ZMP

hbl2

Ensembl ID:

ZFIN ID:

Human Orthologues:

AL512662.2, MBL2, SFTPA1, SFTPA2, SFTPD

Human Descriptions:

Uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:B5MCL0]
mannose-binding lectin (protein C) 2, soluble (opsonic defect) [Source:HGNC Symbol;Acc:6922]
surfactant protein A1 [Source:HGNC Symbol;Acc:10798]
surfactant protein A2 [Source:HGNC Symbol;Acc:10799]
surfactant protein D [Source:HGNC Symbol;Acc:10803]

Mouse Orthologues:

Mbl1, Mbl2, Sftpa1, Sftpd

Mouse Descriptions:

mannose-binding lectin (protein A) 1 Gene [Source:MGI Symbol;Acc:MGI:96923]
mannose-binding lectin (protein C) 2 Gene [Source:MGI Symbol;Acc:MGI:96924]
surfactant associated protein A1 Gene [Source:MGI Symbol;Acc:MGI:109518]
surfactant associated protein D Gene [Source:MGI Symbol;Acc:MGI:109515]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa9228	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9228

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000143027	Nonsense	58	253	1	3

Genomic Location (Zv9):

Chromosome 2 (position 37632147)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	37911279
GRCz11	2	37893736

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCCGGGACACAATGGTCTGCCTGGCAGAGAYGGGAAAGACGGAAGAGAT[G/T]GAGCCACTGGACCCAAAGGAGAGAAGGGAGAGCCAGGTTTGTGTCTGGGA

Long Flanking Sequence:

CAAACATTTCGATAATATTATTCTTAAAGAAGACATAATCACTAATTATAAGTTTTTCAATAATAGACTCCTTCTGCATGGTAAGGCGGCAAGGTTGTAGTTTTGTTTAGGCATGATAAGCAATATAATCGTGCAGAACTGTACTGTATACATTGTAATACCGCTTATATGCTAATAATATACACGGTAATTTATCTTCCAAAAGTTTAACCCCATATTTATCTGCGGTACCTTAAGTTGAAGGATTTAATTTCCACTAAACTTAACAAACGAGTCGTCTTTTACAGGTTGAGGATAAGTTCTGTGAGTTTTCCTGTTTGTCCCAGCAGATGGCGCTGTTGAAGCTGTTCCTCGGGGTTTTTCTGCTCCTTCAGCTTGTTCTGCACGTATTGGTCGGAGCTGCTGAGCCTCAAACCCTGAACTGTCCTATATATGCTGGAGTTCCTGGTGTTCCGGGACACAATGGTCTGCCTGGCAGAGACGGGAAAGACGGAAGAGAT[G/T]GAGCCACTGGACCCAAAGGAGAGAAGGGAGAGCCAGGTTTGTGTCTGGGATTGATGAGCGAGAGAGCATGAGCTTGTTGTTCATTTCAGTTCTTCCTTAATACATGACATTTTTGCTCTTGCTTACAGGAGTGAGTGTGCAGGGACCACCTGGTAAAGCTGGACCACCTGGACTTGATGGGCCGCAGGGTGAAAGGGGTCCACCGGGTATTATTAGTTATTTATAAGTTTATTTACACTTTAGTTTGGGCTCTAATTCAAACTATTAACTAGCTAACATAAACGTCTAATTTGCTCCCCATTCATAGTTAATAAGGTGCTGTTCGGTATAGGTGTGGGGTAGTATCAAGAGATTTGAAAAATAATTATTTTGTAATATTCTGCTAATCAGCCATCATGTATAGTGAGAATTTGTCCTCAAAGTAAAGTATTACCAAAATTCCTCAAGTAAAAATTTGGGGACTTCAGCATATATAATTGTGCATGAACATTAAGTGTGTT

Associated Phenotype:

Not determined