IFT172 (intraflagellar transport 172) - Rat Genome Database

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Gene: IFT172 (intraflagellar transport 172) Sus scrofa
Analyze
Symbol: IFT172
Name: intraflagellar transport 172
RGD ID: 14212021
Description: ENCODES a protein that exhibits transcription factor binding (ortholog); INVOLVED IN cilium assembly (ortholog); negative regulation of transcription by RNA polymerase II (ortholog); PARTICIPATES IN Hedgehog signaling pathway; ASSOCIATED WITH asphyxiating thoracic dystrophy (ortholog); asphyxiating thoracic dystrophy 1 (ortholog); atrioventricular septal defect (ortholog); FOUND IN cell projection (inferred); cilium (inferred); intraciliary transport particle B (inferred); INTERACTS WITH deoxynivalenol
Type: protein-coding
RefSeq Status: MODEL
Previously known as: intraflagellar transport 172 homolog; intraflagellar transport protein 172 homolog
RGD Orthologs
Human
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: Sscrofa11.1 - Pig Sscrofa11.1 Assembly
Position:
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl3111,683,669 - 111,718,970 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.13111,683,674 - 111,718,504 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.23118,754,392 - 118,789,234 (-)NCBISscrofa10.2Sscrofa10.2susScr3
JBrowse: View Region in Genome Browser (JBrowse)
Model


1 to 17 of 17 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172Pigasphyxiating thoracic dystrophy 1  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Short-rib thoracic dysplasia 1 with or without polydactylyClinVarPMID:25741868 and PMID:28492532
IFT172PigBardet-Biedl syndrome  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Bardet-Biedl syndromeClinVarPMID:24033266 more ...
IFT172PigBardet-Biedl syndrome 1  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Bardet-Biedl syndrome 1ClinVarPMID:25741868 and PMID:28492532
IFT172PigBardet-Biedl syndrome 20  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Bardet-Biedl syndrome 20ClinVarPMID:11030072 more ...
IFT172PigBardet-Biedl syndrome 22  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Bardet-Biedl syndrome 22ClinVarPMID:24290075 more ...
IFT172Pigfundus dystrophy  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Retinal dystrophyClinVarPMID:17576681 more ...
IFT172Piggenetic disease  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:24140113 more ...
IFT172PigJoubert syndrome 1  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Familial aplasia of the vermisClinVarPMID:24140113 more ...
IFT172Pignephronophthisis  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: NephronophthisisClinVarPMID:25741868
IFT172PigNeurodevelopmental Disorders  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Neurodevelopmental disorderClinVarPMID:25741868 and PMID:28492532
IFT172Pigoptic atrophy  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Optic atrophyClinVarPMID:25741868 more ...
IFT172Pigretinitis pigmentosa  ISOIFT172 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:11030072 more ...
IFT172Pigretinitis pigmentosa 71  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Retinitis pigmentosa 71ClinVarPMID:11030072 more ...
IFT172Pigshort-rib thoracic dysplasia 10 with or without polydactyly  ISOIFT172 (Homo sapiens)8554872ClinVar more ...ClinVarPMID:11030072 more ...
IFT172Pigshort-rib thoracic dysplasia 6 with or without polydactyly  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Short-rib thoracic dysplasia 6 with or without polydactylyClinVarPMID:24140113 more ...
IFT172Pigsyndromic microphthalmia 5  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Anophthalmia-microphthalmia syndromeClinVarPMID:26893459 and PMID:28492532
IFT172PigTatton-Brown-Rahman syndrome  ISOIFT172 (Homo sapiens)8554872ClinVar Annotator: match by term: Tatton-Brown-Rahman overgrowth syndromeClinVarPMID:28492532
1 to 17 of 17 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172Pigasphyxiating thoracic dystrophy  ISOIFT172 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTD 
IFT172Piggastrointestinal stromal tumor  ISOIFT172 (Homo sapiens)9068941CTD Direct Evidence: marker/mechanismCTDPMID:27793025
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172Pigatrioventricular septal defect  ISOIft172 (Mus musculus)9068941OMIM:600309 more ...MouseDO 
IFT172Pigretinal degeneration  ISOIft172 (Mus musculus)9068941 MouseDO 
IFT172PigVACTERL association  ISOIft172 (Mus musculus)9068941OMIM:192350 more ...MouseDO 


  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172Pigdeoxynivalenol decreases expressionEXP 6480464deoxynivalenol results in decreased expression of IFT172 mRNACTDPMID:35307453


Biological Process
1 to 20 of 32 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172Pigbone development acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigbrain development acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigcilium assembly acts_upstream_of_or_withinISOMGI:26820669068941 PMID:18488998 more ...MGIPMID:18488998 more ...
IFT172Pigcilium assembly acts_upstream_of_or_withinISOMGI:48218249068941 PMID:21653639MGIPMID:21653639
IFT172Pigcilium assembly involved_inIEAUniProtKB:Q6VH22 more ...150520179 EnsemblGO_REF:0000107
IFT172Pigcytoplasmic microtubule organization acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigdetermination of left/right symmetry acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigdorsal/ventral pattern formation acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigembryonic camera-type eye morphogenesis acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigepidermis development acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigheart development acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigheart looping acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pighindgut development acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigintraciliary transport involved_inIBAFB:FBgn0035317 more ...150520179 GO_CentralGO_REF:0000033
IFT172Pigkeratinocyte proliferation acts_upstream_ofIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigleft/right axis specification acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Piglimb development acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pignegative regulation of epithelial cell proliferation acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pignegative regulation of keratinocyte proliferation acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pignegative regulation of smoothened signaling pathway acts_upstream_of_or_withinIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
1 to 20 of 32 rows

Cellular Component
1 to 11 of 11 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172Pigaxoneme is_active_inIBAMGI:2146906 more ...150520179 GO_CentralGO_REF:0000033
IFT172Pigcell projection located_inIEAUniProtKB-KW:KW-0966150520179 UniProtGO_REF:0000043
IFT172Pigciliary basal body is_active_inIBAMGI:2146906 more ...150520179 GO_CentralGO_REF:0000033
IFT172Pigcilium located_inIEAUniProtKB-SubCell:SL-0066150520179 UniProtGO_REF:0000044
IFT172Pigcilium located_inIEAUniProtKB-KW:KW-0969150520179 UniProtGO_REF:0000043
IFT172Pigcilium located_inIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigintraciliary transport particle B part_ofIBAMGI:2682064 more ...150520179 GO_CentralGO_REF:0000033
IFT172Pigintraciliary transport particle B part_ofIEAUniProtKB:Q6VH22 more ...150520179 EnsemblGO_REF:0000107
IFT172Pigsperm cytoplasmic droplet located_inIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigsperm midpiece located_inIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
IFT172Pigsperm principal piece located_inIEAUniProtKB:Q6VH22 and ensembl:ENSMUSP00000049335150520179 EnsemblGO_REF:0000107
1 to 11 of 11 rows

Molecular Function

  

Imported Annotations - PID (archival)

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
IFT172PigHedgehog signaling pathway   ISOIFT172 (Homo sapiens)9068941 PIDPID:200172
PMID:22301074   PMID:30032202  



IFT172
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl3111,683,669 - 111,718,970 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.13111,683,674 - 111,718,504 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.23118,754,392 - 118,789,234 (-)NCBISscrofa10.2Sscrofa10.2susScr3
IFT172
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38227,444,377 - 27,489,743 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl227,444,377 - 27,489,805 (-)EnsemblGRCh38hg38GRCh38
GRCh37227,667,244 - 27,712,610 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36227,520,744 - 27,566,075 (-)NCBINCBI36Build 36hg18NCBI36
Build 34227,578,891 - 27,624,222NCBI
Celera227,513,414 - 27,558,746 (-)NCBICelera
Cytogenetic Map2p23.3NCBI
HuRef227,409,128 - 27,454,460 (-)NCBIHuRef
CHM1_1227,597,152 - 27,642,482 (-)NCBICHM1_1
T2T-CHM13v2.0227,486,730 - 27,532,099 (-)NCBIT2T-CHM13v2.0
Ift172
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39531,410,623 - 31,448,458 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl531,410,621 - 31,448,460 (-)EnsemblGRCm39 Ensembl
GRCm38531,253,279 - 31,291,391 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl531,253,277 - 31,291,116 (-)EnsemblGRCm38mm10GRCm38
MGSCv37531,555,652 - 31,593,487 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36531,529,860 - 31,567,695 (-)NCBIMGSCv36mm8
Celera528,732,431 - 28,770,403 (-)NCBICelera
Cytogenetic Map5B1NCBI
cM Map517.27NCBI
Ift172
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8630,801,841 - 30,841,239 (+)NCBIGRCr8
mRatBN7.2625,081,933 - 25,121,271 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl625,081,980 - 25,120,860 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx625,382,814 - 25,422,109 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0625,698,704 - 25,738,001 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0625,178,064 - 25,217,359 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0626,390,686 - 26,485,459 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0636,210,777 - 36,304,662 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera624,573,352 - 24,613,367 (+)NCBICelera
Cytogenetic Map6q14NCBI
Ift172
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554699,418,609 - 9,455,026 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554699,418,599 - 9,455,026 (-)NCBIChiLan1.0ChiLan1.0
IFT172
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21299,022,173 - 99,066,368 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A99,026,177 - 99,070,336 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A27,448,139 - 27,492,302 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A27,536,534 - 27,580,406 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A27,536,534 - 27,580,406 (-)Ensemblpanpan1.1panPan2
IFT172
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11721,389,462 - 21,426,970 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1721,389,482 - 21,426,796 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1721,281,228 - 21,318,724 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01721,710,828 - 21,748,327 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1721,710,832 - 21,748,293 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11721,397,430 - 21,434,930 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01721,406,908 - 21,444,410 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01721,455,165 - 21,492,664 (-)NCBIUU_Cfam_GSD_1.0
Ift172
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629265,694,405 - 65,731,092 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364935,108,437 - 5,145,160 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364935,108,437 - 5,145,160 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
IFT172
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11480,130,436 - 80,171,259 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604531,982,836 - 32,026,287 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ift172
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247389,510,512 - 9,545,933 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247389,510,452 - 9,546,985 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in IFT172
1237 total Variants



alimentary part of gastrointestinal system
circulatory system
ectoderm
endocrine system
endoderm
hemolymphoid system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
10 4 23 3 2 5 14 12 23 3 6 3



Ensembl Acc Id: ENSSSCT00000028161   ⟹   ENSSSCP00000025952
Type: CODING
Position:
Pig AssemblyChrPosition (strand)Source
Sscrofa11.1 Ensembl3111,683,710 - 111,718,970 (+)Ensembl
Ensembl Acc Id: ENSSSCT00000086891   ⟹   ENSSSCP00000072571
Type: CODING
Position:
Pig AssemblyChrPosition (strand)Source
Sscrofa11.1 Ensembl3111,683,669 - 111,697,838 (+)Ensembl
RefSeq Acc Id: XM_003354889   ⟹   XP_003354937
Type: CODING
Position:
Pig AssemblyChrPosition (strand)Source
Sscrofa11.13111,683,674 - 111,718,504 (+)NCBI
Sequence:
RefSeq Acc Id: XP_003354937   ⟸   XM_003354889
- UniProtKB: A0A8D0WSZ9 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSSSCP00000025952   ⟸   ENSSSCT00000028161
Ensembl Acc Id: ENSSSCP00000072571   ⟸   ENSSSCT00000086891



1 to 40 of 58 rows
Database
Acc Id
Source(s)
Ensembl Genes ENSSSCG00000026367 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
  ENSSSCG00015067999 UniProtKB/TrEMBL
  ENSSSCG00025074182 UniProtKB/TrEMBL
  ENSSSCG00030040587 UniProtKB/TrEMBL
  ENSSSCG00035077552 UniProtKB/TrEMBL
  ENSSSCG00040067993 UniProtKB/TrEMBL
  ENSSSCG00050052293 UniProtKB/TrEMBL
  ENSSSCG00055004510 UniProtKB/TrEMBL
  ENSSSCG00060068983 UniProtKB/TrEMBL
  ENSSSCG00065007156 UniProtKB/TrEMBL
  ENSSSCG00070010371 UniProtKB/TrEMBL
Ensembl Transcript ENSSSCT00000028161 ENTREZGENE
  ENSSSCT00000028161.4 UniProtKB/TrEMBL
  ENSSSCT00000086891.1 UniProtKB/TrEMBL
  ENSSSCT00015091202.1 UniProtKB/TrEMBL
  ENSSSCT00015091953.1 UniProtKB/TrEMBL
  ENSSSCT00025102198.1 UniProtKB/TrEMBL
  ENSSSCT00025102658.1 UniProtKB/TrEMBL
  ENSSSCT00030056461.1 UniProtKB/TrEMBL
  ENSSSCT00030056596.1 UniProtKB/TrEMBL
  ENSSSCT00035105711.1 UniProtKB/TrEMBL
  ENSSSCT00035105969.1 UniProtKB/TrEMBL
  ENSSSCT00040093065.1 UniProtKB/TrEMBL
  ENSSSCT00040093323.1 UniProtKB/TrEMBL
  ENSSSCT00050071227.1 UniProtKB/TrEMBL
  ENSSSCT00050071240.1 UniProtKB/TrEMBL
  ENSSSCT00055008941.1 UniProtKB/TrEMBL
  ENSSSCT00060094496.1 UniProtKB/TrEMBL
  ENSSSCT00065009601.1 UniProtKB/TrEMBL
  ENSSSCT00070020256.1 UniProtKB/TrEMBL
  ENSSSCT00070020269.1 UniProtKB/TrEMBL
Gene3D-CATH 1.25.40.470 UniProtKB/TrEMBL
  2.130.10.10 UniProtKB/TrEMBL
InterPro ARM-type_fold UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom_sf UniProtKB/TrEMBL
  WD40_repeat UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/TrEMBL
KEGG Report ssc:100625100 UniProtKB/TrEMBL
NCBI Gene IFT172 ENTREZGENE
PANTHER IFT140/172-RELATED UniProtKB/TrEMBL
1 to 40 of 58 rows