Incidental Mutation 'IGL01455:Haus8'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Haus8
Ensembl Gene ENSMUSG00000035439
Gene Name4HAUS augmin-like complex, subunit 8
SynonymsHice1, 2410004L22Rik
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.779) question?
Stock #IGL01455
Quality Score
Chromosomal Location71248561-71272934 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 71253231 bp
Amino Acid Change Isoleucine to Valine at position 270 (I270V)
Ref Sequence ENSEMBL: ENSMUSP00000105698 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035960] [ENSMUST00000110071] [ENSMUST00000123495]
Predicted Effect probably benign
Transcript: ENSMUST00000035960
AA Change: I271V

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000040802
Gene: ENSMUSG00000035439
AA Change: I271V

low complexity region 9 19 N/A INTRINSIC
low complexity region 130 142 N/A INTRINSIC
coiled coil region 164 201 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000110071
AA Change: I270V

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
SMART Domains Protein: ENSMUSP00000105698
Gene: ENSMUSG00000035439
AA Change: I270V

low complexity region 9 19 N/A INTRINSIC
low complexity region 129 141 N/A INTRINSIC
coiled coil region 163 200 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000123495
SMART Domains Protein: ENSMUSP00000123517
Gene: ENSMUSG00000035439

low complexity region 9 19 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129455
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134361
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144726
Predicted Effect noncoding transcript
Transcript: ENSMUST00000157039
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] HAUS8 is 1 of 8 subunits of the 390-kD human augmin complex, or HAUS complex. The augmin complex was first identified in Drosophila, and its name comes from the Latin verb 'augmentare,' meaning 'to increase.' The augmin complex is a microtubule-binding complex involved in microtubule generation within the mitotic spindle and is vital to mitotic spindle assembly (Goshima et al., 2008 [PubMed 18443220]; Uehara et al., 2009 [PubMed 19369198]).[supplied by OMIM, Jun 2010]
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl6 A G 11: 54,323,305 D87G possibly damaging Het
Adgra3 G A 5: 49,987,557 R565* probably null Het
Akap12 C T 10: 4,356,886 T1232I probably damaging Het
B3gnt2 A T 11: 22,837,042 W49R probably damaging Het
Ccdc112 T A 18: 46,293,444 K137N possibly damaging Het
Ccdc117 G T 11: 5,534,297 T181K possibly damaging Het
Cfh T C 1: 140,105,539 K756E possibly damaging Het
Clca1 C T 3: 145,007,778 M697I probably benign Het
Cyp2c29 T A 19: 39,329,117 I349K possibly damaging Het
Dcaf15 T C 8: 84,098,590 T434A probably benign Het
Entpd5 T C 12: 84,394,677 I106V probably benign Het
Eps8l1 T A 7: 4,478,923 probably benign Het
Erbin G T 13: 103,859,387 P269Q probably damaging Het
Fam172a A T 13: 77,902,647 probably benign Het
Fbxw22 C T 9: 109,384,994 M251I probably benign Het
Fgd4 T A 16: 16,490,490 T9S probably benign Het
Gm17689 T A 9: 36,581,363 H82L probably benign Het
Herc4 T A 10: 63,286,143 probably null Het
Hspg2 G A 4: 137,553,817 V3367M probably damaging Het
Htr1f A T 16: 64,926,022 F302L probably damaging Het
Inpp5f T C 7: 128,678,049 C458R probably damaging Het
Klhl18 T C 9: 110,432,443 E411G probably damaging Het
Krt20 A T 11: 99,431,943 F289I probably benign Het
Mical1 T C 10: 41,479,069 probably null Het
Nav1 T C 1: 135,469,635 D932G probably benign Het
Nme4 A T 17: 26,092,062 D176E probably benign Het
Nox4 C T 7: 87,376,216 S517L possibly damaging Het
Olfr341 A T 2: 36,479,356 L258H probably damaging Het
Pip5k1a T C 3: 95,068,160 D333G probably benign Het
Polb T C 8: 22,653,072 Y36C probably damaging Het
Spta1 T C 1: 174,203,311 I953T possibly damaging Het
Sptb A T 12: 76,612,912 D1071E probably damaging Het
Stxbp3-ps T C 19: 9,558,007 noncoding transcript Het
Tmcc3 A T 10: 94,586,755 I356F probably damaging Het
Tmem262 G T 19: 6,080,159 R6L probably damaging Het
Tnks C A 8: 34,940,900 V225L probably damaging Het
Other mutations in Haus8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Haus8 APN 8 71255645 critical splice donor site probably null
IGL01298:Haus8 APN 8 71253113 missense probably damaging 1.00
IGL02034:Haus8 APN 8 71255558 missense probably damaging 1.00
IGL02112:Haus8 APN 8 71255561 missense probably damaging 1.00
IGL02188:Haus8 APN 8 71257415 missense probably damaging 1.00
IGL02871:Haus8 APN 8 71256494 missense probably benign 0.00
IGL02939:Haus8 APN 8 71255717 splice site probably benign
R0486:Haus8 UTSW 8 71256537 missense probably damaging 1.00
R0486:Haus8 UTSW 8 71256538 missense probably benign 0.01
R0648:Haus8 UTSW 8 71256530 missense probably damaging 1.00
R1848:Haus8 UTSW 8 71256123 intron probably benign
R2327:Haus8 UTSW 8 71255645 critical splice donor site probably null
R4575:Haus8 UTSW 8 71263092 missense probably damaging 0.99
R5294:Haus8 UTSW 8 71255710 missense unknown
R6424:Haus8 UTSW 8 71251436 nonsense probably null
Posted On2013-11-11