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Protein

Protein FAM135A

Gene

FAM135A

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score: Annotation score: 3 out of 5-Experimental evidence at protein leveli

Functioni

GO - Molecular functioni

GO - Biological processi

Complete GO annotation...

Protein family/group databases

ESTHERihuman-FAM135A. Duf_676.

Names & Taxonomyi

Protein namesi
Recommended name:
Protein FAM135A
Gene namesi
Name:FAM135A
Synonyms:KIAA1411
OrganismiHomo sapiens (Human)
Taxonomic identifieri9606 [NCBI]
Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
Proteomesi
  • UP000005640 Componenti: Chromosome 6

Organism-specific databases

HGNCiHGNC:21084. FAM135A.

Pathology & Biotechi

Organism-specific databases

PharmGKBiPA162386230.

Polymorphism and mutation databases

BioMutaiFAM135A.
DMDMi166233529.

PTM / Processingi

Molecule processing

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Chaini1 – 15151515Protein FAM135APRO_0000314168Add
BLAST

Proteomic databases

EPDiQ9P2D6.
MaxQBiQ9P2D6.
PaxDbiQ9P2D6.
PRIDEiQ9P2D6.

PTM databases

iPTMnetiQ9P2D6.
PhosphoSiteiQ9P2D6.

Expressioni

Tissue specificityi

Ubiquitous.1 Publication

Gene expression databases

BgeeiQ9P2D6.
CleanExiHS_FAM135A.
ExpressionAtlasiQ9P2D6. baseline and differential.
GenevisibleiQ9P2D6. HS.

Organism-specific databases

HPAiHPA031743.
HPA031744.

Interactioni

Protein-protein interaction databases

IntActiQ9P2D6. 2 interactions.
MINTiMINT-4717076.
STRINGi9606.ENSP00000410768.

Structurei

3D structure databases

ProteinModelPortaliQ9P2D6.
SMRiQ9P2D6. Positions 1243-1341.
ModBaseiSearch...
MobiDBiSearch...

Family & Domainsi

Sequence similaritiesi

Belongs to the FAM135 family.Curated

Phylogenomic databases

eggNOGiKOG2205. Eukaryota.
ENOG410XQFK. LUCA.
GeneTreeiENSGT00390000007885.
HOVERGENiHBG106788.
InParanoidiQ9P2D6.
OMAiEIIQYIQ.
OrthoDBiEOG7C8GGG.
PhylomeDBiQ9P2D6.
TreeFamiTF314837.

Family and domain databases

Gene3Di3.40.50.1820. 1 hit.
InterProiIPR029058. AB_hydrolase.
IPR022122. DUF3657.
IPR007751. DUF676_lipase-like.
[Graphical view]
PfamiPF12394. DUF3657. 1 hit.
PF05057. DUF676. 1 hit.
[Graphical view]
SUPFAMiSSF53474. SSF53474. 1 hit.

Sequences (4)i

Sequence statusi: Complete.

This entry describes 4 isoformsi produced by alternative splicing. AlignAdd to basket

Isoform 1 (identifier: Q9P2D6-1) [UniParc]FASTAAdd to basket

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.

« Hide

        10         20         30         40         50
MTEVQAMVEF SVELNKFYNV DLFQRGFYQI RASMKIPSRI PHRVEASLLH
60 70 80 90 100
ATGMTLAFPA SVHDSLICSK TFQILYKNEE VVLNDVMIFK VKMLLDERKI
110 120 130 140 150
EETLEEMNFL LSLDLHFTDG DYSADDLNAL QLISSRTLKL HFSPHRGLHH
160 170 180 190 200
HVNVMFDYFH LSVVSVTVHA SLVALHQPLI SFPRPVKTTW LNRNAPAQNK
210 220 230 240 250
DSVIPTLESV VFGINYTKQL SPDGCSFIIA DSFLHHAYRF HYTLCATLLL
260 270 280 290 300
AFKGLHSYFI TVTEEIPSCQ KLELEEMDVE ARLTELCEEV KKIENPDELA
310 320 330 340 350
ELINMNLAQL CSLLMALWGQ FLEVITLHEE LRILLAQEHH TLRVRRFSEA
360 370 380 390 400
FFCFEHPREA AIAYQELHAQ SHLQMCTAIK NTSFCSSLPP LPIECSELDG
410 420 430 440 450
DLNSLPIIFE DRYLDSVTED LDAPWMGIQN LQRSESSKMD KYETEESSVA
460 470 480 490 500
GLSSPELKVR PAGASSIWYT EGEKQLTKSL KGKNEESNKS KVKVTKLMKT
510 520 530 540 550
MKSENTKKLI KQNSKDSVVL VGYKCLKSTA SNDLIKCFEG NPSHSQKEGL
560 570 580 590 600
DPTICGYNFD PKTYMRQTSQ KEASCLPTNT ERTEQKSPDI ENVQPDQFDP
610 620 630 640 650
LNSGNLNLCA NLSISGKLDI SQDDSEITQM EHNLASRRSS DDCHDHQTTP
660 670 680 690 700
SLGVRTIEIK PSNKDPFSGE NITVKLGPWT ELRQEEILVD NLLPNFESLE
710 720 730 740 750
SNGKSKSIEI TFEKEALQEA KCLSIGESLT KLRSNLPAPS TKEYHVVVSG
760 770 780 790 800
DTIKLPDISA TYASSRFSDS GVESEPSSFA THPNTDLVFE TVQGQGPCNS
810 820 830 840 850
ERLFPQLLMK PDYNVKFSLG NHCTESTSAI SEIQSSLTSI NSLPSDDELS
860 870 880 890 900
PDENSKKSVV PECHLNDSKT VLNLGTTDLP KCDDTKKSSI TLQQQSVVFS
910 920 930 940 950
GNLDNETVAI HSLNSSIKDP LQFVFSDEET SSDVKSSCSS KPNLDTMCKG
960 970 980 990 1000
FQSPDKSNNS TGTAITLNSK LICLGTPCVI SGSISSNTDV SEDRTMKKNS
1010 1020 1030 1040 1050
DVLNLTQMYS EIPTVESETH LGTSDPFSAS TDIVKQGLVE NYFGSQSSTD
1060 1070 1080 1090 1100
ISDTCAVSYS NALSPQKETS EKEISNLQQE QDKEDEEEEQ DQQMVQNGYY
1110 1120 1130 1140 1150
EETDYSALDG TINAHYTSRD ELMEERLTKS EKINSDYLRD GINMPTVCTS
1160 1170 1180 1190 1200
GCLSFPSAPR ESPCNVKYSS KSKFDAITKQ PSSTSYNFTS SISWYESSPK
1210 1220 1230 1240 1250
PQIQAFLQAK EELKLLKLPG FMYSEVPLLA SSVPYFSVEE EDGSEDGVHL
1260 1270 1280 1290 1300
IVCVHGLDGN SADLRLVKTY IELGLPGGRI DFLMSERNQN DTFADFDSMT
1310 1320 1330 1340 1350
DRLLDEIIQY IQIYSLTVSK ISFIGHSLGN LIIRSVLTRP RFKYYLNKLH
1360 1370 1380 1390 1400
TFLSLSGPHL GTLYNSSALV NTGLWFMQKW KKSGSLLQLT CRDHSDPRQT
1410 1420 1430 1440 1450
FLYKLSNKAG LHYFKNVVLV GSLQDRYVPY HSARIEMCKT ALKDKQSGQI
1460 1470 1480 1490 1500
YSEMIHNLLR PVLQSKDCNL VRYNVINALP NTADSLIGRA AHIAVLDSEI
1510
FLEKFFLVAA LKYFQ
Length:1,515
Mass (Da):169,840
Last modified:January 15, 2008 - v2
Checksum:i43DB6301DE0F907F
GO
Isoform 2 (identifier: Q9P2D6-2) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     420-615: Missing.

Show »
Length:1,319
Mass (Da):148,065
Checksum:iDEA7ED3DC0993467
GO
Isoform 3 (identifier: Q9P2D6-3) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     27-69: Missing.
     273-273: E → ELAKANMQLLYERLLRRKQLRTQKDNH
     420-615: Missing.

Show »
Length:1,302
Mass (Da):146,549
Checksum:iEAD715D6E55E0B48
GO
Isoform 4 (identifier: Q9P2D6-4) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     1449-1515: QIYSEMIHNL...FLVAALKYFQ → NGIKLFQRVIGINELFPKFFL

Note: No experimental confirmation available.
Show »
Length:1,469
Mass (Da):164,684
Checksum:i43057A50D33D6B94
GO

Sequence cautioni

The sequence AAH65767.1 differs from that shown.Intron retention.Curated
The sequence BAA90995.1 differs from that shown.Intron retention.Curated
The sequence BAA92649.1 differs from that shown. Reason: Erroneous initiation. Curated
The sequence CAB66754.1 differs from that shown. Reason: Erroneous initiation. Curated
The sequence CAI42417.1 differs from that shown. Reason: Erroneous gene model prediction. Curated

Experimental Info

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Sequence conflicti738 – 7381A → T in CAH18110 (PubMed:17974005).Curated
Sequence conflicti1330 – 13301N → D in CAH18110 (PubMed:17974005).Curated

Natural variant

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Natural varianti725 – 7251I → V.
Corresponds to variant rs9455142 [ dbSNP | Ensembl ].
VAR_037854
Natural varianti954 – 9541P → S.
Corresponds to variant rs16869301 [ dbSNP | Ensembl ].
VAR_037855
Natural varianti1242 – 12421D → G.3 Publications
Corresponds to variant rs2747701 [ dbSNP | Ensembl ].
VAR_037856

Alternative sequence

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifierActions
Alternative sequencei27 – 6943Missing in isoform 3. 2 PublicationsVSP_030225Add
BLAST
Alternative sequencei273 – 2731E → ELAKANMQLLYERLLRRKQL RTQKDNH in isoform 3. 2 PublicationsVSP_030226
Alternative sequencei420 – 615196Missing in isoform 2 and isoform 3. 3 PublicationsVSP_030227Add
BLAST
Alternative sequencei1449 – 151567QIYSE…LKYFQ → NGIKLFQRVIGINELFPKFF L in isoform 4. 1 PublicationVSP_030230Add
BLAST

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AB037832 mRNA. Translation: BAA92649.1. Different initiation.
CR749254 mRNA. Translation: CAH18110.1.
AL078591 Genomic DNA. Translation: CAB89265.1.
AL078591 Genomic DNA. Translation: CAI42417.1. Sequence problems.
CH471051 Genomic DNA. Translation: EAW48820.1.
BC065767 mRNA. Translation: AAH65767.1. Sequence problems.
BC131782 mRNA. Translation: AAI31783.1.
AK000183 mRNA. Translation: BAA90995.1. Sequence problems.
AK002067 mRNA. Translation: BAA92066.1.
AK023639 mRNA. No translation available.
AL136820 mRNA. Translation: CAB66754.1. Different initiation.
CCDSiCCDS34481.1. [Q9P2D6-3]
CCDS47448.1. [Q9P2D6-2]
CCDS55028.1. [Q9P2D6-1]
RefSeqiNP_001099001.1. NM_001105531.2. [Q9P2D6-2]
NP_001156001.1. NM_001162529.1. [Q9P2D6-1]
NP_065870.3. NM_020819.4. [Q9P2D6-3]
XP_005248802.1. XM_005248745.1. [Q9P2D6-1]
UniGeneiHs.211700.

Genome annotation databases

EnsembliENST00000361499; ENSP00000354913; ENSG00000082269. [Q9P2D6-2]
ENST00000370479; ENSP00000359510; ENSG00000082269. [Q9P2D6-1]
ENST00000418814; ENSP00000410768; ENSG00000082269. [Q9P2D6-1]
ENST00000457062; ENSP00000409201; ENSG00000082269. [Q9P2D6-3]
ENST00000505868; ENSP00000423307; ENSG00000082269. [Q9P2D6-4]
GeneIDi57579.
KEGGihsa:57579.
UCSCiuc003pfh.4. human. [Q9P2D6-1]

Keywords - Coding sequence diversityi

Alternative splicing, Polymorphism

Cross-referencesi

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AB037832 mRNA. Translation: BAA92649.1. Different initiation.
CR749254 mRNA. Translation: CAH18110.1.
AL078591 Genomic DNA. Translation: CAB89265.1.
AL078591 Genomic DNA. Translation: CAI42417.1. Sequence problems.
CH471051 Genomic DNA. Translation: EAW48820.1.
BC065767 mRNA. Translation: AAH65767.1. Sequence problems.
BC131782 mRNA. Translation: AAI31783.1.
AK000183 mRNA. Translation: BAA90995.1. Sequence problems.
AK002067 mRNA. Translation: BAA92066.1.
AK023639 mRNA. No translation available.
AL136820 mRNA. Translation: CAB66754.1. Different initiation.
CCDSiCCDS34481.1. [Q9P2D6-3]
CCDS47448.1. [Q9P2D6-2]
CCDS55028.1. [Q9P2D6-1]
RefSeqiNP_001099001.1. NM_001105531.2. [Q9P2D6-2]
NP_001156001.1. NM_001162529.1. [Q9P2D6-1]
NP_065870.3. NM_020819.4. [Q9P2D6-3]
XP_005248802.1. XM_005248745.1. [Q9P2D6-1]
UniGeneiHs.211700.

3D structure databases

ProteinModelPortaliQ9P2D6.
SMRiQ9P2D6. Positions 1243-1341.
ModBaseiSearch...
MobiDBiSearch...

Protein-protein interaction databases

IntActiQ9P2D6. 2 interactions.
MINTiMINT-4717076.
STRINGi9606.ENSP00000410768.

Protein family/group databases

ESTHERihuman-FAM135A. Duf_676.

PTM databases

iPTMnetiQ9P2D6.
PhosphoSiteiQ9P2D6.

Polymorphism and mutation databases

BioMutaiFAM135A.
DMDMi166233529.

Proteomic databases

EPDiQ9P2D6.
MaxQBiQ9P2D6.
PaxDbiQ9P2D6.
PRIDEiQ9P2D6.

Protocols and materials databases

DNASUi57579.
Structural Biology KnowledgebaseSearch...

Genome annotation databases

EnsembliENST00000361499; ENSP00000354913; ENSG00000082269. [Q9P2D6-2]
ENST00000370479; ENSP00000359510; ENSG00000082269. [Q9P2D6-1]
ENST00000418814; ENSP00000410768; ENSG00000082269. [Q9P2D6-1]
ENST00000457062; ENSP00000409201; ENSG00000082269. [Q9P2D6-3]
ENST00000505868; ENSP00000423307; ENSG00000082269. [Q9P2D6-4]
GeneIDi57579.
KEGGihsa:57579.
UCSCiuc003pfh.4. human. [Q9P2D6-1]

Organism-specific databases

CTDi57579.
GeneCardsiFAM135A.
H-InvDBHIX0005996.
HGNCiHGNC:21084. FAM135A.
HPAiHPA031743.
HPA031744.
neXtProtiNX_Q9P2D6.
PharmGKBiPA162386230.
HUGEiSearch...
GenAtlasiSearch...

Phylogenomic databases

eggNOGiKOG2205. Eukaryota.
ENOG410XQFK. LUCA.
GeneTreeiENSGT00390000007885.
HOVERGENiHBG106788.
InParanoidiQ9P2D6.
OMAiEIIQYIQ.
OrthoDBiEOG7C8GGG.
PhylomeDBiQ9P2D6.
TreeFamiTF314837.

Miscellaneous databases

ChiTaRSiFAM135A. human.
GeneWikiiFAM135A.
GenomeRNAii57579.
PROiQ9P2D6.

Gene expression databases

BgeeiQ9P2D6.
CleanExiHS_FAM135A.
ExpressionAtlasiQ9P2D6. baseline and differential.
GenevisibleiQ9P2D6. HS.

Family and domain databases

Gene3Di3.40.50.1820. 1 hit.
InterProiIPR029058. AB_hydrolase.
IPR022122. DUF3657.
IPR007751. DUF676_lipase-like.
[Graphical view]
PfamiPF12394. DUF3657. 1 hit.
PF05057. DUF676. 1 hit.
[Graphical view]
SUPFAMiSSF53474. SSF53474. 1 hit.
ProtoNetiSearch...

Publicationsi

« Hide 'large scale' publications
  1. "Prediction of the coding sequences of unidentified human genes. XVI. The complete sequences of 150 new cDNA clones from brain which code for large proteins in vitro."
    Nagase T., Kikuno R., Ishikawa K., Hirosawa M., Ohara O.
    DNA Res. 7:65-73(2000) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
    Tissue: Brain.
  2. Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3).
    Tissue: Testis.
  3. "DNA sequence and analysis of human chromosome 8."
    Nusbaum C., Mikkelsen T.S., Zody M.C., Asakawa S., Taudien S., Garber M., Kodira C.D., Schueler M.G., Shimizu A., Whittaker C.A., Chang J.L., Cuomo C.A., Dewar K., FitzGerald M.G., Yang X., Allen N.R., Anderson S., Asakawa T.
    , Blechschmidt K., Bloom T., Borowsky M.L., Butler J., Cook A., Corum B., DeArellano K., DeCaprio D., Dooley K.T., Dorris L. III, Engels R., Gloeckner G., Hafez N., Hagopian D.S., Hall J.L., Ishikawa S.K., Jaffe D.B., Kamat A., Kudoh J., Lehmann R., Lokitsang T., Macdonald P., Major J.E., Matthews C.D., Mauceli E., Menzel U., Mihalev A.H., Minoshima S., Murayama Y., Naylor J.W., Nicol R., Nguyen C., O'Leary S.B., O'Neill K., Parker S.C.J., Polley A., Raymond C.K., Reichwald K., Rodriguez J., Sasaki T., Schilhabel M., Siddiqui R., Smith C.L., Sneddon T.P., Talamas J.A., Tenzin P., Topham K., Venkataraman V., Wen G., Yamazaki S., Young S.K., Zeng Q., Zimmer A.R., Rosenthal A., Birren B.W., Platzer M., Shimizu N., Lander E.S.
    Nature 439:331-335(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
  4. Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
  5. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1410-1515 (ISOFORMS 1/2/3), VARIANT GLY-1242.
    Tissue: Placenta.
  6. "Complete sequencing and characterization of 21,243 full-length human cDNAs."
    Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.
    , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
    Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 17-419 (ISOFORM 3), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 902-1515 (ISOFORM 4), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1324-1515 (ISOFORM 1).
    Tissue: Colon and Placenta.
  7. Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 415-1515 (ISOFORM 1), VARIANT GLY-1242.
    Tissue: Testis.
  8. "Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa."
    Abd El-Aziz M.M., Patel R.J., El-Ashry M.F., Barragan I., Marcos I., Borrego S., Antinolo G., Bhattacharya S.S.
    Ophthalmic Res. 38:19-23(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: TISSUE SPECIFICITY, VARIANT GLY-1242.
  9. "Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach."
    Gauci S., Helbig A.O., Slijper M., Krijgsveld J., Heck A.J., Mohammed S.
    Anal. Chem. 81:4493-4501(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].

Entry informationi

Entry nameiF135A_HUMAN
AccessioniPrimary (citable) accession number: Q9P2D6
Secondary accession number(s): A2RRQ5
, Q3C0H3, Q5JXK0, Q5JXK1, Q68DW0, Q6P081, Q9H0F2, Q9NU48, Q9NUQ5, Q9NXL5
Entry historyi
Integrated into UniProtKB/Swiss-Prot: January 15, 2008
Last sequence update: January 15, 2008
Last modified: June 8, 2016
This is version 101 of the entry and version 2 of the sequence. [Complete history]
Entry statusiReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Miscellaneousi

Keywords - Technical termi

Complete proteome, Reference proteome

Documents

  1. Human chromosome 6
    Human chromosome 6: entries, gene names and cross-references to MIM
  2. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
  3. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations
  4. SIMILARITY comments
    Index of protein domains and families

Similar proteinsi

Links to similar proteins from the UniProt Reference Clusters (UniRef) at 100%, 90% and 50% sequence identity:
100%UniRef100 combines identical sequences and sub-fragments with 11 or more residues from any organism into one UniRef entry.
90%UniRef90 is built by clustering UniRef100 sequences that have at least 90% sequence identity to, and 80% overlap with, the longest sequence (a.k.a seed sequence).
50%UniRef50 is built by clustering UniRef90 seed sequences that have at least 50% sequence identity to, and 80% overlap with, the longest sequence in the cluster.