ZMP

ENSDARG00000087133

Ensembl ID:

ENSDARG00000087133

Human Orthologues:

NLGN4X, NLGN4Y

Human Descriptions:

neuroligin 4, X-linked [Source:HGNC Symbol;Acc:14287]
neuroligin 4, Y-linked [Source:HGNC Symbol;Acc:15529]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35029	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa35028	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35029

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123359	Essential Splice Site	166	304	1	3

Genomic Location (Zv9):

Chromosome 11 (position 10037417)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	9964373
GRCz11	11	9947990

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGAGTGAGGACTGCTTATTCTTAAACATATACGTGCCAACGGAGGATGG[T/A]GAGTAAATGTGCGGGCAGGATGGACAGACCTGCCTTTGTCATCTCACTGT

Long Flanking Sequence:

ACCATGCCCTTCCAACAACCAAACCGCCTGAGCAGCATCTGGAAGGCCATGTGTCCGAGGCTAGGCCTCAGTGCTAGCCTGGATCTGCCATTCTTGTGTTGGATAGTAGGCTTGGCCCTGCATGCCCAGCTGGCCGCTTCGGAAAAACTGGATGAAACGGACCCCATTGTCACTACCACTTACGGAAAAGTGCGGGGATTCAAAAAAGAACTCAATAATGAGATCTTGGGGCCTGTTATTCAGTTCCTGGGGGTTCCCTACGCAGCACCTCCAACAGGCGAAAGGCGCTTCCAGCCACCTGAACCCCCTATTTCGTGGTCAGAAATCCGCAACGCAACTCAGTTTGCCCCTGTTTGTCCACAAACCCTGCTGGAGGGCAGGCTACCGGACGTTATGCTGCCGGTTTGGTTCACCAACAGTATTGAAGTGGTGTCATCTTACGTACAGGACCAGAGTGAGGACTGCTTATTCTTAAACATATACGTGCCAACGGAGGATGG[T/A]GAGTAAATGTGCGGGCAGGATGGACAGACCTGCCTTTGTCATCTCACTGTGTCAGTTTCCTTCATGCAGAGTGTAGTGAGTGCAGCGGGGGATAAAAAAAAAAAAAAAGCATGATTTCTGCATGCCCAATGCATGCCGCTGCTTAATGTGTGAGTGGGTGTGTGAGTGAGGCTGTATGTGTGTCCTAACCTTCCCACCATCCCCTGCACATGCAAATTTTTCTGTGTGCTGCAGCACGTCCATTTTAGGTGGTCGGTTTTCTTTCCCCACCCTATACTTATCATACAGACACAATGATTTTCGAAAGCAAATAGTTTTCAAATAATTTTCAAAAGCCAAATGTGGGGGAATTGTTTTGTACAGTACTTATCATAATGATTTAAGTCCGAGAACTTGTTTTTTGGTTTGTTTGTTTTTTTCTTGATAAACTCTTCGCTTCCTTTTACAGTCTAGTTATGCTGTTGCATGCTCCTAATGTCCATAATGGACTCCCATGTTAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35028

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123359	Essential Splice Site	185	304	2	3

Genomic Location (Zv9):

Chromosome 11 (position 10036830)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	9963786
GRCz11	11	9947403

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCCAAGGAATGTGCCAGAAAACCCGGCAAGAAAATATGTAGAAAAGGAG[G/A]TATGTATCCACCGACATAAAACCCAAAAGAGAACAGGCAAAGATCTCCCC

Long Flanking Sequence:

GGGGGATAAAAAAAAAAAAAAAGCATGATTTCTGCATGCCCAATGCATGCCGCTGCTTAATGTGTGAGTGGGTGTGTGAGTGAGGCTGTATGTGTGTCCTAACCTTCCCACCATCCCCTGCACATGCAAATTTTTCTGTGTGCTGCAGCACGTCCATTTTAGGTGGTCGGTTTTCTTTCCCCACCCTATACTTATCATACAGACACAATGATTTTCGAAAGCAAATAGTTTTCAAATAATTTTCAAAAGCCAAATGTGGGGGAATTGTTTTGTACAGTACTTATCATAATGATTTAAGTCCGAGAACTTGTTTTTTGGTTTGTTTGTTTTTTTCTTGATAAACTCTTCGCTTCCTTTTACAGTCTAGTTATGCTGTTGCATGCTCCTAATGTCCATAATGGACTCCCATGTTATTTTTTAGTCTTCTATTCATTTTGCAGTAAAAAGAATATCCAAGGAATGTGCCAGAAAACCCGGCAAGAAAATATGTAGAAAAGGAG[G/A]TATGTATCCACCGACATAAAACCCAAAAGAGAACAGGCAAAGATCTCCCCCTCCTCATTCTGCAACACTGTCCAGATATCAGCTCCCTGAGGTCAAGAGAAGAAGCCATAATTGATTCCCACCACGAAGAGTTAACAGGGGAGACCGAGCCGTCTCTTAAATCAGATGGGCACACGTTGAACTTGCAGAGTCTAATCTCAATTAAAAGAGATGCTATCTGGATTTCATTGGCTTACACTGGCTATATTGATCACAGCTTCATCAAGATAATGTCTCTAGCTTCCCAACCCTGGCATGCCTTACCTCAGCCCATCGAGTTTGGCGACAGCTCACCTTATATAAAGTATCCCGTTAATACGACCTCTCTGGCGACAAGAACAATCATAAAACGTTCCTGCTGGGGAACATTGTCCAATCTCGATATTGCGAAATAAAACAAATCTACCCCCAAAAACGTATACCTACAGTTAGCCATGCAGTGTTTGAAGGTATAGCTCAAC

Associated Phenotype:

Not determined