KEGG ORTHOLOGY: K24210

ORTHOLOGY: K24210

Entry

K24210                      KO

Symbol

LIPN

Name

lipase member N [EC:3.1.1.-]

Disease

H00734

Autosomal recessive congenital ichthyosis

Brite

KEGG Orthology (KO) [BR:ko00001]
09190 Not Included in Pathway or Brite
  09191 Unclassified: metabolism
   99980 Enzymes with EC numbers
    K24210  LIPN; lipase member N

Genes

HSA:	643418(LIPN)

PTR:	466144(LIPN)

PPS:	100986381(LIPN)

GGO:	101150877(LIPN)

PON:	100445868(LIPN)

PPYG:

129006215(LIPN)

NLE:	100607743(LIPN)

HMH:	116478778(LIPN)

SSYN:

129480477(LIPN)

MCC:	693761(LIPN)

MCF:	102137951(LIPN)

MTHB:

126962339

MNI:	105480813(LIPN)

CSAB:

103216219(LIPN)

CATY:

105587162(LIPN)

PANU:

101020022(LIPN)

TGE:	112632008(LIPN)

MLEU:

105552495(LIPN)

RRO:	104675152(LIPN)

RBB:	108526484(LIPN)

TFN:	117086173(LIPN)

PTEH:

111551324(LIPN)

CANG:

105515925(LIPN)

CJC:	100395520(LIPN)

SBQ:	101037435(LIPN)

CIMI:

108290329(LIPN)

ANAN:

105718901(LIPN)

CSYR:

103260556(LIPN)

MMUR:

105875736(LIPN)

LCAT:

123649906(LIPN)

PCOQ:

105822680(LIPN)

OGA:	100961380(LIPN)

MMU:	70166(Lipn)

MCAL:

110285810

MPAH:

110331914(Lipn)

RNO:	499345(Lipn)

MCOC:

116103753

ANU:

117721308

ASYL:

127677400

MUN:	110561525(Lipn)

CGE:	100761667(Lipn)

MAUA:

101823153(Lipn)

PROB:

127233417(Lipn)

MORG:

121454127(Lipn)

MFOT:

126512838

AAMP:

119806203

NGI:	103738039(Lipn)

HGL:	101717023(Lipn)

CPOC:

100724769(Lipn)

CCAN:

109691147

DORD:

105986225(Lipn)

DSP:	122115935(Lipn)

NCAR:

124985142

MMMA:

107153415(Lipn)

ITI:	101960921(Lipn)

OCU:

100339762

OPI:	101529185(LIPN)

TUP:	102474635(LIPN)

GVR:	103604159(LIPN)

CFA:	610475(LIPN)

CLUD:

112656267(LIPN)

VVP:	112931983(LIPN)

VLG:	121475735(LIPN)

NPO:	129507729(LIPN)

AML:	100472997(LIPN)

UMR:	103661928(LIPN)

UAH:	113258972(LIPN)

UAR:	123795510(LIPN)

ELK:

111145207

LLV:

125085083

MPUF:

101681353(LIPN) 101686111

MNP:	132016395(LIPN)

MLK:	131830075(LIPN)

NVS:	122900652(LIPN)

ORO:	101365234(LIPN)

EJU:	114210313(LIPN)

ZCA:	113923501(LIPN)

MLX:	118012837(LIPN)

NSU:	110585975(LIPN)

LWW:	102743379(LIPN)

FCA:	101092545(LIPN)

PYU:	121016581(LIPN)

PCOO:

112851484(LIPN)

PBG:	122493446(LIPN)

PVIV:

125148434(LIPN)

LRUF:

124518592

LGF:	123577351(LIPN)

AJU:

106980983

PTG:	102949387(LIPN)

PPAD:

109255416(LIPN)

PUC:

125933215

PLEZ:

122202132(LIPN)

BTA:	523964(LIPN)

BOM:	102275330(LIPN)

BBUB:

102406049(LIPN)

BBIS:

104987537(LIPN)

CHX:	108633222(LIPN)

OAS:

101123254

BTAX:

128067870

CSUM:

138070525

ODA:	120873790(LIPN)

CCAD:

122446105(LIPN)

MREE:

136157271(LIPN)

OVR:	110138634(LIPN)

MBEZ:

129555572(LIPN)

SSC:

100156277

CFR:	102518294(LIPN)

CBAI:

105081905(LIPN)

CDK:	105102854(LIPN)

VPC:	102535520(LIPN)

BACU:

103001011(LIPN)

BMUS:

118883043

LVE:	103075427(LIPN)

OOR:	101283773(LIPN)

LALB:

132506740(LIPN)

DLE:

PCAD:

PSIU:

NASI:

ECB:	100071663(LIPN)

EPZ:	103558119(LIPN)

EAI:	106822186(LIPN)

MYB:	102258640(LIPN)

MYD:	102756171(LIPN)

MMYO:

118669997(LIPN)

MLF:	102427360(LIPN)

MDT:	132214971(LIPN)

MYUM:

139021909(LIPN)

PKL:	118719264(LIPN)

EFUS:

103296396(LIPN)

MNA:	107543276(LIPN)

DRO:

112307391

SHON:

118987949

AJM:	119057770(LIPN)

PDIC:

114497720

PHAS:

123828808(LIPN)

MMF:	118632367(LIPN)

PPAM:

129069813(LIPN)

PALE:

PGIG:

PVP:

RAY:

MJV:	108394173(LIPN)

TOD:	119233855(LIPN) 119253974

SARA:

101551029(LIPN)

SFUM:

130029795(LIPN)

SETR:

125995026(LIPN)

LAV:	100659525(LIPN)

TMU:

101356689

ETF:

101641607

DNM:	101418788(LIPN)

MDO:	100021384(LIPN)

GAS:

SHR:

AFZ:

PCW:

TVP:

PBRV:

SBIA:

133496056(lipf)

LBD:

AGB:

PPYR:

DVT:

TPAL:

HAZT:

Reference

PMID:21439540

Authors

Israeli S, Khamaysi Z, Fuchs-Telem D, Nousbeck J, Bergman R, Sarig O, Sprecher E

Title

A mutation in LIPN, encoding epidermal lipase N, causes a late-onset form of autosomal-recessive congenital ichthyosis.

Journal

Am J Hum Genet 88:482-7 (2011)
DOI:10.1016/j.ajhg.2011.02.011

Sequence

[hsa:643418]

LinkDB

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