Busch Lab

ZMP

alcamb

Ensembl ID:
ENSDARG00000058538
ZFIN ID:
ZDB-GENE-030131-1768
Description:
neurolin-like cell adhesion molecule [Source:RefSeq peptide;Acc:NP_997799]
Human Orthologue:
ALCAM
Human Description:
activated leukocyte cell adhesion molecule [Source:HGNC Symbol;Acc:400]
Mouse Orthologue:
Alcam
Mouse Description:
activated leukocyte cell adhesion molecule Gene [Source:MGI Symbol;Acc:MGI:1313266]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa12223 Nonsense Available for shipment Available now
sa42525 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35862 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12223
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101204 Nonsense 78 562 3 16
Genomic Location (Zv9):
Chromosome 15 (position 18824774)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 19927400
GRCz11 15 19863132
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTAAAACACAYGGGTCAGAATGCCTCCTCTCCCACTGATGGTAACTAC[A/T]AGAAYAGAGTCAGWATTAAAAAAGATTTTGGWCTCATCATCACACAAGTG
Long Flanking Sequence:
TAAGCGAGTTTAAACTACTTCTACATTAAGGTAGTGTTCAGAAAAAAACTAAACATCAGTGAAGAAACTTGACAAAGAGGAATTTAACAAGCTACTGCCAGCTAGCATTTCAGAAGTGTTATTACAGAGCAAACCAAACAGCGTGCAAGTATAAATAAGAAGTATAAATGCACAGCAATTCACAAGGCATGTGCCGTGGCACATGTGGATCACTCGACACAGAAGTATAAACCAGGCTTTAGCAGAAAGTCGTACATGTAGTCTTGGCTGATCAGTTTAAAAAACAAAACAAAAAATAGACTACAGAACCACTGTATTTTCACTTAAACATGTATGGAAGAATGACTTTATGAATGGCAATTTTGTCATCTCCTCTGGTAAATGTGCATTTTTATTTATTTATTATTATTATTTATTATTTTTTTTACCAGGACAAAGATGGCAGCATTCTGGTAAAACACACGGGTCAGAATGCCTCCTCTCCCACTGATGGTAACTAC[A/T]AGAACAGAGTCAGTATTAAAAAAGATTTTGGTCTCATCATCACACAAGTGTCCCTGGCGGATCAGAAAACCTTCACCTGCATGGTTGTGGCAGCAGATGACATTTTGGAGTATCCTGTCCAACTGGTCATTTACAGTAAGAATCATTAATTAAATTACTGAAAGAGGCCTAAAACGATTCCATATCTACAGTAGAAGTTTTAGTAACCTAGGCTATCTTAATACTACAATGTTGTACTAAACATTTTTAACATTGTGTACAGATGACAGTTGTCACAATAACCCATTTACACTGAATCACGAAACAACAAAATGTTTTAATAAGATAGTAGATGATGTCGCTGTACAGAAACATTATGCACACATATTACAACAATATTGTTTGCAAAGACGGCTGTTAATAAATGTTATTGAAAAAAATTATATTTCTAGTAGTTGCATTTATGAACTTTAATGTCTAACAATGTCTGTTTTCCTGTTTTTTTTAATTTAATAATAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42525
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101204 Essential Splice Site 273 562 7 16
Genomic Location (Zv9):
Chromosome 15 (position 18828754)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 19931380
GRCz11 15 19867112
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACGGCAGACGGAAACCCCCCACCCTCTCGCTACAACTTCTACATCAAG[G/A]TAAGTCTGAATTACTGTTTGTCTGGAAATTAAAATCTGCTTTTGGATTCT
Long Flanking Sequence:
GCTTATGGTCTCATGTTGAGTATAATTCGTTGCATTTATTCAGAATAACTCTCGTTCCTCCTGAAGTAGCCACAAAAAAGAGGCCTGATCAGAATCAAATAGCATGTCCAATGAGATATGTAATTTGGCCTCTCTGGAGCAGGCCGTTTAGATGGTGAATGGGGTTTTGTCTTGCATCTGGCTGTTGTTGTGAAGCCACTAGCCCCTCTGGTAACTCTCAAAACCATTTCTCATTATGAGAGGGCTCTCAAACCCTCAACTCTTGAGCTGAAGGACCTCTTAAGTATGTTCTCTGAAGTGCCCTTATCTGCATGCACTCTAGCTGGCCTTCTCTAAGCTGCCTTCCCTTGCTTTACACAAACCCTTTCTCCACAGACCCTTCGGAGACGATCAGTTTCCATGTGCTGCCCGATGGTCCTGTTAAAGAAGGAGACAATGTGACCCTCAAATGCACGGCAGACGGAAACCCCCCACCCTCTCGCTACAACTTCTACATCAAG[G/A]TAAGTCTGAATTACTGTTTGTCTGGAAATTAAAATCTGCTTTTGGATTCTCTAACTCTGCCTGTTTTATCCATAGGGAGAGAAGAAGACAGTGGAGAAATCGAACATCTTTATCTTGAGTAATGTAACTAGGCAAAACACCGGAGAATACAAATGTTCATTGGTGGATAATGAGATATTGACGGCGTCTAAAAATATCACCGTTGAATGTAAGGAAATACTTTGCCATACTTTTTGTACCTATGATTGCATTGTGTTTAATAAAAAAAAAAGAAAAAAAAAGAATTTTAAATTAATTTTTAAAAATGTTATCTATTTTCTCTCTCTCTGCCCGAAAGATCTTGATGTGATTCTTAGCACCACTGGTGAGGTTTTCAAGAAACTTGGCGATAGCTTTGAAACAACTCTCGATATTAAAGCTTCAGGAAAAACAGAAACCTTTTGTAAGAAGGTAAAAAAATAATATATTAAAAACTATTCTTTGAGCATAAAATCTATAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35862
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101204 Essential Splice Site 483 562 12 16
Genomic Location (Zv9):
Chromosome 15 (position 18831851)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 19934477
GRCz11 15 19870209
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCTCCAATGATTTGGGTTCTGACACGAGGAGCATCGATGTGTCGTCGC[G/A]TAAGTGTAACTTCTGTCCGCTGCTTCTCTTATTTGACTACTAAACACTCA
Long Flanking Sequence:
CGCTCTTGTATTGTATTGCACAAACCCTGCAATAAATACTTTTCTTTCTTGGAGTAGTATATATTACTTTAGAACTTTTTTTAAACAAGTAGAAAATGTCTCTTCAGAAAAAGGTTGTGTATTTTTCCTTAAACAAGCTAAATAATCTGCCGGTGAGTTGGTGTAAGCAAATTAATCTTGTTTTCAGATTATTTGGCTTGTTTTAGGACTCACTTTATTTGGACTAAAAACAAGAAAAATGCTCAAAGAAAGATTTTTTTTGCAATGCAATTTTAAGTCTGTTATCTTTTAATGGATTTTTTTGTTTTATTTATTTATTTGTTTATTTATTTATTTATTTGTTTATTTTGTTGTGTTATAGGTGAAATTTCAAGAGAGCGAACATGTGAATGGAAAGATCACATACTATATCACTGTCAGTCCAAAGGCCAATGTCACTGTGTCCTGCACAATCTCCAATGATTTGGGTTCTGACACGAGGAGCATCGATGTGTCGTCGC[G/A]TAAGTGTAACTTCTGTCCGCTGCTTCTCTTATTTGACTACTAAACACTCATCCATCACTAGTTCGTCGGCTGTCAACAAAATCATTTAGATGAAACTGTGAAGGATGAAACATTAGTAAATACCATTGCCTGATGACTCCTATTTTTTTTAAATAAGTATTGTCCTGTCAAGACCAAGTTTTTGTTTTAAACCTTATTTATTGTATCGATAATACCAGTGCAAAAGGAGCTTTGTTTACGGATTCTCTTTTTTAAACTTTGTTTATGTTTATAAGTAAATGCAGCGATTTAGTTTAGCCAAATTCTATTTATTCTAATTCTATTCTATCAGCTATTACATTATCATAAGTTTACTAATGTGTTAATAAATGCTGAAATTAGGAACCATTCTGTGAGTAGCCTAAAATGCTACAGTATTACATTCTTTGCTAGGTTATTGTAGCGTTTGTTATTGTTTGTTAAGTGTTAACAAAAGTTACTTTATAGTGATTATGATTATA
Associated Phenotype:
Not determined