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 |
