ZMP

alcama

Ensembl ID:

ENSDARG00000026531

ZFIN ID:

ZDB-GENE-990415-30

Description:

CD166 antigen homolog A [Source:UniProtKB/Swiss-Prot;Acc:Q90460]

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12510	Nonsense	Available for shipment	Available now
sa34926	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12510

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
ENSDART00000030138	Nonsense	261	479	6	13
ENSDART00000100180	Nonsense	206	381	5	10
ENSDART00000100184	Nonsense	290	573	6	14
ENSDART00000129400	Nonsense	260	545	6	15

Genomic Location (Zv9):

Chromosome 10 (position 29430758)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	28862352
GRCz11	10	28748977

KASP Assay ID:

2260-3358.1 (used for ordering genotyping assays)

KASP Sequence:

AATGCCAGGCGGAYGGAAACCCTCCTCCTACYAGCTTCAACTTTAACATT[A/T]AGGTGAGGGACTGCCGGCAGYGTCCACAGCAACCAGACCGCTTTTAAATC

Long Flanking Sequence:

CTCAGCTGCTAGCCAAGCTCAATTTGATGTTTTTTTTTTCTTGGTCTTGTCAGGCATAATGCCGGTAACCAAGTCTGCAGTTGCTGTCTCTCTCTCTGTTATCTGAATGCTGAGAGGTTTGTTCAGTGCCTCGGGCTGAAGATGTGATGTGAAATGCTCTGTGGCTGCTAGGCGCGAAAACGAGGGCGAGAATGAGAGACTGCAAATGGTTGTGGAAATGAAGGCGTTTAAGCCCCTTGGGGTCCTCAGAATGGCCCGGTGTCTTAGAGAATGTTTTTTTTTTTTTTGTAGCTGTTGGAAAGTCACACCACATCTCTTGCGATGACAGCCATCCTCCTCAGTTCATTCTAATGTTTGTTTTCTCTCTTTGTCTTTCAGATCCCACTGAGAAGGTGAGTCTACAGGTTGTCTCTCAGAGCCCCATTAGGGAAGGTGATGATGTGACTCTGAAATGCCAGGCGGACGGAAACCCTCCTCCTACCAGCTTCAACTTTAACATT[A/T]AGGTGAGGGACTGCCGGCAGTGTCCACAGCAACCAGACCGCTTTTAAATCTTCAGGGTCCTGCTGTCTGCCCTGTTTTCTTCTCCTGGTTAATCTCACTGCCTTGATCTCTTCAGGGAAAGAAGGTCACGGTGACGGACAAGGATGTCTACACACTGACCGGCGTCACCCGAGCCGACAGCGGTGTGTACAAGTGCTCTCTGCTTGACAACGATGTGATGGAGTCCACTCAGATCGTCACAGTGAGCTGTGAGTGGACAAATCTGCCCTGTTTCTCTTCCATCTCTCCATAAAAACATCCACACACTTAGAGACAGAAGTGATGGAGCACTTGACAGATGTGGAAAGATTTTTTGGAAAGGGCAGAGTCAGCTGAAATGCAAGCAGCATGACAAAAAAAACTGGACTTTCAAATGCTTTCCATGAAATGTTGTTAGTCAGTGCAGGAAAACTTGGAAAAGTTTCTGAAAGTTTGGTTCTCAAGGCTTTCCCCTCATATAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34926

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
ENSDART00000030138	Essential Splice Site	261	479	6	13
ENSDART00000100180	Essential Splice Site	206	381	5	10
ENSDART00000100184	Essential Splice Site	290	573	6	14
ENSDART00000129400	Essential Splice Site	260	545	6	15

Genomic Location (Zv9):

Chromosome 10 (position 29430755)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	28862349
GRCz11	10	28748974

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCAGGCGGACGGAAACCCTCCTCCTACCAGCTTCAACTTTAACATTAAG[G/A]TGAGGGACTGCCGGCAGTGTCCACAGCAACCAGACCGCTTTTAAATCTTC

Long Flanking Sequence:

AGCTGCTAGCCAAGCTCAATTTGATGTTTTTTTTTTCTTGGTCTTGTCAGGCATAATGCCGGTAACCAAGTCTGCAGTTGCTGTCTCTCTCTCTGTTATCTGAATGCTGAGAGGTTTGTTCAGTGCCTCGGGCTGAAGATGTGATGTGAAATGCTCTGTGGCTGCTAGGCGCGAAAACGAGGGCGAGAATGAGAGACTGCAAATGGTTGTGGAAATGAAGGCGTTTAAGCCCCTTGGGGTCCTCAGAATGGCCCGGTGTCTTAGAGAATGTTTTTTTTTTTTTTGTAGCTGTTGGAAAGTCACACCACATCTCTTGCGATGACAGCCATCCTCCTCAGTTCATTCTAATGTTTGTTTTCTCTCTTTGTCTTTCAGATCCCACTGAGAAGGTGAGTCTACAGGTTGTCTCTCAGAGCCCCATTAGGGAAGGTGATGATGTGACTCTGAAATGCCAGGCGGACGGAAACCCTCCTCCTACCAGCTTCAACTTTAACATTAAG[G/A]TGAGGGACTGCCGGCAGTGTCCACAGCAACCAGACCGCTTTTAAATCTTCAGGGTCCTGCTGTCTGCCCTGTTTTCTTCTCCTGGTTAATCTCACTGCCTTGATCTCTTCAGGGAAAGAAGGTCACGGTGACGGACAAGGATGTCTACACACTGACCGGCGTCACCCGAGCCGACAGCGGTGTGTACAAGTGCTCTCTGCTTGACAACGATGTGATGGAGTCCACTCAGATCGTCACAGTGAGCTGTGAGTGGACAAATCTGCCCTGTTTCTCTTCCATCTCTCCATAAAAACATCCACACACTTAGAGACAGAAGTGATGGAGCACTTGACAGATGTGGAAAGATTTTTTGGAAAGGGCAGAGTCAGCTGAAATGCAAGCAGCATGACAAAAAAAACTGGACTTTCAAATGCTTTCCATGAAATGTTGTTAGTCAGTGCAGGAAAACTTGGAAAAGTTTCTGAAAGTTTGGTTCTCAAGGCTTTCCCCTCATATATGAT

Associated Phenotype:

Not determined