Genes on human chromosome 17

Keratin, type I cuticular Ha5 is a keratin protein that in humans is encoded by the KRT35 gene. The protein is a type I keratin and a hair keratin.

Envoplakin is a protein that in humans is encoded by the EVPL gene.

Protein SOX-15 is a protein that in humans is encoded by the SOX15 gene.

NF-κB inhibitor interacting Ras-like 2 is a protein that in humans is encoded by the NKIRAS2 gene.

KRT38 is a keratin gene. Its corresponding protein is asymmetrically distributed within human hair follicles. It does not have murine or equine orthologs. The encoded protein is a type I keratin and a hair keratin.

protein-coding gene in the species Homo sapiens

protein-coding gene in the species Homo sapiens

Serine/threonine-protein kinase Nek8, also known as never in mitosis A-related kinase 8, is an enzyme that in humans is encoded by the NEK8 gene.

Cytochrome b561 is a protein that in humans is encoded by the CYB561 gene. ==References==

The CD79 receptor complex, also known as CD79A:CD79B or Igα:Igβ, is a heterodimeric signaling component of the B-cell receptor (BCR) complex. This transmembrane heterodimer consists of the B-cell antigen receptor complex-associated protein alpha chain (CD79A/Igα) and the B-cell antigen receptor complex-associated protein beta chain (CD79B/Igβ). The CD79 complex is expressed almost exclusively on B cells and B-cell neoplasms, making it valuable for differential diagnosis of B-cell malignancies from T-cell or myeloid neoplasms.

Transcription factor MafG is a bZip Maf transcription factor protein that in humans is encoded by the MAFG gene.

KRT24 is a keratin gene that also influences cellular responses to apoptotic signals. It produces a cytokeratin-like protein of 525 amino acids.

HID1 domain containing is a protein that in humans is encoded by the HID1 gene.

Keratin, type I cytoskeletal 27 is a keratin belonging to the Type I family of intermediate filament proteins. In humans, in it encoded by a gene with symbol KRT27.

HNF1 homeobox B (hepatocyte nuclear factor 1 homeobox B), also known as HNF1B or transcription factor 2 (TCF2), is a human gene.

Homeobox protein DLX-3 is a protein that in humans is encoded by the DLX3 gene.

protein-coding gene in the species Homo sapiens

Ubiquitin-conjugating enzyme E2 G1 is a protein that in humans is encoded by the UBE2G1 gene.

KRT25 (full name keratin 25) is a gene encoding for a protein in the type I keratin family. The gene is encoded on a region of chromosome 17q21.2.

Ras-related protein Rab-37 is a protein that in humans is encoded by the RAB37 gene.

U3 small nucleolar RNA-associated protein 6 homolog is a protein that in humans is encoded by the UTP6 gene.

Transmembrane and immunoglobulin domain containing 1 is a protein that in humans is encoded by the TMIGD1 gene. TMIGD1 was discovered by the lab of Giancarlo Marra and later cloned by Nader Rahimi. Recent findings suggest functions in brush border formation (intestinal epithelium) and roles as tumor suppressor (kidney and intestine).

protein-coding gene in the species Homo sapiens

KRAB-A domain containing 2 is a protein that in humans is encoded by the KRBA2 gene.

Basic helix-loop-helix family, member a9 is a protein in humans that is encoded by the BHLHA9 gene.

Keratin, type I cuticular Ha7 is a protein that in humans is encoded by the KRT37 gene. KRT37 is a member of the keratin gene family. The protein is a type I keratin and a hair keratin.

Myosin-13 also known as myosin, heavy chain 13 is a protein which in humans is encoded by the MYH13 gene.

Dynein axonemal intermediate chain 2 also known as axonemal dynein intermediate chain 2, is a protein that in humans is encoded by the DNAI2 gene.

RING finger protein 135 is a protein that in humans is encoded by the RNF135 gene.

WD repeat domain phosphoinositide-interacting protein 3 (WIPI-3), also known as WD repeat-containing protein 45-like is a protein that in humans is encoded by the gene.

CASPR also known as Contactin associated protein 1, Paranodin and CASPR1 is a protein that in humans is encoded by the CNTNAP1 gene. CASPR is a part of the neurexin family of proteins, hence its another name "Neurexin IV". CASPR is a membrane protein found in the neuronal membrane in the paranodal section of the axon[[]] in myelinated neurons, between the Nodes of Ranvier containing Na+ channels, and juxtaparanode, which contains K+ channels. During myelination, caspr associates with contactin in a cis complex, though its precise role in myelination is not yet understood.

Gap junction gamma-1 protein (GJC1), also known as gap junction alpha-7 protein (GJA7) and connexin 45 (Cx45) — is a protein that in humans is encoded by the GJC1 gene.

Myosin-3 is a protein that in humans is encoded by the MYH3 gene.

Neuronal pentraxin-1 (NP1) is a protein that in humans is encoded by the NPTX1 gene.

Homeobox protein Hox-B13 is a protein that in humans is encoded by the HOXB13 gene.

PRR29 (proline-rich protein 29) is a protein encoded by the PRR29 gene located in humans on chromosome 17 at 17q23.

WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2 is a protein that in humans is encoded by the WFIKKN2 gene.

Tachykinin-4 is a protein that in humans is encoded by the TAC4 gene.

Protein HEXIM1 is a protein that in humans is encoded by the HEXIM1 gene.

Formin-like protein 1 is a protein that in humans is encoded by the FMNL1 gene.

ABC-type organic anion transporter ABCA8 is a protein that in humans is encoded by the ABCA8 gene.

Retinoic acid-induced protein 1 is a transcription factor that in humans is encoded by the RAI1 gene. Mutations or copy number alterations affecting this gene are associated with neurodevelopmental disorders. Deletions of RAI1 are a primary cause of Smith–Magenis syndrome, whereas duplications of the gene are associated with Potocki–Lupski syndrome.

protein-coding gene in the species Homo sapiens

KRT39 is a keratin gene. The encoded protein is a type I keratin.

CMRF35-like molecule 1, also known as CD300lf, is a protein that in humans is encoded by the CD300LF gene. CD300lf belongs to the protein family of CD300. CD300lf is a membrane glycoprotein that contains an immunoglobulin domain and is expressed by myeloid and mast cells of humans and other mammals. The protein functions in immunoregulation but might also have a role in norovirus infections.

Transmembrane channel-like protein 6 is a protein that in humans is encoded by the TMC6 gene. In vivo, TMC6 and its homolog TMC8, interact and form a complex with the zinc transporter 1 (SLC30A1) and localize mostly to the endoplasmic reticulum, but also to the nuclear membrane and Golgi apparatus.

Neurogenic differentiation factor 2 is a protein that in humans is encoded by the NEUROD2 gene.

Rab effector Noc2 is a protein that in humans is encoded by the RPH3AL gene.

Olfactory receptor 1A1 is a protein that in humans is encoded by the OR1A1 gene.

Tetratricopeptide repeat protein 25 is a protein that in humans is encoded by the TTC25 gene.

Dynein heavy chain 9, axonemal is a protein that in humans is encoded by the DNAH9 gene.

Testis expressed 19 is a protein that in humans is encoded by the TEX19 gene.

Keratin, type I cuticular Ha2 is a protein that in humans is encoded by the KRT32 gene.

protein-coding gene in the species Homo sapiens

Pyrroline-5-carboxylate reductase 1, mitochondrial is an enzyme that in humans is encoded by the PYCR1 gene.

Small G protein signaling modulator 2 is a protein that in humans is encoded by the SGSM2 gene.

Mannose-P-dolichol utilization defect 1 protein is a protein that in humans is encoded by the MPDU1 gene.

Flotillin-2 is a protein that in humans is encoded by the FLOT2 gene. Flotillin 2 (flot-2) is a highly conserved protein isolated from caveolae/lipid raft domains that tether growth factor receptors linked to signal transduction pathways. Flot-2 binds to PAR-1, a known upstream mediator of major signal transduction pathways implicated in cell growth and metastasis, and may influence tumour progression.

protein-coding gene in the species Homo sapiens

Protein phosphatase 1D is an enzyme that in humans is encoded by the PPM1D gene.