ZMP
nlgn3b
Ensembl ID:
ZFIN ID:
Description:
neuroligin 3b [Source:RefSeq peptide;Acc:NP_001159806]
Human Orthologue:
NLGN3
Human Description:
neuroligin 3 [Source:HGNC Symbol;Acc:14289]
Mouse Orthologue:
Nlgn3
Mouse Description:
neuroligin 3 Gene [Source:MGI Symbol;Acc:MGI:2444609]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20395 | Nonsense | Available for shipment | Available now |
sa40413 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17458 | Nonsense | Available for shipment | Available now |
sa1317 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20395
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 |
---|---|---|---|---|---|
ENSDART00000090171 | Nonsense | 112 | 846 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 24985864)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22813129 |
GRCz11 | 5 | 23316929 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCTGGTCTGGTGTGAGGAACGCCACGCGCTTTCCTCCTGTTTGCCCA[C/T]AGACCGTTCGCAACGCAGTGCCAGACATAATGATGCCCGTTTGGGCCACC
Long Flanking Sequence:
CCTTAATTGTGCATACCTGGCTGCGGCGATGCCCACTGGATCTTCCTGAGTGTGTGGCATATGCTTGTTTTTGAGTGCTACATTGTCATTGTGTCAAAGCCGAGAGTGTCATTGAGCTACAGACAGAGCTTTACCAGTGTGTGTGTTTGTGTGCGCCGTAAAGAGGGATGATGATCTACACACAGTCAGCAGCTCACCTGGCGCTCACCCGCCTGCCCTGCCGGCCTCTGAACTCCGCTCTCCGCTGGCTGCTCGTGTGGTTGATGTGGTCAGTCTCTGTGGCATCAACGCTGACCTACCAGCCAACAGTAAACACAGCTCTTGGCAGACTGAGGGGGATGCGGGTCGCTGTTGCCACGGAGGGTCTGGGACCTGTGGATCAATATCTGGGTGTGCCTTACGCCGCTCCGCCTGTGGGAGAGAAGCGATTTATGCCACCCGATGCTCCGTCTGCCTGGTCTGGTGTGAGGAACGCCACGCGCTTTCCTCCTGTTTGCCCA[C/T]AGACCGTTCGCAACGCAGTGCCAGACATAATGATGCCCGTTTGGGCCACCTATAATATGGACACGGTCGCCACATACCTGCAGGAGCAGAGCGAGGACTGTCTGTACATGAATATATACGTGCCAACACAAAGTGGTGAGTACACTTGTTAAATGTGTACATGAGCTTGTTTATGTAATACATAGAACATCAGGGGGTTTGATTATGGAATTCTTCAAATGTTTAACTTACGGTTAATGTCGTAATTCTGATTCTTAGTATTTAAAATCTGTATTTAATGGTGCCATAGATTAAATTTTGCCAATGATTCTAGACTTTGATTGAGTATCTTAAATTGTTCTCTGTCATACAAACATACAGTATGTGGCTTAGGTAAGTTCAAAAATTCTCCAGACACCATTTTATATGCTCATTTAAAACTACAGTAATTACCTCTGGAATGAAAAGCTCACTTTTGACCATATTTGGAATGGTTGATGAATGTTAATGTCTTCTCTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40413
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090171 | Nonsense | 428 | 846 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 24957417)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22784682 |
GRCz11 | 5 | 23288482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGATTTTGACTTCACTGTGTCTGACTTTGTGGACAGTCTCTATGGTTA[T/A]CCAGAAGGGAAGGACACTCTTAGAGAGACCATAAAGTTTATGTACACTGA
Long Flanking Sequence:
GAAAAACGGCAGTGTTGGCAGGTGTGACAGAGATTTCCCTGTATTTCGCTGTCATAATCGGGAGATCACAATAAATTTACTCAGAAAAATCCAGACCAAAGCAAACACTACAGTACTAAGTTACTACAGTAATTTTTTTAATCTCTTAATGCAAATCAGGTTGTGTGAGGAAGCCGATTTAATAGTTTGTGTGTGTGTTTTACGCAGGACCTGGTTCTCTGCATGCAGAAGCGCAGCTACAGGGAGCTGGTGGAGCAGGAAATCCAGCCTGCACGCTTCCATGTGGCCTTTGGTCCAGTCATCGACGGCGACCTCATACCAGATGATCCCGAAGTGCTGATGGAGCAGGGGGAGTTCCTCAACTATGACATCATGCTGGGCGTCAACCAGGGGGAGGGATTCCGCTTCGTGGAGGGCGTGGTGGAGCCTGAAGAGGGTGGAGTTTCTGGCTCCGATTTTGACTTCACTGTGTCTGACTTTGTGGACAGTCTCTATGGTTA[T/A]CCAGAAGGGAAGGACACTCTTAGAGAGACCATAAAGTTTATGTACACTGACTGGGCTGATCGAGACAATCCCGAGACCCGCCGGAAAACCCTCGTGGCCATGTTTACAGATCATCAGTGGGTGGAGCCAGCCGTGGTGACAGCCGACCTGCACGCACGTTACGGCTCTCCGACCTTCTTCTATGCCTTCTACCATCACTGCCAGAGCCCCATGAAGCCCCCATGGGCTGACTCCGCACATGGTGATGAGCTGCCCTACGTTTTTGGTGTTCCGCTTATCGGTCCGACAGAACTCTTTCCCTGCAACTTTTCCCGTAATGATATCATGCTGAGTGCTGTCGTCATGACCTACTGGACCAACTTTGCAAAGACTGGGTAAAACAGACCACAGCATTTCAAAACACCATGCAAAATGACCATACAGTCCGAGATAAAAGCAGTACAAAGTGAAAAATTATAATTGACAATGAATGCAGCAATAAAATATCTAAATTATTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17458
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090171 | Nonsense | 514 | 846 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 24957159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22784424 |
GRCz11 | 5 | 23288224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCATGAAGCCCCCATGGGCTGACTCCGCACATGGTGAYGAGCTGCCCTA[C/A]GTTTTTGGTGTTCCGCTTATCGGTCCGACAGAACTCTTTCCCTGCAACTT
Long Flanking Sequence:
GAAATCCAGCCTGCACGCTTCCATGTGGCCTTTGGTCCAGTCATCGACGGCGACCTCATACCAGATGATCCCGAAGTGCTGATGGAGCAGGGGGAGTTCCTCAACTATGACATCATGCTGGGCGTCAACCAGGGGGAGGGATTCCGCTTCGTGGAGGGCGTGGTGGAGCCTGAAGAGGGTGGAGTTTCTGGCTCCGATTTTGACTTCACTGTGTCTGACTTTGTGGACAGTCTCTATGGTTATCCAGAAGGGAAGGACACTCTTAGAGAGACCATAAAGTTTATGTACACTGACTGGGCTGATCGAGACAATCCCGAGACCCGCCGGAAAACCCTCGTGGCCATGTTTACAGATCATCAGTGGGTGGAGCCAGCCGTGGTGACAGCCGACCTGCACGCACGTTACGGCTCTCCGACCTTCTTCTATGCCTTCTACCATCACTGCCAGAGCCCCATGAAGCCCCCATGGGCTGACTCCGCACATGGTGATGAGCTGCCCTA[C/A]GTTTTTGGTGTTCCGCTTATCGGTCCGACAGAACTCTTTCCCTGCAACTTTTCCCGTAATGATATCATGCTGAGTGCTGTCGTCATGACCTACTGGACCAACTTTGCAAAGACTGGGTAAAACAGACCACAGCATTTCAAAACACCATGCAAAATGACCATACAGTCCGAGATAAAAGCAGTACAAAGTGAAAAATTATAATTGACAATGAATGCAGCAATAAAATATCTAAATTATTTAGATGATAGGTCTCAAACTCAGTTCCTGGAGGGCCACAGCTCGGCACAATTTTGCTCCAACACTGATCAAATACACCTGATCCAAATAATCACACTGCTCAAAAAAATCTTGAACACCTTGATTATTTGGATCAGGTGTGTTTGATCAGGGTTGGAGCAAAACTGCAGAGCTGCGGCCCTCCAGGAATTGAGTTTGAAACCTATGATCTAGATAAGGGGTGGGCAAACTCTATCCTGGAGGGCTGGTGTCCTGCACAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1317
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090171 | Nonsense | 601 | 846 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 5 (position 24955245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 22782510 |
GRCz11 | 5 | 23286310 |
KASP Assay ID:
554-1231.1 (used for ordering genotyping assays)
KASP Sequence:
GACCAACTCTACCTGCACATTGGGCTGAAGCCTCGCGTTCGAGATCACTA[T/A]CGGGCAACTAAAGTGGCCTTCTGGAAGCAYCTGGTACCTCACCTGTACAA
Long Flanking Sequence:
CTTACAGCTGCAACCCATATCTGGGAAACATCTATGCACATTCATTTACACGTACACTACGGACAATTTAGCTTACCCAATTCACCTGTACTGCATGTCTTTGAACTGAGGGGGAAAAAGGAGCACCCAGGGGAACCTGGATGCCACCGCATCGCCCCTAGTTCATTCAATCAAGCATTTATTAGTGATGAAAACAGTTGTACTGCTAAATATTTTTACTAAATATTTCTATGACTTCTAATGTGTAAAAAATGCTTGAAATAAAGGTTTTTAATTTTTTTATCTTACAGACCTTTAGTTTTTAACCATGTGTTGTTATAGTTCAGATCTAATTACTTGTATTTTGTGTGTCTCAGGGATCCGAACAAGCCAGTTCCTCAGGACACCAAATTCATCCACACCAAGGCAAACCGTTTTGAAGAAGTGACATGGGCCAAGTATGGTCCTCATGACCAACTCTACCTGCACATTGGGCTGAAGCCTCGCGTTCGAGATCACTA[T/A]CGGGCAACTAAAGTGGCCTTCTGGAAGCATCTGGTACCTCACCTGTACAACCTGCATGATATGTTCCACTACACGTCCACTACCACACGGGTTCCACCTCTTTTGACCACACACAGCTCTCACAGTGCCACGCCACGCCCAGGAGGTAACAAGGCCCGTACTTCTGGTAAACAACCCCCCCAGTCGACAGCCCGCAGTGGGCCACTAGTCATTGCCAATCCCCGTGATTACTCCACAGAGCTGAGTGTCACGATCGCCGTCGGAGCTTCACTTCTGTTCCTCAACGTCCTGGCCTTTGCTGCACTTTACTACCGCAAAGACAAGCGGAGTCGACAAGACACGCCCCCTCAGCCCGCCCCTCAGCGCCAAACCCCACCTATTGACCTCAACTATGCGCCCACTTCCATCTCAGGGGGGAATCAAGAGGAGTTGTCACTGTGTGACCCCCTGCGTTTGACCCCAGCCTCATCTCCACGGGATTATGCTCTTACACTCCGCCG
Associated Phenotype:
Not determined