Busch Lab

ZMP

ncam2

Ensembl ID:
ENSDARG00000017466
ZFIN ID:
ZDB-GENE-010822-1
Description:
neural cell adhesion molecule 2 [Source:RefSeq peptide;Acc:NP_571905]
Human Orthologue:
NCAM2
Human Description:
neural cell adhesion molecule 2 [Source:HGNC Symbol;Acc:7657]
Mouse Orthologue:
Ncam2
Mouse Description:
neural cell adhesion molecule 2 Gene [Source:MGI Symbol;Acc:MGI:97282]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa34694 Nonsense Mutation detected in F1 DNA Not yet available
sa38754 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18956 Nonsense Mutation detected in F1 DNA Not yet available
sa31734 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa34694
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062137 Nonsense 53 840 3 21
ENSDART00000100681 Nonsense 52 795 3 17
Genomic Location (Zv9):
Chromosome 9 (position 36281171)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35500682
GRCz11 9 35309867
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTGTATTTGTGTTTGTAGTGATCGGGGAGCCTGTGAAATTGGAGTG[G/A]TTTAACCCGCAGGGGGAGCGGATGGTCGCGTCTCCACGGGTGGCCTTGCA
Long Flanking Sequence:
ACACAGGGATTTATGTTACTGATCATAATGCATTTACATTAGTGGGAGTTTCCCTTTAATATGCAAAAGTTATGGGATGAGACTATTTAACTTAAAGTTTTTTGGGCAGACAGTTTTTATTTGTATTTCACACCATTTTTAATGCATTTCTTAGCCAATTTTGCACTTGTGTTGAACATTTCATGCACCTTTTCATCATCACTTTTTTCATTTGTTCTGGTTTATTCACTGCATTGGACATTATGAATTTGCACATTGTCAGTAGATCACTACTAAAACCTTTCACTCCTATCTGTGCATTTATTGTATAGTGATCTTGCACTGATTTGCCCTTTTTAATAACTGTAACCTTCAAAGTCTTACTTTGCTCATGATTTAGTGAAAGAAAACATTAAGCCTGGTCTTATTAAAGTCATCTGAACTACATTTTGTATGTCTCACTATGTCAATGTTTTTGTATTTGTGTTTGTAGTGATCGGGGAGCCTGTGAAATTGGAGTG[G/A]TTTAACCCGCAGGGGGAGCGGATGGTCGCGTCTCCACGGGTGGCCTTGCACAATGAAGGTATTCGTTCCAGACTCACCCTTTACAATGCCAAAATAGAAGACGCTGGCATCTACCGGTGCCAGGCCACCGATGCACAGGGAGAGACACAGGAGGCCACTGTGGTGCTCGAGATCTATCGTGAGTATCCAAAACACACAGACAAATCTGTTATTATTCAAGTTACTTTTTTTTTCAGGTAATAAGTCTGAATAAGTCTGAATAATAAGTAGTAGCCTAAATGGTGTAAATTGTTACTTAAACTAACGTGTTACCAAAATAATAAATAAATAGGTTGCAATGAGCAATCTAAATGCAGTGCAATAAAATCTCAACCAAAAATTGTGTTATCCTAATTTATCAAATTATTTTGTGTTTTATTTACATACTTTATTTGTAACAAACAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38754
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062137 Essential Splice Site 113 840 4 21
ENSDART00000100681 Essential Splice Site 112 795 4 17
Genomic Location (Zv9):
Chromosome 9 (position 36268825)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35488336
GRCz11 9 35297521
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTTTCCAACAATGTAATCATTTTTACTATTTCTTCTCTCTGCCCCTC[A/C]GAGAAGCTGACGTTCAGAGATGTGAGGTCTCCTCAGGAGTTTCGGCAGGG
Long Flanking Sequence:
CACTTCATTCATCCATTAATTTTCTTGTCGGCTTAGTCCCCTTATTAATCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTTTTATGCAGCGGATGCCCTTCCAGCCGCAACCCATCTCTGGAAAACATCCACAAACACATTCACACACTCACACACTACGGACAATTTAGCCTACCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCGGAGAAACCGGAGGAAACCCATGTGAACGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCAGCGGCTCGAACCAGCGACCCAGGGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCTTCGCCTGCTAAAACACTTAAACAAGTTTATTTGGTTGTCCAGTGTAATTGTGTTGTCCATGTCAAATAAATAAATGTTATTTTCCAACAATGTAATCATTTTTACTATTTCTTCTCTCTGCCCCTC[A/C]GAGAAGCTGACGTTCAGAGATGTGAGGTCTCCTCAGGAGTTTCGGCAGGGTGAGGTGGCTGAAGTGGTCTGTGATGTCACCAGTTCCCCTGTGCCTGTGGTCTCCTGGTTTTACAACAACATTGAGATCACTGAAGACACTGAGAGTAAGTAATCTGCCATATTGACCTATTTTCTCTGGCTAAAAAAAGACCTTTGCGGCATTGCTAAATAAGTGAGATATCATTGTCAATTAATACTTGAATGCTTGAAAATTAATGTAGACTTCAAGCTTCTCTGTAGAGGACTGCAGAGAGAGAAAATGACCAGCAAAAATACAAAAAAGGGAATGCATGATAAAATCATTGTCACATTATGAATAATGTATGGCCTCATTTCACTGTAAGACTTTCAAAATGTTATTCCCTTTTTCCAACTCAGTGTTGACAAGCGCTAACAAGCGTGTTGATTAAAAAATGCATGTGCTTCATGTAAATGTGATTTCAGCCAGTTTTAAATATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18956
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062137 Nonsense 475 840 11 21
ENSDART00000100681 Nonsense 471 795 11 17
Genomic Location (Zv9):
Chromosome 9 (position 36199502)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35419013
GRCz11 9 35228198
KASP Assay ID:
2260-2144.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCATGGTTCTCAGGTTACTCCGATGTCAGACAGAGATTTTGGCCGTTA[C/A]AACTGCACAGCCAGAAACAACATCGGGATGCGCTTCCAGGAGTTCATCCT
Long Flanking Sequence:
ATGCATTAAGTAGTGTTAACTAAACGACATTACTTCCAAGTGTTAGCAATAGAAATGTATAGAAATGCCAACTAGTAAAATATTTTTTGTGCAAAAACAACAACAAAAAATATTCAGTGTATTAATTACTGCTGATCATGCAGTTTATGATAGTATACATTTCTTTTGAGTCTTTTTAAAATTGTATTTATTTTGTATGATGAGCAGTTTCTAATATATTCAGAGCGATAGAATATTATTGCAGATTATTTGTACAAGCAGAGTTGTCTTTCTTAGGTAGCCTCATTGATAGAGAGAACTCTGACAAGACTCAATGACGTTTCACTTCTCTGGAAACAAAAAGTTTACCACATATTATCTGTGTCAAATGAGTACAGAACATCAAAACAACATTAATATATGTCAACAAATGTTTAAAATGACACTCATGTAAAAAATTATTGTATGAATGATCATGGTTCTCAGGTTACTCCGATGTCAGACAGAGATTTTGGCCGTTA[C/A]AACTGCACAGCCAGAAACAACATCGGGATGCGCTTCCAGGAGTTCATCCTAGCACAGGCAGGTGCGTGTTCACCATGGGTTCAGCTCATCCATCTCGCTGATGCGTGTCTGTCGGTACAATTGCTGTGTGACAATAATGAATGTAGGTGTGTTGTAGAGGTGAAGTGTGTTATTACAGTTCCAGTTTTAGAAACAGTCATATACCAAATGGAGGGAAATAACTAGGTATAAAAAATAGGTCAAAAGCCCGTATTTTAAATTCTGCTTTTTGTGGTCAATGCCTGTACTATTGACACAATGAATATGAAATCCTATATGTACTAGACTGTTTTAATTATGACGCTTTTAACACCACAAGTACTAAAGTTTTTGTAGTTTGGCCCAATTTCTGTAGTTTTTATACAATGTAAAACATGCCAAAAGCAGCTTAACATAGATAGCAAAAATATTGCCTAGTTACTTTTCTTATGTGCCTATTCGTACTTTTCTCCAACCCTGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31734
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
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062137 Essential Splice Site 554 840 12 21
ENSDART00000100681 Essential Splice Site 550 795 12 17
Genomic Location (Zv9):
Chromosome 9 (position 36192182)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35411693
GRCz11 9 35220878
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACATCAGCTCACAGGACTGGAAGGATGTCAAATCGCTGGGGACGCAGAG[T/C]AAGTACAAAGGTTATCTGCTGCTACACTGAAATAAAAAAATATTAATTGA
Long Flanking Sequence:
ATTAATTGCTTAAATCGTATTTAAGTAATTGTTGGCTTTAACCACATTAAGCAAGGTCAGGATTAATAACCAAGCATTTTCTAATCATTACCGATGGAGTAAAGTCTAGTCATTTTTTATCTGAGTGTTTTTGTGTCTATAAAAGACTCTCACTGGGAGATCCTGGCTTGTAAGACCCTGAAAAGCAGCTCTATAACTCTGTTTTCTAGCCCACAGAAAGACACACAACCAGTTCCTTTGATAGTCTCAGAAAGTGTGGCCTCGGCACATAAATGGAGTTGTTTGTTAGTCTCTCTTCCCCTGACCCATAATTTCTCTGTCACAGATGTTCCCTCAAACCCTTACTCTGTTCGGCTGAGCTCTGTGGCTCAGCGCGTGGCCACAGTTACCTTCACCAAGCCAGACTCTCATGGCGGCGTCCCCATCAGTCACTACCTGGTCAAATACAAAGACATCAGCTCACAGGACTGGAAGGATGTCAAATCGCTGGGGACGCAGAG[T/C]AAGTACAAAGGTTATCTGCTGCTACACTGAAATAAAAAAATATTAATTGAATTTAATACATTATTTAAAGGTAAGTAGTTGCAAATAATTTATATGAGCTGAATTTAAGCAAACAAATTAAATTTAATAATGCTCAACCTTATTTGTGTTCAAATTCTGCCTATATAAATTGTTTACAACTACCTTTATAACTAATTTCAGTGAAGGTTTTATCAATATTCACTCATACAGTTTTATTATTCACTCATACAGACTTTTGCGGAAAATTGCTGGTAAGGCCATTTTTGAAAATAACTGTGTGAACGCAGAAAGAAAATTGTCAAATAGAGTACCGTAAACGTCTGCTCCAGCCAATCTGTTCATGAAAATATACTTTTCCAGACACATTTAGCTACTAGATAACGTTTCTATGTTCATTATATATGCCAACTGTGGATAAAATGATCGATATAATGCTTATGATAAACCGCTGTGAGGTTACCTGCAATCCCTGCATTTAA
Associated Phenotype:
Not determined