ZMP
zgc:152904
Ensembl ID:
ZFIN ID:
Description:
neural cell adhesion molecule 2 [Source:RefSeq peptide;Acc:NP_001070212]
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 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24804 | Nonsense | Available for shipment | Available now |
| sa45866 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38233 | Essential Splice Site | Available for shipment | Available now |
| sa44440 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24804
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078058 | Nonsense | 278 | 810 | 7 | 25 |
Genomic Location (Zv9):
Chromosome Zv9_NA999 (position 47834)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150432.1 | 47834 |
| GRCz11 | KN150432.1 | 47834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGCATTGTAGTCCAGCCTCACATCACT[C/T]AGCTGAGGAACGTGACCGCAGTGGAGGGCAGCGCAGCCATGATCTCCTGT
Long Flanking Sequence:
ACAGCTGCGGTTTACAGCACTGAATGGGCCATGGCTCATTTATTCACTTAGTACAGACAGAAGTGCTGCAGAACATCCATCAAAGTGCAGTCTGAAAACAGCATTTGGCTGAAAGCAAACCACGCAAGAGTCACATATGGACAAACTCACTGATTTTTGGCTTAAGTTACTGTGGCTGTTCAGGTTGTGGGGTGGCACAGTGGCTTGGTGGTTAGCACTGTGGCCTCACAGCAAGAAGGTCACTGGTTCGAGTCTCAGCTGAGTACTGGAAAAATTCCAGAAAAAAAGATTTTGCTCCATATTGACATGATAGCATCACACAGCTGCTGCAGATTTGTCGGCTGCACATCCATGATGCCTACACTACAGCTCACAATAATGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATTGTAGTCCAGCCTCACATCACT[C/T]AGCTGAGGAACGTGACCGCAGTGGAGGGCAGCGCAGCCATGATCTCCTGTACAGCTGAAGGAGAGCCGCTGCCCGAGATCTCCTGGAGGAGAGCCAGCGACGGACACAGCTTCACAGACGGGGAGAAGGTCAGAGTCACTTACTGTAACACTGATATGACCACAATATCATATCACCACACCAGACATCTCATCTGAACACTAATATTGCTGAATGATATGGCTAATAATATTGACCTTTAAATGGTGTTAAAACAATTAAAAACTGCTGTTATTCTAGCCGAAATAAAACCAATCAGACTTTCTCCAGAAGAACAAATATTAGAGGAAATACTGTGGAAATTAGAGGAAATCCATCCGTCCATCCATCCATCCATCCATCCATCCACCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCCATCCATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45866
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078058 | Nonsense | 512 | 810 | 16 | 25 |
Genomic Location (Zv9):
Chromosome Zv9_NA999 (position 27969)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150432.1 | 27969 |
| GRCz11 | KN150432.1 | 27969 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTAATATGCCATGAAGAGGAGCGCTTCACTTCACAGGAGACTTCAGCC[A/T]GCCCTGGAGAATACACACACACACACACACACACACACACTCACACACAC
Long Flanking Sequence:
TTATTAATCATAACTTCATTTGTAAACTAATTAGATGTGTTTTCCTTGCATATATCTGGGGGAAATTTCAAATCAACAGCACCTTTATTAATATGTTTTCTGAGAATTATAGGGATGTGTTCAATACCTATTACCCCTCTGTGTTTACAAGTATTTAGTGTTGATTTTAAGGATGTTTTTAAGACGCAGTTGTGATTAGTATCGTCTCTGTTCTTCTCCTAATGATTGTGTTTGGTTTGCGCTGATAAATGTTGACCTGAGAAGCTGCTTGGCTTTTGATGTAAGTGAGTAGTCATGTGCTCAACGCTGATGTACTGTTGAAATTCTCCATAACAATGTGTCCTTTCCATCCGGCCGCTGCTAATTTAACAAGCTCATCTCCTGTAGTGGCTGTGATTTACTGGAGAGCTCAGTAATAAAGCAGAGTACTGTCCCGTTTACTGTAGAGCTGCTTAATATGCCATGAAGAGGAGCGCTTCACTTCACAGGAGACTTCAGCC[A/T]GCCCTGGAGAATACACACACACACACACACACACACACACTCACACACACTCATTCACACACAAGAATAAGCACTCATTCACATACACAGTCAAAAACACACTCAAGAACGCACACACACACATTCTCTCTTTCTCAAACACACACACACACACACACACACACACACACAAACACACACACAAACATGCACTCAAGAATAAGCACTCATTCACATACACAGTCAAAAACACACTCAAGAACGCACACACACACATTCTCTCTTTCTCACACACACACACACACACACACACACACACACACACACACACACACACACACACATACACAAACACTCACACACACANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNACACATACACACACACACTCTGTCTCTCTCTCTCATAAATACACACACATTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38233
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:
C > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078058 | Essential Splice Site | 512 | 810 | 17 | 25 |
Genomic Location (Zv9):
Chromosome Zv9_NA999 (position 26020)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150432.1 | 26020 |
| GRCz11 | KN150432.1 | 26020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCACATCCACACTTCATCACTGGAGGAAACCCGCGTCTCTTTATTTCA[C/T]ACAGAATGAACGAAGCTGTCGCTCACACACACTTACAATCTGCAGTAAAG
Long Flanking Sequence:
CACACATACAAATGAACCTGCATTAAAGAACACACACATACAAACTCAGAAACACGCTCAAGAACATACTCAATCACACACATTCTCTCTCACACACTCAAGAACAAACACTTACATAAATAACAAACACACACTCAAGAACACACACTCATTTACACACACTCTCAGGGCTGCTGTTTATGCTAATGAGATGGAGAGATGTGCACTAGTGGGCGGGGCTGCTGACACACAAACACACACTGCTGGGTTATAGAAGTGGTTTCTGCATAACAGCTCTTCTTTAAAGTGTGTGAAACAGCAGAACTGAAGTGTGTGTGGTGACGTGGGTGATTCTTCTTCTGCTGGAAGATGAAGTGATGCTGAGAGATGATGCTCCTGTCGCAGCGCAGATGATGATGTATTCTGATCTCCAGCAGTCCGCTGTTCATCTGCTGCTCTGTCCTCTGTTTATTTCACATCCACACTTCATCACTGGAGGAAACCCGCGTCTCTTTATTTCA[C/T]ACAGAATGAACGAAGCTGTCGCTCACACACACTTACAATCTGCAGTAAAGAGGAGGAGTCAGAAACAACCCAGATATGAGTGCATAGTTACAATAAAGTTGCTAGGGTGTTGTCATACCACTGCTTGGGTATTCTAATTGATTGCTAGGGTGTTGTCATACCACTGCTTGGATATTCTAGTTGGTTGCTAGGGTGTTGTCATACCACTGCTTGGATATTCTAGTTGGTTGCTAGGGTGTTGTCATACCACTGCTTGGATATTCTAGTTGGTTGCTAGGGTGTTTTTATACCACTGCTTGGATATTCTAGTTGGTTGCTAGGGTGTTGTCATACCACTGCTTGGGTATTCTAGTTGGTTGCTAGGGTGTTTTTATACCACTGCTTGGATATTCTAGTTGGTTGCTAGGGTGTAGTAATGCTACTGCTTGGGTATTCTAGTTGGTTGCTAGGGTGTTTTTATACCACTGCTTGGATATTCTAGTTGGTTGCTAGGGTGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44440
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000078058 | Essential Splice Site | 605 | 810 | 21 | 25 |
Genomic Location (Zv9):
Chromosome Zv9_NA999 (position 18541)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150432.1 | 18541 |
| GRCz11 | KN150432.1 | 18541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGACGGAGGGATGCCCATCGTCGAGTACATCCTCAAGTATAAAACC[G/T]TGAGTGCAGCACACATCACTCTGCTGTTCATATGAAGGCCAAGTGTGTAG
Long Flanking Sequence:
ACCAAGTGTTTTCTGTCATTGCCGCTGCCTCTATTTCTGCTAGTTTAAATCTGGCGCAGGTATCAGTCTCACATCGTTTAATGAATTTGCTCATTTGTGTTTCCATGAGCATTTGAGTTAAAGCTAGAAATACTCGGCTCTTTTTTGTTTTGTAGATAAAATAACAAGGTAAGAAAGGATTATACACACATTTAGGAAAATTCAGGATATTATAGATATGTGTATTTAATTTCAACTGAGTTATTCAGTTGCCTACACTTTAAAAGGGCTTCCTCAGTAGTGCTAGTGTAAAGAATGTTTAGATATTTGGACTAGAAATGTGATGAAAACTCTTCATAAGAAAAGCATTTGTTAGTTTGTTTGCATTTTGTCCTGCAGGTGAGCCCAGTCCACCAACGGTGCACGGTCAGAGAGGCGTGGGGAAGGCCTACAGACTGGGCCTGGTAAAGCAGGATGACGGAGGGATGCCCATCGTCGAGTACATCCTCAAGTATAAAACC[G/T]TGAGTGCAGCACACATCACTCTGCTGTTCATATGAAGGCCAAGTGTGTAGCATTAGATTGGGTTCTTTAATGCATGTGTGAATGGTAGTACAGAGATGTTTAAATACTTTTCATTTAAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGGATAAAGAGGAGCAGTGGATGACCAAGCTGGTTCCGGGTATGAATGATTTTGCGCTCCTGCAGCCGCTTCAGTGGAACACCAGATATAATGTGGAGATCACAGCGCGCAACGTCAAGGGTCTGACAGAGCCCACGTACTTCCAGTTCCTCATGCCGCAGAAGCCTGATATCACAGGTACACACACACATTCTCATTCTCTCACACACACGCAAAGTTCATAAGGAGCTGTTCACGTTCTGTTTGTGTCTAAAAGTGCAATGCCATTCAAATA
Associated Phenotype:
Not determined