ZMP
ncam1b
Ensembl ID:
ZFIN ID:
Description:
neural cell adhesion molecule 1b [Source:RefSeq peptide;Acc:NP_571906]
Human Orthologue:
NCAM1
Human Description:
neural cell adhesion molecule 1 [Source:HGNC Symbol;Acc:7656]
Mouse Orthologue:
Ncam1
Mouse Description:
neural cell adhesion molecule 1 Gene [Source:MGI Symbol;Acc:MGI:97281]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35855 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35854 | Essential Splice Site | Available for shipment | Available now |
| sa42522 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35855
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019006 | Nonsense | 279 | 1031 | 7 | 20 |
| ENSDART00000101610 | Nonsense | 279 | 718 | 7 | 18 |
| ENSDART00000136208 | None | None | 268 | None | 9 |
| ENSDART00000142010 | Nonsense | 279 | 1031 | 7 | 21 |
| ENSDART00000146853 | None | None | 270 | None | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 17416139)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 18536512 |
| GRCz11 | 15 | 18472534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCAGAGATGACAGTACTAGATGTGACAAAGCTGGACGAGGGAGATTA[C/A]ACATGCATTGCTAAGAACAAAGCTGGGGAGAGCGAACAAGAACTTAGCCT
Long Flanking Sequence:
TCGCATCACAGCAAGGAGGTCACTGGGTCGCTGGTTCGAACCTCGGCTCAGTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCACGTGGGTTTCCTCTGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTTAATTGGGTAGGCGGTTCATTCTGCTGTGGCGATCCTGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATAAATGAATAAATATAATTCAAATGGTCAGCATATCAGTTTTCCTGATACAGTAGTTAACAACTGTAACTCATTCTTCCAACGCGTTTTGCCTTTTAGATCAGACTCTTTGAAGAGAAATGTTCAGATTTGTCTTCCCTAATGCTATATTGTTTTAAATGTTAGTACTTTCTTTCCTCTCAGGAACAATGCTCCACTGGAGAGCGGAAACAAATACAGCTTCAATGAAGACGGCTCAGAGATGACAGTACTAGATGTGACAAAGCTGGACGAGGGAGATTA[C/A]ACATGCATTGCTAAGAACAAAGCTGGGGAGAGCGAACAAGAACTTAGCCTTAAAGTCTTTGGTAAGAATTCAAGAGAGTCTCACCGGAGTCTGGAGGTTTGACAGTACTCTTTTATATTTGATGCTAAAAATCCAGCAATGGAAAAAAAAACAAAGTTTTATTCTGCAGGGAACAATGTGTGGCTGCATGAACATATCGTTTTTATACCTTAAAGAATAATATACTAACTGTTTTTTTTTTCTCTGTGAGGTGTTTTAAAAAACACTTTCACATGGGAAAGTTTTAAAACATCTATTGAACATTAAACTTTCATAATCAGGGTACATTTACATAACTCATGAAAATGTTGCATACACATAAATATGTTCCTCATTTATATAAATTCATAAAAATTACAAATAAATAAATAAATACATAAATAAATAAATACATAAATAAATAAATAAAACTGTTCTATTTATGCCAGGCCAGAAGGTGGCGATATCAATTTAGAAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35854
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019006 | Essential Splice Site | 300 | 1031 | 8 | 20 |
| ENSDART00000101610 | Essential Splice Site | 300 | 718 | 8 | 18 |
| ENSDART00000136208 | None | None | 268 | None | 9 |
| ENSDART00000142010 | Essential Splice Site | 300 | 1031 | 8 | 21 |
| ENSDART00000146853 | None | None | 270 | None | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 17413324)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 18533697 |
| GRCz11 | 15 | 18469719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAATGACAGAAAGTCTCAGTGATCTAACCTTGTCTGTTTTGTTCTCTC[A/G]GTACAACCCAAAATCACATACTTGGAAAGCCAGACGACCACAGAAATGGA
Long Flanking Sequence:
TAATGTTTTTATATTATTAAGTAATATTTTTCCTCAATTGTCTTCAGAACAAGCCATCACTATACTATGACTTGCCTAATTACCCTAACTTGCCTCGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTCAAGCTGAATACTAGTATCTAGAAAATATCAAGTAAAATATTATGTCCTGTCATCATGGCAAATATAATAGAAATTAGTTCTTAGAAGTTAGTTATTAAAACTATGATGTTTAGAAATGGGGAAATTATTATTATTATTATTATTTTTTGCAATAAACAAAAATTGGGTTAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATGGGAGCTAATAATTCCAGAGGGCTAATAACTGTAGGTTTGGATTATGTAAACAATGACAGAAAGTCTCAGTGATCTAACCTTGTCTGTTTTGTTCTCTC[A/G]GTACAACCCAAAATCACATACTTGGAAAGCCAGACGACCACAGAAATGGACGAGCAGGTCACATTAACATGCGAAGCCACTGGAGACCCCACACCCACCATTACATGGAGCTTCGGCACTCGAGTCTTCACCGAAGGAGAGCAGGTAACATCAAAACCCAGGAACCTAGAAGAGTAACCAGAAACCAGGAGCTAGACGAGTAACATGTTCATCAGACAGACTGGCAGACAGACAGACAGGCAGTGAGACAGAAAGACAGACAGACAGCTAGTTGAATGGTGAACCTGCCTCTGGCTGTTTCATGCATACAATTCTTTTTGTCTGCAGGAGCAACAAAAGAGGATTTATCAGGTATGAATTCAGAAGGTCAGGTATAGTAACGGGCCACTTAGACTCTAGTGTTTCCAGAAACGGTTCTGGTGTTGTCTGTATATTACTGCATATACTGTATGTTGGAGACGTTTGCTAATCAGCCGTCTGGTGTTTCGATTTCCTGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42522
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019006 | Nonsense | 542 | 1031 | 13 | 20 |
| ENSDART00000101610 | Nonsense | 550 | 718 | 14 | 18 |
| ENSDART00000136208 | Nonsense | 65 | 268 | 2 | 9 |
| ENSDART00000142010 | Nonsense | 542 | 1031 | 13 | 21 |
| ENSDART00000146853 | Nonsense | 91 | 270 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 15 (position 17372660)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 18493033 |
| GRCz11 | 15 | 18429055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCCCGAGTCCACTGGAGGAGTTCCTGTGCTCAAGTACCGAGCCGAGT[G/A]GAGAGCCGTGGGCCGAGGGAAATGGGTGCAGCGAGTCTATGAGGTGAAAG
Long Flanking Sequence:
AGAGCGACTTTGGCAACTACAACTGCACTACCTCCAACGAGATCGGGACCGAATCCAGAGAGTTCATCATGATCCCAGCTGGTCTGTTTCTCTCTCTATTGATCACAAAAAAAAAACAAAATACAGTAATTTACAGTGGTAGCAAATCACATTGACATTGAGTGTTTGGATGCGTTTTGCTTTCAAGGTAGTGGATTTTTTTCCGTAATTGCTTGCAATTCTAGCTTTTGTTCGGTAAAGTGCAATACAATAGCTCAGAATTTTTCTCCAGCCATCATAACTCTGTGTTTAAAGCGTTACAATCAGGCCATATAATTGGGCATAAGCTGTTAAAGTGCAGTTTTCTCCACTGTGTGTTTTGAAGTGTCTCCCCTGTGGTGCAGATGTGCCCTCGGCGCCGTCCATCGGTGAAGTGCAGCCGTACTCCAGCACAGCTCAGGTGCTTTTCGAAGAGCCCGAGTCCACTGGAGGAGTTCCTGTGCTCAAGTACCGAGCCGAGT[G/A]GAGAGCCGTGGGCCGAGGGAAATGGGTGCAGCGAGTCTATGAGGTGAAAGACGGTAAGTTCAGTCCAGCTCATCAAGTGAAGCAGGAAGCCATTGTTTTAAATGAAATCTCAACATCCTGAGATGAAACAGTATTGATTTTATACTGTTTCAATGCACTAATACTAACTGCACAGAGTCAGACCATGGCCGTACATGGACACACCTCCTGTCATGTACCGATTCTGATTAGGCCTATTTAAAGCATTTTGTTATGCTGTAATTATGCTGTGACTTGACATGGGATGATAACCAGTTTCCATGTAAGGTTTACCTCAGTTTGTAAAAGTCAAGGTTTTAGAACTGCTAGGATGCTCCTATGTTTTATTTTTTATAACTATTTTATTTCGTTTTTTAGAGCAATAGTATATCAAGCAGGAAAGTACACTCAACATCAAGAGCTACTGGTCAGCCCACGATTCACCAAACATCTGAAAAACAAATCACTTATAAACCAACATC
Associated Phenotype:
Not determined