IFT122 intraflagellar transport 122 [Homo sapiens (human)] - Gene

Summary

Official Symbol: IFT122provided by HGNC
Official Full Name: intraflagellar transport 122provided by HGNC
Primary source: HGNC:HGNC:13556
See related: Ensembl:ENSG00000163913 MIM:606045; AllianceGenome:HGNC:13556
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: CED; SPG; CED1; FAP80; WDR10; CFAP80; WDR10p; WDR140
Summary: This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Expression: Broad expression in testis (RPKM 41.7), ovary (RPKM 7.5) and 15 other tissues See more
Orthologs: mouse all
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Genomic context

Location:: 3q21.3-q22.1

Exon count:: 34

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	3	NC_000003.12 (129440224..129520507)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	3	NC_060927.1 (132185050..132264949)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	3	NC_000003.11 (129159067..129239350)

Chromosome 3 - NC_000003.12 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Expression

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See details

Project title: HPA RNA-seq normal tissues
Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
BioProject: PRJEB4337
Publication: PMID 24309898
Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

This study demonstrated that the mutation in SPG 7 gene caused autosomal recessive hereditary spastic paraparesis.
Title: Case series of autosomal recessive hereditary spastic paraparesis with novel mutation in SPG 7 gene.
The C11ORF74, interacts with the IFT-A complex via the IFT122 subunit and is accumulated at the distal tip in the absence of an IFT-A subunit IFT139, suggesting that at least a fraction of C11ORF74 molecules can be transported towards the ciliary tip by associating with the IFT-A complex, although its majority might be out of cilia at steady state.
Title: C11ORF74 interacts with the IFT-A complex and participates in ciliary BBSome localization.
IFT122 mutations associated with cranioectodermal dysplasia 1 cause defects in ciliary protein trafficking, but not ciliogenesis when expressed in cells lacking endogenous IFT122 (IFT122 KO).
Title: Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis.
All the nine probands with syndromic craniosynostosis were found to carry the possibly causative variants, among which three variants including two missense mutations in IFT122 gene, in SMC1A gene and a frameshift mutation in TWIST1 gene have never been reported in patients before.
Title: Identification and analysis of the genetic causes in nine unrelated probands with syndromic craniosynostosis.
Using a panel of skeletal dysplasias genes, including 11 related to SRP, we identified biallelic mutations in IFT122 in a fetus with a typical phenotype of SRP-IV, finally confirmed that this phenotype is a ciliopathy and adding to the list of ciliopathies with major skeletal involvement.
Title: Beemer-Langer syndrome is a ciliopathy due to biallelic mutations in IFT122.
The three patients had different, novel, compound heterozygous mutations in IFT122. Consequently, we compared these three patients to those previously described with IFT122 mutations. Thus, our report serves to add 6 novel mutations to the IFT122 mutation spectrum and to contribute to the IFT122-related clinical characterization.
Title: Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum.
this study was able to find causative IFT122 mutations in a non-consanguineous family with recurrent abortions.
Title: Whole exome sequencing revealed biallelic IFT122 mutations in a family with CED1 and recurrent pregnancy loss.
we found a homozygous missense mutation in the IFT122 (WDR10) gene that cosegregated with Sensenbrenner syndrome
Title: Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene.

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Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description	Tests
Cranioectodermal dysplasia 1 MedGen: C0432235 OMIM: 218330 GeneReviews: Cranioectodermal Dysplasia	Compare labs

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

HIV-1 interactions

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Protein interactions

Protein	Gene	Interaction	Pubs
retropepsin	gag-pol	HIV-1 PR is identified to have a physical interaction with intraflagellar transport 122 homolog (IFT122) in human HEK293 and/or Jurkat cell lines by using affinity tagging and purification mass spectrometry analyses	PubMed

Go to the HIV-1, Human Interaction Database

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

D11S2921 (e-PCR)
- UniSTS:152074

D8S2278 (e-PCR)
- UniSTS:473906

D8S2279 (e-PCR)
- UniSTS:473907

D3S2907E (e-PCR)
- UniSTS:150892

RH45232 (e-PCR)
- UniSTS:47517

RH16296 (e-PCR)
- UniSTS:30156

SHGC-34629 (e-PCR)
- UniSTS:7406

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
enables protein binding	IPI Inferred from Physical Interaction more info	PubMed

Process	Evidence Code	Pubs
involved_in camera-type eye morphogenesis	ISS Inferred from Sequence or Structural Similarity more info
involved_in cilium assembly	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in cilium assembly	ISS Inferred from Sequence or Structural Similarity more info
involved_in cilium assembly	NAS Non-traceable Author Statement more info	PubMed
involved_in embryonic body morphogenesis	ISS Inferred from Sequence or Structural Similarity more info
involved_in embryonic forelimb morphogenesis	ISS Inferred from Sequence or Structural Similarity more info
involved_in embryonic heart tube development	ISS Inferred from Sequence or Structural Similarity more info
involved_in embryonic heart tube left/right pattern formation	ISS Inferred from Sequence or Structural Similarity more info
involved_in establishment of protein localization to organelle	ISS Inferred from Sequence or Structural Similarity more info
involved_in intracellular signal transduction	ISS Inferred from Sequence or Structural Similarity more info
involved_in intraciliary anterograde transport	ISS Inferred from Sequence or Structural Similarity more info
involved_in intraciliary retrograde transport	IBA Inferred from Biological aspect of Ancestor more info
involved_in intraciliary retrograde transport	ISS Inferred from Sequence or Structural Similarity more info
involved_in intraciliary retrograde transport	NAS Non-traceable Author Statement more info	PubMed
involved_in intraciliary transport	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in limb development	ISS Inferred from Sequence or Structural Similarity more info
involved_in negative regulation of smoothened signaling pathway	ISS Inferred from Sequence or Structural Similarity more info
involved_in neural tube closure	ISS Inferred from Sequence or Structural Similarity more info
involved_in non-motile cilium assembly	IBA Inferred from Biological aspect of Ancestor more info
involved_in protein localization to cilium	IBA Inferred from Biological aspect of Ancestor more info
acts_upstream_of_or_within protein localization to cilium	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in protein localization to cilium	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in spinal cord dorsal/ventral patterning	ISS Inferred from Sequence or Structural Similarity more info

Component	Evidence Code	Pubs
located_in ciliary basal body	IDA Inferred from Direct Assay more info	PubMed
located_in ciliary tip	TAS Traceable Author Statement more info
located_in cilium	IDA Inferred from Direct Assay more info	PubMed
located_in cilium	ISS Inferred from Sequence or Structural Similarity more info
located_in cilium	NAS Non-traceable Author Statement more info	PubMed
located_in cilium	TAS Traceable Author Statement more info
located_in cytoplasm	IEA Inferred from Electronic Annotation more info
part_of intraciliary transport particle A	IBA Inferred from Biological aspect of Ancestor more info
part_of intraciliary transport particle A	IDA Inferred from Direct Assay more info	PubMed
part_of intraciliary transport particle A	IPI Inferred from Physical Interaction more info	PubMed
located_in membrane	HDA more info	PubMed
is_active_in non-motile cilium	IBA Inferred from Biological aspect of Ancestor more info
located_in photoreceptor connecting cilium	ISS Inferred from Sequence or Structural Similarity more info

General protein information

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Preferred Names: intraflagellar transport protein 122 homolog

Names: WD repeat domain 10; WD repeat-containing protein 10; WD repeat-containing protein 140; intraflagellar transport 122 homolog

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

NG_023392.1 RefSeqGene

Range

5100..85383

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GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

NM_001280541.2 → NP_001267470.1 intraflagellar transport protein 122 homolog isoform 5

Status: REVIEWED

Description

Transcript Variant: This variant (5) lacks an alternate in-frame exon in the 5' coding region and uses an alternate in-frame splice site in the 3' coding region, compared to variant 1. It encodes isoform 5, which is shorter than isoform 1.

Source sequence(s)

AF244931, AK315103, BC028353, BF941125, DB516647

Consensus CDS

CCDS63770.1

UniProtKB/TrEMBL

A0A8I5KP73

Related

ENSP00000425536.1, ENST00000507564.5

Conserved Domains (3) summary

COG2319
Location:4 → 340

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:49 → 341

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
NM_001280545.2 → NP_001267474.1 intraflagellar transport protein 122 homolog isoform 6

See identical proteins and their annotated locations for NP_001267474.1

Status: REVIEWED

Description

Transcript Variant: This variant (6) lacks an alternate exon and contains an alternate exon in the 5' coding region, and initiates translation at a downstream start codon, compared to variant 1. It encodes isoform 6, which is shorter than isoform 1.

Source sequence(s)

AF244930, AK096891, AK124140, BF941125, DB099554, DB516647

UniProtKB/TrEMBL

B4DST2

Conserved Domains (3) summary

COG2319
Location:2 → 200

WD40; WD40 repeat [General function prediction only]

sd00039
Location:133 → 167

7WD40; WD40 repeat [structural motif]

cl02567
Location:134 → 200

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
NM_001280546.2 → NP_001267475.1 intraflagellar transport protein 122 homolog isoform 7

Status: REVIEWED

Description

Transcript Variant: This variant (7) lacks three alternate exons in the 5' coding region and initiates translation at a downstream start codon, compared to variant 1. It encodes isoform 7, which is shorter than isoform 1.

Source sequence(s)

AK096891, AK124140, AK298526, AK299903, BF941125, DB099554, DB516647

UniProtKB/TrEMBL

B4DST2

Related

ENSP00000509186.1, ENST00000693233.1

Conserved Domains (3) summary

COG2319
Location:24 → 141

WD40; WD40 repeat [General function prediction only]

sd00039
Location:30 → 64

7WD40; WD40 repeat [structural motif]

cl02567
Location:24 → 142

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
NM_001410808.1 → NP_001397737.1 intraflagellar transport protein 122 homolog isoform 8

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93372.1

UniProtKB/TrEMBL

A0A8I5KSG5

Related

ENSP00000509878.1, ENST00000692242.1
NM_001410809.1 → NP_001397738.1 intraflagellar transport protein 122 homolog isoform 9

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93374.1

UniProtKB/TrEMBL

A0A8I5KVC7

Related

ENSP00000509806.1, ENST00000693129.1
NM_001410810.1 → NP_001397739.1 intraflagellar transport protein 122 homolog isoform 10

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93375.1

UniProtKB/TrEMBL

A0A8I5KWK4

Related

ENSP00000510425.1, ENST00000689332.1
NM_001410811.1 → NP_001397740.1 intraflagellar transport protein 122 homolog isoform 11

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93376.1

UniProtKB/TrEMBL

A0A8I5QKX8

Related

ENSP00000509982.1, ENST00000689801.1
NM_001410813.1 → NP_001397742.1 intraflagellar transport protein 122 homolog isoform 12

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93377.1

UniProtKB/TrEMBL

A0A8I5KTL4

Related

ENSP00000510741.1, ENST00000691583.1
NM_001410815.1 → NP_001397744.1 intraflagellar transport protein 122 homolog isoform 13

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93379.1

UniProtKB/TrEMBL

A0A8I5KT04

Related

ENSP00000509216.1, ENST00000693588.1
NM_001410817.1 → NP_001397746.1 intraflagellar transport protein 122 homolog isoform 14

Status: REVIEWED

Source sequence(s)

AC080007, AL449212

Consensus CDS

CCDS93380.1

UniProtKB/TrEMBL

A0A8J9A3C6

Related

ENSP00000422179.2, ENST00000504021.6
NM_018262.4 → NP_060732.2 intraflagellar transport protein 122 homolog isoform 3

See identical proteins and their annotated locations for NP_060732.2

Status: REVIEWED

Description

Transcript Variant: This variant (3) lacks two alternate in-frame exons in the 5' coding region, compared to variant 1. It encodes isoform 3, which lacks two internal segments and is shorter than isoform 1.

Source sequence(s)

AK001759, BC028353, BF941125, DB516647

Consensus CDS

CCDS3059.1

UniProtKB/TrEMBL

A0A8I5KSV0

Related

ENSP00000323973.3, ENST00000347300.6

Conserved Domains (3) summary

COG2319
Location:15 → 289

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:49 → 291

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
NM_052985.4 → NP_443711.2 intraflagellar transport protein 122 homolog isoform 1

See identical proteins and their annotated locations for NP_443711.2

Status: REVIEWED

Description

Transcript Variant: This variant (1) is the longest transcript and encodes the longest isoform (1).

Source sequence(s)

AF244931, AK298526, BF941125, DB516647

Consensus CDS

CCDS3060.1

UniProtKB/TrEMBL

A0A8I5KP73

Related

ENSP00000296266.3, ENST00000296266.7

Conserved Domains (3) summary

COG2319
Location:15 → 240

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:12 → 241

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
NM_052989.3 → NP_443715.1 intraflagellar transport protein 122 homolog isoform 2

See identical proteins and their annotated locations for NP_443715.1

Status: REVIEWED

Description

Transcript Variant: This variant (2) lacks an alternate in-frame exon in the 5' coding region, compared to variant 1. It encodes isoform 2, which lacks an internal segment and is shorter that isoform 1.

Source sequence(s)

AF244931, AF302154, BF941125, DB099554, DB516647

Consensus CDS

CCDS3061.1

UniProtKB/Swiss-Prot

B3KW53, B4DEY9, B4DPW7, E7EQF4, E9PDG2, E9PDX2, G3XAB1, H7C3C0, Q53G36, Q8TC06, Q9BTB9, Q9BTY4, Q9HAT9, Q9HBG5, Q9HBG6, Q9NV68, Q9UF80

UniProtKB/TrEMBL

A0A8I5QKV2

Related

ENSP00000324005.4, ENST00000348417.7

Conserved Domains (3) summary

COG2319
Location:4 → 348

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:15 → 190

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
NM_052990.3 → NP_443716.1 intraflagellar transport protein 122 homolog isoform 4

See identical proteins and their annotated locations for NP_443716.1

Status: REVIEWED

Description

Transcript Variant: This variant (4) lacks four alternate exons in the 5' coding region and uses an alternate in-frame splice site in the 3' coding region, compared to variant 1. It encodes isoform 4, which lacks two in-frame segments and is shorter, compared to isoform 1.

Source sequence(s)

AK298526, BC003045, BF941125, DB099554, DB516647

Consensus CDS

CCDS3062.1

UniProtKB/TrEMBL

A0A8I5QL25

Related

ENSP00000324165.3, ENST00000349441.6

Conserved Domains (3) summary

COG2319
Location:15 → 237

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl26002
Location:599 → 807

TPR_11; TPR repeat

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

NC_000003.12 Reference GRCh38.p14 Primary Assembly

Range

129440224..129520507

Download

GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

XM_006713691.4 → XP_006713754.1 intraflagellar transport protein 122 homolog isoform X1

UniProtKB/TrEMBL

A0A8I5KXT5, A0A8I5QKV2

Related

ENSP00000509225.1, ENST00000687377.1

Conserved Domains (3) summary

COG2319
Location:4 → 348

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:15 → 190

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
XM_047448546.1 → XP_047304502.1 intraflagellar transport protein 122 homolog isoform X2
XM_047448547.1 → XP_047304503.1 intraflagellar transport protein 122 homolog isoform X3

UniProtKB/TrEMBL

A0A8I5KUU2

Related

ENSP00000508904.1, ENST00000688020.1
XM_047448548.1 → XP_047304504.1 intraflagellar transport protein 122 homolog isoform X4
XM_047448549.1 → XP_047304505.1 intraflagellar transport protein 122 homolog isoform X5
XM_017006834.3 → XP_016862323.1 intraflagellar transport protein 122 homolog isoform X6

UniProtKB/TrEMBL

A0A8I5QKR8, A0A8I5QL25

Related

ENSP00000509297.1, ENST00000690663.1
XM_047448552.1 → XP_047304508.1 intraflagellar transport protein 122 homolog isoform X7
XM_011512972.4 → XP_011511274.1 intraflagellar transport protein 122 homolog isoform X8

UniProtKB/TrEMBL

A0A8I5KNX7

Related

ENSP00000508811.1, ENST00000690723.1

Conserved Domains (3) summary

COG2319
Location:4 → 348

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:15 → 190

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
XM_006713695.4 → XP_006713758.1 intraflagellar transport protein 122 homolog isoform X9

UniProtKB/TrEMBL

A0A8I5KS91

Related

ENSP00000508642.1, ENST00000685282.1

Conserved Domains (3) summary

COG2319
Location:4 → 348

WD40; WD40 repeat [General function prediction only]

sd00039
Location:15 → 51

7WD40; WD40 repeat [structural motif]

cl02567
Location:15 → 190

WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
XM_047448553.1 → XP_047304509.1 intraflagellar transport protein 122 homolog isoform X10

Related

ENSP00000509155.1, ENST00000685447.1
XM_047448551.1 → XP_047304507.1 intraflagellar transport protein 122 homolog isoform X7
XM_047448554.1 → XP_047304510.1 intraflagellar transport protein 122 homolog isoform X11

Related

ENSP00000508740.1, ENST00000688527.1

Alternate T2T-CHM13v2.0

Genomic

NC_060927.1 Alternate T2T-CHM13v2.0

Range

132185050..132264949

Download

GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

XM_054347220.1 → XP_054203195.1 intraflagellar transport protein 122 homolog isoform X1
XM_054347221.1 → XP_054203196.1 intraflagellar transport protein 122 homolog isoform X2
XM_054347222.1 → XP_054203197.1 intraflagellar transport protein 122 homolog isoform X3
XM_054347223.1 → XP_054203198.1 intraflagellar transport protein 122 homolog isoform X4
XM_054347224.1 → XP_054203199.1 intraflagellar transport protein 122 homolog isoform X5
XM_054347225.1 → XP_054203200.1 intraflagellar transport protein 122 homolog isoform X6
XM_054347227.1 → XP_054203202.1 intraflagellar transport protein 122 homolog isoform X7
XM_054347228.1 → XP_054203203.1 intraflagellar transport protein 122 homolog isoform X8
XM_054347229.1 → XP_054203204.1 intraflagellar transport protein 122 homolog isoform X9
XM_054347230.1 → XP_054203205.1 intraflagellar transport protein 122 homolog isoform X10
XM_054347226.1 → XP_054203201.1 intraflagellar transport protein 122 homolog isoform X7
XM_054347231.1 → XP_054203206.1 intraflagellar transport protein 122 homolog isoform X11