ZMP

FAM161B

Ensembl ID:

ENSDARG00000089467

Description:

family with sequence similarity 161, member B [Source:HGNC Symbol;Acc:19854]

Human Orthologue:

FAM161B

Human Description:

family with sequence similarity 161, member B [Source:HGNC Symbol;Acc:19854]

Mouse Orthologue:

Fam161b

Mouse Description:

family with sequence similarity 161, member B Gene [Source:MGI Symbol;Acc:MGI:2443027]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23170	Nonsense	Available for shipment	Available now
sa39178	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23170

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000123971	Nonsense	40	577	2	9

Genomic Location (Zv9):

Chromosome 17 (position 45173512)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	44893385
GRCz11	17	45007150

KASP Assay ID:

2261-1510.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGTTTCAGAAAGCCTGCTGTCGCTTATAGAGGACAGGAAGAAGACTGAA[C/T]AATCTATGGAGTTGCATTTGGAGGCTCTGAAGGTCAAACGCAAGCAGCAG

Long Flanking Sequence:

AAAATGAATGAATGAATAAAAATATTATTTAAGGTTTACAATGCAAATCCTAATATATCCACTTATTTGGTAAACAAAGCAAGTCTTTCGTTGAATAGATCTACTTAAAGACAGAAAATATTACTTTACAAATTGTATTGTAAATATTATTTAATAAAAGTAGTGAAACAAATATAAAATCTGAATAAATATAGATTTACATGCAATTACATAATGAAATAAATAGACTGTGTCTTACTGCGTTTGCAGATTCTGTGTGGGCCTAACGATAGCTTATACTGCTTCATAAAGAATGTTGTAGAATTTTGTAGAAAGTACAATACACCTTACAGTAGCATAGAATTTACTATAATTTACTATAGTACTTTTGTTATGTGACTAAATACATATTCTCTGTCCAGATCTCTCCCACTTTAGATTTCTCTAGATCTGAAGAGGGAGACAATGCGCATGTTTCAGAAAGCCTGCTGTCGCTTATAGAGGACAGGAAGAAGACTGAA[C/T]AATCTATGGAGTTGCATTTGGAGGCTCTGAAGGTCAAACGCAAGCAGCAGGTGGAGAATTTAGAGCTTCAGCACCAGACTGGCCTGGAGAAGAGGGTCCTGCAGAACTCACTGCTGACCACCAGCACTGAGTGGATGCTTAAAACCAATATAGTGCAGCAGAGCATCAGCGATCATGATGGGCCGGATCGTAAACACCACAGGTAGCTCATATTGTAAATGTGACAGCAGATTTTCAAAAACATTTGCTCTTCACACTCAAAAAGACTAGAGGCTGTAATTCTTTTTTTTTTCCTCATACATTGTCATTATGGGATTTTGTTCGTCGAATTATGAGTAAAATAATGAATTTCTTCCATTTCGGATTTTCAATATTCAATAAGTCAATGTATCCTGGTTATGAACTGATTCAGTGACAAATGTTTGGAGAAATAATTACTTTTTTAGTTTAATAGTTCAAACGTGAATTTCTAAAAATGTTAATCTGGCCTCCTACATGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39178

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
ENSDART00000123971	Essential Splice Site	107	577	2	9

Genomic Location (Zv9):

Chromosome 17 (position 45173309)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	44893182
GRCz11	17	45006947

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGCAGCAGAGCATCAGCGATCATGATGGGCCGGATCGTAAACACCACAG[G/A]TAGCTCATATTGTAAATGTGACAGCAGATTTTCAAAAACATTTGCTCTTC

Long Flanking Sequence:

CAATTACATAATGAAATAAATAGACTGTGTCTTACTGCGTTTGCAGATTCTGTGTGGGCCTAACGATAGCTTATACTGCTTCATAAAGAATGTTGTAGAATTTTGTAGAAAGTACAATACACCTTACAGTAGCATAGAATTTACTATAATTTACTATAGTACTTTTGTTATGTGACTAAATACATATTCTCTGTCCAGATCTCTCCCACTTTAGATTTCTCTAGATCTGAAGAGGGAGACAATGCGCATGTTTCAGAAAGCCTGCTGTCGCTTATAGAGGACAGGAAGAAGACTGAACAATCTATGGAGTTGCATTTGGAGGCTCTGAAGGTCAAACGCAAGCAGCAGGTGGAGAATTTAGAGCTTCAGCACCAGACTGGCCTGGAGAAGAGGGTCCTGCAGAACTCACTGCTGACCACCAGCACTGAGTGGATGCTTAAAACCAATATAGTGCAGCAGAGCATCAGCGATCATGATGGGCCGGATCGTAAACACCACAG[G/A]TAGCTCATATTGTAAATGTGACAGCAGATTTTCAAAAACATTTGCTCTTCACACTCAAAAAGACTAGAGGCTGTAATTCTTTTTTTTTTCCTCATACATTGTCATTATGGGATTTTGTTCGTCGAATTATGAGTAAAATAATGAATTTCTTCCATTTCGGATTTTCAATATTCAATAAGTCAATGTATCCTGGTTATGAACTGATTCAGTGACAAATGTTTGGAGAAATAATTACTTTTTTAGTTTAATAGTTCAAACGTGAATTTCTAAAAATGTTAATCTGGCCTCCTACATGCTGAAATAATGATTGAAAATTCAGTTAATATGGCTATTGATACTGTGCAATAAGGCTTCAGTAGTTATCATTAGTTAATTTAAATAAACCTGTGATATTTATTTCTTAGTTAATGCTCAATAGCATGGTAAAATCGTAGTCGTAATCTAATTTCAAGTCATAATTGTTTTATTAGTTAATAACTAATAACATTCAGTTATATTTT

Associated Phenotype:

Not determined