ZMP

fam122b

Ensembl ID:

ENSDARG00000036500

ZFIN ID:

ZDB-GENE-040801-204

Description:

hypothetical protein LOC445072 [Source:RefSeq peptide;Acc:NP_001003466]

Human Orthologues:

FAM122A, FAM122B

Human Descriptions:

family with sequence similarity 122A [Source:HGNC Symbol;Acc:23490]
family with sequence similarity 122B [Source:HGNC Symbol;Acc:30490]

Mouse Orthologues:

Fam122a, Fam122b

Mouse Descriptions:

family with sequence similarity 122, member A Gene [Source:MGI Symbol;Acc:MGI:1915284]
family with sequence similarity 122, member B Gene [Source:MGI Symbol;Acc:MGI:1926005]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22506	Splice Site, Nonsense	Available for shipment	Available now
sa15466	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa22506

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053026	Splice Site, Nonsense	100	278	4	10

The following transcripts of ENSDARG00000036500 do not overlap with this mutation:

ENSDART00000128658

Genomic Location (Zv9):

Chromosome 14 (position 32408368)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	31198175
GRCz11	14	31538489

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTTGTAGGAAGAAGGTGTTGATGTGATGAACCGTGAAACTGCTCATGAA[C/T]GGTAAGAGCTCGCATCTGCTGAAGCCCCAGGGCATTGCTTTCTCATTTAT

Long Flanking Sequence:

CAGCAGAAGAAACAGCACTACTGTTGTTCGACCCAATGTGGTATGTTGCAAGCAAGCGGCAGAAAAATGTATAACTGTGTATTGGATAATGCAATTTGCTTATTGGATGTTTTATGATTTTAGGTTCCATCTTCGCCAGTTCGTGTTCCTAGCACAAGACTACAGAGGATCAAACAGGTGCAGAGTTTGCATCAGCATACCATGAAATTTGACTTGAGGATGTAATCTTTATAGCATGTCTAACTCGCTGCTCTTGTGTACGAGCACATGAGAGCATGTGTTAAAAATACATGCTGAAATTGCTTTTGGAGTTTTCGTTAACCACCAGTTTTCCAAATTTAGACTGGTTGGTAGTACCGCACTCCAACATGAGATTATAGATGTATACAGAAAGTCATTTTTGTGCTGGTGATGTTTCCCCTCATGTTAAGGTTTCTTCTATGCTTGCTCGCTTGTAGGAAGAAGGTGTTGATGTGATGAACCGTGAAACTGCTCATGAA[C/T]GGTAAGAGCTCGCATCTGCTGAAGCCCCAGGGCATTGCTTTCTCATTTATCAGTTGTTGACAGCAGGTTTTGTGTGTTTGTAGTGTTCAAAAGCTTCACTGACAGCTGGACATGCTCTGTGCACAATCAAATAAGCACTTTTATTAGACTGCTCTGCTTATTTAGTAATGTTTGTATTTAAAAAAAAAAAATTTCCTCATGTTGAATTTTTTTTGCAGAGAGGTGCAGGCAGCCATGCAGATGAGTCAGTCTTGGGAGGAGAGCCTGAGTTTGGTACACATTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATACAGTGTCATGTTCATTATTGTTGCACTTTATTTAATCAGAAATGCTCTAAAACAATTTAAAAAGCCAGGTAACATTATTATTTTTATTTTTATTGTTAATATCTTTAAAATCTAATCTGTTCATATGACTCAAAGCTGAAGTTTTACCATCAGTACTTGCGTCTTTATTGTCACAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15466

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
Order Allele From EZRC

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053026	Essential Splice Site	152	278	6	10

The following transcripts of ENSDARG00000036500 do not overlap with this mutation:

ENSDART00000128658

Genomic Location (Zv9):

Chromosome 14 (position 32410657)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	31200464
GRCz11	14	31540778

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTGTGCCTGTGTCTCCTGCTCCTTCACCCACTAGAGGGATTGGAAAGAAG[G/A]TATCGCTTTMTTTTCCTTAATAAATGTTTTATTWTTGTTWTGCARGCTTT

Long Flanking Sequence:

CAAGGTAGTGGGCGGCGAGGAACAAACTTCATCAATTGACGAAGTGAAGGGAAAAAAACCTTGAAAAATCAGGCTCAGTTGGGCACAACCATTTTTTTCTCTGGTCAAAATATTTTTATAGGTTTGTATGTGACGTGTTTTTTTTTCACATGCTTAAAAAAAATGATGCATGCGGTAGCAATGTTGCCACACTTCCTCTTTCCCTTGTCAATGAGATTGTGGAAGACAAAATTAAGCATGCTAGAGAAAAGCTCATGGAGTTATCAGGGCCACCAGTCTCTCAAGAACAGACTGGATTGGTAGTATAATACTCCAACACCGTATTAGCCGGCAGTTGGTTAATTATTAGACAAACTGTTATCAAGTTCTGACTTGTGGTATTTTGCTTTGGTCTGTAGAGTGATAATGATCTTGAGAAGTCTTCATCGTCATCTCCGAAGCGGATTGATTTTGTGCCTGTGTCTCCTGCTCCTTCACCCACTAGAGGGATTGGAAAGAAG[G/A]TATCGCTTTCTTTTCCTTAATAAATGTTTTATTATTGTTATGCAAGCTTTTGTGCTTTTTATTTATTTCTCTCCTTTGTATGAGTAGCAGTGCTTCTCTCCATCTCTTCAAATTTTGGTAAGCAGTAACGGTCTGACACCTAGTCCTGTTCCCAGCCCAACACGCCGCTTCAGGTGAGTTCTGTCCAGTTTCCTGCCACAGCAGGATTGTGTCCTGTTATATATAGATATAAGCCAAAATCTTTATAAGGCGGAGTAGCTGATATCATTCTCATCATAAGTTTGCCCAGCAGGAGGAGTCAGAGCCCGATCAACTGCATCAGGCCTGGCATTCTGGGCACTTTAAAACGCAAGGGTAAGATGGCACACTTGACACTTTTTAATAATGTAGTGGCTTTTTGTAATGTGTTTACACCTGTGAGATGCCGATACATGTTTCTGTGTATGCTCAGGTGAAATGGAGACAGAAAGCCAGCCCAAGAGACTCTTTCAGGGAACCAC

Associated Phenotype:

Not determined