ZMP
kal1b
Ensembl ID:
ZFIN ID:
Description:
Kallmann syndrome 1b sequence [Source:RefSeq peptide;Acc:NP_571454]
Human Orthologue:
KAL1
Human Description:
Kallmann syndrome 1 sequence [Source:HGNC Symbol;Acc:6211]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24225 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24225
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000003736 | Essential Splice Site | 530 | 648 | 11 | 14 |
| ENSDART00000144318 | Essential Splice Site | 515 | 633 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 22 (position 41951103)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38919096 |
| GRCz11 | 22 | 38905841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATCGCTAATGGGGAGACGGAAAAAACCCGCTGCCTGCGCCAGAGAGGG[T/C]AAGATGACATCTAGCACATCCAGACAGCTGTATTGAGATCTAAATCCCAG
Long Flanking Sequence:
TGACTCGCGTCTTCTCACATGTCAGATGGCAATAGTGAAGAGATGATGTCACTGCCAAACCTGTGCGTGACCCTCCAATGTACCCTGAGCGTGGCGTTCCTGCATCTGACTTCTTTATGCAGCTGAATAGTGTAGCGGAGAATGGCAGCGCTCTATCTGTCATCACCGGCTCTGGACACAATAGAAACGTGCAACCGAGTCTCAGTATGATATCATTATGATGCAGATGGGGCTTATCTGCTGCATTTTCCAGAGCCTTCAGTGTGGTTCTCATTTCATATTATTCTCGACAGAAAAGATGTAATAACTCTGTGCTGTTCTCTGCTTGTTTTAAAGGGAACACATTATGTGATTACCGGCCTGCTGTTTGCCTGTAAGTACCGTGTGGCAGTGAAGCCCGTTGCAGAGCAGAGGTCAGAGGTCACGACTTCGGTGACCACCCCACTTTGCTTATCGCTAATGGGGAGACGGAAAAAACCCGCTGCCTGCGCCAGAGAGGG[T/C]AAGATGACATCTAGCACATCCAGACAGCTGTATTGAGATCTAAATCCCAGAGAAATGATGACGCCCAGATTTAATTCAAGCTAAATAGTCCAGTCAATTACTGTGTCTGAATATTGTACCTATGAAAGTGTTTATAACTGTGATTTCAGCTGGTTGAAACTAGCATAATTTAAACACTCAATAATAAAATGACAAAATCTATTTAGAAGAATACTGGGAATTGTCAGAATTAAATATATCAGGAAAAAAGATCCTTAAAATACACCGTATGACAAAAATTGCTGAAGGGATGGGACGCACAGCTGAGGTCAGAATTATTCACCCCCCTGTTTATTTTCTCCTTAATGTCTGTGAAGCGGAGAGCAGATTTCTCCAGCACATGTCTAATCATAACAGTGTTAATAACTCATCTCTAATAACTGATTTATTTCCTCTTTGTCATGATGACAGTAAATAATATTAGACTAGATATTCTTCAAGTCTATTGACTAGAAGACTAG
Associated Phenotype:
Not determined