ZMP
nlgn4a
Ensembl ID:
ZFIN IDs:
Description:
neuroligin 4b [Source:RefSeq peptide;Acc:NP_001159803]
Human Orthologues:
NLGN4X, NLGN4Y
Human Descriptions:
neuroligin 4, X-linked [Source:HGNC Symbol;Acc:14287]
neuroligin 4, Y-linked [Source:HGNC Symbol;Acc:15529]
neuroligin 4, Y-linked [Source:HGNC Symbol;Acc:15529]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32702 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32703 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39634 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32704 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18031 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32702
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113818 | Nonsense | 351 | 826 | 4 | 5 |
ENSDART00000128317 | Nonsense | 368 | 843 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 32221580)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31936368 |
GRCz11 | 1 | 32668936 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTGCGTTTGGTCCAGTAATTGACGGTGACGTCATCCCAGATGACCCC[C/T]AAATTCTGATGGAGCAAGGGGAGTTCCTCAACTATGACATCATGCTGGGT
Long Flanking Sequence:
TAGTTGTGCTAGGTAGCCTTTGCAAAGGGTACCCAAAAAGTGGTATGGTATGGTTCGCTTGTAGGTACCTCTTGACAGTGGAAATGGCCAAACCGAACCGTACCACTCTGTACCACTCAGTGGAAACGCCCCTTAGAGGCTTTTGCATCTCAGCTGTTTAAATGCTATATATGTGTTTGTTTCATTTCATGTTTGTTTGTCTGAAATAACAATTTAATATTAATTGATTCTATCAATGTGTTTTATCTTCAGATTTGTTTCAGAAAGCCATCATCCAGAGTGGGACTGCTCTGTCTAGCTGGGCCGTCAACTACCAGCCTGCCAAATACACCCGGATACTAGCTGAGAAAGTGGGCTGTAATATGCTAGATAGCATAGACCTGGTGGAATGTCTACAGAACAAGAACTACAAGGAGCTGATTGAACAGTACATAACACAAGCCAAGTACCACATTGCGTTTGGTCCAGTAATTGACGGTGACGTCATCCCAGATGACCCC[C/T]AAATTCTGATGGAGCAAGGGGAGTTCCTCAACTATGACATCATGCTGGGTGTTAACCAGGGTGAGGGTTTTAAGTTTGTGGATGGCATCGTGGACAGTGAGGATGGTGTGTCTGCAAATGACTTTGACTTCGCCGTGTCTGATTTTGTGGACCATCTTTATGGTTATCCAGAGGGCAAGGACACGCTTCGAGAAACCATCAAGTTCATGTATACTGACTGGGCTGACAAGGAGAACCCGGAGACCAGGCGAAAGACTCTAGTTGCACTTTTCACTGATCACCAATGGGTGGCGCCAGCAGTAGCTACAGCAGACCTTCATGCTCAATATGGATCTCCAACATATTTTTATGCTTTTTACCATCATTGTCAGAGTGAAATGAAACCTAGCTGGTCGGATTCAGCACACGGAGACGAGGTGCCTTATGTGTTTGGAATTCCCATGCTTGGCCCCACTGATCTCTTTAATTGTAATTTCTCCAAGAATGATGTCATGCTTTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32703
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 |
---|---|---|---|---|---|
ENSDART00000113818 | Nonsense | 446 | 826 | 4 | 5 |
ENSDART00000128317 | Nonsense | 463 | 843 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 32221867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31936655 |
GRCz11 | 1 | 32669223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGAGACCAGGCGAAAGACTCTAGTTGCACTTTTCACTGATCACCAATG[G/A]GTGGCGCCAGCAGTAGCTACAGCAGACCTTCATGCTCAATATGGATCTCC
Long Flanking Sequence:
GCTCTGTCTAGCTGGGCCGTCAACTACCAGCCTGCCAAATACACCCGGATACTAGCTGAGAAAGTGGGCTGTAATATGCTAGATAGCATAGACCTGGTGGAATGTCTACAGAACAAGAACTACAAGGAGCTGATTGAACAGTACATAACACAAGCCAAGTACCACATTGCGTTTGGTCCAGTAATTGACGGTGACGTCATCCCAGATGACCCCCAAATTCTGATGGAGCAAGGGGAGTTCCTCAACTATGACATCATGCTGGGTGTTAACCAGGGTGAGGGTTTTAAGTTTGTGGATGGCATCGTGGACAGTGAGGATGGTGTGTCTGCAAATGACTTTGACTTCGCCGTGTCTGATTTTGTGGACCATCTTTATGGTTATCCAGAGGGCAAGGACACGCTTCGAGAAACCATCAAGTTCATGTATACTGACTGGGCTGACAAGGAGAACCCGGAGACCAGGCGAAAGACTCTAGTTGCACTTTTCACTGATCACCAATG[G/A]GTGGCGCCAGCAGTAGCTACAGCAGACCTTCATGCTCAATATGGATCTCCAACATATTTTTATGCTTTTTACCATCATTGTCAGAGTGAAATGAAACCTAGCTGGTCGGATTCAGCACACGGAGACGAGGTGCCTTATGTGTTTGGAATTCCCATGCTTGGCCCCACTGATCTCTTTAATTGTAATTTCTCCAAGAATGATGTCATGCTTTCGGCGGTGGTGATGACGTACTGGACAAATTTCGCTAAAACTGGGTAAGAGCATTTTATTTGAACTATAAATTAAAATTTAATACTGGATAACTAATCTAAGGTCTTAATCAGTTATATATACATATGATAGATAAGATATATAAGTCTACATAGTATTTTTTTTTGGAATCTTGTTTTGTTGCTGTTGCTTGTCTGTTTGTTTTAATTTCTTCAAAAATACATAACATATGAAATACCTACTTACAGTTATTTGGATCATGTTATACATATAATTTGTGTTATGTACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39634
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 |
---|---|---|---|---|---|
ENSDART00000113818 | Nonsense | 465 | 826 | 4 | 5 |
ENSDART00000128317 | Nonsense | 482 | 843 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 32221924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31936712 |
GRCz11 | 1 | 32669280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGCAGTAGCTACAGCAGACCTTCATGCTCAATATGGATCTCCAACATA[T/A]TTTTATGCTTTTTACCATCATTGTCAGAGTGAAATGAAACCTAGCTGGTC
Long Flanking Sequence:
GAGAAAGTGGGCTGTAATATGCTAGATAGCATAGACCTGGTGGAATGTCTACAGAACAAGAACTACAAGGAGCTGATTGAACAGTACATAACACAAGCCAAGTACCACATTGCGTTTGGTCCAGTAATTGACGGTGACGTCATCCCAGATGACCCCCAAATTCTGATGGAGCAAGGGGAGTTCCTCAACTATGACATCATGCTGGGTGTTAACCAGGGTGAGGGTTTTAAGTTTGTGGATGGCATCGTGGACAGTGAGGATGGTGTGTCTGCAAATGACTTTGACTTCGCCGTGTCTGATTTTGTGGACCATCTTTATGGTTATCCAGAGGGCAAGGACACGCTTCGAGAAACCATCAAGTTCATGTATACTGACTGGGCTGACAAGGAGAACCCGGAGACCAGGCGAAAGACTCTAGTTGCACTTTTCACTGATCACCAATGGGTGGCGCCAGCAGTAGCTACAGCAGACCTTCATGCTCAATATGGATCTCCAACATA[T/A]TTTTATGCTTTTTACCATCATTGTCAGAGTGAAATGAAACCTAGCTGGTCGGATTCAGCACACGGAGACGAGGTGCCTTATGTGTTTGGAATTCCCATGCTTGGCCCCACTGATCTCTTTAATTGTAATTTCTCCAAGAATGATGTCATGCTTTCGGCGGTGGTGATGACGTACTGGACAAATTTCGCTAAAACTGGGTAAGAGCATTTTATTTGAACTATAAATTAAAATTTAATACTGGATAACTAATCTAAGGTCTTAATCAGTTATATATACATATGATAGATAAGATATATAAGTCTACATAGTATTTTTTTTTGGAATCTTGTTTTGTTGCTGTTGCTTGTCTGTTTGTTTTAATTTCTTCAAAAATACATAACATATGAAATACCTACTTACAGTTATTTGGATCATGTTATACATATAATTTGTGTTATGTACTTGTGATAAAATAACGTTATATATTTCAATATTTTTGTTTAATTTTTGAATTACATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32704
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 |
---|---|---|---|---|---|
ENSDART00000113818 | Nonsense | 605 | 826 | 5 | 5 |
ENSDART00000128317 | Nonsense | 622 | 843 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 32243683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31958471 |
GRCz11 | 1 | 32691039 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACTGGTACCTCATCTCCATAACATCAACGAACTCTTTCAGTATGTCT[C/A]GACCACTACAAAGATACCTCCTCAGGATACTACACCTTTCCCATACACTA
Long Flanking Sequence:
ATACTTATTGTAAGTCATATTACAGTTACTAACCTTTGTCATTGCATCACTGATTGTTTTTAAGTATAGTGAACAAAGAAAAAAAAAAATAGTTGGATCAGTTATAAGCATGAGTTTTTTAAGATGTCTGATGTCTTTCCCTTTCCACTACCCTTCTAACCAACATAGAATTGAATTCTGAGTAAAATGGAATTGGGCATTGCTCTGTAATGTTATAACACGCATTTCTGAAATATAGATATAAATGTTAATATTTATTTGTTTTTCCTCTCATTTTAGGGATCCGAACCAGCCAGTTCCACAGGACACCAAATTCATACACACAAAGCCCAACCGCTTTGAGGAAGTAGCCTGGTCGAAATACAACCCCAAAGACCAGCTTTACTTACACATCGGACTGAAGCCAAGGGTGAGAGATCACTATCGCGCCACCAAGGTTGCTTTCTGGTTAGAACTGGTACCTCATCTCCATAACATCAACGAACTCTTTCAGTATGTCT[C/A]GACCACTACAAAGATACCTCCTCAGGATACTACACCTTTCCCATACACTAAACGACTAGGTAAAACATGGCCATCCACCACACGACACCCTGGTGTTCCTCCTGCCAACACCAAACAAACCACAGACCAGCGTAAAGGCAATGATTTGAGTGATGACTCAGCAGTGGTTATCGAGACAAAGCGCGATTACTCGACCGAACTCAGTGTGACCATAGCAGTAGGTGCTTCTCTCCTTTTCCTCAACATTCTGGCATTCGCAGCGCTCTACTACAAGAAGGATAAACGTCGACATGAATCCAACCGACGAGGACCAAGCCCGCAGCGGAACTCTGCGCCAGCTAATGTGGTGGCTAACGCTAATGACATAGCACATTTGCAGAGTGATGAGCTGATGTCACTTCAGATGAAACAGCAGCAGATGGAACACGAGCACCATCATGAGTGCGATTCTTTACAAGCTCACGATACGCTTCGTCTTACCTGCCCGGCTGATTATACGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18031
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 |
---|---|---|---|---|---|
ENSDART00000113818 | Nonsense | 695 | 826 | 5 | 5 |
ENSDART00000128317 | Nonsense | 712 | 843 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 32243954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 31958742 |
GRCz11 | 1 | 32691310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGCTTCTCTCCTTTTCCTCAACATTCTGGCATTYGCAGCGCTCTACTA[C/A]AAGAAGGAKAAACGTCGACATGAATCCAACCGACGAGGACCAAGCCCGCA
Long Flanking Sequence:
CATTTTAGGGATCCGAACCAGCCAGTTCCACAGGACACCAAATTCATACACACAAAGCCCAACCGCTTTGAGGAAGTAGCCTGGTCGAAATACAACCCCAAAGACCAGCTTTACTTACACATCGGACTGAAGCCAAGGGTGAGAGATCACTATCGCGCCACCAAGGTTGCTTTCTGGTTAGAACTGGTACCTCATCTCCATAACATCAACGAACTCTTTCAGTATGTCTCGACCACTACAAAGATACCTCCTCAGGATACTACACCTTTCCCATACACTAAACGACTAGGTAAAACATGGCCATCCACCACACGACACCCTGGTGTTCCTCCTGCCAACACCAAACAAACCACAGACCAGCGTAAAGGCAATGATTTGAGTGATGACTCAGCAGTGGTTATCGAGACAAAGCGCGATTACTCGACCGAACTCAGTGTGACCATAGCAGTAGGTGCTTCTCTCCTTTTCCTCAACATTCTGGCATTCGCAGCGCTCTACTA[C/A]AAGAAGGATAAACGTCGACATGAATCCAACCGACGAGGACCAAGCCCGCAGCGGAACTCTGCGCCAGCTAATGTGGTGGCTAACGCTAATGACATAGCACATTTGCAGAGTGATGAGCTGATGTCACTTCAGATGAAACAGCAGCAGATGGAACACGAGCACCATCATGAGTGCGATTCTTTACAAGCTCACGATACGCTTCGTCTTACCTGCCCGGCTGATTATACGCTTACCCTGCGACGTTCACCTGATGACATCCCACTCATGACGCCAAGTACCATAACAATGATTCCTAACACTCTGGCCGGAATGCAGACCCTGCACAATTTCAACACATTCGGAGGCAGTCAGAACAGTACCAACTTGCCCCATGGGCATTCCACCACCAGGGTATAGCTTCTTTTTTTTTTTAGAACTACAGAACATGGTCTGCTAAGGCAGTGGGGGATAAAGGACCTTTGTTTGTTATGGCAAACTGTGCTGACTTTGTTCCACTCTGA
Associated Phenotype:
Not determined