Incidental Mutation 'IGL02696:Htr1d'
ID 303914
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Htr1d
Ensembl Gene ENSMUSG00000070687
Gene Name 5-hydroxytryptamine (serotonin) receptor 1D
Synonyms Htr1db, Gpcr14
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02696
Quality Score
Status
Chromosome 4
Chromosomal Location 136150835-136171709 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 136170722 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 317 (V317A)
Ref Sequence ENSEMBL: ENSMUSP00000112402 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088677] [ENSMUST00000117699] [ENSMUST00000121571]
AlphaFold Q61224
Predicted Effect probably benign
Transcript: ENSMUST00000088677
AA Change: V317A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000086052
Gene: ENSMUSG00000070687
AA Change: V317A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 46 368 1.2e-11 PFAM
Pfam:7tm_1 52 353 1.2e-75 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000117699
AA Change: V317A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000112840
Gene: ENSMUSG00000070687
AA Change: V317A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 46 368 1.2e-11 PFAM
Pfam:7tm_1 52 353 2.7e-86 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000121571
AA Change: V317A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000112402
Gene: ENSMUSG00000070687
AA Change: V317A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 46 368 1.2e-11 PFAM
Pfam:7tm_1 52 353 2.7e-86 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000133818
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for disruptions in this gene display a normal phenotype. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr8 A G 14: 29,704,628 (GRCm39) T43A probably benign Het
Adgrd1 T C 5: 129,217,918 (GRCm39) probably benign Het
Asxl1 T A 2: 153,242,115 (GRCm39) Y888* probably null Het
Atp8b5 T C 4: 43,369,634 (GRCm39) V924A possibly damaging Het
AU040320 T C 4: 126,736,380 (GRCm39) L821P probably damaging Het
Capn11 T C 17: 45,943,635 (GRCm39) N596S probably damaging Het
Cnot1 C A 8: 96,471,645 (GRCm39) V1219F probably benign Het
Cope T C 8: 70,763,143 (GRCm39) probably null Het
Crim1 A G 17: 78,587,402 (GRCm39) E169G probably damaging Het
Csmd3 A T 15: 47,533,065 (GRCm39) F2395I probably benign Het
Ctso A C 3: 81,858,691 (GRCm39) D220A possibly damaging Het
Cttnbp2 G A 6: 18,434,128 (GRCm39) P577S probably benign Het
D930048N14Rik T A 11: 51,544,821 (GRCm39) probably benign Het
Dck T A 5: 88,920,666 (GRCm39) S129T probably damaging Het
Dlc1 A G 8: 37,041,326 (GRCm39) V1301A possibly damaging Het
Dusp16 G A 6: 134,695,398 (GRCm39) R478C probably damaging Het
Ermap C T 4: 119,044,904 (GRCm39) R49K possibly damaging Het
Flnc A G 6: 29,446,697 (GRCm39) K969R probably damaging Het
Gjb2 A T 14: 57,337,769 (GRCm39) F146L probably damaging Het
Hdc A T 2: 126,436,220 (GRCm39) D550E probably damaging Het
Hs6st3 A T 14: 120,106,731 (GRCm39) I380F probably damaging Het
Kalrn A T 16: 34,040,484 (GRCm39) M963K probably damaging Het
Kl T A 5: 150,904,450 (GRCm39) S401T probably benign Het
Lair1 A G 7: 4,013,848 (GRCm39) probably benign Het
Lrp5 C T 19: 3,652,253 (GRCm39) V1206I probably benign Het
Matn4 A G 2: 164,238,758 (GRCm39) F343S probably benign Het
Mrgpra4 G T 7: 47,631,251 (GRCm39) R117S possibly damaging Het
Myh14 T C 7: 44,314,530 (GRCm39) Y131C probably damaging Het
Nap1l4 A T 7: 143,077,898 (GRCm39) N345K possibly damaging Het
Oas1c T C 5: 120,943,528 (GRCm39) R204G probably benign Het
Or52e4 A G 7: 104,705,569 (GRCm39) T39A probably benign Het
Or8k25 T A 2: 86,243,959 (GRCm39) T146S probably benign Het
Pakap T A 4: 57,854,663 (GRCm39) D58E probably damaging Het
Pin1 G A 9: 20,574,531 (GRCm39) G150E probably benign Het
R3hdm2 T C 10: 127,300,888 (GRCm39) probably null Het
Rai1 C A 11: 60,084,782 (GRCm39) H1843Q probably benign Het
Siae G T 9: 37,542,680 (GRCm39) A194S probably damaging Het
Slc6a12 G T 6: 121,340,211 (GRCm39) V485L probably benign Het
Stil T G 4: 114,898,692 (GRCm39) S1107R probably damaging Het
Syt16 T C 12: 74,176,185 (GRCm39) V18A possibly damaging Het
Trpm8 A G 1: 88,275,773 (GRCm39) D457G probably damaging Het
Tshr A T 12: 91,460,103 (GRCm39) T66S possibly damaging Het
Ttn T A 2: 76,537,639 (GRCm39) Q34763L probably benign Het
Ubr2 T A 17: 47,274,691 (GRCm39) M830L probably benign Het
Ulk1 A G 5: 110,940,918 (GRCm39) F337S probably damaging Het
Other mutations in Htr1d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01375:Htr1d APN 4 136,170,484 (GRCm39) missense probably benign 0.03
IGL01818:Htr1d APN 4 136,170,197 (GRCm39) missense probably benign 0.02
IGL01952:Htr1d APN 4 136,170,872 (GRCm39) missense probably benign 0.08
R0112:Htr1d UTSW 4 136,170,311 (GRCm39) missense probably benign 0.05
R0147:Htr1d UTSW 4 136,170,788 (GRCm39) missense probably damaging 1.00
R0148:Htr1d UTSW 4 136,170,788 (GRCm39) missense probably damaging 1.00
R2483:Htr1d UTSW 4 136,170,815 (GRCm39) missense probably damaging 0.97
R2764:Htr1d UTSW 4 136,170,376 (GRCm39) missense possibly damaging 0.89
R3622:Htr1d UTSW 4 136,170,815 (GRCm39) missense probably damaging 0.97
R3623:Htr1d UTSW 4 136,170,815 (GRCm39) missense probably damaging 0.97
R3624:Htr1d UTSW 4 136,170,815 (GRCm39) missense probably damaging 0.97
R3894:Htr1d UTSW 4 136,170,548 (GRCm39) missense probably benign 0.00
R4567:Htr1d UTSW 4 136,170,836 (GRCm39) missense probably benign 0.17
R4735:Htr1d UTSW 4 136,170,197 (GRCm39) missense probably benign 0.02
R6190:Htr1d UTSW 4 136,170,109 (GRCm39) missense probably damaging 1.00
R7011:Htr1d UTSW 4 136,170,317 (GRCm39) missense probably benign 0.10
R7123:Htr1d UTSW 4 136,169,664 (GRCm39) start gained probably benign
R7223:Htr1d UTSW 4 136,170,812 (GRCm39) missense probably damaging 1.00
R7328:Htr1d UTSW 4 136,170,614 (GRCm39) missense probably benign 0.01
R8399:Htr1d UTSW 4 136,170,686 (GRCm39) missense probably damaging 1.00
R8514:Htr1d UTSW 4 136,170,650 (GRCm39) missense probably damaging 1.00
R8829:Htr1d UTSW 4 136,170,554 (GRCm39) missense probably benign
R8982:Htr1d UTSW 4 136,170,866 (GRCm39) missense possibly damaging 0.89
R9497:Htr1d UTSW 4 136,169,663 (GRCm39) start gained probably benign
R9505:Htr1d UTSW 4 136,170,889 (GRCm39) missense probably benign
Posted On 2015-04-16