ZMP

fabp11b

Ensembl ID:

ENSDARG00000002311

ZFIN ID:

ZDB-GENE-050522-391

Description:

fatty acid binding protein 11b [Source:RefSeq peptide;Acc:NP_001018394]

Human Orthologues:

FABP12, FABP4, FABP5, FABP9, PMP2

Human Descriptions:

fatty acid binding protein 12 [Source:HGNC Symbol;Acc:34524]
fatty acid binding protein 4, adipocyte [Source:HGNC Symbol;Acc:3559]
fatty acid binding protein 5 (psoriasis-associated) [Source:HGNC Symbol;Acc:3560]
fatty acid binding protein 9, testis [Source:HGNC Symbol;Acc:3563]
peripheral myelin protein 2 [Source:HGNC Symbol;Acc:9117]

Mouse Orthologues:

Fabp12, Fabp4, Fabp5, Fabp9, Pmp2

Mouse Descriptions:

fatty acid binding protein 12 Gene [Source:MGI Symbol;Acc:MGI:1922747]
fatty acid binding protein 4, adipocyte Gene [Source:MGI Symbol;Acc:MGI:88038]
fatty acid binding protein 5, epidermal Gene [Source:MGI Symbol;Acc:MGI:101790]
fatty acid binding protein 9, testis Gene [Source:MGI Symbol;Acc:MGI:1194881]
peripheral myelin protein 2 Gene [Source:MGI Symbol;Acc:MGI:102667]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa42690	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42690

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
ENSDART00000012718	Essential Splice Site	117	134	3	4

Genomic Location (Zv9):

Chromosome 16 (position 18201511)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	16242748
GRCz11	16	16150725

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGACCACAATAATCGAAAGAGAGATTCAAGACACGAAAATGATAGCGG[T/A]ATGTGTACAAGCCTCATGCAGTTAGCTTTATATCGCTAAGCTGCAGTTTT

Long Flanking Sequence:

GAACTATCCCTTTAAGTTAAAACATTGTTATTGTGTAGTTTAAAATGAATATAAAAATGAAACTTGAACGCTTACATTTCCCAGTTCTGGGTTTCAGCTCGACGGGCATCCGCTAGGTAAAACATATGTTGAAATAATTGGTGGTTCATTCTGCTGTAATTACCCCTAATAAAAACGGGACTAAGCTTACGGAAAATTAATGAATGAATGAAAACGAACAAAAAAAATAAAAATAAAACACCTTTCATTTTAAACAGGATAAAATGTCATCAGTAGTAAAACAAAAAGGATGTTTAAATGCAAACAACAATTACAATTTATTTTGTTTATTTATTTAATCATGAGCATAATTATGTGTCATTTCATATGTTACGCTTTGCTTTGCTTTCCTTTTCAGACTACTATGAGCCTTGCGGATGGTAAACTTATTCAAAAGCAGACCTGGGAAGGAAAGACCACAATAATCGAAAGAGAGATTCAAGACACGAAAATGATAGCGG[T/A]ATGTGTACAAGCCTCATGCAGTTAGCTTTATATCGCTAAGCTGCAGTTTTTTATTATTATTTATTTTTAAATTTGTTTGTGTTTTTACATTTTATGTAATTTTTACAATTTGAGTCTCCCTTTGAATTTTTTTTCCTTTTTGAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTAGCTGGAATGAAAGCAGTTTTACTATTTTTAAACACCATTTTAAGGTCAAATTTATTAGCCTTTTTAAGCCATATTTTTTTCCGATAGTCTACAGACAAACCATCATCTTAAAATAGTTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAATGTCTAGGTTTAAATTTAAATGTCACTTTAAGCTGTATAGAAGTGTGTTAAAAATATCTAG

Associated Phenotype:

Not determined