Incidental Mutation 'R4586:Dnhd1'
ID 344111
Institutional Source Beutler Lab
Gene Symbol Dnhd1
Ensembl Gene ENSMUSG00000030882
Gene Name dynein heavy chain domain 1
Synonyms 8030491N06Rik
MMRRC Submission 041807-MU
Accession Numbers

Variant 1:ENSMUST00000145988; OTTMUST00000062891; Variant 2:  ENSMUST00000106773; Variant 3: ENSMUST00000106776; Variant 4: ENSMUST00000163171; Variant 5: ENSMUST00000142363;OTTMUST00000062869; Variant 6: ENSMUST00000142874; OTTMUST00000062870; Variant 7: ENSMUST00000128388; OTTMUST00000062892; MGI:1924755

Essential gene? Probably non essential (E-score: 0.077) question?
Stock # R4586 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 105650827-105721799 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 105678049 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 735 (L735P)
Ref Sequence ENSEMBL: ENSMUSP00000121261 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106776] [ENSMUST00000142874] [ENSMUST00000145988] [ENSMUST00000210312]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000106776
SMART Domains Protein: ENSMUSP00000102388
Gene: ENSMUSG00000030882

DomainStartEndE-ValueType
low complexity region 205 224 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128388
Predicted Effect probably benign
Transcript: ENSMUST00000142874
Predicted Effect probably damaging
Transcript: ENSMUST00000145988
AA Change: L735P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000121261
Gene: ENSMUSG00000030882
AA Change: L735P

DomainStartEndE-ValueType
low complexity region 5 18 N/A INTRINSIC
low complexity region 102 115 N/A INTRINSIC
low complexity region 183 191 N/A INTRINSIC
low complexity region 253 269 N/A INTRINSIC
low complexity region 943 962 N/A INTRINSIC
Pfam:DHC_N2 1018 1472 4.6e-50 PFAM
Pfam:AAA_6 1652 1875 2.7e-14 PFAM
low complexity region 1906 1918 N/A INTRINSIC
Blast:AAA 1993 2196 1e-34 BLAST
Pfam:AAA_7 2362 2610 3.3e-11 PFAM
low complexity region 2697 2714 N/A INTRINSIC
low complexity region 2722 2733 N/A INTRINSIC
low complexity region 2800 2810 N/A INTRINSIC
low complexity region 3116 3134 N/A INTRINSIC
Pfam:MT 3178 3470 3.9e-16 PFAM
coiled coil region 3590 3642 N/A INTRINSIC
coiled coil region 3816 3843 N/A INTRINSIC
Pfam:Dynein_heavy 3976 4746 7.3e-97 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000210312
Meta Mutation Damage Score 0.6755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.3%
Validation Efficiency 100% (96/96)
Allele List at MGI

All alleles(1) : Gene trapped(1)

Other mutations in this stock
Total: 84 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110004E09Rik A T 16: 90,927,426 (GRCm38) V136D probably damaging Het
Akap9 T C 5: 3,976,151 (GRCm38) S1269P probably benign Het
Aqr T C 2: 114,112,577 (GRCm38) T1172A probably benign Het
Art2a-ps A T 7: 101,554,749 (GRCm38) L194* probably null Het
Atrn T C 2: 130,982,042 (GRCm38) F967S probably damaging Het
Btnl1 A G 17: 34,382,462 (GRCm38) D323G probably damaging Het
Cadps C A 14: 12,505,808 (GRCm38) C754F probably damaging Het
Ccdc7b A G 8: 129,110,920 (GRCm38) T131A probably benign Het
Cic A T 7: 25,272,778 (GRCm38) I645L probably benign Het
Clca1 C A 3: 145,016,858 (GRCm38) C251F probably damaging Het
Cldn16 A T 16: 26,477,558 (GRCm38) T95S probably benign Het
Cntnap4 C T 8: 112,810,710 (GRCm38) H738Y probably benign Het
Col8a2 A T 4: 126,311,019 (GRCm38) probably benign Het
Corin A T 5: 72,329,699 (GRCm38) V706D probably damaging Het
Cuzd1 G A 7: 131,314,800 (GRCm38) P310L probably damaging Het
Cyp4a12a T C 4: 115,327,312 (GRCm38) F295L probably benign Het
Cyp4a12b T G 4: 115,432,506 (GRCm38) M190R probably damaging Het
Dagla A G 19: 10,271,009 (GRCm38) Y96H probably damaging Het
Dapp1 T C 3: 137,939,171 (GRCm38) Q148R probably benign Het
Dcaf17 T A 2: 71,088,580 (GRCm38) S499R probably benign Het
Ddx27 T A 2: 167,019,984 (GRCm38) D135E probably benign Het
Defb3 A T 8: 19,295,156 (GRCm38) I43F possibly damaging Het
Dnajc10 T G 2: 80,347,778 (GRCm38) F710V probably damaging Het
Dnmt1 G A 9: 20,926,693 (GRCm38) P242S probably benign Het
Dync1h1 G A 12: 110,649,483 (GRCm38) D3022N probably benign Het
Ep400 G A 5: 110,753,859 (GRCm38) T464I probably damaging Het
Epc1 T C 18: 6,449,138 (GRCm38) N453S possibly damaging Het
Eral1 A T 11: 78,078,304 (GRCm38) N123K probably damaging Het
Ercc5 G A 1: 44,158,857 (GRCm38) V145I probably benign Het
Evc A G 5: 37,323,713 (GRCm38) S263P probably damaging Het
Fancc A T 13: 63,347,564 (GRCm38) M182K probably benign Het
Fbxl3 G T 14: 103,083,090 (GRCm38) A355E probably damaging Het
Fig4 A C 10: 41,188,632 (GRCm38) S872A probably damaging Het
Gm14393 C A 2: 175,062,704 (GRCm38) probably benign Het
Gm16432 A G 1: 178,122,785 (GRCm38) D734G possibly damaging Het
Gm27013 A T 6: 130,521,040 (GRCm38) noncoding transcript Het
Gprc5a T A 6: 135,083,452 (GRCm38) M313K probably benign Het
H2-T3 T C 17: 36,189,344 (GRCm38) probably null Het
Hap1 G A 11: 100,354,724 (GRCm38) T138M probably benign Het
Hist1h2ak T C 13: 21,753,712 (GRCm38) N39S possibly damaging Het
Hook3 T G 8: 26,032,011 (GRCm38) K679T probably damaging Het
Ints2 G T 11: 86,249,275 (GRCm38) R244S probably damaging Het
Itgb4 T C 11: 115,993,325 (GRCm38) V945A probably damaging Het
Itih2 C T 2: 10,110,400 (GRCm38) S387N probably benign Het
Jmjd7 T A 2: 120,032,168 (GRCm38) M306K probably benign Het
Klra2 T A 6: 131,230,157 (GRCm38) D163V probably benign Het
Kmo T A 1: 175,650,572 (GRCm38) M208K probably damaging Het
Kmo G T 1: 175,650,573 (GRCm38) M208I possibly damaging Het
Masp2 A G 4: 148,613,901 (GRCm38) T480A probably damaging Het
Mogs G T 6: 83,118,638 (GRCm38) R812L possibly damaging Het
Mrpl43 A G 19: 45,005,889 (GRCm38) I97T possibly damaging Het
Myoz1 A G 14: 20,650,595 (GRCm38) W185R probably damaging Het
Ncam2 T A 16: 81,465,569 (GRCm38) H303Q probably benign Het
Nufip2 T C 11: 77,741,728 (GRCm38) V690A unknown Het
Obox1 A T 7: 15,556,227 (GRCm38) N165I possibly damaging Het
Olfr1218 T G 2: 89,055,154 (GRCm38) I91L possibly damaging Het
Olfr3 C T 2: 36,812,525 (GRCm38) C189Y probably damaging Het
Olfr32 T A 2: 90,138,214 (GRCm38) E308D probably benign Het
Olfr781 A G 10: 129,333,273 (GRCm38) T131A probably benign Het
Pex1 A G 5: 3,633,885 (GRCm38) Y1127C probably damaging Het
Pno1 T C 11: 17,211,438 (GRCm38) K24E probably benign Het
Qdpr T A 5: 45,439,327 (GRCm38) N165I possibly damaging Het
Robo2 A G 16: 73,961,873 (GRCm38) V674A probably damaging Het
Runx1t1 A T 4: 13,889,864 (GRCm38) T598S unknown Het
Samd11 A G 4: 156,249,432 (GRCm38) L174P probably damaging Het
Scn2a T A 2: 65,743,051 (GRCm38) probably null Het
Slc4a1 G T 11: 102,361,419 (GRCm38) probably benign Het
Snx25 A T 8: 46,116,437 (GRCm38) probably benign Het
Sox2 A G 3: 34,651,044 (GRCm38) N210S probably benign Het
Spag6 T C 2: 18,732,147 (GRCm38) probably null Het
Speer4b A T 5: 27,498,038 (GRCm38) L154Q probably null Het
Stt3a T A 9: 36,741,793 (GRCm38) Q531L probably damaging Het
Tcl1 A C 12: 105,217,508 (GRCm38) probably benign Het
Trip11 A T 12: 101,883,341 (GRCm38) M1488K possibly damaging Het
Ttn T C 2: 76,968,403 (GRCm38) H509R probably benign Het
Ulk3 C T 9: 57,594,310 (GRCm38) L425F possibly damaging Het
Vmn1r238 T A 18: 3,123,294 (GRCm38) K40M probably damaging Het
Vopp1 G A 6: 57,754,548 (GRCm38) P153S probably damaging Het
Wdyhv1 A T 15: 58,148,344 (GRCm38) I34F probably damaging Het
Zbtb42 C T 12: 112,680,542 (GRCm38) R384W probably damaging Het
Zfp14 G T 7: 30,038,916 (GRCm38) Q215K probably damaging Het
Zfp473 A T 7: 44,732,952 (GRCm38) Y651* probably null Het
Zfp735 G T 11: 73,689,724 (GRCm38) E16D possibly damaging Het
Zfp846 G T 9: 20,593,513 (GRCm38) C223F probably damaging Het
Other mutations in Dnhd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00321:Dnhd1 APN 7 105,677,995 (GRCm38) missense probably damaging 1.00
IGL00516:Dnhd1 APN 7 105,657,211 (GRCm38) missense possibly damaging 0.52
IGL00576:Dnhd1 APN 7 105,692,675 (GRCm38) missense probably damaging 1.00
IGL00990:Dnhd1 APN 7 105,721,688 (GRCm38) missense possibly damaging 0.85
IGL01346:Dnhd1 APN 7 105,713,909 (GRCm38) missense probably benign
IGL01714:Dnhd1 APN 7 105,720,942 (GRCm38) missense probably damaging 1.00
IGL01735:Dnhd1 APN 7 105,713,754 (GRCm38) missense probably benign 0.37
IGL01814:Dnhd1 APN 7 105,652,030 (GRCm38) missense probably benign
IGL01999:Dnhd1 APN 7 105,721,215 (GRCm38) missense possibly damaging 0.50
IGL02022:Dnhd1 APN 7 105,678,309 (GRCm38) missense probably damaging 1.00
IGL02131:Dnhd1 APN 7 105,720,802 (GRCm38) missense probably damaging 1.00
IGL02156:Dnhd1 APN 7 105,721,744 (GRCm38) missense probably damaging 1.00
IGL02674:Dnhd1 APN 7 105,721,481 (GRCm38) missense probably benign 0.00
IGL02966:Dnhd1 APN 7 105,720,741 (GRCm38) missense probably benign 0.00
IGL03066:Dnhd1 APN 7 105,719,882 (GRCm38) missense probably damaging 0.99
IGL03298:Dnhd1 APN 7 105,714,475 (GRCm38) missense probably damaging 0.98
IGL03378:Dnhd1 APN 7 105,713,733 (GRCm38) missense possibly damaging 0.87
IGL02802:Dnhd1 UTSW 7 105,655,723 (GRCm38) missense possibly damaging 0.83
R0060:Dnhd1 UTSW 7 105,668,514 (GRCm38) missense probably damaging 0.99
R0129:Dnhd1 UTSW 7 105,720,924 (GRCm38) missense probably benign 0.19
R0238:Dnhd1 UTSW 7 105,721,531 (GRCm38) missense probably benign 0.06
R0238:Dnhd1 UTSW 7 105,721,531 (GRCm38) missense probably benign 0.06
R0239:Dnhd1 UTSW 7 105,721,531 (GRCm38) missense probably benign 0.06
R0239:Dnhd1 UTSW 7 105,721,531 (GRCm38) missense probably benign 0.06
R0384:Dnhd1 UTSW 7 105,720,114 (GRCm38) missense possibly damaging 0.56
R0453:Dnhd1 UTSW 7 105,674,444 (GRCm38) missense probably benign 0.00
R0540:Dnhd1 UTSW 7 105,720,788 (GRCm38) missense probably benign 0.04
R0554:Dnhd1 UTSW 7 105,694,395 (GRCm38) missense probably benign 0.10
R0576:Dnhd1 UTSW 7 105,714,045 (GRCm38) missense probably damaging 1.00
R0607:Dnhd1 UTSW 7 105,720,788 (GRCm38) missense probably benign 0.04
R0631:Dnhd1 UTSW 7 105,651,624 (GRCm38) missense probably benign 0.17
R0639:Dnhd1 UTSW 7 105,696,464 (GRCm38) missense possibly damaging 0.95
R0668:Dnhd1 UTSW 7 105,695,751 (GRCm38) missense probably benign
R0669:Dnhd1 UTSW 7 105,693,704 (GRCm38) missense probably benign 0.01
R0670:Dnhd1 UTSW 7 105,696,464 (GRCm38) missense possibly damaging 0.95
R0699:Dnhd1 UTSW 7 105,651,906 (GRCm38) missense probably damaging 0.98
R1019:Dnhd1 UTSW 7 105,709,171 (GRCm38) missense probably damaging 1.00
R1144:Dnhd1 UTSW 7 105,713,031 (GRCm38) missense probably damaging 1.00
R1226:Dnhd1 UTSW 7 105,696,899 (GRCm38) missense probably damaging 1.00
R1257:Dnhd1 UTSW 7 105,694,153 (GRCm38) missense probably damaging 1.00
R1391:Dnhd1 UTSW 7 105,720,124 (GRCm38) missense probably damaging 1.00
R1453:Dnhd1 UTSW 7 105,721,273 (GRCm38) critical splice donor site probably null
R1501:Dnhd1 UTSW 7 105,668,463 (GRCm38) missense probably benign 0.00
R1503:Dnhd1 UTSW 7 105,693,660 (GRCm38) missense possibly damaging 0.67
R1515:Dnhd1 UTSW 7 105,704,148 (GRCm38) missense probably benign 0.11
R1615:Dnhd1 UTSW 7 105,713,706 (GRCm38) missense possibly damaging 0.74
R1615:Dnhd1 UTSW 7 105,703,206 (GRCm38) missense probably benign 0.00
R1656:Dnhd1 UTSW 7 105,714,281 (GRCm38) missense probably damaging 1.00
R1720:Dnhd1 UTSW 7 105,693,828 (GRCm38) missense probably benign
R1723:Dnhd1 UTSW 7 105,714,920 (GRCm38) missense possibly damaging 0.60
R1766:Dnhd1 UTSW 7 105,693,972 (GRCm38) missense possibly damaging 0.50
R1799:Dnhd1 UTSW 7 105,655,767 (GRCm38) missense probably benign 0.31
R1860:Dnhd1 UTSW 7 105,704,205 (GRCm38) missense probably benign
R1920:Dnhd1 UTSW 7 105,713,407 (GRCm38) missense probably benign 0.00
R1925:Dnhd1 UTSW 7 105,673,854 (GRCm38) missense probably damaging 0.96
R1925:Dnhd1 UTSW 7 105,652,252 (GRCm38) missense probably damaging 1.00
R1934:Dnhd1 UTSW 7 105,708,582 (GRCm38) missense probably benign 0.05
R1935:Dnhd1 UTSW 7 105,673,976 (GRCm38) missense probably benign 0.09
R1936:Dnhd1 UTSW 7 105,673,976 (GRCm38) missense probably benign 0.09
R2035:Dnhd1 UTSW 7 105,704,921 (GRCm38) missense probably damaging 0.99
R2125:Dnhd1 UTSW 7 105,677,971 (GRCm38) missense probably benign 0.35
R2127:Dnhd1 UTSW 7 105,693,721 (GRCm38) missense possibly damaging 0.56
R2254:Dnhd1 UTSW 7 105,703,772 (GRCm38) missense probably damaging 1.00
R2301:Dnhd1 UTSW 7 105,705,399 (GRCm38) missense probably damaging 1.00
R2316:Dnhd1 UTSW 7 105,674,421 (GRCm38) missense probably damaging 1.00
R2324:Dnhd1 UTSW 7 105,710,090 (GRCm38) missense probably damaging 1.00
R2337:Dnhd1 UTSW 7 105,703,467 (GRCm38) missense probably benign 0.07
R2381:Dnhd1 UTSW 7 105,693,664 (GRCm38) missense probably benign 0.42
R2394:Dnhd1 UTSW 7 105,720,231 (GRCm38) missense probably benign 0.19
R2862:Dnhd1 UTSW 7 105,712,559 (GRCm38) missense probably benign 0.01
R3038:Dnhd1 UTSW 7 105,720,229 (GRCm38) missense probably damaging 0.99
R3114:Dnhd1 UTSW 7 105,696,565 (GRCm38) critical splice donor site probably null
R3404:Dnhd1 UTSW 7 105,694,761 (GRCm38) nonsense probably null
R3405:Dnhd1 UTSW 7 105,694,761 (GRCm38) nonsense probably null
R3439:Dnhd1 UTSW 7 105,694,785 (GRCm38) missense probably damaging 1.00
R3959:Dnhd1 UTSW 7 105,713,122 (GRCm38) missense probably benign 0.21
R4014:Dnhd1 UTSW 7 105,714,838 (GRCm38) missense probably damaging 0.99
R4084:Dnhd1 UTSW 7 105,709,588 (GRCm38) missense probably damaging 1.00
R4181:Dnhd1 UTSW 7 105,693,954 (GRCm38) missense probably damaging 1.00
R4255:Dnhd1 UTSW 7 105,712,998 (GRCm38) missense probably damaging 1.00
R4302:Dnhd1 UTSW 7 105,693,954 (GRCm38) missense probably damaging 1.00
R4440:Dnhd1 UTSW 7 105,696,728 (GRCm38) nonsense probably null
R4565:Dnhd1 UTSW 7 105,651,956 (GRCm38) missense possibly damaging 0.92
R4569:Dnhd1 UTSW 7 105,657,166 (GRCm38) splice site probably null
R4584:Dnhd1 UTSW 7 105,678,049 (GRCm38) missense probably damaging 1.00
R4590:Dnhd1 UTSW 7 105,714,030 (GRCm38) missense probably damaging 1.00
R4593:Dnhd1 UTSW 7 105,715,446 (GRCm38) missense probably benign 0.02
R4600:Dnhd1 UTSW 7 105,703,644 (GRCm38) missense probably damaging 1.00
R4705:Dnhd1 UTSW 7 105,655,741 (GRCm38) missense probably damaging 1.00
R4731:Dnhd1 UTSW 7 105,673,849 (GRCm38) missense probably benign 0.00
R4732:Dnhd1 UTSW 7 105,673,849 (GRCm38) missense probably benign 0.00
R4733:Dnhd1 UTSW 7 105,673,849 (GRCm38) missense probably benign 0.00
R4786:Dnhd1 UTSW 7 105,674,444 (GRCm38) missense probably benign 0.00
R4791:Dnhd1 UTSW 7 105,721,117 (GRCm38) missense probably damaging 1.00
R4811:Dnhd1 UTSW 7 105,714,281 (GRCm38) missense probably damaging 0.99
R4822:Dnhd1 UTSW 7 105,703,964 (GRCm38) missense probably benign 0.00
R4886:Dnhd1 UTSW 7 105,714,808 (GRCm38) missense probably benign 0.00
R4890:Dnhd1 UTSW 7 105,656,957 (GRCm38) missense possibly damaging 0.47
R4973:Dnhd1 UTSW 7 105,713,633 (GRCm38) missense probably benign 0.24
R5007:Dnhd1 UTSW 7 105,713,076 (GRCm38) missense probably damaging 1.00
R5048:Dnhd1 UTSW 7 105,693,697 (GRCm38) missense probably benign 0.01
R5151:Dnhd1 UTSW 7 105,713,440 (GRCm38) missense probably benign 0.22
R5179:Dnhd1 UTSW 7 105,714,552 (GRCm38) missense probably damaging 1.00
R5182:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5183:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5185:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5209:Dnhd1 UTSW 7 105,696,460 (GRCm38) missense probably benign 0.00
R5225:Dnhd1 UTSW 7 105,703,923 (GRCm38) missense possibly damaging 0.73
R5250:Dnhd1 UTSW 7 105,685,761 (GRCm38) missense probably damaging 1.00
R5257:Dnhd1 UTSW 7 105,674,037 (GRCm38) missense probably benign
R5258:Dnhd1 UTSW 7 105,674,037 (GRCm38) missense probably benign
R5273:Dnhd1 UTSW 7 105,714,482 (GRCm38) missense probably damaging 0.99
R5288:Dnhd1 UTSW 7 105,714,437 (GRCm38) missense possibly damaging 0.94
R5396:Dnhd1 UTSW 7 105,713,684 (GRCm38) missense probably benign 0.00
R5453:Dnhd1 UTSW 7 105,710,123 (GRCm38) missense probably damaging 1.00
R5511:Dnhd1 UTSW 7 105,714,156 (GRCm38) missense probably damaging 1.00
R5518:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5523:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5528:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5529:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5561:Dnhd1 UTSW 7 105,714,821 (GRCm38) missense probably damaging 0.99
R5681:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5682:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5683:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5684:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5686:Dnhd1 UTSW 7 105,703,209 (GRCm38) missense probably damaging 1.00
R5697:Dnhd1 UTSW 7 105,674,188 (GRCm38) missense probably damaging 1.00
R5789:Dnhd1 UTSW 7 105,705,010 (GRCm38) missense possibly damaging 0.50
R5790:Dnhd1 UTSW 7 105,655,774 (GRCm38) missense probably damaging 1.00
R5814:Dnhd1 UTSW 7 105,719,895 (GRCm38) missense possibly damaging 0.69
R5828:Dnhd1 UTSW 7 105,720,181 (GRCm38) missense probably benign 0.00
R5852:Dnhd1 UTSW 7 105,695,748 (GRCm38) missense probably damaging 1.00
R5883:Dnhd1 UTSW 7 105,720,504 (GRCm38) missense probably damaging 0.98
R6115:Dnhd1 UTSW 7 105,713,987 (GRCm38) missense probably benign 0.00
R6119:Dnhd1 UTSW 7 105,709,440 (GRCm38) missense probably benign 0.18
R6212:Dnhd1 UTSW 7 105,704,048 (GRCm38) missense probably damaging 1.00
R6243:Dnhd1 UTSW 7 105,652,009 (GRCm38) missense probably damaging 1.00
R6265:Dnhd1 UTSW 7 105,693,370 (GRCm38) missense probably benign 0.07
R6332:Dnhd1 UTSW 7 105,694,066 (GRCm38) missense probably benign 0.02
R6344:Dnhd1 UTSW 7 105,694,610 (GRCm38) missense probably benign 0.38
R6477:Dnhd1 UTSW 7 105,677,886 (GRCm38) missense probably benign 0.05
R6642:Dnhd1 UTSW 7 105,703,799 (GRCm38) missense probably benign
R6663:Dnhd1 UTSW 7 105,685,692 (GRCm38) splice site probably null
R6730:Dnhd1 UTSW 7 105,703,875 (GRCm38) missense probably benign 0.00
R6748:Dnhd1 UTSW 7 105,720,637 (GRCm38) missense probably benign 0.03
R6833:Dnhd1 UTSW 7 105,703,373 (GRCm38) missense probably benign 0.01
R6850:Dnhd1 UTSW 7 105,719,930 (GRCm38) missense possibly damaging 0.68
R6853:Dnhd1 UTSW 7 105,703,728 (GRCm38) missense probably benign
R6860:Dnhd1 UTSW 7 105,678,266 (GRCm38) missense probably benign
R6898:Dnhd1 UTSW 7 105,687,377 (GRCm38) missense probably damaging 0.99
R6927:Dnhd1 UTSW 7 105,715,563 (GRCm38) missense probably damaging 1.00
R6952:Dnhd1 UTSW 7 105,713,688 (GRCm38) missense probably damaging 1.00
R6987:Dnhd1 UTSW 7 105,704,585 (GRCm38) missense probably damaging 0.98
R6988:Dnhd1 UTSW 7 105,714,210 (GRCm38) missense probably damaging 1.00
R7022:Dnhd1 UTSW 7 105,720,798 (GRCm38) missense probably benign 0.36
R7053:Dnhd1 UTSW 7 105,694,954 (GRCm38) missense probably damaging 1.00
R7085:Dnhd1 UTSW 7 105,715,261 (GRCm38) missense probably benign 0.26
R7086:Dnhd1 UTSW 7 105,708,532 (GRCm38) missense probably benign 0.03
R7112:Dnhd1 UTSW 7 105,713,985 (GRCm38) missense probably damaging 1.00
R7140:Dnhd1 UTSW 7 105,693,766 (GRCm38) missense probably benign 0.00
R7151:Dnhd1 UTSW 7 105,710,027 (GRCm38) missense probably benign 0.03
R7178:Dnhd1 UTSW 7 105,694,993 (GRCm38) missense probably damaging 0.98
R7326:Dnhd1 UTSW 7 105,720,930 (GRCm38) missense probably damaging 0.96
R7345:Dnhd1 UTSW 7 105,703,967 (GRCm38) missense probably benign 0.17
R7349:Dnhd1 UTSW 7 105,710,123 (GRCm38) missense probably damaging 1.00
R7397:Dnhd1 UTSW 7 105,705,297 (GRCm38) missense possibly damaging 0.87
R7520:Dnhd1 UTSW 7 105,696,048 (GRCm38) missense probably benign 0.07
R7536:Dnhd1 UTSW 7 105,709,561 (GRCm38) missense probably damaging 1.00
R7539:Dnhd1 UTSW 7 105,720,912 (GRCm38) missense probably damaging 1.00
R7541:Dnhd1 UTSW 7 105,678,309 (GRCm38) missense probably damaging 1.00
R7619:Dnhd1 UTSW 7 105,674,268 (GRCm38) missense probably benign 0.01
R7676:Dnhd1 UTSW 7 105,684,087 (GRCm38) missense probably benign 0.09
R7689:Dnhd1 UTSW 7 105,713,963 (GRCm38) missense probably benign 0.07
R7712:Dnhd1 UTSW 7 105,651,624 (GRCm38) missense probably benign 0.17
R7729:Dnhd1 UTSW 7 105,705,265 (GRCm38) missense probably damaging 1.00
R7767:Dnhd1 UTSW 7 105,694,610 (GRCm38) missense probably benign 0.38
R7768:Dnhd1 UTSW 7 105,721,095 (GRCm38) missense possibly damaging 0.87
R7779:Dnhd1 UTSW 7 105,677,915 (GRCm38) missense probably benign 0.01
R7879:Dnhd1 UTSW 7 105,703,439 (GRCm38) missense probably benign 0.09
R7922:Dnhd1 UTSW 7 105,668,514 (GRCm38) missense probably damaging 1.00
R7951:Dnhd1 UTSW 7 105,678,004 (GRCm38) missense probably damaging 1.00
R8259:Dnhd1 UTSW 7 105,694,788 (GRCm38) missense probably benign 0.38
R8350:Dnhd1 UTSW 7 105,678,024 (GRCm38) missense probably damaging 0.99
R8380:Dnhd1 UTSW 7 105,677,866 (GRCm38) missense probably benign 0.31
R8392:Dnhd1 UTSW 7 105,703,343 (GRCm38) missense possibly damaging 0.84
R8478:Dnhd1 UTSW 7 105,682,794 (GRCm38) missense probably benign 0.00
R8708:Dnhd1 UTSW 7 105,694,280 (GRCm38) nonsense probably null
R8767:Dnhd1 UTSW 7 105,652,123 (GRCm38) missense probably damaging 1.00
R8825:Dnhd1 UTSW 7 105,693,967 (GRCm38) missense possibly damaging 0.95
R8849:Dnhd1 UTSW 7 105,721,516 (GRCm38) missense probably benign 0.00
R8903:Dnhd1 UTSW 7 105,713,648 (GRCm38) nonsense probably null
R8910:Dnhd1 UTSW 7 105,683,697 (GRCm38) missense possibly damaging 0.92
R8940:Dnhd1 UTSW 7 105,714,647 (GRCm38) intron probably benign
R8954:Dnhd1 UTSW 7 105,694,779 (GRCm38) missense probably benign 0.35
R8956:Dnhd1 UTSW 7 105,692,645 (GRCm38) missense probably damaging 0.99
R8971:Dnhd1 UTSW 7 105,709,321 (GRCm38) nonsense probably null
R8996:Dnhd1 UTSW 7 105,674,035 (GRCm38) missense probably damaging 1.00
R9051:Dnhd1 UTSW 7 105,692,726 (GRCm38) missense possibly damaging 0.54
R9058:Dnhd1 UTSW 7 105,684,063 (GRCm38) missense probably benign 0.01
R9109:Dnhd1 UTSW 7 105,683,966 (GRCm38) missense probably damaging 0.98
R9284:Dnhd1 UTSW 7 105,651,884 (GRCm38) missense probably damaging 1.00
R9295:Dnhd1 UTSW 7 105,714,141 (GRCm38) missense probably benign
R9298:Dnhd1 UTSW 7 105,683,966 (GRCm38) missense probably damaging 0.98
R9299:Dnhd1 UTSW 7 105,720,599 (GRCm38) missense probably benign 0.00
R9308:Dnhd1 UTSW 7 105,704,277 (GRCm38) missense probably damaging 1.00
R9337:Dnhd1 UTSW 7 105,720,599 (GRCm38) missense probably benign 0.00
R9385:Dnhd1 UTSW 7 105,712,765 (GRCm38) missense probably damaging 1.00
R9463:Dnhd1 UTSW 7 105,695,016 (GRCm38) missense probably benign
R9463:Dnhd1 UTSW 7 105,657,247 (GRCm38) missense probably benign 0.00
R9476:Dnhd1 UTSW 7 105,703,682 (GRCm38) missense possibly damaging 0.74
R9489:Dnhd1 UTSW 7 105,651,597 (GRCm38) missense probably benign
R9500:Dnhd1 UTSW 7 105,704,502 (GRCm38) missense probably benign
R9510:Dnhd1 UTSW 7 105,703,682 (GRCm38) missense possibly damaging 0.74
R9513:Dnhd1 UTSW 7 105,704,972 (GRCm38) missense probably damaging 1.00
R9537:Dnhd1 UTSW 7 105,695,533 (GRCm38) missense probably damaging 0.99
R9567:Dnhd1 UTSW 7 105,704,266 (GRCm38) missense probably benign 0.03
R9622:Dnhd1 UTSW 7 105,704,135 (GRCm38) missense probably benign
R9623:Dnhd1 UTSW 7 105,694,927 (GRCm38) missense probably damaging 1.00
R9623:Dnhd1 UTSW 7 105,686,566 (GRCm38) missense probably damaging 1.00
R9674:Dnhd1 UTSW 7 105,714,222 (GRCm38) missense probably damaging 1.00
R9756:Dnhd1 UTSW 7 105,703,928 (GRCm38) missense probably benign 0.19
R9777:Dnhd1 UTSW 7 105,720,249 (GRCm38) missense probably benign 0.14
R9778:Dnhd1 UTSW 7 105,704,033 (GRCm38) missense probably benign
R9781:Dnhd1 UTSW 7 105,703,710 (GRCm38) missense probably benign 0.31
R9796:Dnhd1 UTSW 7 105,693,330 (GRCm38) missense probably damaging 1.00
Z1088:Dnhd1 UTSW 7 105,712,727 (GRCm38) missense probably benign 0.00
Z1176:Dnhd1 UTSW 7 105,703,036 (GRCm38) critical splice acceptor site probably null
Z1176:Dnhd1 UTSW 7 105,678,299 (GRCm38) missense probably benign
Z1176:Dnhd1 UTSW 7 105,668,547 (GRCm38) missense probably damaging 0.98
Z1176:Dnhd1 UTSW 7 105,703,580 (GRCm38) frame shift probably null
Z1177:Dnhd1 UTSW 7 105,682,841 (GRCm38) missense possibly damaging 0.90
Predicted Primers PCR Primer
(F):5'- ATTCCTGATGCCCAAGTTTCATG -3'
(R):5'- CTCCAGGCTTTCAGGAACTC -3'

Sequencing Primer
(F):5'- CCTGATGCCCAAGTTTCATGGAAAG -3'
(R):5'- GGCTTTCAGGAACTCATAGATGCC -3'
Posted On 2015-09-24