Human ORFeome, Internal ID: 15551
BC number:  N/AEntrez Gene ID:  54903
Length: 1129Symbol:  MKS1
Resource Plate: GDEhISO11003Resource Plate Position:  G06
Forward Primer:  GGGGACAACTTTGTACAAAAAAGTTGGCACCATGACCACTGCAGCCAGCGA
Reverse Primer:  GGGGACAACTTTGTACAAGAAAGTTGGCAACACTTACTCAGAAATAACTCATATC
Description:  Meckel syndrome, type 1 CHROMOSOME: 17
Template Information: 
Vendor Plate:  N/AVendor Position:  N/A
Collection:  Vendor Name: N/A
Vector: N/ACatalog Number: 
Information Source: N/A Library: N/A
Clone ID:  N/A Genbank Accession: N/A
GI:  1800000146
MGC Coding Sequence: 
atgaccactgcagccagcgaggtgccttcattcttggtcgagcgaatggcaaatgtcaggcgtcgccggcaggacaggcgagggatggagggcggcatcc
tcaagtcacgcatcgtcacctgggagccctcagaagagtttgtcaggaacaaccacgtcattaacacccctcttcagacaatgcacatcatggcagacct
ggggccctataaaaagcttggctataagaagtatgaacatgtcctgtgtactctgaaggtggatagcaatggtgtgatcacagtaaagcctgacttcacg
ggcctcaaaggaccctacaggattgagacggagggggagaagcaggagctgtggaaatatacgatcgacaatgtttccccccacgcacagccggaggagg
aggagcgggaacggcgagtgttcaaggatctttatggccggcacaaggagtatctcagcagcctcgtaggcaccgactttgagatgactgtcccaggtgc
cctccggctctttgtaaatggagaggtcgtttcagcccaaggctatgagtatgacaatctctacgtccacttctttgtagaattgccaactgctcactgg
tcaagcccagcattccagcagctctcaggagtaacacagacctgcaccaccaagtccctggcaatggacaaggtggctcacttctcctacccattcacgt
ttgaagccttcttcctccatgaggatgaatcttctgatgcactcccggagtggcctgtgctctactgtgaggtcctctcgctggacttctggcagaggta
ccgtgtggaaggctatggggctgtggtgctgcctgccactccaggctcacacaccctgacagtctccacgtggagacctgtggagcttggcacggtggct
gagctgaggaggtttttcattggcggttctctggaactggaggacctctcctatgtacggataccaggatccttcaagcctttcatcttccaagaccaaa
gaaggaaggaaggtggacggtgagagggtcttaaatccccagcctgtgagtctcagcctctttccagggaagcctcattctactgcttggggcttgctga
ggttgagatatgagttatttctgagtaag
cDNA Sequence (including UTRs): 
n/a