ZMP

zgc:158651

Ensembl ID:

ENSDARG00000061215

ZFIN ID:

ZDB-GENE-070112-2102

Description:

Protein FAM149B1 [Source:UniProtKB/Swiss-Prot;Acc:A1L253]

Human Orthologue:

FAM149B1

Human Description:

family with sequence similarity 149, member B1 [Source:HGNC Symbol;Acc:29162]

Mouse Orthologue:

Fam149b

Mouse Description:

family with sequence similarity 149, member B Gene [Source:MGI Symbol;Acc:MGI:2145567]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36425	Nonsense	Mutation detected in F1 DNA	Not yet available
sa6478	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36425

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087062	Nonsense	393	644	9	15
ENSDART00000127224	Nonsense	416	667	10	16

Genomic Location (Zv9):

Chromosome 17 (position 26438110)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26578029
GRCz11	17	26596420

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGGCATTCCACTGCAGCAAAGGAACCTGGGAACTCTGGACCGATTAAAT[C/T]AGTATGAACCACACAGAAACACAAATAGATACAGCGTTTACTGTGTATTG

Long Flanking Sequence:

AGTGTATCTGTCTGTGGACCCGTTTCTCTCTCTTTTTCGGATACTTTCACACTCTGTTTTTAACACACACATCACATTTCTAACAGCCTTTTAAACATGACTTCACTTTTAGTTGCTTTCTCTGTTTTTTAATCCTGTGGATGTGATTAGAATGCTTGTTCTGCACTCTTAGTTCTGTTTCTATTCTCTTTGTTTAGTTTTTTCACTGTCTTTTTGTCTGTTTTCACACGTCATCGCATGCTGTACAAATGATGGATGTCAGATGCTGTGAATGCCATCATTTTTTATTTATCAGTGAGATAAATATGCATTCTAGGACATTAAATGAAAACCTCAATTTGTTTAATGTTTTCTCTTTCCTCTTCTCTCTGTCTTTGTTTCCACAGACCAGTCGAGTGCCTGTAGGACCGGCGGTTGCTCATCACAATCTTAATGACCTCATCATGATACATGGCATTCCACTGCAGCAAAGGAACCTGGGAACTCTGGACCGATTAAAT[C/T]AGTATGAACCACACAGAAACACAAATAGATACAGCGTTTACTGTGTATTGTATGCTTATATTGCATTTTGTTTTTAGGACAGTGCAATACTTATCATCTTTGATAATATCTCAATTATTATGTTGTCATTATGCTTTTGGTATGTTGCTCACTTTACAATTAACAAGCTAATACATTGAGAGTCGAAAGCAGAGGTCACCAATCTCGGTCCAGGAGGGCTGGTGTCCCTGCAGGGTTTAGCTCCAACTTGCCTCAATACACCTGCCTGTGTTTGATTAGGGTTGCAGGACACCGGCCCTCCAGGAACAAGTTTGGTGACCACTGGTCCAAAGCATCAACTGTGTGATGAAGACTATTAGAATTAAGTTAGAATAACATTGTTATTAAATTTATCAAAACTCTGTTTGATTTTATATATTTTAAAATAAATGGTGAAGTGATCACACAAGCAAAATGCAAGTTTTTCATGGAAATTAGGATATGAGTGATCACAAATAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6478

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087062	Nonsense	445	644	10	15
ENSDART00000127224	Nonsense	468	667	11	16

Genomic Location (Zv9):

Chromosome 17 (position 26436528)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26576447
GRCz11	17	26594838

KASP Assay ID:

554-4576.1 (used for ordering genotyping assays)

KASP Sequence:

CATCTTTGACTCGCCCCCCTCAGTCTGCACGGCGACGGAACCCACCTCCT[C/T]GAAATCTGATGCCAATTACGTCCAGCGTAACACAGCCAATCACAACCATG

Long Flanking Sequence:

TGGTGTTTTGTTCTTGAATGAATAATTAGGAACAAATAATTTAAGAAAATATTTAATGGTTCAATAATAAAGACAAATCAATTGAATGACAGAATATCAATGTATAGTTTTTTTGTCCAATTAATTACACAAATTCTTTTATTGCTTGTGTTAAAGACTGGAGTAATTGTATTATACATTTGTTTTCTTTGCAACAGGTAATAACTTGTTTATTTTTTTGTCTTTACATTATTTTCCAAAACTAAGTCTTTTTATTCAGTCCATAATTTTTTTAAACATGTTTTTGTAGATGAAATGCGTATATTTTCTTCTTCTTTGACAGAGAATGTCCTCTCTCTGTCTGTAGGTCTGACTGTAGGGACTCTGAGGACAAAGTGTCTCATCGTCCTGGCTCTAGTGTGATCCCTGCCGGTAAACCCCGGCCCCGCAGGGCACTGGATCAAAGCACTTCATCTTTGACTCGCCCCCCTCAGTCTGCACGGCGACGGAACCCACCTCCT[C/T]GAAATCTGATGCCAATTACGTCCAGCGTAACACAGCCAATCACAACCATGGAGGAGGTGGTCAGAGGCACTAGACTGTAAGACCATCATTTAATTCCAGTGGTTCAGTATATTTTGTTACACAAAAACAATTTTCTCACAATACTGTCTGTGTGTGTGTTTGTGTTTCAGGACAACTCCCAGTGATCGTTTGACTTCACCTCCAATGCATCTCAGTAGAAACACACTCCTTCCTCCCATTGGCACAGGAGACATAGACCATGTATACTCCGGACAACACACACGGCTTATACAGGTGCTTTAACTACACAATAAACCCAATCAGATGGTAGTAATAAATTCCAGCAAACAATTTTGCTTGGCTAAAACAAGGCTAAACTTGGCCTTTCAGTGAAAATCTAATAGACATCTTAGAATAGCCCAAAACTAGACTAGTCGTCAAATAGACAGATTTGACAGACTTTATATGTGCAGTCATTCATTTTTGTTTATTTGATGACT

Associated Phenotype:

Not determined