSW 9 7,147,731 (GRCm38) missense probably benign 0.15
R1081:Dync2h1 UTSW 9 7,005,488 (GRCm38) critical splice donor site probably null
R1178:Dync2h1 UTSW 9 7,101,193 (GRCm38) splice site probably benign
R1243:Dync2h1 UTSW 9 7,120,882 (GRCm38) missense probably benign
R1295:Dync2h1 UTSW 9 7,075,752 (GRCm38) splice site probably benign
R1304:Dync2h1 UTSW 9 7,102,318 (GRCm38) missense probably damaging 1.00
R1387:Dync2h1 UTSW 9 7,125,816 (GRCm38) missense probably benign
R1513:Dync2h1 UTSW 9 7,103,663 (GRCm38) missense possibly damaging 0.74
R1557:Dync2h1 UTSW 9 7,140,911 (GRCm38) missense probably damaging 1.00
R1568:Dync2h1 UTSW 9 7,157,553 (GRCm38) missense probably null 0.02
R1570:Dync2h1 UTSW 9 7,176,926 (GRCm38) missense probably benign 0.12
R1670:Dync2h1 UTSW 9 6,993,942 (GRCm38) missense possibly damaging 0.82
R1713:Dync2h1 UTSW 9 7,131,891 (GRCm38) missense probably benign
R1766:Dync2h1 UTSW 9 7,015,526 (GRCm38) critical splice acceptor site probably null
R1773:Dync2h1 UTSW 9 7,128,256 (GRCm38) missense probably damaging 1.00
R1786:Dync2h1 UTSW 9 7,081,084 (GRCm38) missense probably damaging 1.00
R1848:Dync2h1 UTSW 9 7,049,166 (GRCm38) missense probably benign 0.01
R1850:Dync2h1 UTSW 9 7,001,448 (GRCm38) missense probably benign 0.00
R1935:Dync2h1 UTSW 9 7,139,159 (GRCm38) critical splice donor site probably null
R1936:Dync2h1 UTSW 9 7,139,159 (GRCm38) critical splice donor site probably null
R1937:Dync2h1 UTSW 9 7,139,159 (GRCm38) critical splice donor site probably null
R1939:Dync2h1 UTSW 9 7,139,159 (GRCm38) critical splice donor site probably null
R1940:Dync2h1 UTSW 9 7,139,159 (GRCm38) critical splice donor site probably null
R1944:Dync2h1 UTSW 9 7,001,377 (GRCm38) missense probably damaging 1.00
R1976:Dync2h1 UTSW 9 7,129,045 (GRCm38) missense probably benign
R2012:Dync2h1 UTSW 9 7,169,589 (GRCm38) missense probably benign 0.00
R2020:Dync2h1 UTSW 9 7,162,925 (GRCm38) missense probably benign 0.25
R2020:Dync2h1 UTSW 9 7,122,772 (GRCm38) missense probably damaging 0.99
R2024:Dync2h1 UTSW 9 7,129,062 (GRCm38) missense probably damaging 0.97
R2038:Dync2h1 UTSW 9 6,967,226 (GRCm38) missense probably damaging 0.99
R2045:Dync2h1 UTSW 9 7,160,171 (GRCm38) missense probably damaging 1.00
R2060:Dync2h1 UTSW 9 7,162,802 (GRCm38) missense possibly damaging 0.92
R2094:Dync2h1 UTSW 9 7,148,735 (GRCm38) missense probably benign 0.18
R2129:Dync2h1 UTSW 9 7,175,289 (GRCm38) missense possibly damaging 0.94
R2130:Dync2h1 UTSW 9 7,011,253 (GRCm38) missense probably damaging 1.00
R2136:Dync2h1 UTSW 9 7,122,772 (GRCm38) missense probably damaging 0.99
R2164:Dync2h1 UTSW 9 7,124,797 (GRCm38) missense probably damaging 1.00
R2242:Dync2h1 UTSW 9 7,037,828 (GRCm38) splice site probably null
R2255:Dync2h1 UTSW 9 6,955,905 (GRCm38) critical splice donor site probably null
R2357:Dync2h1 UTSW 9 7,081,053 (GRCm38) missense probably benign 0.03
R2389:Dync2h1 UTSW 9 7,122,618 (GRCm38) missense possibly damaging 0.82
R2412:Dync2h1 UTSW 9 7,144,246 (GRCm38) missense probably benign 0.01
R2885:Dync2h1 UTSW 9 7,102,329 (GRCm38) missense probably damaging 1.00
R2909:Dync2h1 UTSW 9 7,049,114 (GRCm38) missense probably damaging 1.00
R3434:Dync2h1 UTSW 9 7,011,236 (GRCm38) missense probably benign
R3719:Dync2h1 UTSW 9 7,006,882 (GRCm38) splice site probably benign
R3723:Dync2h1 UTSW 9 7,041,658 (GRCm38) missense probably benign 0.17
R3800:Dync2h1 UTSW 9 7,101,525 (GRCm38) missense possibly damaging 0.90
R3803:Dync2h1 UTSW 9 6,935,293 (GRCm38) missense probably benign 0.00
R3936:Dync2h1 UTSW 9 7,001,482 (GRCm38) missense probably damaging 1.00
R3941:Dync2h1 UTSW 9 7,124,825 (GRCm38) missense probably benign
R3950:Dync2h1 UTSW 9 7,112,061 (GRCm38) nonsense probably null
R4004:Dync2h1 UTSW 9 7,117,404 (GRCm38) missense probably damaging 1.00
R4091:Dync2h1 UTSW 9 7,131,881 (GRCm38) missense probably benign 0.01
R4233:Dync2h1 UTSW 9 7,134,360 (GRCm38) missense probably benign 0.02
R4302:Dync2h1 UTSW 9 7,077,880 (GRCm38) missense probably benign 0.02
R4451:Dync2h1 UTSW 9 6,983,477 (GRCm38) missense probably benign 0.02
R4512:Dync2h1 UTSW 9 7,085,009 (GRCm38) nonsense probably null
R4596:Dync2h1 UTSW 9 6,992,595 (GRCm38) missense probably benign
R4604:Dync2h1 UTSW 9 7,140,995 (GRCm38) missense probably benign 0.00
R4614:Dync2h1 UTSW 9 7,011,290 (GRCm38) missense probably benign 0.03
R4667:Dync2h1 UTSW 9 7,051,411 (GRCm38) missense probably benign 0.00
R4671:Dync2h1 UTSW 9 7,169,640 (GRCm38) missense possibly damaging 0.82
R4714:Dync2h1 UTSW 9 7,118,932 (GRCm38) missense possibly damaging 0.86
R4716:Dync2h1 UTSW 9 7,142,648 (GRCm38) critical splice donor site probably null
R4736:Dync2h1 UTSW 9 7,006,862 (GRCm38) missense probably benign 0.00
R4807:Dync2h1 UTSW 9 7,139,422 (GRCm38) missense probably benign 0.31
R4850:Dync2h1 UTSW 9 7,134,364 (GRCm38) missense probably benign 0.14
R4862:Dync2h1 UTSW 9 7,147,717 (GRCm38) missense probably benign
R4899:Dync2h1 UTSW 9 7,131,921 (GRCm38) nonsense probably null
R4971:Dync2h1 UTSW 9 7,131,949 (GRCm38) missense probably benign
R5040:Dync2h1 UTSW 9 6,992,625 (GRCm38) missense probably benign 0.09
R5054:Dync2h1 UTSW 9 7,085,007 (GRCm38) missense possibly damaging 0.63
R5274:Dync2h1 UTSW 9 7,116,540 (GRCm38) missense probably benign 0.00
R5307:Dync2h1 UTSW 9 7,155,099 (GRCm38) missense probably damaging 1.00
R5347:Dync2h1 UTSW 9 7,129,727 (GRCm38) missense probably damaging 1.00
R5372:Dync2h1 UTSW 9 7,176,962 (GRCm38) unclassified probably benign
R5384:Dync2h1 UTSW 9 7,016,791 (GRCm38) missense probably damaging 0.99
R5385:Dync2h1 UTSW 9 7,016,791 (GRCm38) missense probably damaging 0.99
R5394:Dync2h1 UTSW 9 7,120,899 (GRCm38) nonsense probably null
R5402:Dync2h1 UTSW 9 7,114,949 (GRCm38) missense probably damaging 1.00
R5446:Dync2h1 UTSW 9 7,144,217 (GRCm38) missense probably benign
R5538:Dync2h1 UTSW 9 7,168,630 (GRCm38) intron probably benign
R5551:Dync2h1 UTSW 9 7,031,718 (GRCm38) missense possibly damaging 0.74
R5619:Dync2h1 UTSW 9 7,118,885 (GRCm38) missense probably benign 0.02
R5621:Dync2h1 UTSW 9 7,120,909 (GRCm38) missense possibly damaging 0.86
R5652:Dync2h1 UTSW 9 7,116,638 (GRCm38) missense probably benign 0.45
R5655:Dync2h1 UTSW 9 7,148,659 (GRCm38) missense probably benign 0.01
R5689:Dync2h1 UTSW 9 7,169,689 (GRCm38) missense probably damaging 1.00
R5725:Dync2h1 UTSW 9 7,169,528 (GRCm38) missense probably benign 0.21
R5742:Dync2h1 UTSW 9 7,165,762 (GRCm38) missense possibly damaging 0.64
R5817:Dync2h1 UTSW 9 6,996,905 (GRCm38) missense probably damaging 1.00
R5852:Dync2h1 UTSW 9 7,011,290 (GRCm38) missense probably benign 0.03
R5898:Dync2h1 UTSW 9 7,148,717 (GRCm38) missense probably benign 0.00
R5916:Dync2h1 UTSW 9 7,102,309 (GRCm38) critical splice donor site probably null
R5939:Dync2h1 UTSW 9 7,037,801 (GRCm38) missense probably damaging 0.99
R5942:Dync2h1 UTSW 9 7,117,466 (GRCm38) nonsense probably null
R5982:Dync2h1 UTSW 9 6,955,986 (GRCm38) missense probably benign 0.00
R6029:Dync2h1 UTSW 9 7,157,646 (GRCm38) missense probably benign
R6125:Dync2h1 UTSW 9 7,168,706 (GRCm38) missense probably damaging 1.00
R6209:Dync2h1 UTSW 9 7,165,677 (GRCm38) missense probably benign 0.01
R6247:Dync2h1 UTSW 9 7,135,078 (GRCm38) missense probably damaging 1.00
R6294:Dync2h1 UTSW 9 7,084,986 (GRCm38) missense probably benign 0.01
R6328:Dync2h1 UTSW 9 7,165,717 (GRCm38) missense probably benign 0.00
R6376:Dync2h1 UTSW 9 7,165,703 (GRCm38) missense probably benign 0.21
R6394:Dync2h1 UTSW 9 7,168,331 (GRCm38) missense probably damaging 0.99
R6539:Dync2h1 UTSW 9 7,159,478 (GRCm38) splice site probably null
R6554:Dync2h1 UTSW 9 7,037,699 (GRCm38) missense probably benign 0.39
R6559:Dync2h1 UTSW 9 7,139,501 (GRCm38) missense possibly damaging 0.72
R6563:Dync2h1 UTSW 9 7,120,819 (GRCm38) missense probably benign 0.27
R6807:Dync2h1 UTSW 9 7,041,718 (GRCm38) missense probably benign 0.10
R6848:Dync2h1 UTSW 9 7,159,632 (GRCm38) missense probably benign 0.22
R6901:Dync2h1 UTSW 9 7,131,855 (GRCm38) missense probably damaging 1.00
R6921:Dync2h1 UTSW 9 7,102,549 (GRCm38) missense probably benign
R6997:Dync2h1 UTSW 9 7,168,743 (GRCm38) missense probably null 0.00
R7084:Dync2h1 UTSW 9 7,113,214 (GRCm38) missense possibly damaging 0.72
R7113:Dync2h1 UTSW 9 7,075,788 (GRCm38) missense probably benign 0.03
R7131:Dync2h1 UTSW 9 7,075,786 (GRCm38) missense probably damaging 1.00
R7165:Dync2h1 UTSW 9 7,050,479 (GRCm38) missense probably benign
R7196:Dync2h1 UTSW 9 7,147,715 (GRCm38) nonsense probably null
R7208:Dync2h1 UTSW 9 7,141,059 (GRCm38) missense probably damaging 1.00
R7225:Dync2h1 UTSW 9 7,142,756 (GRCm38) missense probably benign
R7237:Dync2h1 UTSW 9 6,993,966 (GRCm38) missense probably benign 0.00
R7243:Dync2h1 UTSW 9 7,102,405 (GRCm38) missense possibly damaging 0.64
R7291:Dync2h1 UTSW 9 6,929,590 (GRCm38) missense possibly damaging 0.69
R7293:Dync2h1 UTSW 9 7,001,454 (GRCm38) missense possibly damaging 0.88
R7329:Dync2h1 UTSW 9 7,011,247 (GRCm38) missense probably benign
R7351:Dync2h1 UTSW 9 7,167,145 (GRCm38) missense probably damaging 1.00
R7358:Dync2h1 UTSW 9 7,159,479 (GRCm38) critical splice donor site probably null
R7387:Dync2h1 UTSW 9 7,157,932 (GRCm38) missense possibly damaging 0.68
R7446:Dync2h1 UTSW 9 7,041,720 (GRCm38) missense probably benign 0.03
R7487:Dync2h1 UTSW 9 7,132,041 (GRCm38) missense probably benign 0.26
R7488:Dync2h1 UTSW 9 7,124,855 (GRCm38) missense probably benign 0.03
R7496:Dync2h1 UTSW 9 7,135,015 (GRCm38) splice site probably null
R7501:Dync2h1 UTSW 9 7,175,336 (GRCm38) missense possibly damaging 0.82
R7571:Dync2h1 UTSW 9 7,002,623 (GRCm38) missense probably damaging 1.00
R7627:Dync2h1 UTSW 9 7,101,111 (GRCm38) missense probably benign 0.00
R7639:Dync2h1 UTSW 9 7,141,254 (GRCm38) missense probably damaging 0.97
R7653:Dync2h1 UTSW 9 7,117,570 (GRCm38) missense probably benign
R7654:Dync2h1 UTSW 9 7,122,664 (GRCm38) missense probably damaging 1.00
R7742:Dync2h1 UTSW 9 7,076,232 (GRCm38) missense probably benign 0.00
R7755:Dync2h1 UTSW 9 7,015,490 (GRCm38) missense probably benign 0.00
R7762:Dync2h1 UTSW 9 7,129,719 (GRCm38) missense probably benign 0.01
R7790:Dync2h1 UTSW 9 7,114,914 (GRCm38) missense probably damaging 0.96
R7834:Dync2h1 UTSW 9 7,118,953 (GRCm38) missense probably benign 0.04
R7883:Dync2h1 UTSW 9 7,005,566 (GRCm38) missense possibly damaging 0.80
R7952:Dync2h1 UTSW 9 7,129,802 (GRCm38) missense possibly damaging 0.63
R8111:Dync2h1 UTSW 9 7,148,688 (GRCm38) missense probably benign 0.03
R8157:Dync2h1 UTSW 9 7,001,473 (GRCm38) missense possibly damaging 0.47
R8166:Dync2h1 UTSW 9 7,129,089 (GRCm38) nonsense probably null
R8236:Dync2h1 UTSW 9 7,080,363 (GRCm38) intron probably benign
R8326:Dync2h1 UTSW 9 7,147,771 (GRCm38) missense probably benign
R8335:Dync2h1 UTSW 9 7,084,941 (GRCm38) missense probably benign 0.28
R8347:Dync2h1 UTSW 9 7,116,578 (GRCm38) missense possibly damaging 0.81
R8372:Dync2h1 UTSW 9 7,111,514 (GRCm38) missense possibly damaging 0.90
R8421:Dync2h1 UTSW 9 7,102,477 (GRCm38) missense probably damaging 1.00
R8518:Dync2h1 UTSW 9 7,051,452 (GRCm38) missense probably benign 0.04
R8556:Dync2h1 UTSW 9 7,113,198 (GRCm38) missense probably benign 0.32
R8690:Dync2h1 UTSW 9 7,075,824 (GRCm38) missense probably damaging 1.00
R8713:Dync2h1 UTSW 9 7,141,008 (GRCm38) nonsense probably null
R8719:Dync2h1 UTSW 9 7,041,641 (GRCm38) missense probably benign 0.05
R8732:Dync2h1 UTSW 9 7,168,326 (GRCm38) missense probably damaging 1.00
R8744:Dync2h1 UTSW 9 7,011,220 (GRCm38) nonsense probably null
R8749:Dync2h1 UTSW 9 7,035,063 (GRCm38) missense probably benign 0.32
R8795:Dync2h1 UTSW 9 7,137,087 (GRCm38) missense probably benign 0.00
R8853:Dync2h1 UTSW 9 7,117,645 (GRCm38) missense possibly damaging 0.94
R8923:Dync2h1 UTSW 9 7,168,515 (GRCm38) missense probably benign
R8969:Dync2h1 UTSW 9 7,130,723 (GRCm38) missense probably damaging 1.00
R8988:Dync2h1 UTSW 9 7,037,727 (GRCm38) missense probably benign 0.00
R8997:Dync2h1 UTSW 9 7,129,003 (GRCm38) missense probably benign
R9025:Dync2h1 UTSW 9 7,139,462 (GRCm38) nonsense probably null
R9036:Dync2h1 UTSW 9 7,051,495 (GRCm38) missense probably damaging 1.00
R9055:Dync2h1 UTSW 9 6,996,641 (GRCm38) intron probably benign
R9165:Dync2h1 UTSW 9 7,114,883 (GRCm38) missense probably damaging 0.99
R9172:Dync2h1 UTSW 9 7,031,771 (GRCm38) missense probably damaging 1.00
R9286:Dync2h1 UTSW 9 6,941,668 (GRCm38) missense probably benign 0.01
R9312:Dync2h1 UTSW 9 7,050,413 (GRCm38) missense probably damaging 1.00
R9335:Dync2h1 UTSW 9 7,112,149 (GRCm38) missense possibly damaging 0.88
R9344:Dync2h1 UTSW 9 7,148,659 (GRCm38) missense probably benign 0.01
R9351:Dync2h1 UTSW 9 7,176,911 (GRCm38) missense probably damaging 0.98
R9367:Dync2h1 UTSW 9 7,125,730 (GRCm38) critical splice donor site probably null
R9613:Dync2h1 UTSW 9 7,075,769 (GRCm38) missense probably damaging 0.99
R9650:Dync2h1 UTSW 9 7,174,849 (GRCm38) missense possibly damaging 0.83
R9726:Dync2h1 UTSW 9 7,077,999 (GRCm38) missense possibly damaging 0.94
R9731:Dync2h1 UTSW 9 7,141,166 (GRCm38) missense probably benign
X0009:Dync2h1 UTSW 9 7,117,576 (GRCm38) missense possibly damaging 0.81
Z1176:Dync2h1 UTSW 9 7,168,730 (GRCm38) frame shift probably null
Z1176:Dync2h1 UTSW 9 7,142,361 (GRCm38) missense probably damaging 0.99
Z1177:Dync2h1 UTSW 9 7,102,427 (GRCm38) missense probably damaging 1.00
Posted On 2015-04-16