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2.A.7.24.9 SLC family 35 member F1 (SLC35F1; also called DUF914) of 412 aas and 10 TMSs. Expression in the mouse brain has been reported (Farenholtz et al. 2019). It is a candidate gene for neurodevelopmental disorders resembling Rett syndrome (Di Fede et al. 2021).
Accession Number:	Q5T1Q4
Protein Name:	Solute carrier family 35 member F1
Length:	408
Molecular Weight:	45346.00
Species:	Homo sapiens (Human) [9606]
Number of TMSs:	10
Location¹ / Topology² / Orientation³:	Membrane¹ / Multi-pass membrane protein²
Substrate

Entrez Gene ID:	222553
Pfam:	PF06027
KEGG:	hsa:222553 hsa:222553
Gene Ontology GO:0016021 C:integral to membrane GO:0006810 P:transport
References (6) [1] “The DNA sequence and analysis of human chromosome 6.” Mungall A.J.et.al. 14574404 [2] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” The MGC Project Teamet.al. 15489334 [3] “The full-ORF clone resource of the German cDNA consortium.” Bechtel S.et.al. 17974005 [4] “The DNA sequence and analysis of human chromosome 6.” Mungall A.J.et.al. 14574404 [5] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” The MGC Project Teamet.al. 15489334 [6] “The full-ORF clone resource of the German cDNA consortium.” Bechtel S.et.al. 17974005

UniProt (Universal Protein Resource)
CDD Search (Conserved Domain Database)

Predict TMSs (Predict number of transmembrane segments)

FASTA formatted sequence

1:	MIPPEQPQQQ LQPPSPAPPN HVVTTIENLP AEGSGGGGSL SASSRAGVRQ RIRKVLNREM 
61:	LISVALGQVL SLLICGIGLT SKYLSEDFHA NTPVFQSFLN YILLFLVYTT TLAVRQGEEN 
121:	LLAILRRRWW KYMILGLIDL EANYLVVKAY QYTTLTSIQL LDCFVIPVVI LLSWFFLLIR 
181:	YKAVHFIGIV VCILGMGCMV GADVLVGRHQ GAGENKLVGD LLVLGGATLY GISNVWEEYI 
241:	IRTLSRVEFL GMIGLFGAFF SGIQLAIMEH KELLKVPWDW QIGLLYVGFS ACMFGLYSFM 
301:	PVVIKKTSAT SVNLSLLTAD LYSLFCGLFL FHYKFSGLYL LSFFTILIGL VLYSSTSTYI 
361:	AQDPRVYKQF RNPSGPVVDL PTTAQVEPSV TYTSLGQETE EEPHVRVA

2.A.7.24.9
SLC family 35 member F1 (SLC35F1; also called DUF914) of 412 aas and 10 TMSs. Expression in the mouse brain has been reported (Farenholtz et al. 2019). It is a candidate gene for neurodevelopmental disorders resembling Rett syndrome (Di Fede et al. 2021).

Cross database links:

Gene Ontology

References (6)

External Searches:

Analyze:

2.A.7.24.9SLC family 35 member F1 (SLC35F1; also called DUF914) of 412 aas and 10 TMSs. Expression in the mouse brain has been reported (Farenholtz et al. 2019). It is a candidate gene for neurodevelopmental disorders resembling Rett syndrome (Di Fede et al. 2021).

Cross database links:

Gene Ontology

References (6)

External Searches:

Analyze:

2.A.7.24.9
SLC family 35 member F1 (SLC35F1; also called DUF914) of 412 aas and 10 TMSs. Expression in the mouse brain has been reported (Farenholtz et al. 2019). It is a candidate gene for neurodevelopmental disorders resembling Rett syndrome (Di Fede et al. 2021).