Gene: [0Xp2232/KAL1] Kallmann syndrome 1 sequence (hypogonadotropic hypogonadism and anosmia); adhesion molecule-like peptide KAL1, X-linked; [KAL ADMLX ]


CAG

There are three genetic forms of Kallmann syndrome: KAL1 - X-linked form, KAL2 - autosomal dominant form (GEM:00.0/KAL2), KAL3 - autosomal recessive form (GEM:00.0/KAL3)."

PSG

GEM:0Yq11/KALP

REF

LOC,LIN,MAP "Ballabio A &: Genomics, 4, 36-40, 1989
LOC,LIN,MAP "Ballabio A &: Clin Genet, 34, 31-37, 1988
LOC,LIN,MAP "Ballabio A &: Hum Genet, 77, 338-341, 1987
LOC,LIN,MAP "Ballabio A &: Hum Genet, 72, 237-240, 1986
CLO,SEQ,STR "del Castillo I &: Nature Genet, 2, 305-310, 1992
CLO,SEQ,STR "Franco B &: Nature, 353, 529-536, 1991
HET "Guioli S &: Nature Genet, 1, 337-340, 1992
CLO,LOC,HET "Incerti B &: Nature Genet, 2, 311-314, 1992
LOC,LIN,MAP "Legouis R &: CCG, 58, 2074, 1991a
CLO,SEQ,STR "Legouis R &: Cell, 67, 423-435, 1991b
LOC,LIN,MAP "Meitinger T &: AJHG, 47, 664-669, 1990
HET "Parenti G &: Am J Med Genet, 57, 476-478, 1995
LOC,LIN,MAP "Petit C &: PNAS, 87, 3680-3684, 1990
LOC,LIN,MAP "Petit C &: CCG, 51, 1059, 1989

SWI

SWISSPROT: P23352

KEY

mem, sex

CLA

coding, basic

LOC

0X p22.32

MIM

MIM: 308700

SYN

KAL ADMLX

鸯铗痂蝈 蜞赕:

  • Gene: [08p/GNRH1] gonadotropin-releasing hormone 1 (GNRH1; gonadoliberin); luteinizing hormone, releasing hormone (LHRH; gonadoliberin); prolactin release-inhibiting factor; adrenal hypoplasia with absent luteinizing hormone? (MIM:202150);